| geneid | 9577 |
|---|---|
| ensemblid | ENSG00000158019.21 |
| hgncid | 1106 |
| symbol | BABAM2 |
| name | BRISC and BRCA1 A complex member 2 |
| refseq_nuc | NM_199191.3 |
| refseq_prot | NP_954661.1 |
| ensembl_nuc | ENST00000379624.6 |
| ensembl_prot | ENSP00000368945.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 27890729 |
| end | 28338901 |
| strand | + |
| ver | v1.2 |
| region | chr2:27890729-28338901 |
| region5000 | chr2:27885729-28343901 |
| regionname0 | BABAM2_chr2_27890729_28338901 |
| regionname5000 | BABAM2_chr2_27885729_28343901 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 383 | 157 | 68 | 37 | 32 | 2 | 16 | 20 | BABAM2_chr2_27885729_28343901 | BABAM2 | copy fasta | chr2 | 27885729 | 28343901 |
| a0002 | 0/0 | 383 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | copy fasta | chr2 | 27885729 | 28343901 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1152 | 157 | 68 | 37 | 32 | 2 | 16 | BABAM2_chr2_27885729_28343901 | BABAM2 | copy fasta | chr2 | 27885729 | 28343901 |
| c0002 | 0/0 | 1152 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | copy fasta | chr2 | 27885729 | 28343901 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 527 | 79 | 26 | 20 | 18 | 2 | 11 | BABAM2_chr2_27885729_28343901 | BABAM2 | copy fasta | chr2 | 27885729 | 28343901 |
| t0002 | 0/0 | 527 | 66 | 32 | 16 | 13 | 0 | 5 | BABAM2_chr2_27885729_28343901 | BABAM2 | copy fasta | chr2 | 27885729 | 28343901 |
| t0003 | 0/0 | 527 | 11 | 8 | 2 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | copy fasta | chr2 | 27885729 | 28343901 |
| t0004 | 0/0 | 527 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | copy fasta | chr2 | 27885729 | 28343901 |
| t0005 | 0/0 | 527 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | copy fasta | chr2 | 27885729 | 28343901 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0073 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0129 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1152 | 157 | 68 | 37 | 32 | 2 | 16 | BABAM2_chr2_27885729_28343901 | BABAM2 | copy fasta | chr2 | 27885729 | 28343901 |
| a0002c0002 | 0/0 | 1152 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | copy fasta | chr2 | 27885729 | 28343901 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1678 | 78 | 26 | 19 | 18 | 2 | 11 | BABAM2_chr2_27885729_28343901 | BABAM2 | copy fasta | chr2 | 27885729 | 28343901 |
| a0001c0001t0002 | 0/0 | 1678 | 66 | 32 | 16 | 13 | 0 | 5 | BABAM2_chr2_27885729_28343901 | BABAM2 | copy fasta | chr2 | 27885729 | 28343901 |
| a0001c0001t0003 | 0/0 | 1678 | 11 | 8 | 2 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | copy fasta | chr2 | 27885729 | 28343901 |
| a0001c0001t0004 | 0/0 | 1678 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | copy fasta | chr2 | 27885729 | 28343901 |
| a0001c0001t0005 | 0/0 | 1678 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | copy fasta | chr2 | 27885729 | 28343901 |
| a0002c0002t0001 | 0/0 | 1678 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | copy fasta | chr2 | 27885729 | 28343901 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0073 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0129 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0001c0001t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | GBR | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0082 | EUR | GBR | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0135 | AMR | PUR | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0136 | AMR | PUR | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0100 | AMR | PUR | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | CLM | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0085 | AMR | CLM | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0137 | AFR | ACB | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PEL | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PEL | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | KHV | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | KHV | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PEL | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CDX | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CDX | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | CDX | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CDX | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | ACB | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | ACB | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | ACB | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0121 | AFR | GWD | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0148 | AFR | GWD | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | GWD | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | GWD | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | ESN | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ESN | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | ESN | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0106 | AFR | GWD | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | ESN | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | ESN | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0089 | AFR | MSL | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0118 | AFR | MSL | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | GWD | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | STU | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | STU | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | YRI | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | YRI | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0090 | AFR | LWK | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | LWK | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | LWK | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | LWK | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ASW | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | ASW | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | GIH | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | GIH | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0119 | AFR | ACB | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | ACB | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | ACB | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | ACB | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | MSL | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | MSL | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0073 | REF | REF | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0129 | REF | REF | BABAM2_chr2_27885729_28343901 | BABAM2 | chr2 | 27885729 | 28343901 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:28025355
|
A | G | 1 | a0002 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.430A>G | p.Thr144Ala | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/12 | 568/1678 | 430/1152 | 144/383 | chr2 | 28025355 | ||
| chr2:28025356
|
C | A | 1 | a0002 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.431C>A | p.Thr144Lys | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/12 | 569/1678 | 431/1152 | 144/383 | chr2 | 28025356 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:28338559
|
T | C | 1 | a0001c0001t0004 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*46T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 12/12 | 46 | chr2 | 28338559 | |||||
| chr2:28338753
|
T | C | 1 | a0001c0001t0005 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*240T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 12/12 | 240 | chr2 | 28338753 | |||||
| chr2:28338890
|
C | T | 3 | a0001c0001t0002a0001c0001t0003a0001c0001t0005 | 78 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*377C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 12/12 | 377 | chr2 | 28338890 | |||||
| chr2:28338891
|
T | C | 2 | a0001c0001t0002a0001c0001t0005 | 67 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*378T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 12/12 | 378 | chr2 | 28338891 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:27891044
|
A | G | 16 | a0001c0001t0001g0143a0001c0001t0001g0146a0001c0001t0001g0150others(13): Show | 16 | HG00733.hp1 HG00741.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.-25+202A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 1/11 | chr2 | 27891044 | ||||||
| chr2:27891242
|
C | G | 1 | a0001c0001t0001g0142 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-25+400C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 1/11 | chr2 | 27891242 | ||||||
| chr2:27891281
|
G | A | 2 | a0001c0001t0002g0001a0001c0001t0002g0002 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-25+439G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 1/11 | chr2 | 27891281 | ||||||
| chr2:27891684
|
G | A | 14 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(11): Show | 14 | HG01109.hp2 HG01346.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-25+842G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 1/11 | chr2 | 27891684 | ||||||
| chr2:27891741
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-25+899G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 1/11 | chr2 | 27891741 | ||||||
| chr2:27891987
|
G | A | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-25+1145G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 1/11 | chr2 | 27891987 | ||||||
| chr2:27892822
|
C | G | 12 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0138others(9): Show | 12 | HG00733.hp2 HG01167.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.-24-1711C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 1/11 | chr2 | 27892822 | ||||||
| chr2:27892834
|
G | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-24-1699G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 1/11 | chr2 | 27892834 | ||||||
| chr2:27892998
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-24-1535T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 1/11 | chr2 | 27892998 | ||||||
| chr2:27893029
|
T | C | 14 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(11): Show | 14 | HG01109.hp2 HG01346.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-24-1504T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 1/11 | chr2 | 27893029 | ||||||
| chr2:27893043
|
T | C | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG01109.hp1 HG02735.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-1490T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 1/11 | chr2 | 27893043 | ||||||
| chr2:27893332
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-24-1201G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 1/11 | chr2 | 27893332 | ||||||
| chr2:27893446
|
C | A | 14 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(11): Show | 14 | HG01109.hp2 HG01346.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-24-1087C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 1/11 | chr2 | 27893446 | ||||||
| chr2:27893992
|
C | CA | 20 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0023others(17): Show | 20 | HG01106.hp1 HG01109.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-24-531dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 27893992 | |||||
| chr2:27894003
|
G | A | 154 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(151): Show | 154 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(151): Show |
intron_variant | MODIFIER | c.-24-530G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 1/11 | chr2 | 27894003 | ||||||
| chr2:27894037
|
T | C | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-24-496T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 1/11 | chr2 | 27894037 | ||||||
| chr2:27894098
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-24-435C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 1/11 | chr2 | 27894098 | ||||||
| chr2:27894162
|
T | G | 1 | a0001c0001t0001g0035 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-24-371T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 1/11 | chr2 | 27894162 | ||||||
| chr2:27894167
|
T | G | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG00738.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24-366T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 1/11 | chr2 | 27894167 | ||||||
| chr2:27894411
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02630.hp1 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-24-122G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 1/11 | chr2 | 27894411 | ||||||
| chr2:27894509
|
A | G | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-24-24A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 1/11 | chr2 | 27894509 | ||||||
| chr2:27895106
|
G | A | 1 | a0001c0001t0002g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.128+422G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27895106 | ||||||
| chr2:27895155
|
A | AT | 22 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(19): Show | 22 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.128+481dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 27895155 | |||||
| chr2:27895267
|
G | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(16): Show | 19 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.128+583G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27895267 | ||||||
| chr2:27895795
|
G | A | 91 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(88): Show | 91 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.128+1111G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27895795 | ||||||
| chr2:27895896
|
G | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(16): Show | 19 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.128+1212G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27895896 | ||||||
| chr2:27896035
|
T | G | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 5 | HG01106.hp1 HG01243.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.128+1351T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27896035 | ||||||
| chr2:27896053
|
C | G | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02027.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.128+1369C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27896053 | ||||||
| chr2:27896733
|
C | G | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.128+2049C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27896733 | ||||||
| chr2:27897036
|
T | G | 157 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(154): Show | 157 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(154): Show |
intron_variant | MODIFIER | c.128+2352T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27897036 | ||||||
| chr2:27897401
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.128+2717A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27897401 | ||||||
| chr2:27897490
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0044 | 2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.128+2806G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27897490 | ||||||
| chr2:27897550
|
T | C | 1 | a0001c0001t0002g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.128+2866T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27897550 | ||||||
| chr2:27897920
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.128+3236C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27897920 | ||||||
| chr2:27898249
|
C | T | 1 | a0001c0001t0002g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.128+3565C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27898249 | ||||||
| chr2:27898323
|
C | T | 46 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0088others(43): Show | 46 | HG00140.hp1 HG01069.hp2 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.128+3639C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27898323 | ||||||
| chr2:27898345
|
G | A | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG00738.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.128+3661G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27898345 | ||||||
| chr2:27898376
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.128+3692C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27898376 | ||||||
| chr2:27898666
|
CTAAG | C | 2 | a0001c0001t0002g0122a0001c0001t0003g0121 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.128+3984_128+3987d others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 27898666 | |||||
| chr2:27898752
|
CAGAA | C | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG00738.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.128+4071_128+4074d others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 27898752 | |||||
| chr2:27899476
|
GT | G | 82 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0017others(79): Show | 82 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.128+4806delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 27899476 | |||||
| chr2:27899489
|
T | A | 1 | a0001c0001t0001g0045 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.128+4805T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27899489 | ||||||
| chr2:27899611
|
G | A | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.128+4927G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27899611 | ||||||
| chr2:27900085
|
C | A | 1 | a0001c0001t0001g0127 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.128+5401C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27900085 | ||||||
| chr2:27900312
|
T | C | 7 | a0001c0001t0002g0029a0001c0001t0002g0046a0001c0001t0002g0047others(4): Show | 7 | HG00639.hp1 HG01167.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.128+5628T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27900312 | ||||||
| chr2:27900368
|
C | CT | 8 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(5): Show | 8 | HG01109.hp1 HG01109.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.128+5698dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 27900368 | |||||
| chr2:27900507
|
T | G | 70 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0032others(67): Show | 70 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.128+5823T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27900507 | ||||||
| chr2:27900542
|
G | A | 3 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132 | 3 | HG02280.hp2 HG02723.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.128+5858G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27900542 | ||||||
| chr2:27900795
|
G | A | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.128+6111G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27900795 | ||||||
| chr2:27900809
|
C | T | 1 | a0002c0002t0001g0085 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.128+6125C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27900809 | ||||||
| chr2:27900853
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.128+6169C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27900853 | ||||||
| chr2:27900893
|
A | T | 70 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0032others(67): Show | 70 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.128+6209A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27900893 | ||||||
| chr2:27900904
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.128+6220A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27900904 | ||||||
| chr2:27901042
|
CA | C | 82 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(79): Show | 82 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.128+6378delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 27901042 | |||||
| chr2:27901304
|
G | A | 72 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(69): Show | 72 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.128+6620G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27901304 | ||||||
| chr2:27901739
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.128+7055C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27901739 | ||||||
| chr2:27901872
|
A | C | 1 | a0001c0001t0004g0118 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.128+7188A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27901872 | ||||||
| chr2:27902041
|
G | A | 1 | a0001c0001t0002g0087 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.128+7357G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27902041 | ||||||
| chr2:27902905
|
T | TTG | 75 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(72): Show | 75 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.128+8240_128+8241d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 27902905 | |||||
| chr2:27902924
|
T | A | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG01109.hp1 HG02735.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.128+8240T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27902924 | ||||||
| chr2:27902924
|
TGA | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.128+8261_128+8262d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 27902924 | |||||
| chr2:27902926
|
A | T | 6 | a0001c0001t0001g0017a0001c0001t0001g0053a0001c0001t0001g0082others(3): Show | 6 | HG00140.hp2 HG01099.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.128+8242A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27902926 | ||||||
| chr2:27902988
|
A | G | 1 | a0001c0001t0002g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.128+8304A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27902988 | ||||||
| chr2:27903067
|
A | T | 1 | a0001c0001t0002g0116 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.128+8383A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27903067 | ||||||
| chr2:27903093
|
A | AC | 10 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(7): Show | 10 | HG01099.hp1 HG01099.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.128+8417dupC | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 27903093 | |||||
| chr2:27903490
|
G | A | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.128+8806G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27903490 | ||||||
| chr2:27903663
|
C | G | 1 | a0001c0001t0001g0111 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.128+8979C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27903663 | ||||||
| chr2:27903730
|
T | C | 156 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(153): Show |
intron_variant | MODIFIER | c.128+9046T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27903730 | ||||||
| chr2:27903781
|
A | C | 1 | a0001c0001t0002g0110 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.128+9097A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27903781 | ||||||
| chr2:27903832
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.128+9148G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27903832 | ||||||
| chr2:27903873
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.128+9189T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27903873 | ||||||
| chr2:27903884
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.128+9200G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27903884 | ||||||
| chr2:27904152
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.128+9468A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27904152 | ||||||
| chr2:27904348
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.128+9664C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27904348 | ||||||
| chr2:27904614
|
AAGAC | A | 3 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0016 | 3 | HG01109.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.128+9934_128+9937d others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 27904614 | |||||
| chr2:27905375
|
C | T | 14 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(11): Show | 14 | HG01109.hp2 HG01346.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.128+10691C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27905375 | ||||||
| chr2:27905419
|
C | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.128+10735C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27905419 | ||||||
| chr2:27905844
|
C | T | 1 | a0001c0001t0002g0077 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.128+11160C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27905844 | ||||||
| chr2:27906291
|
A | G | 2 | a0001c0001t0001g0045a0001c0001t0002g0076 | 2 | HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.128+11607A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27906291 | ||||||
| chr2:27906524
|
G | A | 42 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0088others(39): Show | 42 | HG00140.hp1 HG01069.hp2 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.128+11840G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27906524 | ||||||
| chr2:27906606
|
G | C | 3 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056 | 3 | HG02280.hp1 HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.128+11922G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27906606 | ||||||
| chr2:27906673
|
C | T | 14 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(11): Show | 14 | HG01109.hp2 HG01346.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.128+11989C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27906673 | ||||||
| chr2:27906809
|
GA | G | 14 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(11): Show | 14 | HG01109.hp2 HG01346.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.128+12135delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 27906809 | |||||
| chr2:27907113
|
C | T | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.128+12429C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27907113 | ||||||
| chr2:27907431
|
C | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(7): Show | 10 | HG01346.hp1 HG01891.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.128+12747C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27907431 | ||||||
| chr2:27907518
|
TGTG | T | 2 | a0001c0001t0002g0046a0001c0001t0002g0047 | 2 | HG00639.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.128+12837_128+1283 others(7): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 27907518 | |||||
| chr2:27907898
|
G | A | 157 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(154): Show | 157 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(154): Show |
intron_variant | MODIFIER | c.128+13214G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27907898 | ||||||
| chr2:27908024
|
G | A | 3 | a0001c0001t0001g0057a0001c0001t0002g0003a0001c0001t0002g0012 | 3 | HG02135.hp1 HG02698.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.128+13340G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27908024 | ||||||
| chr2:27908086
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0044 | 2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.128+13402C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27908086 | ||||||
| chr2:27908239
|
C | T | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.128+13555C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27908239 | ||||||
| chr2:27908366
|
G | C | 94 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(91): Show | 94 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.128+13682G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27908366 | ||||||
| chr2:27908367
|
G | A | 1 | a0001c0001t0002g0030 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.128+13683G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27908367 | ||||||
| chr2:27908376
|
A | G | 75 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(72): Show | 75 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.128+13692A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27908376 | ||||||
| chr2:27908425
|
C | G | 1 | a0001c0001t0001g0075 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.128+13741C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27908425 | ||||||
| chr2:27908457
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.128+13773G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27908457 | ||||||
| chr2:27908522
|
C | G | 3 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056 | 3 | HG02280.hp1 HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.128+13838C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27908522 | ||||||
| chr2:27908567
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.128+13883C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27908567 | ||||||
| chr2:27909107
|
A | G | 1 | a0001c0001t0002g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.128+14423A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27909107 | ||||||
| chr2:27909121
|
T | G | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.128+14437T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27909121 | ||||||
| chr2:27909275
|
G | A | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG01496.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.128+14591G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27909275 | ||||||
| chr2:27909383
|
G | A | 88 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(85): Show | 88 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.128+14699G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27909383 | ||||||
| chr2:27909398
|
C | T | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.128+14714C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27909398 | ||||||
| chr2:27909582
|
C | A | 2 | a0001c0001t0001g0146a0001c0001t0002g0147 | 2 | HG01168.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.128+14898C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27909582 | ||||||
| chr2:27909917
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.128+15233A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27909917 | ||||||
| chr2:27909963
|
G | A | 13 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(10): Show | 13 | HG01109.hp2 HG01346.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.128+15279G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27909963 | ||||||
| chr2:27910308
|
A | G | 1 | a0001c0001t0005g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.128+15624A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27910308 | ||||||
| chr2:27910319
|
T | TAGAAAGC others(337): Show |
1 | a0001c0001t0002g0039 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.128+15654_128+1565 others(348): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 27910319 | |||||
| chr2:27910319
|
T | TAGAAAGC others(356): Show |
2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG00738.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.128+15654_128+1565 others(367): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 27910319 | |||||
| chr2:27910319
|
T | TAGAAAGC others(359): Show |
1 | a0001c0001t0002g0036 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.128+15654_128+1565 others(370): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 27910319 | |||||
| chr2:27910773
|
T | C | 1 | a0001c0001t0002g0009 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.128+16089T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27910773 | ||||||
| chr2:27911170
|
A | G | 73 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0032others(70): Show | 73 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.128+16486A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27911170 | ||||||
| chr2:27912419
|
A | G | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG01109.hp1 HG02735.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.129-17413A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27912419 | ||||||
| chr2:27912526
|
G | A | 2 | a0001c0001t0002g0010a0001c0001t0002g0016 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.129-17306G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27912526 | ||||||
| chr2:27912566
|
TATAG | T | 2 | a0001c0001t0002g0107a0001c0001t0003g0106 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.129-17265_129-1726 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27912566 | ||||||
| chr2:27912617
|
A | G | 154 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(151): Show | 154 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(151): Show |
intron_variant | MODIFIER | c.129-17215A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27912617 | ||||||
| chr2:27912629
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.129-17203G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27912629 | ||||||
| chr2:27912869
|
G | C | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.129-16963G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27912869 | ||||||
| chr2:27912966
|
C | A | 1 | a0001c0001t0002g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.129-16866C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27912966 | ||||||
| chr2:27913339
|
C | A | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.129-16493C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27913339 | ||||||
| chr2:27913484
|
A | G | 72 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0032others(69): Show | 72 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.129-16348A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27913484 | ||||||
| chr2:27913818
|
T | A | 1 | a0001c0001t0002g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.129-16014T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27913818 | ||||||
| chr2:27913832
|
C | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0081 | 2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.129-16000C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27913832 | ||||||
| chr2:27914044
|
G | A | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0075others(1): Show | 4 | HG00735.hp2 HG01081.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.129-15788G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27914044 | ||||||
| chr2:27914120
|
T | C | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG00738.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.129-15712T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27914120 | ||||||
| chr2:27914419
|
G | T | 157 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(154): Show | 157 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(154): Show |
intron_variant | MODIFIER | c.129-15413G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27914419 | ||||||
| chr2:27914551
|
A | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02630.hp1 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.129-15281A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27914551 | ||||||
| chr2:27914667
|
C | T | 14 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(11): Show | 14 | HG01109.hp2 HG01346.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.129-15165C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27914667 | ||||||
| chr2:27914847
|
A | T | 3 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132 | 3 | HG02280.hp2 HG02723.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.129-14985A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27914847 | ||||||
| chr2:27914863
|
G | A | 14 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(11): Show | 14 | HG01109.hp2 HG01346.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.129-14969G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27914863 | ||||||
| chr2:27914869
|
T | TAAAAATT others(331): Show |
1 | a0001c0001t0001g0073 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.129-14952_129-1495 others(342): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 27914869 | |||||
| chr2:27915228
|
C | T | 1 | a0001c0001t0002g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.129-14604C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27915228 | ||||||
| chr2:27915427
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.129-14405C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27915427 | ||||||
| chr2:27915520
|
C | CA | 157 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(154): Show | 157 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(154): Show |
intron_variant | MODIFIER | c.129-14312_129-1431 others(5): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27915520 | ||||||
| chr2:27915565
|
A | G | 1 | a0001c0001t0002g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.129-14267A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27915565 | ||||||
| chr2:27915670
|
T | C | 1 | a0001c0001t0003g0148 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.129-14162T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27915670 | ||||||
| chr2:27915677
|
CG | C | 13 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(10): Show | 13 | HG01109.hp2 HG01346.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.129-14154delG | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27915677 | ||||||
| chr2:27915678
|
GT | G | 144 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0023others(141): Show | 144 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(141): Show |
intron_variant | MODIFIER | c.129-14146delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 27915678 | |||||
| chr2:27915914
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0044 | 2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.129-13918C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27915914 | ||||||
| chr2:27916092
|
A | G | 19 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(16): Show | 19 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.129-13740A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27916092 | ||||||
| chr2:27916095
|
C | G | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.129-13737C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27916095 | ||||||
| chr2:27916281
|
TA | T | 36 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0093others(33): Show | 36 | HG00140.hp1 HG01069.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.129-13546delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 27916281 | |||||
| chr2:27916530
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.129-13302C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27916530 | ||||||
| chr2:27916936
|
T | G | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 5 | HG01106.hp1 HG01243.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.129-12896T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27916936 | ||||||
| chr2:27917014
|
CT | C | 76 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(73): Show | 76 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.129-12796delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 27917014 | |||||
| chr2:27917019
|
T | C | 1 | a0001c0001t0002g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.129-12813T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27917019 | ||||||
| chr2:27917307
|
C | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.129-12525C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27917307 | ||||||
| chr2:27917312
|
G | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.129-12520G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27917312 | ||||||
| chr2:27917482
|
G | A | 43 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0088others(40): Show | 43 | HG00140.hp1 HG01069.hp2 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.129-12350G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27917482 | ||||||
| chr2:27918066
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.129-11766C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27918066 | ||||||
| chr2:27918503
|
T | C | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG00738.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.129-11329T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27918503 | ||||||
| chr2:27918700
|
T | C | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.129-11132T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27918700 | ||||||
| chr2:27918755
|
G | C | 14 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(11): Show | 14 | HG01109.hp2 HG01346.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.129-11077G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27918755 | ||||||
| chr2:27918773
|
T | C | 153 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(150): Show | 153 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(150): Show |
intron_variant | MODIFIER | c.129-11059T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27918773 | ||||||
| chr2:27919017
|
A | T | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.129-10815A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27919017 | ||||||
| chr2:27919370
|
C | A | 1 | a0001c0001t0001g0142 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.129-10462C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27919370 | ||||||
| chr2:27919372
|
T | C | 14 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(11): Show | 14 | HG01109.hp2 HG01346.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.129-10460T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27919372 | ||||||
| chr2:27919526
|
C | G | 10 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(7): Show | 10 | HG01346.hp1 HG01891.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.129-10306C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27919526 | ||||||
| chr2:27920083
|
T | C | 1 | a0001c0001t0002g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.129-9749T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27920083 | ||||||
| chr2:27920102
|
A | G | 3 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0009 | 3 | HG01346.hp1 HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.129-9730A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27920102 | ||||||
| chr2:27920150
|
G | T | 88 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(85): Show | 88 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.129-9682G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27920150 | ||||||
| chr2:27920293
|
A | G | 2 | a0001c0001t0002g0001a0001c0001t0002g0002 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.129-9539A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27920293 | ||||||
| chr2:27920320
|
GATGCCTT others(10): Show |
G | 3 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0016 | 3 | HG01109.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.129-9507_129-9491d others(19): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 27920320 | |||||
| chr2:27920454
|
A | C | 1 | a0001c0001t0001g0066 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.129-9378A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27920454 | ||||||
| chr2:27921139
|
A | G | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG00738.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.129-8693A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27921139 | ||||||
| chr2:27921200
|
G | A | 88 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(85): Show | 88 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.129-8632G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27921200 | ||||||
| chr2:27921379
|
CATTT | C | 2 | a0001c0001t0003g0089a0001c0001t0003g0090 | 2 | HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.129-8450_129-8447d others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 27921379 | |||||
| chr2:27921469
|
A | G | 1 | a0001c0001t0001g0094 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.129-8363A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27921469 | ||||||
| chr2:27921652
|
A | G | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.129-8180A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27921652 | ||||||
| chr2:27921854
|
T | C | 2 | a0001c0001t0002g0107a0001c0001t0003g0106 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.129-7978T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27921854 | ||||||
| chr2:27921948
|
G | A | 3 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0016 | 3 | HG01109.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.129-7884G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27921948 | ||||||
| chr2:27922029
|
C | T | 2 | a0001c0001t0003g0089a0001c0001t0003g0090 | 2 | HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.129-7803C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27922029 | ||||||
| chr2:27922090
|
T | C | 1 | a0001c0001t0003g0067 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.129-7742T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27922090 | ||||||
| chr2:27922148
|
C | G | 1 | a0001c0001t0002g0077 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.129-7684C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27922148 | ||||||
| chr2:27922153
|
A | G | 6 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0092others(3): Show | 6 | HG02615.hp2 HG03209.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.129-7679A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27922153 | ||||||
| chr2:27922292
|
G | T | 10 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0065others(7): Show | 10 | HG00735.hp1 HG00738.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.129-7540G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27922292 | ||||||
| chr2:27922299
|
A | G | 19 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(16): Show | 19 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.129-7533A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27922299 | ||||||
| chr2:27922446
|
A | G | 19 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(16): Show | 19 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.129-7386A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27922446 | ||||||
| chr2:27922920
|
A | T | 2 | a0001c0001t0002g0010a0001c0001t0002g0016 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.129-6912A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27922920 | ||||||
| chr2:27922949
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.129-6883T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27922949 | ||||||
| chr2:27923697
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.129-6135G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27923697 | ||||||
| chr2:27923796
|
C | A | 1 | a0001c0001t0002g0068 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.129-6036C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27923796 | ||||||
| chr2:27923897
|
G | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(16): Show | 19 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.129-5935G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27923897 | ||||||
| chr2:27924315
|
T | C | 1 | a0001c0001t0004g0118 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.129-5517T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27924315 | ||||||
| chr2:27924674
|
T | C | 93 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(90): Show | 93 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.129-5158T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27924674 | ||||||
| chr2:27924910
|
A | T | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 5 | HG01106.hp1 HG01243.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.129-4922A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27924910 | ||||||
| chr2:27925004
|
A | G | 5 | a0001c0001t0001g0045a0001c0001t0001g0054a0001c0001t0001g0055others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.129-4828A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27925004 | ||||||
| chr2:27925855
|
G | A | 2 | a0001c0001t0002g0010a0001c0001t0002g0016 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.129-3977G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27925855 | ||||||
| chr2:27925960
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.129-3872G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27925960 | ||||||
| chr2:27926093
|
C | CT | 20 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(17): Show | 20 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.129-3726dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 27926093 | |||||
| chr2:27926176
|
G | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02630.hp1 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.129-3656G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27926176 | ||||||
| chr2:27926372
|
A | C | 1 | a0001c0001t0001g0138 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.129-3460A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27926372 | ||||||
| chr2:27926512
|
A | G | 4 | a0001c0001t0001g0040a0001c0001t0002g0010a0001c0001t0002g0011others(1): Show | 4 | HG01109.hp2 HG01243.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.129-3320A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27926512 | ||||||
| chr2:27926630
|
A | G | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.129-3202A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27926630 | ||||||
| chr2:27927224
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.129-2608A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27927224 | ||||||
| chr2:27927460
|
G | T | 1 | a0001c0001t0001g0123 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.129-2372G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27927460 | ||||||
| chr2:27927499
|
C | G | 1 | a0001c0001t0002g0016 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.129-2333C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27927499 | ||||||
| chr2:27927564
|
C | G | 1 | a0001c0001t0002g0030 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.129-2268C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27927564 | ||||||
| chr2:27927693
|
G | C | 1 | a0001c0001t0002g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.129-2139G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27927693 | ||||||
| chr2:27927716
|
A | G | 10 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(7): Show | 10 | HG01346.hp1 HG01891.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.129-2116A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27927716 | ||||||
| chr2:27927838
|
G | GT | 78 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(75): Show | 78 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.129-1978dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 27927838 | |||||
| chr2:27927931
|
C | T | 28 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0093others(25): Show | 28 | HG00140.hp1 HG01069.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.129-1901C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27927931 | ||||||
| chr2:27927995
|
C | A | 1 | a0001c0001t0001g0075 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.129-1837C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27927995 | ||||||
| chr2:27928163
|
G | A | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.129-1669G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27928163 | ||||||
| chr2:27928173
|
G | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0081 | 2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.129-1659G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27928173 | ||||||
| chr2:27928174
|
C | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0081 | 2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.129-1658C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27928174 | ||||||
| chr2:27928256
|
C | T | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG01109.hp1 HG02735.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.129-1576C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27928256 | ||||||
| chr2:27928302
|
C | G | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.129-1530C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27928302 | ||||||
| chr2:27928413
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.129-1419G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27928413 | ||||||
| chr2:27928463
|
T | TTTCTC | 93 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(90): Show | 93 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.129-1367_129-1366i others(7): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 27928463 | |||||
| chr2:27928487
|
G | A | 88 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(85): Show | 88 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.129-1345G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27928487 | ||||||
| chr2:27928552
|
T | G | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.129-1280T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27928552 | ||||||
| chr2:27928889
|
T | C | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.129-943T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27928889 | ||||||
| chr2:27928967
|
A | G | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(3): Show | 6 | HG01109.hp1 HG02735.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.129-865A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27928967 | ||||||
| chr2:27928993
|
A | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.129-839A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27928993 | ||||||
| chr2:27929051
|
T | TA | 78 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(75): Show | 78 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.129-761dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 27929051 | |||||
| chr2:27929051
|
T | TAA | 5 | a0001c0001t0001g0053a0001c0001t0001g0081a0001c0001t0002g0144others(2): Show | 5 | HG00733.hp2 HG01167.hp2 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.129-762_129-761dup others(2): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 27929051 | |||||
| chr2:27929051
|
TA | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(5): Show | 8 | HG01109.hp2 HG01891.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.129-761delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 27929051 | |||||
| chr2:27929192
|
G | A | 3 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132 | 3 | HG02280.hp2 HG02723.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.129-640G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 2/11 | chr2 | 27929192 | ||||||
| chr2:27930234
|
C | T | 10 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0065others(7): Show | 10 | HG00735.hp1 HG00738.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.205+326C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27930234 | ||||||
| chr2:27930493
|
G | A | 154 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(151): Show | 154 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(151): Show |
intron_variant | MODIFIER | c.205+585G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27930493 | ||||||
| chr2:27930621
|
A | G | 19 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(16): Show | 19 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.205+713A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27930621 | ||||||
| chr2:27930737
|
A | G | 3 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0016 | 3 | HG01109.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.205+829A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27930737 | ||||||
| chr2:27930840
|
G | A | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.205+932G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27930840 | ||||||
| chr2:27931031
|
G | C | 1 | a0001c0001t0001g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.205+1123G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27931031 | ||||||
| chr2:27931208
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.205+1300C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27931208 | ||||||
| chr2:27931286
|
C | T | 13 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(10): Show | 13 | HG01109.hp2 HG01346.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.205+1378C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27931286 | ||||||
| chr2:27931287
|
G | A | 1 | a0002c0002t0001g0085 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.205+1379G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27931287 | ||||||
| chr2:27931371
|
T | C | 3 | a0001c0001t0002g0087a0001c0001t0002g0095a0001c0001t0002g0096 | 3 | HG01106.hp2 HG01192.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.205+1463T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27931371 | ||||||
| chr2:27931474
|
T | C | 1 | a0001c0001t0002g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.205+1566T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27931474 | ||||||
| chr2:27931508
|
G | A | 14 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(11): Show | 14 | HG01109.hp2 HG01346.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.205+1600G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27931508 | ||||||
| chr2:27931579
|
G | A | 2 | a0001c0001t0001g0150a0001c0001t0002g0149 | 2 | HG02165.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.205+1671G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27931579 | ||||||
| chr2:27931783
|
C | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.205+1875C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27931783 | ||||||
| chr2:27932104
|
G | C | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.205+2196G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27932104 | ||||||
| chr2:27932328
|
T | A | 88 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(85): Show | 88 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.205+2420T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27932328 | ||||||
| chr2:27932350
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.205+2442G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27932350 | ||||||
| chr2:27932812
|
C | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(16): Show | 19 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.205+2904C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27932812 | ||||||
| chr2:27932881
|
A | C | 60 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0088others(57): Show | 60 | HG00140.hp1 HG00733.hp2 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.205+2973A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27932881 | ||||||
| chr2:27932998
|
G | A | 12 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0138others(9): Show | 12 | HG00733.hp2 HG01167.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.205+3090G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27932998 | ||||||
| chr2:27933040
|
C | G | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.205+3132C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27933040 | ||||||
| chr2:27933462
|
A | T | 2 | a0001c0001t0002g0147a0001c0001t0003g0148 | 2 | HG02258.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.205+3554A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27933462 | ||||||
| chr2:27933527
|
T | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(16): Show | 19 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.205+3619T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27933527 | ||||||
| chr2:27933753
|
A | G | 93 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(90): Show | 93 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.205+3845A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27933753 | ||||||
| chr2:27933764
|
G | GT | 24 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(21): Show | 24 | HG01069.hp1 HG01109.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.205+3879dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27933764 | |||||
| chr2:27933772
|
T | TG | 2 | a0001c0001t0001g0109a0001c0001t0002g0105 | 2 | HG02970.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.205+3864_205+3865i others(3): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27933772 | ||||||
| chr2:27933773
|
T | G | 31 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0093others(28): Show | 31 | HG00140.hp1 HG01069.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.205+3865T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27933773 | ||||||
| chr2:27933980
|
TA | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.205+4076delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27933980 | |||||
| chr2:27934449
|
C | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.205+4541C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27934449 | ||||||
| chr2:27934464
|
C | T | 1 | a0001c0001t0002g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.205+4556C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27934464 | ||||||
| chr2:27934849
|
T | C | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG01109.hp1 HG02735.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.205+4941T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27934849 | ||||||
| chr2:27934924
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0104 | 2 | NA18954.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.205+5016C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27934924 | ||||||
| chr2:27935145
|
G | A | 1 | a0001c0001t0002g0158 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.205+5237G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27935145 | ||||||
| chr2:27935396
|
A | G | 4 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0092others(1): Show | 4 | HG02615.hp2 HG03225.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.205+5488A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27935396 | ||||||
| chr2:27935515
|
T | C | 1 | a0001c0001t0002g0140 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.205+5607T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27935515 | ||||||
| chr2:27935751
|
T | C | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.205+5843T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27935751 | ||||||
| chr2:27935783
|
C | A | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.205+5875C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27935783 | ||||||
| chr2:27935977
|
G | A | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.205+6069G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27935977 | ||||||
| chr2:27936042
|
C | G | 1 | a0001c0001t0001g0075 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.205+6134C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27936042 | ||||||
| chr2:27936044
|
A | G | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.205+6136A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27936044 | ||||||
| chr2:27936112
|
G | T | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.205+6204G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27936112 | ||||||
| chr2:27936212
|
G | A | 72 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0032others(69): Show | 72 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.205+6304G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27936212 | ||||||
| chr2:27936228
|
G | A | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.205+6320G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27936228 | ||||||
| chr2:27936498
|
C | A | 3 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132 | 3 | HG02280.hp2 HG02723.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.205+6590C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27936498 | ||||||
| chr2:27936515
|
A | G | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.205+6607A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27936515 | ||||||
| chr2:27936705
|
G | A | 88 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(85): Show | 88 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.205+6797G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27936705 | ||||||
| chr2:27936715
|
G | A | 3 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132 | 3 | HG02280.hp2 HG02723.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.205+6807G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27936715 | ||||||
| chr2:27936765
|
A | G | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG00738.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.205+6857A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27936765 | ||||||
| chr2:27936777
|
A | G | 74 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0032others(71): Show | 74 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.205+6869A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27936777 | ||||||
| chr2:27936879
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0044 | 2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.205+6971C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27936879 | ||||||
| chr2:27936909
|
T | C | 1 | a0001c0001t0002g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.205+7001T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27936909 | ||||||
| chr2:27936915
|
T | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.205+7007T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27936915 | ||||||
| chr2:27936920
|
T | C | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.205+7012T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27936920 | ||||||
| chr2:27936957
|
CAAAT | C | 12 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0138others(9): Show | 12 | HG00733.hp2 HG01167.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.205+7054_205+7057d others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27936957 | |||||
| chr2:27937287
|
T | C | 2 | a0001c0001t0002g0006a0001c0001t0002g0009 | 2 | HG01346.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.205+7379T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27937287 | ||||||
| chr2:27937595
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.205+7687G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27937595 | ||||||
| chr2:27937623
|
G | A | 157 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(154): Show | 157 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(154): Show |
intron_variant | MODIFIER | c.205+7715G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27937623 | ||||||
| chr2:27937645
|
C | A | 1 | a0001c0001t0002g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.205+7737C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27937645 | ||||||
| chr2:27937685
|
A | G | 1 | a0001c0001t0002g0026 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.205+7777A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27937685 | ||||||
| chr2:27937822
|
A | G | 1 | a0001c0001t0002g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.205+7914A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27937822 | ||||||
| chr2:27937957
|
T | C | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.205+8049T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27937957 | ||||||
| chr2:27938026
|
T | G | 10 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(7): Show | 10 | HG01346.hp1 HG01891.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.205+8118T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27938026 | ||||||
| chr2:27938119
|
G | A | 1 | a0001c0001t0002g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.205+8211G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27938119 | ||||||
| chr2:27938495
|
G | A | 4 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0092others(1): Show | 4 | HG02615.hp2 HG03225.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.205+8587G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27938495 | ||||||
| chr2:27938606
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.205+8698G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27938606 | ||||||
| chr2:27938760
|
G | A | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.205+8852G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27938760 | ||||||
| chr2:27938811
|
CCTT | C | 16 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0001t0001g0053others(13): Show | 16 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.205+8906_205+8908d others(5): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27938811 | |||||
| chr2:27938871
|
C | T | 3 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0016 | 3 | HG01109.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.205+8963C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27938871 | ||||||
| chr2:27939202
|
C | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(16): Show | 19 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.205+9294C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27939202 | ||||||
| chr2:27939203
|
G | T | 1 | a0001c0001t0001g0155 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.205+9295G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27939203 | ||||||
| chr2:27939242
|
C | T | 72 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0032others(69): Show | 72 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.205+9334C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27939242 | ||||||
| chr2:27939407
|
T | C | 74 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(71): Show | 74 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.205+9499T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27939407 | ||||||
| chr2:27939457
|
A | C | 1 | a0001c0001t0002g0140 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.205+9549A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27939457 | ||||||
| chr2:27939994
|
T | C | 72 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0032others(69): Show | 72 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.205+10086T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27939994 | ||||||
| chr2:27940074
|
A | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(7): Show | 10 | HG01346.hp1 HG01891.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.205+10166A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27940074 | ||||||
| chr2:27940089
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.205+10181A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27940089 | ||||||
| chr2:27940623
|
C | CAGTTTGC others(10): Show |
93 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(90): Show | 93 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.205+10716_205+1073 others(21): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27940623 | |||||
| chr2:27940862
|
T | G | 2 | a0001c0001t0001g0031a0001c0001t0002g0030 | 2 | HG02698.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.205+10954T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27940862 | ||||||
| chr2:27940941
|
C | T | 1 | a0001c0001t0002g0112 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.205+11033C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27940941 | ||||||
| chr2:27941012
|
C | G | 2 | a0001c0001t0001g0005a0001c0001t0002g0004 | 2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.205+11104C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27941012 | ||||||
| chr2:27941268
|
C | G | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.205+11360C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27941268 | ||||||
| chr2:27941512
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.205+11604C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27941512 | ||||||
| chr2:27941649
|
A | G | 1 | a0001c0001t0003g0067 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.205+11741A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27941649 | ||||||
| chr2:27941686
|
C | T | 76 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(73): Show | 76 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.205+11778C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27941686 | ||||||
| chr2:27942131
|
G | A | 2 | a0001c0001t0002g0068a0001c0001t0003g0067 | 2 | NA18974.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.205+12223G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27942131 | ||||||
| chr2:27942349
|
A | ATTATT | 2 | a0001c0001t0001g0071a0001c0001t0001g0154 | 2 | HG00741.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.205+12458_205+1246 others(9): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27942349 | |||||
| chr2:27942423
|
C | T | 1 | a0001c0001t0002g0077 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.205+12515C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27942423 | ||||||
| chr2:27942456
|
G | A | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.205+12548G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27942456 | ||||||
| chr2:27942534
|
AT | A | 24 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(21): Show | 24 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.205+12641delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27942534 | |||||
| chr2:27942695
|
T | G | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG00738.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.205+12787T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27942695 | ||||||
| chr2:27942701
|
T | G | 1 | a0001c0001t0001g0097 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.205+12793T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27942701 | ||||||
| chr2:27942791
|
A | AATTT | 60 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0017others(57): Show | 60 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.205+12919_205+1292 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27942791 | |||||
| chr2:27942791
|
A | AATTTATT others(1): Show |
79 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(76): Show | 79 | HG00639.hp1 HG00733.hp1 HG00738.hp1 others(76): Show |
intron_variant | MODIFIER | c.205+12915_205+1292 others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27942791 | |||||
| chr2:27942791
|
A | AATTTATT others(5): Show |
7 | a0001c0001t0001g0041a0001c0001t0001g0044a0001c0001t0001g0070others(4): Show | 7 | HG00733.hp2 HG01167.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.205+12911_205+1292 others(16): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27942791 | |||||
| chr2:27942791
|
AATTT | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0004g0118 | 3 | HG03225.hp1 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.205+12919_205+1292 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27942791 | |||||
| chr2:27942954
|
TC | T | 2 | a0001c0001t0001g0078a0001c0001t0002g0061 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.205+13047delC | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27942954 | ||||||
| chr2:27943459
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.205+13551C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27943459 | ||||||
| chr2:27943858
|
T | C | 1 | a0001c0001t0002g0048 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.205+13950T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27943858 | ||||||
| chr2:27943921
|
G | A | 5 | a0001c0001t0001g0045a0001c0001t0001g0054a0001c0001t0001g0055others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.205+14013G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27943921 | ||||||
| chr2:27944217
|
C | T | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.205+14309C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27944217 | ||||||
| chr2:27944583
|
C | T | 96 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(93): Show | 96 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.205+14675C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27944583 | ||||||
| chr2:27944820
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.205+14912A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27944820 | ||||||
| chr2:27944910
|
A | G | 6 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0002g0004others(3): Show | 6 | HG01346.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.205+15002A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27944910 | ||||||
| chr2:27945159
|
A | T | 1 | a0001c0001t0002g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.205+15251A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27945159 | ||||||
| chr2:27945210
|
G | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.205+15302G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27945210 | ||||||
| chr2:27945548
|
A | G | 77 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(74): Show | 77 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.205+15640A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27945548 | ||||||
| chr2:27945616
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.205+15708A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27945616 | ||||||
| chr2:27946623
|
C | T | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.205+16715C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27946623 | ||||||
| chr2:27946730
|
T | C | 97 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(94): Show | 97 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.205+16822T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27946730 | ||||||
| chr2:27947276
|
C | CT | 10 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(7): Show | 10 | HG01346.hp1 HG01891.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.205+17369dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27947276 | |||||
| chr2:27948213
|
A | G | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG01109.hp1 HG02735.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.205+18305A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27948213 | ||||||
| chr2:27948245
|
A | G | 15 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0001t0001g0053others(12): Show | 15 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.205+18337A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27948245 | ||||||
| chr2:27948291
|
A | T | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.205+18383A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27948291 | ||||||
| chr2:27948563
|
G | A | 2 | a0001c0001t0003g0089a0001c0001t0003g0090 | 2 | HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.205+18655G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27948563 | ||||||
| chr2:27948877
|
A | G | 2 | a0001c0001t0002g0107a0001c0001t0003g0106 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.205+18969A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27948877 | ||||||
| chr2:27948992
|
G | A | 1 | a0001c0001t0001g0027 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.205+19084G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27948992 | ||||||
| chr2:27949258
|
A | T | 97 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(94): Show | 97 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.205+19350A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27949258 | ||||||
| chr2:27949270
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.205+19362C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27949270 | ||||||
| chr2:27949426
|
T | C | 97 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(94): Show | 97 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.205+19518T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27949426 | ||||||
| chr2:27949548
|
A | C | 1 | a0001c0001t0002g0029 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.205+19640A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27949548 | ||||||
| chr2:27949604
|
A | G | 1 | a0001c0001t0002g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.205+19696A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27949604 | ||||||
| chr2:27950176
|
T | A | 78 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(75): Show | 78 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.205+20268T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27950176 | ||||||
| chr2:27950305
|
A | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0044 | 2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.205+20397A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27950305 | ||||||
| chr2:27951214
|
G | A | 35 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0093others(32): Show | 35 | HG00140.hp1 HG01069.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.205+21306G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27951214 | ||||||
| chr2:27951226
|
C | T | 1 | a0001c0001t0003g0148 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.205+21318C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27951226 | ||||||
| chr2:27951453
|
A | C | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.205+21545A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27951453 | ||||||
| chr2:27951540
|
A | C | 58 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0088others(55): Show | 58 | HG00140.hp1 HG00733.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.205+21632A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27951540 | ||||||
| chr2:27951598
|
G | A | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.205+21690G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27951598 | ||||||
| chr2:27951837
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.205+21929C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27951837 | ||||||
| chr2:27951877
|
A | T | 1 | a0001c0001t0002g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.205+21969A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27951877 | ||||||
| chr2:27952164
|
C | G | 1 | a0001c0001t0002g0077 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.205+22256C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27952164 | ||||||
| chr2:27952354
|
A | G | 2 | a0001c0001t0001g0093a0001c0001t0002g0117 | 2 | HG01168.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.205+22446A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27952354 | ||||||
| chr2:27952383
|
C | T | 1 | a0001c0001t0002g0110 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.205+22475C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27952383 | ||||||
| chr2:27952556
|
T | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(16): Show | 19 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.205+22648T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27952556 | ||||||
| chr2:27952776
|
GTC | G | 3 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132 | 3 | HG02280.hp2 HG02723.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.205+22870_205+2287 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27952776 | |||||
| chr2:27953189
|
A | T | 78 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(75): Show | 78 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.205+23281A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27953189 | ||||||
| chr2:27953220
|
G | A | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.205+23312G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27953220 | ||||||
| chr2:27953242
|
A | G | 97 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(94): Show | 97 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.205+23334A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27953242 | ||||||
| chr2:27953511
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.205+23603C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27953511 | ||||||
| chr2:27953536
|
C | T | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.205+23628C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27953536 | ||||||
| chr2:27953572
|
A | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.205+23664A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27953572 | ||||||
| chr2:27953576
|
A | C | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.205+23668A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27953576 | ||||||
| chr2:27953644
|
CA | C | 8 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0092others(5): Show | 8 | HG00738.hp1 HG02615.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.205+23750delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27953644 | |||||
| chr2:27953660
|
A | C | 97 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(94): Show | 97 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.205+23752A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27953660 | ||||||
| chr2:27953699
|
A | T | 1 | a0001c0001t0002g0158 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.205+23791A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27953699 | ||||||
| chr2:27953724
|
G | A | 7 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0002g0140others(4): Show | 7 | HG00733.hp2 HG01167.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.205+23816G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27953724 | ||||||
| chr2:27954831
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.205+24923T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27954831 | ||||||
| chr2:27954979
|
A | G | 4 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0092others(1): Show | 4 | HG02615.hp2 HG03225.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.205+25071A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27954979 | ||||||
| chr2:27954982
|
G | C | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.205+25074G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27954982 | ||||||
| chr2:27955385
|
C | T | 3 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132 | 3 | HG02280.hp2 HG02723.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.205+25477C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27955385 | ||||||
| chr2:27955450
|
A | G | 2 | a0001c0001t0001g0031a0001c0001t0002g0030 | 2 | HG02698.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.205+25542A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27955450 | ||||||
| chr2:27955792
|
C | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(16): Show | 19 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.205+25884C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27955792 | ||||||
| chr2:27955981
|
G | GT | 97 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(94): Show | 97 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.205+26083dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27955981 | |||||
| chr2:27956405
|
T | G | 1 | a0001c0001t0002g0098 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.205+26497T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27956405 | ||||||
| chr2:27956519
|
G | A | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.205+26611G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27956519 | ||||||
| chr2:27956523
|
A | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0044 | 2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.205+26615A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27956523 | ||||||
| chr2:27956991
|
C | T | 2 | a0001c0001t0002g0001a0001c0001t0002g0002 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.205+27083C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27956991 | ||||||
| chr2:27957358
|
G | A | 1 | a0001c0001t0002g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.205+27450G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27957358 | ||||||
| chr2:27957401
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.205+27493A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27957401 | ||||||
| chr2:27957606
|
G | A | 2 | a0001c0001t0001g0058a0001c0001t0001g0073 | 2 | HG02155.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.205+27698G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27957606 | ||||||
| chr2:27957700
|
C | A | 1 | a0001c0001t0001g0113 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.205+27792C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27957700 | ||||||
| chr2:27958052
|
C | G | 19 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(16): Show | 19 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.205+28144C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27958052 | ||||||
| chr2:27958465
|
TTA | T | 41 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0088others(38): Show | 41 | HG00140.hp1 HG01069.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.205+28566_205+2856 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27958465 | |||||
| chr2:27958511
|
T | C | 1 | a0001c0001t0002g0140 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.205+28603T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27958511 | ||||||
| chr2:27958808
|
G | C | 1 | a0001c0001t0001g0099 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.205+28900G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27958808 | ||||||
| chr2:27959034
|
G | C | 75 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0032others(72): Show | 75 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.206-28959G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27959034 | ||||||
| chr2:27959139
|
T | C | 61 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0040others(58): Show | 61 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.206-28854T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27959139 | ||||||
| chr2:27959500
|
A | G | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG00738.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.206-28493A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27959500 | ||||||
| chr2:27959545
|
TTC | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02630.hp1 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.206-28446_206-2844 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27959545 | |||||
| chr2:27959549
|
GT | G | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(3): Show | 6 | HG01109.hp1 HG02735.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.206-28433delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27959549 | |||||
| chr2:27959887
|
G | A | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.206-28106G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27959887 | ||||||
| chr2:27959915
|
T | A | 1 | a0001c0001t0002g0009 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.206-28078T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27959915 | ||||||
| chr2:27959962
|
T | C | 3 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0016 | 3 | HG01109.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.206-28031T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27959962 | ||||||
| chr2:27959965
|
A | G | 2 | a0001c0001t0002g0006a0001c0001t0002g0009 | 2 | HG01346.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.206-28028A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27959965 | ||||||
| chr2:27960136
|
T | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(7): Show | 10 | HG01346.hp1 HG01891.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.206-27857T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27960136 | ||||||
| chr2:27960266
|
G | A | 1 | a0001c0001t0002g0149 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.206-27727G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27960266 | ||||||
| chr2:27960273
|
G | A | 3 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056 | 3 | HG02280.hp1 HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.206-27720G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27960273 | ||||||
| chr2:27960310
|
T | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(16): Show | 19 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.206-27683T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27960310 | ||||||
| chr2:27960700
|
A | G | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG01109.hp1 HG02735.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.206-27293A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27960700 | ||||||
| chr2:27961098
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.206-26895T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27961098 | ||||||
| chr2:27961128
|
C | T | 2 | a0001c0001t0003g0135a0001c0001t0003g0136 | 2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.206-26865C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27961128 | ||||||
| chr2:27961181
|
G | A | 12 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0138others(9): Show | 12 | HG00733.hp2 HG01167.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.206-26812G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27961181 | ||||||
| chr2:27961207
|
G | T | 1 | a0001c0001t0002g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.206-26786G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27961207 | ||||||
| chr2:27961359
|
A | G | 3 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0016 | 3 | HG01109.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.206-26634A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27961359 | ||||||
| chr2:27961438
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.206-26555A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27961438 | ||||||
| chr2:27961667
|
A | C | 1 | a0001c0001t0002g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.206-26326A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27961667 | ||||||
| chr2:27961722
|
CT | C | 66 | a0001c0001t0001g0022a0001c0001t0001g0031a0001c0001t0001g0032others(63): Show | 66 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.206-26250delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27961722 | |||||
| chr2:27961722
|
CTT | C | 22 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(19): Show | 22 | HG00733.hp2 HG01106.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.206-26251_206-2625 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27961722 | |||||
| chr2:27961722
|
CTTT | C | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(3): Show | 6 | HG01109.hp1 HG01109.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.206-26252_206-2625 others(7): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27961722 | |||||
| chr2:27961899
|
T | A | 54 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0040others(51): Show | 54 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.206-26094T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27961899 | ||||||
| chr2:27962470
|
C | T | 1 | a0001c0001t0002g0110 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.206-25523C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27962470 | ||||||
| chr2:27962647
|
G | C | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.206-25346G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27962647 | ||||||
| chr2:27962695
|
A | G | 1 | a0001c0001t0002g0144 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.206-25298A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27962695 | ||||||
| chr2:27962941
|
G | C | 96 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(93): Show | 96 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.206-25052G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27962941 | ||||||
| chr2:27962982
|
T | C | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.206-25011T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27962982 | ||||||
| chr2:27962991
|
A | T | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.206-25002A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27962991 | ||||||
| chr2:27963149
|
A | G | 1 | a0001c0001t0002g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.206-24844A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27963149 | ||||||
| chr2:27963157
|
G | A | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.206-24836G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27963157 | ||||||
| chr2:27963246
|
G | A | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.206-24747G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27963246 | ||||||
| chr2:27963469
|
C | CA | 10 | a0001c0001t0001g0057a0001c0001t0001g0079a0001c0001t0001g0088others(7): Show | 10 | HG02027.hp1 HG02135.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.206-24500dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27963469 | |||||
| chr2:27963469
|
CA | C | 26 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0023others(23): Show | 26 | HG01081.hp1 HG01109.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.206-24500delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27963469 | |||||
| chr2:27963485
|
A | G | 1 | a0001c0001t0002g0007 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.206-24508A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27963485 | ||||||
| chr2:27963488
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.206-24505A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27963488 | ||||||
| chr2:27963600
|
C | G | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.206-24393C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27963600 | ||||||
| chr2:27964026
|
A | G | 19 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(16): Show | 19 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.206-23967A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27964026 | ||||||
| chr2:27964077
|
A | G | 2 | a0001c0001t0002g0107a0001c0001t0003g0106 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.206-23916A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27964077 | ||||||
| chr2:27964270
|
C | T | 10 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0065others(7): Show | 10 | HG00735.hp1 HG00738.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.206-23723C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27964270 | ||||||
| chr2:27964462
|
G | T | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG00738.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.206-23531G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27964462 | ||||||
| chr2:27964826
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.206-23167C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27964826 | ||||||
| chr2:27965271
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0002g0030 | 2 | HG02698.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.206-22722C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27965271 | ||||||
| chr2:27965272
|
G | A | 2 | a0001c0001t0002g0122a0001c0001t0003g0121 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.206-22721G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27965272 | ||||||
| chr2:27965494
|
C | T | 1 | a0001c0001t0001g0073 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.206-22499C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27965494 | ||||||
| chr2:27965666
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.206-22327C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27965666 | ||||||
| chr2:27965667
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0082a0002c0002t0001g0085 | 3 | HG00140.hp2 HG01433.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.206-22326G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27965667 | ||||||
| chr2:27965895
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.206-22098C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27965895 | ||||||
| chr2:27966013
|
T | C | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG01109.hp1 HG02735.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.206-21980T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27966013 | ||||||
| chr2:27966214
|
TTTC | T | 76 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(73): Show | 76 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.206-21772_206-2177 others(7): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27966214 | |||||
| chr2:27966408
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.206-21585C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27966408 | ||||||
| chr2:27966413
|
G | A | 76 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(73): Show | 76 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.206-21580G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27966413 | ||||||
| chr2:27966870
|
C | T | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.206-21123C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27966870 | ||||||
| chr2:27968084
|
T | C | 1 | a0001c0001t0002g0108 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.206-19909T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27968084 | ||||||
| chr2:27968762
|
C | T | 78 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(75): Show | 78 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.206-19231C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27968762 | ||||||
| chr2:27969238
|
T | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(16): Show | 19 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.206-18755T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27969238 | ||||||
| chr2:27969612
|
C | T | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 5 | HG01106.hp1 HG01243.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.206-18381C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27969612 | ||||||
| chr2:27969688
|
C | G | 95 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(92): Show | 95 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.206-18305C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27969688 | ||||||
| chr2:27969730
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.206-18263A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27969730 | ||||||
| chr2:27970342
|
T | C | 1 | a0001c0001t0002g0114 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.206-17651T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27970342 | ||||||
| chr2:27970607
|
C | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02630.hp1 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.206-17386C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27970607 | ||||||
| chr2:27970622
|
G | A | 156 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(153): Show |
intron_variant | MODIFIER | c.206-17371G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27970622 | ||||||
| chr2:27970860
|
T | G | 1 | a0001c0001t0002g0108 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.206-17133T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27970860 | ||||||
| chr2:27971055
|
C | G | 1 | a0001c0001t0002g0152 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.206-16938C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27971055 | ||||||
| chr2:27971180
|
G | A | 2 | a0001c0001t0002g0010a0001c0001t0002g0016 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.206-16813G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27971180 | ||||||
| chr2:27971513
|
A | G | 1 | a0001c0001t0001g0032 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.206-16480A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27971513 | ||||||
| chr2:27971690
|
A | T | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.206-16303A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27971690 | ||||||
| chr2:27971694
|
G | GT | 6 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(3): Show | 6 | HG01106.hp1 HG01243.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.206-16288dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27971694 | |||||
| chr2:27972151
|
C | T | 1 | a0001c0001t0002g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.206-15842C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27972151 | ||||||
| chr2:27972274
|
C | T | 3 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0016 | 3 | HG01109.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.206-15719C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27972274 | ||||||
| chr2:27972445
|
G | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.206-15548G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27972445 | ||||||
| chr2:27972540
|
C | T | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.206-15453C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27972540 | ||||||
| chr2:27972740
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.206-15253A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27972740 | ||||||
| chr2:27972773
|
C | CT | 151 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(148): Show | 151 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(148): Show |
intron_variant | MODIFIER | c.206-15206dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27972773 | |||||
| chr2:27973114
|
C | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.206-14879C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27973114 | ||||||
| chr2:27973271
|
T | G | 2 | a0001c0001t0003g0089a0001c0001t0003g0090 | 2 | HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.206-14722T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27973271 | ||||||
| chr2:27973437
|
T | C | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.206-14556T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27973437 | ||||||
| chr2:27973444
|
T | C | 77 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(74): Show | 77 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.206-14549T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27973444 | ||||||
| chr2:27973465
|
C | T | 1 | a0001c0001t0002g0030 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.206-14528C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27973465 | ||||||
| chr2:27973889
|
A | G | 2 | a0001c0001t0002g0107a0001c0001t0003g0106 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.206-14104A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27973889 | ||||||
| chr2:27974062
|
C | A | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.206-13931C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27974062 | ||||||
| chr2:27974076
|
A | G | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.206-13917A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27974076 | ||||||
| chr2:27974202
|
A | G | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG00738.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.206-13791A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27974202 | ||||||
| chr2:27974268
|
G | A | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.206-13725G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27974268 | ||||||
| chr2:27974361
|
A | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.206-13632A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27974361 | ||||||
| chr2:27974418
|
G | A | 3 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0151 | 3 | HG02074.hp1 NA18968.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.206-13575G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27974418 | ||||||
| chr2:27974974
|
G | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0004g0118 | 3 | HG03225.hp1 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.206-13019G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27974974 | ||||||
| chr2:27975147
|
G | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.206-12846G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27975147 | ||||||
| chr2:27975457
|
C | T | 2 | a0001c0001t0003g0089a0001c0001t0003g0090 | 2 | HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.206-12536C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27975457 | ||||||
| chr2:27975743
|
A | C | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.206-12250A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27975743 | ||||||
| chr2:27975752
|
AG | A | 156 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(153): Show |
intron_variant | MODIFIER | c.206-12239delG | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27975752 | |||||
| chr2:27975881
|
G | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.206-12112G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27975881 | ||||||
| chr2:27976308
|
T | C | 2 | a0001c0001t0001g0065a0001c0001t0001g0083 | 2 | HG00735.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.206-11685T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27976308 | ||||||
| chr2:27976479
|
C | T | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG00738.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.206-11514C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27976479 | ||||||
| chr2:27976507
|
A | C | 1 | a0001c0001t0002g0114 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.206-11486A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27976507 | ||||||
| chr2:27976557
|
G | A | 74 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0032others(71): Show | 74 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.206-11436G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27976557 | ||||||
| chr2:27976838
|
A | G | 2 | a0001c0001t0003g0089a0001c0001t0003g0090 | 2 | HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.206-11155A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27976838 | ||||||
| chr2:27976869
|
G | C | 77 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(74): Show | 77 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.206-11124G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27976869 | ||||||
| chr2:27976920
|
A | G | 1 | a0001c0001t0002g0151 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.206-11073A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27976920 | ||||||
| chr2:27977071
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.206-10922C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27977071 | ||||||
| chr2:27977261
|
T | C | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG00738.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.206-10732T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27977261 | ||||||
| chr2:27977285
|
G | A | 76 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(73): Show | 76 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.206-10708G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27977285 | ||||||
| chr2:27977482
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.206-10511G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27977482 | ||||||
| chr2:27977983
|
T | G | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG01109.hp1 HG02735.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.206-10010T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27977983 | ||||||
| chr2:27978032
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.206-9961C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27978032 | ||||||
| chr2:27978033
|
G | A | 3 | a0001c0001t0002g0012a0001c0001t0003g0018a0001c0001t0003g0019 | 3 | HG02486.hp1 HG02698.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.206-9960G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27978033 | ||||||
| chr2:27978447
|
C | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.206-9546C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27978447 | ||||||
| chr2:27978562
|
A | C | 1 | a0001c0001t0002g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.206-9431A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27978562 | ||||||
| chr2:27978774
|
T | G | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.206-9219T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27978774 | ||||||
| chr2:27978865
|
C | G | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.206-9128C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27978865 | ||||||
| chr2:27979003
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.206-8990G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27979003 | ||||||
| chr2:27979032
|
C | CT | 153 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0017others(150): Show | 153 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(150): Show |
intron_variant | MODIFIER | c.206-8948dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27979032 | |||||
| chr2:27979130
|
C | T | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG01109.hp1 HG02735.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.206-8863C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27979130 | ||||||
| chr2:27979340
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.206-8653C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27979340 | ||||||
| chr2:27979394
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.206-8599T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27979394 | ||||||
| chr2:27979580
|
A | G | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.206-8413A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27979580 | ||||||
| chr2:27979964
|
G | A | 1 | a0001c0001t0003g0148 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.206-8029G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27979964 | ||||||
| chr2:27980069
|
C | G | 74 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0032others(71): Show | 74 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.206-7924C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27980069 | ||||||
| chr2:27980427
|
C | T | 35 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0040others(32): Show | 35 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.206-7566C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27980427 | ||||||
| chr2:27980516
|
A | G | 1 | a0001c0001t0002g0107 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.206-7477A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27980516 | ||||||
| chr2:27980619
|
T | C | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG01496.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.206-7374T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27980619 | ||||||
| chr2:27980735
|
TA | T | 156 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(153): Show |
intron_variant | MODIFIER | c.206-7246delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27980735 | |||||
| chr2:27980895
|
T | A | 1 | a0001c0001t0001g0111 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.206-7098T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27980895 | ||||||
| chr2:27980896
|
T | A | 1 | a0001c0001t0001g0111 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.206-7097T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27980896 | ||||||
| chr2:27981076
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.206-6917C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27981076 | ||||||
| chr2:27981128
|
T | C | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.206-6865T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27981128 | ||||||
| chr2:27981129
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.206-6864C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27981129 | ||||||
| chr2:27981250
|
CTG | C | 3 | a0001c0001t0003g0135a0001c0001t0003g0136a0001c0001t0003g0137 | 3 | HG00733.hp2 HG01167.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.206-6739_206-6738d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27981250 | |||||
| chr2:27981372
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.206-6621C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27981372 | ||||||
| chr2:27981464
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.206-6529T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27981464 | ||||||
| chr2:27981859
|
G | A | 1 | a0001c0001t0002g0103 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.206-6134G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27981859 | ||||||
| chr2:27981961
|
T | G | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.206-6032T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27981961 | ||||||
| chr2:27982081
|
A | C | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.206-5912A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27982081 | ||||||
| chr2:27982100
|
G | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.206-5893G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27982100 | ||||||
| chr2:27982450
|
T | G | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.206-5543T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27982450 | ||||||
| chr2:27982714
|
C | T | 78 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0032others(75): Show | 78 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.206-5279C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27982714 | ||||||
| chr2:27982843
|
G | GTA | 29 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(26): Show | 29 | HG00639.hp1 HG01106.hp1 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.206-5149_206-5148d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27982843 | |||||
| chr2:27982844
|
T | TAC | 22 | a0001c0001t0001g0109a0001c0001t0001g0120a0001c0001t0001g0123others(19): Show | 22 | HG00140.hp1 HG00733.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.206-5111_206-5110d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27982844 | |||||
| chr2:27982844
|
T | TACAC | 20 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0094others(17): Show | 20 | HG01192.hp1 HG01496.hp1 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.206-5113_206-5110d others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27982844 | |||||
| chr2:27982844
|
T | TACACAC | 6 | a0001c0001t0001g0142a0001c0001t0002g0087a0001c0001t0002g0100others(3): Show | 6 | HG01106.hp2 HG01243.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.206-5115_206-5110d others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27982844 | |||||
| chr2:27982844
|
T | TATAC | 26 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(23): Show | 26 | HG00140.hp2 HG00735.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.206-5148_206-5147i others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27982844 | |||||
| chr2:27982844
|
T | TATACAC | 12 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0025others(9): Show | 12 | HG00639.hp2 HG01109.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.206-5148_206-5147i others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27982844 | |||||
| chr2:27982844
|
T | TATACACA others(1): Show |
5 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0002g0004others(2): Show | 5 | HG01891.hp1 HG02145.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.206-5148_206-5147i others(10): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27982844 | |||||
| chr2:27982844
|
T | TATACACA others(3): Show |
1 | a0001c0001t0001g0023 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.206-5148_206-5147i others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27982844 | |||||
| chr2:27982844
|
TAC | T | 17 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0065others(14): Show | 17 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.206-5111_206-5110d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27982844 | |||||
| chr2:27982844
|
TACACAC | T | 3 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0004g0118 | 3 | HG03225.hp1 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.206-5115_206-5110d others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27982844 | |||||
| chr2:27982844
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0001g0146 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.206-5119_206-5110d others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27982844 | |||||
| chr2:27982846
|
C | T | 8 | a0001c0001t0001g0072a0001c0001t0001g0150a0001c0001t0001g0155others(5): Show | 8 | HG00738.hp2 HG01069.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.206-5147C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27982846 | ||||||
| chr2:27982848
|
C | T | 13 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0065others(10): Show | 13 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.206-5145C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27982848 | ||||||
| chr2:27982856
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.206-5137C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27982856 | ||||||
| chr2:27982882
|
C | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.206-5111C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27982882 | ||||||
| chr2:27982884
|
T | C | 3 | a0001c0001t0002g0051a0001c0001t0002g0122a0001c0001t0003g0121 | 3 | HG02572.hp2 HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.206-5109T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27982884 | ||||||
| chr2:27983048
|
C | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.206-4945C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27983048 | ||||||
| chr2:27983147
|
A | G | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.206-4846A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27983147 | ||||||
| chr2:27983283
|
A | C | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.206-4710A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27983283 | ||||||
| chr2:27983401
|
C | T | 14 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0001t0001g0053others(11): Show | 14 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.206-4592C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27983401 | ||||||
| chr2:27983511
|
G | A | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.206-4482G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27983511 | ||||||
| chr2:27983939
|
T | C | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG01496.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.206-4054T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27983939 | ||||||
| chr2:27983942
|
C | CTTTTTTT others(1): Show |
6 | a0001c0001t0002g0029a0001c0001t0002g0046a0001c0001t0002g0047others(3): Show | 6 | HG00639.hp1 HG01167.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.206-4039_206-4032d others(10): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27983942 | |||||
| chr2:27983942
|
C | CTTTTTTT others(3): Show |
12 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(9): Show | 12 | HG00733.hp2 HG01109.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.206-4041_206-4032d others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27983942 | |||||
| chr2:27983942
|
C | CTTTTTTT others(4): Show |
9 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0139others(6): Show | 9 | HG01167.hp2 HG02280.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.206-4042_206-4032d others(13): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27983942 | |||||
| chr2:27983942
|
C | CTTTTTTT others(5): Show |
5 | a0001c0001t0001g0013a0001c0001t0001g0091a0001c0001t0002g0033others(2): Show | 5 | HG01891.hp2 HG02622.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.206-4043_206-4032d others(14): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27983942 | |||||
| chr2:27983942
|
C | CTTTTTTT others(6): Show |
11 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0043others(8): Show | 11 | HG00738.hp1 HG00741.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.206-4044_206-4032d others(15): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27983942 | |||||
| chr2:27983942
|
C | CTTTTTTT others(7): Show |
23 | a0001c0001t0001g0022a0001c0001t0001g0031a0001c0001t0001g0041others(20): Show | 23 | HG00733.hp1 HG00738.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.206-4045_206-4032d others(16): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27983942 | |||||
| chr2:27983942
|
C | CTTTTTTT others(8): Show |
21 | a0001c0001t0001g0005a0001c0001t0001g0040a0001c0001t0001g0052others(18): Show | 21 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.206-4046_206-4032d others(17): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27983942 | |||||
| chr2:27983942
|
C | CTTTTTTT others(9): Show |
14 | a0001c0001t0001g0045a0001c0001t0001g0055a0001c0001t0001g0057others(11): Show | 14 | HG00735.hp2 HG01081.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.206-4047_206-4032d others(18): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27983942 | |||||
| chr2:27983942
|
C | CTTTTTTT others(10): Show |
8 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0056others(5): Show | 8 | HG00140.hp2 HG01433.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.206-4048_206-4032d others(19): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27983942 | |||||
| chr2:27983942
|
C | CTTTTTTT others(11): Show |
5 | a0001c0001t0001g0053a0001c0001t0001g0080a0001c0001t0002g0004others(2): Show | 5 | HG01099.hp2 HG02109.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.206-4049_206-4032d others(20): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27983942 | |||||
| chr2:27983942
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0002g0009 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.206-4050_206-4032d others(21): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27983942 | |||||
| chr2:27983942
|
CT | C | 26 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0093others(23): Show | 26 | HG00140.hp1 HG01069.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.206-4032delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27983942 | |||||
| chr2:27983942
|
CTT | C | 9 | a0001c0001t0001g0094a0001c0001t0001g0109a0001c0001t0002g0107others(6): Show | 9 | HG02451.hp1 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.206-4033_206-4032d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27983942 | |||||
| chr2:27984101
|
A | T | 1 | a0001c0001t0002g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.206-3892A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27984101 | ||||||
| chr2:27984205
|
G | A | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG00738.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.206-3788G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27984205 | ||||||
| chr2:27984466
|
T | C | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.206-3527T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27984466 | ||||||
| chr2:27984607
|
T | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.206-3386T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27984607 | ||||||
| chr2:27984665
|
G | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.206-3328G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27984665 | ||||||
| chr2:27984699
|
A | G | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.206-3294A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27984699 | ||||||
| chr2:27984935
|
G | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.206-3058G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27984935 | ||||||
| chr2:27985057
|
A | ATG | 62 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0032others(59): Show | 62 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.206-2896_206-2895d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27985057 | |||||
| chr2:27985057
|
A | ATGTG | 47 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0034others(44): Show | 47 | HG00639.hp2 HG01069.hp2 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.206-2898_206-2895d others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27985057 | |||||
| chr2:27985057
|
A | ATGTGTG | 9 | a0001c0001t0001g0082a0001c0001t0001g0111a0001c0001t0001g0138others(6): Show | 9 | HG00140.hp2 HG01106.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.206-2900_206-2895d others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27985057 | |||||
| chr2:27985057
|
A | ATGTGTGT others(1): Show |
10 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0017others(7): Show | 10 | HG00735.hp2 HG01346.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.206-2902_206-2895d others(10): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27985057 | |||||
| chr2:27985057
|
A | ATGTGTGT others(3): Show |
4 | a0001c0001t0001g0015a0001c0001t0001g0139a0001c0001t0002g0007others(1): Show | 4 | HG00738.hp1 HG02109.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.206-2904_206-2895d others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27985057 | |||||
| chr2:27985057
|
A | ATGTGTGT others(5): Show |
2 | a0001c0001t0001g0013a0001c0001t0002g0003 | 2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.206-2906_206-2895d others(14): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27985057 | |||||
| chr2:27985057
|
A | ATGTGTGT others(7): Show |
1 | a0001c0001t0002g0004 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.206-2908_206-2895d others(16): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27985057 | |||||
| chr2:27985057
|
A | ATGTGTGT others(15): Show |
1 | a0001c0001t0002g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.206-2916_206-2895d others(24): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27985057 | |||||
| chr2:27985057
|
ATG | A | 8 | a0001c0001t0001g0022a0001c0001t0001g0031a0001c0001t0001g0043others(5): Show | 8 | HG01081.hp1 HG02486.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.206-2896_206-2895d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27985057 | |||||
| chr2:27985162
|
A | G | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.206-2831A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27985162 | ||||||
| chr2:27985241
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.206-2752C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27985241 | ||||||
| chr2:27985377
|
G | A | 2 | a0001c0001t0003g0089a0001c0001t0003g0090 | 2 | HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.206-2616G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27985377 | ||||||
| chr2:27985439
|
C | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0002g0004others(3): Show | 6 | HG01346.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.206-2554C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27985439 | ||||||
| chr2:27985613
|
T | C | 2 | a0001c0001t0001g0022a0001c0001t0001g0044 | 2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.206-2380T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27985613 | ||||||
| chr2:27985982
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.206-2011G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27985982 | ||||||
| chr2:27986053
|
A | G | 74 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0032others(71): Show | 74 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.206-1940A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27986053 | ||||||
| chr2:27986352
|
GT | G | 7 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0002g0003others(4): Show | 7 | HG01346.hp1 HG01891.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.206-1631delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27986352 | |||||
| chr2:27986416
|
C | T | 76 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(73): Show | 76 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.206-1577C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27986416 | ||||||
| chr2:27986612
|
G | A | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG01109.hp1 HG02735.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.206-1381G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27986612 | ||||||
| chr2:27986780
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.206-1213G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27986780 | ||||||
| chr2:27987122
|
C | G | 1 | a0001c0001t0001g0005 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.206-871C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27987122 | ||||||
| chr2:27987347
|
C | T | 3 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132 | 3 | HG02280.hp2 HG02723.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.206-646C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27987347 | ||||||
| chr2:27987621
|
C | T | 1 | a0001c0001t0005g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.206-372C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27987621 | ||||||
| chr2:27987709
|
G | C | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02630.hp1 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.206-284G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27987709 | ||||||
| chr2:27987806
|
C | A | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.206-187C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27987806 | ||||||
| chr2:27987809
|
T | G | 3 | a0001c0001t0003g0135a0001c0001t0003g0136a0001c0001t0003g0137 | 3 | HG00733.hp2 HG01167.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.206-184T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | chr2 | 27987809 | ||||||
| chr2:27987814
|
C | CA | 5 | a0001c0001t0001g0022a0001c0001t0001g0044a0001c0001t0002g0068others(2): Show | 5 | HG02258.hp2 HG03209.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.206-161dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 27987814 | |||||
| chr2:27988418
|
A | C | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG00738.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.300+331A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27988418 | ||||||
| chr2:27988471
|
T | G | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG00738.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.300+384T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27988471 | ||||||
| chr2:27988851
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.300+764T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27988851 | ||||||
| chr2:27989013
|
T | C | 1 | a0001c0001t0001g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.300+926T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27989013 | ||||||
| chr2:27989156
|
G | T | 8 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(5): Show | 8 | HG01109.hp1 HG01109.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.300+1069G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27989156 | ||||||
| chr2:27989164
|
C | G | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.300+1077C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27989164 | ||||||
| chr2:27989165
|
G | A | 7 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0002g0140others(4): Show | 7 | HG00733.hp2 HG01167.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.300+1078G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27989165 | ||||||
| chr2:27989291
|
T | G | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.300+1204T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27989291 | ||||||
| chr2:27989325
|
G | A | 8 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(5): Show | 8 | HG01109.hp1 HG01109.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.300+1238G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27989325 | ||||||
| chr2:27989379
|
T | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0091 | 2 | HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.300+1292T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27989379 | ||||||
| chr2:27989546
|
A | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.300+1459A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27989546 | ||||||
| chr2:27990008
|
A | G | 1 | a0001c0001t0002g0063 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.300+1921A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27990008 | ||||||
| chr2:27990023
|
A | G | 33 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0093others(30): Show | 33 | HG00140.hp1 HG01069.hp2 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.300+1936A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27990023 | ||||||
| chr2:27990176
|
G | A | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.300+2089G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27990176 | ||||||
| chr2:27990227
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.300+2140C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27990227 | ||||||
| chr2:27990465
|
A | C | 1 | a0001c0001t0001g0083 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.300+2378A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27990465 | ||||||
| chr2:27990557
|
C | T | 76 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(73): Show | 76 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.300+2470C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27990557 | ||||||
| chr2:27990753
|
T | A | 1 | a0001c0001t0002g0108 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.300+2666T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27990753 | ||||||
| chr2:27990858
|
GA | G | 4 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0012others(1): Show | 4 | HG01109.hp2 HG02698.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.300+2780delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 27990858 | |||||
| chr2:27991252
|
TG | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(7): Show | 10 | HG01346.hp1 HG01891.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.300+3168delG | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 27991252 | |||||
| chr2:27991734
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.300+3647G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27991734 | ||||||
| chr2:27991883
|
A | T | 3 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0151 | 3 | HG02074.hp1 NA18968.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.300+3796A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27991883 | ||||||
| chr2:27992063
|
G | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.300+3976G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27992063 | ||||||
| chr2:27992099
|
C | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0081 | 2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.300+4012C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27992099 | ||||||
| chr2:27992298
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.300+4211C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27992298 | ||||||
| chr2:27992602
|
A | G | 4 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0092others(1): Show | 4 | HG02615.hp2 HG03225.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.300+4515A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27992602 | ||||||
| chr2:27992743
|
C | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.300+4656C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27992743 | ||||||
| chr2:27992806
|
A | C | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.300+4719A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27992806 | ||||||
| chr2:27992941
|
A | G | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG01109.hp1 HG02735.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+4854A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27992941 | ||||||
| chr2:27993369
|
G | C | 5 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0003g0135others(2): Show | 5 | HG00733.hp2 HG01167.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.300+5282G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27993369 | ||||||
| chr2:27993725
|
G | A | 1 | a0001c0001t0002g0108 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.300+5638G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27993725 | ||||||
| chr2:27993905
|
C | T | 5 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0003g0135others(2): Show | 5 | HG00733.hp2 HG01167.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.300+5818C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27993905 | ||||||
| chr2:27994008
|
A | G | 3 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0016 | 3 | HG01109.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.300+5921A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27994008 | ||||||
| chr2:27994185
|
T | G | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG01109.hp1 HG02735.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+6098T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27994185 | ||||||
| chr2:27994450
|
G | C | 1 | a0001c0001t0002g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.300+6363G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27994450 | ||||||
| chr2:27994460
|
T | C | 71 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(68): Show | 71 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.300+6373T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27994460 | ||||||
| chr2:27994474
|
A | G | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.300+6387A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27994474 | ||||||
| chr2:27994552
|
G | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.300+6465G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27994552 | ||||||
| chr2:27994566
|
A | G | 1 | a0001c0001t0002g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.300+6479A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27994566 | ||||||
| chr2:27995047
|
T | C | 156 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(153): Show |
intron_variant | MODIFIER | c.300+6960T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27995047 | ||||||
| chr2:27995081
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.300+6994G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27995081 | ||||||
| chr2:27995267
|
A | G | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.300+7180A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27995267 | ||||||
| chr2:27995508
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.300+7421C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27995508 | ||||||
| chr2:27995672
|
C | T | 1 | a0001c0001t0003g0089 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.300+7585C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27995672 | ||||||
| chr2:27996042
|
A | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.300+7955A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27996042 | ||||||
| chr2:27996071
|
C | T | 1 | a0001c0001t0001g0032 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.300+7984C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27996071 | ||||||
| chr2:27996214
|
C | A | 1 | a0001c0001t0001g0024 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.300+8127C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27996214 | ||||||
| chr2:27996504
|
G | A | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.300+8417G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27996504 | ||||||
| chr2:27996567
|
G | A | 3 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132 | 3 | HG02280.hp2 HG02723.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.300+8480G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27996567 | ||||||
| chr2:27996625
|
A | G | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.300+8538A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27996625 | ||||||
| chr2:27996741
|
T | C | 95 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(92): Show | 95 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.300+8654T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27996741 | ||||||
| chr2:27996828
|
GC | G | 2 | a0001c0001t0003g0089a0001c0001t0003g0090 | 2 | HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.300+8743delC | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 27996828 | |||||
| chr2:27996939
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.300+8852C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27996939 | ||||||
| chr2:27997074
|
A | G | 76 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(73): Show | 76 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.300+8987A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27997074 | ||||||
| chr2:27997152
|
G | A | 1 | a0001c0001t0002g0087 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.300+9065G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27997152 | ||||||
| chr2:27997265
|
G | GTTGAATG others(4): Show |
18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.300+9181_300+9182i others(13): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 27997265 | |||||
| chr2:27997299
|
C | G | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.300+9212C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27997299 | ||||||
| chr2:27997305
|
G | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.300+9218G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27997305 | ||||||
| chr2:27997909
|
T | C | 156 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(153): Show |
intron_variant | MODIFIER | c.300+9822T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27997909 | ||||||
| chr2:27998058
|
G | C | 95 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(92): Show | 95 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.300+9971G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27998058 | ||||||
| chr2:27998087
|
A | C | 13 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0065others(10): Show | 13 | HG00735.hp1 HG00738.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.300+10000A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27998087 | ||||||
| chr2:27998315
|
A | T | 95 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(92): Show | 95 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.300+10228A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27998315 | ||||||
| chr2:27998331
|
A | C | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG00738.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.300+10244A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27998331 | ||||||
| chr2:27998670
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.300+10583G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27998670 | ||||||
| chr2:27998913
|
A | G | 3 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056 | 3 | HG02280.hp1 HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.300+10826A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27998913 | ||||||
| chr2:27998933
|
G | T | 3 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0016 | 3 | HG01109.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.300+10846G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27998933 | ||||||
| chr2:27999812
|
A | G | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.300+11725A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27999812 | ||||||
| chr2:27999861
|
A | T | 1 | a0001c0001t0002g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.300+11774A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27999861 | ||||||
| chr2:27999988
|
G | A | 1 | a0001c0001t0002g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.300+11901G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 27999988 | ||||||
| chr2:28000159
|
G | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.300+12072G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28000159 | ||||||
| chr2:28000342
|
T | C | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.300+12255T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28000342 | ||||||
| chr2:28001249
|
G | T | 11 | a0001c0001t0001g0035a0001c0001t0001g0094a0001c0001t0001g0104others(8): Show | 11 | HG01106.hp2 HG01192.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.300+13162G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28001249 | ||||||
| chr2:28001345
|
T | C | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.300+13258T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28001345 | ||||||
| chr2:28001435
|
C | A | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.300+13348C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28001435 | ||||||
| chr2:28001598
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.300+13511A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28001598 | ||||||
| chr2:28001861
|
T | C | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.300+13774T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28001861 | ||||||
| chr2:28002060
|
T | TA | 70 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0032others(67): Show | 70 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.300+13989dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28002060 | |||||
| chr2:28002060
|
TA | T | 58 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0027others(55): Show | 58 | HG00140.hp1 HG00733.hp2 HG01069.hp2 others(55): Show |
intron_variant | MODIFIER | c.300+13989delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28002060 | |||||
| chr2:28002132
|
C | T | 1 | a0001c0001t0002g0108 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.300+14045C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28002132 | ||||||
| chr2:28002498
|
G | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(7): Show | 10 | HG01346.hp1 HG01891.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.300+14411G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28002498 | ||||||
| chr2:28002630
|
T | A | 1 | a0001c0001t0001g0102 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.300+14543T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28002630 | ||||||
| chr2:28002812
|
G | T | 157 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(154): Show | 157 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(154): Show |
intron_variant | MODIFIER | c.300+14725G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28002812 | ||||||
| chr2:28002881
|
C | T | 1 | a0001c0001t0003g0121 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.300+14794C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28002881 | ||||||
| chr2:28002994
|
G | T | 5 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0071others(2): Show | 5 | HG00735.hp1 HG00738.hp2 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.300+14907G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28002994 | ||||||
| chr2:28003062
|
G | C | 1 | a0001c0001t0002g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.300+14975G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28003062 | ||||||
| chr2:28003491
|
A | G | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.300+15404A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28003491 | ||||||
| chr2:28003505
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.300+15418G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28003505 | ||||||
| chr2:28004131
|
C | CA | 96 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(93): Show | 96 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.300+16058dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28004131 | |||||
| chr2:28004261
|
A | G | 1 | a0001c0001t0001g0027 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.300+16174A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28004261 | ||||||
| chr2:28004268
|
C | T | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG00738.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.300+16181C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28004268 | ||||||
| chr2:28004291
|
T | C | 1 | a0001c0001t0002g0077 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.300+16204T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28004291 | ||||||
| chr2:28004480
|
A | T | 1 | a0001c0001t0002g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.300+16393A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28004480 | ||||||
| chr2:28004689
|
CT | C | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.300+16617delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28004689 | |||||
| chr2:28004747
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.300+16660C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28004747 | ||||||
| chr2:28005000
|
G | A | 1 | a0001c0001t0002g0029 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.300+16913G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28005000 | ||||||
| chr2:28005108
|
A | T | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 5 | HG01106.hp1 HG01243.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.300+17021A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28005108 | ||||||
| chr2:28005168
|
G | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0002g0004 | 3 | HG01891.hp1 HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.300+17081G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28005168 | ||||||
| chr2:28005282
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.300+17195T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28005282 | ||||||
| chr2:28005513
|
T | G | 1 | a0001c0001t0002g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.300+17426T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28005513 | ||||||
| chr2:28005541
|
T | A | 95 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(92): Show | 95 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.300+17454T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28005541 | ||||||
| chr2:28005554
|
G | A | 1 | a0001c0001t0002g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.300+17467G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28005554 | ||||||
| chr2:28006181
|
T | G | 1 | a0001c0001t0003g0019 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.300+18094T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28006181 | ||||||
| chr2:28006425
|
A | G | 1 | a0001c0001t0003g0121 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.300+18338A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28006425 | ||||||
| chr2:28006667
|
A | C | 2 | a0001c0001t0002g0001a0001c0001t0002g0002 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.301-18559A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28006667 | ||||||
| chr2:28006687
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0044 | 2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.301-18539G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28006687 | ||||||
| chr2:28006689
|
A | G | 2 | a0001c0001t0002g0122a0001c0001t0003g0121 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.301-18537A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28006689 | ||||||
| chr2:28007018
|
G | C | 1 | a0001c0001t0002g0062 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.301-18208G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28007018 | ||||||
| chr2:28007182
|
G | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0044 | 2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.301-18044G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28007182 | ||||||
| chr2:28007770
|
A | G | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG00738.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.301-17456A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28007770 | ||||||
| chr2:28007857
|
A | C | 1 | a0001c0001t0001g0086 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.301-17369A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28007857 | ||||||
| chr2:28008188
|
G | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.301-17038G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28008188 | ||||||
| chr2:28008297
|
A | G | 1 | a0001c0001t0002g0103 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.301-16929A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28008297 | ||||||
| chr2:28008641
|
A | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0044 | 2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.301-16585A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28008641 | ||||||
| chr2:28009115
|
G | A | 1 | a0001c0001t0002g0009 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.301-16111G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28009115 | ||||||
| chr2:28009121
|
G | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(16): Show | 19 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.301-16105G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28009121 | ||||||
| chr2:28009181
|
T | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(16): Show | 19 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.301-16045T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28009181 | ||||||
| chr2:28009220
|
A | G | 95 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(92): Show | 95 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.301-16006A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28009220 | ||||||
| chr2:28009279
|
A | G | 1 | a0001c0001t0002g0095 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.301-15947A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28009279 | ||||||
| chr2:28009356
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.301-15870A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28009356 | ||||||
| chr2:28009412
|
A | C | 76 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(73): Show | 76 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.301-15814A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28009412 | ||||||
| chr2:28009529
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.301-15697G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28009529 | ||||||
| chr2:28009720
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.301-15506G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28009720 | ||||||
| chr2:28010266
|
T | G | 1 | a0001c0001t0002g0149 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.301-14960T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28010266 | ||||||
| chr2:28010344
|
T | G | 2 | a0001c0001t0002g0122a0001c0001t0003g0121 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.301-14882T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28010344 | ||||||
| chr2:28010531
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.301-14695C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28010531 | ||||||
| chr2:28010540
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.301-14686A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28010540 | ||||||
| chr2:28010632
|
T | A | 3 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0016 | 3 | HG01109.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.301-14594T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28010632 | ||||||
| chr2:28010968
|
G | A | 1 | a0001c0001t0002g0029 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.301-14258G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28010968 | ||||||
| chr2:28011259
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0044 | 2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.301-13967G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28011259 | ||||||
| chr2:28011439
|
C | A | 1 | a0001c0001t0003g0067 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.301-13787C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28011439 | ||||||
| chr2:28011440
|
A | T | 1 | a0001c0001t0003g0067 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.301-13786A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28011440 | ||||||
| chr2:28011441
|
T | G | 1 | a0001c0001t0003g0067 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.301-13785T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28011441 | ||||||
| chr2:28011479
|
T | A | 1 | a0001c0001t0003g0067 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.301-13747T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28011479 | ||||||
| chr2:28011481
|
A | G | 1 | a0001c0001t0003g0067 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.301-13745A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28011481 | ||||||
| chr2:28011482
|
G | A | 1 | a0001c0001t0003g0067 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.301-13744G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28011482 | ||||||
| chr2:28011502
|
A | AGCTGGGG others(55): Show |
1 | a0001c0001t0003g0067 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.301-13724_301-1372 others(66): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28011502 | ||||||
| chr2:28011537
|
G | C | 1 | a0001c0001t0003g0067 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.301-13689G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28011537 | ||||||
| chr2:28011538
|
C | A | 1 | a0001c0001t0003g0067 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.301-13688C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28011538 | ||||||
| chr2:28011539
|
A | T | 1 | a0001c0001t0003g0067 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.301-13687A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28011539 | ||||||
| chr2:28011829
|
G | GA | 96 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(93): Show | 96 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.301-13393dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28011829 | |||||
| chr2:28011834
|
T | A | 96 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(93): Show | 96 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.301-13392T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28011834 | ||||||
| chr2:28011972
|
G | A | 2 | a0001c0001t0002g0122a0001c0001t0003g0121 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.301-13254G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28011972 | ||||||
| chr2:28012008
|
TC | T | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG00738.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.301-13216delC | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28012008 | |||||
| chr2:28012141
|
T | C | 2 | a0001c0001t0002g0122a0001c0001t0003g0121 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.301-13085T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28012141 | ||||||
| chr2:28012148
|
C | T | 1 | a0001c0001t0002g0048 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.301-13078C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28012148 | ||||||
| chr2:28012317
|
G | A | 76 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(73): Show | 76 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.301-12909G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28012317 | ||||||
| chr2:28012641
|
T | A | 1 | a0001c0001t0001g0022 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.301-12585T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28012641 | ||||||
| chr2:28012896
|
C | T | 37 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0093others(34): Show | 37 | HG00140.hp1 HG01069.hp2 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.301-12330C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28012896 | ||||||
| chr2:28012897
|
G | A | 1 | a0001c0001t0002g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.301-12329G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28012897 | ||||||
| chr2:28013088
|
T | C | 44 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0088others(41): Show | 44 | HG00140.hp1 HG01069.hp2 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.301-12138T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28013088 | ||||||
| chr2:28013253
|
C | T | 28 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0093others(25): Show | 28 | HG00140.hp1 HG01069.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.301-11973C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28013253 | ||||||
| chr2:28013297
|
G | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(7): Show | 10 | HG01346.hp1 HG01891.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.301-11929G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28013297 | ||||||
| chr2:28013665
|
TA | T | 91 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(88): Show | 91 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.301-11538delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28013665 | |||||
| chr2:28013667
|
A | T | 1 | a0001c0001t0002g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.301-11559A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28013667 | ||||||
| chr2:28013694
|
T | TAC | 31 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0054others(28): Show | 31 | HG00639.hp2 HG01069.hp2 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.301-11497_301-1149 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28013694 | |||||
| chr2:28013694
|
T | TACAC | 17 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0053others(14): Show | 17 | HG00140.hp2 HG00639.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.301-11499_301-1149 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28013694 | |||||
| chr2:28013694
|
T | TACACAC | 13 | a0001c0001t0001g0031a0001c0001t0001g0042a0001c0001t0001g0043others(10): Show | 13 | HG00735.hp1 HG01099.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.301-11501_301-1149 others(10): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28013694 | |||||
| chr2:28013694
|
T | TACACACA others(1): Show |
13 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0153others(10): Show | 13 | HG00733.hp1 HG00733.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.301-11503_301-1149 others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28013694 | |||||
| chr2:28013694
|
T | TACACACA others(3): Show |
6 | a0001c0001t0001g0041a0001c0001t0001g0070a0001c0001t0001g0071others(3): Show | 6 | HG00741.hp1 HG00741.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.301-11505_301-1149 others(14): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28013694 | |||||
| chr2:28013694
|
T | TACACACA others(5): Show |
3 | a0001c0001t0001g0146a0001c0001t0001g0157a0001c0001t0002g0033 | 3 | HG01168.hp2 HG02040.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.301-11507_301-1149 others(16): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28013694 | |||||
| chr2:28013694
|
T | TACACACA others(11): Show |
1 | a0001c0001t0001g0143 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.301-11513_301-1149 others(22): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28013694 | |||||
| chr2:28013694
|
TAC | T | 17 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0044others(14): Show | 17 | HG00738.hp1 HG01934.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.301-11497_301-1149 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28013694 | |||||
| chr2:28013694
|
TACAC | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.301-11499_301-1149 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28013694 | |||||
| chr2:28013694
|
TACACAC | T | 4 | a0001c0001t0001g0027a0001c0001t0002g0010a0001c0001t0002g0011others(1): Show | 4 | HG01109.hp2 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.301-11501_301-1149 others(10): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28013694 | |||||
| chr2:28013694
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.301-11505_301-1149 others(14): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28013694 | |||||
| chr2:28013766
|
G | A | 1 | a0001c0001t0002g0062 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.301-11460G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28013766 | ||||||
| chr2:28013931
|
T | A | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.301-11295T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28013931 | ||||||
| chr2:28014668
|
G | GT | 60 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0088others(57): Show | 60 | HG00140.hp1 HG00733.hp2 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.301-10544dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28014668 | |||||
| chr2:28014668
|
GT | G | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.301-10544delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28014668 | |||||
| chr2:28014787
|
C | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.301-10439C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28014787 | ||||||
| chr2:28015118
|
C | T | 74 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0032others(71): Show | 74 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.301-10108C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28015118 | ||||||
| chr2:28016078
|
C | T | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG00738.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.301-9148C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28016078 | ||||||
| chr2:28016239
|
T | C | 1 | a0001c0001t0002g0156 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.301-8987T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28016239 | ||||||
| chr2:28016527
|
C | T | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG01109.hp1 HG02735.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.301-8699C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28016527 | ||||||
| chr2:28016595
|
A | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.301-8631A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28016595 | ||||||
| chr2:28016943
|
G | A | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG01109.hp1 HG02735.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.301-8283G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28016943 | ||||||
| chr2:28017210
|
C | G | 1 | a0001c0001t0002g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.301-8016C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28017210 | ||||||
| chr2:28017352
|
ATGT | A | 76 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0032others(73): Show | 76 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.301-7868_301-7866d others(5): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28017352 | |||||
| chr2:28017495
|
A | C | 3 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0016 | 3 | HG01109.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.301-7731A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28017495 | ||||||
| chr2:28017592
|
C | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.301-7634C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28017592 | ||||||
| chr2:28017592
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.301-7634C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28017592 | ||||||
| chr2:28017636
|
A | G | 2 | a0001c0001t0002g0001a0001c0001t0002g0002 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.301-7590A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28017636 | ||||||
| chr2:28017658
|
T | C | 94 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(91): Show | 94 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.301-7568T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28017658 | ||||||
| chr2:28017995
|
T | A | 3 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056 | 3 | HG02280.hp1 HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.301-7231T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28017995 | ||||||
| chr2:28019215
|
A | G | 19 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(16): Show | 19 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.301-6011A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28019215 | ||||||
| chr2:28019320
|
C | T | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0075others(1): Show | 4 | HG00735.hp2 HG01081.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.301-5906C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28019320 | ||||||
| chr2:28019341
|
A | AT | 149 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(146): Show | 149 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(146): Show |
intron_variant | MODIFIER | c.301-5875dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28019341 | |||||
| chr2:28019441
|
G | A | 76 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(73): Show | 76 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.301-5785G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28019441 | ||||||
| chr2:28019585
|
G | T | 28 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0093others(25): Show | 28 | HG00140.hp1 HG01069.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.301-5641G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28019585 | ||||||
| chr2:28019714
|
C | T | 1 | a0001c0001t0002g0158 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.301-5512C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28019714 | ||||||
| chr2:28019732
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.301-5494A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28019732 | ||||||
| chr2:28019781
|
C | T | 14 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(11): Show | 14 | HG01109.hp2 HG01346.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.301-5445C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28019781 | ||||||
| chr2:28020015
|
A | G | 3 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056 | 3 | HG02280.hp1 HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.301-5211A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28020015 | ||||||
| chr2:28020493
|
C | CA | 4 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0092others(1): Show | 4 | HG02615.hp2 HG03225.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.301-4731dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28020493 | |||||
| chr2:28020675
|
T | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(7): Show | 10 | HG01346.hp1 HG01891.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.301-4551T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28020675 | ||||||
| chr2:28020952
|
G | GAC | 30 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0031others(27): Show | 30 | HG00733.hp2 HG01106.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.301-4236_301-4235d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28020952 | |||||
| chr2:28020952
|
G | GACAC | 34 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0058others(31): Show | 34 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.301-4238_301-4235d others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28020952 | |||||
| chr2:28020952
|
G | GACACAC | 27 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0094others(24): Show | 27 | HG00140.hp1 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.301-4240_301-4235d others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28020952 | |||||
| chr2:28020952
|
G | GACACACA others(1): Show |
11 | a0001c0001t0001g0023a0001c0001t0001g0057a0001c0001t0001g0099others(8): Show | 11 | HG02135.hp1 HG02155.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.301-4242_301-4235d others(10): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28020952 | |||||
| chr2:28020952
|
G | GACACACA others(3): Show |
7 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0093others(4): Show | 7 | HG01168.hp1 HG03209.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.301-4244_301-4235d others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28020952 | |||||
| chr2:28020952
|
G | GACACACA others(5): Show |
3 | a0001c0001t0001g0044a0001c0001t0001g0120a0001c0001t0001g0142 | 3 | HG02258.hp2 NA18969.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.301-4246_301-4235d others(14): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28020952 | |||||
| chr2:28020952
|
GAC | G | 12 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0001t0001g0053others(9): Show | 12 | HG00140.hp2 HG00735.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.301-4236_301-4235d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28020952 | |||||
| chr2:28020952
|
GACAC | G | 6 | a0001c0001t0001g0078a0001c0001t0002g0006a0001c0001t0002g0010others(3): Show | 6 | HG02622.hp1 HG02622.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.301-4238_301-4235d others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28020952 | |||||
| chr2:28020991
|
A | ACACAC | 2 | a0001c0001t0001g0045a0001c0001t0002g0020 | 2 | HG02897.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.301-4235_301-4234i others(7): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28020991 | ||||||
| chr2:28020991
|
A | ACACACAC | 2 | a0001c0001t0001g0034a0001c0001t0002g0048 | 2 | HG02074.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.301-4235_301-4234i others(9): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28020991 | ||||||
| chr2:28021023
|
T | TA | 14 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(11): Show | 14 | HG01109.hp2 HG01346.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.301-4199dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28021023 | |||||
| chr2:28021066
|
G | A | 1 | a0001c0001t0002g0114 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.301-4160G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28021066 | ||||||
| chr2:28021139
|
T | C | 3 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0016 | 3 | HG01109.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.301-4087T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28021139 | ||||||
| chr2:28021370
|
C | T | 156 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(153): Show |
intron_variant | MODIFIER | c.301-3856C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28021370 | ||||||
| chr2:28021747
|
C | G | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.301-3479C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28021747 | ||||||
| chr2:28021783
|
C | T | 5 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0002g0010others(2): Show | 5 | HG01109.hp2 HG03139.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.301-3443C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28021783 | ||||||
| chr2:28021923
|
C | T | 1 | a0001c0001t0002g0046 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.301-3303C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28021923 | ||||||
| chr2:28021924
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.301-3302G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28021924 | ||||||
| chr2:28022059
|
G | C | 5 | a0001c0001t0001g0017a0001c0001t0001g0053a0001c0001t0001g0080others(2): Show | 5 | HG00140.hp2 HG01099.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.301-3167G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28022059 | ||||||
| chr2:28022084
|
T | C | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.301-3142T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28022084 | ||||||
| chr2:28022163
|
T | TGAGGGGT others(15): Show |
3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02630.hp1 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.301-3062_301-3041d others(24): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 28022163 | |||||
| chr2:28022283
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.301-2943G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28022283 | ||||||
| chr2:28022357
|
A | C | 4 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0092others(1): Show | 4 | HG02615.hp2 HG03225.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.301-2869A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28022357 | ||||||
| chr2:28022378
|
G | T | 1 | a0001c0001t0002g0114 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.301-2848G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28022378 | ||||||
| chr2:28023731
|
T | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(16): Show | 19 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.301-1495T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28023731 | ||||||
| chr2:28023831
|
T | C | 1 | a0001c0001t0002g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.301-1395T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28023831 | ||||||
| chr2:28023974
|
G | A | 5 | a0001c0001t0001g0017a0001c0001t0001g0053a0001c0001t0001g0080others(2): Show | 5 | HG00140.hp2 HG01099.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.301-1252G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28023974 | ||||||
| chr2:28024143
|
G | A | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.301-1083G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28024143 | ||||||
| chr2:28024793
|
AC | A | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.301-432delC | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28024793 | ||||||
| chr2:28025127
|
T | G | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.301-99T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | chr2 | 28025127 | ||||||
| chr2:28026001
|
A | G | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.495+581A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026001 | ||||||
| chr2:28026340
|
T | C | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.495+920T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026340 | ||||||
| chr2:28026388
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.495+968A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026388 | ||||||
| chr2:28026582
|
G | T | 1 | a0001c0001t0002g0112 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.495+1162G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026582 | ||||||
| chr2:28026583
|
T | G | 1 | a0001c0001t0002g0112 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.495+1163T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026583 | ||||||
| chr2:28026761
|
C | CTA | 80 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0023others(77): Show | 80 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.495+1346_495+1347d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026761 | |||||
| chr2:28026761
|
C | CTATATAT others(31): Show |
1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.495+1347_495+1348i others(40): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026761 | |||||
| chr2:28026761
|
C | CTATATAT others(67): Show |
2 | a0001c0001t0002g0010a0001c0001t0002g0016 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.495+1347_495+1348i others(76): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026761 | |||||
| chr2:28026768
|
A | T | 12 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(9): Show | 12 | HG01167.hp1 HG01346.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.495+1348A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026768 | ||||||
| chr2:28026770
|
T | A | 12 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(9): Show | 12 | HG01167.hp1 HG01346.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.495+1350T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026770 | ||||||
| chr2:28026775
|
A | AAAAAAAT others(44): Show |
2 | a0001c0001t0002g0122a0001c0001t0003g0121 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.495+1381_495+1382i others(53): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026775 | |||||
| chr2:28026775
|
A | AT | 12 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(9): Show | 12 | HG01167.hp1 HG01346.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.495+1355_495+1356i others(3): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026775 | ||||||
| chr2:28026800
|
TA | T | 16 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0001t0001g0053others(13): Show | 16 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.495+1386delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026800 | |||||
| chr2:28026801
|
A | AT | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.495+1381_495+1382i others(3): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026801 | ||||||
| chr2:28026805
|
AATATATA others(13): Show |
A | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.495+1402_495+1421d others(22): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026805 | |||||
| chr2:28026814
|
A | ATT | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG00738.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+1395_495+1396i others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026814 | |||||
| chr2:28026822
|
T | A | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG00738.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+1402T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026822 | ||||||
| chr2:28026822
|
T | TTA | 2 | a0001c0001t0001g0027a0001c0001t0002g0007 | 2 | HG02109.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.495+1411_495+1412d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026822 | |||||
| chr2:28026822
|
T | TTATA | 13 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0023others(10): Show | 13 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.495+1409_495+1412d others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026822 | |||||
| chr2:28026823
|
T | G | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG00738.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+1403T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026823 | ||||||
| chr2:28026823
|
T | TATATATA others(133): Show |
1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.495+1421_495+1422i others(142): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026823 | |||||
| chr2:28026832
|
A | ATATAAAT others(17): Show |
3 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02630.hp1 HG02723.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.495+1412_495+1413i others(26): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026832 | ||||||
| chr2:28026833
|
A | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02630.hp1 HG02723.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.495+1413A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026833 | ||||||
| chr2:28026843
|
A | AATATATA others(15): Show |
2 | a0001c0001t0001g0022a0001c0001t0001g0044 | 2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.495+1442_495+1443i others(24): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026843 | |||||
| chr2:28026843
|
A | AATATATA others(17): Show |
3 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0086 | 3 | HG01192.hp2 HG02735.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.495+1442_495+1443i others(26): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026843 | |||||
| chr2:28026843
|
A | AATATATA others(39): Show |
1 | a0001c0001t0002g0108 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.495+1442_495+1443i others(48): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026843 | |||||
| chr2:28026843
|
A | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02630.hp1 HG02723.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.495+1423A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026843 | ||||||
| chr2:28026843
|
AATATATA others(3): Show |
A | 1 | a0001c0001t0002g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.495+1432_495+1441d others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026843 | |||||
| chr2:28026852
|
T | TTA | 58 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0032others(55): Show | 58 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.495+1441_495+1442d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026852 | |||||
| chr2:28026852
|
T | TTATATAT others(25): Show |
1 | a0001c0001t0002g0046 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.495+1442_495+1443i others(34): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026852 | |||||
| chr2:28026853
|
T | A | 5 | a0001c0001t0002g0012a0001c0001t0002g0036a0001c0001t0002g0037others(2): Show | 5 | HG00738.hp1 HG02698.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.495+1433T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026853 | ||||||
| chr2:28026863
|
G | A | 5 | a0001c0001t0002g0012a0001c0001t0002g0036a0001c0001t0002g0037others(2): Show | 5 | HG00738.hp1 HG02698.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.495+1443G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026863 | ||||||
| chr2:28026863
|
G | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0112a0001c0001t0002g0147 | 3 | HG02258.hp1 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.495+1443G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026863 | ||||||
| chr2:28026863
|
GAT | G | 8 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0002g0003others(5): Show | 8 | HG01109.hp2 HG01346.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.495+1452_495+1453d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026863 | |||||
| chr2:28026865
|
T | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0112a0001c0001t0002g0147 | 3 | HG02258.hp1 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.495+1445T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026865 | ||||||
| chr2:28026865
|
T | TATATATT others(29): Show |
1 | a0001c0001t0002g0010 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.495+1451_495+1452i others(38): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026865 | |||||
| chr2:28026865
|
T | TATATATT others(31): Show |
5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG01109.hp1 HG02735.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.495+1451_495+1452i others(40): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026865 | |||||
| chr2:28026865
|
T | TATATATT others(85): Show |
1 | a0001c0001t0002g0007 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.495+1451_495+1452i others(94): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026865 | |||||
| chr2:28026865
|
TATATATA others(25): Show |
T | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG00738.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+1454_495+1485d others(34): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026865 | |||||
| chr2:28026867
|
T | TATATATA others(1): Show |
3 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02630.hp1 HG02723.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.495+1453_495+1454i others(10): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026867 | |||||
| chr2:28026872
|
A | T | 1 | a0001c0001t0002g0112 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.495+1452A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026872 | ||||||
| chr2:28026874
|
T | A | 6 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG02258.hp1 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+1454T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026874 | ||||||
| chr2:28026874
|
TTA | T | 8 | a0001c0001t0001g0078a0001c0001t0001g0133a0001c0001t0002g0130others(5): Show | 8 | HG02109.hp2 HG02280.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.495+1465_495+1466d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026874 | |||||
| chr2:28026875
|
T | A | 7 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(4): Show | 7 | HG01109.hp1 HG02109.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.495+1455T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026875 | ||||||
| chr2:28026875
|
T | TATATATA others(3): Show |
7 | a0001c0001t0001g0017a0001c0001t0001g0053a0001c0001t0001g0080others(4): Show | 7 | HG00140.hp2 HG00639.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.495+1464_495+1465i others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026875 | |||||
| chr2:28026876
|
A | T | 2 | a0001c0001t0002g0021a0001c0001t0002g0147 | 2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.495+1456A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026876 | ||||||
| chr2:28026877
|
T | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02630.hp1 HG02698.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+1457T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026877 | ||||||
| chr2:28026884
|
A | AGATATAT others(5): Show |
4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0075others(1): Show | 4 | HG00735.hp2 HG01081.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+1464_495+1465i others(14): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026884 | ||||||
| chr2:28026885
|
T | A | 7 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(4): Show | 7 | HG01109.hp1 HG02109.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.495+1465T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026885 | ||||||
| chr2:28026885
|
T | G | 6 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0002g0003others(3): Show | 6 | HG01346.hp1 HG01891.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.495+1465T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026885 | ||||||
| chr2:28026886
|
A | T | 12 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0015others(9): Show | 12 | HG00140.hp2 HG00639.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.495+1466A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026886 | ||||||
| chr2:28026887
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0002g0012 | 2 | HG02698.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.495+1467G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026887 | ||||||
| chr2:28026887
|
G | T | 27 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(24): Show | 27 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.495+1467G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026887 | ||||||
| chr2:28026887
|
GAT | G | 2 | a0001c0001t0002g0011a0001c0001t0002g0016 | 2 | HG01109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.495+1475_495+1476d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026887 | |||||
| chr2:28026889
|
T | G | 1 | a0001c0001t0002g0116 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.495+1469T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026889 | ||||||
| chr2:28026894
|
A | ATATT | 7 | a0001c0001t0002g0029a0001c0001t0002g0046a0001c0001t0002g0047others(4): Show | 7 | HG00639.hp1 HG01167.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.495+1476_495+1477i others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026894 | |||||
| chr2:28026897
|
A | AATATATA others(25): Show |
2 | a0001c0001t0002g0130a0001c0001t0002g0132 | 2 | HG02723.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.495+1527_495+1558d others(34): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026897 | |||||
| chr2:28026897
|
A | AATATATA others(19): Show |
1 | a0001c0001t0002g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.495+1486_495+1487i others(28): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026897 | |||||
| chr2:28026897
|
A | G | 11 | a0001c0001t0001g0017a0001c0001t0001g0053a0001c0001t0001g0059others(8): Show | 11 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.495+1477A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026897 | ||||||
| chr2:28026897
|
A | T | 7 | a0001c0001t0002g0029a0001c0001t0002g0046a0001c0001t0002g0047others(4): Show | 7 | HG00639.hp1 HG01167.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.495+1477A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026897 | ||||||
| chr2:28026906
|
A | T | 52 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0040others(49): Show | 52 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.495+1486A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026906 | ||||||
| chr2:28026907
|
A | G | 7 | a0001c0001t0002g0029a0001c0001t0002g0046a0001c0001t0002g0047others(4): Show | 7 | HG00639.hp1 HG01167.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.495+1487A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026907 | ||||||
| chr2:28026916
|
T | A | 18 | a0001c0001t0001g0017a0001c0001t0001g0053a0001c0001t0001g0059others(15): Show | 18 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.495+1496T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026916 | ||||||
| chr2:28026926
|
A | T | 22 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0001t0001g0053others(19): Show | 22 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.495+1506A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026926 | ||||||
| chr2:28026927
|
A | T | 52 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0040others(49): Show | 52 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.495+1507A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026927 | ||||||
| chr2:28026927
|
AAT | A | 3 | a0001c0001t0001g0109a0001c0001t0002g0010a0001c0001t0005g0119 | 3 | HG02109.hp2 HG02970.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.495+1517_495+1518d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026927 | |||||
| chr2:28026929
|
T | A | 53 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0040others(50): Show | 53 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.495+1509T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026929 | ||||||
| chr2:28026934
|
A | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.495+1514A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026934 | ||||||
| chr2:28026936
|
A | T | 18 | a0001c0001t0001g0017a0001c0001t0001g0053a0001c0001t0001g0059others(15): Show | 18 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.495+1516A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026936 | ||||||
| chr2:28026937
|
T | A | 18 | a0001c0001t0001g0017a0001c0001t0001g0053a0001c0001t0001g0059others(15): Show | 18 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.495+1517T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026937 | ||||||
| chr2:28026939
|
A | T | 18 | a0001c0001t0001g0017a0001c0001t0001g0053a0001c0001t0001g0059others(15): Show | 18 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.495+1519A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026939 | ||||||
| chr2:28026941
|
TATATATT others(11): Show |
T | 51 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0040others(48): Show | 51 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.495+1528_495+1545d others(20): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026941 | |||||
| chr2:28026943
|
TATATTAA others(9): Show |
T | 1 | a0001c0001t0001g0066 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.495+1528_495+1543d others(18): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026943 | |||||
| chr2:28026947
|
T | A | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.495+1527T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026947 | ||||||
| chr2:28026948
|
T | A | 34 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0017others(31): Show | 34 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.495+1528T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026948 | ||||||
| chr2:28026949
|
A | AATATATA others(49): Show |
1 | a0001c0001t0002g0004 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.495+1537_495+1538i others(58): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026949 | |||||
| chr2:28026951
|
TATATATA others(1): Show |
T | 4 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0086others(1): Show | 4 | HG01192.hp2 HG02735.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+1539_495+1546d others(10): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026951 | |||||
| chr2:28026957
|
T | TTAATATA others(79): Show |
2 | a0001c0001t0002g0011a0001c0001t0002g0016 | 2 | HG01109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.495+1537_495+1538i others(88): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026957 | ||||||
| chr2:28026957
|
T | TTAATATA others(91): Show |
1 | a0001c0001t0002g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.495+1537_495+1538i others(100): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026957 | ||||||
| chr2:28026957
|
T | TTAATATA others(49): Show |
1 | a0001c0001t0002g0009 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.495+1537_495+1538i others(58): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026957 | ||||||
| chr2:28026957
|
T | TTAATATA others(51): Show |
1 | a0001c0001t0001g0005 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.495+1537_495+1538i others(60): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026957 | ||||||
| chr2:28026957
|
T | TTAATATA others(51): Show |
1 | a0001c0001t0001g0013 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.495+1537_495+1538i others(60): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026957 | ||||||
| chr2:28026957
|
T | TTTATATA others(51): Show |
1 | a0001c0001t0002g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.495+1537_495+1538i others(60): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026957 | ||||||
| chr2:28026958
|
A | T | 1 | a0001c0001t0003g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.495+1538A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026958 | ||||||
| chr2:28026959
|
A | AAT | 20 | a0001c0001t0001g0017a0001c0001t0001g0044a0001c0001t0001g0053others(17): Show | 20 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.495+1549_495+1550d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026959 | |||||
| chr2:28026959
|
A | AATATATA others(39): Show |
1 | a0001c0001t0002g0010 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.495+1548_495+1549i others(48): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026959 | |||||
| chr2:28026959
|
A | AATATATA others(7): Show |
2 | a0001c0001t0001g0024a0001c0001t0002g0026 | 2 | HG01109.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.495+1545_495+1558d others(16): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026959 | |||||
| chr2:28026959
|
A | AATATATA others(9): Show |
3 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02630.hp1 HG02723.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.495+1550_495+1551i others(18): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026959 | |||||
| chr2:28026959
|
A | T | 7 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0002g0003others(4): Show | 7 | HG01109.hp2 HG01346.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.495+1539A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026959 | ||||||
| chr2:28026963
|
T | TATATATA others(35): Show |
1 | a0001c0001t0002g0007 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.495+1558_495+1559i others(44): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026963 | |||||
| chr2:28026963
|
TATATATA others(1): Show |
T | 12 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0092others(9): Show | 12 | HG02451.hp1 HG02486.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.495+1559_495+1566d others(10): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026963 | |||||
| chr2:28026967
|
T | TAA | 28 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0093others(25): Show | 28 | HG00140.hp1 HG01069.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.495+1548_495+1549i others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026967 | |||||
| chr2:28026967
|
T | TAAATATA others(27): Show |
1 | a0001c0001t0003g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.495+1548_495+1549i others(36): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026967 | |||||
| chr2:28026969
|
T | TATAAATA others(15): Show |
1 | a0001c0001t0001g0022 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.495+1550_495+1551i others(24): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026969 | |||||
| chr2:28026971
|
A | AATATATA others(9): Show |
2 | a0001c0001t0001g0023a0001c0001t0001g0025 | 2 | HG02735.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.495+1558_495+1559i others(18): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026971 | |||||
| chr2:28026971
|
A | AATATATA others(11): Show |
1 | a0001c0001t0001g0027 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.495+1558_495+1559i others(20): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026971 | |||||
| chr2:28026971
|
A | AATATATA others(17): Show |
3 | a0001c0001t0001g0109a0001c0001t0002g0112a0001c0001t0005g0119 | 3 | HG02109.hp2 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.495+1558_495+1559i others(26): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28026971 | |||||
| chr2:28026971
|
A | T | 30 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0093others(27): Show | 30 | HG00140.hp1 HG01069.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.495+1551A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026971 | ||||||
| chr2:28026973
|
T | A | 1 | a0001c0001t0002g0004 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.495+1553T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026973 | ||||||
| chr2:28026979
|
A | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.495+1559A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026979 | ||||||
| chr2:28026989
|
A | T | 8 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(5): Show | 8 | HG01109.hp1 HG01109.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.495+1569A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28026989 | ||||||
| chr2:28027022
|
A | C | 1 | a0001c0001t0002g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.495+1602A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28027022 | ||||||
| chr2:28027522
|
A | G | 42 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0088others(39): Show | 42 | HG00140.hp1 HG01069.hp2 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.495+2102A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28027522 | ||||||
| chr2:28027523
|
T | G | 1 | a0001c0001t0002g0112 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.495+2103T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28027523 | ||||||
| chr2:28027771
|
C | T | 1 | a0001c0001t0002g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.495+2351C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28027771 | ||||||
| chr2:28027973
|
A | G | 3 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056 | 3 | HG02280.hp1 HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.495+2553A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28027973 | ||||||
| chr2:28028123
|
T | G | 95 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(92): Show | 95 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.495+2703T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28028123 | ||||||
| chr2:28028204
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.495+2784C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28028204 | ||||||
| chr2:28028457
|
G | A | 1 | a0001c0001t0002g0116 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.495+3037G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28028457 | ||||||
| chr2:28028479
|
C | T | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.495+3059C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28028479 | ||||||
| chr2:28028834
|
T | C | 2 | a0001c0001t0002g0107a0001c0001t0003g0106 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.495+3414T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28028834 | ||||||
| chr2:28029180
|
A | G | 2 | a0001c0001t0002g0122a0001c0001t0003g0121 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.495+3760A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28029180 | ||||||
| chr2:28029562
|
T | C | 1 | a0001c0001t0004g0118 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.495+4142T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28029562 | ||||||
| chr2:28029660
|
A | G | 8 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(5): Show | 8 | HG01109.hp1 HG01109.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.495+4240A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28029660 | ||||||
| chr2:28029664
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.495+4244G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28029664 | ||||||
| chr2:28030005
|
G | C | 1 | a0001c0001t0001g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.495+4585G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28030005 | ||||||
| chr2:28030734
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.495+5314C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28030734 | ||||||
| chr2:28030883
|
C | T | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.495+5463C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28030883 | ||||||
| chr2:28031169
|
C | T | 3 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132 | 3 | HG02280.hp2 HG02723.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.495+5749C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28031169 | ||||||
| chr2:28031457
|
G | A | 2 | a0001c0001t0002g0122a0001c0001t0003g0121 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.495+6037G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28031457 | ||||||
| chr2:28031707
|
A | C | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG01109.hp1 HG02735.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.495+6287A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28031707 | ||||||
| chr2:28031825
|
G | A | 7 | a0001c0001t0001g0057a0001c0001t0001g0069a0001c0001t0001g0074others(4): Show | 7 | HG02135.hp1 HG02572.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.495+6405G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28031825 | ||||||
| chr2:28031902
|
T | C | 12 | a0001c0001t0001g0035a0001c0001t0001g0094a0001c0001t0001g0104others(9): Show | 12 | HG01106.hp2 HG01192.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.495+6482T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28031902 | ||||||
| chr2:28031967
|
A | T | 3 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0009 | 3 | HG01346.hp1 HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.495+6547A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28031967 | ||||||
| chr2:28032027
|
A | G | 3 | a0001c0001t0001g0143a0001c0001t0001g0154a0001c0001t0001g0157 | 3 | HG00741.hp2 HG02040.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.495+6607A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28032027 | ||||||
| chr2:28032435
|
C | T | 76 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(73): Show | 76 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.495+7015C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28032435 | ||||||
| chr2:28032875
|
T | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02630.hp1 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.495+7455T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28032875 | ||||||
| chr2:28033055
|
A | T | 1 | a0001c0001t0001g0083 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.495+7635A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28033055 | ||||||
| chr2:28033591
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.495+8171A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28033591 | ||||||
| chr2:28033624
|
A | C | 8 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(5): Show | 8 | HG01109.hp1 HG01109.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.495+8204A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28033624 | ||||||
| chr2:28033651
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.495+8231A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28033651 | ||||||
| chr2:28033800
|
G | GT | 71 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0032others(68): Show | 71 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.495+8391dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28033800 | |||||
| chr2:28033800
|
G | GTT | 6 | a0001c0001t0001g0031a0001c0001t0001g0054a0001c0001t0001g0055others(3): Show | 6 | HG02280.hp1 HG02451.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.495+8390_495+8391d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28033800 | |||||
| chr2:28033953
|
G | A | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.495+8533G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28033953 | ||||||
| chr2:28033964
|
A | G | 76 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(73): Show | 76 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.495+8544A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28033964 | ||||||
| chr2:28034036
|
C | G | 1 | a0001c0001t0002g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.495+8616C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28034036 | ||||||
| chr2:28034111
|
A | C | 1 | a0001c0001t0001g0125 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.495+8691A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28034111 | ||||||
| chr2:28034557
|
T | C | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.495+9137T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28034557 | ||||||
| chr2:28034602
|
G | A | 1 | a0001c0001t0001g0142 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.495+9182G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28034602 | ||||||
| chr2:28034864
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.495+9444C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28034864 | ||||||
| chr2:28034981
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.495+9561C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28034981 | ||||||
| chr2:28035160
|
G | A | 76 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(73): Show | 76 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.495+9740G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28035160 | ||||||
| chr2:28035275
|
C | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.495+9855C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28035275 | ||||||
| chr2:28035430
|
C | G | 1 | a0001c0001t0003g0148 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.495+10010C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28035430 | ||||||
| chr2:28035601
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.496-10124G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28035601 | ||||||
| chr2:28035704
|
G | T | 1 | a0001c0001t0002g0051 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.496-10021G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28035704 | ||||||
| chr2:28036718
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.496-9007A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28036718 | ||||||
| chr2:28036776
|
T | C | 1 | a0001c0001t0002g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.496-8949T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28036776 | ||||||
| chr2:28036828
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0044 | 2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.496-8897G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28036828 | ||||||
| chr2:28036868
|
C | G | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.496-8857C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28036868 | ||||||
| chr2:28037063
|
T | C | 1 | a0001c0001t0002g0151 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.496-8662T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28037063 | ||||||
| chr2:28037109
|
A | G | 22 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(19): Show | 22 | HG00738.hp1 HG01109.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.496-8616A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28037109 | ||||||
| chr2:28037219
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.496-8506T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28037219 | ||||||
| chr2:28037224
|
A | T | 1 | a0001c0001t0002g0108 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.496-8501A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28037224 | ||||||
| chr2:28037269
|
G | A | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG01109.hp1 HG02735.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.496-8456G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28037269 | ||||||
| chr2:28037311
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.496-8414C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28037311 | ||||||
| chr2:28037431
|
A | G | 22 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(19): Show | 22 | HG00738.hp1 HG01109.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.496-8294A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28037431 | ||||||
| chr2:28037511
|
TAATA | T | 2 | a0001c0001t0002g0107a0001c0001t0003g0106 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.496-8208_496-8205d others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28037511 | |||||
| chr2:28038131
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.496-7594C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28038131 | ||||||
| chr2:28038296
|
C | A | 76 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(73): Show | 76 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.496-7429C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28038296 | ||||||
| chr2:28038413
|
C | T | 14 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(11): Show | 14 | HG01109.hp2 HG01346.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.496-7312C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28038413 | ||||||
| chr2:28038517
|
G | A | 90 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(87): Show | 90 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.496-7208G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28038517 | ||||||
| chr2:28038784
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.496-6941C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28038784 | ||||||
| chr2:28038807
|
C | T | 34 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0040others(31): Show | 34 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.496-6918C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28038807 | ||||||
| chr2:28039068
|
T | G | 5 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0002g0006others(2): Show | 5 | HG01346.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.496-6657T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28039068 | ||||||
| chr2:28039141
|
G | A | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.496-6584G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28039141 | ||||||
| chr2:28039867
|
T | A | 1 | a0001c0001t0001g0053 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.496-5858T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28039867 | ||||||
| chr2:28039959
|
CA | C | 140 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(137): Show | 140 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(137): Show |
intron_variant | MODIFIER | c.496-5754delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28039959 | |||||
| chr2:28039995
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.496-5730G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28039995 | ||||||
| chr2:28040153
|
C | G | 3 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0016 | 3 | HG01109.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.496-5572C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28040153 | ||||||
| chr2:28040162
|
T | G | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG01109.hp1 HG02735.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.496-5563T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28040162 | ||||||
| chr2:28040294
|
C | CTT | 6 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0029others(3): Show | 6 | HG00639.hp1 HG01109.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.496-5408_496-5407d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28040294 | |||||
| chr2:28040294
|
C | CTTT | 19 | a0001c0001t0001g0125a0001c0001t0001g0143a0001c0001t0001g0146others(16): Show | 19 | HG00733.hp1 HG00741.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.496-5409_496-5407d others(5): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28040294 | |||||
| chr2:28040294
|
C | CTTTTTTT | 7 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(4): Show | 7 | HG01891.hp1 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.496-5413_496-5407d others(9): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28040294 | |||||
| chr2:28040294
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0024 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.496-5418_496-5407d others(14): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28040294 | |||||
| chr2:28040294
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0002g0026 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.496-5419_496-5407d others(15): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28040294 | |||||
| chr2:28040294
|
C | CTTTTTTT others(8): Show |
5 | a0001c0001t0001g0022a0001c0001t0001g0044a0001c0001t0001g0070others(2): Show | 5 | HG00741.hp1 HG01099.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.496-5421_496-5407d others(17): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28040294 | |||||
| chr2:28040294
|
C | CTTTTTTT others(9): Show |
11 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0065others(8): Show | 11 | HG00735.hp1 HG01081.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.496-5422_496-5407d others(18): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28040294 | |||||
| chr2:28040294
|
C | CTTTTTTT others(10): Show |
6 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0057others(3): Show | 6 | HG02135.hp1 HG03139.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.496-5423_496-5407d others(19): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28040294 | |||||
| chr2:28040294
|
C | CTTTTTTT others(11): Show |
2 | a0001c0001t0001g0069a0001c0001t0002g0064 | 2 | NA19043.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.496-5424_496-5407d others(20): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28040294 | |||||
| chr2:28040294
|
C | CTTTTTTT others(12): Show |
3 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0021 | 3 | HG02486.hp2 HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.496-5425_496-5407d others(21): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28040294 | |||||
| chr2:28040294
|
C | CTTTTTTT others(13): Show |
2 | a0001c0001t0001g0058a0001c0001t0001g0072 | 2 | HG00738.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.496-5426_496-5407d others(22): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28040294 | |||||
| chr2:28040294
|
C | CTTTTTTT others(18): Show |
1 | a0001c0001t0001g0031 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.496-5407_496-5406i others(27): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28040294 | |||||
| chr2:28040294
|
C | CTTTTTTT others(28): Show |
1 | a0001c0001t0001g0066 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.496-5407_496-5406i others(37): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28040294 | |||||
| chr2:28040294
|
CT | C | 56 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0054others(53): Show | 56 | HG00140.hp1 HG00733.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.496-5407delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28040294 | |||||
| chr2:28040294
|
CTT | C | 5 | a0001c0001t0001g0041a0001c0001t0001g0078a0001c0001t0001g0079others(2): Show | 5 | HG00639.hp2 HG01934.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.496-5408_496-5407d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28040294 | |||||
| chr2:28040294
|
CTTT | C | 15 | a0001c0001t0001g0017a0001c0001t0001g0045a0001c0001t0001g0052others(12): Show | 15 | HG00140.hp2 HG01081.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.496-5409_496-5407d others(5): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28040294 | |||||
| chr2:28040323
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.496-5402C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28040323 | ||||||
| chr2:28040363
|
G | C | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.496-5362G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28040363 | ||||||
| chr2:28040461
|
C | T | 15 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(12): Show | 15 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.496-5264C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28040461 | ||||||
| chr2:28040575
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.496-5150C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28040575 | ||||||
| chr2:28040590
|
G | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(7): Show | 10 | HG01109.hp2 HG01891.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.496-5135G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28040590 | ||||||
| chr2:28040625
|
C | T | 15 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(12): Show | 15 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.496-5100C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28040625 | ||||||
| chr2:28041215
|
A | G | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.496-4510A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28041215 | ||||||
| chr2:28041723
|
C | G | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.496-4002C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28041723 | ||||||
| chr2:28041743
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.496-3982A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28041743 | ||||||
| chr2:28041987
|
T | C | 1 | a0001c0001t0002g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.496-3738T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28041987 | ||||||
| chr2:28042011
|
A | C | 1 | a0001c0001t0002g0112 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.496-3714A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28042011 | ||||||
| chr2:28042391
|
A | T | 1 | a0001c0001t0001g0060 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.496-3334A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28042391 | ||||||
| chr2:28042855
|
T | C | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02630.hp1 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.496-2870T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28042855 | ||||||
| chr2:28042921
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.496-2804G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28042921 | ||||||
| chr2:28043168
|
G | A | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.496-2557G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28043168 | ||||||
| chr2:28043177
|
A | G | 92 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(89): Show | 92 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.496-2548A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28043177 | ||||||
| chr2:28043202
|
C | T | 76 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(73): Show | 76 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.496-2523C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28043202 | ||||||
| chr2:28043339
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.496-2386C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28043339 | ||||||
| chr2:28043516
|
C | A | 1 | a0001c0001t0002g0112 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.496-2209C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28043516 | ||||||
| chr2:28043747
|
C | A | 1 | a0001c0001t0001g0083 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.496-1978C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28043747 | ||||||
| chr2:28044354
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.496-1371C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28044354 | ||||||
| chr2:28044373
|
G | A | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 5 | HG01106.hp1 HG01243.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.496-1352G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28044373 | ||||||
| chr2:28044499
|
G | A | 15 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(12): Show | 15 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.496-1226G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28044499 | ||||||
| chr2:28044842
|
G | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0081 | 2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.496-883G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28044842 | ||||||
| chr2:28044995
|
T | TA | 6 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0092others(3): Show | 6 | HG01168.hp1 HG02615.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.496-716dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 28044995 | |||||
| chr2:28045400
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.496-325G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28045400 | ||||||
| chr2:28045600
|
C | T | 76 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(73): Show | 76 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.496-125C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | chr2 | 28045600 | ||||||
| chr2:28045875
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.570+76C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28045875 | ||||||
| chr2:28045955
|
G | A | 155 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(152): Show | 155 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(152): Show |
intron_variant | MODIFIER | c.570+156G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28045955 | ||||||
| chr2:28046230
|
A | G | 157 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(154): Show | 157 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(154): Show |
intron_variant | MODIFIER | c.570+431A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28046230 | ||||||
| chr2:28046334
|
C | G | 1 | a0001c0001t0002g0112 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.570+535C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28046334 | ||||||
| chr2:28046547
|
TA | T | 3 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132 | 3 | HG02280.hp2 HG02723.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.570+750delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28046547 | |||||
| chr2:28046766
|
A | AT | 15 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(12): Show | 15 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.570+975dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28046766 | |||||
| chr2:28046835
|
T | A | 37 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0093others(34): Show | 37 | HG00140.hp1 HG01069.hp2 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.570+1036T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28046835 | ||||||
| chr2:28046848
|
C | A | 15 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(12): Show | 15 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.570+1049C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28046848 | ||||||
| chr2:28046883
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.570+1084C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28046883 | ||||||
| chr2:28047086
|
A | G | 1 | a0001c0001t0003g0089 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.570+1287A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28047086 | ||||||
| chr2:28047157
|
G | A | 15 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(12): Show | 15 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.570+1358G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28047157 | ||||||
| chr2:28047238
|
T | A | 1 | a0001c0001t0001g0154 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.570+1439T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28047238 | ||||||
| chr2:28047459
|
T | A | 15 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(12): Show | 15 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.570+1660T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28047459 | ||||||
| chr2:28047594
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.570+1795T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28047594 | ||||||
| chr2:28047610
|
T | TAAGAATT others(314): Show |
1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.570+1827_570+1828i others(323): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28047610 | |||||
| chr2:28048021
|
T | C | 15 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(12): Show | 15 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.570+2222T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28048021 | ||||||
| chr2:28048242
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.570+2443A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28048242 | ||||||
| chr2:28048264
|
T | C | 15 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(12): Show | 15 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.570+2465T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28048264 | ||||||
| chr2:28048568
|
T | G | 77 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(74): Show | 77 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.570+2769T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28048568 | ||||||
| chr2:28048647
|
G | T | 3 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0004g0118 | 3 | HG03225.hp1 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.570+2848G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28048647 | ||||||
| chr2:28049632
|
T | C | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02630.hp1 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.570+3833T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28049632 | ||||||
| chr2:28049861
|
G | A | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.570+4062G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28049861 | ||||||
| chr2:28050578
|
A | C | 1 | a0002c0002t0001g0085 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.570+4779A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28050578 | ||||||
| chr2:28050728
|
A | G | 15 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(12): Show | 15 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.570+4929A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28050728 | ||||||
| chr2:28050827
|
G | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0004g0118 | 3 | HG03225.hp1 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.570+5028G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28050827 | ||||||
| chr2:28051026
|
T | C | 1 | a0001c0001t0002g0048 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.570+5227T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28051026 | ||||||
| chr2:28051145
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.570+5346G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28051145 | ||||||
| chr2:28051250
|
C | T | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.570+5451C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28051250 | ||||||
| chr2:28051635
|
T | C | 1 | a0001c0001t0002g0030 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.570+5836T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28051635 | ||||||
| chr2:28051789
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.570+5990C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28051789 | ||||||
| chr2:28052240
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.570+6441A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28052240 | ||||||
| chr2:28052287
|
C | CT | 5 | a0001c0001t0001g0040a0001c0001t0001g0057a0001c0001t0001g0079others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.570+6502dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28052287 | |||||
| chr2:28052370
|
C | T | 7 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(4): Show | 7 | HG01891.hp1 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.570+6571C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28052370 | ||||||
| chr2:28052433
|
A | G | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.570+6634A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28052433 | ||||||
| chr2:28052530
|
T | C | 15 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(12): Show | 15 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.570+6731T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28052530 | ||||||
| chr2:28052627
|
C | G | 1 | a0001c0001t0002g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.570+6828C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28052627 | ||||||
| chr2:28052627
|
C | T | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.570+6828C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28052627 | ||||||
| chr2:28052667
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.570+6868C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28052667 | ||||||
| chr2:28052936
|
A | G | 1 | a0001c0001t0002g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.570+7137A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28052936 | ||||||
| chr2:28052962
|
T | A | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.570+7163T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28052962 | ||||||
| chr2:28052964
|
G | T | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.570+7165G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28052964 | ||||||
| chr2:28053032
|
A | T | 1 | a0001c0001t0002g0036 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.570+7233A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28053032 | ||||||
| chr2:28053139
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.570+7340C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28053139 | ||||||
| chr2:28053331
|
T | G | 3 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0016 | 3 | HG01109.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.570+7532T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28053331 | ||||||
| chr2:28053433
|
G | A | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.570+7634G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28053433 | ||||||
| chr2:28053776
|
C | G | 76 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(73): Show | 76 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.570+7977C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28053776 | ||||||
| chr2:28054001
|
A | G | 1 | a0001c0001t0002g0114 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.570+8202A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28054001 | ||||||
| chr2:28054025
|
A | G | 1 | a0001c0001t0002g0108 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.570+8226A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28054025 | ||||||
| chr2:28054547
|
T | C | 9 | a0001c0001t0001g0125a0001c0001t0001g0146a0001c0001t0001g0150others(6): Show | 9 | HG01069.hp1 HG01168.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.570+8748T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28054547 | ||||||
| chr2:28054664
|
C | T | 3 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0016 | 3 | HG01109.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.570+8865C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28054664 | ||||||
| chr2:28054694
|
A | G | 2 | a0001c0001t0002g0122a0001c0001t0003g0121 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.570+8895A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28054694 | ||||||
| chr2:28054700
|
A | T | 157 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(154): Show | 157 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(154): Show |
intron_variant | MODIFIER | c.570+8901A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28054700 | ||||||
| chr2:28054712
|
A | G | 15 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(12): Show | 15 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.570+8913A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28054712 | ||||||
| chr2:28055059
|
T | C | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.570+9260T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28055059 | ||||||
| chr2:28055301
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.570+9502A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28055301 | ||||||
| chr2:28055571
|
T | C | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.570+9772T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28055571 | ||||||
| chr2:28055661
|
G | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0002g0004 | 3 | HG01891.hp1 HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.570+9862G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28055661 | ||||||
| chr2:28055946
|
G | A | 1 | a0001c0001t0002g0063 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.570+10147G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28055946 | ||||||
| chr2:28056015
|
C | T | 15 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(12): Show | 15 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.570+10216C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28056015 | ||||||
| chr2:28056055
|
T | C | 156 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(153): Show |
intron_variant | MODIFIER | c.570+10256T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28056055 | ||||||
| chr2:28056214
|
G | C | 15 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(12): Show | 15 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.570+10415G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28056214 | ||||||
| chr2:28056336
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.570+10537A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28056336 | ||||||
| chr2:28056684
|
A | C | 4 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(1): Show | 4 | HG00738.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+10885A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28056684 | ||||||
| chr2:28056782
|
T | G | 93 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(90): Show | 93 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.570+10983T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28056782 | ||||||
| chr2:28056826
|
G | A | 93 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(90): Show | 93 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.570+11027G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28056826 | ||||||
| chr2:28057302
|
A | G | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.570+11503A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28057302 | ||||||
| chr2:28057384
|
G | A | 1 | a0001c0001t0003g0019 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.570+11585G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28057384 | ||||||
| chr2:28057529
|
A | C | 1 | a0001c0001t0001g0032 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.570+11730A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28057529 | ||||||
| chr2:28057530
|
T | C | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.570+11731T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28057530 | ||||||
| chr2:28057652
|
A | C | 1 | a0001c0001t0001g0057 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.570+11853A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28057652 | ||||||
| chr2:28057734
|
A | G | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.570+11935A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28057734 | ||||||
| chr2:28057853
|
A | G | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.570+12054A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28057853 | ||||||
| chr2:28058108
|
C | T | 4 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0092others(1): Show | 4 | HG02615.hp2 HG03225.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+12309C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28058108 | ||||||
| chr2:28058126
|
A | G | 1 | a0001c0001t0002g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.570+12327A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28058126 | ||||||
| chr2:28058141
|
C | CA | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(3): Show | 6 | HG01106.hp1 HG01109.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+12354dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28058141 | |||||
| chr2:28058210
|
A | G | 4 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0092others(1): Show | 4 | HG02615.hp2 HG03225.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+12411A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28058210 | ||||||
| chr2:28058239
|
A | C | 3 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0016 | 3 | HG01109.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.570+12440A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28058239 | ||||||
| chr2:28058678
|
G | A | 87 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(84): Show | 87 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.570+12879G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28058678 | ||||||
| chr2:28058703
|
T | C | 1 | a0001c0001t0002g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.570+12904T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28058703 | ||||||
| chr2:28058823
|
G | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(7): Show | 10 | HG01109.hp2 HG01891.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.570+13024G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28058823 | ||||||
| chr2:28058890
|
G | C | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.570+13091G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28058890 | ||||||
| chr2:28058891
|
G | T | 1 | a0001c0001t0002g0114 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.570+13092G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28058891 | ||||||
| chr2:28058896
|
G | A | 1 | a0001c0001t0002g0016 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.570+13097G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28058896 | ||||||
| chr2:28059022
|
G | C | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.570+13223G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28059022 | ||||||
| chr2:28059843
|
A | T | 1 | a0001c0001t0001g0013 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.570+14044A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28059843 | ||||||
| chr2:28059860
|
A | T | 1 | a0001c0001t0001g0120 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.570+14061A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28059860 | ||||||
| chr2:28060125
|
A | G | 1 | a0001c0001t0002g0010 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.570+14326A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28060125 | ||||||
| chr2:28060252
|
T | G | 1 | a0001c0001t0001g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.570+14453T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28060252 | ||||||
| chr2:28060372
|
A | G | 7 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(4): Show | 7 | HG01891.hp1 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.570+14573A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28060372 | ||||||
| chr2:28060642
|
T | G | 2 | a0001c0001t0001g0045a0001c0001t0002g0021 | 2 | HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.570+14843T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28060642 | ||||||
| chr2:28060663
|
A | G | 7 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(4): Show | 7 | HG01891.hp1 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.570+14864A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28060663 | ||||||
| chr2:28060666
|
A | C | 2 | a0001c0001t0001g0045a0001c0001t0002g0021 | 2 | HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.570+14867A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28060666 | ||||||
| chr2:28060813
|
T | C | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.570+15014T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28060813 | ||||||
| chr2:28061091
|
C | A | 157 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(154): Show | 157 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(154): Show |
intron_variant | MODIFIER | c.570+15292C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28061091 | ||||||
| chr2:28061188
|
G | A | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.570+15389G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28061188 | ||||||
| chr2:28061357
|
G | T | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0075others(1): Show | 4 | HG00735.hp2 HG01081.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+15558G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28061357 | ||||||
| chr2:28061501
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.570+15702C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28061501 | ||||||
| chr2:28061516
|
C | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(7): Show | 10 | HG01109.hp2 HG01891.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.570+15717C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28061516 | ||||||
| chr2:28061584
|
C | CA | 19 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(16): Show | 19 | HG01109.hp1 HG01109.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.570+15804dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28061584 | |||||
| chr2:28061584
|
C | CAA | 7 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(4): Show | 7 | HG01891.hp1 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.570+15803_570+1580 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28061584 | |||||
| chr2:28061584
|
CA | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0104a0001c0001t0002g0009others(2): Show | 5 | HG01069.hp1 HG01346.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.570+15804delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28061584 | |||||
| chr2:28061766
|
T | C | 92 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(89): Show | 92 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.570+15967T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28061766 | ||||||
| chr2:28061774
|
CT | C | 5 | a0001c0001t0001g0045a0001c0001t0002g0098a0001c0001t0003g0018others(2): Show | 5 | HG02486.hp1 HG02818.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.570+15986delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28061774 | |||||
| chr2:28061785
|
T | A | 15 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(12): Show | 15 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.570+15986T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28061785 | ||||||
| chr2:28061884
|
C | T | 1 | a0001c0001t0002g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.570+16085C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28061884 | ||||||
| chr2:28061951
|
A | G | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.570+16152A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28061951 | ||||||
| chr2:28061987
|
G | A | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.570+16188G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28061987 | ||||||
| chr2:28062074
|
G | A | 156 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(153): Show |
intron_variant | MODIFIER | c.570+16275G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28062074 | ||||||
| chr2:28062084
|
C | G | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.570+16285C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28062084 | ||||||
| chr2:28062253
|
G | A | 156 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(153): Show |
intron_variant | MODIFIER | c.570+16454G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28062253 | ||||||
| chr2:28062257
|
C | CA | 10 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0071others(7): Show | 10 | HG00733.hp1 HG00741.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.570+16474dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28062257 | |||||
| chr2:28062257
|
CA | C | 9 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(6): Show | 9 | HG01109.hp1 HG01109.hp2 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.570+16474delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28062257 | |||||
| chr2:28062433
|
C | T | 2 | a0001c0001t0002g0112a0001c0001t0005g0119 | 2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.570+16634C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28062433 | ||||||
| chr2:28062574
|
C | A | 11 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(8): Show | 11 | HG01109.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.570+16775C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28062574 | ||||||
| chr2:28062575
|
CA | C | 73 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(70): Show | 73 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.570+16790delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28062575 | |||||
| chr2:28062576
|
A | C | 11 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(8): Show | 11 | HG01109.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.570+16777A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28062576 | ||||||
| chr2:28063298
|
C | T | 2 | a0001c0001t0002g0107a0001c0001t0003g0106 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.570+17499C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28063298 | ||||||
| chr2:28063818
|
T | C | 15 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(12): Show | 15 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.570+18019T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28063818 | ||||||
| chr2:28063839
|
A | T | 1 | a0001c0001t0001g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.570+18040A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28063839 | ||||||
| chr2:28064670
|
A | G | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.570+18871A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28064670 | ||||||
| chr2:28064767
|
G | A | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.570+18968G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28064767 | ||||||
| chr2:28064777
|
G | A | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.570+18978G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28064777 | ||||||
| chr2:28065002
|
CA | C | 11 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(8): Show | 11 | HG01109.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.570+19219delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28065002 | |||||
| chr2:28065034
|
G | A | 2 | a0001c0001t0001g0115a0001c0001t0002g0110 | 2 | HG02135.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.570+19235G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28065034 | ||||||
| chr2:28065153
|
C | T | 2 | a0001c0001t0001g0093a0001c0001t0001g0102 | 2 | HG01069.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.570+19354C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28065153 | ||||||
| chr2:28065509
|
T | C | 3 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056 | 3 | HG02280.hp1 HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.570+19710T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28065509 | ||||||
| chr2:28065525
|
C | T | 59 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(56): Show | 59 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.570+19726C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28065525 | ||||||
| chr2:28065535
|
G | T | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.570+19736G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28065535 | ||||||
| chr2:28065839
|
A | C | 15 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0138others(12): Show | 15 | HG00733.hp2 HG01167.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.570+20040A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28065839 | ||||||
| chr2:28065911
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.570+20112C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28065911 | ||||||
| chr2:28065978
|
T | TA | 9 | a0001c0001t0001g0043a0001c0001t0001g0066a0001c0001t0001g0115others(6): Show | 9 | HG00733.hp2 HG01109.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.570+20201dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28065978 | |||||
| chr2:28066108
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.570+20309G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28066108 | ||||||
| chr2:28066137
|
C | T | 1 | a0001c0001t0003g0106 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.570+20338C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28066137 | ||||||
| chr2:28066170
|
A | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0071 | 2 | HG00741.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.570+20371A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28066170 | ||||||
| chr2:28066174
|
T | A | 15 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0001t0001g0053others(12): Show | 15 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.570+20375T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28066174 | ||||||
| chr2:28066263
|
C | T | 1 | a0001c0001t0002g0152 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.570+20464C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28066263 | ||||||
| chr2:28066480
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.570+20681C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28066480 | ||||||
| chr2:28066708
|
G | A | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG01496.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.570+20909G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28066708 | ||||||
| chr2:28066942
|
G | A | 16 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(13): Show | 16 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.570+21143G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28066942 | ||||||
| chr2:28066987
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.570+21188G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28066987 | ||||||
| chr2:28067224
|
G | A | 15 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(12): Show | 15 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.570+21425G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28067224 | ||||||
| chr2:28067480
|
T | C | 69 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0040others(66): Show | 69 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.570+21681T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28067480 | ||||||
| chr2:28067660
|
C | G | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG01109.hp1 HG02735.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.570+21861C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28067660 | ||||||
| chr2:28067783
|
G | A | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.570+21984G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28067783 | ||||||
| chr2:28068042
|
C | CT | 16 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(13): Show | 16 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.570+22253dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28068042 | |||||
| chr2:28068196
|
A | G | 1 | a0001c0001t0002g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.570+22397A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28068196 | ||||||
| chr2:28068327
|
C | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0002g0004 | 3 | HG01891.hp1 HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.570+22528C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28068327 | ||||||
| chr2:28068423
|
T | C | 157 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(154): Show | 157 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(154): Show |
intron_variant | MODIFIER | c.570+22624T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28068423 | ||||||
| chr2:28068489
|
A | T | 1 | a0001c0001t0001g0088 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.570+22690A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28068489 | ||||||
| chr2:28068527
|
G | A | 15 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(12): Show | 15 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.570+22728G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28068527 | ||||||
| chr2:28069017
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.570+23218C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28069017 | ||||||
| chr2:28069905
|
C | T | 1 | a0001c0001t0002g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.570+24106C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28069905 | ||||||
| chr2:28069906
|
G | A | 5 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0071others(2): Show | 5 | HG00735.hp1 HG00738.hp2 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.570+24107G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28069906 | ||||||
| chr2:28070109
|
A | G | 2 | a0001c0001t0003g0089a0001c0001t0003g0090 | 2 | HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.570+24310A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28070109 | ||||||
| chr2:28070116
|
G | A | 1 | a0001c0001t0001g0155 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.570+24317G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28070116 | ||||||
| chr2:28070139
|
G | A | 15 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(12): Show | 15 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.570+24340G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28070139 | ||||||
| chr2:28070432
|
C | A | 78 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(75): Show | 78 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.570+24633C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28070432 | ||||||
| chr2:28070551
|
C | CTTTTT | 12 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0023others(9): Show | 12 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.570+24756_570+2475 others(9): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28070551 | |||||
| chr2:28070556
|
C | CTT | 77 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0031others(74): Show | 77 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.570+24767_570+2476 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28070556 | |||||
| chr2:28070556
|
C | CTTTTCTT others(6): Show |
1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.570+24761_570+2476 others(17): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28070556 | |||||
| chr2:28070556
|
C | T | 15 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(12): Show | 15 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.570+24757C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28070556 | ||||||
| chr2:28070827
|
T | A | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.570+25028T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28070827 | ||||||
| chr2:28070832
|
T | A | 1 | a0001c0001t0002g0101 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.570+25033T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28070832 | ||||||
| chr2:28070999
|
G | T | 1 | a0001c0001t0002g0112 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.570+25200G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28070999 | ||||||
| chr2:28071035
|
A | G | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.570+25236A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28071035 | ||||||
| chr2:28071174
|
C | G | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.570+25375C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28071174 | ||||||
| chr2:28071200
|
A | G | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.570+25401A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28071200 | ||||||
| chr2:28071232
|
A | G | 15 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(12): Show | 15 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.570+25433A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28071232 | ||||||
| chr2:28071509
|
C | T | 157 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(154): Show | 157 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(154): Show |
intron_variant | MODIFIER | c.570+25710C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28071509 | ||||||
| chr2:28071657
|
C | T | 3 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132 | 3 | HG02280.hp2 HG02723.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.570+25858C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28071657 | ||||||
| chr2:28072155
|
G | A | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.570+26356G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28072155 | ||||||
| chr2:28072329
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.570+26530C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28072329 | ||||||
| chr2:28072478
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.570+26679C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28072478 | ||||||
| chr2:28072562
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.570+26763T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28072562 | ||||||
| chr2:28072822
|
G | A | 1 | a0001c0001t0002g0098 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.570+27023G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28072822 | ||||||
| chr2:28073086
|
A | G | 1 | a0001c0001t0001g0032 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.570+27287A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28073086 | ||||||
| chr2:28073141
|
C | T | 3 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0016 | 3 | HG01109.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.570+27342C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28073141 | ||||||
| chr2:28073763
|
A | T | 56 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0034others(53): Show | 56 | HG00140.hp1 HG01069.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.570+27964A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28073763 | ||||||
| chr2:28073990
|
C | T | 1 | a0001c0001t0002g0062 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.570+28191C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28073990 | ||||||
| chr2:28074000
|
TACACATA others(7): Show |
T | 3 | a0001c0001t0003g0135a0001c0001t0003g0136a0001c0001t0003g0137 | 3 | HG00733.hp2 HG01167.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.570+28217_570+2823 others(18): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28074000 | |||||
| chr2:28074010
|
TAC | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0015 | 2 | HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.570+28219_570+2822 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28074010 | |||||
| chr2:28074215
|
A | G | 1 | a0001c0001t0002g0068 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.570+28416A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28074215 | ||||||
| chr2:28074467
|
A | T | 1 | a0001c0001t0001g0086 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.570+28668A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28074467 | ||||||
| chr2:28074553
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.570+28754A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28074553 | ||||||
| chr2:28074554
|
T | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.570+28755T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28074554 | ||||||
| chr2:28074987
|
G | C | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.570+29188G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28074987 | ||||||
| chr2:28075034
|
A | T | 1 | a0001c0001t0002g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.570+29235A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28075034 | ||||||
| chr2:28075062
|
G | T | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.570+29263G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28075062 | ||||||
| chr2:28075445
|
A | C | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.570+29646A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28075445 | ||||||
| chr2:28075528
|
T | TTCTC | 12 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(9): Show | 12 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.570+29745_570+2974 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28075528 | |||||
| chr2:28075528
|
TTCTC | T | 13 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0088others(10): Show | 13 | HG02280.hp1 HG02280.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.570+29745_570+2974 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28075528 | |||||
| chr2:28075544
|
C | T | 2 | a0001c0001t0003g0089a0001c0001t0003g0090 | 2 | HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.570+29745C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28075544 | ||||||
| chr2:28075558
|
A | ATGTG | 18 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0088others(15): Show | 18 | HG00738.hp1 HG02280.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.570+29776_570+2977 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28075558 | |||||
| chr2:28075580
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.570+29781G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28075580 | ||||||
| chr2:28076011
|
C | A | 14 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0088others(11): Show | 14 | HG02280.hp1 HG02280.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.570+30212C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28076011 | ||||||
| chr2:28076044
|
A | C | 2 | a0001c0001t0003g0089a0001c0001t0003g0090 | 2 | HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.570+30245A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28076044 | ||||||
| chr2:28076055
|
C | G | 34 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(31): Show | 34 | HG00639.hp2 HG01109.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.570+30256C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28076055 | ||||||
| chr2:28076117
|
A | G | 112 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 112 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(109): Show |
intron_variant | MODIFIER | c.570+30318A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28076117 | ||||||
| chr2:28076168
|
G | T | 1 | a0001c0001t0002g0141 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.570+30369G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28076168 | ||||||
| chr2:28076307
|
C | T | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.570+30508C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28076307 | ||||||
| chr2:28076400
|
A | G | 75 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0031others(72): Show | 75 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.570+30601A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28076400 | ||||||
| chr2:28076458
|
A | ATATTTAT others(5): Show |
2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG01496.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.570+30674_570+3068 others(16): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28076458 | |||||
| chr2:28076458
|
ATATT | A | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG01192.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+30682_570+3068 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28076458 | |||||
| chr2:28076473
|
T | TTTAG | 61 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0031others(58): Show | 61 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.570+30677_570+3067 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28076473 | |||||
| chr2:28076477
|
T | G | 1 | a0001c0001t0001g0071 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.570+30678T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28076477 | ||||||
| chr2:28076481
|
T | G | 72 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0022others(69): Show | 72 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.570+30682T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28076481 | ||||||
| chr2:28076481
|
T | TTTAG | 3 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0004g0118 | 3 | HG02615.hp2 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.570+30706_570+3070 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28076481 | |||||
| chr2:28076481
|
TTTAG | T | 19 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(16): Show | 19 | HG00639.hp2 HG01109.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.570+30706_570+3070 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28076481 | |||||
| chr2:28076485
|
G | T | 4 | a0001c0001t0001g0045a0001c0001t0002g0126a0001c0001t0002g0140others(1): Show | 4 | HG01496.hp1 HG02559.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+30686G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28076485 | ||||||
| chr2:28076489
|
G | T | 12 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(9): Show | 12 | HG00639.hp2 HG01109.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.570+30690G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28076489 | ||||||
| chr2:28076493
|
G | T | 7 | a0001c0001t0001g0024a0001c0001t0002g0026a0001c0001t0002g0077others(4): Show | 7 | HG00639.hp2 HG01109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.570+30694G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28076493 | ||||||
| chr2:28076509
|
T | G | 1 | a0001c0001t0002g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.570+30710T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28076509 | ||||||
| chr2:28076588
|
C | T | 3 | a0001c0001t0001g0045a0001c0001t0002g0140a0001c0001t0002g0141 | 3 | HG01496.hp1 HG02559.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.570+30789C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28076588 | ||||||
| chr2:28076701
|
T | G | 14 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0088others(11): Show | 14 | HG02280.hp1 HG02280.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.570+30902T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28076701 | ||||||
| chr2:28076758
|
G | A | 1 | a0001c0001t0002g0049 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.570+30959G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28076758 | ||||||
| chr2:28076774
|
A | G | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(7): Show | 10 | HG00639.hp2 HG01109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.570+30975A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28076774 | ||||||
| chr2:28076792
|
C | T | 30 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(27): Show | 30 | HG00639.hp2 HG01109.hp1 HG02280.hp1 others(27): Show |
intron_variant | MODIFIER | c.570+30993C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28076792 | ||||||
| chr2:28076838
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.570+31039A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28076838 | ||||||
| chr2:28077055
|
T | G | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.570+31256T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28077055 | ||||||
| chr2:28077124
|
C | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.570+31325C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28077124 | ||||||
| chr2:28077302
|
A | G | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.570+31503A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28077302 | ||||||
| chr2:28077352
|
G | T | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(7): Show | 10 | HG00639.hp2 HG01109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.570+31553G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28077352 | ||||||
| chr2:28077447
|
A | G | 35 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(32): Show | 35 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.570+31648A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28077447 | ||||||
| chr2:28077511
|
G | A | 1 | a0001c0001t0002g0108 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.570+31712G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28077511 | ||||||
| chr2:28077518
|
T | C | 8 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(5): Show | 8 | HG00639.hp2 HG01109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.570+31719T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28077518 | ||||||
| chr2:28077867
|
A | C | 3 | a0001c0001t0001g0045a0001c0001t0002g0140a0001c0001t0002g0141 | 3 | HG01496.hp1 HG02559.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.570+32068A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28077867 | ||||||
| chr2:28077891
|
A | T | 34 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(31): Show | 34 | HG00639.hp2 HG01109.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.570+32092A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28077891 | ||||||
| chr2:28078102
|
A | G | 2 | a0001c0001t0001g0032a0001c0001t0001g0072 | 2 | HG00738.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.570+32303A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28078102 | ||||||
| chr2:28078304
|
A | G | 8 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0002g0010others(5): Show | 8 | HG02280.hp1 HG02451.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.570+32505A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28078304 | ||||||
| chr2:28078328
|
T | C | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.570+32529T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28078328 | ||||||
| chr2:28078343
|
GC | G | 55 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0032others(52): Show | 55 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.570+32548delC | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28078343 | |||||
| chr2:28078395
|
C | T | 1 | a0001c0001t0002g0108 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.570+32596C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28078395 | ||||||
| chr2:28078673
|
T | C | 13 | a0001c0001t0001g0066a0001c0001t0001g0111a0001c0001t0001g0125others(10): Show | 13 | HG00741.hp2 HG02074.hp1 HG02148.hp1 others(10): Show |
intron_variant | MODIFIER | c.570+32874T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28078673 | ||||||
| chr2:28079102
|
A | T | 12 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(9): Show | 12 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.570+33303A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28079102 | ||||||
| chr2:28079166
|
G | A | 32 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(29): Show | 32 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.570+33367G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28079166 | ||||||
| chr2:28079322
|
A | G | 14 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(11): Show | 14 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.570+33523A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28079322 | ||||||
| chr2:28079592
|
C | T | 1 | a0001c0001t0002g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.570+33793C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28079592 | ||||||
| chr2:28079839
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.570+34040A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28079839 | ||||||
| chr2:28080090
|
A | G | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.570+34291A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28080090 | ||||||
| chr2:28080132
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.570+34333A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28080132 | ||||||
| chr2:28080148
|
G | A | 1 | a0001c0001t0002g0007 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.570+34349G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28080148 | ||||||
| chr2:28080383
|
A | G | 1 | a0001c0001t0002g0063 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.570+34584A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28080383 | ||||||
| chr2:28080450
|
T | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02630.hp1 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.570+34651T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28080450 | ||||||
| chr2:28080568
|
T | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.570+34769T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28080568 | ||||||
| chr2:28080669
|
A | G | 1 | a0001c0001t0001g0120 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.570+34870A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28080669 | ||||||
| chr2:28080682
|
G | A | 12 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0088others(9): Show | 12 | HG02280.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.570+34883G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28080682 | ||||||
| chr2:28080789
|
A | G | 4 | a0001c0001t0001g0138a0001c0001t0002g0006a0001c0001t0002g0007others(1): Show | 4 | HG01346.hp1 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+34990A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28080789 | ||||||
| chr2:28080846
|
C | T | 91 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(88): Show | 91 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.570+35047C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28080846 | ||||||
| chr2:28080889
|
C | G | 14 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(11): Show | 14 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.570+35090C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28080889 | ||||||
| chr2:28081160
|
A | T | 12 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0088others(9): Show | 12 | HG02280.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.570+35361A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28081160 | ||||||
| chr2:28081172
|
A | C | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.570+35373A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28081172 | ||||||
| chr2:28081194
|
G | A | 44 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0032others(41): Show | 44 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.570+35395G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28081194 | ||||||
| chr2:28081293
|
T | C | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.570+35494T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28081293 | ||||||
| chr2:28081336
|
T | G | 1 | a0001c0001t0001g0138 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.570+35537T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28081336 | ||||||
| chr2:28081506
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.570+35707A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28081506 | ||||||
| chr2:28081513
|
C | A | 8 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0002g0010others(5): Show | 8 | HG02280.hp1 HG02451.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.570+35714C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28081513 | ||||||
| chr2:28081763
|
A | G | 39 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(36): Show | 39 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.570+35964A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28081763 | ||||||
| chr2:28081793
|
C | T | 12 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0088others(9): Show | 12 | HG02280.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.570+35994C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28081793 | ||||||
| chr2:28081843
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.570+36044A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28081843 | ||||||
| chr2:28081929
|
A | G | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.570+36130A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28081929 | ||||||
| chr2:28082048
|
T | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.570+36249T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28082048 | ||||||
| chr2:28082090
|
A | G | 1 | a0001c0001t0001g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.570+36291A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28082090 | ||||||
| chr2:28082112
|
GA | G | 44 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0032others(41): Show | 44 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.570+36321delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28082112 | |||||
| chr2:28082288
|
T | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02559.hp2 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+36489T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28082288 | ||||||
| chr2:28082448
|
C | G | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.570+36649C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28082448 | ||||||
| chr2:28082546
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.570+36747G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28082546 | ||||||
| chr2:28082796
|
C | T | 44 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0032others(41): Show | 44 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.570+36997C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28082796 | ||||||
| chr2:28082919
|
C | G | 1 | a0001c0001t0001g0071 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.570+37120C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28082919 | ||||||
| chr2:28083068
|
T | A | 2 | a0001c0001t0003g0089a0001c0001t0003g0090 | 2 | HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.570+37269T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28083068 | ||||||
| chr2:28083090
|
G | C | 1 | a0001c0001t0001g0073 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.570+37291G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28083090 | ||||||
| chr2:28083138
|
A | G | 1 | a0001c0001t0003g0148 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.570+37339A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28083138 | ||||||
| chr2:28083190
|
C | A | 21 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(18): Show | 21 | HG01109.hp2 HG02280.hp1 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.570+37391C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28083190 | ||||||
| chr2:28083419
|
T | C | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.570+37620T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28083419 | ||||||
| chr2:28083426
|
C | T | 8 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0002g0010others(5): Show | 8 | HG02280.hp1 HG02451.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.570+37627C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28083426 | ||||||
| chr2:28083742
|
A | G | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.570+37943A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28083742 | ||||||
| chr2:28083756
|
C | G | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.570+37957C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28083756 | ||||||
| chr2:28084041
|
A | T | 1 | a0001c0001t0002g0050 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.570+38242A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28084041 | ||||||
| chr2:28084062
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0002g0004 | 2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.570+38263G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28084062 | ||||||
| chr2:28084076
|
G | A | 35 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0001g0035others(32): Show | 35 | HG00140.hp1 HG01069.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.570+38277G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28084076 | ||||||
| chr2:28084111
|
T | C | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.570+38312T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28084111 | ||||||
| chr2:28084595
|
A | T | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02559.hp2 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+38796A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28084595 | ||||||
| chr2:28084924
|
G | A | 72 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0031others(69): Show | 72 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.570+39125G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28084924 | ||||||
| chr2:28085166
|
C | G | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.570+39367C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28085166 | ||||||
| chr2:28085300
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.570+39501C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28085300 | ||||||
| chr2:28085368
|
A | G | 1 | a0001c0001t0001g0155 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.570+39569A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28085368 | ||||||
| chr2:28085377
|
G | C | 2 | a0001c0001t0003g0089a0001c0001t0003g0090 | 2 | HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.570+39578G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28085377 | ||||||
| chr2:28085580
|
T | G | 149 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(146): Show | 149 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(146): Show |
intron_variant | MODIFIER | c.570+39781T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28085580 | ||||||
| chr2:28085595
|
A | G | 27 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(24): Show | 27 | HG01109.hp2 HG01496.hp1 HG02280.hp1 others(24): Show |
intron_variant | MODIFIER | c.570+39796A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28085595 | ||||||
| chr2:28086287
|
T | G | 157 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(154): Show | 157 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(154): Show |
intron_variant | MODIFIER | c.570+40488T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28086287 | ||||||
| chr2:28086411
|
G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02559.hp2 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+40612G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28086411 | ||||||
| chr2:28086710
|
A | G | 61 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0031others(58): Show | 61 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.570+40911A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28086710 | ||||||
| chr2:28086785
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02630.hp1 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.570+40986C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28086785 | ||||||
| chr2:28086862
|
T | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.570+41063T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28086862 | ||||||
| chr2:28087078
|
T | A | 4 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0003g0089others(1): Show | 4 | HG03209.hp2 NA18906.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+41279T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28087078 | ||||||
| chr2:28087209
|
A | G | 12 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0088others(9): Show | 12 | HG02280.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.570+41410A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28087209 | ||||||
| chr2:28087227
|
A | T | 24 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(21): Show | 24 | HG01109.hp2 HG02280.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.570+41428A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28087227 | ||||||
| chr2:28087235
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.570+41436G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28087235 | ||||||
| chr2:28087741
|
T | C | 137 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(134): Show | 137 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(134): Show |
intron_variant | MODIFIER | c.571-41530T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28087741 | ||||||
| chr2:28087794
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.571-41477G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28087794 | ||||||
| chr2:28087889
|
A | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02630.hp1 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.571-41382A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28087889 | ||||||
| chr2:28088018
|
C | A | 14 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0088others(11): Show | 14 | HG02280.hp1 HG02280.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.571-41253C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28088018 | ||||||
| chr2:28088140
|
T | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.571-41131T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28088140 | ||||||
| chr2:28088254
|
A | G | 16 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(13): Show | 16 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.571-41017A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28088254 | ||||||
| chr2:28088597
|
C | T | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.571-40674C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28088597 | ||||||
| chr2:28088761
|
G | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.571-40510G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28088761 | ||||||
| chr2:28088817
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02630.hp1 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.571-40454G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28088817 | ||||||
| chr2:28088875
|
A | C | 7 | a0001c0001t0001g0045a0001c0001t0001g0133a0001c0001t0001g0134others(4): Show | 7 | HG01496.hp1 HG02559.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-40396A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28088875 | ||||||
| chr2:28088925
|
A | G | 23 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(20): Show | 23 | HG01496.hp1 HG02280.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.571-40346A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28088925 | ||||||
| chr2:28089038
|
G | GT | 4 | a0001c0001t0001g0088a0001c0001t0002g0130a0001c0001t0002g0131others(1): Show | 4 | HG02280.hp2 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-40233_571-4023 others(5): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28089038 | ||||||
| chr2:28089039
|
G | GT | 10 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0060others(7): Show | 10 | HG01081.hp2 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.571-40222dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28089039 | |||||
| chr2:28089039
|
G | T | 4 | a0001c0001t0001g0088a0001c0001t0002g0130a0001c0001t0002g0131others(1): Show | 4 | HG02280.hp2 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-40232G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28089039 | ||||||
| chr2:28089075
|
C | T | 5 | a0001c0001t0002g0087a0001c0001t0002g0095a0001c0001t0002g0098others(2): Show | 5 | HG01106.hp2 HG01192.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-40196C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28089075 | ||||||
| chr2:28089268
|
G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02559.hp2 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-40003G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28089268 | ||||||
| chr2:28089269
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0044a0001c0001t0001g0139 | 3 | HG02258.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.571-40002C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28089269 | ||||||
| chr2:28089270
|
G | A | 3 | a0001c0001t0001g0045a0001c0001t0002g0140a0001c0001t0002g0141 | 3 | HG01496.hp1 HG02559.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.571-40001G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28089270 | ||||||
| chr2:28089271
|
C | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.571-40000C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28089271 | ||||||
| chr2:28089319
|
G | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0083 | 2 | HG00735.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.571-39952G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28089319 | ||||||
| chr2:28089331
|
A | G | 24 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(21): Show | 24 | HG01109.hp2 HG01496.hp1 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.571-39940A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28089331 | ||||||
| chr2:28089628
|
G | A | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.571-39643G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28089628 | ||||||
| chr2:28089889
|
G | T | 23 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(20): Show | 23 | HG01496.hp1 HG02280.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.571-39382G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28089889 | ||||||
| chr2:28089891
|
A | AT | 129 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(126): Show | 129 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(126): Show |
intron_variant | MODIFIER | c.571-39372dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28089891 | |||||
| chr2:28089906
|
G | A | 13 | a0001c0001t0001g0066a0001c0001t0001g0111a0001c0001t0001g0125others(10): Show | 13 | HG00741.hp2 HG02074.hp1 HG02148.hp1 others(10): Show |
intron_variant | MODIFIER | c.571-39365G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28089906 | ||||||
| chr2:28089965
|
A | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.571-39306A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28089965 | ||||||
| chr2:28089971
|
A | G | 9 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0065others(6): Show | 9 | HG00735.hp1 HG00738.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.571-39300A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28089971 | ||||||
| chr2:28090003
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.571-39268C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28090003 | ||||||
| chr2:28090241
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.571-39030A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28090241 | ||||||
| chr2:28090329
|
C | G | 3 | a0001c0001t0001g0097a0001c0001t0001g0123a0001c0001t0002g0114 | 3 | HG00140.hp1 HG01433.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.571-38942C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28090329 | ||||||
| chr2:28090435
|
G | T | 23 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(20): Show | 23 | HG01496.hp1 HG02280.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.571-38836G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28090435 | ||||||
| chr2:28090443
|
C | T | 1 | a0001c0001t0002g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.571-38828C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28090443 | ||||||
| chr2:28090623
|
A | T | 3 | a0001c0001t0003g0135a0001c0001t0003g0136a0001c0001t0003g0137 | 3 | HG00733.hp2 HG01167.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.571-38648A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28090623 | ||||||
| chr2:28090766
|
C | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.571-38505C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28090766 | ||||||
| chr2:28090771
|
G | C | 1 | a0001c0001t0001g0072 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.571-38500G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28090771 | ||||||
| chr2:28090778
|
G | A | 2 | a0001c0001t0003g0089a0001c0001t0003g0090 | 2 | HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.571-38493G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28090778 | ||||||
| chr2:28090806
|
C | T | 1 | a0001c0001t0002g0140 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.571-38465C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28090806 | ||||||
| chr2:28091069
|
A | T | 1 | a0001c0001t0002g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.571-38202A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28091069 | ||||||
| chr2:28091214
|
A | G | 1 | a0001c0001t0002g0077 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.571-38057A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28091214 | ||||||
| chr2:28091451
|
G | T | 1 | a0001c0001t0002g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.571-37820G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28091451 | ||||||
| chr2:28091495
|
T | C | 1 | a0001c0001t0002g0095 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.571-37776T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28091495 | ||||||
| chr2:28091497
|
C | T | 4 | a0001c0001t0001g0088a0001c0001t0002g0130a0001c0001t0002g0131others(1): Show | 4 | HG02280.hp2 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-37774C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28091497 | ||||||
| chr2:28091627
|
C | G | 2 | a0001c0001t0001g0094a0001c0001t0002g0101 | 2 | NA18955.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.571-37644C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28091627 | ||||||
| chr2:28091991
|
G | T | 60 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0031others(57): Show | 60 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.571-37280G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28091991 | ||||||
| chr2:28092055
|
C | T | 11 | a0001c0001t0001g0066a0001c0001t0001g0111a0001c0001t0001g0125others(8): Show | 11 | HG02074.hp1 HG02165.hp2 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.571-37216C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28092055 | ||||||
| chr2:28092138
|
A | T | 1 | a0001c0001t0002g0016 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.571-37133A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28092138 | ||||||
| chr2:28092227
|
G | A | 137 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(134): Show | 137 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(134): Show |
intron_variant | MODIFIER | c.571-37044G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28092227 | ||||||
| chr2:28092252
|
T | C | 2 | a0001c0001t0001g0008a0001c0001t0002g0004 | 2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.571-37019T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28092252 | ||||||
| chr2:28092263
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.571-37008G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28092263 | ||||||
| chr2:28092277
|
G | T | 60 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0031others(57): Show | 60 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.571-36994G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28092277 | ||||||
| chr2:28092278
|
C | T | 60 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0031others(57): Show | 60 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.571-36993C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28092278 | ||||||
| chr2:28092597
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.571-36674G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28092597 | ||||||
| chr2:28092691
|
A | G | 65 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(62): Show | 65 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.571-36580A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28092691 | ||||||
| chr2:28092749
|
C | CCT | 111 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(108): Show | 111 | HG00140.hp1 HG00639.hp1 HG00733.hp1 others(108): Show |
intron_variant | MODIFIER | c.571-36500_571-3649 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28092749 | |||||
| chr2:28092749
|
C | CCTCT | 3 | a0001c0001t0001g0082a0001c0001t0001g0139a0001c0001t0002g0110 | 3 | HG00140.hp2 HG02165.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.571-36502_571-3649 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28092749 | |||||
| chr2:28092860
|
AG | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.571-36409delG | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28092860 | |||||
| chr2:28092903
|
T | C | 2 | a0001c0001t0001g0093a0001c0001t0001g0102 | 2 | HG01069.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.571-36368T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28092903 | ||||||
| chr2:28093027
|
C | A | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.571-36244C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28093027 | ||||||
| chr2:28093124
|
T | C | 1 | a0001c0001t0002g0009 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.571-36147T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28093124 | ||||||
| chr2:28093150
|
C | A | 3 | a0001c0001t0001g0045a0001c0001t0002g0140a0001c0001t0002g0141 | 3 | HG01496.hp1 HG02559.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.571-36121C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28093150 | ||||||
| chr2:28093796
|
CAGTT | C | 11 | a0001c0001t0001g0066a0001c0001t0001g0111a0001c0001t0001g0125others(8): Show | 11 | HG02074.hp1 HG02165.hp2 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.571-35471_571-3546 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28093796 | |||||
| chr2:28093889
|
A | C | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.571-35382A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28093889 | ||||||
| chr2:28094219
|
A | G | 10 | a0001c0001t0001g0066a0001c0001t0001g0111a0001c0001t0001g0125others(7): Show | 10 | HG02074.hp1 HG02165.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.571-35052A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28094219 | ||||||
| chr2:28094338
|
T | C | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.571-34933T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28094338 | ||||||
| chr2:28094574
|
A | G | 65 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(62): Show | 65 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.571-34697A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28094574 | ||||||
| chr2:28094660
|
A | G | 2 | a0001c0001t0001g0008a0001c0001t0002g0004 | 2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.571-34611A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28094660 | ||||||
| chr2:28094774
|
G | A | 11 | a0001c0001t0001g0066a0001c0001t0001g0111a0001c0001t0001g0125others(8): Show | 11 | HG02074.hp1 HG02165.hp2 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.571-34497G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28094774 | ||||||
| chr2:28094907
|
C | CT | 13 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0088others(10): Show | 13 | HG02280.hp1 HG02280.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.571-34348dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28094907 | |||||
| chr2:28094942
|
A | G | 61 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0031others(58): Show | 61 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.571-34329A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28094942 | ||||||
| chr2:28095013
|
T | G | 1 | a0001c0001t0001g0080 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.571-34258T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28095013 | ||||||
| chr2:28095141
|
A | G | 17 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(14): Show | 17 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.571-34130A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28095141 | ||||||
| chr2:28095152
|
C | T | 4 | a0001c0001t0001g0088a0001c0001t0002g0130a0001c0001t0002g0131others(1): Show | 4 | HG02280.hp2 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-34119C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28095152 | ||||||
| chr2:28095191
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.571-34080G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28095191 | ||||||
| chr2:28095775
|
C | T | 1 | a0001c0001t0002g0108 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.571-33496C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28095775 | ||||||
| chr2:28095989
|
T | G | 1 | a0001c0001t0002g0095 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.571-33282T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28095989 | ||||||
| chr2:28096012
|
G | A | 45 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0066others(42): Show | 45 | HG00140.hp1 HG01069.hp2 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.571-33259G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28096012 | ||||||
| chr2:28096049
|
C | T | 48 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(45): Show | 48 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.571-33222C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28096049 | ||||||
| chr2:28096267
|
A | G | 44 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0032others(41): Show | 44 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.571-33004A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28096267 | ||||||
| chr2:28096316
|
T | C | 12 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0088others(9): Show | 12 | HG02280.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.571-32955T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28096316 | ||||||
| chr2:28096375
|
A | G | 14 | a0001c0001t0001g0022a0001c0001t0001g0044a0001c0001t0001g0066others(11): Show | 14 | HG02074.hp1 HG02165.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.571-32896A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28096375 | ||||||
| chr2:28096377
|
CA | C | 9 | a0001c0001t0001g0045a0001c0001t0001g0074a0001c0001t0001g0081others(6): Show | 9 | HG01168.hp2 HG01496.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.571-32880delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28096377 | |||||
| chr2:28096377
|
CAA | C | 76 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(73): Show | 76 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.571-32881_571-3288 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28096377 | |||||
| chr2:28096429
|
C | T | 80 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(77): Show | 80 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.571-32842C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28096429 | ||||||
| chr2:28096442
|
G | A | 3 | a0001c0001t0003g0135a0001c0001t0003g0136a0001c0001t0003g0137 | 3 | HG00733.hp2 HG01167.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.571-32829G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28096442 | ||||||
| chr2:28096453
|
T | C | 121 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(118): Show | 121 | HG00140.hp1 HG00639.hp1 HG00735.hp1 others(118): Show |
intron_variant | MODIFIER | c.571-32818T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28096453 | ||||||
| chr2:28096471
|
G | GAATATGA others(3): Show |
1 | a0001c0001t0002g0062 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.571-32799_571-3279 others(14): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28096471 | |||||
| chr2:28096807
|
G | A | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.571-32464G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28096807 | ||||||
| chr2:28096872
|
C | T | 44 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0032others(41): Show | 44 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.571-32399C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28096872 | ||||||
| chr2:28097007
|
G | A | 8 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0002g0010others(5): Show | 8 | HG02280.hp1 HG02451.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.571-32264G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28097007 | ||||||
| chr2:28097032
|
A | T | 1 | a0001c0001t0001g0083 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.571-32239A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28097032 | ||||||
| chr2:28097090
|
A | G | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02559.hp2 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-32181A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28097090 | ||||||
| chr2:28097094
|
G | T | 34 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0091others(31): Show | 34 | HG00140.hp1 HG01069.hp2 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.571-32177G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28097094 | ||||||
| chr2:28097166
|
T | C | 34 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0091others(31): Show | 34 | HG00140.hp1 HG01069.hp2 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.571-32105T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28097166 | ||||||
| chr2:28097314
|
C | T | 80 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(77): Show | 80 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.571-31957C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28097314 | ||||||
| chr2:28097474
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.571-31797A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28097474 | ||||||
| chr2:28097809
|
G | A | 5 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012others(2): Show | 5 | HG02572.hp1 HG02698.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-31462G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28097809 | ||||||
| chr2:28097922
|
T | A | 3 | a0001c0001t0003g0135a0001c0001t0003g0136a0001c0001t0003g0137 | 3 | HG00733.hp2 HG01167.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.571-31349T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28097922 | ||||||
| chr2:28097986
|
T | C | 5 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012others(2): Show | 5 | HG02572.hp1 HG02698.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-31285T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28097986 | ||||||
| chr2:28098143
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.571-31128T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28098143 | ||||||
| chr2:28098189
|
A | G | 34 | a0001c0001t0001g0022a0001c0001t0001g0044a0001c0001t0001g0045others(31): Show | 34 | HG00741.hp2 HG01109.hp2 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.571-31082A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28098189 | ||||||
| chr2:28098506
|
G | A | 8 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0002g0010others(5): Show | 8 | HG02280.hp1 HG02451.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.571-30765G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28098506 | ||||||
| chr2:28098606
|
A | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.571-30665A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28098606 | ||||||
| chr2:28098731
|
T | C | 3 | a0001c0001t0001g0045a0001c0001t0002g0140a0001c0001t0002g0141 | 3 | HG01496.hp1 HG02559.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.571-30540T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28098731 | ||||||
| chr2:28099170
|
A | T | 14 | a0001c0001t0001g0022a0001c0001t0001g0044a0001c0001t0001g0066others(11): Show | 14 | HG02074.hp1 HG02165.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.571-30101A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28099170 | ||||||
| chr2:28099455
|
C | T | 5 | a0001c0001t0001g0045a0001c0001t0001g0133a0001c0001t0001g0134others(2): Show | 5 | HG01496.hp1 HG02559.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-29816C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28099455 | ||||||
| chr2:28099593
|
G | A | 48 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(45): Show | 48 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.571-29678G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28099593 | ||||||
| chr2:28099726
|
G | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.571-29545G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28099726 | ||||||
| chr2:28099872
|
T | A | 1 | a0001c0001t0002g0116 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.571-29399T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28099872 | ||||||
| chr2:28100123
|
G | C | 1 | a0001c0001t0001g0102 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.571-29148G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28100123 | ||||||
| chr2:28100140
|
G | A | 11 | a0001c0001t0001g0066a0001c0001t0001g0111a0001c0001t0001g0125others(8): Show | 11 | HG02074.hp1 HG02165.hp2 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.571-29131G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28100140 | ||||||
| chr2:28100303
|
A | G | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.571-28968A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28100303 | ||||||
| chr2:28100328
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.571-28943C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28100328 | ||||||
| chr2:28100353
|
G | A | 14 | a0001c0001t0001g0022a0001c0001t0001g0044a0001c0001t0001g0066others(11): Show | 14 | HG02074.hp1 HG02165.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.571-28918G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28100353 | ||||||
| chr2:28100415
|
G | A | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.571-28856G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28100415 | ||||||
| chr2:28100446
|
C | T | 32 | a0001c0001t0001g0022a0001c0001t0001g0044a0001c0001t0001g0045others(29): Show | 32 | HG01109.hp2 HG01496.hp1 HG02074.hp1 others(29): Show |
intron_variant | MODIFIER | c.571-28825C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28100446 | ||||||
| chr2:28100462
|
C | CA | 93 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0022others(90): Show | 93 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(90): Show |
intron_variant | MODIFIER | c.571-28789dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28100462 | |||||
| chr2:28100474
|
A | G | 2 | a0001c0001t0003g0089a0001c0001t0003g0090 | 2 | HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.571-28797A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28100474 | ||||||
| chr2:28100730
|
G | A | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.571-28541G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28100730 | ||||||
| chr2:28100962
|
A | C | 1 | a0001c0001t0002g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.571-28309A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28100962 | ||||||
| chr2:28100972
|
T | C | 1 | a0001c0001t0002g0063 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.571-28299T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28100972 | ||||||
| chr2:28101002
|
C | T | 12 | a0001c0001t0001g0066a0001c0001t0001g0111a0001c0001t0001g0125others(9): Show | 12 | HG00741.hp2 HG02074.hp1 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.571-28269C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28101002 | ||||||
| chr2:28101190
|
C | T | 1 | a0001c0001t0002g0103 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.571-28081C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28101190 | ||||||
| chr2:28101263
|
A | G | 65 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(62): Show | 65 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.571-28008A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28101263 | ||||||
| chr2:28101379
|
G | C | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02559.hp2 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-27892G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28101379 | ||||||
| chr2:28101563
|
C | T | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.571-27708C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28101563 | ||||||
| chr2:28101842
|
TC | T | 49 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(46): Show | 49 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.571-27425delC | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28101842 | |||||
| chr2:28101888
|
T | C | 1 | a0001c0001t0002g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.571-27383T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28101888 | ||||||
| chr2:28101969
|
C | G | 2 | a0001c0001t0002g0001a0001c0001t0002g0002 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.571-27302C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28101969 | ||||||
| chr2:28102169
|
C | T | 4 | a0001c0001t0001g0088a0001c0001t0002g0130a0001c0001t0002g0131others(1): Show | 4 | HG02280.hp2 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-27102C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28102169 | ||||||
| chr2:28102219
|
C | T | 1 | a0001c0001t0002g0114 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.571-27052C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28102219 | ||||||
| chr2:28102220
|
G | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.571-27051G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28102220 | ||||||
| chr2:28102263
|
A | C | 2 | a0001c0001t0003g0089a0001c0001t0003g0090 | 2 | HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.571-27008A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28102263 | ||||||
| chr2:28102334
|
C | T | 86 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(83): Show | 86 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(83): Show |
intron_variant | MODIFIER | c.571-26937C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28102334 | ||||||
| chr2:28102664
|
A | C | 1 | a0001c0001t0002g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.571-26607A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28102664 | ||||||
| chr2:28102678
|
C | T | 3 | a0001c0001t0003g0135a0001c0001t0003g0136a0001c0001t0003g0137 | 3 | HG00733.hp2 HG01167.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.571-26593C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28102678 | ||||||
| chr2:28102831
|
A | G | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.571-26440A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28102831 | ||||||
| chr2:28103142
|
T | TA | 9 | a0001c0001t0001g0022a0001c0001t0001g0044a0001c0001t0001g0075others(6): Show | 9 | HG00735.hp2 HG01346.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.571-26114dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28103142 | |||||
| chr2:28103158
|
T | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02559.hp2 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-26113T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28103158 | ||||||
| chr2:28103232
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.571-26039A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28103232 | ||||||
| chr2:28103301
|
T | TTTTTG | 20 | a0001c0001t0001g0066a0001c0001t0001g0074a0001c0001t0001g0081others(17): Show | 20 | HG00741.hp2 HG01109.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.571-25945_571-2594 others(9): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28103301 | |||||
| chr2:28103301
|
T | TTTTTGTT others(3): Show |
74 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(71): Show | 74 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.571-25950_571-2594 others(14): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28103301 | |||||
| chr2:28103301
|
T | TTTTTGTT others(8): Show |
6 | a0001c0001t0001g0065a0001c0001t0001g0083a0001c0001t0001g0088others(3): Show | 6 | HG00735.hp1 HG01099.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-25955_571-2594 others(19): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28103301 | |||||
| chr2:28103301
|
TTTTTG | T | 3 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039 | 3 | HG02922.hp1 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.571-25945_571-2594 others(9): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28103301 | |||||
| chr2:28103388
|
C | G | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.571-25883C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28103388 | ||||||
| chr2:28103391
|
G | C | 98 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(95): Show | 98 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(95): Show |
intron_variant | MODIFIER | c.571-25880G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28103391 | ||||||
| chr2:28103982
|
AT | A | 4 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012others(1): Show | 4 | HG02572.hp1 HG02647.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-25282delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28103982 | |||||
| chr2:28104349
|
A | C | 18 | a0001c0001t0001g0045a0001c0001t0001g0066a0001c0001t0001g0111others(15): Show | 18 | HG00741.hp2 HG01496.hp1 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.571-24922A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28104349 | ||||||
| chr2:28104374
|
C | A | 1 | a0001c0001t0001g0066 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.571-24897C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28104374 | ||||||
| chr2:28104403
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.571-24868G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28104403 | ||||||
| chr2:28104404
|
A | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.571-24867A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28104404 | ||||||
| chr2:28104468
|
G | A | 1 | a0001c0001t0002g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.571-24803G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28104468 | ||||||
| chr2:28104515
|
T | C | 1 | a0001c0001t0002g0001 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.571-24756T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28104515 | ||||||
| chr2:28104585
|
T | C | 2 | a0001c0001t0001g0008a0001c0001t0002g0004 | 2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.571-24686T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28104585 | ||||||
| chr2:28104647
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.571-24624T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28104647 | ||||||
| chr2:28104719
|
G | T | 60 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0031others(57): Show | 60 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.571-24552G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28104719 | ||||||
| chr2:28104869
|
A | G | 2 | a0001c0001t0003g0089a0001c0001t0003g0090 | 2 | HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.571-24402A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28104869 | ||||||
| chr2:28104916
|
C | A | 5 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012others(2): Show | 5 | HG02572.hp1 HG02698.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-24355C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28104916 | ||||||
| chr2:28104938
|
G | A | 3 | a0001c0001t0001g0045a0001c0001t0002g0140a0001c0001t0002g0141 | 3 | HG01496.hp1 HG02559.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.571-24333G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28104938 | ||||||
| chr2:28104955
|
T | C | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.571-24316T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28104955 | ||||||
| chr2:28104963
|
C | G | 42 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0032others(39): Show | 42 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.571-24308C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28104963 | ||||||
| chr2:28104965
|
C | T | 12 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(9): Show | 12 | HG02280.hp1 HG02451.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.571-24306C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28104965 | ||||||
| chr2:28105052
|
T | TG | 9 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(6): Show | 9 | HG02559.hp2 HG02572.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.571-24214dupG | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28105052 | |||||
| chr2:28105160
|
C | T | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(7): Show | 10 | HG00639.hp2 HG01109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.571-24111C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28105160 | ||||||
| chr2:28105444
|
G | A | 12 | a0001c0001t0001g0066a0001c0001t0001g0111a0001c0001t0001g0125others(9): Show | 12 | HG02074.hp1 HG02165.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.571-23827G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28105444 | ||||||
| chr2:28105570
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02630.hp1 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.571-23701C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28105570 | ||||||
| chr2:28105593
|
T | G | 5 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012others(2): Show | 5 | HG02572.hp1 HG02698.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-23678T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28105593 | ||||||
| chr2:28105629
|
G | A | 5 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012others(2): Show | 5 | HG02572.hp1 HG02698.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-23642G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28105629 | ||||||
| chr2:28105631
|
T | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.571-23640T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28105631 | ||||||
| chr2:28105721
|
G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02559.hp2 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-23550G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28105721 | ||||||
| chr2:28105735
|
G | A | 5 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012others(2): Show | 5 | HG02572.hp1 HG02698.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-23536G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28105735 | ||||||
| chr2:28105940
|
C | CT | 24 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(21): Show | 24 | HG00733.hp2 HG01167.hp2 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.571-23318dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28105940 | |||||
| chr2:28106219
|
T | C | 1 | a0001c0001t0002g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.571-23052T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28106219 | ||||||
| chr2:28106225
|
T | A | 6 | a0001c0001t0002g0010a0001c0001t0002g0016a0001c0001t0002g0020others(3): Show | 6 | HG02451.hp1 HG02897.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-23046T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28106225 | ||||||
| chr2:28106315
|
G | A | 1 | a0001c0001t0002g0130 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.571-22956G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28106315 | ||||||
| chr2:28106446
|
A | C | 12 | a0001c0001t0001g0066a0001c0001t0001g0070a0001c0001t0001g0111others(9): Show | 12 | HG02074.hp1 HG02165.hp2 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.571-22825A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28106446 | ||||||
| chr2:28106534
|
A | G | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(7): Show | 10 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.571-22737A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28106534 | ||||||
| chr2:28106721
|
TA | T | 2 | a0001c0001t0002g0130a0001c0001t0002g0131 | 2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.571-22547delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28106721 | |||||
| chr2:28106735
|
T | C | 152 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(149): Show | 152 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(149): Show |
intron_variant | MODIFIER | c.571-22536T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28106735 | ||||||
| chr2:28106736
|
C | A | 1 | a0001c0001t0001g0057 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.571-22535C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28106736 | ||||||
| chr2:28106775
|
C | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.571-22496C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28106775 | ||||||
| chr2:28106927
|
T | C | 3 | a0001c0001t0001g0045a0001c0001t0002g0140a0001c0001t0002g0141 | 3 | HG01496.hp1 HG02559.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.571-22344T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28106927 | ||||||
| chr2:28106963
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-22308C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28106963 | ||||||
| chr2:28107002
|
C | G | 1 | a0001c0001t0001g0057 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.571-22269C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28107002 | ||||||
| chr2:28107028
|
A | G | 92 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(89): Show | 92 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.571-22243A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28107028 | ||||||
| chr2:28107049
|
G | A | 152 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(149): Show | 152 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(149): Show |
intron_variant | MODIFIER | c.571-22222G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28107049 | ||||||
| chr2:28107071
|
G | A | 6 | a0001c0001t0001g0008a0001c0001t0001g0111a0001c0001t0001g0125others(3): Show | 6 | HG01168.hp2 HG02602.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-22200G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28107071 | ||||||
| chr2:28107092
|
T | C | 3 | a0001c0001t0001g0044a0001c0001t0002g0001a0001c0001t0002g0002 | 3 | HG02258.hp2 HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.571-22179T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28107092 | ||||||
| chr2:28107204
|
A | G | 18 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(15): Show | 18 | HG01168.hp2 HG02074.hp1 HG02165.hp2 others(15): Show |
intron_variant | MODIFIER | c.571-22067A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28107204 | ||||||
| chr2:28107550
|
C | G | 4 | a0001c0001t0002g0010a0001c0001t0002g0016a0001c0001t0002g0020others(1): Show | 4 | HG02897.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-21721C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28107550 | ||||||
| chr2:28107566
|
T | C | 15 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(12): Show | 15 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.571-21705T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28107566 | ||||||
| chr2:28107634
|
C | A | 1 | a0001c0001t0001g0086 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.571-21637C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28107634 | ||||||
| chr2:28107772
|
C | A | 15 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(12): Show | 15 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.571-21499C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28107772 | ||||||
| chr2:28107791
|
G | C | 2 | a0001c0001t0002g0122a0001c0001t0003g0121 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.571-21480G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28107791 | ||||||
| chr2:28107977
|
A | T | 1 | a0001c0001t0001g0138 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.571-21294A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28107977 | ||||||
| chr2:28108138
|
G | A | 1 | a0001c0001t0002g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.571-21133G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28108138 | ||||||
| chr2:28108346
|
C | T | 4 | a0001c0001t0002g0010a0001c0001t0002g0016a0001c0001t0002g0020others(1): Show | 4 | HG02897.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-20925C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28108346 | ||||||
| chr2:28108927
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.571-20344G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28108927 | ||||||
| chr2:28108985
|
GT | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.571-20285delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28108985 | ||||||
| chr2:28109045
|
G | T | 1 | a0001c0001t0001g0041 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.571-20226G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28109045 | ||||||
| chr2:28109074
|
A | G | 1 | a0001c0001t0002g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.571-20197A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28109074 | ||||||
| chr2:28109184
|
C | CT | 30 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(27): Show | 30 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.571-20065dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28109184 | |||||
| chr2:28109184
|
C | CTT | 10 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(7): Show | 10 | HG00735.hp2 HG01081.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.571-20066_571-2006 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28109184 | |||||
| chr2:28109184
|
C | CTTT | 8 | a0001c0001t0001g0079a0001c0001t0001g0088a0001c0001t0002g0108others(5): Show | 8 | HG00733.hp2 HG01167.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.571-20067_571-2006 others(7): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28109184 | |||||
| chr2:28109184
|
CT | C | 10 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0001g0094others(7): Show | 10 | HG02572.hp1 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.571-20065delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28109184 | |||||
| chr2:28109228
|
G | A | 1 | a0001c0001t0002g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.571-20043G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28109228 | ||||||
| chr2:28109281
|
T | C | 152 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(149): Show | 152 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(149): Show |
intron_variant | MODIFIER | c.571-19990T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28109281 | ||||||
| chr2:28109350
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0025 | 2 | HG02735.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.571-19921G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28109350 | ||||||
| chr2:28109521
|
A | G | 5 | a0001c0001t0001g0045a0001c0001t0002g0140a0001c0001t0002g0141others(2): Show | 5 | HG00733.hp2 HG01167.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-19750A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28109521 | ||||||
| chr2:28109546
|
C | T | 1 | a0001c0001t0002g0116 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.571-19725C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28109546 | ||||||
| chr2:28109562
|
T | A | 1 | a0001c0001t0001g0155 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.571-19709T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28109562 | ||||||
| chr2:28109703
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.571-19568G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28109703 | ||||||
| chr2:28109884
|
A | G | 21 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(18): Show | 21 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.571-19387A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28109884 | ||||||
| chr2:28109913
|
G | A | 2 | a0001c0001t0003g0135a0001c0001t0003g0136 | 2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.571-19358G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28109913 | ||||||
| chr2:28110081
|
G | A | 3 | a0001c0001t0001g0097a0001c0001t0001g0123a0001c0001t0002g0114 | 3 | HG00140.hp1 HG01433.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.571-19190G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28110081 | ||||||
| chr2:28110209
|
TG | T | 35 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(32): Show | 35 | HG00639.hp1 HG00639.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.571-19061delG | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28110209 | ||||||
| chr2:28110242
|
A | G | 35 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(32): Show | 35 | HG00639.hp1 HG00639.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.571-19029A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28110242 | ||||||
| chr2:28110320
|
A | G | 5 | a0001c0001t0001g0088a0001c0001t0002g0108a0001c0001t0002g0130others(2): Show | 5 | HG02280.hp2 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-18951A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28110320 | ||||||
| chr2:28110517
|
G | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.571-18754G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28110517 | ||||||
| chr2:28110838
|
C | G | 2 | a0001c0001t0002g0001a0001c0001t0002g0002 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.571-18433C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28110838 | ||||||
| chr2:28110970
|
C | CT | 8 | a0001c0001t0001g0044a0001c0001t0001g0078a0001c0001t0001g0123others(5): Show | 8 | HG00140.hp1 HG02148.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.571-18285dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28110970 | |||||
| chr2:28111132
|
CTATTTTT others(11): Show |
C | 30 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(27): Show | 30 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.571-18126_571-1810 others(22): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28111132 | |||||
| chr2:28111134
|
A | AT | 12 | a0001c0001t0001g0032a0001c0001t0001g0069a0001c0001t0001g0074others(9): Show | 12 | HG00140.hp2 HG00738.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.571-18122dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28111134 | |||||
| chr2:28111424
|
G | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0054a0001c0001t0001g0055others(1): Show | 4 | HG02280.hp1 HG02451.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-17847G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28111424 | ||||||
| chr2:28111488
|
T | A | 5 | a0001c0001t0001g0088a0001c0001t0002g0108a0001c0001t0002g0130others(2): Show | 5 | HG02280.hp2 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-17783T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28111488 | ||||||
| chr2:28111578
|
C | G | 21 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(18): Show | 21 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.571-17693C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28111578 | ||||||
| chr2:28111652
|
CT | C | 16 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(13): Show | 16 | HG01168.hp2 HG02074.hp1 HG02165.hp2 others(13): Show |
intron_variant | MODIFIER | c.571-17615delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28111652 | |||||
| chr2:28111830
|
G | A | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG02074.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.571-17441G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28111830 | ||||||
| chr2:28111916
|
C | G | 4 | a0001c0001t0002g0010a0001c0001t0002g0016a0001c0001t0002g0020others(1): Show | 4 | HG02897.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-17355C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28111916 | ||||||
| chr2:28112083
|
C | CTCTT | 23 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0040others(20): Show | 23 | HG00140.hp1 HG01069.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.571-17126_571-1712 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112083 | |||||
| chr2:28112083
|
C | CTCTTTCT others(1): Show |
18 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0041others(15): Show | 18 | HG00639.hp2 HG00733.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.571-17130_571-1712 others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112083 | |||||
| chr2:28112083
|
C | CTCTTTCT others(5): Show |
15 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0034others(12): Show | 15 | HG00735.hp1 HG00738.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.571-17134_571-1712 others(16): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112083 | |||||
| chr2:28112083
|
C | CTCTTTCT others(9): Show |
11 | a0001c0001t0001g0060a0001c0001t0001g0072a0001c0001t0001g0082others(8): Show | 11 | HG00140.hp2 HG00738.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.571-17138_571-1712 others(20): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112083 | |||||
| chr2:28112083
|
C | CTCTTTCT others(13): Show |
5 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0001g0153others(2): Show | 5 | HG00733.hp1 HG02145.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-17142_571-1712 others(24): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112083 | |||||
| chr2:28112083
|
C | CTCTTTCT others(17): Show |
3 | a0001c0001t0001g0008a0001c0001t0001g0017a0002c0002t0001g0085 | 3 | HG01433.hp1 HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.571-17146_571-1712 others(28): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112083 | |||||
| chr2:28112083
|
C | CTCTTTCT others(21): Show |
1 | a0001c0001t0002g0036 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.571-17150_571-1712 others(32): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112083 | |||||
| chr2:28112106
|
T | C | 1 | a0001c0001t0002g0007 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.571-17165T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112106 | ||||||
| chr2:28112135
|
TTCTTTCT others(25): Show |
T | 1 | a0001c0001t0001g0142 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.571-17133_571-1710 others(36): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112135 | |||||
| chr2:28112137
|
C | CTTTCTTT others(11): Show |
1 | a0001c0001t0001g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.571-17123_571-1712 others(22): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112137 | |||||
| chr2:28112138
|
T | C | 1 | a0001c0001t0003g0067 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.571-17133T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112138 | ||||||
| chr2:28112139
|
T | C | 1 | a0001c0001t0003g0067 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.571-17132T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112139 | ||||||
| chr2:28112142
|
T | C | 5 | a0001c0001t0001g0044a0001c0001t0001g0139a0001c0001t0002g0002others(2): Show | 5 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-17129T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112142 | ||||||
| chr2:28112143
|
T | C | 5 | a0001c0001t0001g0044a0001c0001t0001g0139a0001c0001t0002g0002others(2): Show | 5 | HG02258.hp2 HG02486.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-17128T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112143 | ||||||
| chr2:28112143
|
TTCTTTAC others(5): Show |
T | 1 | a0001c0001t0001g0104 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.571-17125_571-1711 others(16): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112143 | |||||
| chr2:28112145
|
C | CTTTCTTT others(11): Show |
1 | a0001c0001t0001g0056 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.571-17123_571-1712 others(22): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112145 | |||||
| chr2:28112146
|
T | C | 14 | a0001c0001t0001g0027a0001c0001t0001g0043a0001c0001t0001g0044others(11): Show | 14 | HG00741.hp2 HG02135.hp1 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.571-17125T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112146 | ||||||
| chr2:28112146
|
T | TTTCTTTC others(5): Show |
1 | a0001c0001t0002g0028 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.571-17123_571-1712 others(16): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112146 | |||||
| chr2:28112146
|
T | TTTCTTTC others(9): Show |
1 | a0001c0001t0001g0052 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.571-17123_571-1712 others(20): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112146 | |||||
| chr2:28112146
|
T | TTTCTTTC others(21): Show |
1 | a0001c0001t0001g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.571-17123_571-1712 others(32): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112146 | |||||
| chr2:28112147
|
T | C | 14 | a0001c0001t0001g0027a0001c0001t0001g0043a0001c0001t0001g0044others(11): Show | 14 | HG00741.hp2 HG02135.hp1 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.571-17124T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112147 | ||||||
| chr2:28112147
|
T | TTCTTTCC others(17): Show |
1 | a0001c0001t0002g0046 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.571-17123_571-1712 others(28): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112147 | |||||
| chr2:28112147
|
T | TTCTTTCT others(9): Show |
1 | a0001c0001t0001g0054 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.571-17123_571-1712 others(20): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112147 | |||||
| chr2:28112147
|
T | TTCTTTCT others(9): Show |
1 | a0001c0001t0001g0071 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.571-17123_571-1712 others(20): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112147 | |||||
| chr2:28112147
|
T | TTCTTTCT others(29): Show |
1 | a0001c0001t0001g0055 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.571-17123_571-1712 others(40): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112147 | |||||
| chr2:28112147
|
T | TTCTTTCT others(36): Show |
1 | a0001c0001t0003g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.571-17123_571-1712 others(47): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112147 | |||||
| chr2:28112147
|
T | TTCTTTCT others(17): Show |
1 | a0001c0001t0002g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.571-17123_571-1712 others(28): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112147 | |||||
| chr2:28112147
|
T | TTCTTTCT others(41): Show |
1 | a0001c0001t0002g0049 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.571-17123_571-1712 others(52): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112147 | |||||
| chr2:28112147
|
T | TTCTTTCT others(33): Show |
1 | a0001c0001t0001g0086 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.571-17123_571-1712 others(44): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112147 | |||||
| chr2:28112147
|
T | TTCTTTCT others(33): Show |
1 | a0001c0001t0002g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.571-17123_571-1712 others(44): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112147 | |||||
| chr2:28112147
|
T | TTCTTTCT others(49): Show |
2 | a0001c0001t0002g0048a0001c0001t0002g0051 | 2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.571-17123_571-1712 others(60): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112147 | |||||
| chr2:28112147
|
T | TTCTTTCT others(29): Show |
1 | a0001c0001t0002g0158 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.571-17123_571-1712 others(40): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112147 | |||||
| chr2:28112147
|
TTACC | T | 4 | a0001c0001t0002g0016a0001c0001t0002g0076a0001c0001t0002g0108others(1): Show | 4 | HG03516.hp1 HG03540.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-17122_571-1711 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112147 | |||||
| chr2:28112147
|
TTACCTCC others(1): Show |
T | 2 | a0001c0001t0001g0035a0001c0001t0002g0009 | 2 | HG01346.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.571-17122_571-1711 others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112147 | |||||
| chr2:28112147
|
TTACCTCC others(9): Show |
T | 1 | a0001c0001t0002g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.571-17122_571-1710 others(20): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112147 | |||||
| chr2:28112147
|
TTACCTCC others(17): Show |
T | 1 | a0001c0001t0002g0098 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.571-17122_571-1709 others(28): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112147 | |||||
| chr2:28112148
|
T | TCTTTCTT others(14): Show |
1 | a0001c0001t0001g0073 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.571-17123_571-1712 others(25): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112148 | ||||||
| chr2:28112148
|
TAC | T | 5 | a0001c0001t0001g0059a0001c0001t0001g0075a0001c0001t0001g0097others(2): Show | 5 | HG00735.hp2 HG01346.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-17122_571-1712 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112148 | ||||||
| chr2:28112149
|
A | C | 138 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(135): Show | 138 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(135): Show |
intron_variant | MODIFIER | c.571-17122A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112149 | ||||||
| chr2:28112149
|
ACCTCCCT others(1): Show |
A | 2 | a0001c0001t0002g0122a0001c0001t0003g0121 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.571-17078_571-1707 others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112149 | |||||
| chr2:28112149
|
ACCTCCCT others(9): Show |
A | 1 | a0001c0001t0001g0138 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.571-17086_571-1707 others(20): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112149 | |||||
| chr2:28112150
|
C | T | 62 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0024others(59): Show | 62 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.571-17121C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112150 | ||||||
| chr2:28112151
|
C | CTTTCTTT others(15): Show |
2 | a0001c0001t0001g0075a0001c0001t0002g0117 | 2 | HG00735.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.571-17119_571-1711 others(26): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112151 | |||||
| chr2:28112151
|
C | CTTTCTTT others(19): Show |
2 | a0001c0001t0001g0059a0001c0001t0001g0097 | 2 | HG01346.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.571-17119_571-1711 others(30): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112151 | |||||
| chr2:28112151
|
C | CTTTCTTT others(21): Show |
1 | a0001c0001t0001g0133 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.571-17119_571-1711 others(32): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112151 | |||||
| chr2:28112151
|
C | T | 67 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(64): Show | 67 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.571-17120C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112151 | ||||||
| chr2:28112154
|
C | T | 53 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0032others(50): Show | 53 | HG00140.hp1 HG01069.hp2 HG01106.hp2 others(50): Show |
intron_variant | MODIFIER | c.571-17117C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112154 | ||||||
| chr2:28112155
|
C | T | 57 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0032others(54): Show | 57 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.571-17116C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112155 | ||||||
| chr2:28112158
|
C | T | 30 | a0001c0001t0001g0015a0001c0001t0001g0078a0001c0001t0001g0088others(27): Show | 30 | HG01106.hp2 HG01192.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.571-17113C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112158 | ||||||
| chr2:28112159
|
C | T | 31 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0078others(28): Show | 31 | HG01106.hp2 HG01192.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.571-17112C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112159 | ||||||
| chr2:28112162
|
C | T | 17 | a0001c0001t0001g0015a0001c0001t0001g0078a0001c0001t0001g0088others(14): Show | 17 | HG01346.hp1 HG02109.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.571-17109C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112162 | ||||||
| chr2:28112163
|
C | T | 20 | a0001c0001t0001g0015a0001c0001t0001g0078a0001c0001t0001g0088others(17): Show | 20 | HG01167.hp1 HG01346.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.571-17108C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112163 | ||||||
| chr2:28112166
|
C | T | 8 | a0001c0001t0002g0010a0001c0001t0002g0016a0001c0001t0002g0020others(5): Show | 8 | HG02897.hp1 HG03139.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.571-17105C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112166 | ||||||
| chr2:28112167
|
C | T | 10 | a0001c0001t0001g0078a0001c0001t0002g0010a0001c0001t0002g0016others(7): Show | 10 | HG02818.hp1 HG02897.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.571-17104C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112167 | ||||||
| chr2:28112169
|
C | CCCTTCCT others(16): Show |
1 | a0001c0001t0001g0154 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.571-17099_571-1709 others(27): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112169 | |||||
| chr2:28112169
|
C | CCCTTCCT others(20): Show |
1 | a0001c0001t0001g0150 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.571-17099_571-1709 others(31): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112169 | |||||
| chr2:28112169
|
C | CCCTTCCT others(24): Show |
1 | a0001c0001t0001g0125 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.571-17099_571-1709 others(35): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112169 | |||||
| chr2:28112169
|
C | CCCTTCCT others(36): Show |
1 | a0001c0001t0001g0155 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.571-17099_571-1709 others(47): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112169 | |||||
| chr2:28112170
|
C | T | 3 | a0001c0001t0002g0010a0001c0001t0002g0016a0001c0001t0002g0112 | 3 | HG03139.hp1 HG03516.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.571-17101C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112170 | ||||||
| chr2:28112171
|
C | T | 3 | a0001c0001t0002g0010a0001c0001t0002g0016a0001c0001t0002g0112 | 3 | HG03139.hp1 HG03516.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.571-17100C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112171 | ||||||
| chr2:28112173
|
C | CCCTTCCT others(20): Show |
1 | a0001c0001t0001g0043 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.571-17095_571-1709 others(31): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112173 | |||||
| chr2:28112173
|
C | CCCTTCCT others(24): Show |
1 | a0001c0001t0001g0008 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.571-17095_571-1709 others(35): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112173 | |||||
| chr2:28112173
|
C | CCCTTCCT others(32): Show |
1 | a0001c0001t0002g0145 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.571-17095_571-1709 others(43): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112173 | |||||
| chr2:28112173
|
C | T | 4 | a0001c0001t0001g0125a0001c0001t0001g0150a0001c0001t0001g0154others(1): Show | 4 | HG00741.hp2 HG02165.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-17098C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112173 | ||||||
| chr2:28112177
|
C | CCCTTCCT others(24): Show |
1 | a0001c0001t0003g0148 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.571-17091_571-1709 others(35): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112177 | |||||
| chr2:28112177
|
C | CCCTTCCT others(28): Show |
1 | a0001c0001t0001g0013 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.571-17091_571-1709 others(39): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112177 | |||||
| chr2:28112177
|
C | CCCTTCCT others(32): Show |
2 | a0001c0001t0001g0143a0001c0001t0002g0151 | 2 | HG02148.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.571-17091_571-1709 others(43): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112177 | |||||
| chr2:28112177
|
C | CCCTTCCT others(36): Show |
1 | a0001c0001t0002g0144 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.571-17091_571-1709 others(47): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112177 | |||||
| chr2:28112177
|
C | T | 7 | a0001c0001t0001g0008a0001c0001t0001g0043a0001c0001t0001g0125others(4): Show | 7 | HG00741.hp2 HG02165.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-17094C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112177 | ||||||
| chr2:28112179
|
C | T | 2 | a0001c0001t0002g0046a0001c0001t0002g0126 | 2 | HG00639.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.571-17092C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112179 | ||||||
| chr2:28112181
|
C | CCCTTCCT others(20): Show |
1 | a0001c0001t0001g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.571-17087_571-1708 others(31): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112181 | |||||
| chr2:28112181
|
C | CCCTTCCT others(36): Show |
1 | a0001c0001t0001g0146 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.571-17087_571-1708 others(47): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112181 | |||||
| chr2:28112181
|
C | T | 16 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0043others(13): Show | 16 | HG00741.hp2 HG01167.hp1 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.571-17090C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112181 | ||||||
| chr2:28112185
|
C | CCCTTCCT others(13): Show |
1 | a0001c0001t0003g0067 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.571-17083_571-1708 others(24): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112185 | |||||
| chr2:28112185
|
C | CCCTTCCT others(32): Show |
1 | a0001c0001t0001g0111 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.571-17083_571-1708 others(43): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112185 | |||||
| chr2:28112185
|
C | T | 18 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(15): Show | 18 | HG00741.hp2 HG01167.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.571-17086C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112185 | ||||||
| chr2:28112187
|
C | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0002g0002 | 3 | HG02258.hp2 HG02486.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.571-17084C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112187 | ||||||
| chr2:28112189
|
C | CCCTTCCT others(5): Show |
1 | a0001c0001t0002g0140 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.571-17079_571-1707 others(16): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112189 | |||||
| chr2:28112189
|
C | CCCTTCCT others(13): Show |
1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.571-17079_571-1707 others(24): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112189 | |||||
| chr2:28112189
|
C | CCCTTCCT others(21): Show |
1 | a0001c0001t0002g0068 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.571-17079_571-1707 others(32): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112189 | |||||
| chr2:28112189
|
C | CCCTTCCT others(29): Show |
2 | a0001c0001t0002g0038a0001c0001t0002g0152 | 2 | HG02922.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.571-17079_571-1707 others(40): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112189 | |||||
| chr2:28112189
|
C | CCCTTCCT others(41): Show |
1 | a0001c0001t0001g0065 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.571-17079_571-1707 others(52): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112189 | |||||
| chr2:28112189
|
C | T | 24 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(21): Show | 24 | HG00741.hp2 HG01167.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.571-17082C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112189 | ||||||
| chr2:28112191
|
C | T | 2 | a0001c0001t0001g0023a0001c0001t0002g0001 | 2 | HG02630.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.571-17080C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112191 | ||||||
| chr2:28112193
|
C | CCCTTCCT others(9): Show |
1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-17075_571-1707 others(20): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112193 | |||||
| chr2:28112193
|
C | CCCTTCCT others(17): Show |
1 | a0001c0001t0003g0136 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.571-17075_571-1707 others(28): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112193 | |||||
| chr2:28112193
|
C | CCCTTCCT others(25): Show |
4 | a0001c0001t0001g0084a0001c0001t0002g0033a0001c0001t0002g0037others(1): Show | 4 | HG00738.hp1 HG01081.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-17075_571-1707 others(36): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112193 | |||||
| chr2:28112193
|
C | CCCTTCCT others(29): Show |
1 | a0001c0001t0002g0004 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.571-17075_571-1707 others(40): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112193 | |||||
| chr2:28112193
|
C | CCCTTCCT others(36): Show |
1 | a0001c0001t0001g0015 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.571-17075_571-1707 others(47): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112193 | |||||
| chr2:28112193
|
C | CCTTCCCT others(21): Show |
2 | a0001c0001t0002g0050a0001c0001t0003g0019 | 2 | HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.571-17077_571-1707 others(32): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112193 | |||||
| chr2:28112193
|
C | CCTTCCCT others(25): Show |
1 | a0001c0001t0002g0047 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.571-17077_571-1707 others(36): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112193 | |||||
| chr2:28112193
|
C | CCTTCCCT others(29): Show |
1 | a0001c0001t0002g0077 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.571-17077_571-1707 others(40): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112193 | |||||
| chr2:28112193
|
C | CCTTCCCT others(33): Show |
1 | a0001c0001t0002g0026 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.571-17077_571-1707 others(44): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112193 | |||||
| chr2:28112193
|
C | T | 34 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(31): Show | 34 | HG00735.hp1 HG00741.hp2 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.571-17078C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112193 | ||||||
| chr2:28112197
|
C | CCCTCCCT others(29): Show |
1 | a0001c0001t0002g0028 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.571-17071_571-1707 others(40): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112197 | |||||
| chr2:28112197
|
C | CCCTCCCT others(21): Show |
1 | a0001c0001t0001g0139 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.571-17071_571-1707 others(32): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112197 | |||||
| chr2:28112197
|
C | CCCTCCCT others(25): Show |
1 | a0001c0001t0001g0005 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.571-17071_571-1707 others(36): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112197 | |||||
| chr2:28112197
|
C | CCCTCCCT others(29): Show |
2 | a0001c0001t0001g0041a0001c0001t0001g0069 | 2 | HG03225.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.571-17071_571-1707 others(40): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112197 | |||||
| chr2:28112197
|
C | CCCTCCCT others(41): Show |
1 | a0001c0001t0002g0001 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.571-17071_571-1707 others(52): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112197 | |||||
| chr2:28112197
|
C | CCCTCCCT others(29): Show |
2 | a0001c0001t0001g0025a0001c0001t0001g0042 | 2 | HG02735.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.571-17071_571-1707 others(40): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112197 | |||||
| chr2:28112197
|
C | CCCTCCCT others(37): Show |
1 | a0001c0001t0002g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.571-17071_571-1707 others(48): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112197 | |||||
| chr2:28112197
|
C | CCCTCCCT others(41): Show |
1 | a0001c0001t0001g0044 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.571-17071_571-1707 others(52): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112197 | |||||
| chr2:28112197
|
C | CCCTCCCT others(17): Show |
1 | a0001c0001t0001g0022 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.571-17071_571-1707 others(28): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112197 | |||||
| chr2:28112197
|
C | CCCTCCCT others(21): Show |
1 | a0001c0001t0001g0023 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.571-17071_571-1707 others(32): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112197 | |||||
| chr2:28112197
|
C | CCCTCCCT others(25): Show |
1 | a0001c0001t0001g0066 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.571-17071_571-1707 others(36): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112197 | |||||
| chr2:28112197
|
C | CCCTCCCT others(29): Show |
1 | a0001c0001t0001g0057 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.571-17071_571-1707 others(40): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112197 | |||||
| chr2:28112197
|
C | CCCTCCCT others(37): Show |
2 | a0001c0001t0002g0147a0001c0001t0003g0106 | 2 | HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.571-17071_571-1707 others(48): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112197 | |||||
| chr2:28112197
|
C | CCCTCCCT others(21): Show |
1 | a0001c0001t0002g0156 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.571-17071_571-1707 others(32): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112197 | |||||
| chr2:28112197
|
C | CCCTCCCT others(25): Show |
1 | a0001c0001t0001g0027 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.571-17071_571-1707 others(36): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112197 | |||||
| chr2:28112197
|
C | CCCTCCCT others(45): Show |
1 | a0001c0001t0002g0107 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.571-17071_571-1707 others(56): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112197 | |||||
| chr2:28112197
|
C | CCCTTCCT others(5): Show |
1 | a0001c0001t0001g0054 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.571-17053_571-1704 others(16): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112197 | |||||
| chr2:28112197
|
C | CCCTTCCT others(21): Show |
1 | a0001c0001t0003g0135 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.571-17069_571-1704 others(32): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112197 | |||||
| chr2:28112197
|
C | CCCTTCCT others(25): Show |
4 | a0001c0001t0002g0036a0001c0001t0002g0063a0001c0001t0002g0064others(1): Show | 4 | HG02027.hp1 HG02970.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-17073_571-1704 others(36): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112197 | |||||
| chr2:28112197
|
C | CCCTTCCT others(33): Show |
1 | a0001c0001t0001g0073 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.571-17042_571-1704 others(44): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112197 | |||||
| chr2:28112197
|
C | CCCTTCCT others(41): Show |
1 | a0001c0001t0001g0083 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.571-17042_571-1704 others(52): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112197 | |||||
| chr2:28112197
|
C | CCCTTCCT others(44): Show |
1 | a0001c0001t0003g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.571-17057_571-1705 others(55): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112197 | |||||
| chr2:28112197
|
C | CCCTTCCT others(48): Show |
1 | a0001c0001t0003g0089 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.571-17057_571-1705 others(59): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112197 | |||||
| chr2:28112197
|
C | CCTTCCCT others(49): Show |
1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.571-17073_571-1707 others(60): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112197 | |||||
| chr2:28112197
|
C | CCTTCCCT others(29): Show |
2 | a0001c0001t0002g0021a0001c0001t0002g0029 | 2 | HG01934.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.571-17073_571-1707 others(40): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112197 | |||||
| chr2:28112197
|
C | CCTTCCCT others(33): Show |
1 | a0001c0001t0001g0024 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.571-17073_571-1707 others(44): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112197 | |||||
| chr2:28112197
|
C | T | 50 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(47): Show | 50 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.571-17074C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112197 | ||||||
| chr2:28112201
|
T | C | 42 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(39): Show | 42 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.571-17070T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112201 | ||||||
| chr2:28112206
|
C | CCTTCCTT others(16): Show |
1 | a0001c0001t0001g0071 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.571-17064_571-1704 others(27): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28112206 | |||||
| chr2:28112303
|
A | G | 2 | a0001c0001t0003g0135a0001c0001t0003g0136 | 2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.571-16968A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112303 | ||||||
| chr2:28112325
|
T | A | 2 | a0001c0001t0003g0135a0001c0001t0003g0136 | 2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.571-16946T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112325 | ||||||
| chr2:28112363
|
C | A | 77 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(74): Show | 77 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.571-16908C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112363 | ||||||
| chr2:28112469
|
G | A | 21 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(18): Show | 21 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.571-16802G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112469 | ||||||
| chr2:28112486
|
C | T | 40 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(37): Show | 40 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.571-16785C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112486 | ||||||
| chr2:28112600
|
G | T | 35 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(32): Show | 35 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.571-16671G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112600 | ||||||
| chr2:28112667
|
T | C | 1 | a0001c0001t0002g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.571-16604T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112667 | ||||||
| chr2:28112689
|
G | C | 3 | a0001c0001t0001g0045a0001c0001t0002g0140a0001c0001t0002g0141 | 3 | HG01496.hp1 HG02559.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.571-16582G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112689 | ||||||
| chr2:28112690
|
T | A | 1 | a0001c0001t0001g0139 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.571-16581T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112690 | ||||||
| chr2:28112714
|
TATATACC others(11): Show |
T | 2 | a0001c0001t0003g0135a0001c0001t0003g0136 | 2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.571-16556_571-1653 others(22): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28112714 | ||||||
| chr2:28113056
|
A | T | 35 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(32): Show | 35 | HG00639.hp1 HG00639.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.571-16215A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28113056 | ||||||
| chr2:28113372
|
G | A | 1 | a0001c0001t0001g0027 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.571-15899G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28113372 | ||||||
| chr2:28113377
|
G | A | 29 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(26): Show | 29 | HG00741.hp2 HG01168.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.571-15894G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28113377 | ||||||
| chr2:28113391
|
C | T | 23 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(20): Show | 23 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.571-15880C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28113391 | ||||||
| chr2:28113533
|
T | C | 1 | a0001c0001t0005g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.571-15738T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28113533 | ||||||
| chr2:28113818
|
T | G | 1 | a0001c0001t0001g0023 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.571-15453T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28113818 | ||||||
| chr2:28113871
|
T | C | 23 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(20): Show | 23 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.571-15400T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28113871 | ||||||
| chr2:28113914
|
G | A | 1 | a0001c0001t0002g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.571-15357G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28113914 | ||||||
| chr2:28113934
|
T | C | 33 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(30): Show | 33 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.571-15337T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28113934 | ||||||
| chr2:28113994
|
A | G | 13 | a0001c0001t0001g0005a0001c0001t0001g0041a0001c0001t0001g0042others(10): Show | 13 | HG00639.hp1 HG01106.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.571-15277A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28113994 | ||||||
| chr2:28114054
|
A | C | 33 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(30): Show | 33 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.571-15217A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28114054 | ||||||
| chr2:28114225
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.571-15046T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28114225 | ||||||
| chr2:28114312
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-14959C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28114312 | ||||||
| chr2:28114429
|
C | T | 4 | a0001c0001t0002g0010a0001c0001t0002g0016a0001c0001t0002g0020others(1): Show | 4 | HG02897.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-14842C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28114429 | ||||||
| chr2:28114612
|
C | T | 30 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(27): Show | 30 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.571-14659C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28114612 | ||||||
| chr2:28114808
|
T | G | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.571-14463T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28114808 | ||||||
| chr2:28114874
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.571-14397A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28114874 | ||||||
| chr2:28115182
|
A | AAC | 13 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0001g0060others(10): Show | 13 | HG00738.hp2 HG01081.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.571-14047_571-1404 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28115182 | |||||
| chr2:28115182
|
A | AACAC | 10 | a0001c0001t0001g0057a0001c0001t0001g0070a0001c0001t0001g0074others(7): Show | 10 | HG02135.hp1 HG02572.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.571-14049_571-1404 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28115182 | |||||
| chr2:28115182
|
A | AACACACA others(3): Show |
1 | a0001c0001t0001g0008 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.571-14055_571-1404 others(14): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28115182 | |||||
| chr2:28115182
|
AAC | A | 35 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0034others(32): Show | 35 | HG00140.hp1 HG01069.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.571-14047_571-1404 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28115182 | |||||
| chr2:28115182
|
AACAC | A | 5 | a0001c0001t0001g0142a0001c0001t0002g0101a0001c0001t0002g0147others(2): Show | 5 | HG00733.hp2 HG01167.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-14049_571-1404 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28115182 | |||||
| chr2:28115182
|
AACACAC | A | 6 | a0001c0001t0001g0035a0001c0001t0001g0157a0001c0001t0002g0010others(3): Show | 6 | HG01891.hp2 HG02040.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-14051_571-1404 others(10): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28115182 | |||||
| chr2:28115182
|
AACACACA others(1): Show |
A | 10 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(7): Show | 10 | HG02486.hp2 HG02630.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.571-14053_571-1404 others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28115182 | |||||
| chr2:28115182
|
AACACACA others(3): Show |
A | 30 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(27): Show | 30 | HG00639.hp1 HG00639.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.571-14055_571-1404 others(14): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28115182 | |||||
| chr2:28115182
|
AACACACA others(5): Show |
A | 9 | a0001c0001t0001g0052a0001c0001t0001g0111a0001c0001t0001g0125others(6): Show | 9 | HG01168.hp2 HG02074.hp1 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.571-14057_571-1404 others(16): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28115182 | |||||
| chr2:28115182
|
AACACACA others(17): Show |
A | 1 | a0001c0001t0002g0103 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.571-14069_571-1404 others(28): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28115182 | |||||
| chr2:28115397
|
C | T | 32 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(29): Show | 32 | HG00639.hp1 HG00639.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.571-13874C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28115397 | ||||||
| chr2:28115402
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.571-13869G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28115402 | ||||||
| chr2:28115499
|
G | A | 3 | a0001c0001t0001g0045a0001c0001t0002g0140a0001c0001t0002g0141 | 3 | HG01496.hp1 HG02559.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.571-13772G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28115499 | ||||||
| chr2:28115591
|
A | G | 3 | a0001c0001t0001g0045a0001c0001t0002g0140a0001c0001t0002g0141 | 3 | HG01496.hp1 HG02559.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.571-13680A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28115591 | ||||||
| chr2:28115768
|
A | C | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.571-13503A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28115768 | ||||||
| chr2:28115769
|
T | A | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.571-13502T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28115769 | ||||||
| chr2:28115880
|
C | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.571-13391C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28115880 | ||||||
| chr2:28115996
|
A | T | 18 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(15): Show | 18 | HG00741.hp2 HG01168.hp2 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.571-13275A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28115996 | ||||||
| chr2:28116111
|
G | A | 2 | a0001c0001t0003g0135a0001c0001t0003g0136 | 2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.571-13160G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28116111 | ||||||
| chr2:28116220
|
C | T | 1 | a0001c0001t0002g0151 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.571-13051C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28116220 | ||||||
| chr2:28116775
|
G | C | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.571-12496G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28116775 | ||||||
| chr2:28117017
|
T | TA | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.571-12253dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28117017 | |||||
| chr2:28117039
|
A | G | 15 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0099others(12): Show | 15 | HG01106.hp2 HG01192.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.571-12232A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28117039 | ||||||
| chr2:28117458
|
G | A | 1 | a0001c0001t0002g0007 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.571-11813G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28117458 | ||||||
| chr2:28117775
|
C | T | 30 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(27): Show | 30 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.571-11496C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28117775 | ||||||
| chr2:28117981
|
A | G | 18 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(15): Show | 18 | HG00741.hp2 HG01168.hp2 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.571-11290A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28117981 | ||||||
| chr2:28118088
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.571-11183G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28118088 | ||||||
| chr2:28118187
|
G | C | 1 | a0001c0001t0002g0009 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.571-11084G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28118187 | ||||||
| chr2:28118313
|
T | G | 1 | a0001c0001t0002g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.571-10958T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28118313 | ||||||
| chr2:28118508
|
C | T | 64 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(61): Show | 64 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.571-10763C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28118508 | ||||||
| chr2:28118555
|
T | C | 2 | a0001c0001t0002g0062a0001c0001t0002g0096 | 2 | HG01934.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.571-10716T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28118555 | ||||||
| chr2:28118570
|
TG | T | 2 | a0001c0001t0003g0135a0001c0001t0003g0136 | 2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.571-10700delG | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28118570 | ||||||
| chr2:28118609
|
C | T | 38 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(35): Show | 38 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.571-10662C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28118609 | ||||||
| chr2:28118750
|
A | G | 3 | a0001c0001t0001g0045a0001c0001t0002g0140a0001c0001t0002g0141 | 3 | HG01496.hp1 HG02559.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.571-10521A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28118750 | ||||||
| chr2:28118767
|
A | G | 4 | a0001c0001t0002g0010a0001c0001t0002g0016a0001c0001t0002g0020others(1): Show | 4 | HG02897.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-10504A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28118767 | ||||||
| chr2:28119155
|
A | G | 156 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(153): Show |
intron_variant | MODIFIER | c.571-10116A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28119155 | ||||||
| chr2:28119216
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.571-10055G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28119216 | ||||||
| chr2:28119286
|
A | G | 40 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(37): Show | 40 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.571-9985A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28119286 | ||||||
| chr2:28119669
|
C | T | 18 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(15): Show | 18 | HG00741.hp2 HG01168.hp2 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.571-9602C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28119669 | ||||||
| chr2:28119789
|
C | G | 8 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(5): Show | 8 | HG00639.hp2 HG01109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.571-9482C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28119789 | ||||||
| chr2:28120011
|
T | C | 2 | a0001c0001t0003g0135a0001c0001t0003g0136 | 2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.571-9260T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28120011 | ||||||
| chr2:28120167
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0025 | 2 | HG02735.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.571-9104G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28120167 | ||||||
| chr2:28120347
|
T | C | 2 | a0001c0001t0003g0135a0001c0001t0003g0136 | 2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.571-8924T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28120347 | ||||||
| chr2:28120413
|
C | T | 33 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(30): Show | 33 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.571-8858C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28120413 | ||||||
| chr2:28120428
|
T | C | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.571-8843T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28120428 | ||||||
| chr2:28120583
|
G | A | 8 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(5): Show | 8 | HG00639.hp2 HG01109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.571-8688G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28120583 | ||||||
| chr2:28120729
|
A | G | 3 | a0001c0001t0001g0045a0001c0001t0002g0140a0001c0001t0002g0141 | 3 | HG01496.hp1 HG02559.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.571-8542A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28120729 | ||||||
| chr2:28120869
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0043 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.571-8402A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28120869 | ||||||
| chr2:28120996
|
A | G | 1 | a0001c0001t0002g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.571-8275A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28120996 | ||||||
| chr2:28121013
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.571-8258C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28121013 | ||||||
| chr2:28121354
|
C | T | 1 | a0001c0001t0002g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.571-7917C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28121354 | ||||||
| chr2:28121418
|
G | A | 8 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0053others(5): Show | 8 | HG00140.hp2 HG00733.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.571-7853G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28121418 | ||||||
| chr2:28121494
|
A | G | 2 | a0001c0001t0002g0147a0001c0001t0002g0156 | 2 | HG01069.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.571-7777A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28121494 | ||||||
| chr2:28121696
|
C | A | 6 | a0001c0001t0001g0088a0001c0001t0002g0108a0001c0001t0002g0130others(3): Show | 6 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-7575C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28121696 | ||||||
| chr2:28121722
|
TA | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.571-7548delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28121722 | ||||||
| chr2:28121996
|
T | C | 77 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(74): Show | 77 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.571-7275T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28121996 | ||||||
| chr2:28122075
|
C | G | 35 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(32): Show | 35 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.571-7196C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28122075 | ||||||
| chr2:28122107
|
T | G | 2 | a0001c0001t0001g0127a0001c0001t0002g0110 | 2 | HG02040.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.571-7164T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28122107 | ||||||
| chr2:28122109
|
G | A | 3 | a0001c0001t0001g0045a0001c0001t0002g0140a0001c0001t0002g0141 | 3 | HG01496.hp1 HG02559.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.571-7162G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28122109 | ||||||
| chr2:28122121
|
C | T | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG02630.hp1 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-7150C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28122121 | ||||||
| chr2:28122132
|
C | G | 5 | a0001c0001t0001g0065a0001c0001t0001g0070a0001c0001t0001g0071others(2): Show | 5 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-7139C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28122132 | ||||||
| chr2:28122242
|
A | G | 2 | a0001c0001t0003g0135a0001c0001t0003g0136 | 2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.571-7029A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28122242 | ||||||
| chr2:28122385
|
C | T | 3 | a0001c0001t0001g0045a0001c0001t0002g0140a0001c0001t0002g0141 | 3 | HG01496.hp1 HG02559.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.571-6886C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28122385 | ||||||
| chr2:28122397
|
T | A | 74 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(71): Show | 74 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.571-6874T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28122397 | ||||||
| chr2:28122573
|
C | T | 1 | a0001c0001t0002g0063 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.571-6698C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28122573 | ||||||
| chr2:28122599
|
T | G | 35 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(32): Show | 35 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.571-6672T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28122599 | ||||||
| chr2:28122632
|
T | C | 2 | a0001c0001t0002g0001a0001c0001t0002g0002 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.571-6639T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28122632 | ||||||
| chr2:28122733
|
G | A | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(3): Show | 6 | HG00639.hp2 HG01109.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-6538G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28122733 | ||||||
| chr2:28122778
|
ATTG | A | 3 | a0001c0001t0001g0045a0001c0001t0002g0140a0001c0001t0002g0141 | 3 | HG01496.hp1 HG02559.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.571-6484_571-6482d others(5): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28122778 | |||||
| chr2:28122827
|
G | T | 3 | a0001c0001t0001g0045a0001c0001t0002g0140a0001c0001t0002g0141 | 3 | HG01496.hp1 HG02559.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.571-6444G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28122827 | ||||||
| chr2:28122850
|
AT | A | 33 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(30): Show | 33 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.571-6419delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28122850 | |||||
| chr2:28122922
|
T | G | 12 | a0001c0001t0001g0008a0001c0001t0001g0111a0001c0001t0001g0125others(9): Show | 12 | HG00741.hp2 HG01168.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.571-6349T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28122922 | ||||||
| chr2:28123084
|
T | G | 2 | a0001c0001t0003g0135a0001c0001t0003g0136 | 2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.571-6187T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28123084 | ||||||
| chr2:28123127
|
C | T | 1 | a0001c0001t0003g0089 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.571-6144C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28123127 | ||||||
| chr2:28123165
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.571-6106C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28123165 | ||||||
| chr2:28123207
|
C | T | 1 | a0001c0001t0002g0029 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.571-6064C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28123207 | ||||||
| chr2:28123327
|
G | A | 33 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(30): Show | 33 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.571-5944G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28123327 | ||||||
| chr2:28123413
|
C | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.571-5858C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28123413 | ||||||
| chr2:28123469
|
C | CT | 21 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(18): Show | 21 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.571-5800dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28123469 | |||||
| chr2:28123472
|
G | A | 21 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(18): Show | 21 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.571-5799G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28123472 | ||||||
| chr2:28123616
|
G | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0054a0001c0001t0001g0055others(1): Show | 4 | HG02280.hp1 HG02451.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-5655G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28123616 | ||||||
| chr2:28123938
|
T | G | 5 | a0001c0001t0001g0088a0001c0001t0002g0108a0001c0001t0002g0130others(2): Show | 5 | HG02280.hp2 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-5333T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28123938 | ||||||
| chr2:28123957
|
T | C | 3 | a0001c0001t0001g0022a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | HG02280.hp1 HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.571-5314T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28123957 | ||||||
| chr2:28124021
|
C | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.571-5250C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28124021 | ||||||
| chr2:28124286
|
T | C | 3 | a0001c0001t0001g0045a0001c0001t0002g0140a0001c0001t0002g0141 | 3 | HG01496.hp1 HG02559.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.571-4985T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28124286 | ||||||
| chr2:28124409
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.571-4862A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28124409 | ||||||
| chr2:28124628
|
C | A | 152 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(149): Show | 152 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(149): Show |
intron_variant | MODIFIER | c.571-4643C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28124628 | ||||||
| chr2:28124659
|
A | G | 7 | a0001c0001t0001g0088a0001c0001t0002g0108a0001c0001t0002g0128others(4): Show | 7 | HG01891.hp2 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-4612A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28124659 | ||||||
| chr2:28124806
|
G | T | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-4465G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28124806 | ||||||
| chr2:28124815
|
C | T | 18 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(15): Show | 18 | HG01168.hp2 HG02074.hp1 HG02165.hp2 others(15): Show |
intron_variant | MODIFIER | c.571-4456C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28124815 | ||||||
| chr2:28124865
|
G | A | 1 | a0001c0001t0002g0063 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.571-4406G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28124865 | ||||||
| chr2:28125011
|
A | G | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.571-4260A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28125011 | ||||||
| chr2:28125220
|
G | T | 3 | a0001c0001t0001g0044a0001c0001t0002g0001a0001c0001t0002g0002 | 3 | HG02258.hp2 HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.571-4051G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28125220 | ||||||
| chr2:28125238
|
G | A | 4 | a0001c0001t0001g0138a0001c0001t0002g0006a0001c0001t0002g0007others(1): Show | 4 | HG01346.hp1 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-4033G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28125238 | ||||||
| chr2:28125303
|
A | T | 32 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(29): Show | 32 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.571-3968A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28125303 | ||||||
| chr2:28125493
|
G | A | 16 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(13): Show | 16 | HG01168.hp2 HG01496.hp1 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.571-3778G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28125493 | ||||||
| chr2:28125617
|
T | C | 27 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(24): Show | 27 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.571-3654T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28125617 | ||||||
| chr2:28126048
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.571-3223G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28126048 | ||||||
| chr2:28126087
|
T | C | 156 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(153): Show |
intron_variant | MODIFIER | c.571-3184T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28126087 | ||||||
| chr2:28126119
|
G | GT | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.571-3151dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28126119 | |||||
| chr2:28126138
|
T | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.571-3133T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28126138 | ||||||
| chr2:28126147
|
TTTA | T | 4 | a0001c0001t0001g0138a0001c0001t0002g0006a0001c0001t0002g0007others(1): Show | 4 | HG01346.hp1 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-3113_571-3111d others(5): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28126147 | |||||
| chr2:28126196
|
G | C | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-3075G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28126196 | ||||||
| chr2:28126327
|
T | C | 1 | a0001c0001t0001g0080 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.571-2944T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28126327 | ||||||
| chr2:28126434
|
A | G | 36 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(33): Show | 36 | HG00639.hp1 HG00639.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.571-2837A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28126434 | ||||||
| chr2:28126546
|
T | A | 25 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(22): Show | 25 | HG00639.hp1 HG00639.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.571-2725T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28126546 | ||||||
| chr2:28126580
|
C | G | 15 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(12): Show | 15 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.571-2691C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28126580 | ||||||
| chr2:28126593
|
G | A | 26 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(23): Show | 26 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.571-2678G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28126593 | ||||||
| chr2:28126741
|
C | G | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.571-2530C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28126741 | ||||||
| chr2:28126754
|
C | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.571-2517C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28126754 | ||||||
| chr2:28126771
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.571-2500G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28126771 | ||||||
| chr2:28126800
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.571-2471C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28126800 | ||||||
| chr2:28126801
|
G | C | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.571-2470G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28126801 | ||||||
| chr2:28126839
|
T | C | 156 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(153): Show |
intron_variant | MODIFIER | c.571-2432T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28126839 | ||||||
| chr2:28126860
|
C | T | 156 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(153): Show |
intron_variant | MODIFIER | c.571-2411C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28126860 | ||||||
| chr2:28126903
|
G | A | 6 | a0001c0001t0001g0088a0001c0001t0002g0108a0001c0001t0002g0130others(3): Show | 6 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-2368G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28126903 | ||||||
| chr2:28126957
|
G | T | 1 | a0001c0001t0002g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.571-2314G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28126957 | ||||||
| chr2:28126969
|
C | T | 5 | a0001c0001t0001g0065a0001c0001t0001g0083a0001c0001t0002g0064others(2): Show | 5 | HG00735.hp1 HG01099.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-2302C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28126969 | ||||||
| chr2:28127007
|
T | C | 1 | a0001c0001t0001g0111 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.571-2264T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28127007 | ||||||
| chr2:28127099
|
C | G | 2 | a0001c0001t0003g0135a0001c0001t0003g0136 | 2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.571-2172C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28127099 | ||||||
| chr2:28127135
|
T | G | 1 | a0001c0001t0002g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.571-2136T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28127135 | ||||||
| chr2:28127260
|
A | G | 106 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(103): Show | 106 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.571-2011A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28127260 | ||||||
| chr2:28127272
|
C | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0139 | 2 | HG02897.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.571-1999C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28127272 | ||||||
| chr2:28127353
|
C | T | 26 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(23): Show | 26 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.571-1918C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28127353 | ||||||
| chr2:28127376
|
C | G | 1 | a0001c0001t0002g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.571-1895C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28127376 | ||||||
| chr2:28127380
|
A | G | 112 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(109): Show | 112 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(109): Show |
intron_variant | MODIFIER | c.571-1891A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28127380 | ||||||
| chr2:28127390
|
G | C | 1 | a0001c0001t0002g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.571-1881G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28127390 | ||||||
| chr2:28127508
|
C | T | 7 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0053others(4): Show | 7 | HG00140.hp2 HG00733.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.571-1763C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28127508 | ||||||
| chr2:28127744
|
A | G | 112 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(109): Show | 112 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(109): Show |
intron_variant | MODIFIER | c.571-1527A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28127744 | ||||||
| chr2:28127808
|
C | CT | 26 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(23): Show | 26 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.571-1447dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28127808 | |||||
| chr2:28127808
|
C | CTT | 5 | a0001c0001t0002g0004a0001c0001t0002g0036a0001c0001t0002g0037others(2): Show | 5 | HG00738.hp1 HG02145.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-1448_571-1447d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28127808 | |||||
| chr2:28127811
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.571-1460T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28127811 | ||||||
| chr2:28127845
|
T | C | 150 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(147): Show | 150 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(147): Show |
intron_variant | MODIFIER | c.571-1426T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28127845 | ||||||
| chr2:28127876
|
C | T | 29 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(26): Show | 29 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.571-1395C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28127876 | ||||||
| chr2:28127900
|
G | A | 2 | a0001c0001t0002g0006a0001c0001t0002g0009 | 2 | HG01346.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.571-1371G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28127900 | ||||||
| chr2:28127926
|
C | T | 5 | a0001c0001t0001g0088a0001c0001t0002g0108a0001c0001t0002g0130others(2): Show | 5 | HG02280.hp2 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-1345C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28127926 | ||||||
| chr2:28127978
|
GT | G | 6 | a0001c0001t0001g0088a0001c0001t0002g0108a0001c0001t0002g0130others(3): Show | 6 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-1286delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28127978 | |||||
| chr2:28128055
|
G | A | 29 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(26): Show | 29 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.571-1216G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28128055 | ||||||
| chr2:28128101
|
C | T | 38 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(35): Show | 38 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.571-1170C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28128101 | ||||||
| chr2:28128144
|
T | C | 156 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(153): Show |
intron_variant | MODIFIER | c.571-1127T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28128144 | ||||||
| chr2:28128210
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.571-1061T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28128210 | ||||||
| chr2:28128246
|
G | T | 2 | a0001c0001t0003g0135a0001c0001t0003g0136 | 2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.571-1025G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28128246 | ||||||
| chr2:28128264
|
A | G | 17 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(14): Show | 17 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.571-1007A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28128264 | ||||||
| chr2:28128871
|
AAGGT | A | 15 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(12): Show | 15 | HG01168.hp2 HG02074.hp1 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.571-395_571-392del others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 28128871 | |||||
| chr2:28128905
|
TG | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.571-365delG | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28128905 | ||||||
| chr2:28129014
|
C | T | 29 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(26): Show | 29 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.571-257C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | chr2 | 28129014 | ||||||
| chr2:28130219
|
T | G | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.680+839T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28130219 | ||||||
| chr2:28130277
|
T | C | 3 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0009 | 3 | HG01346.hp1 HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.680+897T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28130277 | ||||||
| chr2:28130651
|
G | A | 2 | a0001c0001t0001g0093a0001c0001t0001g0102 | 2 | HG01069.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.680+1271G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28130651 | ||||||
| chr2:28130808
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.680+1428C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28130808 | ||||||
| chr2:28130963
|
A | G | 2 | a0001c0001t0003g0135a0001c0001t0003g0136 | 2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.680+1583A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28130963 | ||||||
| chr2:28131053
|
TTATTATT others(320): Show |
T | 104 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(101): Show | 104 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.680+1681_680+2007d others(2): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28131053 | |||||
| chr2:28131067
|
A | AT | 2 | a0001c0001t0002g0101a0001c0001t0002g0149 | 2 | NA18955.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.680+1689dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28131067 | |||||
| chr2:28131070
|
A | AT | 14 | a0001c0001t0001g0032a0001c0001t0001g0072a0001c0001t0001g0093others(11): Show | 14 | HG00738.hp2 HG01168.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.680+1692dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28131070 | |||||
| chr2:28131070
|
A | ATT | 7 | a0001c0001t0001g0058a0001c0001t0001g0097a0001c0001t0001g0127others(4): Show | 7 | HG01106.hp2 HG01192.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.680+1691_680+1692d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28131070 | |||||
| chr2:28131070
|
A | T | 3 | a0001c0001t0001g0109a0001c0001t0002g0101a0001c0001t0002g0149 | 3 | HG02970.hp1 NA18955.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.680+1690A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28131070 | ||||||
| chr2:28131073
|
A | AT | 7 | a0001c0001t0001g0099a0001c0001t0001g0104a0001c0001t0001g0133others(4): Show | 7 | HG02109.hp2 HG02155.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.680+1695dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28131073 | |||||
| chr2:28131073
|
A | ATT | 4 | a0001c0001t0001g0092a0001c0001t0001g0123a0001c0001t0003g0135others(1): Show | 4 | HG00140.hp1 HG00733.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.680+1694_680+1695d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28131073 | |||||
| chr2:28131073
|
A | T | 28 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0058others(25): Show | 28 | HG00738.hp2 HG01069.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.680+1693A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28131073 | ||||||
| chr2:28131076
|
A | AT | 4 | a0001c0001t0001g0031a0001c0001t0001g0113a0001c0001t0001g0134others(1): Show | 4 | HG02738.hp1 HG03688.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.680+1698dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28131076 | |||||
| chr2:28131076
|
A | T | 43 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0058others(40): Show | 43 | HG00140.hp1 HG00733.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.680+1696A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28131076 | ||||||
| chr2:28131079
|
A | T | 51 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(48): Show | 51 | HG00140.hp1 HG00733.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.680+1699A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28131079 | ||||||
| chr2:28131175
|
G | A | 4 | a0001c0001t0002g0010a0001c0001t0002g0016a0001c0001t0002g0020others(1): Show | 4 | HG02897.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.680+1795G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28131175 | ||||||
| chr2:28131239
|
G | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.680+1859G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28131239 | ||||||
| chr2:28131501
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.680+2121G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28131501 | ||||||
| chr2:28131577
|
A | G | 5 | a0001c0001t0002g0004a0001c0001t0002g0036a0001c0001t0002g0037others(2): Show | 5 | HG00738.hp1 HG02145.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.680+2197A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28131577 | ||||||
| chr2:28131878
|
A | G | 32 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(29): Show | 32 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.680+2498A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28131878 | ||||||
| chr2:28131941
|
A | G | 3 | a0001c0001t0001g0044a0001c0001t0002g0001a0001c0001t0002g0002 | 3 | HG02258.hp2 HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.680+2561A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28131941 | ||||||
| chr2:28131945
|
G | A | 1 | a0001c0001t0005g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.680+2565G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28131945 | ||||||
| chr2:28132049
|
A | T | 1 | a0001c0001t0001g0069 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.680+2669A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28132049 | ||||||
| chr2:28132142
|
C | CT | 39 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(36): Show | 39 | HG00639.hp1 HG00639.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.680+2776dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28132142 | |||||
| chr2:28132199
|
C | G | 1 | a0001c0001t0001g0123 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.680+2819C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28132199 | ||||||
| chr2:28132261
|
C | G | 1 | a0001c0001t0002g0114 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.680+2881C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28132261 | ||||||
| chr2:28132300
|
G | A | 44 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(41): Show | 44 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.680+2920G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28132300 | ||||||
| chr2:28132357
|
C | G | 44 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(41): Show | 44 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.680+2977C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28132357 | ||||||
| chr2:28132373
|
C | T | 15 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(12): Show | 15 | HG01168.hp2 HG02074.hp1 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.680+2993C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28132373 | ||||||
| chr2:28132386
|
C | T | 5 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0001g0054others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.680+3006C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28132386 | ||||||
| chr2:28132428
|
A | G | 44 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(41): Show | 44 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.680+3048A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28132428 | ||||||
| chr2:28132539
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.680+3159A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28132539 | ||||||
| chr2:28132560
|
C | T | 13 | a0001c0001t0001g0005a0001c0001t0001g0041a0001c0001t0001g0042others(10): Show | 13 | HG00639.hp1 HG01106.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.680+3180C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28132560 | ||||||
| chr2:28132689
|
C | A | 6 | a0001c0001t0001g0088a0001c0001t0002g0108a0001c0001t0002g0130others(3): Show | 6 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.680+3309C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28132689 | ||||||
| chr2:28132689
|
C | T | 5 | a0001c0001t0001g0066a0001c0001t0001g0073a0001c0001t0002g0063others(2): Show | 5 | HG02027.hp1 HG03017.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.680+3309C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28132689 | ||||||
| chr2:28132963
|
G | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.680+3583G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28132963 | ||||||
| chr2:28133029
|
G | A | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG01496.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.680+3649G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28133029 | ||||||
| chr2:28133052
|
C | T | 1 | a0001c0001t0005g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.680+3672C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28133052 | ||||||
| chr2:28133363
|
T | C | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG01496.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.680+3983T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28133363 | ||||||
| chr2:28133479
|
C | T | 5 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0001g0054others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.680+4099C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28133479 | ||||||
| chr2:28133519
|
G | T | 44 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(41): Show | 44 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.680+4139G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28133519 | ||||||
| chr2:28133528
|
A | G | 15 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(12): Show | 15 | HG01168.hp2 HG02074.hp1 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.680+4148A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28133528 | ||||||
| chr2:28133557
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.680+4177C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28133557 | ||||||
| chr2:28134015
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.680+4635G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28134015 | ||||||
| chr2:28134117
|
C | T | 1 | a0001c0001t0002g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.680+4737C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28134117 | ||||||
| chr2:28134155
|
G | A | 6 | a0001c0001t0001g0088a0001c0001t0002g0108a0001c0001t0002g0130others(3): Show | 6 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.680+4775G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28134155 | ||||||
| chr2:28134204
|
CA | C | 112 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(109): Show | 112 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(109): Show |
intron_variant | MODIFIER | c.680+4841delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28134204 | |||||
| chr2:28134204
|
CAA | C | 41 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(38): Show | 41 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.680+4840_680+4841d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28134204 | |||||
| chr2:28134369
|
A | G | 1 | a0001c0001t0002g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.680+4989A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28134369 | ||||||
| chr2:28134403
|
T | G | 29 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(26): Show | 29 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.680+5023T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28134403 | ||||||
| chr2:28134460
|
A | G | 29 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(26): Show | 29 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.680+5080A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28134460 | ||||||
| chr2:28134684
|
G | A | 5 | a0001c0001t0001g0017a0001c0001t0001g0053a0001c0001t0001g0082others(2): Show | 5 | HG00140.hp2 HG00733.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.680+5304G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28134684 | ||||||
| chr2:28134715
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.680+5335A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28134715 | ||||||
| chr2:28134812
|
A | C | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.680+5432A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28134812 | ||||||
| chr2:28134841
|
A | G | 26 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(23): Show | 26 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.680+5461A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28134841 | ||||||
| chr2:28135003
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.680+5623G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28135003 | ||||||
| chr2:28135467
|
C | T | 104 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(101): Show | 104 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.680+6087C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28135467 | ||||||
| chr2:28135507
|
C | T | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG01496.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.680+6127C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28135507 | ||||||
| chr2:28135570
|
G | A | 1 | a0001c0001t0002g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.680+6190G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28135570 | ||||||
| chr2:28135612
|
T | C | 116 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(113): Show | 116 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.680+6232T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28135612 | ||||||
| chr2:28135788
|
C | G | 34 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(31): Show | 34 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.680+6408C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28135788 | ||||||
| chr2:28135836
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.680+6456C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28135836 | ||||||
| chr2:28135863
|
G | A | 6 | a0001c0001t0001g0088a0001c0001t0002g0108a0001c0001t0002g0130others(3): Show | 6 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.680+6483G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28135863 | ||||||
| chr2:28135884
|
C | T | 26 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(23): Show | 26 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.680+6504C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28135884 | ||||||
| chr2:28135907
|
T | C | 104 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(101): Show | 104 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.680+6527T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28135907 | ||||||
| chr2:28136016
|
G | A | 1 | a0001c0001t0002g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.680+6636G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28136016 | ||||||
| chr2:28136095
|
G | A | 65 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(62): Show | 65 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.680+6715G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28136095 | ||||||
| chr2:28136114
|
C | T | 29 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(26): Show | 29 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.680+6734C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28136114 | ||||||
| chr2:28136149
|
T | C | 5 | a0001c0001t0001g0017a0001c0001t0001g0053a0001c0001t0001g0082others(2): Show | 5 | HG00140.hp2 HG00733.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.680+6769T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28136149 | ||||||
| chr2:28136206
|
C | T | 1 | a0001c0001t0001g0155 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.680+6826C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28136206 | ||||||
| chr2:28136207
|
G | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 5 | HG01106.hp1 HG01891.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.680+6827G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28136207 | ||||||
| chr2:28136282
|
C | T | 28 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(25): Show | 28 | HG00639.hp1 HG00639.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.680+6902C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28136282 | ||||||
| chr2:28136629
|
A | G | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG01496.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.680+7249A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28136629 | ||||||
| chr2:28136753
|
G | A | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.680+7373G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28136753 | ||||||
| chr2:28136815
|
G | A | 1 | a0001c0001t0002g0103 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.680+7435G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28136815 | ||||||
| chr2:28136888
|
A | T | 1 | a0001c0001t0002g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.680+7508A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28136888 | ||||||
| chr2:28136893
|
T | C | 6 | a0001c0001t0001g0088a0001c0001t0002g0108a0001c0001t0002g0130others(3): Show | 6 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.680+7513T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28136893 | ||||||
| chr2:28136894
|
G | T | 1 | a0001c0001t0002g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.680+7514G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28136894 | ||||||
| chr2:28136895
|
A | C | 1 | a0001c0001t0002g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.680+7515A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28136895 | ||||||
| chr2:28136896
|
ATGAGTAA others(579): Show |
A | 1 | a0001c0001t0002g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.680+7517_680+8102d others(2): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28136896 | ||||||
| chr2:28137127
|
C | T | 4 | a0001c0001t0001g0138a0001c0001t0002g0006a0001c0001t0002g0007others(1): Show | 4 | HG01346.hp1 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.680+7747C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28137127 | ||||||
| chr2:28137216
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.680+7836G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28137216 | ||||||
| chr2:28137237
|
T | A | 15 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(12): Show | 15 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.680+7857T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28137237 | ||||||
| chr2:28137329
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.680+7949G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28137329 | ||||||
| chr2:28137331
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.680+7951A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28137331 | ||||||
| chr2:28137361
|
T | C | 29 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(26): Show | 29 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.680+7981T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28137361 | ||||||
| chr2:28137773
|
T | C | 157 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(154): Show | 157 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(154): Show |
intron_variant | MODIFIER | c.680+8393T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28137773 | ||||||
| chr2:28137791
|
A | G | 1 | a0001c0001t0002g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.680+8411A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28137791 | ||||||
| chr2:28137823
|
T | C | 2 | a0001c0001t0001g0040a0001c0001t0001g0078 | 2 | HG01243.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.680+8443T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28137823 | ||||||
| chr2:28138229
|
A | G | 1 | a0001c0001t0002g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.680+8849A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28138229 | ||||||
| chr2:28138258
|
T | C | 15 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(12): Show | 15 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.680+8878T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28138258 | ||||||
| chr2:28138439
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.680+9059C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28138439 | ||||||
| chr2:28138547
|
G | A | 2 | a0001c0001t0003g0089a0001c0001t0003g0090 | 2 | HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.680+9167G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28138547 | ||||||
| chr2:28138571
|
T | C | 1 | a0001c0001t0003g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.680+9191T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28138571 | ||||||
| chr2:28138594
|
A | G | 29 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(26): Show | 29 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.680+9214A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28138594 | ||||||
| chr2:28138693
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0072 | 2 | HG00738.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.680+9313C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28138693 | ||||||
| chr2:28138964
|
T | C | 38 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(35): Show | 38 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.680+9584T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28138964 | ||||||
| chr2:28139053
|
A | G | 2 | a0001c0001t0001g0070a0001c0001t0001g0084 | 2 | HG01081.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.680+9673A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28139053 | ||||||
| chr2:28139071
|
G | A | 29 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(26): Show | 29 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.680+9691G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28139071 | ||||||
| chr2:28139111
|
G | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.680+9731G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28139111 | ||||||
| chr2:28139127
|
T | C | 29 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(26): Show | 29 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.680+9747T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28139127 | ||||||
| chr2:28139135
|
C | A | 46 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.680+9755C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28139135 | ||||||
| chr2:28139147
|
G | A | 29 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(26): Show | 29 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.680+9767G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28139147 | ||||||
| chr2:28139152
|
G | T | 17 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(14): Show | 17 | HG00741.hp2 HG01168.hp2 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.680+9772G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28139152 | ||||||
| chr2:28139201
|
G | A | 38 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(35): Show | 38 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.680+9821G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28139201 | ||||||
| chr2:28139244
|
C | T | 17 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(14): Show | 17 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.680+9864C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28139244 | ||||||
| chr2:28139275
|
C | T | 5 | a0001c0001t0001g0088a0001c0001t0002g0108a0001c0001t0002g0130others(2): Show | 5 | HG02280.hp2 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.680+9895C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28139275 | ||||||
| chr2:28139316
|
C | T | 19 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(16): Show | 19 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.680+9936C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28139316 | ||||||
| chr2:28139320
|
T | C | 5 | a0001c0001t0002g0087a0001c0001t0002g0095a0001c0001t0002g0098others(2): Show | 5 | HG01106.hp2 HG01192.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.680+9940T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28139320 | ||||||
| chr2:28139321
|
C | CA | 14 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0027others(11): Show | 14 | HG01109.hp2 HG02074.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.680+9965dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28139321 | |||||
| chr2:28139321
|
C | CAA | 18 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(15): Show | 18 | HG00639.hp1 HG01109.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.680+9964_680+9965d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28139321 | |||||
| chr2:28139340
|
A | G | 16 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(13): Show | 16 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.680+9960A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28139340 | ||||||
| chr2:28139340
|
AAAAAAG | A | 5 | a0001c0001t0001g0088a0001c0001t0002g0108a0001c0001t0002g0131others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.680+9972_680+9977d others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28139340 | |||||
| chr2:28139341
|
A | AG | 27 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(24): Show | 27 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.680+9961_680+9962i others(3): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28139341 | ||||||
| chr2:28139341
|
A | G | 1 | a0001c0001t0003g0067 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.680+9961A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28139341 | ||||||
| chr2:28139383
|
A | G | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.680+10003A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28139383 | ||||||
| chr2:28139395
|
C | T | 31 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(28): Show | 31 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.680+10015C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28139395 | ||||||
| chr2:28139451
|
C | G | 29 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(26): Show | 29 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.680+10071C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28139451 | ||||||
| chr2:28139685
|
G | A | 12 | a0001c0001t0001g0111a0001c0001t0001g0125a0001c0001t0001g0142others(9): Show | 12 | HG00741.hp2 HG01168.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.680+10305G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28139685 | ||||||
| chr2:28139872
|
G | T | 31 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(28): Show | 31 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.680+10492G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28139872 | ||||||
| chr2:28139985
|
A | AAAACAGA others(22): Show |
2 | a0001c0001t0001g0142a0001c0001t0002g0145 | 2 | NA18969.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.680+10629_680+1065 others(33): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28139985 | |||||
| chr2:28139987
|
AAC | A | 6 | a0001c0001t0001g0088a0001c0001t0002g0108a0001c0001t0002g0130others(3): Show | 6 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.680+10609_680+1061 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28139987 | |||||
| chr2:28140102
|
CT | C | 5 | a0001c0001t0001g0088a0001c0001t0002g0108a0001c0001t0002g0130others(2): Show | 5 | HG02280.hp2 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.680+10730delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28140102 | |||||
| chr2:28140273
|
A | G | 5 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0001g0054others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.680+10893A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28140273 | ||||||
| chr2:28140287
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.680+10907G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28140287 | ||||||
| chr2:28140475
|
C | T | 15 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(12): Show | 15 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.680+11095C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28140475 | ||||||
| chr2:28140657
|
A | G | 23 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(20): Show | 23 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.680+11277A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28140657 | ||||||
| chr2:28140718
|
A | G | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02630.hp1 HG02723.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.680+11338A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28140718 | ||||||
| chr2:28140730
|
A | T | 89 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0022others(86): Show | 89 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.680+11350A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28140730 | ||||||
| chr2:28140760
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.680+11380G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28140760 | ||||||
| chr2:28140771
|
A | T | 1 | a0001c0001t0001g0044 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.680+11391A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28140771 | ||||||
| chr2:28140789
|
G | A | 6 | a0001c0001t0001g0088a0001c0001t0002g0108a0001c0001t0002g0130others(3): Show | 6 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.680+11409G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28140789 | ||||||
| chr2:28140813
|
A | G | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.680+11433A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28140813 | ||||||
| chr2:28140874
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.680+11494G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28140874 | ||||||
| chr2:28141176
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.680+11796C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28141176 | ||||||
| chr2:28141309
|
CCCCATGA others(1): Show |
C | 23 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(20): Show | 23 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.680+11930_680+1193 others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28141309 | ||||||
| chr2:28141405
|
T | C | 38 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(35): Show | 38 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.680+12025T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28141405 | ||||||
| chr2:28141416
|
C | T | 104 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(101): Show | 104 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.680+12036C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28141416 | ||||||
| chr2:28141485
|
A | G | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(7): Show | 10 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.680+12105A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28141485 | ||||||
| chr2:28141559
|
C | T | 23 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(20): Show | 23 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.680+12179C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28141559 | ||||||
| chr2:28142060
|
C | CTGT | 23 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(20): Show | 23 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.680+12686_680+1268 others(7): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28142060 | |||||
| chr2:28142224
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.680+12844G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28142224 | ||||||
| chr2:28142315
|
A | G | 2 | a0001c0001t0002g0107a0001c0001t0003g0106 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.680+12935A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28142315 | ||||||
| chr2:28142530
|
A | G | 1 | a0001c0001t0002g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.680+13150A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28142530 | ||||||
| chr2:28142797
|
C | T | 29 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(26): Show | 29 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.680+13417C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28142797 | ||||||
| chr2:28142853
|
A | T | 2 | a0001c0001t0002g0062a0001c0001t0002g0096 | 2 | HG01934.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.680+13473A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28142853 | ||||||
| chr2:28142900
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.680+13520A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28142900 | ||||||
| chr2:28143047
|
G | A | 26 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(23): Show | 26 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.680+13667G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28143047 | ||||||
| chr2:28143144
|
A | AAT | 46 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(43): Show | 46 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.680+13780_680+1378 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28143144 | |||||
| chr2:28143144
|
A | AATAT | 2 | a0001c0001t0003g0089a0001c0001t0003g0090 | 2 | HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.680+13778_680+1378 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28143144 | |||||
| chr2:28143200
|
T | C | 2 | a0001c0001t0001g0109a0001c0001t0002g0061 | 2 | HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.680+13820T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28143200 | ||||||
| chr2:28143317
|
GA | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0139 | 2 | HG02897.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.680+13938delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28143317 | ||||||
| chr2:28143817
|
T | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.680+14437T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28143817 | ||||||
| chr2:28143917
|
G | A | 1 | a0001c0001t0001g0155 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.680+14537G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28143917 | ||||||
| chr2:28144055
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0154 | 2 | HG00741.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.680+14675C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28144055 | ||||||
| chr2:28144137
|
A | G | 1 | a0001c0001t0002g0152 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.680+14757A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28144137 | ||||||
| chr2:28144284
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.680+14904C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28144284 | ||||||
| chr2:28144382
|
G | A | 101 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(98): Show | 101 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.680+15002G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28144382 | ||||||
| chr2:28144478
|
A | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0139 | 2 | HG02897.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.680+15098A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28144478 | ||||||
| chr2:28144665
|
C | T | 31 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(28): Show | 31 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.680+15285C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28144665 | ||||||
| chr2:28144752
|
T | C | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG01496.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.680+15372T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28144752 | ||||||
| chr2:28144894
|
T | G | 17 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(14): Show | 17 | HG00741.hp2 HG01168.hp2 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.680+15514T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28144894 | ||||||
| chr2:28144919
|
A | G | 2 | a0001c0001t0003g0135a0001c0001t0003g0136 | 2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.680+15539A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28144919 | ||||||
| chr2:28144968
|
G | A | 1 | a0001c0001t0001g0155 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.680+15588G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28144968 | ||||||
| chr2:28145054
|
A | G | 4 | a0001c0001t0001g0138a0001c0001t0002g0006a0001c0001t0002g0007others(1): Show | 4 | HG01346.hp1 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.680+15674A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28145054 | ||||||
| chr2:28145208
|
CACAG | C | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02630.hp1 HG02723.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.680+15834_680+1583 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28145208 | |||||
| chr2:28145408
|
G | A | 26 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(23): Show | 26 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.680+16028G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28145408 | ||||||
| chr2:28145437
|
T | A | 1 | a0001c0001t0001g0034 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.680+16057T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28145437 | ||||||
| chr2:28145642
|
T | C | 108 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(105): Show | 108 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.680+16262T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28145642 | ||||||
| chr2:28145665
|
A | C | 1 | a0001c0001t0001g0143 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.680+16285A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28145665 | ||||||
| chr2:28145869
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.680+16489A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28145869 | ||||||
| chr2:28146062
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.680+16682G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28146062 | ||||||
| chr2:28146158
|
A | T | 3 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0009 | 3 | HG01346.hp1 HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.680+16778A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28146158 | ||||||
| chr2:28146275
|
C | G | 1 | a0001c0001t0002g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.680+16895C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28146275 | ||||||
| chr2:28146367
|
AT | A | 3 | a0001c0001t0001g0044a0001c0001t0002g0001a0001c0001t0002g0002 | 3 | HG02258.hp2 HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.680+16989delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28146367 | |||||
| chr2:28146385
|
A | G | 1 | a0001c0001t0002g0110 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.680+17005A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28146385 | ||||||
| chr2:28146459
|
C | T | 1 | a0001c0001t0002g0145 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.680+17079C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28146459 | ||||||
| chr2:28146569
|
C | T | 32 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(29): Show | 32 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.680+17189C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28146569 | ||||||
| chr2:28146892
|
C | T | 53 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(50): Show | 53 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.680+17512C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28146892 | ||||||
| chr2:28146893
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.680+17513G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28146893 | ||||||
| chr2:28147114
|
T | C | 15 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(12): Show | 15 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.680+17734T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28147114 | ||||||
| chr2:28147345
|
A | G | 2 | a0001c0001t0002g0107a0001c0001t0003g0106 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.680+17965A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28147345 | ||||||
| chr2:28147517
|
A | G | 15 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(12): Show | 15 | HG01168.hp2 HG02074.hp1 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.680+18137A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28147517 | ||||||
| chr2:28147622
|
C | T | 6 | a0001c0001t0001g0088a0001c0001t0002g0108a0001c0001t0002g0130others(3): Show | 6 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.680+18242C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28147622 | ||||||
| chr2:28147664
|
G | A | 1 | a0001c0001t0002g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.680+18284G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28147664 | ||||||
| chr2:28147816
|
G | A | 15 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(12): Show | 15 | HG01168.hp2 HG02074.hp1 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.680+18436G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28147816 | ||||||
| chr2:28148029
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.680+18649C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28148029 | ||||||
| chr2:28148225
|
C | G | 1 | a0001c0001t0002g0098 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.680+18845C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28148225 | ||||||
| chr2:28148327
|
T | C | 33 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(30): Show | 33 | HG00639.hp1 HG00639.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.680+18947T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28148327 | ||||||
| chr2:28148412
|
A | G | 1 | a0001c0001t0003g0089 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.680+19032A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28148412 | ||||||
| chr2:28148413
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0002g0068 | 3 | HG02922.hp2 HG03195.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.680+19033C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28148413 | ||||||
| chr2:28148608
|
A | G | 15 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(12): Show | 15 | HG01168.hp2 HG02074.hp1 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.680+19228A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28148608 | ||||||
| chr2:28148899
|
A | G | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.680+19519A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28148899 | ||||||
| chr2:28149380
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.680+20000G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28149380 | ||||||
| chr2:28149411
|
T | A | 2 | a0001c0001t0002g0001a0001c0001t0002g0002 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.680+20031T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28149411 | ||||||
| chr2:28149497
|
G | A | 6 | a0001c0001t0001g0088a0001c0001t0002g0108a0001c0001t0002g0130others(3): Show | 6 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.680+20117G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28149497 | ||||||
| chr2:28149639
|
C | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.680+20259C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28149639 | ||||||
| chr2:28149654
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.680+20274G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28149654 | ||||||
| chr2:28150033
|
C | T | 53 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(50): Show | 53 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.680+20653C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28150033 | ||||||
| chr2:28150109
|
T | C | 3 | a0001c0001t0002g0064a0001c0001t0003g0089a0001c0001t0003g0090 | 3 | HG03209.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.680+20729T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28150109 | ||||||
| chr2:28150210
|
C | G | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.680+20830C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28150210 | ||||||
| chr2:28150344
|
G | A | 1 | a0001c0001t0001g0120 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.680+20964G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28150344 | ||||||
| chr2:28150507
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.680+21127G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28150507 | ||||||
| chr2:28150580
|
A | T | 2 | a0001c0001t0002g0011a0001c0001t0002g0128 | 2 | HG01109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.680+21200A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28150580 | ||||||
| chr2:28150685
|
A | G | 112 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(109): Show | 112 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(109): Show |
intron_variant | MODIFIER | c.680+21305A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28150685 | ||||||
| chr2:28150886
|
A | C | 17 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(14): Show | 17 | HG00741.hp2 HG01168.hp2 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.680+21506A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28150886 | ||||||
| chr2:28150951
|
A | T | 15 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(12): Show | 15 | HG01168.hp2 HG02074.hp1 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.680+21571A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28150951 | ||||||
| chr2:28151054
|
G | T | 3 | a0001c0001t0002g0064a0001c0001t0003g0089a0001c0001t0003g0090 | 3 | HG03209.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.680+21674G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28151054 | ||||||
| chr2:28151231
|
T | A | 33 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(30): Show | 33 | HG00639.hp1 HG00639.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.680+21851T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28151231 | ||||||
| chr2:28151287
|
A | G | 2 | a0001c0001t0001g0070a0001c0001t0001g0084 | 2 | HG01081.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.680+21907A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28151287 | ||||||
| chr2:28151532
|
G | A | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.680+22152G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28151532 | ||||||
| chr2:28151552
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.680+22172G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28151552 | ||||||
| chr2:28151677
|
A | ATACT | 104 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(101): Show | 104 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.680+22300_680+2230 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28151677 | |||||
| chr2:28151707
|
G | A | 1 | a0001c0001t0002g0141 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.680+22327G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28151707 | ||||||
| chr2:28151903
|
C | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.680+22523C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28151903 | ||||||
| chr2:28151904
|
A | C | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG01496.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.680+22524A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28151904 | ||||||
| chr2:28151954
|
G | A | 1 | a0001c0001t0002g0001 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.680+22574G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28151954 | ||||||
| chr2:28152010
|
A | AG | 48 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(45): Show | 48 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.680+22635dupG | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28152010 | |||||
| chr2:28152015
|
G | T | 34 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(31): Show | 34 | HG00639.hp1 HG00639.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.680+22635G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28152015 | ||||||
| chr2:28152069
|
T | G | 1 | a0001c0001t0002g0016 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.680+22689T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28152069 | ||||||
| chr2:28152093
|
T | A | 3 | a0001c0001t0002g0064a0001c0001t0003g0089a0001c0001t0003g0090 | 3 | HG03209.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.680+22713T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28152093 | ||||||
| chr2:28152322
|
A | G | 3 | a0001c0001t0001g0022a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | HG02280.hp1 HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.680+22942A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28152322 | ||||||
| chr2:28152502
|
C | T | 5 | a0001c0001t0001g0017a0001c0001t0001g0053a0001c0001t0001g0082others(2): Show | 5 | HG00140.hp2 HG00733.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.680+23122C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28152502 | ||||||
| chr2:28152783
|
G | A | 1 | a0001c0001t0002g0130 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.680+23403G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28152783 | ||||||
| chr2:28152905
|
G | A | 88 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0022others(85): Show | 88 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.680+23525G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28152905 | ||||||
| chr2:28153095
|
C | G | 1 | a0001c0001t0001g0080 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.680+23715C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28153095 | ||||||
| chr2:28153115
|
GT | G | 16 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(13): Show | 16 | HG01168.hp2 HG02074.hp1 HG02165.hp2 others(13): Show |
intron_variant | MODIFIER | c.680+23737delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28153115 | |||||
| chr2:28153133
|
C | A | 23 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(20): Show | 23 | HG00639.hp1 HG00639.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.680+23753C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28153133 | ||||||
| chr2:28153342
|
T | G | 16 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(13): Show | 16 | HG01168.hp2 HG02074.hp1 HG02165.hp2 others(13): Show |
intron_variant | MODIFIER | c.680+23962T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28153342 | ||||||
| chr2:28153662
|
A | C | 15 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(12): Show | 15 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.680+24282A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28153662 | ||||||
| chr2:28153805
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.680+24425C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28153805 | ||||||
| chr2:28153869
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.680+24489G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28153869 | ||||||
| chr2:28153943
|
G | T | 23 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(20): Show | 23 | HG00639.hp1 HG00639.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.680+24563G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28153943 | ||||||
| chr2:28153981
|
A | C | 3 | a0001c0001t0001g0044a0001c0001t0002g0001a0001c0001t0002g0002 | 3 | HG02258.hp2 HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.680+24601A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28153981 | ||||||
| chr2:28154243
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.680+24863A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28154243 | ||||||
| chr2:28154439
|
GTAAGGTG others(5): Show |
G | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.680+25062_680+2507 others(16): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28154439 | |||||
| chr2:28154565
|
T | C | 2 | a0001c0001t0002g0001a0001c0001t0002g0002 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.680+25185T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28154565 | ||||||
| chr2:28154715
|
A | G | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG01496.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.680+25335A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28154715 | ||||||
| chr2:28154786
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0043 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.680+25406A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28154786 | ||||||
| chr2:28154828
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.680+25448G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28154828 | ||||||
| chr2:28155674
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.680+26294G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28155674 | ||||||
| chr2:28155677
|
A | G | 3 | a0001c0001t0002g0064a0001c0001t0003g0089a0001c0001t0003g0090 | 3 | HG03209.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.680+26297A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28155677 | ||||||
| chr2:28155692
|
T | C | 52 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(49): Show | 52 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.680+26312T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28155692 | ||||||
| chr2:28155704
|
A | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0154 | 2 | HG00741.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.680+26324A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28155704 | ||||||
| chr2:28155715
|
G | C | 1 | a0001c0001t0001g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.680+26335G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28155715 | ||||||
| chr2:28155734
|
A | G | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.680+26354A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28155734 | ||||||
| chr2:28155815
|
T | C | 104 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(101): Show | 104 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.680+26435T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28155815 | ||||||
| chr2:28155939
|
T | C | 157 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(154): Show | 157 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(154): Show |
intron_variant | MODIFIER | c.680+26559T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28155939 | ||||||
| chr2:28156268
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.680+26888A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28156268 | ||||||
| chr2:28156424
|
A | G | 1 | a0001c0001t0002g0020 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.680+27044A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28156424 | ||||||
| chr2:28156463
|
A | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.680+27083A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28156463 | ||||||
| chr2:28156576
|
A | G | 49 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(46): Show | 49 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.680+27196A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28156576 | ||||||
| chr2:28156789
|
G | A | 15 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(12): Show | 15 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.680+27409G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28156789 | ||||||
| chr2:28156828
|
C | T | 5 | a0001c0001t0001g0088a0001c0001t0002g0108a0001c0001t0002g0130others(2): Show | 5 | HG02280.hp2 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.680+27448C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28156828 | ||||||
| chr2:28156878
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.680+27498C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28156878 | ||||||
| chr2:28157000
|
G | A | 1 | a0001c0001t0002g0116 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.680+27620G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28157000 | ||||||
| chr2:28157049
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.680+27669C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28157049 | ||||||
| chr2:28157109
|
A | C | 53 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(50): Show | 53 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.680+27729A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28157109 | ||||||
| chr2:28157125
|
T | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.680+27745T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28157125 | ||||||
| chr2:28157408
|
T | A | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.680+28028T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28157408 | ||||||
| chr2:28157428
|
A | G | 40 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(37): Show | 40 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.680+28048A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28157428 | ||||||
| chr2:28157795
|
A | T | 1 | a0001c0001t0002g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.680+28415A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28157795 | ||||||
| chr2:28158009
|
G | A | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.680+28629G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28158009 | ||||||
| chr2:28158108
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.680+28728G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28158108 | ||||||
| chr2:28158134
|
A | G | 16 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(13): Show | 16 | HG01168.hp2 HG02074.hp1 HG02165.hp2 others(13): Show |
intron_variant | MODIFIER | c.680+28754A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28158134 | ||||||
| chr2:28158159
|
G | A | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.680+28779G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28158159 | ||||||
| chr2:28158687
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.680+29307A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28158687 | ||||||
| chr2:28158905
|
G | A | 16 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(13): Show | 16 | HG01168.hp2 HG02074.hp1 HG02165.hp2 others(13): Show |
intron_variant | MODIFIER | c.680+29525G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28158905 | ||||||
| chr2:28158966
|
A | G | 25 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(22): Show | 25 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.680+29586A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28158966 | ||||||
| chr2:28158988
|
T | A | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.680+29608T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28158988 | ||||||
| chr2:28159211
|
T | A | 1 | a0001c0001t0001g0008 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.680+29831T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28159211 | ||||||
| chr2:28159218
|
C | T | 1 | a0001c0001t0002g0114 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.680+29838C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28159218 | ||||||
| chr2:28159355
|
A | G | 1 | a0001c0001t0002g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.680+29975A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28159355 | ||||||
| chr2:28159421
|
G | A | 16 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(13): Show | 16 | HG01168.hp2 HG02074.hp1 HG02165.hp2 others(13): Show |
intron_variant | MODIFIER | c.680+30041G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28159421 | ||||||
| chr2:28159815
|
G | A | 15 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(12): Show | 15 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.680+30435G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28159815 | ||||||
| chr2:28159882
|
GA | G | 9 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(6): Show | 9 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.680+30517delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28159882 | |||||
| chr2:28159911
|
G | A | 3 | a0001c0001t0001g0044a0001c0001t0002g0001a0001c0001t0002g0002 | 3 | HG02258.hp2 HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.680+30531G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28159911 | ||||||
| chr2:28159989
|
G | A | 1 | a0001c0001t0002g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.680+30609G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28159989 | ||||||
| chr2:28160022
|
C | T | 15 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(12): Show | 15 | HG01168.hp2 HG02074.hp1 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.680+30642C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28160022 | ||||||
| chr2:28160261
|
A | T | 33 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(30): Show | 33 | HG00639.hp1 HG00639.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.680+30881A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28160261 | ||||||
| chr2:28160498
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.680+31118C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28160498 | ||||||
| chr2:28160546
|
C | T | 16 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(13): Show | 16 | HG01168.hp2 HG02074.hp1 HG02165.hp2 others(13): Show |
intron_variant | MODIFIER | c.680+31166C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28160546 | ||||||
| chr2:28160735
|
G | GT | 54 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0040others(51): Show | 54 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.680+31373dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28160735 | |||||
| chr2:28160735
|
GT | G | 32 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(29): Show | 32 | HG00639.hp1 HG00639.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.680+31373delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28160735 | |||||
| chr2:28160757
|
TAAAG | T | 2 | a0001c0001t0003g0135a0001c0001t0003g0136 | 2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.680+31379_680+3138 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28160757 | |||||
| chr2:28160820
|
T | G | 49 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(46): Show | 49 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.680+31440T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28160820 | ||||||
| chr2:28160881
|
A | G | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG01496.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.680+31501A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28160881 | ||||||
| chr2:28160974
|
G | A | 25 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(22): Show | 25 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.680+31594G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28160974 | ||||||
| chr2:28160986
|
C | G | 25 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(22): Show | 25 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.680+31606C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28160986 | ||||||
| chr2:28161006
|
G | A | 16 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(13): Show | 16 | HG01168.hp2 HG02074.hp1 HG02165.hp2 others(13): Show |
intron_variant | MODIFIER | c.680+31626G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28161006 | ||||||
| chr2:28161105
|
A | G | 16 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(13): Show | 16 | HG01168.hp2 HG02074.hp1 HG02165.hp2 others(13): Show |
intron_variant | MODIFIER | c.680+31725A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28161105 | ||||||
| chr2:28161167
|
G | T | 1 | a0001c0001t0001g0143 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.680+31787G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28161167 | ||||||
| chr2:28161265
|
T | C | 48 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(45): Show | 48 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.680+31885T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28161265 | ||||||
| chr2:28161404
|
G | A | 5 | a0001c0001t0001g0057a0001c0001t0001g0069a0001c0001t0002g0068others(2): Show | 5 | HG02135.hp1 HG02602.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.680+32024G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28161404 | ||||||
| chr2:28161509
|
A | G | 3 | a0001c0001t0002g0064a0001c0001t0003g0089a0001c0001t0003g0090 | 3 | HG03209.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.680+32129A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28161509 | ||||||
| chr2:28161661
|
C | T | 2 | a0001c0001t0003g0089a0001c0001t0003g0090 | 2 | HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.680+32281C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28161661 | ||||||
| chr2:28161913
|
T | C | 8 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(5): Show | 8 | HG00639.hp2 HG01109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.680+32533T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28161913 | ||||||
| chr2:28161996
|
A | C | 1 | a0001c0001t0001g0146 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.680+32616A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28161996 | ||||||
| chr2:28162150
|
A | G | 15 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(12): Show | 15 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.680+32770A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28162150 | ||||||
| chr2:28162162
|
G | A | 48 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(45): Show | 48 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.680+32782G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28162162 | ||||||
| chr2:28162280
|
G | A | 48 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(45): Show | 48 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.680+32900G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28162280 | ||||||
| chr2:28162282
|
A | T | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG01496.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.680+32902A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28162282 | ||||||
| chr2:28162289
|
T | C | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.680+32909T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28162289 | ||||||
| chr2:28162290
|
C | G | 1 | a0001c0001t0001g0146 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.680+32910C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28162290 | ||||||
| chr2:28162577
|
C | T | 1 | a0001c0001t0003g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.680+33197C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28162577 | ||||||
| chr2:28162936
|
C | T | 52 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(49): Show | 52 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.680+33556C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28162936 | ||||||
| chr2:28163257
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0139 | 2 | HG02897.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.680+33877C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28163257 | ||||||
| chr2:28163278
|
C | T | 1 | a0001c0001t0001g0073 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.680+33898C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28163278 | ||||||
| chr2:28163370
|
G | A | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.680+33990G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28163370 | ||||||
| chr2:28163669
|
A | G | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.680+34289A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28163669 | ||||||
| chr2:28163760
|
T | A | 1 | a0001c0001t0001g0142 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.680+34380T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28163760 | ||||||
| chr2:28163839
|
T | TGAGGCC | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG01496.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.680+34460_680+3446 others(10): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28163839 | |||||
| chr2:28163971
|
A | C | 7 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0001g0054others(4): Show | 7 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.680+34591A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28163971 | ||||||
| chr2:28164171
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.680+34791G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28164171 | ||||||
| chr2:28164221
|
A | G | 155 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(152): Show | 155 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(152): Show |
intron_variant | MODIFIER | c.680+34841A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28164221 | ||||||
| chr2:28164250
|
C | T | 2 | a0001c0001t0002g0001a0001c0001t0002g0002 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.680+34870C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28164250 | ||||||
| chr2:28164333
|
G | A | 13 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(10): Show | 13 | HG01168.hp2 HG02074.hp1 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.680+34953G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28164333 | ||||||
| chr2:28164472
|
C | T | 14 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(11): Show | 14 | HG01168.hp2 HG02074.hp1 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.680+35092C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28164472 | ||||||
| chr2:28164535
|
T | TA | 16 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(13): Show | 16 | HG00639.hp2 HG01168.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.680+35165dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28164535 | |||||
| chr2:28164989
|
T | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.680+35609T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28164989 | ||||||
| chr2:28165076
|
G | A | 2 | a0001c0001t0002g0152a0001c0001t0002g0158 | 2 | HG02027.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.680+35696G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28165076 | ||||||
| chr2:28165114
|
G | A | 4 | a0001c0001t0002g0010a0001c0001t0002g0016a0001c0001t0002g0020others(1): Show | 4 | HG02897.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.680+35734G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28165114 | ||||||
| chr2:28165191
|
A | G | 2 | a0001c0001t0001g0123a0001c0001t0002g0114 | 2 | HG00140.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.680+35811A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28165191 | ||||||
| chr2:28165529
|
C | CT | 75 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0017others(72): Show | 75 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.680+36172dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28165529 | |||||
| chr2:28165620
|
C | T | 13 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(10): Show | 13 | HG01168.hp2 HG02074.hp1 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.680+36240C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28165620 | ||||||
| chr2:28165744
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.680+36364A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28165744 | ||||||
| chr2:28165823
|
G | A | 1 | a0001c0001t0002g0114 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.680+36443G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28165823 | ||||||
| chr2:28165949
|
A | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.680+36569A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28165949 | ||||||
| chr2:28166218
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.680+36838T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28166218 | ||||||
| chr2:28166261
|
A | G | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.680+36881A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28166261 | ||||||
| chr2:28166368
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0139 | 2 | HG02897.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.680+36988G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28166368 | ||||||
| chr2:28166625
|
G | A | 14 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(11): Show | 14 | HG01168.hp2 HG01891.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.680+37245G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28166625 | ||||||
| chr2:28166765
|
C | G | 1 | a0001c0001t0002g0116 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.680+37385C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28166765 | ||||||
| chr2:28166792
|
G | T | 13 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(10): Show | 13 | HG01168.hp2 HG02074.hp1 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.680+37412G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28166792 | ||||||
| chr2:28166917
|
C | T | 13 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(10): Show | 13 | HG01168.hp2 HG02074.hp1 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.680+37537C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28166917 | ||||||
| chr2:28166979
|
A | C | 25 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(22): Show | 25 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.680+37599A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28166979 | ||||||
| chr2:28166981
|
A | G | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.680+37601A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28166981 | ||||||
| chr2:28167145
|
T | C | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.680+37765T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28167145 | ||||||
| chr2:28167386
|
G | A | 1 | a0001c0001t0003g0067 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.680+38006G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28167386 | ||||||
| chr2:28167448
|
C | A | 50 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(47): Show | 50 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.680+38068C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28167448 | ||||||
| chr2:28167693
|
C | CAAAA | 7 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0066others(4): Show | 7 | HG00140.hp2 HG00733.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.680+38317_680+3832 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28167693 | |||||
| chr2:28167697
|
A | AAAAT | 33 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0069others(30): Show | 33 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.680+38356_680+3835 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28167697 | |||||
| chr2:28167697
|
AAAAT | A | 35 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(32): Show | 35 | HG00639.hp1 HG00639.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.680+38356_680+3835 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28167697 | |||||
| chr2:28167697
|
AAAATAAA others(1): Show |
A | 64 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(61): Show | 64 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.680+38352_680+3835 others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28167697 | |||||
| chr2:28167701
|
T | A | 14 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(11): Show | 14 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.680+38321T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28167701 | ||||||
| chr2:28167705
|
T | A | 5 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0075others(2): Show | 5 | HG00735.hp2 HG01081.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.680+38325T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28167705 | ||||||
| chr2:28167709
|
T | A | 1 | a0001c0001t0001g0060 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.680+38329T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28167709 | ||||||
| chr2:28167889
|
A | T | 1 | a0001c0001t0002g0149 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.680+38509A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28167889 | ||||||
| chr2:28168106
|
CAAG | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0025 | 2 | HG02735.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.680+38727_680+3872 others(7): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28168106 | ||||||
| chr2:28168159
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.680+38779C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28168159 | ||||||
| chr2:28168160
|
G | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0078 | 2 | HG01243.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.680+38780G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28168160 | ||||||
| chr2:28168170
|
C | T | 1 | a0001c0001t0002g0007 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.680+38790C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28168170 | ||||||
| chr2:28168176
|
A | G | 2 | a0001c0001t0002g0006a0001c0001t0002g0009 | 2 | HG01346.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.680+38796A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28168176 | ||||||
| chr2:28168417
|
G | A | 1 | a0001c0001t0003g0089 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.680+39037G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28168417 | ||||||
| chr2:28168461
|
G | A | 16 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(13): Show | 16 | HG00639.hp1 HG00639.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.680+39081G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28168461 | ||||||
| chr2:28168462
|
A | G | 157 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(154): Show | 157 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(154): Show |
intron_variant | MODIFIER | c.680+39082A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28168462 | ||||||
| chr2:28168463
|
T | A | 1 | a0001c0001t0001g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.680+39083T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28168463 | ||||||
| chr2:28168964
|
G | C | 154 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(151): Show | 154 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(151): Show |
intron_variant | MODIFIER | c.680+39584G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28168964 | ||||||
| chr2:28169042
|
C | T | 2 | a0001c0001t0002g0001a0001c0001t0002g0002 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.680+39662C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28169042 | ||||||
| chr2:28169075
|
T | C | 1 | a0001c0001t0003g0089 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.680+39695T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28169075 | ||||||
| chr2:28169595
|
A | G | 49 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0032others(46): Show | 49 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.680+40215A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28169595 | ||||||
| chr2:28169643
|
C | T | 15 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(12): Show | 15 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.680+40263C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28169643 | ||||||
| chr2:28169707
|
T | C | 3 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0151 | 3 | HG02074.hp1 NA18968.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.680+40327T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28169707 | ||||||
| chr2:28169775
|
CA | C | 38 | a0001c0001t0001g0044a0001c0001t0001g0057a0001c0001t0001g0065others(35): Show | 38 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.680+40412delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28169775 | |||||
| chr2:28169884
|
T | G | 1 | a0001c0001t0002g0068 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.680+40504T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28169884 | ||||||
| chr2:28169905
|
G | A | 1 | a0001c0001t0002g0095 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.680+40525G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28169905 | ||||||
| chr2:28169927
|
T | C | 54 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(51): Show | 54 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.680+40547T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28169927 | ||||||
| chr2:28170248
|
T | A | 2 | a0001c0001t0001g0093a0001c0001t0001g0102 | 2 | HG01069.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.680+40868T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28170248 | ||||||
| chr2:28170344
|
T | C | 6 | a0001c0001t0001g0138a0001c0001t0002g0001a0001c0001t0002g0002others(3): Show | 6 | HG01346.hp1 HG02109.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.680+40964T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28170344 | ||||||
| chr2:28170376
|
GTC | G | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG01496.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.680+40998_680+4099 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28170376 | |||||
| chr2:28170414
|
C | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.680+41034C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28170414 | ||||||
| chr2:28170462
|
A | G | 4 | a0001c0001t0002g0010a0001c0001t0002g0016a0001c0001t0002g0020others(1): Show | 4 | HG02897.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.680+41082A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28170462 | ||||||
| chr2:28170578
|
C | T | 52 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(49): Show | 52 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.680+41198C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28170578 | ||||||
| chr2:28170675
|
G | A | 2 | a0001c0001t0001g0143a0001c0001t0001g0154 | 2 | HG00741.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.680+41295G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28170675 | ||||||
| chr2:28170839
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.680+41459T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28170839 | ||||||
| chr2:28171072
|
G | A | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG01496.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.680+41692G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28171072 | ||||||
| chr2:28171112
|
A | AAT | 79 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0023others(76): Show | 79 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.680+41749_680+4175 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28171112 | |||||
| chr2:28171112
|
A | AATAT | 5 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012others(2): Show | 5 | HG02572.hp1 HG02698.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.680+41747_680+4175 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28171112 | |||||
| chr2:28171320
|
T | A | 154 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(151): Show | 154 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(151): Show |
intron_variant | MODIFIER | c.680+41940T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28171320 | ||||||
| chr2:28171426
|
T | C | 16 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(13): Show | 16 | HG00741.hp2 HG01168.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.680+42046T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28171426 | ||||||
| chr2:28171593
|
T | C | 46 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(43): Show | 46 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.680+42213T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28171593 | ||||||
| chr2:28171768
|
G | C | 1 | a0001c0001t0001g0127 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.680+42388G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28171768 | ||||||
| chr2:28171859
|
C | CA | 54 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(51): Show | 54 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.680+42479_680+4248 others(5): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28171859 | ||||||
| chr2:28172016
|
A | G | 154 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(151): Show | 154 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(151): Show |
intron_variant | MODIFIER | c.680+42636A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28172016 | ||||||
| chr2:28172087
|
A | ATG | 8 | a0001c0001t0001g0045a0001c0001t0001g0094a0001c0001t0002g0062others(5): Show | 8 | HG01934.hp1 HG02572.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.680+42734_680+4273 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28172087 | |||||
| chr2:28172087
|
ATG | A | 42 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(39): Show | 42 | HG00639.hp1 HG00639.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.680+42734_680+4273 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28172087 | |||||
| chr2:28172087
|
ATGTGTG | A | 55 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(52): Show | 55 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.680+42730_680+4273 others(10): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28172087 | |||||
| chr2:28172221
|
A | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.680+42841A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28172221 | ||||||
| chr2:28172243
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.680+42863G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28172243 | ||||||
| chr2:28172334
|
G | A | 1 | a0001c0001t0001g0073 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.680+42954G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28172334 | ||||||
| chr2:28172778
|
C | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.680+43398C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28172778 | ||||||
| chr2:28173135
|
T | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.680+43755T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28173135 | ||||||
| chr2:28173438
|
G | A | 2 | a0001c0001t0003g0089a0001c0001t0003g0090 | 2 | HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.680+44058G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28173438 | ||||||
| chr2:28173444
|
G | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0025 | 2 | HG02735.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.680+44064G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28173444 | ||||||
| chr2:28173532
|
AC | A | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG01496.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.680+44153delC | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28173532 | ||||||
| chr2:28173582
|
C | T | 17 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(14): Show | 17 | HG00639.hp1 HG00639.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.680+44202C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28173582 | ||||||
| chr2:28173613
|
T | G | 2 | a0001c0001t0001g0074a0001c0001t0001g0081 | 2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.680+44233T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28173613 | ||||||
| chr2:28173616
|
G | A | 83 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(80): Show | 83 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.680+44236G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28173616 | ||||||
| chr2:28173655
|
C | G | 1 | a0001c0001t0001g0073 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.680+44275C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28173655 | ||||||
| chr2:28173663
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.680+44283T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28173663 | ||||||
| chr2:28173764
|
G | A | 1 | a0001c0001t0002g0001 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.680+44384G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28173764 | ||||||
| chr2:28174393
|
G | A | 4 | a0001c0001t0002g0010a0001c0001t0002g0016a0001c0001t0002g0020others(1): Show | 4 | HG02897.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.680+45013G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28174393 | ||||||
| chr2:28174581
|
GA | G | 31 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(28): Show | 31 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.680+45204delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28174581 | |||||
| chr2:28174597
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.680+45217C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28174597 | ||||||
| chr2:28174824
|
C | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.680+45444C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28174824 | ||||||
| chr2:28175171
|
A | C | 1 | a0001c0001t0001g0111 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.680+45791A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28175171 | ||||||
| chr2:28175241
|
C | T | 2 | a0001c0001t0003g0135a0001c0001t0003g0136 | 2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.680+45861C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28175241 | ||||||
| chr2:28175297
|
A | C | 4 | a0001c0001t0001g0138a0001c0001t0002g0006a0001c0001t0002g0007others(1): Show | 4 | HG01346.hp1 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.680+45917A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28175297 | ||||||
| chr2:28175322
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0104a0001c0001t0002g0105 | 3 | NA18954.hp2 NA18986.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.680+45942G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28175322 | ||||||
| chr2:28175374
|
G | A | 16 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(13): Show | 16 | HG00639.hp1 HG00639.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.680+45994G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28175374 | ||||||
| chr2:28175457
|
G | A | 83 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(80): Show | 83 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.680+46077G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28175457 | ||||||
| chr2:28175528
|
A | G | 15 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(12): Show | 15 | HG01168.hp2 HG02074.hp1 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.680+46148A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28175528 | ||||||
| chr2:28175897
|
C | A | 5 | a0001c0001t0001g0088a0001c0001t0002g0108a0001c0001t0002g0130others(2): Show | 5 | HG02280.hp2 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.680+46517C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28175897 | ||||||
| chr2:28176054
|
A | G | 15 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(12): Show | 15 | HG01168.hp2 HG02074.hp1 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.680+46674A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28176054 | ||||||
| chr2:28176329
|
G | T | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG01496.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.680+46949G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28176329 | ||||||
| chr2:28176343
|
G | A | 31 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(28): Show | 31 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.680+46963G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28176343 | ||||||
| chr2:28176401
|
C | G | 1 | a0001c0001t0002g0158 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.680+47021C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28176401 | ||||||
| chr2:28176524
|
T | C | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG01496.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.680+47144T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28176524 | ||||||
| chr2:28176569
|
C | CA | 24 | a0001c0001t0001g0056a0001c0001t0001g0065a0001c0001t0001g0066others(21): Show | 24 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.680+47216dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28176569 | |||||
| chr2:28176569
|
C | CAA | 8 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0036others(5): Show | 8 | HG02027.hp1 HG02074.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.680+47215_680+4721 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28176569 | |||||
| chr2:28176569
|
C | CAAA | 7 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0002g0006others(4): Show | 7 | HG01168.hp2 HG01346.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.680+47214_680+4721 others(7): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28176569 | |||||
| chr2:28176569
|
C | CAAAA | 12 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0023others(9): Show | 12 | HG00733.hp2 HG00741.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.680+47213_680+4721 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28176569 | |||||
| chr2:28176569
|
C | CAAAAA | 10 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0143others(7): Show | 10 | HG00639.hp1 HG00639.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.680+47212_680+4721 others(9): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28176569 | |||||
| chr2:28176569
|
C | CAAAAAA | 7 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0054others(4): Show | 7 | HG01109.hp1 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.680+47211_680+4721 others(10): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28176569 | |||||
| chr2:28176569
|
C | CAAAAAAA others(1): Show |
6 | a0001c0001t0001g0075a0001c0001t0001g0088a0001c0001t0002g0064others(3): Show | 6 | HG00735.hp2 HG02280.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.680+47209_680+4721 others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28176569 | |||||
| chr2:28176569
|
C | CAAAAAAA others(2): Show |
10 | a0001c0001t0001g0045a0001c0001t0001g0059a0001c0001t0001g0060others(7): Show | 10 | HG01081.hp2 HG01099.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.680+47208_680+4721 others(13): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28176569 | |||||
| chr2:28176569
|
C | CAAAAAAA others(3): Show |
10 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0078others(7): Show | 10 | HG00140.hp2 HG01243.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.680+47207_680+4721 others(14): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28176569 | |||||
| chr2:28176569
|
C | CAAAAAAA others(4): Show |
2 | a0001c0001t0001g0053a0001c0001t0001g0153 | 2 | HG00733.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.680+47206_680+4721 others(15): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28176569 | |||||
| chr2:28176569
|
C | CAAAAAAA others(5): Show |
3 | a0001c0001t0001g0017a0001c0001t0001g0044a0001c0001t0003g0121 | 3 | HG01433.hp1 HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.680+47205_680+4721 others(16): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28176569 | |||||
| chr2:28176569
|
C | CAAAAAAA others(7): Show |
2 | a0001c0001t0001g0134a0001c0001t0005g0119 | 2 | HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.680+47203_680+4721 others(18): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28176569 | |||||
| chr2:28176569
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0002g0028 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.680+47202_680+4721 others(19): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28176569 | |||||
| chr2:28176569
|
C | CAAAAAAA others(9): Show |
9 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0102others(6): Show | 9 | HG01069.hp2 HG01106.hp2 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.680+47201_680+4721 others(20): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28176569 | |||||
| chr2:28176569
|
C | CAAAAAAA others(10): Show |
11 | a0001c0001t0001g0035a0001c0001t0001g0058a0001c0001t0001g0072others(8): Show | 11 | HG00738.hp2 HG01168.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.680+47200_680+4721 others(21): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28176569 | |||||
| chr2:28176569
|
C | CAAAAAAA others(11): Show |
3 | a0001c0001t0001g0113a0001c0001t0002g0030a0001c0001t0002g0114 | 3 | HG02698.hp2 HG02738.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.680+47199_680+4721 others(22): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28176569 | |||||
| chr2:28176569
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0001g0073 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.680+47197_680+4721 others(24): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28176569 | |||||
| chr2:28176569
|
C | CAAAAAAA others(14): Show |
2 | a0001c0001t0001g0041a0001c0001t0002g0095 | 2 | HG01192.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.680+47196_680+4721 others(25): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28176569 | |||||
| chr2:28176569
|
C | CAAAAAAA others(15): Show |
3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0002g0061 | 3 | HG02027.hp2 HG02602.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.680+47195_680+4721 others(26): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28176569 | |||||
| chr2:28176569
|
C | CAAAAAAA others(16): Show |
2 | a0001c0001t0002g0062a0001c0001t0004g0118 | 2 | HG03486.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.680+47194_680+4721 others(27): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28176569 | |||||
| chr2:28176569
|
C | CAAAAAAA others(17): Show |
2 | a0001c0001t0001g0111a0001c0001t0001g0115 | 2 | HG02135.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.680+47193_680+4721 others(28): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28176569 | |||||
| chr2:28176569
|
C | CAAAAAAA others(18): Show |
2 | a0001c0001t0001g0109a0001c0001t0002g0149 | 2 | HG02970.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.680+47192_680+4721 others(29): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28176569 | |||||
| chr2:28176569
|
C | CAAAAAAA others(20): Show |
3 | a0001c0001t0001g0042a0001c0001t0001g0091a0001c0001t0002g0103 | 3 | HG02148.hp2 HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.680+47190_680+4721 others(31): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28176569 | |||||
| chr2:28176569
|
C | CAAAAAAA others(26): Show |
1 | a0001c0001t0001g0097 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.680+47216_680+4721 others(37): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28176569 | |||||
| chr2:28176569
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0002g0110 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.680+47205_680+4721 others(16): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28176569 | |||||
| chr2:28176841
|
C | CA | 10 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0074others(7): Show | 10 | HG01109.hp2 HG01891.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.680+47477dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28176841 | |||||
| chr2:28176841
|
CA | C | 9 | a0001c0001t0001g0155a0001c0001t0002g0029a0001c0001t0002g0046others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.680+47477delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28176841 | |||||
| chr2:28176854
|
AAAAG | A | 15 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(12): Show | 15 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.680+47477_680+4748 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28176854 | |||||
| chr2:28176890
|
A | G | 1 | a0001c0001t0002g0098 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.680+47510A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28176890 | ||||||
| chr2:28177083
|
A | G | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.680+47703A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28177083 | ||||||
| chr2:28177113
|
C | A | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG01496.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.680+47733C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28177113 | ||||||
| chr2:28177264
|
GA | G | 7 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(4): Show | 7 | HG00741.hp2 HG01109.hp1 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.680+47896delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28177264 | |||||
| chr2:28177332
|
A | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.680+47952A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28177332 | ||||||
| chr2:28177436
|
A | T | 1 | a0001c0001t0001g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.680+48056A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28177436 | ||||||
| chr2:28177439
|
TCTATCAT others(57): Show |
T | 5 | a0001c0001t0001g0088a0001c0001t0002g0108a0001c0001t0002g0130others(2): Show | 5 | HG02280.hp2 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.680+48060_680+4812 others(68): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28177439 | ||||||
| chr2:28177706
|
C | CA | 7 | a0001c0001t0001g0088a0001c0001t0002g0046a0001c0001t0002g0077others(4): Show | 7 | HG00639.hp1 HG00639.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.680+48339dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28177706 | |||||
| chr2:28177706
|
CA | C | 25 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(22): Show | 25 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.680+48339delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28177706 | |||||
| chr2:28177708
|
A | G | 31 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(28): Show | 31 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.680+48328A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28177708 | ||||||
| chr2:28177732
|
A | T | 2 | a0001c0001t0002g0001a0001c0001t0002g0002 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.680+48352A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28177732 | ||||||
| chr2:28177977
|
TGGA | T | 4 | a0001c0001t0002g0010a0001c0001t0002g0016a0001c0001t0002g0020others(1): Show | 4 | HG02897.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.680+48599_680+4860 others(7): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28177977 | |||||
| chr2:28178150
|
A | G | 2 | a0001c0001t0001g0023a0001c0001t0001g0025 | 2 | HG02735.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.680+48770A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28178150 | ||||||
| chr2:28178439
|
A | G | 84 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(81): Show | 84 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.680+49059A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28178439 | ||||||
| chr2:28178558
|
T | C | 1 | a0001c0001t0002g0116 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.680+49178T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28178558 | ||||||
| chr2:28178699
|
G | GT | 136 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0022others(133): Show | 136 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(133): Show |
intron_variant | MODIFIER | c.680+49329dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28178699 | |||||
| chr2:28178699
|
G | GTT | 15 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(12): Show | 15 | HG01168.hp2 HG02074.hp1 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.680+49328_680+4932 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28178699 | |||||
| chr2:28178727
|
C | CA | 5 | a0001c0001t0001g0088a0001c0001t0002g0108a0001c0001t0002g0130others(2): Show | 5 | HG02280.hp2 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.680+49354dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28178727 | |||||
| chr2:28178818
|
T | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.680+49438T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28178818 | ||||||
| chr2:28178990
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.680+49610C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28178990 | ||||||
| chr2:28179091
|
C | T | 5 | a0001c0001t0001g0088a0001c0001t0002g0108a0001c0001t0002g0130others(2): Show | 5 | HG02280.hp2 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.680+49711C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28179091 | ||||||
| chr2:28179137
|
A | G | 2 | a0001c0001t0003g0135a0001c0001t0003g0136 | 2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.680+49757A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28179137 | ||||||
| chr2:28179228
|
T | C | 154 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(151): Show | 154 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(151): Show |
intron_variant | MODIFIER | c.680+49848T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28179228 | ||||||
| chr2:28179348
|
C | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0025 | 2 | HG02735.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.680+49968C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28179348 | ||||||
| chr2:28179349
|
G | T | 1 | a0001c0001t0002g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.680+49969G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28179349 | ||||||
| chr2:28179427
|
C | T | 16 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(13): Show | 16 | HG00741.hp2 HG01168.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.680+50047C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28179427 | ||||||
| chr2:28179431
|
G | A | 154 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(151): Show | 154 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(151): Show |
intron_variant | MODIFIER | c.680+50051G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28179431 | ||||||
| chr2:28179530
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.680+50150G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28179530 | ||||||
| chr2:28179691
|
C | G | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG01496.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.680+50311C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28179691 | ||||||
| chr2:28179759
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.680+50379G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28179759 | ||||||
| chr2:28179838
|
G | A | 154 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(151): Show | 154 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(151): Show |
intron_variant | MODIFIER | c.680+50458G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28179838 | ||||||
| chr2:28179996
|
C | A | 50 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(47): Show | 50 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.680+50616C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28179996 | ||||||
| chr2:28180106
|
G | GA | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.680+50732dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28180106 | |||||
| chr2:28180117
|
C | G | 1 | a0001c0001t0002g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.680+50737C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28180117 | ||||||
| chr2:28180307
|
A | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.680+50927A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28180307 | ||||||
| chr2:28180378
|
T | C | 1 | a0001c0001t0002g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.680+50998T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28180378 | ||||||
| chr2:28180424
|
C | T | 25 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(22): Show | 25 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.680+51044C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28180424 | ||||||
| chr2:28180524
|
G | A | 154 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(151): Show | 154 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(151): Show |
intron_variant | MODIFIER | c.680+51144G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28180524 | ||||||
| chr2:28180535
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.680+51155G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28180535 | ||||||
| chr2:28180593
|
G | T | 2 | a0001c0001t0002g0122a0001c0001t0003g0121 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.680+51213G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28180593 | ||||||
| chr2:28180746
|
G | A | 54 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(51): Show | 54 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.680+51366G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28180746 | ||||||
| chr2:28180778
|
AT | A | 2 | a0001c0001t0002g0122a0001c0001t0003g0121 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.680+51399delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28180778 | ||||||
| chr2:28180832
|
G | A | 54 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(51): Show | 54 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.680+51452G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28180832 | ||||||
| chr2:28180916
|
T | C | 54 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(51): Show | 54 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.680+51536T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28180916 | ||||||
| chr2:28180951
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.680+51571A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28180951 | ||||||
| chr2:28181450
|
A | G | 2 | a0001c0001t0002g0006a0001c0001t0002g0009 | 2 | HG01346.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.680+52070A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28181450 | ||||||
| chr2:28181540
|
A | C | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.680+52160A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28181540 | ||||||
| chr2:28181793
|
T | A | 49 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0032others(46): Show | 49 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.680+52413T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28181793 | ||||||
| chr2:28181794
|
T | A | 115 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0022others(112): Show | 115 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(112): Show |
intron_variant | MODIFIER | c.680+52414T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28181794 | ||||||
| chr2:28181795
|
A | T | 19 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(16): Show | 19 | HG01168.hp2 HG01496.hp1 HG02074.hp1 others(16): Show |
intron_variant | MODIFIER | c.680+52415A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28181795 | ||||||
| chr2:28181796
|
A | T | 17 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(14): Show | 17 | HG01168.hp2 HG01496.hp1 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.680+52416A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28181796 | ||||||
| chr2:28181807
|
CAAAAT | C | 10 | a0001c0001t0001g0092a0001c0001t0001g0142a0001c0001t0001g0143others(7): Show | 10 | HG00741.hp2 HG01168.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.680+52431_680+5243 others(9): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28181807 | |||||
| chr2:28181995
|
A | G | 17 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(14): Show | 17 | HG00741.hp2 HG01168.hp2 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.680+52615A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28181995 | ||||||
| chr2:28182241
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.680+52861G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28182241 | ||||||
| chr2:28182278
|
T | C | 19 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(16): Show | 19 | HG00741.hp2 HG01168.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.680+52898T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28182278 | ||||||
| chr2:28182428
|
C | T | 7 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0001g0054others(4): Show | 7 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.680+53048C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28182428 | ||||||
| chr2:28182446
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.680+53066G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28182446 | ||||||
| chr2:28182519
|
C | T | 18 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(15): Show | 18 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.680+53139C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28182519 | ||||||
| chr2:28182638
|
G | C | 2 | a0001c0001t0002g0122a0001c0001t0003g0121 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.680+53258G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28182638 | ||||||
| chr2:28182696
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.680+53316T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28182696 | ||||||
| chr2:28182789
|
A | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.680+53409A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28182789 | ||||||
| chr2:28183165
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.680+53785G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28183165 | ||||||
| chr2:28183174
|
C | T | 2 | a0001c0001t0001g0091a0001c0001t0004g0118 | 2 | HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.680+53794C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28183174 | ||||||
| chr2:28183396
|
G | A | 1 | a0001c0001t0002g0122 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.681-53806G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28183396 | ||||||
| chr2:28183739
|
T | TCA | 5 | a0001c0001t0001g0088a0001c0001t0002g0108a0001c0001t0002g0130others(2): Show | 5 | HG02280.hp2 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.681-53429_681-5342 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28183739 | |||||
| chr2:28183739
|
T | TCACACA | 5 | a0001c0001t0001g0022a0001c0001t0001g0054a0001c0001t0001g0055others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.681-53433_681-5342 others(10): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28183739 | |||||
| chr2:28183739
|
T | TCACACAC others(1): Show |
12 | a0001c0001t0001g0045a0001c0001t0001g0073a0001c0001t0001g0113others(9): Show | 12 | HG00140.hp1 HG02165.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.681-53435_681-5342 others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28183739 | |||||
| chr2:28183739
|
T | TCACACAC others(3): Show |
8 | a0001c0001t0001g0027a0001c0001t0001g0074a0001c0001t0001g0091others(5): Show | 8 | HG00741.hp2 HG02148.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.681-53437_681-5342 others(14): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28183739 | |||||
| chr2:28183739
|
T | TCACACAC others(5): Show |
36 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(33): Show | 36 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.681-53439_681-5342 others(16): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28183739 | |||||
| chr2:28183739
|
T | TCACACAC others(7): Show |
13 | a0001c0001t0001g0023a0001c0001t0001g0093a0001c0001t0001g0097others(10): Show | 13 | HG01109.hp1 HG01168.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.681-53441_681-5342 others(18): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28183739 | |||||
| chr2:28183739
|
T | TCACACAC others(9): Show |
8 | a0001c0001t0001g0032a0001c0001t0001g0035a0001c0001t0001g0102others(5): Show | 8 | HG01069.hp2 HG02615.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.681-53443_681-5342 others(20): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28183739 | |||||
| chr2:28183739
|
T | TCACACAC others(11): Show |
2 | a0001c0001t0002g0029a0001c0001t0002g0096 | 2 | HG01934.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.681-53445_681-5342 others(22): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28183739 | |||||
| chr2:28183739
|
T | TCACACAC others(13): Show |
1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.681-53447_681-5342 others(24): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28183739 | |||||
| chr2:28183739
|
T | TCTCACA | 6 | a0001c0001t0001g0092a0001c0001t0001g0146a0001c0001t0001g0150others(3): Show | 6 | HG01168.hp2 HG02165.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.681-53462_681-5346 others(10): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28183739 | |||||
| chr2:28183739
|
T | TCTCACAC others(1): Show |
6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG02074.hp1 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.681-53462_681-5346 others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28183739 | |||||
| chr2:28183739
|
T | TCTCACAC others(3): Show |
1 | a0001c0001t0003g0089 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.681-53462_681-5346 others(14): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28183739 | |||||
| chr2:28183739
|
T | TCTCACAC others(5): Show |
6 | a0001c0001t0001g0008a0001c0001t0002g0064a0001c0001t0002g0140others(3): Show | 6 | HG00733.hp2 HG01167.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.681-53462_681-5346 others(16): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28183739 | |||||
| chr2:28183739
|
T | TCTCACAC others(7): Show |
13 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0053others(10): Show | 13 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.681-53462_681-5346 others(18): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28183739 | |||||
| chr2:28183739
|
T | TCTCTCAC others(3): Show |
18 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0001g0070others(15): Show | 18 | HG00738.hp1 HG00741.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.681-53462_681-5346 others(14): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28183739 | |||||
| chr2:28183739
|
T | TCTCTCAC others(5): Show |
5 | a0001c0001t0001g0057a0001c0001t0002g0001a0001c0001t0002g0002others(2): Show | 5 | HG02135.hp1 HG02486.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.681-53462_681-5346 others(16): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28183739 | |||||
| chr2:28183739
|
T | TCTCTCAC others(7): Show |
1 | a0001c0001t0002g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.681-53462_681-5346 others(18): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28183739 | |||||
| chr2:28183739
|
T | TCTCTCAC others(11): Show |
1 | a0001c0001t0001g0065 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.681-53462_681-5346 others(22): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28183739 | |||||
| chr2:28183739
|
TCA | T | 3 | a0001c0001t0002g0011a0001c0001t0002g0063a0001c0001t0003g0137 | 3 | HG01109.hp2 HG01891.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.681-53429_681-5342 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28183739 | |||||
| chr2:28183739
|
TCACACAC others(1): Show |
T | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.681-53435_681-5342 others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28183739 | |||||
| chr2:28183740
|
C | CTCACACA others(9): Show |
2 | a0001c0001t0001g0017a0002c0002t0001g0085 | 2 | HG01433.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.681-53462_681-5346 others(20): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28183740 | ||||||
| chr2:28183742
|
C | T | 13 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0053others(10): Show | 13 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.681-53460C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28183742 | ||||||
| chr2:28183743
|
A | T | 1 | a0001c0001t0002g0063 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.681-53459A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28183743 | ||||||
| chr2:28183744
|
C | T | 3 | a0001c0001t0002g0064a0001c0001t0003g0135a0001c0001t0003g0136 | 3 | HG00733.hp2 HG01167.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.681-53458C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28183744 | ||||||
| chr2:28183745
|
A | T | 1 | a0001c0001t0002g0063 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.681-53457A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28183745 | ||||||
| chr2:28183827
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.681-53375A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28183827 | ||||||
| chr2:28183966
|
A | G | 1 | a0001c0001t0002g0116 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.681-53236A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28183966 | ||||||
| chr2:28184263
|
C | CCT | 33 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(30): Show | 33 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.681-52917_681-5291 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28184263 | |||||
| chr2:28184263
|
C | CCTCT | 30 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(27): Show | 30 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.681-52919_681-5291 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28184263 | |||||
| chr2:28184263
|
C | CCTCTCT | 24 | a0001c0001t0001g0053a0001c0001t0001g0057a0001c0001t0001g0065others(21): Show | 24 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.681-52921_681-5291 others(10): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28184263 | |||||
| chr2:28184263
|
C | CCTCTCTC others(3): Show |
1 | a0001c0001t0001g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.681-52925_681-5291 others(14): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28184263 | |||||
| chr2:28184263
|
CCTCTCT | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.681-52921_681-5291 others(10): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28184263 | |||||
| chr2:28184285
|
T | TCC | 22 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0041others(19): Show | 22 | HG00140.hp1 HG01069.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.681-52911_681-5291 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28184285 | |||||
| chr2:28184285
|
T | TCCC | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(23): Show | 26 | HG00738.hp2 HG01433.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.681-52912_681-5291 others(7): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28184285 | |||||
| chr2:28184292
|
C | T | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.681-52910C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28184292 | ||||||
| chr2:28184305
|
T | A | 3 | a0001c0001t0002g0010a0001c0001t0002g0016a0001c0001t0002g0112 | 3 | HG03139.hp1 HG03516.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.681-52897T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28184305 | ||||||
| chr2:28184335
|
T | C | 2 | a0001c0001t0001g0091a0001c0001t0004g0118 | 2 | HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.681-52867T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28184335 | ||||||
| chr2:28184351
|
T | A | 25 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(22): Show | 25 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.681-52851T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28184351 | ||||||
| chr2:28184477
|
T | C | 66 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(63): Show | 66 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.681-52725T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28184477 | ||||||
| chr2:28184485
|
C | T | 2 | a0001c0001t0002g0006a0001c0001t0002g0009 | 2 | HG01346.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.681-52717C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28184485 | ||||||
| chr2:28184532
|
A | G | 3 | a0001c0001t0002g0064a0001c0001t0003g0135a0001c0001t0003g0136 | 3 | HG00733.hp2 HG01167.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.681-52670A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28184532 | ||||||
| chr2:28184549
|
G | C | 3 | a0001c0001t0002g0064a0001c0001t0003g0135a0001c0001t0003g0136 | 3 | HG00733.hp2 HG01167.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.681-52653G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28184549 | ||||||
| chr2:28184625
|
A | G | 7 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0001g0054others(4): Show | 7 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.681-52577A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28184625 | ||||||
| chr2:28184672
|
G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02630.hp1 HG02723.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.681-52530G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28184672 | ||||||
| chr2:28184901
|
T | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.681-52301T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28184901 | ||||||
| chr2:28184949
|
T | C | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.681-52253T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28184949 | ||||||
| chr2:28185340
|
T | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.681-51862T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28185340 | ||||||
| chr2:28185429
|
C | T | 15 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(12): Show | 15 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.681-51773C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28185429 | ||||||
| chr2:28185570
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.681-51632A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28185570 | ||||||
| chr2:28185605
|
G | T | 1 | a0001c0001t0001g0146 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.681-51597G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28185605 | ||||||
| chr2:28185795
|
T | C | 18 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(15): Show | 18 | HG00741.hp2 HG01168.hp2 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.681-51407T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28185795 | ||||||
| chr2:28185831
|
C | T | 14 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(11): Show | 14 | HG01168.hp2 HG02074.hp1 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.681-51371C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28185831 | ||||||
| chr2:28185962
|
A | T | 154 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(151): Show | 154 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(151): Show |
intron_variant | MODIFIER | c.681-51240A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28185962 | ||||||
| chr2:28186315
|
C | A | 2 | a0001c0001t0002g0001a0001c0001t0002g0002 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.681-50887C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28186315 | ||||||
| chr2:28186576
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.681-50626G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28186576 | ||||||
| chr2:28186607
|
G | A | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG01496.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.681-50595G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28186607 | ||||||
| chr2:28186808
|
A | AT | 6 | a0001c0001t0001g0138a0001c0001t0002g0006a0001c0001t0002g0007others(3): Show | 6 | HG01346.hp1 HG02109.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.681-50379dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28186808 | |||||
| chr2:28186808
|
AT | A | 64 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(61): Show | 64 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.681-50379delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28186808 | |||||
| chr2:28187021
|
G | A | 1 | a0001c0001t0001g0035 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.681-50181G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28187021 | ||||||
| chr2:28187195
|
A | G | 2 | a0001c0001t0001g0032a0001c0001t0001g0072 | 2 | HG00738.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.681-50007A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28187195 | ||||||
| chr2:28187287
|
G | C | 154 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(151): Show | 154 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(151): Show |
intron_variant | MODIFIER | c.681-49915G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28187287 | ||||||
| chr2:28187322
|
T | C | 156 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(153): Show |
intron_variant | MODIFIER | c.681-49880T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28187322 | ||||||
| chr2:28187531
|
A | C | 1 | a0001c0001t0001g0094 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.681-49671A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28187531 | ||||||
| chr2:28187531
|
A | G | 45 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(42): Show | 45 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.681-49671A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28187531 | ||||||
| chr2:28187662
|
A | AT | 35 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(32): Show | 35 | HG00639.hp1 HG00639.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.681-49517dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28187662 | |||||
| chr2:28187662
|
A | ATT | 12 | a0001c0001t0001g0031a0001c0001t0001g0058a0001c0001t0001g0099others(9): Show | 12 | HG02148.hp1 HG02155.hp1 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.681-49518_681-4951 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28187662 | |||||
| chr2:28187662
|
A | ATTT | 36 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0034others(33): Show | 36 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.681-49519_681-4951 others(7): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28187662 | |||||
| chr2:28187662
|
A | ATTTT | 5 | a0001c0001t0001g0097a0001c0001t0001g0125a0001c0001t0001g0127others(2): Show | 5 | HG01433.hp2 HG01934.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.681-49520_681-4951 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28187662 | |||||
| chr2:28187662
|
AT | A | 44 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0053others(41): Show | 44 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.681-49517delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28187662 | |||||
| chr2:28187662
|
ATT | A | 14 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(11): Show | 14 | HG01168.hp2 HG01433.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.681-49518_681-4951 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28187662 | |||||
| chr2:28188035
|
C | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02258.hp2 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.681-49167C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28188035 | ||||||
| chr2:28188088
|
A | C | 89 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(86): Show | 89 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.681-49114A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28188088 | ||||||
| chr2:28188102
|
G | T | 1 | a0001c0001t0002g0051 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.681-49100G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28188102 | ||||||
| chr2:28188155
|
G | A | 61 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(58): Show | 61 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.681-49047G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28188155 | ||||||
| chr2:28188159
|
C | A | 27 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(24): Show | 27 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.681-49043C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28188159 | ||||||
| chr2:28188231
|
A | T | 2 | a0001c0001t0001g0123a0001c0001t0002g0114 | 2 | HG00140.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.681-48971A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28188231 | ||||||
| chr2:28188288
|
G | A | 64 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(61): Show | 64 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.681-48914G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28188288 | ||||||
| chr2:28188323
|
T | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.681-48879T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28188323 | ||||||
| chr2:28188604
|
C | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.681-48598C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28188604 | ||||||
| chr2:28188645
|
A | C | 1 | a0001c0001t0004g0118 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.681-48557A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28188645 | ||||||
| chr2:28188773
|
G | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.681-48429G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28188773 | ||||||
| chr2:28188894
|
C | T | 1 | a0001c0001t0002g0049 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.681-48308C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28188894 | ||||||
| chr2:28188971
|
C | T | 15 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(12): Show | 15 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.681-48231C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28188971 | ||||||
| chr2:28188990
|
C | T | 4 | a0001c0001t0002g0010a0001c0001t0002g0016a0001c0001t0002g0020others(1): Show | 4 | HG02897.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.681-48212C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28188990 | ||||||
| chr2:28188998
|
C | T | 1 | a0001c0001t0002g0107 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.681-48204C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28188998 | ||||||
| chr2:28189034
|
C | T | 18 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(15): Show | 18 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.681-48168C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28189034 | ||||||
| chr2:28189167
|
C | T | 25 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(22): Show | 25 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.681-48035C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28189167 | ||||||
| chr2:28189199
|
C | CA | 9 | a0001c0001t0001g0005a0001c0001t0001g0041a0001c0001t0001g0042others(6): Show | 9 | HG01106.hp2 HG01891.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.681-47990dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28189199 | |||||
| chr2:28189199
|
CA | C | 27 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(24): Show | 27 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.681-47990delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28189199 | |||||
| chr2:28189565
|
T | G | 154 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(151): Show | 154 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(151): Show |
intron_variant | MODIFIER | c.681-47637T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28189565 | ||||||
| chr2:28189632
|
C | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.681-47570C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28189632 | ||||||
| chr2:28189691
|
A | G | 17 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(14): Show | 17 | HG00741.hp2 HG01168.hp2 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.681-47511A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28189691 | ||||||
| chr2:28189785
|
C | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.681-47417C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28189785 | ||||||
| chr2:28189968
|
A | G | 1 | a0001c0001t0001g0027 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.681-47234A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28189968 | ||||||
| chr2:28190330
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.681-46872C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28190330 | ||||||
| chr2:28190756
|
A | G | 1 | a0001c0001t0002g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.681-46446A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28190756 | ||||||
| chr2:28190763
|
A | G | 1 | a0001c0001t0001g0094 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.681-46439A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28190763 | ||||||
| chr2:28191100
|
T | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.681-46102T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28191100 | ||||||
| chr2:28191214
|
A | G | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.681-45988A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28191214 | ||||||
| chr2:28191435
|
C | A | 36 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(33): Show | 36 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.681-45767C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28191435 | ||||||
| chr2:28191672
|
A | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.681-45530A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28191672 | ||||||
| chr2:28191721
|
T | C | 7 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0001g0054others(4): Show | 7 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.681-45481T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28191721 | ||||||
| chr2:28191834
|
A | G | 1 | a0001c0001t0002g0062 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.681-45368A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28191834 | ||||||
| chr2:28191886
|
A | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.681-45316A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28191886 | ||||||
| chr2:28192058
|
A | G | 4 | a0001c0001t0001g0138a0001c0001t0002g0006a0001c0001t0002g0007others(1): Show | 4 | HG01346.hp1 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.681-45144A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28192058 | ||||||
| chr2:28192117
|
C | A | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.681-45085C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28192117 | ||||||
| chr2:28192184
|
G | A | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.681-45018G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28192184 | ||||||
| chr2:28192224
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.681-44978C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28192224 | ||||||
| chr2:28192256
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.681-44946G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28192256 | ||||||
| chr2:28192395
|
C | G | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.681-44807C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28192395 | ||||||
| chr2:28192395
|
C | T | 17 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(14): Show | 17 | HG01168.hp2 HG01496.hp1 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.681-44807C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28192395 | ||||||
| chr2:28192403
|
A | T | 6 | a0001c0001t0001g0138a0001c0001t0002g0006a0001c0001t0002g0007others(3): Show | 6 | HG01346.hp1 HG02109.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.681-44799A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28192403 | ||||||
| chr2:28192445
|
TAA | T | 64 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(61): Show | 64 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.681-44747_681-4474 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28192445 | |||||
| chr2:28192517
|
CTTTTTT | C | 17 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0053others(14): Show | 17 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.681-44668_681-4466 others(10): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28192517 | |||||
| chr2:28192517
|
CTTTTTTT | C | 6 | a0001c0001t0001g0017a0001c0001t0001g0088a0001c0001t0002g0108others(3): Show | 6 | HG01433.hp1 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.681-44669_681-4466 others(11): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28192517 | |||||
| chr2:28192531
|
T | C | 16 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(13): Show | 16 | HG01168.hp2 HG01496.hp1 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.681-44671T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28192531 | ||||||
| chr2:28192731
|
C | T | 3 | a0001c0001t0001g0052a0001c0001t0001g0080a0001c0001t0001g0157 | 3 | HG01099.hp2 HG02040.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.681-44471C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28192731 | ||||||
| chr2:28192771
|
C | A | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.681-44431C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28192771 | ||||||
| chr2:28193032
|
G | A | 1 | a0001c0001t0003g0089 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.681-44170G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28193032 | ||||||
| chr2:28193379
|
G | A | 25 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(22): Show | 25 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.681-43823G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28193379 | ||||||
| chr2:28193614
|
A | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.681-43588A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28193614 | ||||||
| chr2:28193933
|
G | T | 1 | a0001c0001t0001g0080 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.681-43269G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28193933 | ||||||
| chr2:28194017
|
G | T | 57 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0032others(54): Show | 57 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.681-43185G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28194017 | ||||||
| chr2:28194362
|
G | C | 2 | a0001c0001t0003g0089a0001c0001t0003g0090 | 2 | HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.681-42840G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28194362 | ||||||
| chr2:28194575
|
C | CT | 81 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(78): Show | 81 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.681-42606dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28194575 | |||||
| chr2:28194575
|
C | CTT | 59 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0015others(56): Show | 59 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.681-42607_681-4260 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28194575 | |||||
| chr2:28194575
|
C | CTTT | 5 | a0001c0001t0001g0014a0001c0001t0001g0040a0001c0001t0001g0074others(2): Show | 5 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.681-42608_681-4260 others(7): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28194575 | |||||
| chr2:28194613
|
T | C | 154 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(151): Show | 154 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(151): Show |
intron_variant | MODIFIER | c.681-42589T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28194613 | ||||||
| chr2:28194636
|
C | T | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.681-42566C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28194636 | ||||||
| chr2:28194637
|
G | A | 86 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(83): Show | 86 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.681-42565G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28194637 | ||||||
| chr2:28194648
|
C | A | 1 | a0001c0001t0003g0089 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.681-42554C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28194648 | ||||||
| chr2:28194651
|
G | A | 25 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(22): Show | 25 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.681-42551G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28194651 | ||||||
| chr2:28194849
|
T | G | 87 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(84): Show | 87 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.681-42353T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28194849 | ||||||
| chr2:28194931
|
C | T | 18 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(15): Show | 18 | HG00741.hp2 HG01168.hp2 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.681-42271C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28194931 | ||||||
| chr2:28194932
|
G | A | 3 | a0001c0001t0001g0069a0001c0001t0002g0068a0001c0001t0003g0067 | 3 | NA18974.hp2 NA18986.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.681-42270G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28194932 | ||||||
| chr2:28195036
|
A | G | 1 | a0001c0001t0002g0050 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.681-42166A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28195036 | ||||||
| chr2:28195102
|
A | G | 2 | a0001c0001t0002g0107a0001c0001t0003g0106 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.681-42100A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28195102 | ||||||
| chr2:28195164
|
T | C | 87 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(84): Show | 87 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.681-42038T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28195164 | ||||||
| chr2:28195322
|
G | A | 87 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(84): Show | 87 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.681-41880G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28195322 | ||||||
| chr2:28195401
|
G | A | 1 | a0001c0001t0002g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.681-41801G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28195401 | ||||||
| chr2:28195681
|
C | T | 5 | a0001c0001t0001g0088a0001c0001t0002g0108a0001c0001t0002g0130others(2): Show | 5 | HG02280.hp2 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.681-41521C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28195681 | ||||||
| chr2:28195724
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.681-41478C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28195724 | ||||||
| chr2:28195826
|
C | T | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG01496.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.681-41376C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28195826 | ||||||
| chr2:28195858
|
A | G | 1 | a0001c0001t0002g0098 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.681-41344A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28195858 | ||||||
| chr2:28195870
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.681-41332T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28195870 | ||||||
| chr2:28196094
|
G | A | 25 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(22): Show | 25 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.681-41108G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28196094 | ||||||
| chr2:28196188
|
A | G | 18 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(15): Show | 18 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.681-41014A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28196188 | ||||||
| chr2:28196247
|
A | G | 18 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(15): Show | 18 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.681-40955A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28196247 | ||||||
| chr2:28196281
|
T | C | 1 | a0001c0001t0001g0111 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.681-40921T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28196281 | ||||||
| chr2:28196288
|
C | T | 2 | a0001c0001t0002g0140a0001c0001t0002g0141 | 2 | HG01496.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.681-40914C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28196288 | ||||||
| chr2:28196306
|
A | G | 18 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(15): Show | 18 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.681-40896A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28196306 | ||||||
| chr2:28196314
|
A | G | 18 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(15): Show | 18 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.681-40888A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28196314 | ||||||
| chr2:28196321
|
C | CGTCTCAA others(1): Show |
3 | a0001c0001t0001g0052a0001c0001t0001g0080a0001c0001t0001g0157 | 3 | HG01099.hp2 HG02040.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.681-40881_681-4088 others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28196321 | ||||||
| chr2:28196321
|
C | CGTCTCAA others(18): Show |
1 | a0001c0001t0003g0136 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.681-40881_681-4088 others(29): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28196321 | ||||||
| chr2:28196321
|
C | CGTCTCAA others(19): Show |
1 | a0001c0001t0003g0135 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.681-40881_681-4088 others(30): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28196321 | ||||||
| chr2:28196321
|
C | CGTCTCAA others(21): Show |
4 | a0001c0001t0001g0078a0001c0001t0001g0153a0001c0001t0002g0064others(1): Show | 4 | HG00733.hp1 HG01496.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.681-40881_681-4088 others(32): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28196321 | ||||||
| chr2:28196321
|
C | CGTCTCAA others(22): Show |
2 | a0001c0001t0001g0017a0001c0001t0001g0082 | 2 | HG00140.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.681-40881_681-4088 others(33): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28196321 | ||||||
| chr2:28196321
|
C | CGTCTCAA others(23): Show |
4 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0079others(1): Show | 4 | HG01081.hp2 HG01192.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.681-40881_681-4088 others(34): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28196321 | ||||||
| chr2:28196321
|
C | CGTCTCAA others(24): Show |
1 | a0001c0001t0001g0059 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.681-40881_681-4088 others(35): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28196321 | ||||||
| chr2:28196321
|
C | CGTCTCAA others(25): Show |
1 | a0001c0001t0001g0075 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.681-40881_681-4088 others(36): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28196321 | ||||||
| chr2:28196321
|
C | CGTCTCAA others(26): Show |
1 | a0001c0001t0001g0040 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.681-40881_681-4088 others(37): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28196321 | ||||||
| chr2:28196323
|
T | A | 18 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(15): Show | 18 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.681-40879T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28196323 | ||||||
| chr2:28196325
|
T | A | 18 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(15): Show | 18 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.681-40877T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28196325 | ||||||
| chr2:28196420
|
G | C | 2 | a0001c0001t0001g0074a0001c0001t0001g0081 | 2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.681-40782G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28196420 | ||||||
| chr2:28196459
|
A | C | 25 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0066others(22): Show | 25 | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.681-40743A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28196459 | ||||||
| chr2:28196520
|
G | C | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.681-40682G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28196520 | ||||||
| chr2:28196709
|
C | T | 1 | a0001c0001t0002g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.681-40493C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28196709 | ||||||
| chr2:28196836
|
C | CT | 17 | a0001c0001t0001g0056a0001c0001t0001g0065a0001c0001t0001g0083others(14): Show | 17 | HG00735.hp1 HG00738.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.681-40339dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28196836 | |||||
| chr2:28196836
|
C | CTT | 21 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0015others(18): Show | 21 | HG00741.hp1 HG01069.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.681-40340_681-4033 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28196836 | |||||
| chr2:28196836
|
C | CTTT | 22 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0045others(19): Show | 22 | HG01346.hp1 HG02027.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.681-40341_681-4033 others(7): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28196836 | |||||
| chr2:28196836
|
C | CTTTT | 8 | a0001c0001t0001g0035a0001c0001t0001g0093a0001c0001t0001g0142others(5): Show | 8 | HG01168.hp1 HG02818.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.681-40342_681-4033 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28196836 | |||||
| chr2:28196836
|
C | CTTTTT | 34 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0042others(31): Show | 34 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.681-40343_681-4033 others(9): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28196836 | |||||
| chr2:28196836
|
C | CTTTTTT | 20 | a0001c0001t0001g0032a0001c0001t0001g0041a0001c0001t0001g0052others(17): Show | 20 | HG00733.hp2 HG01167.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.681-40344_681-4033 others(10): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28196836 | |||||
| chr2:28196836
|
C | CTTTTTTT | 8 | a0001c0001t0001g0040a0001c0001t0001g0059a0001c0001t0001g0075others(5): Show | 8 | HG00733.hp1 HG00735.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.681-40345_681-4033 others(11): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28196836 | |||||
| chr2:28196836
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0044 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.681-40348_681-4033 others(14): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28196836 | |||||
| chr2:28196836
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0082a0001c0001t0001g0134 | 2 | HG00140.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.681-40349_681-4033 others(15): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28196836 | |||||
| chr2:28196836
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0133 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.681-40350_681-4033 others(16): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28196836 | |||||
| chr2:28196836
|
CTTTTTTT | C | 6 | a0001c0001t0002g0029a0001c0001t0002g0047a0001c0001t0002g0048others(3): Show | 6 | HG00639.hp2 HG01167.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.681-40345_681-4033 others(11): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28196836 | |||||
| chr2:28196836
|
CTTTTTTT others(1): Show |
C | 7 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(4): Show | 7 | HG00639.hp1 HG01109.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.681-40346_681-4033 others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28196836 | |||||
| chr2:28197259
|
A | T | 1 | a0001c0001t0001g0083 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.681-39943A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28197259 | ||||||
| chr2:28197572
|
G | T | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.681-39630G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28197572 | ||||||
| chr2:28197595
|
T | C | 2 | a0001c0001t0001g0143a0001c0001t0001g0154 | 2 | HG00741.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.681-39607T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28197595 | ||||||
| chr2:28198137
|
C | T | 1 | a0001c0001t0002g0156 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.681-39065C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28198137 | ||||||
| chr2:28198138
|
G | A | 3 | a0001c0001t0002g0064a0001c0001t0003g0135a0001c0001t0003g0136 | 3 | HG00733.hp2 HG01167.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.681-39064G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28198138 | ||||||
| chr2:28198201
|
C | T | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.681-39001C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28198201 | ||||||
| chr2:28198233
|
G | A | 5 | a0001c0001t0001g0088a0001c0001t0002g0108a0001c0001t0002g0130others(2): Show | 5 | HG02280.hp2 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.681-38969G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28198233 | ||||||
| chr2:28198250
|
G | A | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0138others(2): Show | 5 | HG01346.hp1 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.681-38952G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28198250 | ||||||
| chr2:28198418
|
A | G | 151 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0017others(148): Show | 151 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(148): Show |
intron_variant | MODIFIER | c.681-38784A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28198418 | ||||||
| chr2:28198487
|
T | G | 1 | a0001c0001t0002g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.681-38715T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28198487 | ||||||
| chr2:28198514
|
C | T | 49 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0023others(46): Show | 49 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.681-38688C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28198514 | ||||||
| chr2:28198529
|
C | T | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.681-38673C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28198529 | ||||||
| chr2:28198594
|
G | A | 102 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(99): Show | 102 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.681-38608G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28198594 | ||||||
| chr2:28198606
|
T | C | 26 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(23): Show | 26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.681-38596T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28198606 | ||||||
| chr2:28198785
|
T | C | 8 | a0001c0001t0002g0029a0001c0001t0002g0047a0001c0001t0002g0048others(5): Show | 8 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.681-38417T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28198785 | ||||||
| chr2:28198888
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0002g0012 | 2 | HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.681-38314C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28198888 | ||||||
| chr2:28198903
|
C | T | 1 | a0001c0001t0002g0096 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.681-38299C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28198903 | ||||||
| chr2:28198926
|
G | A | 89 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0017others(86): Show | 89 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.681-38276G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28198926 | ||||||
| chr2:28198927
|
TA | T | 10 | a0001c0001t0001g0092a0001c0001t0002g0029a0001c0001t0002g0038others(7): Show | 10 | HG00639.hp2 HG01106.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.681-38269delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28198927 | |||||
| chr2:28198959
|
T | C | 10 | a0001c0001t0002g0021a0001c0001t0002g0029a0001c0001t0002g0047others(7): Show | 10 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.681-38243T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28198959 | ||||||
| chr2:28199122
|
T | C | 30 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0025others(27): Show | 30 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.681-38080T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28199122 | ||||||
| chr2:28199189
|
G | A | 6 | a0001c0001t0001g0022a0001c0001t0001g0054a0001c0001t0001g0055others(3): Show | 6 | HG01109.hp2 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.681-38013G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28199189 | ||||||
| chr2:28199191
|
T | C | 2 | a0001c0001t0002g0122a0001c0001t0003g0121 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.681-38011T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28199191 | ||||||
| chr2:28199691
|
A | T | 1 | a0001c0001t0001g0034 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.681-37511A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28199691 | ||||||
| chr2:28199700
|
C | G | 147 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(144): Show | 147 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(144): Show |
intron_variant | MODIFIER | c.681-37502C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28199700 | ||||||
| chr2:28199702
|
G | A | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.681-37500G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28199702 | ||||||
| chr2:28199744
|
G | A | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.681-37458G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28199744 | ||||||
| chr2:28199763
|
T | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.681-37439T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28199763 | ||||||
| chr2:28199883
|
C | G | 1 | a0001c0001t0001g0125 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.681-37319C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28199883 | ||||||
| chr2:28199981
|
G | A | 8 | a0001c0001t0002g0029a0001c0001t0002g0047a0001c0001t0002g0048others(5): Show | 8 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.681-37221G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28199981 | ||||||
| chr2:28200041
|
T | C | 1 | a0001c0001t0005g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.681-37161T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28200041 | ||||||
| chr2:28200202
|
T | G | 125 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0023others(122): Show | 125 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(122): Show |
intron_variant | MODIFIER | c.681-37000T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28200202 | ||||||
| chr2:28200222
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.681-36980C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28200222 | ||||||
| chr2:28200511
|
A | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.681-36691A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28200511 | ||||||
| chr2:28200571
|
G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG01891.hp2 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.681-36631G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28200571 | ||||||
| chr2:28200608
|
C | T | 1 | a0001c0001t0002g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.681-36594C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28200608 | ||||||
| chr2:28200654
|
T | G | 6 | a0001c0001t0001g0035a0001c0001t0001g0115a0001c0001t0001g0127others(3): Show | 6 | HG02040.hp1 HG02135.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.681-36548T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28200654 | ||||||
| chr2:28200729
|
G | A | 2 | a0001c0001t0002g0122a0001c0001t0003g0121 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.681-36473G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28200729 | ||||||
| chr2:28200758
|
T | TTTTG | 21 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(18): Show | 21 | HG00733.hp2 HG01167.hp2 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.681-36420_681-3641 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28200758 | |||||
| chr2:28200758
|
T | TTTTGTTT others(1): Show |
26 | a0001c0001t0001g0008a0001c0001t0001g0023a0001c0001t0001g0044others(23): Show | 26 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.681-36424_681-3641 others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28200758 | |||||
| chr2:28200758
|
T | TTTTGTTT others(5): Show |
1 | a0001c0001t0002g0029 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.681-36428_681-3641 others(16): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28200758 | |||||
| chr2:28200758
|
TTTTG | T | 104 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0025others(101): Show | 104 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.681-36420_681-3641 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28200758 | |||||
| chr2:28201055
|
G | A | 18 | a0001c0001t0001g0008a0001c0001t0001g0023a0001c0001t0001g0044others(15): Show | 18 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.681-36147G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28201055 | ||||||
| chr2:28201077
|
A | G | 147 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(144): Show | 147 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(144): Show |
intron_variant | MODIFIER | c.681-36125A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28201077 | ||||||
| chr2:28201078
|
G | A | 111 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0025others(108): Show | 111 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.681-36124G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28201078 | ||||||
| chr2:28201159
|
AGT | A | 8 | a0001c0001t0002g0029a0001c0001t0002g0047a0001c0001t0002g0048others(5): Show | 8 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.681-36042_681-3604 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28201159 | ||||||
| chr2:28201315
|
T | C | 1 | a0001c0001t0002g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.681-35887T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28201315 | ||||||
| chr2:28201605
|
C | T | 7 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0053others(4): Show | 7 | HG00140.hp2 HG00733.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.681-35597C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28201605 | ||||||
| chr2:28201809
|
A | G | 4 | a0001c0001t0001g0017a0001c0001t0001g0053a0001c0001t0001g0082others(1): Show | 4 | HG00140.hp2 HG01433.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.681-35393A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28201809 | ||||||
| chr2:28201852
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.681-35350A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28201852 | ||||||
| chr2:28201912
|
T | A | 148 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(145): Show | 148 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(145): Show |
intron_variant | MODIFIER | c.681-35290T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28201912 | ||||||
| chr2:28201939
|
C | CG | 147 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(144): Show | 147 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(144): Show |
intron_variant | MODIFIER | c.681-35261dupG | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28201939 | |||||
| chr2:28201948
|
G | A | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.681-35254G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28201948 | ||||||
| chr2:28201965
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.681-35237A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28201965 | ||||||
| chr2:28202221
|
A | T | 1 | a0001c0001t0003g0067 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.681-34981A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28202221 | ||||||
| chr2:28202222
|
T | A | 1 | a0001c0001t0003g0067 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.681-34980T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28202222 | ||||||
| chr2:28202239
|
G | T | 1 | a0001c0001t0003g0067 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.681-34963G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28202239 | ||||||
| chr2:28202339
|
C | T | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG01891.hp2 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.681-34863C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28202339 | ||||||
| chr2:28202500
|
A | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.681-34702A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28202500 | ||||||
| chr2:28202606
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | HG02280.hp1 HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.681-34596C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28202606 | ||||||
| chr2:28202614
|
A | C | 68 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(65): Show | 68 | HG00140.hp1 HG00738.hp2 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.681-34588A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28202614 | ||||||
| chr2:28202643
|
T | G | 148 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(145): Show | 148 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(145): Show |
intron_variant | MODIFIER | c.681-34559T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28202643 | ||||||
| chr2:28202758
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.681-34444T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28202758 | ||||||
| chr2:28202873
|
G | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.681-34329G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28202873 | ||||||
| chr2:28202980
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.681-34222C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28202980 | ||||||
| chr2:28203195
|
G | T | 1 | a0001c0001t0003g0067 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.681-34007G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28203195 | ||||||
| chr2:28203295
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.681-33907A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28203295 | ||||||
| chr2:28203352
|
C | G | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.681-33850C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28203352 | ||||||
| chr2:28203654
|
T | C | 1 | a0001c0001t0002g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.681-33548T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28203654 | ||||||
| chr2:28203693
|
T | C | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.681-33509T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28203693 | ||||||
| chr2:28203858
|
A | G | 104 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0025others(101): Show | 104 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.681-33344A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28203858 | ||||||
| chr2:28203922
|
G | A | 103 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0025others(100): Show | 103 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.681-33280G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28203922 | ||||||
| chr2:28204132
|
A | G | 16 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(13): Show | 16 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.681-33070A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28204132 | ||||||
| chr2:28204385
|
A | G | 2 | a0001c0001t0002g0107a0001c0001t0003g0106 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.681-32817A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28204385 | ||||||
| chr2:28204432
|
G | T | 1 | a0001c0001t0001g0123 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.681-32770G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28204432 | ||||||
| chr2:28204547
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.681-32655G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28204547 | ||||||
| chr2:28204674
|
T | C | 1 | a0001c0001t0002g0140 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.681-32528T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28204674 | ||||||
| chr2:28205047
|
C | G | 4 | a0001c0001t0002g0062a0001c0001t0002g0096a0001c0001t0002g0101others(1): Show | 4 | HG01934.hp1 NA18955.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.681-32155C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28205047 | ||||||
| chr2:28205063
|
A | G | 2 | a0001c0001t0002g0108a0001c0001t0002g0132 | 2 | HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.681-32139A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28205063 | ||||||
| chr2:28205080
|
T | C | 3 | a0001c0001t0001g0052a0001c0001t0001g0080a0001c0001t0001g0157 | 3 | HG01099.hp2 HG02040.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.681-32122T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28205080 | ||||||
| chr2:28205181
|
T | A | 148 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(145): Show | 148 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(145): Show |
intron_variant | MODIFIER | c.681-32021T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28205181 | ||||||
| chr2:28205395
|
C | T | 1 | a0001c0001t0002g0140 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.681-31807C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28205395 | ||||||
| chr2:28205434
|
TAGAGGTC others(2): Show |
T | 14 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(11): Show | 14 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.681-31765_681-3175 others(13): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28205434 | |||||
| chr2:28205599
|
A | G | 18 | a0001c0001t0001g0008a0001c0001t0001g0023a0001c0001t0001g0044others(15): Show | 18 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.681-31603A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28205599 | ||||||
| chr2:28205818
|
A | G | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.681-31384A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28205818 | ||||||
| chr2:28205863
|
G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG01891.hp2 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.681-31339G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28205863 | ||||||
| chr2:28205922
|
G | A | 8 | a0001c0001t0002g0029a0001c0001t0002g0047a0001c0001t0002g0048others(5): Show | 8 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.681-31280G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28205922 | ||||||
| chr2:28205970
|
C | T | 16 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(13): Show | 16 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.681-31232C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28205970 | ||||||
| chr2:28205971
|
G | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | HG02280.hp1 HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.681-31231G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28205971 | ||||||
| chr2:28206198
|
A | G | 8 | a0001c0001t0002g0029a0001c0001t0002g0047a0001c0001t0002g0048others(5): Show | 8 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.681-31004A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28206198 | ||||||
| chr2:28206261
|
G | A | 7 | a0001c0001t0001g0035a0001c0001t0001g0099a0001c0001t0001g0155others(4): Show | 7 | HG02155.hp2 HG02165.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.681-30941G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28206261 | ||||||
| chr2:28206371
|
G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG01891.hp2 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.681-30831G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28206371 | ||||||
| chr2:28206540
|
A | G | 8 | a0001c0001t0002g0029a0001c0001t0002g0047a0001c0001t0002g0048others(5): Show | 8 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.681-30662A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28206540 | ||||||
| chr2:28206588
|
A | G | 147 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(144): Show | 147 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(144): Show |
intron_variant | MODIFIER | c.681-30614A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28206588 | ||||||
| chr2:28206728
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.681-30474G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28206728 | ||||||
| chr2:28206814
|
T | C | 8 | a0001c0001t0002g0029a0001c0001t0002g0047a0001c0001t0002g0048others(5): Show | 8 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.681-30388T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28206814 | ||||||
| chr2:28206927
|
A | G | 16 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(13): Show | 16 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.681-30275A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28206927 | ||||||
| chr2:28207343
|
TA | T | 144 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(141): Show | 144 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(141): Show |
intron_variant | MODIFIER | c.681-29843delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28207343 | |||||
| chr2:28207391
|
G | A | 2 | a0001c0001t0002g0122a0001c0001t0003g0121 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.681-29811G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28207391 | ||||||
| chr2:28207394
|
G | A | 119 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(116): Show | 119 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.681-29808G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28207394 | ||||||
| chr2:28207486
|
A | G | 2 | a0001c0001t0001g0139a0001c0001t0002g0002 | 2 | HG02486.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.681-29716A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28207486 | ||||||
| chr2:28207488
|
G | GGAA | 8 | a0001c0001t0002g0029a0001c0001t0002g0047a0001c0001t0002g0048others(5): Show | 8 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.681-29712_681-2971 others(7): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28207488 | |||||
| chr2:28207488
|
G | T | 2 | a0001c0001t0001g0139a0001c0001t0002g0002 | 2 | HG02486.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.681-29714G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28207488 | ||||||
| chr2:28207533
|
A | T | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG01891.hp2 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.681-29669A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28207533 | ||||||
| chr2:28207664
|
T | C | 115 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0025others(112): Show | 115 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.681-29538T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28207664 | ||||||
| chr2:28207677
|
GA | G | 6 | a0001c0001t0001g0023a0001c0001t0001g0065a0001c0001t0001g0070others(3): Show | 6 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.681-29517delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28207677 | |||||
| chr2:28207924
|
G | T | 122 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0017others(119): Show | 122 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(119): Show |
intron_variant | MODIFIER | c.681-29278G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28207924 | ||||||
| chr2:28208023
|
T | C | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02630.hp1 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.681-29179T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28208023 | ||||||
| chr2:28208029
|
C | CTG | 5 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(2): Show | 5 | HG02135.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.681-29137_681-2913 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28208029 | |||||
| chr2:28208029
|
C | CTGTG | 2 | a0001c0001t0001g0043a0001c0001t0002g0020 | 2 | HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.681-29139_681-2913 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28208029 | |||||
| chr2:28208029
|
CTG | C | 9 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0069others(6): Show | 9 | HG02258.hp2 HG02818.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.681-29137_681-2913 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28208029 | |||||
| chr2:28208029
|
CTGTG | C | 86 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0017others(83): Show | 86 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.681-29139_681-2913 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28208029 | |||||
| chr2:28208029
|
CTGTGTG | C | 27 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(24): Show | 27 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.681-29141_681-2913 others(10): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28208029 | |||||
| chr2:28208029
|
CTGTGTGT others(1): Show |
C | 5 | a0001c0001t0001g0139a0001c0001t0002g0002a0001c0001t0002g0064others(2): Show | 5 | HG01496.hp1 HG02486.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.681-29143_681-2913 others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28208029 | |||||
| chr2:28208029
|
CTGTGTGT others(3): Show |
C | 9 | a0001c0001t0002g0029a0001c0001t0002g0047a0001c0001t0002g0048others(6): Show | 9 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.681-29145_681-2913 others(14): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28208029 | |||||
| chr2:28208029
|
CTGTGTGT others(7): Show |
C | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.681-29149_681-2913 others(18): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28208029 | |||||
| chr2:28208170
|
T | C | 30 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(27): Show | 30 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.681-29032T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28208170 | ||||||
| chr2:28208198
|
A | G | 7 | a0001c0001t0002g0029a0001c0001t0002g0047a0001c0001t0002g0048others(4): Show | 7 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.681-29004A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28208198 | ||||||
| chr2:28208279
|
A | G | 1 | a0001c0001t0002g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.681-28923A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28208279 | ||||||
| chr2:28208387
|
A | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.681-28815A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28208387 | ||||||
| chr2:28208592
|
T | C | 147 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(144): Show | 147 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(144): Show |
intron_variant | MODIFIER | c.681-28610T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28208592 | ||||||
| chr2:28208598
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.681-28604T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28208598 | ||||||
| chr2:28208606
|
C | T | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG01891.hp2 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.681-28596C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28208606 | ||||||
| chr2:28208635
|
CTTTCTTT others(7): Show |
C | 1 | a0001c0001t0002g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.681-28552_681-2853 others(18): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28208635 | |||||
| chr2:28208687
|
G | A | 127 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0023others(124): Show | 127 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(124): Show |
intron_variant | MODIFIER | c.681-28515G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28208687 | ||||||
| chr2:28209074
|
A | T | 8 | a0001c0001t0002g0029a0001c0001t0002g0047a0001c0001t0002g0048others(5): Show | 8 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.681-28128A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28209074 | ||||||
| chr2:28209313
|
T | C | 1 | a0001c0001t0002g0140 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.681-27889T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28209313 | ||||||
| chr2:28209370
|
A | G | 31 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0022others(28): Show | 31 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.681-27832A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28209370 | ||||||
| chr2:28209459
|
GA | G | 14 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(11): Show | 14 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.681-27742delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28209459 | ||||||
| chr2:28209461
|
G | T | 14 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(11): Show | 14 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.681-27741G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28209461 | ||||||
| chr2:28209478
|
G | C | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG01891.hp2 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.681-27724G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28209478 | ||||||
| chr2:28209668
|
A | G | 8 | a0001c0001t0002g0029a0001c0001t0002g0047a0001c0001t0002g0048others(5): Show | 8 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.681-27534A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28209668 | ||||||
| chr2:28209879
|
C | G | 19 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(16): Show | 19 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.681-27323C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28209879 | ||||||
| chr2:28209926
|
T | C | 111 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(108): Show | 111 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.681-27276T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28209926 | ||||||
| chr2:28210272
|
T | C | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.681-26930T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28210272 | ||||||
| chr2:28210305
|
T | C | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.681-26897T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28210305 | ||||||
| chr2:28210313
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.681-26889G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28210313 | ||||||
| chr2:28210658
|
G | A | 8 | a0001c0001t0002g0029a0001c0001t0002g0047a0001c0001t0002g0048others(5): Show | 8 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.681-26544G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28210658 | ||||||
| chr2:28210797
|
A | G | 105 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0025others(102): Show | 105 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.681-26405A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28210797 | ||||||
| chr2:28211309
|
A | G | 15 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(12): Show | 15 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.681-25893A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28211309 | ||||||
| chr2:28211316
|
G | C | 105 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0025others(102): Show | 105 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.681-25886G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28211316 | ||||||
| chr2:28211386
|
C | CTT | 36 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0023others(33): Show | 36 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.681-25799_681-2579 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28211386 | |||||
| chr2:28211386
|
C | CTTT | 5 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(2): Show | 5 | HG01496.hp1 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.681-25800_681-2579 others(7): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28211386 | |||||
| chr2:28211386
|
C | CTTTTTTT | 77 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0025others(74): Show | 77 | HG00140.hp1 HG00639.hp1 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.681-25804_681-2579 others(11): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28211386 | |||||
| chr2:28211386
|
C | CTTTTTTT others(1): Show |
16 | a0001c0001t0001g0040a0001c0001t0001g0059a0001c0001t0001g0078others(13): Show | 16 | HG00140.hp2 HG00733.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.681-25805_681-2579 others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28211386 | |||||
| chr2:28211386
|
C | CTTTTTTT others(2): Show |
5 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0075others(2): Show | 5 | HG00735.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.681-25806_681-2579 others(13): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28211386 | |||||
| chr2:28211405
|
G | T | 2 | a0001c0001t0002g0130a0001c0001t0002g0131 | 2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.681-25797G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28211405 | ||||||
| chr2:28211406
|
A | T | 2 | a0001c0001t0002g0130a0001c0001t0002g0131 | 2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.681-25796A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28211406 | ||||||
| chr2:28211407
|
G | T | 2 | a0001c0001t0002g0130a0001c0001t0002g0131 | 2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.681-25795G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28211407 | ||||||
| chr2:28211408
|
A | T | 2 | a0001c0001t0002g0130a0001c0001t0002g0131 | 2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.681-25794A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28211408 | ||||||
| chr2:28211409
|
A | G | 2 | a0001c0001t0002g0130a0001c0001t0002g0131 | 2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.681-25793A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28211409 | ||||||
| chr2:28211456
|
C | T | 105 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0025others(102): Show | 105 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.681-25746C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28211456 | ||||||
| chr2:28211527
|
A | G | 31 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(28): Show | 31 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.681-25675A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28211527 | ||||||
| chr2:28211546
|
C | A | 1 | a0001c0001t0005g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.681-25656C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28211546 | ||||||
| chr2:28211610
|
A | G | 105 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0025others(102): Show | 105 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.681-25592A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28211610 | ||||||
| chr2:28211612
|
C | T | 18 | a0001c0001t0001g0008a0001c0001t0001g0023a0001c0001t0001g0044others(15): Show | 18 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.681-25590C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28211612 | ||||||
| chr2:28211804
|
A | T | 2 | a0001c0001t0002g0108a0001c0001t0002g0132 | 2 | HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.681-25398A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28211804 | ||||||
| chr2:28211823
|
A | G | 2 | a0001c0001t0002g0122a0001c0001t0003g0121 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.681-25379A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28211823 | ||||||
| chr2:28212302
|
G | A | 1 | a0001c0001t0002g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.681-24900G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28212302 | ||||||
| chr2:28212397
|
T | C | 97 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0032others(94): Show | 97 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.681-24805T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28212397 | ||||||
| chr2:28212858
|
G | GATT | 148 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(145): Show | 148 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(145): Show |
intron_variant | MODIFIER | c.681-24344_681-2434 others(7): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28212858 | ||||||
| chr2:28212859
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.681-24343G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28212859 | ||||||
| chr2:28213011
|
C | A | 18 | a0001c0001t0001g0008a0001c0001t0001g0023a0001c0001t0001g0044others(15): Show | 18 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.681-24191C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28213011 | ||||||
| chr2:28213152
|
A | C | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.681-24050A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28213152 | ||||||
| chr2:28213303
|
C | G | 18 | a0001c0001t0001g0008a0001c0001t0001g0023a0001c0001t0001g0044others(15): Show | 18 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.681-23899C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28213303 | ||||||
| chr2:28213441
|
G | A | 94 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0032others(91): Show | 94 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.681-23761G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28213441 | ||||||
| chr2:28213946
|
T | TA | 102 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0022others(99): Show | 102 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.681-23242dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28213946 | |||||
| chr2:28213946
|
T | TAA | 24 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(21): Show | 24 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.681-23243_681-2324 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28213946 | |||||
| chr2:28214544
|
G | A | 2 | a0001c0001t0001g0043a0001c0001t0002g0020 | 2 | HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.681-22658G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28214544 | ||||||
| chr2:28214757
|
C | T | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG01891.hp2 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.681-22445C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28214757 | ||||||
| chr2:28215018
|
A | G | 3 | a0001c0001t0001g0022a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | HG02280.hp1 HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.681-22184A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28215018 | ||||||
| chr2:28215087
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.681-22115G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28215087 | ||||||
| chr2:28215192
|
A | G | 8 | a0001c0001t0002g0029a0001c0001t0002g0047a0001c0001t0002g0048others(5): Show | 8 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.681-22010A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28215192 | ||||||
| chr2:28215664
|
AT | A | 148 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(145): Show | 148 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(145): Show |
intron_variant | MODIFIER | c.681-21533delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28215664 | |||||
| chr2:28215670
|
C | G | 1 | a0001c0001t0001g0150 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.681-21532C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28215670 | ||||||
| chr2:28215744
|
G | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0150 | 2 | HG02165.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.681-21458G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28215744 | ||||||
| chr2:28215978
|
A | G | 148 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(145): Show | 148 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(145): Show |
intron_variant | MODIFIER | c.681-21224A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28215978 | ||||||
| chr2:28216035
|
T | C | 118 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(115): Show | 118 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(115): Show |
intron_variant | MODIFIER | c.681-21167T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28216035 | ||||||
| chr2:28216179
|
A | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.681-21023A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28216179 | ||||||
| chr2:28216404
|
C | G | 1 | a0001c0001t0002g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.681-20798C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28216404 | ||||||
| chr2:28216853
|
C | T | 29 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0022others(26): Show | 29 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.681-20349C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28216853 | ||||||
| chr2:28216883
|
C | T | 2 | a0001c0001t0002g0101a0001c0001t0002g0149 | 2 | NA18955.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.681-20319C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28216883 | ||||||
| chr2:28216917
|
A | G | 113 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0025others(110): Show | 113 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(110): Show |
intron_variant | MODIFIER | c.681-20285A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28216917 | ||||||
| chr2:28216934
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.681-20268C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28216934 | ||||||
| chr2:28216937
|
C | A | 6 | a0001c0001t0001g0023a0001c0001t0001g0065a0001c0001t0001g0070others(3): Show | 6 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.681-20265C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28216937 | ||||||
| chr2:28216978
|
A | G | 2 | a0001c0001t0001g0065a0001c0001t0001g0083 | 2 | HG00735.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.681-20224A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28216978 | ||||||
| chr2:28217078
|
A | G | 113 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0025others(110): Show | 113 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(110): Show |
intron_variant | MODIFIER | c.681-20124A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28217078 | ||||||
| chr2:28217088
|
A | G | 113 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0025others(110): Show | 113 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(110): Show |
intron_variant | MODIFIER | c.681-20114A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28217088 | ||||||
| chr2:28217159
|
CT | C | 113 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0025others(110): Show | 113 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(110): Show |
intron_variant | MODIFIER | c.681-20039delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28217159 | |||||
| chr2:28218025
|
T | C | 16 | a0001c0001t0001g0008a0001c0001t0001g0023a0001c0001t0001g0044others(13): Show | 16 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.681-19177T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28218025 | ||||||
| chr2:28218200
|
A | G | 19 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(16): Show | 19 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.681-19002A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28218200 | ||||||
| chr2:28218305
|
C | G | 5 | a0001c0001t0002g0004a0001c0001t0002g0036a0001c0001t0002g0037others(2): Show | 5 | HG00738.hp1 HG02145.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.681-18897C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28218305 | ||||||
| chr2:28218549
|
C | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.681-18653C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28218549 | ||||||
| chr2:28218645
|
G | A | 105 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0025others(102): Show | 105 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.681-18557G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28218645 | ||||||
| chr2:28218692
|
T | A | 118 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(115): Show | 118 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(115): Show |
intron_variant | MODIFIER | c.681-18510T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28218692 | ||||||
| chr2:28218937
|
G | T | 1 | a0001c0001t0001g0034 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.681-18265G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28218937 | ||||||
| chr2:28219329
|
A | G | 18 | a0001c0001t0001g0008a0001c0001t0001g0023a0001c0001t0001g0044others(15): Show | 18 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.681-17873A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28219329 | ||||||
| chr2:28219399
|
T | C | 9 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0054others(6): Show | 9 | HG01346.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.681-17803T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28219399 | ||||||
| chr2:28219431
|
C | G | 1 | a0001c0001t0002g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.681-17771C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28219431 | ||||||
| chr2:28219540
|
A | G | 85 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0032others(82): Show | 85 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.681-17662A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28219540 | ||||||
| chr2:28219658
|
G | GA | 10 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(7): Show | 10 | HG01109.hp2 HG01891.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.681-17532dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28219658 | |||||
| chr2:28219679
|
A | G | 3 | a0001c0001t0001g0022a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | HG02280.hp1 HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.681-17523A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28219679 | ||||||
| chr2:28219821
|
G | T | 1 | a0001c0001t0001g0150 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.681-17381G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28219821 | ||||||
| chr2:28219826
|
G | A | 1 | a0001c0001t0002g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.681-17376G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28219826 | ||||||
| chr2:28220013
|
C | T | 2 | a0001c0001t0002g0130a0001c0001t0002g0131 | 2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.681-17189C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28220013 | ||||||
| chr2:28220051
|
TTTC | T | 7 | a0001c0001t0001g0005a0001c0001t0001g0133a0001c0001t0001g0134others(4): Show | 7 | HG01346.hp1 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.681-17144_681-1714 others(7): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28220051 | |||||
| chr2:28220183
|
C | T | 77 | a0001c0001t0001g0008a0001c0001t0001g0023a0001c0001t0001g0031others(74): Show | 77 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.681-17019C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28220183 | ||||||
| chr2:28220184
|
G | A | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.681-17018G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28220184 | ||||||
| chr2:28220206
|
G | A | 2 | a0001c0001t0001g0043a0001c0001t0002g0020 | 2 | HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.681-16996G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28220206 | ||||||
| chr2:28220522
|
C | CCT | 2 | a0001c0001t0001g0035a0001c0001t0002g0152 | 2 | NA18954.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.681-16664_681-1666 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28220522 | |||||
| chr2:28220592
|
G | A | 7 | a0001c0001t0001g0005a0001c0001t0001g0133a0001c0001t0001g0134others(4): Show | 7 | HG01346.hp1 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.681-16610G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28220592 | ||||||
| chr2:28220618
|
C | CA | 24 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(21): Show | 24 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.681-16574dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28220618 | |||||
| chr2:28220618
|
CA | C | 113 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0022others(110): Show | 113 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(110): Show |
intron_variant | MODIFIER | c.681-16574delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28220618 | |||||
| chr2:28220625
|
A | AT | 3 | a0001c0001t0002g0126a0001c0001t0002g0130a0001c0001t0002g0131 | 3 | HG02280.hp2 HG02723.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.681-16577_681-1657 others(5): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28220625 | ||||||
| chr2:28220819
|
C | G | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.681-16383C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28220819 | ||||||
| chr2:28220820
|
G | A | 14 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(11): Show | 14 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.681-16382G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28220820 | ||||||
| chr2:28221111
|
C | CCT | 5 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0133others(2): Show | 5 | HG01891.hp1 HG03516.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.681-16071_681-1607 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28221111 | |||||
| chr2:28221111
|
CCTCT | C | 15 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0045others(12): Show | 15 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.681-16073_681-1607 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28221111 | |||||
| chr2:28221181
|
C | CT | 24 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(21): Show | 24 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.681-16020dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28221181 | |||||
| chr2:28221251
|
A | G | 33 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(30): Show | 33 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.681-15951A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28221251 | ||||||
| chr2:28221274
|
G | A | 2 | a0001c0001t0002g0130a0001c0001t0002g0131 | 2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.681-15928G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28221274 | ||||||
| chr2:28221562
|
T | A | 13 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0045others(10): Show | 13 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.681-15640T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28221562 | ||||||
| chr2:28221684
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.681-15518T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28221684 | ||||||
| chr2:28221812
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.681-15390C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28221812 | ||||||
| chr2:28221929
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.681-15273T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28221929 | ||||||
| chr2:28221994
|
G | A | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.681-15208G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28221994 | ||||||
| chr2:28222021
|
G | A | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.681-15181G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28222021 | ||||||
| chr2:28222025
|
T | C | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.681-15177T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28222025 | ||||||
| chr2:28222297
|
A | G | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.681-14905A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28222297 | ||||||
| chr2:28222363
|
C | G | 1 | a0001c0001t0001g0057 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.681-14839C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28222363 | ||||||
| chr2:28222474
|
A | G | 4 | a0001c0001t0001g0142a0001c0001t0001g0146a0001c0001t0002g0144others(1): Show | 4 | HG01168.hp2 HG02074.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.681-14728A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28222474 | ||||||
| chr2:28222541
|
A | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0113 | 2 | HG03688.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.681-14661A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28222541 | ||||||
| chr2:28222571
|
C | T | 72 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0031others(69): Show | 72 | HG00140.hp1 HG00738.hp2 HG01069.hp1 others(69): Show |
intron_variant | MODIFIER | c.681-14631C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28222571 | ||||||
| chr2:28222751
|
C | A | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.681-14451C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28222751 | ||||||
| chr2:28222772
|
C | A | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.681-14430C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28222772 | ||||||
| chr2:28222856
|
C | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.681-14346C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28222856 | ||||||
| chr2:28222890
|
A | G | 1 | a0001c0001t0001g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.681-14312A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28222890 | ||||||
| chr2:28222986
|
A | G | 37 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(34): Show | 37 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.681-14216A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28222986 | ||||||
| chr2:28223324
|
G | A | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.681-13878G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28223324 | ||||||
| chr2:28223814
|
C | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.681-13388C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28223814 | ||||||
| chr2:28223896
|
A | G | 41 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(38): Show | 41 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.681-13306A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28223896 | ||||||
| chr2:28223983
|
G | T | 2 | a0001c0001t0001g0093a0001c0001t0001g0102 | 2 | HG01069.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.681-13219G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28223983 | ||||||
| chr2:28224027
|
A | G | 3 | a0001c0001t0001g0022a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | HG02280.hp1 HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.681-13175A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28224027 | ||||||
| chr2:28224188
|
C | G | 1 | a0001c0001t0001g0073 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.681-13014C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28224188 | ||||||
| chr2:28224379
|
T | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.681-12823T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28224379 | ||||||
| chr2:28224482
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.681-12720A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28224482 | ||||||
| chr2:28224485
|
T | C | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.681-12717T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28224485 | ||||||
| chr2:28224529
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | HG02280.hp1 HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.681-12673C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28224529 | ||||||
| chr2:28224549
|
T | G | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.681-12653T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28224549 | ||||||
| chr2:28224598
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | HG02280.hp1 HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.681-12604C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28224598 | ||||||
| chr2:28224609
|
A | G | 2 | a0001c0001t0002g0130a0001c0001t0002g0131 | 2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.681-12593A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28224609 | ||||||
| chr2:28224641
|
C | A | 3 | a0001c0001t0002g0064a0001c0001t0002g0130a0001c0001t0002g0131 | 3 | HG02280.hp2 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.681-12561C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28224641 | ||||||
| chr2:28224669
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.681-12533C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28224669 | ||||||
| chr2:28224769
|
A | G | 42 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(39): Show | 42 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.681-12433A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28224769 | ||||||
| chr2:28224849
|
G | GA | 6 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0027others(3): Show | 6 | HG00639.hp1 HG01109.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.681-12352dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28224849 | |||||
| chr2:28224849
|
G | GAA | 18 | a0001c0001t0001g0025a0001c0001t0001g0143a0001c0001t0002g0004others(15): Show | 18 | HG00639.hp2 HG00738.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.681-12352_681-1235 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28224849 | |||||
| chr2:28224849
|
G | GAAA | 8 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0154others(5): Show | 8 | HG00741.hp2 HG01346.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.681-12352_681-1235 others(7): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28224849 | |||||
| chr2:28224851
|
C | A | 32 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(29): Show | 32 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.681-12351C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28224851 | ||||||
| chr2:28224851
|
C | CA | 17 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(14): Show | 17 | HG01069.hp2 HG01081.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.681-12328dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28224851 | |||||
| chr2:28224851
|
CA | C | 18 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0040others(15): Show | 18 | HG00140.hp2 HG00733.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.681-12328delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28224851 | |||||
| chr2:28225147
|
G | A | 13 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0045others(10): Show | 13 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.681-12055G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28225147 | ||||||
| chr2:28225178
|
C | A | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.681-12024C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28225178 | ||||||
| chr2:28225178
|
C | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.681-12024C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28225178 | ||||||
| chr2:28225245
|
G | A | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.681-11957G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28225245 | ||||||
| chr2:28225276
|
G | T | 1 | a0001c0001t0001g0091 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.681-11926G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28225276 | ||||||
| chr2:28225294
|
G | T | 1 | a0001c0001t0004g0118 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.681-11908G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28225294 | ||||||
| chr2:28225341
|
G | C | 4 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0009others(1): Show | 4 | HG01346.hp1 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.681-11861G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28225341 | ||||||
| chr2:28225347
|
G | A | 27 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0027others(24): Show | 27 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.681-11855G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28225347 | ||||||
| chr2:28225371
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.681-11831G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28225371 | ||||||
| chr2:28225415
|
G | T | 73 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0025others(70): Show | 73 | HG00140.hp1 HG00738.hp2 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.681-11787G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28225415 | ||||||
| chr2:28225477
|
A | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.681-11725A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28225477 | ||||||
| chr2:28225553
|
G | A | 4 | a0001c0001t0001g0142a0001c0001t0001g0146a0001c0001t0002g0144others(1): Show | 4 | HG01168.hp2 HG02074.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.681-11649G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28225553 | ||||||
| chr2:28225828
|
C | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.681-11374C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28225828 | ||||||
| chr2:28225967
|
G | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.681-11235G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28225967 | ||||||
| chr2:28226143
|
G | A | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.681-11059G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28226143 | ||||||
| chr2:28226316
|
G | C | 13 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0045others(10): Show | 13 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.681-10886G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28226316 | ||||||
| chr2:28226554
|
G | A | 6 | a0001c0001t0001g0142a0001c0001t0001g0146a0001c0001t0002g0107others(3): Show | 6 | HG01168.hp2 HG02074.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.681-10648G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28226554 | ||||||
| chr2:28226572
|
T | C | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.681-10630T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28226572 | ||||||
| chr2:28226708
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.681-10494G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28226708 | ||||||
| chr2:28226712
|
C | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.681-10490C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28226712 | ||||||
| chr2:28227089
|
G | C | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG01891.hp2 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.681-10113G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28227089 | ||||||
| chr2:28227165
|
T | C | 2 | a0001c0001t0002g0030a0001c0001t0002g0063 | 2 | HG02698.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.681-10037T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28227165 | ||||||
| chr2:28227209
|
C | T | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 8 | HG01891.hp2 HG02572.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.681-9993C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28227209 | ||||||
| chr2:28227288
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.681-9914C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28227288 | ||||||
| chr2:28227345
|
G | A | 3 | a0001c0001t0002g0064a0001c0001t0002g0130a0001c0001t0002g0131 | 3 | HG02280.hp2 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.681-9857G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28227345 | ||||||
| chr2:28227506
|
C | G | 1 | a0001c0001t0002g0110 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.681-9696C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28227506 | ||||||
| chr2:28227533
|
A | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.681-9669A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28227533 | ||||||
| chr2:28227562
|
T | C | 1 | a0001c0001t0002g0141 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.681-9640T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28227562 | ||||||
| chr2:28227626
|
C | T | 1 | a0001c0001t0003g0148 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.681-9576C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28227626 | ||||||
| chr2:28227722
|
TC | T | 3 | a0001c0001t0002g0064a0001c0001t0002g0130a0001c0001t0002g0131 | 3 | HG02280.hp2 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.681-9478delC | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28227722 | |||||
| chr2:28227734
|
C | T | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG01891.hp2 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.681-9468C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28227734 | ||||||
| chr2:28227844
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.681-9358G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28227844 | ||||||
| chr2:28227860
|
C | G | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.681-9342C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28227860 | ||||||
| chr2:28227882
|
G | T | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.681-9320G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28227882 | ||||||
| chr2:28228115
|
T | C | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.681-9087T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28228115 | ||||||
| chr2:28228355
|
G | A | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.681-8847G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28228355 | ||||||
| chr2:28228544
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.681-8658C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28228544 | ||||||
| chr2:28228691
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.681-8511C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28228691 | ||||||
| chr2:28228982
|
A | G | 2 | a0001c0001t0002g0101a0001c0001t0002g0149 | 2 | NA18955.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.681-8220A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28228982 | ||||||
| chr2:28229193
|
G | C | 1 | a0001c0001t0001g0025 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.681-8009G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28229193 | ||||||
| chr2:28229324
|
G | A | 2 | a0001c0001t0002g0122a0001c0001t0003g0121 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.681-7878G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28229324 | ||||||
| chr2:28229411
|
A | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.681-7791A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28229411 | ||||||
| chr2:28229564
|
A | G | 1 | a0001c0001t0002g0158 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.681-7638A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28229564 | ||||||
| chr2:28229589
|
CT | C | 119 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(116): Show | 119 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.681-7600delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28229589 | |||||
| chr2:28229667
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.681-7535C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28229667 | ||||||
| chr2:28229809
|
A | T | 1 | a0001c0001t0001g0155 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.681-7393A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28229809 | ||||||
| chr2:28229825
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.681-7377G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28229825 | ||||||
| chr2:28230089
|
T | G | 119 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(116): Show | 119 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.681-7113T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28230089 | ||||||
| chr2:28230091
|
A | C | 119 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(116): Show | 119 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.681-7111A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28230091 | ||||||
| chr2:28230339
|
G | A | 2 | a0001c0001t0002g0122a0001c0001t0003g0121 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.681-6863G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28230339 | ||||||
| chr2:28230343
|
A | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.681-6859A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28230343 | ||||||
| chr2:28230468
|
C | T | 24 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(21): Show | 24 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.681-6734C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28230468 | ||||||
| chr2:28230513
|
G | A | 18 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0044others(15): Show | 18 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.681-6689G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28230513 | ||||||
| chr2:28230560
|
C | CA | 116 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0022others(113): Show | 116 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.681-6628dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28230560 | |||||
| chr2:28230560
|
C | CAAA | 13 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(10): Show | 13 | HG01346.hp1 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.681-6630_681-6628d others(5): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28230560 | |||||
| chr2:28230560
|
C | CAAAA | 17 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(14): Show | 17 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.681-6631_681-6628d others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28230560 | |||||
| chr2:28230588
|
T | G | 30 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(27): Show | 30 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.681-6614T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28230588 | ||||||
| chr2:28230718
|
G | GA | 106 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(103): Show | 106 | HG00140.hp1 HG00639.hp2 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.681-6471dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28230718 | |||||
| chr2:28230718
|
G | GAA | 16 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(13): Show | 16 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.681-6472_681-6471d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28230718 | |||||
| chr2:28230718
|
G | GAAA | 24 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(21): Show | 24 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.681-6473_681-6471d others(5): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28230718 | |||||
| chr2:28230848
|
G | A | 30 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(27): Show | 30 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.681-6354G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28230848 | ||||||
| chr2:28230879
|
G | A | 2 | a0001c0001t0002g0007a0001c0001t0002g0128 | 2 | HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.681-6323G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28230879 | ||||||
| chr2:28231143
|
G | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | HG02280.hp1 HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.681-6059G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28231143 | ||||||
| chr2:28231174
|
G | C | 22 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(19): Show | 22 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.681-6028G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28231174 | ||||||
| chr2:28231372
|
G | A | 3 | a0001c0001t0002g0064a0001c0001t0002g0130a0001c0001t0002g0131 | 3 | HG02280.hp2 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.681-5830G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28231372 | ||||||
| chr2:28231461
|
C | G | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.681-5741C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28231461 | ||||||
| chr2:28231461
|
C | T | 22 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(19): Show | 22 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.681-5741C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28231461 | ||||||
| chr2:28231490
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.681-5712C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28231490 | ||||||
| chr2:28231493
|
G | C | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.681-5709G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28231493 | ||||||
| chr2:28231594
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.681-5608C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28231594 | ||||||
| chr2:28231614
|
G | A | 1 | a0001c0001t0004g0118 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.681-5588G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28231614 | ||||||
| chr2:28231625
|
A | T | 1 | a0001c0001t0003g0148 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.681-5577A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28231625 | ||||||
| chr2:28231785
|
CTT | C | 6 | a0001c0001t0001g0086a0001c0001t0002g0001a0001c0001t0002g0130others(3): Show | 6 | HG01192.hp2 HG02486.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.681-5380_681-5379d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28231785 | |||||
| chr2:28231785
|
CTTT | C | 15 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(12): Show | 15 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.681-5381_681-5379d others(5): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28231785 | |||||
| chr2:28231785
|
CTTTT | C | 6 | a0001c0001t0001g0043a0001c0001t0001g0075a0001c0001t0001g0157others(3): Show | 6 | HG00735.hp2 HG01167.hp2 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.681-5382_681-5379d others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28231785 | |||||
| chr2:28231785
|
CTTTTTT | C | 13 | a0001c0001t0001g0008a0001c0001t0001g0032a0001c0001t0001g0058others(10): Show | 13 | HG00741.hp2 HG01496.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.681-5384_681-5379d others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28231785 | |||||
| chr2:28231785
|
CTTTTTTT | C | 60 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0041others(57): Show | 60 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.681-5385_681-5379d others(9): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28231785 | |||||
| chr2:28231785
|
CTTTTTTT others(1): Show |
C | 9 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 9 | HG01891.hp1 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.681-5386_681-5379d others(10): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28231785 | |||||
| chr2:28231785
|
CTTTTTTT others(2): Show |
C | 8 | a0001c0001t0001g0055a0001c0001t0001g0133a0001c0001t0001g0134others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.681-5387_681-5379d others(11): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28231785 | |||||
| chr2:28231785
|
CTTTTTTT others(3): Show |
C | 17 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0025others(14): Show | 17 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.681-5388_681-5379d others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28231785 | |||||
| chr2:28231785
|
CTTTTTTT others(14): Show |
C | 11 | a0001c0001t0001g0023a0001c0001t0001g0065a0001c0001t0001g0070others(8): Show | 11 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.681-5399_681-5379d others(23): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28231785 | |||||
| chr2:28231785
|
CTTTTTTT others(15): Show |
C | 2 | a0001c0001t0001g0088a0001c0001t0001g0139 | 2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.681-5400_681-5379d others(24): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28231785 | |||||
| chr2:28231801
|
T | TAAGAGAC others(66): Show |
1 | a0001c0001t0001g0045 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.681-5401_681-5400i others(75): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28231801 | ||||||
| chr2:28231802
|
T | A | 1 | a0001c0001t0001g0045 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.681-5400T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28231802 | ||||||
| chr2:28231802
|
T | TAAGAGAC others(67): Show |
2 | a0001c0001t0001g0044a0001c0001t0001g0091 | 2 | HG02258.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.681-5400_681-5399i others(76): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28231802 | ||||||
| chr2:28231804
|
T | G | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0091 | 3 | HG02258.hp2 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.681-5398T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28231804 | ||||||
| chr2:28231806
|
T | C | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0091 | 3 | HG02258.hp2 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.681-5396T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28231806 | ||||||
| chr2:28231917
|
C | T | 1 | a0001c0001t0003g0089 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.681-5285C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28231917 | ||||||
| chr2:28232503
|
G | A | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.681-4699G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28232503 | ||||||
| chr2:28232655
|
T | C | 1 | a0001c0001t0002g0030 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.681-4547T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28232655 | ||||||
| chr2:28232900
|
A | G | 3 | a0001c0001t0002g0064a0001c0001t0002g0130a0001c0001t0002g0131 | 3 | HG02280.hp2 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.681-4302A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28232900 | ||||||
| chr2:28233267
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.681-3935C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28233267 | ||||||
| chr2:28233619
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.681-3583G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28233619 | ||||||
| chr2:28233669
|
G | A | 3 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0016 | 3 | HG01109.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.681-3533G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28233669 | ||||||
| chr2:28233708
|
G | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.681-3494G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28233708 | ||||||
| chr2:28233949
|
C | T | 1 | a0001c0001t0002g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.681-3253C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28233949 | ||||||
| chr2:28233979
|
T | TG | 146 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(143): Show | 146 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(143): Show |
intron_variant | MODIFIER | c.681-3223_681-3222i others(3): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28233979 | ||||||
| chr2:28234220
|
G | A | 3 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0009 | 3 | HG01346.hp1 HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.681-2982G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28234220 | ||||||
| chr2:28234424
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.681-2778G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28234424 | ||||||
| chr2:28234519
|
T | A | 1 | a0001c0001t0001g0146 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.681-2683T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28234519 | ||||||
| chr2:28234631
|
C | A | 2 | a0001c0001t0002g0122a0001c0001t0003g0121 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.681-2571C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28234631 | ||||||
| chr2:28234909
|
A | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0133a0001c0001t0001g0134others(1): Show | 4 | HG01891.hp1 HG03540.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.681-2293A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28234909 | ||||||
| chr2:28235080
|
T | C | 3 | a0001c0001t0002g0064a0001c0001t0002g0130a0001c0001t0002g0131 | 3 | HG02280.hp2 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.681-2122T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28235080 | ||||||
| chr2:28235235
|
T | G | 156 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(153): Show |
intron_variant | MODIFIER | c.681-1967T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28235235 | ||||||
| chr2:28235239
|
G | A | 2 | a0001c0001t0002g0108a0001c0001t0002g0132 | 2 | HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.681-1963G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28235239 | ||||||
| chr2:28235322
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.681-1880G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28235322 | ||||||
| chr2:28235417
|
C | T | 1 | a0001c0001t0002g0141 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.681-1785C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28235417 | ||||||
| chr2:28235578
|
G | A | 143 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(140): Show | 143 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(140): Show |
intron_variant | MODIFIER | c.681-1624G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28235578 | ||||||
| chr2:28235646
|
T | TTTTG | 13 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(10): Show | 13 | HG01891.hp2 HG02486.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.681-1532_681-1529d others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28235646 | |||||
| chr2:28235719
|
C | T | 6 | a0001c0001t0002g0001a0001c0001t0003g0089a0001c0001t0003g0090others(3): Show | 6 | HG00733.hp2 HG01167.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.681-1483C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28235719 | ||||||
| chr2:28235720
|
G | A | 1 | a0001c0001t0003g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.681-1482G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28235720 | ||||||
| chr2:28235756
|
A | G | 137 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0017others(134): Show | 137 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(134): Show |
intron_variant | MODIFIER | c.681-1446A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28235756 | ||||||
| chr2:28235824
|
T | G | 119 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(116): Show | 119 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.681-1378T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28235824 | ||||||
| chr2:28235826
|
T | G | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.681-1376T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28235826 | ||||||
| chr2:28235875
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.681-1327G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28235875 | ||||||
| chr2:28235955
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0069 | 2 | HG01081.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.681-1247C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28235955 | ||||||
| chr2:28235960
|
A | G | 143 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(140): Show | 143 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(140): Show |
intron_variant | MODIFIER | c.681-1242A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28235960 | ||||||
| chr2:28236066
|
A | G | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.681-1136A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28236066 | ||||||
| chr2:28236257
|
GTGATAAA | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.681-941_681-935del others(7): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 28236257 | |||||
| chr2:28236274
|
C | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0009 | 3 | HG01346.hp1 HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.681-928C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28236274 | ||||||
| chr2:28236462
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.681-740C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28236462 | ||||||
| chr2:28236519
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.681-683A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28236519 | ||||||
| chr2:28236794
|
G | C | 115 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0022others(112): Show | 115 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(112): Show |
intron_variant | MODIFIER | c.681-408G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28236794 | ||||||
| chr2:28236901
|
A | G | 143 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(140): Show | 143 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(140): Show |
intron_variant | MODIFIER | c.681-301A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28236901 | ||||||
| chr2:28237114
|
A | G | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.681-88A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | chr2 | 28237114 | ||||||
| chr2:28237308
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0055 | 2 | HG02280.hp1 HG03453.hp2 |
splice_region_variant&intron_variant | LOW | c.780+7G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | chr2 | 28237308 | ||||||
| chr2:28237399
|
G | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(2): Show | 5 | HG02486.hp1 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.780+98G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | chr2 | 28237399 | ||||||
| chr2:28237506
|
T | G | 6 | a0001c0001t0001g0054a0001c0001t0001g0109a0001c0001t0002g0010others(3): Show | 6 | HG02451.hp2 HG02818.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.780+205T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | chr2 | 28237506 | ||||||
| chr2:28237524
|
GTCTTA | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0055 | 2 | HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.780+228_780+232del others(5): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 28237524 | |||||
| chr2:28237644
|
T | C | 2 | a0001c0001t0002g0007a0001c0001t0002g0128 | 2 | HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.780+343T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | chr2 | 28237644 | ||||||
| chr2:28237707
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.780+406C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | chr2 | 28237707 | ||||||
| chr2:28237741
|
T | C | 148 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(145): Show | 148 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(145): Show |
intron_variant | MODIFIER | c.780+440T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | chr2 | 28237741 | ||||||
| chr2:28237999
|
G | A | 85 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0031others(82): Show | 85 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.780+698G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | chr2 | 28237999 | ||||||
| chr2:28238118
|
G | A | 105 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0022others(102): Show | 105 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(102): Show |
intron_variant | MODIFIER | c.780+817G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | chr2 | 28238118 | ||||||
| chr2:28238670
|
A | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.780+1369A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | chr2 | 28238670 | ||||||
| chr2:28238763
|
T | A | 2 | a0001c0001t0002g0108a0001c0001t0002g0132 | 2 | HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.780+1462T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | chr2 | 28238763 | ||||||
| chr2:28238840
|
C | CA | 142 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(139): Show | 142 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(139): Show |
intron_variant | MODIFIER | c.780+1548dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 28238840 | |||||
| chr2:28238939
|
A | G | 143 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(140): Show | 143 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(140): Show |
intron_variant | MODIFIER | c.780+1638A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | chr2 | 28238939 | ||||||
| chr2:28239268
|
G | A | 14 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0045others(11): Show | 14 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.780+1967G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | chr2 | 28239268 | ||||||
| chr2:28239383
|
G | T | 1 | a0001c0001t0003g0148 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.781-1940G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | chr2 | 28239383 | ||||||
| chr2:28239481
|
G | A | 14 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0045others(11): Show | 14 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.781-1842G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | chr2 | 28239481 | ||||||
| chr2:28239858
|
G | C | 1 | a0001c0001t0001g0111 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.781-1465G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | chr2 | 28239858 | ||||||
| chr2:28239861
|
C | A | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.781-1462C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | chr2 | 28239861 | ||||||
| chr2:28240005
|
G | T | 2 | a0001c0001t0001g0142a0001c0001t0002g0145 | 2 | NA18969.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.781-1318G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | chr2 | 28240005 | ||||||
| chr2:28240122
|
T | A | 2 | a0001c0001t0002g0108a0001c0001t0002g0132 | 2 | HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.781-1201T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | chr2 | 28240122 | ||||||
| chr2:28240245
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.781-1078C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | chr2 | 28240245 | ||||||
| chr2:28240373
|
T | C | 146 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(143): Show | 146 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(143): Show |
intron_variant | MODIFIER | c.781-950T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | chr2 | 28240373 | ||||||
| chr2:28240663
|
A | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.781-660A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | chr2 | 28240663 | ||||||
| chr2:28240870
|
CA | C | 134 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0017others(131): Show | 134 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(131): Show |
intron_variant | MODIFIER | c.781-438delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 28240870 | |||||
| chr2:28240881
|
A | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.781-442A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | chr2 | 28240881 | ||||||
| chr2:28240883
|
A | C | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.781-440A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | chr2 | 28240883 | ||||||
| chr2:28240885
|
A | C | 1 | a0001c0001t0001g0154 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.781-438A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | chr2 | 28240885 | ||||||
| chr2:28240886
|
C | A | 2 | a0001c0001t0001g0154a0001c0001t0002g0126 | 2 | HG00741.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.781-437C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | chr2 | 28240886 | ||||||
| chr2:28240895
|
C | A | 117 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0022others(114): Show | 117 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(114): Show |
intron_variant | MODIFIER | c.781-428C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | chr2 | 28240895 | ||||||
| chr2:28240942
|
T | A | 116 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0022others(113): Show | 116 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.781-381T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | chr2 | 28240942 | ||||||
| chr2:28241066
|
A | C | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.781-257A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | chr2 | 28241066 | ||||||
| chr2:28241107
|
C | G | 22 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(19): Show | 22 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.781-216C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 8/11 | chr2 | 28241107 | ||||||
| chr2:28241423
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0154 | 2 | HG00741.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.851+30C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | chr2 | 28241423 | ||||||
| chr2:28241521
|
G | A | 7 | a0001c0001t0001g0005a0001c0001t0001g0133a0001c0001t0001g0134others(4): Show | 7 | HG01346.hp1 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.851+128G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | chr2 | 28241521 | ||||||
| chr2:28241568
|
T | C | 157 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(154): Show | 157 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(154): Show |
intron_variant | MODIFIER | c.851+175T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | chr2 | 28241568 | ||||||
| chr2:28241656
|
A | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.851+263A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | chr2 | 28241656 | ||||||
| chr2:28241860
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.851+467A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | chr2 | 28241860 | ||||||
| chr2:28241864
|
C | CT | 12 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(9): Show | 12 | HG00733.hp2 HG01167.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.851+490dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 28241864 | |||||
| chr2:28241864
|
CT | C | 107 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0023others(104): Show | 107 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.851+490delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 28241864 | |||||
| chr2:28241864
|
CTT | C | 28 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(25): Show | 28 | HG00639.hp1 HG00735.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.851+489_851+490del others(2): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 28241864 | |||||
| chr2:28242128
|
G | A | 2 | a0001c0001t0002g0108a0001c0001t0002g0132 | 2 | HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.851+735G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | chr2 | 28242128 | ||||||
| chr2:28242151
|
G | T | 1 | a0001c0001t0001g0099 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.851+758G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | chr2 | 28242151 | ||||||
| chr2:28242481
|
C | T | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.851+1088C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | chr2 | 28242481 | ||||||
| chr2:28242677
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.851+1284C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | chr2 | 28242677 | ||||||
| chr2:28242812
|
C | G | 1 | a0001c0001t0002g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.851+1419C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | chr2 | 28242812 | ||||||
| chr2:28242838
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.851+1445T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | chr2 | 28242838 | ||||||
| chr2:28243280
|
T | G | 1 | a0001c0001t0001g0045 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.852-1500T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | chr2 | 28243280 | ||||||
| chr2:28243308
|
C | T | 22 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(19): Show | 22 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.852-1472C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | chr2 | 28243308 | ||||||
| chr2:28243557
|
A | G | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.852-1223A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | chr2 | 28243557 | ||||||
| chr2:28243564
|
G | T | 1 | a0001c0001t0001g0139 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.852-1216G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | chr2 | 28243564 | ||||||
| chr2:28243600
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0138 | 2 | HG01891.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.852-1180G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | chr2 | 28243600 | ||||||
| chr2:28243611
|
G | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.852-1169G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | chr2 | 28243611 | ||||||
| chr2:28243684
|
G | T | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.852-1096G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | chr2 | 28243684 | ||||||
| chr2:28243706
|
CA | C | 14 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0045others(11): Show | 14 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.852-1064delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 28243706 | |||||
| chr2:28243713
|
A | T | 1 | a0001c0001t0001g0008 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.852-1067A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | chr2 | 28243713 | ||||||
| chr2:28243717
|
T | A | 1 | a0001c0001t0002g0101 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.852-1063T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | chr2 | 28243717 | ||||||
| chr2:28243754
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0055 | 2 | HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.852-1026G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | chr2 | 28243754 | ||||||
| chr2:28243868
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0055 | 2 | HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.852-912C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | chr2 | 28243868 | ||||||
| chr2:28243883
|
G | A | 30 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(27): Show | 30 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.852-897G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | chr2 | 28243883 | ||||||
| chr2:28244086
|
C | G | 30 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(27): Show | 30 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.852-694C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | chr2 | 28244086 | ||||||
| chr2:28244167
|
G | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.852-613G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | chr2 | 28244167 | ||||||
| chr2:28244344
|
A | T | 2 | a0001c0001t0001g0043a0001c0001t0002g0020 | 2 | HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.852-436A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | chr2 | 28244344 | ||||||
| chr2:28244354
|
C | T | 1 | a0001c0001t0001g0073 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.852-426C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | chr2 | 28244354 | ||||||
| chr2:28244420
|
A | ATGT | 4 | a0001c0001t0001g0017a0001c0001t0001g0053a0001c0001t0001g0082others(1): Show | 4 | HG00140.hp2 HG01433.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.852-359_852-357dup others(3): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 28244420 | |||||
| chr2:28244430
|
T | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.852-350T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | chr2 | 28244430 | ||||||
| chr2:28244459
|
CTTAT | C | 88 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0031others(85): Show | 88 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.852-318_852-315del others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 28244459 | |||||
| chr2:28244460
|
T | C | 30 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(27): Show | 30 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.852-320T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 9/11 | chr2 | 28244460 | ||||||
| chr2:28244928
|
A | T | 1 | a0001c0001t0002g0110 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.934+66A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28244928 | ||||||
| chr2:28245187
|
C | T | 32 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(29): Show | 32 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.934+325C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28245187 | ||||||
| chr2:28245204
|
C | A | 112 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 112 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(109): Show |
intron_variant | MODIFIER | c.934+342C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28245204 | ||||||
| chr2:28245230
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.934+368A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28245230 | ||||||
| chr2:28245314
|
A | G | 3 | a0001c0001t0001g0088a0001c0001t0001g0092a0001c0001t0004g0118 | 3 | HG02615.hp2 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.934+452A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28245314 | ||||||
| chr2:28245321
|
G | C | 32 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(29): Show | 32 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.934+459G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28245321 | ||||||
| chr2:28245537
|
G | A | 2 | a0001c0001t0002g0011a0001c0001t0002g0064 | 2 | HG01109.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.934+675G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28245537 | ||||||
| chr2:28245647
|
A | G | 14 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(11): Show | 14 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.934+785A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28245647 | ||||||
| chr2:28245652
|
G | A | 14 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(11): Show | 14 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.934+790G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28245652 | ||||||
| chr2:28245818
|
C | A | 1 | a0001c0001t0002g0114 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.934+956C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28245818 | ||||||
| chr2:28245836
|
T | C | 8 | a0001c0001t0002g0029a0001c0001t0002g0047a0001c0001t0002g0048others(5): Show | 8 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.934+974T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28245836 | ||||||
| chr2:28245894
|
G | A | 32 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(29): Show | 32 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.934+1032G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28245894 | ||||||
| chr2:28246220
|
G | C | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.934+1358G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28246220 | ||||||
| chr2:28246360
|
T | A | 1 | a0001c0001t0002g0037 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.934+1498T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28246360 | ||||||
| chr2:28246474
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0133a0001c0001t0001g0134others(1): Show | 4 | HG01891.hp1 HG03540.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.934+1612G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28246474 | ||||||
| chr2:28246589
|
G | A | 106 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0022others(103): Show | 106 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(103): Show |
intron_variant | MODIFIER | c.934+1727G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28246589 | ||||||
| chr2:28247096
|
C | T | 112 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 112 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(109): Show |
intron_variant | MODIFIER | c.934+2234C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28247096 | ||||||
| chr2:28247109
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.934+2247A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28247109 | ||||||
| chr2:28247182
|
C | T | 4 | a0001c0001t0002g0062a0001c0001t0002g0096a0001c0001t0002g0101others(1): Show | 4 | HG01934.hp1 NA18955.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.934+2320C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28247182 | ||||||
| chr2:28247224
|
C | G | 108 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0022others(105): Show | 108 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(105): Show |
intron_variant | MODIFIER | c.934+2362C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28247224 | ||||||
| chr2:28247249
|
C | T | 14 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0045others(11): Show | 14 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.934+2387C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28247249 | ||||||
| chr2:28247343
|
T | C | 32 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(29): Show | 32 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.934+2481T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28247343 | ||||||
| chr2:28247365
|
T | G | 17 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(14): Show | 17 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.934+2503T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28247365 | ||||||
| chr2:28247374
|
G | A | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.934+2512G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28247374 | ||||||
| chr2:28247439
|
T | A | 1 | a0001c0001t0001g0025 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.934+2577T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28247439 | ||||||
| chr2:28247685
|
A | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.934+2823A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28247685 | ||||||
| chr2:28248207
|
C | CTTTTTCT others(3): Show |
3 | a0001c0001t0001g0111a0001c0001t0002g0098a0001c0001t0002g0149 | 3 | NA18955.hp1 NA18964.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.934+3350_934+3351i others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28248207 | |||||
| chr2:28248207
|
C | CTTTTTCT others(4): Show |
38 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0035others(35): Show | 38 | HG00140.hp1 HG01069.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.934+3350_934+3351i others(13): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28248207 | |||||
| chr2:28248207
|
C | CTTTTTCT others(5): Show |
9 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0072others(6): Show | 9 | HG00738.hp2 HG01168.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.934+3350_934+3351i others(14): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28248207 | |||||
| chr2:28248207
|
C | CTTTTTCT others(6): Show |
25 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(22): Show | 25 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.934+3350_934+3351i others(15): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28248207 | |||||
| chr2:28248207
|
C | CTTTTTCT others(7): Show |
13 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0044others(10): Show | 13 | HG01081.hp1 HG01099.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.934+3350_934+3351i others(16): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28248207 | |||||
| chr2:28248207
|
C | CTTTTTCT others(8): Show |
6 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0055others(3): Show | 6 | HG00735.hp1 HG00741.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.934+3350_934+3351i others(17): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28248207 | |||||
| chr2:28248207
|
C | CTTTTTCT others(9): Show |
1 | a0001c0001t0001g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.934+3350_934+3351i others(18): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28248207 | |||||
| chr2:28248207
|
C | CTTTTTCT others(10): Show |
1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.934+3350_934+3351i others(19): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28248207 | |||||
| chr2:28248207
|
C | G | 14 | a0001c0001t0001g0057a0001c0001t0001g0099a0001c0001t0001g0113others(11): Show | 14 | HG01069.hp1 HG02027.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.934+3345C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28248207 | ||||||
| chr2:28248207
|
CT | C | 25 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(22): Show | 25 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.934+3364delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28248207 | |||||
| chr2:28248207
|
CTT | C | 7 | a0001c0001t0002g0029a0001c0001t0002g0047a0001c0001t0002g0048others(4): Show | 7 | HG00639.hp2 HG01106.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.934+3363_934+3364d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28248207 | |||||
| chr2:28248209
|
T | TTTTC | 13 | a0001c0001t0001g0057a0001c0001t0001g0099a0001c0001t0001g0113others(10): Show | 13 | HG01069.hp1 HG02027.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.934+3350_934+3351i others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28248209 | |||||
| chr2:28248211
|
T | TTCTTTTT others(6): Show |
1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.934+3350_934+3351i others(15): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28248211 | |||||
| chr2:28248381
|
G | A | 15 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0045others(12): Show | 15 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.934+3519G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28248381 | ||||||
| chr2:28248383
|
A | G | 89 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0022others(86): Show | 89 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(86): Show |
intron_variant | MODIFIER | c.934+3521A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28248383 | ||||||
| chr2:28248923
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0055 | 2 | HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.934+4061G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28248923 | ||||||
| chr2:28248958
|
T | C | 122 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(119): Show | 122 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(119): Show |
intron_variant | MODIFIER | c.934+4096T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28248958 | ||||||
| chr2:28249024
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.934+4162C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28249024 | ||||||
| chr2:28249075
|
G | A | 30 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(27): Show | 30 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.934+4213G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28249075 | ||||||
| chr2:28249087
|
G | GT | 7 | a0001c0001t0001g0066a0001c0001t0001g0143a0001c0001t0001g0154others(4): Show | 7 | HG00741.hp2 HG01167.hp2 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.934+4242dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28249087 | |||||
| chr2:28249087
|
GT | G | 10 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(7): Show | 10 | HG01891.hp2 HG02572.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.934+4242delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28249087 | |||||
| chr2:28249137
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.934+4275G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28249137 | ||||||
| chr2:28249214
|
G | A | 30 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(27): Show | 30 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.934+4352G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28249214 | ||||||
| chr2:28249325
|
G | T | 2 | a0001c0001t0002g0130a0001c0001t0002g0131 | 2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.934+4463G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28249325 | ||||||
| chr2:28249937
|
G | T | 108 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0022others(105): Show | 108 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(105): Show |
intron_variant | MODIFIER | c.934+5075G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28249937 | ||||||
| chr2:28250131
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.934+5269A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28250131 | ||||||
| chr2:28250216
|
G | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0009 | 3 | HG01346.hp1 HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.934+5354G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28250216 | ||||||
| chr2:28250318
|
C | CT | 104 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0017others(101): Show | 104 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.934+5477dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28250318 | |||||
| chr2:28250318
|
C | CTT | 7 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(4): Show | 7 | HG01243.hp1 HG02622.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.934+5476_934+5477d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28250318 | |||||
| chr2:28250339
|
T | TAGC | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.934+5478_934+5480d others(5): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28250339 | |||||
| chr2:28250450
|
G | A | 1 | a0001c0001t0002g0095 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.934+5588G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28250450 | ||||||
| chr2:28250453
|
A | G | 15 | a0001c0001t0001g0005a0001c0001t0001g0133a0001c0001t0001g0134others(12): Show | 15 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.934+5591A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28250453 | ||||||
| chr2:28250554
|
A | C | 7 | a0001c0001t0002g0029a0001c0001t0002g0047a0001c0001t0002g0048others(4): Show | 7 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.934+5692A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28250554 | ||||||
| chr2:28250584
|
C | CT | 51 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(48): Show | 51 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.934+5732dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28250584 | |||||
| chr2:28250584
|
C | CTT | 86 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0022others(83): Show | 86 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.934+5731_934+5732d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28250584 | |||||
| chr2:28250584
|
C | CTTT | 7 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.934+5730_934+5732d others(5): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28250584 | |||||
| chr2:28250595
|
G | T | 128 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(125): Show | 128 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(125): Show |
intron_variant | MODIFIER | c.934+5733G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28250595 | ||||||
| chr2:28250630
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.934+5768C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28250630 | ||||||
| chr2:28250701
|
G | A | 1 | a0001c0001t0002g0096 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.934+5839G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28250701 | ||||||
| chr2:28250846
|
G | T | 69 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032others(66): Show | 69 | HG00140.hp1 HG00738.hp2 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.934+5984G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28250846 | ||||||
| chr2:28250891
|
G | T | 1 | a0001c0001t0001g0073 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.934+6029G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28250891 | ||||||
| chr2:28251086
|
T | C | 2 | a0001c0001t0002g0130a0001c0001t0002g0131 | 2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.934+6224T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28251086 | ||||||
| chr2:28251456
|
G | A | 144 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(141): Show | 144 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(141): Show |
intron_variant | MODIFIER | c.934+6594G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28251456 | ||||||
| chr2:28251484
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.934+6622A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28251484 | ||||||
| chr2:28251556
|
G | A | 87 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0022others(84): Show | 87 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.934+6694G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28251556 | ||||||
| chr2:28251628
|
T | A | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0091 | 3 | HG02258.hp2 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.934+6766T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28251628 | ||||||
| chr2:28251699
|
T | A | 144 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(141): Show | 144 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(141): Show |
intron_variant | MODIFIER | c.934+6837T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28251699 | ||||||
| chr2:28251725
|
C | T | 144 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(141): Show | 144 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(141): Show |
intron_variant | MODIFIER | c.934+6863C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28251725 | ||||||
| chr2:28251851
|
A | T | 1 | a0001c0001t0003g0089 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.934+6989A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28251851 | ||||||
| chr2:28251854
|
T | G | 1 | a0001c0001t0001g0097 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.934+6992T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28251854 | ||||||
| chr2:28251965
|
T | C | 93 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0031others(90): Show | 93 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.934+7103T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28251965 | ||||||
| chr2:28252064
|
A | T | 6 | a0001c0001t0001g0023a0001c0001t0001g0065a0001c0001t0001g0070others(3): Show | 6 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.934+7202A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28252064 | ||||||
| chr2:28252096
|
G | T | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.934+7234G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28252096 | ||||||
| chr2:28252186
|
C | CA | 5 | a0001c0001t0002g0002a0001c0001t0002g0122a0001c0001t0002g0130others(2): Show | 5 | HG02280.hp2 HG02486.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.934+7337dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28252186 | |||||
| chr2:28252228
|
G | GA | 34 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(31): Show | 34 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.934+7370dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28252228 | |||||
| chr2:28252480
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0138 | 2 | HG01891.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.934+7618G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28252480 | ||||||
| chr2:28252612
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.934+7750A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28252612 | ||||||
| chr2:28252796
|
T | C | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.934+7934T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28252796 | ||||||
| chr2:28252864
|
A | C | 15 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0045others(12): Show | 15 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.934+8002A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28252864 | ||||||
| chr2:28253368
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.934+8506C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28253368 | ||||||
| chr2:28253401
|
C | CA | 35 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0044others(32): Show | 35 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.934+8554dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28253401 | |||||
| chr2:28253463
|
A | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.934+8601A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28253463 | ||||||
| chr2:28253493
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.934+8631C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28253493 | ||||||
| chr2:28253500
|
A | T | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.934+8638A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28253500 | ||||||
| chr2:28253528
|
C | T | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.934+8666C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28253528 | ||||||
| chr2:28253624
|
G | A | 112 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 112 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(109): Show |
intron_variant | MODIFIER | c.934+8762G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28253624 | ||||||
| chr2:28253682
|
C | A | 32 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(29): Show | 32 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.934+8820C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28253682 | ||||||
| chr2:28253696
|
G | A | 7 | a0001c0001t0001g0142a0001c0001t0001g0146a0001c0001t0002g0107others(4): Show | 7 | HG01168.hp2 HG02074.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.934+8834G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28253696 | ||||||
| chr2:28253761
|
G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG01891.hp2 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.934+8899G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28253761 | ||||||
| chr2:28253874
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.934+9012A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28253874 | ||||||
| chr2:28254173
|
C | A | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.934+9311C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28254173 | ||||||
| chr2:28254252
|
C | T | 112 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 112 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(109): Show |
intron_variant | MODIFIER | c.934+9390C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28254252 | ||||||
| chr2:28254290
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.934+9428C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28254290 | ||||||
| chr2:28254309
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.934+9447G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28254309 | ||||||
| chr2:28254326
|
G | A | 5 | a0001c0001t0001g0142a0001c0001t0001g0146a0001c0001t0002g0116others(2): Show | 5 | HG01168.hp2 HG02074.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.934+9464G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28254326 | ||||||
| chr2:28254428
|
C | T | 87 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0022others(84): Show | 87 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.934+9566C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28254428 | ||||||
| chr2:28254444
|
ATTG | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02630.hp1 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.934+9588_934+9590d others(5): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28254444 | |||||
| chr2:28254515
|
T | TA | 16 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0044others(13): Show | 16 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.934+9666dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28254515 | |||||
| chr2:28254553
|
G | A | 3 | a0001c0001t0002g0107a0001c0001t0003g0019a0001c0001t0003g0106 | 3 | HG02451.hp1 HG02486.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.934+9691G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28254553 | ||||||
| chr2:28254728
|
A | AT | 21 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0040others(18): Show | 21 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.934+9887dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28254728 | |||||
| chr2:28254906
|
A | T | 86 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0031others(83): Show | 86 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.934+10044A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28254906 | ||||||
| chr2:28255071
|
T | C | 2 | a0001c0001t0002g0122a0001c0001t0003g0121 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.934+10209T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28255071 | ||||||
| chr2:28255103
|
C | T | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.934+10241C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28255103 | ||||||
| chr2:28255150
|
G | GT | 9 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0146others(6): Show | 9 | HG00741.hp2 HG01168.hp2 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.934+10296dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28255150 | |||||
| chr2:28255227
|
G | C | 1 | a0001c0001t0002g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.934+10365G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28255227 | ||||||
| chr2:28255305
|
A | G | 144 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(141): Show | 144 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(141): Show |
intron_variant | MODIFIER | c.934+10443A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28255305 | ||||||
| chr2:28255909
|
G | A | 30 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(27): Show | 30 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.934+11047G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28255909 | ||||||
| chr2:28255957
|
C | T | 30 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(27): Show | 30 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.934+11095C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28255957 | ||||||
| chr2:28256282
|
G | A | 15 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0045others(12): Show | 15 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.934+11420G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28256282 | ||||||
| chr2:28256287
|
A | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.934+11425A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28256287 | ||||||
| chr2:28256502
|
C | T | 2 | a0001c0001t0001g0043a0001c0001t0002g0020 | 2 | HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.934+11640C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28256502 | ||||||
| chr2:28256508
|
C | G | 2 | a0001c0001t0002g0101a0001c0001t0002g0149 | 2 | NA18955.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.934+11646C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28256508 | ||||||
| chr2:28256567
|
A | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.934+11705A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28256567 | ||||||
| chr2:28256605
|
A | G | 30 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(27): Show | 30 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.934+11743A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28256605 | ||||||
| chr2:28256675
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.934+11813T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28256675 | ||||||
| chr2:28256693
|
C | CT | 86 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(83): Show | 86 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.934+11850dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28256693 | |||||
| chr2:28256757
|
C | T | 3 | a0001c0001t0001g0052a0001c0001t0001g0080a0001c0001t0001g0157 | 3 | HG01099.hp2 HG02040.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.934+11895C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28256757 | ||||||
| chr2:28256840
|
G | A | 107 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0022others(104): Show | 107 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(104): Show |
intron_variant | MODIFIER | c.934+11978G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28256840 | ||||||
| chr2:28256942
|
A | G | 2 | a0001c0001t0002g0130a0001c0001t0002g0131 | 2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.934+12080A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28256942 | ||||||
| chr2:28257378
|
G | A | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.934+12516G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28257378 | ||||||
| chr2:28257427
|
G | A | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.934+12565G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28257427 | ||||||
| chr2:28257466
|
A | G | 17 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(14): Show | 17 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.934+12604A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28257466 | ||||||
| chr2:28257646
|
A | G | 1 | a0001c0001t0002g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.934+12784A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28257646 | ||||||
| chr2:28257909
|
G | A | 15 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(12): Show | 15 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.934+13047G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28257909 | ||||||
| chr2:28258113
|
G | T | 1 | a0001c0001t0001g0150 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.934+13251G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28258113 | ||||||
| chr2:28258154
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0138 | 2 | HG01891.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.934+13292G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28258154 | ||||||
| chr2:28258264
|
G | A | 1 | a0001c0001t0003g0067 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.934+13402G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28258264 | ||||||
| chr2:28258615
|
C | CT | 6 | a0001c0001t0001g0043a0001c0001t0002g0020a0001c0001t0002g0130others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.934+13769dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28258615 | |||||
| chr2:28258615
|
C | CTTTTCTT others(7): Show |
2 | a0001c0001t0002g0122a0001c0001t0003g0121 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.934+13757_934+1375 others(18): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28258615 | |||||
| chr2:28258615
|
C | CTTTTTT | 24 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(21): Show | 24 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.934+13764_934+1376 others(10): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28258615 | |||||
| chr2:28258615
|
C | CTTTTTTT | 88 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0017others(85): Show | 88 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.934+13763_934+1376 others(11): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28258615 | |||||
| chr2:28258615
|
C | CTTTTTTT others(1): Show |
5 | a0001c0001t0001g0053a0001c0001t0001g0086a0001c0001t0001g0124others(2): Show | 5 | HG01192.hp2 HG01934.hp1 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.934+13762_934+1376 others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28258615 | |||||
| chr2:28258615
|
C | CTTTTTTT others(2): Show |
5 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.934+13761_934+1376 others(13): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28258615 | |||||
| chr2:28258615
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.934+13760_934+1376 others(14): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28258615 | |||||
| chr2:28258622
|
T | TTTTTTTC | 18 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0045others(15): Show | 18 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.934+13766_934+1376 others(11): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28258622 | |||||
| chr2:28258662
|
G | A | 3 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0009 | 3 | HG01346.hp1 HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.934+13800G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28258662 | ||||||
| chr2:28258706
|
A | G | 17 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(14): Show | 17 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.934+13844A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28258706 | ||||||
| chr2:28258707
|
G | C | 15 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0045others(12): Show | 15 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.934+13845G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28258707 | ||||||
| chr2:28258764
|
C | T | 1 | a0001c0001t0002g0108 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.934+13902C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28258764 | ||||||
| chr2:28258765
|
G | A | 32 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(29): Show | 32 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.934+13903G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28258765 | ||||||
| chr2:28258778
|
A | C | 32 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(29): Show | 32 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.934+13916A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28258778 | ||||||
| chr2:28258807
|
C | T | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 8 | HG01891.hp2 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.934+13945C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28258807 | ||||||
| chr2:28258997
|
G | C | 6 | a0001c0001t0001g0043a0001c0001t0002g0020a0001c0001t0002g0130others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.934+14135G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28258997 | ||||||
| chr2:28259074
|
C | CT | 13 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0045others(10): Show | 13 | HG01081.hp1 HG01433.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.934+14244dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28259074 | |||||
| chr2:28259074
|
C | CTT | 5 | a0001c0001t0001g0044a0001c0001t0001g0086a0001c0001t0002g0011others(2): Show | 5 | HG01109.hp2 HG01192.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.934+14243_934+1424 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28259074 | |||||
| chr2:28259074
|
C | CTTT | 25 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(22): Show | 25 | HG00140.hp1 HG01069.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.934+14242_934+1424 others(7): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28259074 | |||||
| chr2:28259074
|
C | CTTTT | 27 | a0001c0001t0001g0008a0001c0001t0001g0058a0001c0001t0001g0072others(24): Show | 27 | HG00738.hp2 HG01069.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.934+14241_934+1424 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28259074 | |||||
| chr2:28259074
|
C | CTTTTT | 18 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0034others(15): Show | 18 | HG01106.hp1 HG01891.hp2 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.934+14240_934+1424 others(9): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28259074 | |||||
| chr2:28259074
|
CT | C | 31 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(28): Show | 31 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.934+14244delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28259074 | |||||
| chr2:28259074
|
CTT | C | 9 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0026others(6): Show | 9 | HG00639.hp2 HG01109.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.934+14243_934+1424 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28259074 | |||||
| chr2:28259074
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0002g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.934+14235_934+1424 others(14): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28259074 | |||||
| chr2:28259074
|
CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.934+14230_934+1424 others(19): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28259074 | |||||
| chr2:28259125
|
G | A | 46 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(43): Show | 46 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.934+14263G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28259125 | ||||||
| chr2:28259304
|
T | C | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.934+14442T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28259304 | ||||||
| chr2:28259388
|
A | T | 2 | a0001c0001t0002g0130a0001c0001t0002g0131 | 2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.934+14526A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28259388 | ||||||
| chr2:28259615
|
A | G | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.934+14753A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28259615 | ||||||
| chr2:28259834
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.934+14972C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28259834 | ||||||
| chr2:28259905
|
C | CT | 87 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0031others(84): Show | 87 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.934+15055dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28259905 | |||||
| chr2:28259989
|
T | C | 149 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(146): Show | 149 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(146): Show |
intron_variant | MODIFIER | c.934+15127T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28259989 | ||||||
| chr2:28260167
|
A | T | 15 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(12): Show | 15 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.934+15305A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28260167 | ||||||
| chr2:28260243
|
C | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.934+15381C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28260243 | ||||||
| chr2:28260299
|
CT | C | 8 | a0001c0001t0001g0013a0001c0001t0001g0027a0001c0001t0001g0045others(5): Show | 8 | HG02572.hp1 HG02622.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.934+15457delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28260299 | |||||
| chr2:28260304
|
T | C | 1 | a0001c0001t0002g0049 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.934+15442T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28260304 | ||||||
| chr2:28260305
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.934+15443T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28260305 | ||||||
| chr2:28260376
|
ACTGCAAC others(92): Show |
A | 1 | a0001c0001t0001g0139 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.934+15515_934+1561 others(103): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28260376 | ||||||
| chr2:28260443
|
A | G | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.934+15581A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28260443 | ||||||
| chr2:28260528
|
C | G | 4 | a0001c0001t0001g0043a0001c0001t0002g0020a0001c0001t0002g0130others(1): Show | 4 | HG02280.hp2 HG02723.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.934+15666C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28260528 | ||||||
| chr2:28260663
|
G | A | 17 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0045others(14): Show | 17 | HG00735.hp1 HG00741.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.934+15801G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28260663 | ||||||
| chr2:28260767
|
C | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.934+15905C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28260767 | ||||||
| chr2:28260825
|
A | G | 70 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032others(67): Show | 70 | HG00140.hp1 HG00738.hp2 HG00741.hp2 others(67): Show |
intron_variant | MODIFIER | c.934+15963A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28260825 | ||||||
| chr2:28260851
|
T | C | 15 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0045others(12): Show | 15 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.934+15989T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28260851 | ||||||
| chr2:28260852
|
A | G | 2 | a0001c0001t0001g0043a0001c0001t0002g0020 | 2 | HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.934+15990A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28260852 | ||||||
| chr2:28260906
|
C | T | 1 | a0001c0001t0002g0050 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.934+16044C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28260906 | ||||||
| chr2:28260941
|
C | CT | 32 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(29): Show | 32 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.934+16097dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28260941 | |||||
| chr2:28260941
|
CT | C | 102 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(99): Show | 102 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(99): Show |
intron_variant | MODIFIER | c.934+16097delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28260941 | |||||
| chr2:28260945
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.934+16083T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28260945 | ||||||
| chr2:28260946
|
T | C | 15 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0045others(12): Show | 15 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.934+16084T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28260946 | ||||||
| chr2:28260968
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.934+16106G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28260968 | ||||||
| chr2:28261049
|
C | T | 2 | a0001c0001t0002g0130a0001c0001t0002g0131 | 2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.934+16187C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28261049 | ||||||
| chr2:28261170
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.934+16308G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28261170 | ||||||
| chr2:28261218
|
G | A | 31 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(28): Show | 31 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.934+16356G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28261218 | ||||||
| chr2:28261293
|
G | T | 1 | a0001c0001t0003g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.934+16431G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28261293 | ||||||
| chr2:28261328
|
AT | A | 72 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0024others(69): Show | 72 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.934+16482delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28261328 | |||||
| chr2:28261350
|
G | A | 3 | a0001c0001t0001g0025a0001c0001t0001g0088a0001c0001t0001g0092 | 3 | HG02615.hp2 HG02735.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.934+16488G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28261350 | ||||||
| chr2:28261351
|
G | A | 2 | a0001c0001t0002g0130a0001c0001t0002g0131 | 2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.934+16489G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28261351 | ||||||
| chr2:28261365
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.934+16503C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28261365 | ||||||
| chr2:28261408
|
C | T | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 8 | HG01891.hp2 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.934+16546C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28261408 | ||||||
| chr2:28261454
|
C | G | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.934+16592C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28261454 | ||||||
| chr2:28261491
|
G | A | 1 | a0001c0001t0002g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.934+16629G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28261491 | ||||||
| chr2:28261570
|
T | C | 6 | a0001c0001t0001g0043a0001c0001t0002g0020a0001c0001t0002g0130others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.934+16708T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28261570 | ||||||
| chr2:28261633
|
C | T | 1 | a0001c0001t0002g0145 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.934+16771C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28261633 | ||||||
| chr2:28261816
|
GACCTGAC others(1): Show |
G | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.934+16955_934+1696 others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28261816 | ||||||
| chr2:28262055
|
C | T | 7 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(4): Show | 7 | HG00639.hp1 HG01109.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.934+17193C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28262055 | ||||||
| chr2:28262154
|
T | C | 2 | a0001c0001t0001g0022a0001c0001t0001g0055 | 2 | HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.934+17292T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28262154 | ||||||
| chr2:28262345
|
T | G | 1 | a0001c0001t0001g0123 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.934+17483T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28262345 | ||||||
| chr2:28262415
|
A | T | 14 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(11): Show | 14 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.934+17553A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28262415 | ||||||
| chr2:28262548
|
G | A | 2 | a0001c0001t0002g0130a0001c0001t0002g0131 | 2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.934+17686G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28262548 | ||||||
| chr2:28262577
|
G | A | 82 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0031others(79): Show | 82 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.934+17715G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28262577 | ||||||
| chr2:28262617
|
A | G | 32 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(29): Show | 32 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.934+17755A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28262617 | ||||||
| chr2:28262669
|
G | A | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.934+17807G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28262669 | ||||||
| chr2:28262721
|
A | G | 1 | a0001c0001t0002g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.934+17859A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28262721 | ||||||
| chr2:28262914
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.934+18052T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28262914 | ||||||
| chr2:28263033
|
C | T | 32 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(29): Show | 32 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.934+18171C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28263033 | ||||||
| chr2:28263105
|
T | C | 1 | a0001c0001t0002g0140 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.934+18243T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28263105 | ||||||
| chr2:28263131
|
C | CA | 18 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(15): Show | 18 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.934+18285dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28263131 | |||||
| chr2:28263131
|
CA | C | 28 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(25): Show | 28 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.934+18285delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28263131 | |||||
| chr2:28263144
|
AAAAG | A | 7 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.934+18285_934+1828 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28263144 | |||||
| chr2:28263145
|
AAAG | A | 16 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0045others(13): Show | 16 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.934+18289_934+1829 others(7): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28263145 | |||||
| chr2:28263185
|
GATT | G | 2 | a0001c0001t0001g0043a0001c0001t0002g0020 | 2 | HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.934+18334_934+1833 others(7): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28263185 | |||||
| chr2:28263291
|
A | G | 2 | a0001c0001t0003g0135a0001c0001t0003g0136 | 2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.934+18429A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28263291 | ||||||
| chr2:28263387
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.934+18525C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28263387 | ||||||
| chr2:28263470
|
A | G | 6 | a0001c0001t0001g0142a0001c0001t0001g0146a0001c0001t0002g0107others(3): Show | 6 | HG01168.hp2 HG02074.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.934+18608A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28263470 | ||||||
| chr2:28263549
|
G | A | 15 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0045others(12): Show | 15 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.934+18687G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28263549 | ||||||
| chr2:28263590
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.934+18728C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28263590 | ||||||
| chr2:28263653
|
A | G | 34 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(31): Show | 34 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.934+18791A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28263653 | ||||||
| chr2:28263677
|
T | A | 32 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(29): Show | 32 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.934+18815T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28263677 | ||||||
| chr2:28263708
|
C | A | 34 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(31): Show | 34 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.934+18846C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28263708 | ||||||
| chr2:28263953
|
C | G | 32 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(29): Show | 32 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.934+19091C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28263953 | ||||||
| chr2:28264058
|
C | T | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.934+19196C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28264058 | ||||||
| chr2:28264316
|
A | G | 2 | a0001c0001t0002g0130a0001c0001t0002g0131 | 2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.934+19454A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28264316 | ||||||
| chr2:28264521
|
G | A | 15 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0045others(12): Show | 15 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.934+19659G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28264521 | ||||||
| chr2:28264839
|
A | T | 58 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0032others(55): Show | 58 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.934+19977A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28264839 | ||||||
| chr2:28264984
|
T | G | 6 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0009others(3): Show | 6 | HG01346.hp1 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.934+20122T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28264984 | ||||||
| chr2:28265337
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.934+20475G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28265337 | ||||||
| chr2:28265566
|
G | A | 4 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0009others(1): Show | 4 | HG01346.hp1 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.934+20704G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28265566 | ||||||
| chr2:28265942
|
T | C | 23 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(20): Show | 23 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.934+21080T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28265942 | ||||||
| chr2:28266019
|
A | G | 12 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(9): Show | 12 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.934+21157A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28266019 | ||||||
| chr2:28266141
|
C | T | 21 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0133others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.934+21279C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28266141 | ||||||
| chr2:28266652
|
A | T | 36 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0057others(33): Show | 36 | HG01069.hp1 HG01106.hp1 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.934+21790A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28266652 | ||||||
| chr2:28266682
|
G | A | 31 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(28): Show | 31 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.934+21820G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28266682 | ||||||
| chr2:28266696
|
A | G | 31 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(28): Show | 31 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.934+21834A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28266696 | ||||||
| chr2:28266721
|
T | G | 2 | a0001c0001t0002g0007a0001c0001t0002g0128 | 2 | HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.934+21859T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28266721 | ||||||
| chr2:28266893
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.934+22031C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28266893 | ||||||
| chr2:28266925
|
G | A | 22 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(19): Show | 22 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.934+22063G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28266925 | ||||||
| chr2:28266937
|
G | C | 31 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(28): Show | 31 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.934+22075G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28266937 | ||||||
| chr2:28267087
|
C | T | 1 | a0001c0001t0002g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.934+22225C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28267087 | ||||||
| chr2:28267167
|
GGAAA | G | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.934+22321_934+2232 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28267167 | |||||
| chr2:28267366
|
A | G | 24 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(21): Show | 24 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.934+22504A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28267366 | ||||||
| chr2:28267384
|
C | T | 2 | a0001c0001t0002g0147a0001c0001t0002g0156 | 2 | HG01069.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.934+22522C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28267384 | ||||||
| chr2:28267436
|
CAT | C | 7 | a0001c0001t0002g0029a0001c0001t0002g0047a0001c0001t0002g0048others(4): Show | 7 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.934+22576_934+2257 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28267436 | |||||
| chr2:28267438
|
T | C | 1 | a0001c0001t0002g0051 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.934+22576T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28267438 | ||||||
| chr2:28267438
|
T | TAC | 11 | a0001c0001t0001g0053a0001c0001t0001g0057a0001c0001t0001g0058others(8): Show | 11 | HG00733.hp1 HG01106.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.934+22603_934+2260 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28267438 | |||||
| chr2:28267438
|
T | TACAC | 3 | a0001c0001t0002g0122a0001c0001t0002g0140a0001c0001t0003g0121 | 3 | HG01496.hp1 HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.934+22601_934+2260 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28267438 | |||||
| chr2:28267438
|
TAC | T | 24 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0075others(21): Show | 24 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.934+22603_934+2260 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28267438 | |||||
| chr2:28267438
|
TACACACA others(1): Show |
T | 6 | a0001c0001t0001g0027a0001c0001t0001g0074a0001c0001t0001g0081others(3): Show | 6 | HG02486.hp1 HG02572.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.934+22597_934+2260 others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28267438 | |||||
| chr2:28267438
|
TACACACA others(5): Show |
T | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG01891.hp2 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.934+22593_934+2260 others(16): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28267438 | |||||
| chr2:28267597
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.934+22735A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28267597 | ||||||
| chr2:28268009
|
C | A | 22 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(19): Show | 22 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.934+23147C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28268009 | ||||||
| chr2:28268020
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.934+23158C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28268020 | ||||||
| chr2:28268021
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.934+23159G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28268021 | ||||||
| chr2:28269231
|
G | A | 15 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(12): Show | 15 | HG00733.hp2 HG01167.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.934+24369G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28269231 | ||||||
| chr2:28269743
|
C | T | 13 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(10): Show | 13 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.934+24881C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28269743 | ||||||
| chr2:28269802
|
G | A | 2 | a0001c0001t0003g0135a0001c0001t0003g0136 | 2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.934+24940G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28269802 | ||||||
| chr2:28269850
|
A | AT | 35 | a0001c0001t0001g0057a0001c0001t0001g0073a0001c0001t0001g0113others(32): Show | 35 | HG00639.hp2 HG01069.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.934+25001dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28269850 | |||||
| chr2:28269850
|
AT | A | 15 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(12): Show | 15 | HG00733.hp2 HG01167.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.934+25001delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28269850 | |||||
| chr2:28270370
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.934+25508C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28270370 | ||||||
| chr2:28270503
|
C | T | 24 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(21): Show | 24 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.934+25641C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28270503 | ||||||
| chr2:28270568
|
G | A | 1 | a0001c0001t0003g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.934+25706G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28270568 | ||||||
| chr2:28270649
|
T | A | 24 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(21): Show | 24 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.934+25787T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28270649 | ||||||
| chr2:28270822
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.934+25960A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28270822 | ||||||
| chr2:28270842
|
C | A | 61 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0031others(58): Show | 61 | HG00140.hp1 HG00738.hp2 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.934+25980C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28270842 | ||||||
| chr2:28271024
|
A | T | 39 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(36): Show | 39 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.934+26162A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28271024 | ||||||
| chr2:28271133
|
T | C | 39 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(36): Show | 39 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.934+26271T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28271133 | ||||||
| chr2:28271158
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.934+26296A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28271158 | ||||||
| chr2:28271282
|
G | C | 3 | a0001c0001t0001g0052a0001c0001t0001g0080a0001c0001t0001g0157 | 3 | HG01099.hp2 HG02040.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.934+26420G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28271282 | ||||||
| chr2:28271324
|
TC | T | 6 | a0001c0001t0002g0004a0001c0001t0002g0036a0001c0001t0002g0037others(3): Show | 6 | HG00738.hp1 HG02145.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.934+26465delC | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28271324 | |||||
| chr2:28271406
|
CTCTCCTC others(276): Show |
C | 1 | a0001c0001t0002g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.934+26546_935-2664 others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28271406 | |||||
| chr2:28271427
|
TCA | T | 23 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(20): Show | 23 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.934+26568_934+2656 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28271427 | |||||
| chr2:28271658
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.935-26680G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28271658 | ||||||
| chr2:28272005
|
T | C | 17 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(14): Show | 17 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.935-26333T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28272005 | ||||||
| chr2:28272043
|
A | G | 24 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(21): Show | 24 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.935-26295A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28272043 | ||||||
| chr2:28272290
|
T | A | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.935-26048T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28272290 | ||||||
| chr2:28272651
|
G | GT | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.935-25686dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28272651 | |||||
| chr2:28272697
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.935-25641A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28272697 | ||||||
| chr2:28272780
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.935-25558G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28272780 | ||||||
| chr2:28273079
|
C | A | 1 | a0001c0001t0004g0118 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.935-25259C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28273079 | ||||||
| chr2:28273115
|
C | T | 8 | a0001c0001t0002g0029a0001c0001t0002g0047a0001c0001t0002g0048others(5): Show | 8 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.935-25223C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28273115 | ||||||
| chr2:28273135
|
C | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG01891.hp2 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.935-25203C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28273135 | ||||||
| chr2:28273191
|
A | G | 2 | a0001c0001t0001g0115a0001c0001t0002g0158 | 2 | HG02027.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.935-25147A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28273191 | ||||||
| chr2:28273286
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02630.hp1 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.935-25052G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28273286 | ||||||
| chr2:28273872
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02630.hp1 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.935-24466G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28273872 | ||||||
| chr2:28274009
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.935-24329G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28274009 | ||||||
| chr2:28274264
|
C | G | 1 | a0001c0001t0002g0122 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.935-24074C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28274264 | ||||||
| chr2:28274409
|
C | T | 14 | a0001c0001t0001g0023a0001c0001t0001g0043a0001c0001t0001g0044others(11): Show | 14 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.935-23929C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28274409 | ||||||
| chr2:28274683
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02630.hp1 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.935-23655C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28274683 | ||||||
| chr2:28274879
|
G | A | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.935-23459G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28274879 | ||||||
| chr2:28274963
|
G | A | 8 | a0001c0001t0002g0029a0001c0001t0002g0047a0001c0001t0002g0048others(5): Show | 8 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.935-23375G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28274963 | ||||||
| chr2:28275035
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.935-23303G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28275035 | ||||||
| chr2:28275383
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.935-22955A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28275383 | ||||||
| chr2:28275454
|
T | C | 39 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(36): Show | 39 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.935-22884T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28275454 | ||||||
| chr2:28275600
|
T | C | 156 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(153): Show |
intron_variant | MODIFIER | c.935-22738T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28275600 | ||||||
| chr2:28275785
|
G | A | 8 | a0001c0001t0002g0001a0001c0001t0003g0018a0001c0001t0003g0019others(5): Show | 8 | HG00733.hp2 HG01167.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.935-22553G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28275785 | ||||||
| chr2:28275927
|
G | A | 2 | a0001c0001t0001g0043a0001c0001t0002g0020 | 2 | HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.935-22411G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28275927 | ||||||
| chr2:28275950
|
T | G | 13 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(10): Show | 13 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.935-22388T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28275950 | ||||||
| chr2:28276007
|
C | CAA | 5 | a0001c0001t0002g0001a0001c0001t0003g0089a0001c0001t0003g0135others(2): Show | 5 | HG00733.hp2 HG01167.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.935-22318_935-2231 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28276007 | |||||
| chr2:28276021
|
AG | A | 11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0074others(8): Show | 11 | HG01346.hp1 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.935-22316delG | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28276021 | ||||||
| chr2:28276022
|
G | A | 24 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(21): Show | 24 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.935-22316G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28276022 | ||||||
| chr2:28276286
|
TTCTC | T | 3 | a0001c0001t0002g0010a0001c0001t0002g0016a0001c0001t0002g0112 | 3 | HG03139.hp1 HG03516.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.935-22049_935-2204 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28276286 | |||||
| chr2:28276307
|
G | A | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.935-22031G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28276307 | ||||||
| chr2:28276473
|
T | C | 1 | a0001c0001t0001g0080 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.935-21865T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28276473 | ||||||
| chr2:28276544
|
C | T | 1 | a0001c0001t0002g0029 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.935-21794C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28276544 | ||||||
| chr2:28276566
|
A | G | 3 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0002g0021 | 3 | HG03041.hp2 HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.935-21772A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28276566 | ||||||
| chr2:28276650
|
T | A | 24 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(21): Show | 24 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.935-21688T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28276650 | ||||||
| chr2:28276737
|
T | A | 39 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(36): Show | 39 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.935-21601T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28276737 | ||||||
| chr2:28276934
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02630.hp1 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.935-21404G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28276934 | ||||||
| chr2:28277919
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.935-20419A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28277919 | ||||||
| chr2:28278298
|
C | G | 1 | a0001c0001t0002g0130 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.935-20040C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28278298 | ||||||
| chr2:28278393
|
C | T | 13 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(10): Show | 13 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.935-19945C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28278393 | ||||||
| chr2:28278501
|
C | G | 3 | a0001c0001t0001g0022a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | HG02280.hp1 HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.935-19837C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28278501 | ||||||
| chr2:28278694
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0138 | 2 | HG01891.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.935-19644G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28278694 | ||||||
| chr2:28278777
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.935-19561G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28278777 | ||||||
| chr2:28278906
|
G | A | 1 | a0001c0001t0002g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.935-19432G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28278906 | ||||||
| chr2:28279226
|
G | A | 7 | a0001c0001t0002g0001a0001c0001t0003g0089a0001c0001t0003g0090others(4): Show | 7 | HG00733.hp2 HG01167.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.935-19112G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28279226 | ||||||
| chr2:28279246
|
C | T | 2 | a0001c0001t0002g0130a0001c0001t0002g0131 | 2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.935-19092C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28279246 | ||||||
| chr2:28279341
|
C | T | 1 | a0001c0001t0002g0144 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.935-18997C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28279341 | ||||||
| chr2:28279362
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.935-18976C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28279362 | ||||||
| chr2:28279393
|
C | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.935-18945C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28279393 | ||||||
| chr2:28279478
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.935-18860G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28279478 | ||||||
| chr2:28279660
|
C | CT | 46 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0056others(43): Show | 46 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.935-18656dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28279660 | |||||
| chr2:28279779
|
C | G | 1 | a0001c0001t0003g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.935-18559C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28279779 | ||||||
| chr2:28280011
|
T | C | 8 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0146others(5): Show | 8 | HG00741.hp2 HG01168.hp2 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.935-18327T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28280011 | ||||||
| chr2:28280020
|
T | C | 2 | a0001c0001t0002g0062a0001c0001t0002g0096 | 2 | HG01934.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.935-18318T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28280020 | ||||||
| chr2:28280033
|
G | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02630.hp1 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.935-18305G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28280033 | ||||||
| chr2:28280180
|
T | C | 22 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(19): Show | 22 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.935-18158T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28280180 | ||||||
| chr2:28280187
|
C | T | 35 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(32): Show | 35 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.935-18151C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28280187 | ||||||
| chr2:28280452
|
T | C | 13 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(10): Show | 13 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.935-17886T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28280452 | ||||||
| chr2:28280564
|
T | C | 7 | a0001c0001t0002g0001a0001c0001t0003g0089a0001c0001t0003g0090others(4): Show | 7 | HG00733.hp2 HG01167.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.935-17774T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28280564 | ||||||
| chr2:28281074
|
G | A | 25 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0031others(22): Show | 25 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.935-17264G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28281074 | ||||||
| chr2:28281101
|
A | G | 23 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(20): Show | 23 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.935-17237A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28281101 | ||||||
| chr2:28281283
|
G | C | 17 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0042others(14): Show | 17 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.935-17055G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28281283 | ||||||
| chr2:28281931
|
A | G | 5 | a0001c0001t0002g0004a0001c0001t0002g0036a0001c0001t0002g0037others(2): Show | 5 | HG00738.hp1 HG02145.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.935-16407A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28281931 | ||||||
| chr2:28282507
|
A | G | 6 | a0001c0001t0002g0001a0001c0001t0003g0089a0001c0001t0003g0090others(3): Show | 6 | HG00733.hp2 HG01167.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.935-15831A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28282507 | ||||||
| chr2:28282526
|
G | A | 13 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(10): Show | 13 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.935-15812G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28282526 | ||||||
| chr2:28282754
|
T | C | 36 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(33): Show | 36 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.935-15584T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28282754 | ||||||
| chr2:28282781
|
C | T | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.935-15557C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28282781 | ||||||
| chr2:28282795
|
C | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.935-15543C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28282795 | ||||||
| chr2:28282997
|
C | CA | 88 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(85): Show | 88 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(85): Show |
intron_variant | MODIFIER | c.935-15320dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28282997 | |||||
| chr2:28282997
|
C | CAA | 7 | a0001c0001t0001g0057a0001c0001t0001g0088a0001c0001t0001g0115others(4): Show | 7 | HG02027.hp1 HG02135.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.935-15321_935-1532 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28282997 | |||||
| chr2:28283018
|
A | AAAGGAAA others(13): Show |
2 | a0001c0001t0001g0109a0001c0001t0003g0121 | 2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.935-15320_935-1531 others(24): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28283018 | ||||||
| chr2:28283018
|
A | AAGGAAAG others(12): Show |
25 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(22): Show | 25 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.935-15320_935-1531 others(23): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28283018 | ||||||
| chr2:28283018
|
A | G | 29 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(26): Show | 29 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.935-15320A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28283018 | ||||||
| chr2:28283019
|
G | A | 27 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(24): Show | 27 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.935-15319G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28283019 | ||||||
| chr2:28283019
|
G | GAAAGAAA others(10): Show |
29 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(26): Show | 29 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.935-15319_935-1531 others(21): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28283019 | ||||||
| chr2:28283019
|
G | GGAAAGAA others(11): Show |
3 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0003g0090 | 3 | HG01346.hp1 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.935-15316_935-1531 others(22): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28283019 | |||||
| chr2:28283084
|
C | T | 34 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(31): Show | 34 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.935-15254C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28283084 | ||||||
| chr2:28283832
|
C | A | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.935-14506C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28283832 | ||||||
| chr2:28284070
|
G | A | 3 | a0001c0001t0001g0052a0001c0001t0001g0080a0001c0001t0001g0157 | 3 | HG01099.hp2 HG02040.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.935-14268G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28284070 | ||||||
| chr2:28284277
|
G | T | 2 | a0001c0001t0002g0122a0001c0001t0003g0121 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.935-14061G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28284277 | ||||||
| chr2:28284306
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.935-14032G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28284306 | ||||||
| chr2:28284387
|
T | C | 35 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(32): Show | 35 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.935-13951T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28284387 | ||||||
| chr2:28284487
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.935-13851T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28284487 | ||||||
| chr2:28284551
|
CA | C | 11 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0001others(8): Show | 11 | HG00733.hp2 HG01167.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.935-13786delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28284551 | ||||||
| chr2:28284554
|
A | T | 23 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(20): Show | 23 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.935-13784A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28284554 | ||||||
| chr2:28284777
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.935-13561C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28284777 | ||||||
| chr2:28285363
|
A | AT | 9 | a0001c0001t0002g0001a0001c0001t0003g0018a0001c0001t0003g0019others(6): Show | 9 | HG00733.hp2 HG01167.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.935-12969dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28285363 | |||||
| chr2:28285482
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.935-12856G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28285482 | ||||||
| chr2:28285737
|
CT | C | 6 | a0001c0001t0002g0001a0001c0001t0003g0089a0001c0001t0003g0090others(3): Show | 6 | HG00733.hp2 HG01167.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.935-12589delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28285737 | |||||
| chr2:28285955
|
CT | C | 23 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(20): Show | 23 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.935-12365delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28285955 | |||||
| chr2:28286042
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.935-12296A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28286042 | ||||||
| chr2:28286244
|
G | A | 1 | a0001c0001t0002g0107 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.935-12094G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28286244 | ||||||
| chr2:28286246
|
G | A | 1 | a0001c0001t0004g0118 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.935-12092G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28286246 | ||||||
| chr2:28287346
|
T | C | 2 | a0001c0001t0002g0021a0001c0001t0005g0119 | 2 | HG02109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.935-10992T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28287346 | ||||||
| chr2:28287429
|
G | A | 5 | a0001c0001t0002g0004a0001c0001t0002g0036a0001c0001t0002g0037others(2): Show | 5 | HG00738.hp1 HG02145.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.935-10909G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28287429 | ||||||
| chr2:28287480
|
A | G | 18 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(15): Show | 18 | HG00639.hp1 HG00741.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.935-10858A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28287480 | ||||||
| chr2:28287684
|
A | C | 1 | a0001c0001t0002g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.935-10654A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28287684 | ||||||
| chr2:28287710
|
T | C | 1 | a0001c0001t0003g0067 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.935-10628T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28287710 | ||||||
| chr2:28287738
|
C | T | 1 | a0001c0001t0005g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.935-10600C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28287738 | ||||||
| chr2:28288080
|
G | T | 1 | a0001c0001t0001g0091 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.935-10258G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28288080 | ||||||
| chr2:28288329
|
CT | C | 27 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(24): Show | 27 | HG00639.hp1 HG00733.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.935-9993delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28288329 | |||||
| chr2:28288334
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.935-10004T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28288334 | ||||||
| chr2:28288404
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.935-9934C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28288404 | ||||||
| chr2:28288510
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.935-9828C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28288510 | ||||||
| chr2:28288663
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.935-9675T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28288663 | ||||||
| chr2:28288683
|
G | T | 28 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(25): Show | 28 | HG00639.hp1 HG00733.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.935-9655G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28288683 | ||||||
| chr2:28288720
|
C | T | 8 | a0001c0001t0002g0029a0001c0001t0002g0047a0001c0001t0002g0048others(5): Show | 8 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.935-9618C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28288720 | ||||||
| chr2:28288822
|
C | T | 2 | a0001c0001t0002g0122a0001c0001t0003g0121 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.935-9516C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28288822 | ||||||
| chr2:28288867
|
G | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | HG02280.hp1 HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.935-9471G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28288867 | ||||||
| chr2:28288962
|
G | GT | 9 | a0001c0001t0001g0142a0001c0001t0002g0029a0001c0001t0002g0047others(6): Show | 9 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.935-9362dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28288962 | |||||
| chr2:28288964
|
T | G | 3 | a0001c0001t0001g0052a0001c0001t0001g0080a0001c0001t0001g0157 | 3 | HG01099.hp2 HG02040.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.935-9374T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28288964 | ||||||
| chr2:28289044
|
G | A | 47 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(44): Show | 47 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.935-9294G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28289044 | ||||||
| chr2:28289333
|
G | A | 3 | a0001c0001t0002g0007a0001c0001t0002g0128a0001c0001t0002g0140 | 3 | HG01496.hp1 HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.935-9005G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28289333 | ||||||
| chr2:28289341
|
A | G | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.935-8997A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28289341 | ||||||
| chr2:28289588
|
A | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0138 | 2 | HG01891.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.935-8750A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28289588 | ||||||
| chr2:28289636
|
C | G | 1 | a0001c0001t0001g0154 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.935-8702C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28289636 | ||||||
| chr2:28289765
|
C | T | 4 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0001g0125others(1): Show | 4 | HG02572.hp1 HG02602.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.935-8573C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28289765 | ||||||
| chr2:28289972
|
C | G | 3 | a0001c0001t0002g0107a0001c0001t0002g0130a0001c0001t0002g0131 | 3 | HG02280.hp2 HG02451.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.935-8366C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28289972 | ||||||
| chr2:28290149
|
C | T | 1 | a0001c0001t0002g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.935-8189C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28290149 | ||||||
| chr2:28290316
|
CAT | C | 8 | a0001c0001t0002g0029a0001c0001t0002g0047a0001c0001t0002g0048others(5): Show | 8 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.935-8021_935-8020d others(4): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28290316 | ||||||
| chr2:28290562
|
GT | G | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.935-7775delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28290562 | ||||||
| chr2:28290581
|
C | T | 1 | a0001c0001t0002g0112 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.935-7757C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28290581 | ||||||
| chr2:28290633
|
T | C | 1 | a0001c0001t0002g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.935-7705T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28290633 | ||||||
| chr2:28290653
|
T | C | 5 | a0001c0001t0002g0004a0001c0001t0002g0036a0001c0001t0002g0037others(2): Show | 5 | HG00738.hp1 HG02145.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.935-7685T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28290653 | ||||||
| chr2:28290695
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.935-7643G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28290695 | ||||||
| chr2:28290907
|
T | A | 4 | a0001c0001t0001g0142a0001c0001t0002g0116a0001c0001t0002g0144others(1): Show | 4 | HG02074.hp1 NA18968.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.935-7431T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28290907 | ||||||
| chr2:28291168
|
G | T | 1 | a0001c0001t0002g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.935-7170G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28291168 | ||||||
| chr2:28291267
|
G | A | 16 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(13): Show | 16 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.935-7071G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28291267 | ||||||
| chr2:28291524
|
G | C | 2 | a0001c0001t0002g0147a0001c0001t0002g0156 | 2 | HG01069.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.935-6814G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28291524 | ||||||
| chr2:28291595
|
CA | C | 8 | a0001c0001t0002g0001a0001c0001t0003g0018a0001c0001t0003g0019others(5): Show | 8 | HG00733.hp2 HG01167.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.935-6731delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28291595 | |||||
| chr2:28291832
|
A | C | 2 | a0001c0001t0002g0101a0001c0001t0002g0149 | 2 | NA18955.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.935-6506A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28291832 | ||||||
| chr2:28291836
|
G | A | 14 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(11): Show | 14 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.935-6502G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28291836 | ||||||
| chr2:28291850
|
G | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0072 | 2 | HG00738.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.935-6488G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28291850 | ||||||
| chr2:28291893
|
G | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | HG02280.hp1 HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.935-6445G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28291893 | ||||||
| chr2:28292016
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0072 | 2 | HG00738.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.935-6322C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28292016 | ||||||
| chr2:28292056
|
ACTGGAGC others(3): Show |
A | 11 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0001others(8): Show | 11 | HG00733.hp2 HG01167.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.935-6278_935-6269d others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 28292056 | |||||
| chr2:28292180
|
G | A | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.935-6158G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28292180 | ||||||
| chr2:28292267
|
C | T | 1 | a0001c0001t0003g0067 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.935-6071C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28292267 | ||||||
| chr2:28292296
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.935-6042G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28292296 | ||||||
| chr2:28292413
|
T | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0092 | 2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.935-5925T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28292413 | ||||||
| chr2:28292428
|
C | T | 16 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(13): Show | 16 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.935-5910C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28292428 | ||||||
| chr2:28292468
|
C | T | 1 | a0001c0001t0002g0144 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.935-5870C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28292468 | ||||||
| chr2:28292581
|
T | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012 | 3 | HG02572.hp1 HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.935-5757T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28292581 | ||||||
| chr2:28292606
|
G | A | 1 | a0001c0001t0003g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.935-5732G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28292606 | ||||||
| chr2:28293379
|
G | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.935-4959G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28293379 | ||||||
| chr2:28293404
|
G | A | 61 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(58): Show | 61 | HG00733.hp2 HG01069.hp1 HG01106.hp1 others(58): Show |
intron_variant | MODIFIER | c.935-4934G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28293404 | ||||||
| chr2:28293584
|
C | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0078 | 2 | HG01243.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.935-4754C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28293584 | ||||||
| chr2:28293739
|
C | T | 82 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(79): Show | 82 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.935-4599C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28293739 | ||||||
| chr2:28293959
|
G | T | 1 | a0001c0001t0003g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.935-4379G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28293959 | ||||||
| chr2:28294156
|
A | T | 1 | a0001c0001t0002g0051 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.935-4182A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28294156 | ||||||
| chr2:28294162
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.935-4176C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28294162 | ||||||
| chr2:28294444
|
A | G | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.935-3894A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28294444 | ||||||
| chr2:28294472
|
G | A | 1 | a0001c0001t0002g0141 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.935-3866G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28294472 | ||||||
| chr2:28294543
|
G | C | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02630.hp1 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.935-3795G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28294543 | ||||||
| chr2:28294994
|
A | G | 113 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(110): Show | 113 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(110): Show |
intron_variant | MODIFIER | c.935-3344A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28294994 | ||||||
| chr2:28295212
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.935-3126C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28295212 | ||||||
| chr2:28295236
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.935-3102C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28295236 | ||||||
| chr2:28295286
|
T | C | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.935-3052T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28295286 | ||||||
| chr2:28295351
|
A | G | 14 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(11): Show | 14 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.935-2987A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28295351 | ||||||
| chr2:28295623
|
G | A | 17 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(14): Show | 17 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.935-2715G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28295623 | ||||||
| chr2:28295716
|
C | T | 1 | a0001c0001t0002g0062 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.935-2622C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28295716 | ||||||
| chr2:28296290
|
A | G | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.935-2048A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28296290 | ||||||
| chr2:28296321
|
C | A | 2 | a0001c0001t0001g0088a0001c0001t0001g0092 | 2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.935-2017C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28296321 | ||||||
| chr2:28296321
|
C | G | 1 | a0001c0001t0002g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.935-2017C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28296321 | ||||||
| chr2:28296535
|
C | G | 14 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0052others(11): Show | 14 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.935-1803C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28296535 | ||||||
| chr2:28296537
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.935-1801C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28296537 | ||||||
| chr2:28296538
|
G | A | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.935-1800G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28296538 | ||||||
| chr2:28296696
|
A | G | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.935-1642A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28296696 | ||||||
| chr2:28296714
|
G | A | 1 | a0001c0001t0002g0077 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.935-1624G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28296714 | ||||||
| chr2:28296791
|
G | A | 1 | a0001c0001t0001g0035 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.935-1547G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28296791 | ||||||
| chr2:28297014
|
A | G | 1 | a0001c0001t0002g0039 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.935-1324A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28297014 | ||||||
| chr2:28297216
|
A | G | 113 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(110): Show | 113 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(110): Show |
intron_variant | MODIFIER | c.935-1122A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28297216 | ||||||
| chr2:28297244
|
A | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0081 | 2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.935-1094A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28297244 | ||||||
| chr2:28297258
|
G | A | 1 | a0001c0001t0002g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.935-1080G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28297258 | ||||||
| chr2:28297418
|
G | A | 1 | a0001c0001t0002g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.935-920G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28297418 | ||||||
| chr2:28297440
|
G | A | 1 | a0001c0001t0002g0141 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.935-898G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28297440 | ||||||
| chr2:28297651
|
G | A | 9 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0003g0018others(6): Show | 9 | HG00733.hp2 HG01167.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.935-687G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28297651 | ||||||
| chr2:28297898
|
A | G | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.935-440A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28297898 | ||||||
| chr2:28298179
|
TC | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0083 | 2 | HG00735.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.935-158delC | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28298179 | ||||||
| chr2:28298190
|
C | T | 77 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(74): Show | 77 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.935-148C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | chr2 | 28298190 | ||||||
| chr2:28298642
|
A | G | 8 | a0001c0001t0002g0001a0001c0001t0003g0018a0001c0001t0003g0019others(5): Show | 8 | HG00733.hp2 HG01167.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1088+151A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28298642 | ||||||
| chr2:28299458
|
A | G | 19 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(16): Show | 19 | HG00639.hp1 HG00741.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1088+967A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28299458 | ||||||
| chr2:28299927
|
T | TTTTTA | 3 | a0001c0001t0001g0138a0001c0001t0002g0011a0001c0001t0003g0137 | 3 | HG01109.hp2 HG01891.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1088+1461_1088+146 others(9): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28299927 | |||||
| chr2:28300179
|
T | A | 2 | a0001c0001t0002g0003a0001c0001t0002g0126 | 2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1088+1688T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28300179 | ||||||
| chr2:28300314
|
T | A | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1088+1823T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28300314 | ||||||
| chr2:28300516
|
G | A | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1088+2025G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28300516 | ||||||
| chr2:28300878
|
A | G | 8 | a0001c0001t0002g0001a0001c0001t0003g0018a0001c0001t0003g0019others(5): Show | 8 | HG00733.hp2 HG01167.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1088+2387A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28300878 | ||||||
| chr2:28300913
|
G | T | 1 | a0001c0001t0003g0019 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1088+2422G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28300913 | ||||||
| chr2:28300967
|
C | T | 96 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(93): Show | 96 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.1088+2476C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28300967 | ||||||
| chr2:28301128
|
T | C | 50 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(47): Show | 50 | HG00741.hp2 HG01069.hp1 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.1088+2637T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28301128 | ||||||
| chr2:28301179
|
A | G | 1 | a0001c0001t0002g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1088+2688A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28301179 | ||||||
| chr2:28301410
|
G | A | 1 | a0001c0001t0002g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1088+2919G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28301410 | ||||||
| chr2:28301508
|
C | G | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1088+3017C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28301508 | ||||||
| chr2:28302139
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1088+3648C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28302139 | ||||||
| chr2:28302146
|
A | C | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1088+3655A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28302146 | ||||||
| chr2:28302191
|
C | T | 17 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(14): Show | 17 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.1088+3700C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28302191 | ||||||
| chr2:28302349
|
G | A | 79 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(76): Show | 79 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.1088+3858G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28302349 | ||||||
| chr2:28302416
|
CA | C | 106 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(103): Show | 106 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.1088+3941delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28302416 | |||||
| chr2:28302573
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1088+4082G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28302573 | ||||||
| chr2:28302592
|
T | C | 26 | a0001c0001t0001g0073a0001c0001t0001g0113a0001c0001t0001g0115others(23): Show | 26 | HG01069.hp1 HG01106.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1088+4101T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28302592 | ||||||
| chr2:28302947
|
G | C | 1 | a0001c0001t0001g0102 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1088+4456G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28302947 | ||||||
| chr2:28303061
|
C | T | 8 | a0001c0001t0002g0029a0001c0001t0002g0047a0001c0001t0002g0048others(5): Show | 8 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.1088+4570C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28303061 | ||||||
| chr2:28303399
|
A | T | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1088+4908A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28303399 | ||||||
| chr2:28303550
|
C | G | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1088+5059C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28303550 | ||||||
| chr2:28303850
|
A | T | 1 | a0001c0001t0001g0142 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1088+5359A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28303850 | ||||||
| chr2:28303973
|
C | A | 1 | a0001c0001t0001g0080 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1088+5482C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28303973 | ||||||
| chr2:28304308
|
G | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | HG02280.hp1 HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1088+5817G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28304308 | ||||||
| chr2:28304343
|
A | G | 3 | a0001c0001t0001g0024a0001c0001t0002g0026a0001c0001t0002g0046 | 3 | HG00639.hp1 HG01109.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1088+5852A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28304343 | ||||||
| chr2:28304543
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0138 | 2 | HG01891.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1088+6052T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28304543 | ||||||
| chr2:28304585
|
C | A | 2 | a0001c0001t0001g0032a0001c0001t0001g0072 | 2 | HG00738.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1088+6094C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28304585 | ||||||
| chr2:28304600
|
G | A | 8 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(5): Show | 8 | HG00639.hp1 HG01109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1088+6109G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28304600 | ||||||
| chr2:28304638
|
A | G | 109 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(106): Show | 109 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(106): Show |
intron_variant | MODIFIER | c.1088+6147A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28304638 | ||||||
| chr2:28304692
|
C | T | 79 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(76): Show | 79 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.1088+6201C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28304692 | ||||||
| chr2:28304751
|
A | AT | 8 | a0001c0001t0002g0029a0001c0001t0002g0047a0001c0001t0002g0048others(5): Show | 8 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.1088+6270dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28304751 | |||||
| chr2:28305134
|
A | G | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1088+6643A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28305134 | ||||||
| chr2:28305829
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1088+7338A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28305829 | ||||||
| chr2:28306005
|
G | A | 1 | a0001c0001t0002g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1088+7514G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28306005 | ||||||
| chr2:28306067
|
C | A | 45 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(42): Show | 45 | HG01069.hp1 HG01106.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.1088+7576C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28306067 | ||||||
| chr2:28306097
|
A | G | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0091 | 3 | HG02258.hp2 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1088+7606A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28306097 | ||||||
| chr2:28306298
|
G | A | 107 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(104): Show | 107 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.1088+7807G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28306298 | ||||||
| chr2:28306393
|
T | C | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1088+7902T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28306393 | ||||||
| chr2:28306557
|
A | G | 109 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(106): Show | 109 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(106): Show |
intron_variant | MODIFIER | c.1088+8066A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28306557 | ||||||
| chr2:28306766
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1088+8275G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28306766 | ||||||
| chr2:28306770
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0154 | 2 | HG00741.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1088+8279C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28306770 | ||||||
| chr2:28306843
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1088+8352C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28306843 | ||||||
| chr2:28306950
|
C | A | 2 | a0001c0001t0001g0088a0001c0001t0001g0092 | 2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1088+8459C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28306950 | ||||||
| chr2:28306994
|
C | CG | 2 | a0001c0001t0001g0143a0001c0001t0001g0154 | 2 | HG00741.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1088+8503_1088+850 others(5): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28306994 | ||||||
| chr2:28306995
|
C | CT | 43 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(40): Show | 43 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.1088+8533dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28306995 | |||||
| chr2:28306995
|
C | CTT | 11 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0031others(8): Show | 11 | HG00741.hp1 HG01891.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.1088+8532_1088+853 others(6): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28306995 | |||||
| chr2:28306995
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0154 | 2 | HG00741.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1088+8504C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28306995 | ||||||
| chr2:28306995
|
CT | C | 42 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(39): Show | 42 | HG00140.hp2 HG00733.hp1 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.1088+8533delT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28306995 | |||||
| chr2:28307056
|
G | A | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1088+8565G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28307056 | ||||||
| chr2:28307058
|
G | A | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1088+8567G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28307058 | ||||||
| chr2:28307099
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | HG02280.hp1 HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1088+8608C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28307099 | ||||||
| chr2:28307503
|
A | G | 3 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0126 | 3 | HG01346.hp1 HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1088+9012A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28307503 | ||||||
| chr2:28307524
|
T | C | 1 | a0001c0001t0001g0031 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1088+9033T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28307524 | ||||||
| chr2:28307666
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1088+9175C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28307666 | ||||||
| chr2:28307852
|
C | T | 9 | a0001c0001t0002g0001a0001c0001t0003g0018a0001c0001t0003g0019others(6): Show | 9 | HG00733.hp2 HG01167.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1088+9361C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28307852 | ||||||
| chr2:28307853
|
A | G | 110 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(107): Show | 110 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(107): Show |
intron_variant | MODIFIER | c.1088+9362A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28307853 | ||||||
| chr2:28308058
|
G | T | 3 | a0001c0001t0002g0107a0001c0001t0002g0130a0001c0001t0002g0131 | 3 | HG02280.hp2 HG02451.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1088+9567G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28308058 | ||||||
| chr2:28308821
|
C | A | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1088+10330C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28308821 | ||||||
| chr2:28309036
|
A | G | 80 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(77): Show | 80 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.1088+10545A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28309036 | ||||||
| chr2:28309442
|
A | G | 114 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(111): Show | 114 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(111): Show |
intron_variant | MODIFIER | c.1088+10951A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28309442 | ||||||
| chr2:28309524
|
T | A | 1 | a0001c0001t0003g0067 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1088+11033T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28309524 | ||||||
| chr2:28309887
|
A | G | 25 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(22): Show | 25 | HG00639.hp1 HG00741.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.1088+11396A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28309887 | ||||||
| chr2:28309921
|
G | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0083 | 2 | HG00735.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1088+11430G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28309921 | ||||||
| chr2:28309924
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1088+11433C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28309924 | ||||||
| chr2:28310415
|
C | A | 2 | a0001c0001t0001g0088a0001c0001t0001g0092 | 2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1088+11924C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28310415 | ||||||
| chr2:28310516
|
G | C | 2 | a0001c0001t0002g0108a0001c0001t0002g0132 | 2 | HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1088+12025G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28310516 | ||||||
| chr2:28310794
|
G | A | 2 | a0001c0001t0002g0130a0001c0001t0002g0131 | 2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1088+12303G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28310794 | ||||||
| chr2:28310879
|
G | A | 2 | a0001c0001t0001g0143a0001c0001t0001g0154 | 2 | HG00741.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1088+12388G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28310879 | ||||||
| chr2:28310990
|
G | A | 65 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(62): Show | 65 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.1088+12499G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28310990 | ||||||
| chr2:28311077
|
T | A | 1 | a0001c0001t0002g0039 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1088+12586T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28311077 | ||||||
| chr2:28311115
|
G | T | 2 | a0001c0001t0001g0088a0001c0001t0001g0092 | 2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1088+12624G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28311115 | ||||||
| chr2:28311137
|
T | G | 1 | a0001c0001t0002g0050 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1088+12646T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28311137 | ||||||
| chr2:28311177
|
C | T | 1 | a0001c0001t0002g0016 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1088+12686C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28311177 | ||||||
| chr2:28311216
|
G | A | 5 | a0001c0001t0002g0004a0001c0001t0002g0036a0001c0001t0002g0037others(2): Show | 5 | HG00738.hp1 HG02145.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1088+12725G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28311216 | ||||||
| chr2:28311260
|
CA | C | 98 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(95): Show | 98 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.1088+12788delA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28311260 | |||||
| chr2:28311593
|
G | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1088+13102G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28311593 | ||||||
| chr2:28311779
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1088+13288T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28311779 | ||||||
| chr2:28311806
|
G | A | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1088+13315G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28311806 | ||||||
| chr2:28311865
|
T | G | 77 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(74): Show | 77 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.1088+13374T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28311865 | ||||||
| chr2:28311919
|
G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02630.hp1 HG02723.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1088+13428G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28311919 | ||||||
| chr2:28312077
|
A | T | 1 | a0001c0001t0002g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1088+13586A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28312077 | ||||||
| chr2:28312194
|
A | G | 77 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(74): Show | 77 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.1088+13703A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28312194 | ||||||
| chr2:28312835
|
A | G | 2 | a0001c0001t0001g0065a0001c0001t0001g0083 | 2 | HG00735.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1088+14344A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28312835 | ||||||
| chr2:28312936
|
C | A | 1 | a0001c0001t0002g0158 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1088+14445C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28312936 | ||||||
| chr2:28313203
|
TCTAAAAA others(3): Show |
T | 2 | a0001c0001t0001g0088a0001c0001t0001g0092 | 2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1088+14713_1088+14 others(16): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28313203 | ||||||
| chr2:28313216
|
T | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0092 | 2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1088+14725T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28313216 | ||||||
| chr2:28313217
|
A | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0092 | 2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1088+14726A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28313217 | ||||||
| chr2:28313218
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0001g0092 | 2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1088+14727C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28313218 | ||||||
| chr2:28313265
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1088+14774G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28313265 | ||||||
| chr2:28313597
|
G | A | 22 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(19): Show | 22 | HG00639.hp1 HG00741.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.1088+15106G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28313597 | ||||||
| chr2:28313665
|
A | C | 1 | a0001c0001t0002g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1088+15174A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28313665 | ||||||
| chr2:28313683
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1088+15192T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28313683 | ||||||
| chr2:28313886
|
G | A | 5 | a0001c0001t0001g0142a0001c0001t0002g0116a0001c0001t0002g0144others(2): Show | 5 | HG02074.hp1 HG03041.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1088+15395G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28313886 | ||||||
| chr2:28313899
|
A | G | 2 | a0001c0001t0002g0122a0001c0001t0003g0121 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1088+15408A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28313899 | ||||||
| chr2:28314920
|
G | A | 1 | a0001c0001t0002g0009 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1088+16429G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28314920 | ||||||
| chr2:28315023
|
GGAGA | G | 123 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(120): Show | 123 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(120): Show |
intron_variant | MODIFIER | c.1088+16541_1088+16 others(10): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28315023 | |||||
| chr2:28315030
|
GAGAGAAG others(1): Show |
G | 2 | a0001c0001t0001g0088a0001c0001t0001g0092 | 2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1088+16541_1088+16 others(14): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28315030 | |||||
| chr2:28315072
|
GAGGGAAG others(40): Show |
G | 2 | a0001c0001t0002g0001a0001c0001t0003g0148 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1088+16590_1088+16 others(53): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28315072 | |||||
| chr2:28315130
|
GAGA | G | 16 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0040others(13): Show | 16 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1088+16642_1088+16 others(9): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28315130 | |||||
| chr2:28315232
|
T | TTTTG | 5 | a0001c0001t0002g0010a0001c0001t0002g0016a0001c0001t0002g0112others(2): Show | 5 | HG02572.hp2 HG02647.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1088+16765_1088+16 others(10): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28315232 | |||||
| chr2:28315420
|
TTTTTTC | T | 5 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0002g0026others(2): Show | 5 | HG00639.hp1 HG01109.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1088+16934_1088+16 others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28315420 | |||||
| chr2:28315420
|
TTTTTTCT others(4): Show |
T | 1 | a0001c0001t0002g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1088+16934_1088+16 others(17): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28315420 | |||||
| chr2:28315421
|
T | TTTTC | 6 | a0001c0001t0001g0027a0001c0001t0001g0052a0001c0001t0001g0080others(3): Show | 6 | HG01099.hp2 HG02040.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1088+16933_1088+16 others(10): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28315421 | |||||
| chr2:28315421
|
T | TTTTTC | 11 | a0001c0001t0001g0022a0001c0001t0001g0043a0001c0001t0001g0044others(8): Show | 11 | HG00741.hp1 HG01081.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.1088+16991_1088+16 others(11): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28315421 | |||||
| chr2:28315421
|
T | TTTTTCTT others(3): Show |
18 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0041others(15): Show | 18 | HG00735.hp1 HG00738.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1088+16986_1088+16 others(16): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28315421 | |||||
| chr2:28315421
|
T | TTTTTCTT others(8): Show |
4 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0001g0111others(1): Show | 4 | HG02970.hp2 HG03688.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.1088+16981_1088+16 others(21): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28315421 | |||||
| chr2:28315421
|
TTTTTC | T | 10 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0045others(7): Show | 10 | HG02155.hp1 HG02165.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.1088+16991_1088+16 others(11): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28315421 | |||||
| chr2:28315421
|
TTTTTCTT others(3): Show |
T | 14 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0035others(11): Show | 14 | HG01168.hp2 HG01346.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.1088+16986_1088+16 others(16): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28315421 | |||||
| chr2:28315421
|
TTTTTCTT others(8): Show |
T | 23 | a0001c0001t0001g0059a0001c0001t0001g0072a0001c0001t0001g0075others(20): Show | 23 | HG00733.hp2 HG00735.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.1088+16981_1088+16 others(21): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28315421 | |||||
| chr2:28315421
|
TTTTTCTT others(13): Show |
T | 40 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0040others(37): Show | 40 | HG00639.hp2 HG01069.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.1088+16976_1088+16 others(26): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28315421 | |||||
| chr2:28315421
|
TTTTTCTT others(18): Show |
T | 8 | a0001c0001t0001g0053a0001c0001t0001g0082a0001c0001t0001g0109others(5): Show | 8 | HG00140.hp2 HG00733.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1088+16971_1088+16 others(31): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28315421 | |||||
| chr2:28315421
|
TTTTTCTT others(23): Show |
T | 1 | a0001c0001t0001g0079 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1088+16966_1088+16 others(36): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28315421 | |||||
| chr2:28315446
|
CTTTTCTT others(10): Show |
C | 2 | a0001c0001t0001g0005a0001c0001t0001g0138 | 2 | HG01891.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1088+16958_1088+16 others(23): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28315446 | |||||
| chr2:28315569
|
G | C | 1 | a0001c0001t0001g0133 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1088+17078G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28315569 | ||||||
| chr2:28315609
|
A | G | 1 | a0001c0001t0002g0141 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1088+17118A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28315609 | ||||||
| chr2:28315657
|
A | T | 6 | a0001c0001t0001g0027a0001c0001t0001g0080a0001c0001t0001g0157others(3): Show | 6 | HG01099.hp2 HG02040.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1088+17166A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28315657 | ||||||
| chr2:28315661
|
T | A | 9 | a0001c0001t0002g0001a0001c0001t0003g0018a0001c0001t0003g0019others(6): Show | 9 | HG00733.hp2 HG01167.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1088+17170T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28315661 | ||||||
| chr2:28315664
|
A | AT | 15 | a0001c0001t0001g0088a0001c0001t0001g0092a0001c0001t0002g0001others(12): Show | 15 | HG00733.hp2 HG01167.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.1088+17184dupT | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28315664 | |||||
| chr2:28315824
|
G | T | 6 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0036others(3): Show | 6 | HG00738.hp1 HG01109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1088+17333G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28315824 | ||||||
| chr2:28316219
|
C | G | 1 | a0001c0001t0002g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1088+17728C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28316219 | ||||||
| chr2:28316396
|
A | ATGGGGG | 8 | a0001c0001t0002g0021a0001c0001t0002g0047a0001c0001t0002g0048others(5): Show | 8 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.1088+17910_1088+17 others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28316396 | |||||
| chr2:28316407
|
A | G | 1 | a0001c0001t0002g0029 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1088+17916A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28316407 | ||||||
| chr2:28316407
|
AGTGGGG | A | 28 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0091others(25): Show | 28 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1088+17946_1088+17 others(12): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28316407 | |||||
| chr2:28316413
|
G | A | 1 | a0001c0001t0002g0029 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1088+17922G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28316413 | ||||||
| chr2:28316445
|
T | G | 5 | a0001c0001t0002g0004a0001c0001t0002g0036a0001c0001t0002g0037others(2): Show | 5 | HG00738.hp1 HG02145.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1088+17954T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28316445 | ||||||
| chr2:28316520
|
C | T | 1 | a0001c0001t0002g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1088+18029C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28316520 | ||||||
| chr2:28316524
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1088+18033T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28316524 | ||||||
| chr2:28316652
|
G | A | 14 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(11): Show | 14 | HG01168.hp2 HG01433.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1088+18161G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28316652 | ||||||
| chr2:28316743
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1088+18252G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28316743 | ||||||
| chr2:28317010
|
C | T | 81 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0022others(78): Show | 81 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.1088+18519C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28317010 | ||||||
| chr2:28317079
|
G | A | 37 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(34): Show | 37 | HG00639.hp2 HG00733.hp2 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.1088+18588G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28317079 | ||||||
| chr2:28317176
|
C | T | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1088+18685C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28317176 | ||||||
| chr2:28317260
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1088+18769A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28317260 | ||||||
| chr2:28317277
|
C | T | 35 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(32): Show | 35 | HG01069.hp1 HG01106.hp1 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.1088+18786C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28317277 | ||||||
| chr2:28317353
|
A | AATAGC | 3 | a0001c0001t0001g0022a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | HG02280.hp1 HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1088+18864_1088+18 others(11): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28317353 | |||||
| chr2:28317420
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1088+18929C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28317420 | ||||||
| chr2:28317708
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1088+19217G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28317708 | ||||||
| chr2:28318122
|
C | T | 2 | a0001c0001t0002g0003a0001c0001t0002g0126 | 2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1088+19631C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28318122 | ||||||
| chr2:28318268
|
A | G | 28 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0034others(25): Show | 28 | HG00140.hp1 HG00741.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1088+19777A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28318268 | ||||||
| chr2:28318268
|
AAAC | A | 12 | a0001c0001t0001g0025a0001c0001t0002g0021a0001c0001t0002g0029others(9): Show | 12 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.1088+19782_1088+19 others(9): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28318268 | |||||
| chr2:28318448
|
G | T | 1 | a0001c0001t0001g0123 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1088+19957G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28318448 | ||||||
| chr2:28318863
|
G | A | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1089-19587G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28318863 | ||||||
| chr2:28319299
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1089-19151G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28319299 | ||||||
| chr2:28319406
|
C | T | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1089-19044C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28319406 | ||||||
| chr2:28319478
|
T | C | 74 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(71): Show | 74 | HG00639.hp1 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.1089-18972T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28319478 | ||||||
| chr2:28319577
|
C | A | 6 | a0001c0001t0003g0089a0001c0001t0003g0090a0001c0001t0003g0121others(3): Show | 6 | HG00733.hp2 HG01167.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1089-18873C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28319577 | ||||||
| chr2:28319649
|
G | A | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1089-18801G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28319649 | ||||||
| chr2:28319891
|
G | A | 5 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0049others(2): Show | 5 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.1089-18559G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28319891 | ||||||
| chr2:28319959
|
TCCA | T | 6 | a0001c0001t0003g0089a0001c0001t0003g0090a0001c0001t0003g0121others(3): Show | 6 | HG00733.hp2 HG01167.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1089-18488_1089-18 others(9): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28319959 | |||||
| chr2:28320014
|
CTG | C | 3 | a0001c0001t0001g0025a0001c0001t0002g0114a0001c0001t0002g0141 | 3 | HG02559.hp1 HG02735.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1089-18433_1089-18 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28320014 | |||||
| chr2:28320067
|
A | G | 39 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(36): Show | 39 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.1089-18383A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28320067 | ||||||
| chr2:28320526
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1089-17924A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28320526 | ||||||
| chr2:28320588
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02922.hp2 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1089-17862G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28320588 | ||||||
| chr2:28320596
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1089-17854C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28320596 | ||||||
| chr2:28320598
|
C | G | 3 | a0001c0001t0002g0012a0001c0001t0003g0067a0001c0001t0003g0106 | 3 | HG02698.hp1 HG03041.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1089-17852C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28320598 | ||||||
| chr2:28320780
|
C | T | 25 | a0001c0001t0001g0109a0001c0001t0001g0139a0001c0001t0002g0004others(22): Show | 25 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.1089-17670C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28320780 | ||||||
| chr2:28321006
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1089-17444A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28321006 | ||||||
| chr2:28321143
|
T | G | 4 | a0001c0001t0002g0003a0001c0001t0002g0126a0001c0001t0003g0018others(1): Show | 4 | HG02486.hp1 HG02818.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1089-17307T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28321143 | ||||||
| chr2:28321216
|
G | A | 1 | a0001c0001t0003g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1089-17234G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28321216 | ||||||
| chr2:28321328
|
C | T | 1 | a0001c0001t0005g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1089-17122C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28321328 | ||||||
| chr2:28321508
|
A | T | 1 | a0001c0001t0002g0029 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1089-16942A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28321508 | ||||||
| chr2:28321573
|
G | A | 2 | a0001c0001t0002g0062a0001c0001t0002g0096 | 2 | HG01934.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1089-16877G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28321573 | ||||||
| chr2:28321584
|
G | A | 1 | a0001c0001t0002g0144 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1089-16866G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28321584 | ||||||
| chr2:28321712
|
G | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1089-16738G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28321712 | ||||||
| chr2:28321728
|
C | T | 6 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0107others(3): Show | 6 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1089-16722C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28321728 | ||||||
| chr2:28321779
|
CTT | C | 6 | a0001c0001t0003g0089a0001c0001t0003g0090a0001c0001t0003g0121others(3): Show | 6 | HG00733.hp2 HG01167.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1089-16670_1089-16 others(8): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28321779 | ||||||
| chr2:28321942
|
T | TA | 5 | a0001c0001t0002g0003a0001c0001t0002g0108a0001c0001t0002g0126others(2): Show | 5 | HG02486.hp1 HG02818.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1089-16494dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28321942 | |||||
| chr2:28322242
|
G | T | 62 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(59): Show | 62 | HG00639.hp1 HG00733.hp2 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.1089-16208G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28322242 | ||||||
| chr2:28322321
|
G | A | 4 | a0001c0001t0001g0025a0001c0001t0002g0114a0001c0001t0002g0122others(1): Show | 4 | HG02559.hp1 HG02647.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1089-16129G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28322321 | ||||||
| chr2:28322542
|
G | A | 2 | a0001c0001t0003g0067a0001c0001t0003g0106 | 2 | HG03041.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1089-15908G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28322542 | ||||||
| chr2:28322668
|
G | A | 1 | a0001c0001t0002g0122 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1089-15782G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28322668 | ||||||
| chr2:28323048
|
G | A | 2 | a0001c0001t0002g0021a0001c0001t0002g0050 | 2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1089-15402G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28323048 | ||||||
| chr2:28323156
|
G | A | 43 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0027others(40): Show | 43 | HG00639.hp1 HG00741.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.1089-15294G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28323156 | ||||||
| chr2:28323364
|
A | AGGCTCTT others(326): Show |
1 | a0001c0001t0001g0115 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1089-15072_1089-15 others(339): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28323364 | |||||
| chr2:28323414
|
T | G | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1089-15036T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28323414 | ||||||
| chr2:28323657
|
T | A | 4 | a0001c0001t0002g0003a0001c0001t0002g0126a0001c0001t0003g0018others(1): Show | 4 | HG02486.hp1 HG02818.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1089-14793T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28323657 | ||||||
| chr2:28323815
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1089-14635C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28323815 | ||||||
| chr2:28324113
|
A | C | 1 | a0001c0001t0003g0121 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1089-14337A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28324113 | ||||||
| chr2:28324273
|
C | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1089-14177C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28324273 | ||||||
| chr2:28324320
|
C | T | 7 | a0001c0001t0002g0003a0001c0001t0002g0012a0001c0001t0002g0126others(4): Show | 7 | HG02486.hp1 HG02698.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1089-14130C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28324320 | ||||||
| chr2:28324612
|
A | G | 7 | a0001c0001t0002g0003a0001c0001t0002g0012a0001c0001t0002g0126others(4): Show | 7 | HG02486.hp1 HG02698.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1089-13838A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28324612 | ||||||
| chr2:28324627
|
C | CA | 23 | a0001c0001t0001g0127a0001c0001t0002g0004a0001c0001t0002g0011others(20): Show | 23 | HG00639.hp2 HG00738.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.1089-13809dupA | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28324627 | |||||
| chr2:28324677
|
C | A | 2 | a0001c0001t0002g0130a0001c0001t0002g0131 | 2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1089-13773C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28324677 | ||||||
| chr2:28325189
|
T | C | 3 | a0001c0001t0002g0012a0001c0001t0003g0067a0001c0001t0003g0106 | 3 | HG02698.hp1 HG03041.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1089-13261T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28325189 | ||||||
| chr2:28325259
|
G | A | 7 | a0001c0001t0002g0003a0001c0001t0002g0012a0001c0001t0002g0126others(4): Show | 7 | HG02486.hp1 HG02698.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1089-13191G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28325259 | ||||||
| chr2:28325288
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1089-13162C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28325288 | ||||||
| chr2:28325392
|
T | C | 7 | a0001c0001t0002g0003a0001c0001t0002g0012a0001c0001t0002g0126others(4): Show | 7 | HG02486.hp1 HG02698.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1089-13058T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28325392 | ||||||
| chr2:28325424
|
T | C | 7 | a0001c0001t0002g0003a0001c0001t0002g0012a0001c0001t0002g0126others(4): Show | 7 | HG02486.hp1 HG02698.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1089-13026T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28325424 | ||||||
| chr2:28325437
|
A | G | 1 | a0001c0001t0003g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1089-13013A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28325437 | ||||||
| chr2:28325496
|
T | A | 4 | a0001c0001t0002g0003a0001c0001t0002g0126a0001c0001t0003g0018others(1): Show | 4 | HG02486.hp1 HG02818.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1089-12954T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28325496 | ||||||
| chr2:28325591
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0139 | 2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1089-12859C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28325591 | ||||||
| chr2:28325642
|
C | T | 4 | a0001c0001t0002g0003a0001c0001t0002g0126a0001c0001t0003g0018others(1): Show | 4 | HG02486.hp1 HG02818.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1089-12808C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28325642 | ||||||
| chr2:28325738
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1089-12712G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28325738 | ||||||
| chr2:28325784
|
A | G | 5 | a0001c0001t0002g0004a0001c0001t0002g0036a0001c0001t0002g0037others(2): Show | 5 | HG00738.hp1 HG02145.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1089-12666A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28325784 | ||||||
| chr2:28325862
|
G | C | 156 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(153): Show |
intron_variant | MODIFIER | c.1089-12588G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28325862 | ||||||
| chr2:28325887
|
A | G | 2 | a0001c0001t0001g0109a0001c0001t0001g0139 | 2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1089-12563A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28325887 | ||||||
| chr2:28326042
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1089-12408C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28326042 | ||||||
| chr2:28326118
|
C | G | 155 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(152): Show | 155 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(152): Show |
intron_variant | MODIFIER | c.1089-12332C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28326118 | ||||||
| chr2:28326284
|
C | A | 1 | a0001c0001t0002g0029 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1089-12166C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28326284 | ||||||
| chr2:28326441
|
T | C | 3 | a0001c0001t0002g0012a0001c0001t0003g0067a0001c0001t0003g0106 | 3 | HG02698.hp1 HG03041.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1089-12009T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28326441 | ||||||
| chr2:28326483
|
C | A | 65 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0017others(62): Show | 65 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.1089-11967C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28326483 | ||||||
| chr2:28326593
|
G | A | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1089-11857G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28326593 | ||||||
| chr2:28326646
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1089-11804C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28326646 | ||||||
| chr2:28326662
|
G | T | 4 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0009others(1): Show | 4 | HG01346.hp1 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1089-11788G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28326662 | ||||||
| chr2:28326732
|
T | C | 4 | a0001c0001t0002g0003a0001c0001t0002g0126a0001c0001t0003g0018others(1): Show | 4 | HG02486.hp1 HG02818.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1089-11718T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28326732 | ||||||
| chr2:28326782
|
C | T | 3 | a0001c0001t0001g0092a0001c0001t0001g0109a0001c0001t0001g0139 | 3 | HG02615.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1089-11668C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28326782 | ||||||
| chr2:28326791
|
A | G | 6 | a0001c0001t0002g0003a0001c0001t0002g0126a0001c0001t0003g0018others(3): Show | 6 | HG02486.hp1 HG02818.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1089-11659A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28326791 | ||||||
| chr2:28326819
|
C | T | 1 | a0001c0001t0002g0051 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089-11631C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28326819 | ||||||
| chr2:28326834
|
C | G | 11 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0002g0007others(8): Show | 11 | HG00639.hp1 HG01109.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1089-11616C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28326834 | ||||||
| chr2:28326890
|
T | C | 89 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0014others(86): Show | 89 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.1089-11560T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28326890 | ||||||
| chr2:28326927
|
TATTA | T | 155 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(152): Show | 155 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(152): Show |
intron_variant | MODIFIER | c.1089-11518_1089-11 others(10): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28326927 | |||||
| chr2:28326948
|
A | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1089-11502A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28326948 | ||||||
| chr2:28327177
|
G | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1089-11273G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28327177 | ||||||
| chr2:28327214
|
C | G | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1089-11236C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28327214 | ||||||
| chr2:28327267
|
G | A | 1 | a0001c0001t0004g0118 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1089-11183G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28327267 | ||||||
| chr2:28327463
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1089-10987T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28327463 | ||||||
| chr2:28327674
|
A | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1089-10776A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28327674 | ||||||
| chr2:28328206
|
G | A | 3 | a0001c0001t0001g0052a0001c0001t0001g0080a0001c0001t0001g0157 | 3 | HG01099.hp2 HG02040.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1089-10244G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28328206 | ||||||
| chr2:28328556
|
A | G | 1 | a0001c0001t0004g0118 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1089-9894A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28328556 | ||||||
| chr2:28328562
|
A | G | 1 | a0001c0001t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1089-9888A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28328562 | ||||||
| chr2:28328567
|
G | T | 24 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(21): Show | 24 | HG00639.hp1 HG01109.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1089-9883G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28328567 | ||||||
| chr2:28328582
|
T | C | 4 | a0001c0001t0002g0028a0001c0001t0002g0095a0001c0001t0002g0100others(1): Show | 4 | HG01106.hp1 HG01192.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.1089-9868T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28328582 | ||||||
| chr2:28328690
|
G | A | 1 | a0001c0001t0003g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1089-9760G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28328690 | ||||||
| chr2:28328735
|
A | C | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1089-9715A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28328735 | ||||||
| chr2:28328961
|
A | G | 3 | a0001c0001t0001g0022a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | HG02280.hp1 HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1089-9489A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28328961 | ||||||
| chr2:28328974
|
G | T | 1 | a0001c0001t0001g0091 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1089-9476G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28328974 | ||||||
| chr2:28328996
|
T | C | 4 | a0001c0001t0002g0003a0001c0001t0002g0126a0001c0001t0003g0018others(1): Show | 4 | HG02486.hp1 HG02818.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1089-9454T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28328996 | ||||||
| chr2:28329120
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1089-9330C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28329120 | ||||||
| chr2:28329243
|
C | T | 1 | a0001c0001t0002g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1089-9207C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28329243 | ||||||
| chr2:28329903
|
T | C | 156 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(153): Show |
intron_variant | MODIFIER | c.1089-8547T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28329903 | ||||||
| chr2:28329907
|
G | C | 1 | a0001c0001t0002g0116 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1089-8543G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28329907 | ||||||
| chr2:28330231
|
G | A | 38 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0133others(35): Show | 38 | HG01069.hp1 HG01106.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.1089-8219G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28330231 | ||||||
| chr2:28330310
|
A | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1089-8140A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28330310 | ||||||
| chr2:28330518
|
G | A | 85 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0015others(82): Show | 85 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.1089-7932G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28330518 | ||||||
| chr2:28330711
|
A | G | 1 | a0001c0001t0002g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1089-7739A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28330711 | ||||||
| chr2:28330722
|
A | T | 1 | a0001c0001t0001g0146 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1089-7728A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28330722 | ||||||
| chr2:28330758
|
C | T | 1 | a0001c0001t0002g0062 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1089-7692C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28330758 | ||||||
| chr2:28330826
|
A | T | 88 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0015others(85): Show | 88 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.1089-7624A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28330826 | ||||||
| chr2:28330869
|
G | A | 85 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0015others(82): Show | 85 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.1089-7581G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28330869 | ||||||
| chr2:28330993
|
G | C | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1089-7457G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28330993 | ||||||
| chr2:28331081
|
C | T | 5 | a0001c0001t0002g0004a0001c0001t0002g0036a0001c0001t0002g0037others(2): Show | 5 | HG00738.hp1 HG02145.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1089-7369C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28331081 | ||||||
| chr2:28331142
|
G | C | 156 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(153): Show |
intron_variant | MODIFIER | c.1089-7308G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28331142 | ||||||
| chr2:28331144
|
C | T | 17 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(14): Show | 17 | HG00639.hp1 HG01109.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1089-7306C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28331144 | ||||||
| chr2:28331283
|
G | A | 1 | a0001c0001t0004g0118 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1089-7167G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28331283 | ||||||
| chr2:28331292
|
A | T | 1 | a0001c0001t0001g0071 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1089-7158A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28331292 | ||||||
| chr2:28331335
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1089-7115T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28331335 | ||||||
| chr2:28331557
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1089-6893T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28331557 | ||||||
| chr2:28331865
|
C | T | 9 | a0001c0001t0001g0027a0001c0001t0002g0011a0001c0001t0002g0020others(6): Show | 9 | HG00639.hp1 HG01109.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1089-6585C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28331865 | ||||||
| chr2:28331955
|
G | A | 1 | a0001c0001t0002g0122 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1089-6495G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28331955 | ||||||
| chr2:28332031
|
A | G | 4 | a0001c0001t0002g0003a0001c0001t0002g0126a0001c0001t0003g0018others(1): Show | 4 | HG02486.hp1 HG02818.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1089-6419A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28332031 | ||||||
| chr2:28332114
|
G | T | 63 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0054others(60): Show | 63 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.1089-6336G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28332114 | ||||||
| chr2:28332282
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1089-6168C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28332282 | ||||||
| chr2:28332307
|
A | C | 1 | a0001c0001t0002g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1089-6143A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28332307 | ||||||
| chr2:28332436
|
A | G | 25 | a0001c0001t0001g0027a0001c0001t0001g0092a0001c0001t0001g0109others(22): Show | 25 | HG00639.hp1 HG00741.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1089-6014A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28332436 | ||||||
| chr2:28332627
|
C | G | 4 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0009others(1): Show | 4 | HG01346.hp1 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1089-5823C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28332627 | ||||||
| chr2:28332650
|
G | A | 2 | a0001c0001t0001g0120a0001c0001t0001g0127 | 2 | HG02040.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1089-5800G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28332650 | ||||||
| chr2:28332700
|
C | T | 33 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0016others(30): Show | 33 | HG01069.hp1 HG01106.hp1 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.1089-5750C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28332700 | ||||||
| chr2:28332736
|
C | A | 1 | a0001c0001t0001g0097 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1089-5714C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28332736 | ||||||
| chr2:28332973
|
C | G | 1 | a0001c0001t0001g0058 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1089-5477C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28332973 | ||||||
| chr2:28333042
|
C | T | 12 | a0001c0001t0001g0027a0001c0001t0002g0007a0001c0001t0002g0011others(9): Show | 12 | HG00639.hp1 HG01109.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1089-5408C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28333042 | ||||||
| chr2:28333242
|
T | C | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1089-5208T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28333242 | ||||||
| chr2:28333409
|
G | A | 128 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(125): Show | 128 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(125): Show |
intron_variant | MODIFIER | c.1089-5041G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28333409 | ||||||
| chr2:28333542
|
A | C | 5 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0009others(2): Show | 5 | HG01346.hp1 HG01891.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1089-4908A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28333542 | ||||||
| chr2:28333730
|
A | G | 1 | a0001c0001t0002g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1089-4720A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28333730 | ||||||
| chr2:28333823
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1089-4627C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28333823 | ||||||
| chr2:28333931
|
T | G | 8 | a0001c0001t0002g0021a0001c0001t0002g0029a0001c0001t0002g0047others(5): Show | 8 | HG00639.hp2 HG01106.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.1089-4519T>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28333931 | ||||||
| chr2:28334023
|
A | C | 135 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(132): Show | 135 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(132): Show |
intron_variant | MODIFIER | c.1089-4427A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28334023 | ||||||
| chr2:28334213
|
C | T | 125 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0017others(122): Show | 125 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(122): Show |
intron_variant | MODIFIER | c.1089-4237C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28334213 | ||||||
| chr2:28334295
|
C | A | 1 | a0001c0001t0002g0047 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1089-4155C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28334295 | ||||||
| chr2:28334389
|
C | A | 1 | a0001c0001t0002g0141 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1089-4061C>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28334389 | ||||||
| chr2:28334550
|
G | T | 1 | a0001c0001t0002g0046 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1089-3900G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28334550 | ||||||
| chr2:28334730
|
C | G | 1 | a0001c0001t0002g0144 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1089-3720C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28334730 | ||||||
| chr2:28334782
|
C | G | 15 | a0001c0001t0002g0004a0001c0001t0002g0021a0001c0001t0002g0029others(12): Show | 15 | HG00639.hp2 HG00738.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.1089-3668C>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28334782 | ||||||
| chr2:28335102
|
T | A | 1 | a0001c0001t0002g0145 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1089-3348T>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28335102 | ||||||
| chr2:28335123
|
C | T | 23 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0027others(20): Show | 23 | HG00639.hp1 HG01109.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1089-3327C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28335123 | ||||||
| chr2:28335129
|
C | T | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1089-3321C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28335129 | ||||||
| chr2:28335133
|
A | G | 155 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(152): Show | 155 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(152): Show |
intron_variant | MODIFIER | c.1089-3317A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28335133 | ||||||
| chr2:28335154
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0002g0051 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1089-3278_1089-326 others(14): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28335154 | |||||
| chr2:28335154
|
C | CTTTTTTT others(4): Show |
4 | a0001c0001t0001g0027a0001c0001t0002g0026a0001c0001t0002g0046others(1): Show | 4 | HG00639.hp1 HG01109.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1089-3279_1089-326 others(15): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28335154 | |||||
| chr2:28335154
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0002g0007 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1089-3280_1089-326 others(16): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28335154 | |||||
| chr2:28335154
|
CTTTTT | C | 53 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0040others(50): Show | 53 | HG00140.hp1 HG00140.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.1089-3273_1089-326 others(9): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28335154 | |||||
| chr2:28335154
|
CTTTTTT | C | 78 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(75): Show | 78 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.1089-3274_1089-326 others(10): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 28335154 | |||||
| chr2:28335263
|
G | T | 2 | a0001c0001t0003g0067a0001c0001t0003g0106 | 2 | HG03041.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1089-3187G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28335263 | ||||||
| chr2:28335624
|
G | A | 4 | a0001c0001t0002g0003a0001c0001t0002g0126a0001c0001t0003g0018others(1): Show | 4 | HG02486.hp1 HG02818.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1089-2826G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28335624 | ||||||
| chr2:28335668
|
T | C | 1 | a0001c0001t0002g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1089-2782T>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28335668 | ||||||
| chr2:28335698
|
G | A | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1089-2752G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28335698 | ||||||
| chr2:28335758
|
A | C | 4 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0009others(1): Show | 4 | HG01346.hp1 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1089-2692A>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28335758 | ||||||
| chr2:28336105
|
C | T | 1 | a0001c0001t0001g0035 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1089-2345C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28336105 | ||||||
| chr2:28336441
|
G | T | 4 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0009others(1): Show | 4 | HG01346.hp1 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1089-2009G>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28336441 | ||||||
| chr2:28336443
|
G | A | 4 | a0001c0001t0002g0001a0001c0001t0002g0107a0001c0001t0002g0130others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1089-2007G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28336443 | ||||||
| chr2:28336525
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1089-1925G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28336525 | ||||||
| chr2:28336618
|
A | T | 5 | a0001c0001t0002g0004a0001c0001t0002g0036a0001c0001t0002g0037others(2): Show | 5 | HG00738.hp1 HG02145.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1089-1832A>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28336618 | ||||||
| chr2:28336623
|
G | C | 1 | a0001c0001t0003g0121 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1089-1827G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28336623 | ||||||
| chr2:28336647
|
G | A | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1089-1803G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28336647 | ||||||
| chr2:28336653
|
G | C | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1089-1797G>C | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28336653 | ||||||
| chr2:28336818
|
G | A | 2 | a0001c0001t0003g0067a0001c0001t0003g0106 | 2 | HG03041.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1089-1632G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28336818 | ||||||
| chr2:28336850
|
C | T | 60 | a0001c0001t0001g0013a0001c0001t0001g0092a0001c0001t0001g0109others(57): Show | 60 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.1089-1600C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28336850 | ||||||
| chr2:28336851
|
G | A | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1089-1599G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28336851 | ||||||
| chr2:28336861
|
C | T | 128 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(125): Show | 128 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(125): Show |
intron_variant | MODIFIER | c.1089-1589C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28336861 | ||||||
| chr2:28337167
|
G | A | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1089-1283G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28337167 | ||||||
| chr2:28337236
|
C | T | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1089-1214C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28337236 | ||||||
| chr2:28337343
|
G | A | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1089-1107G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28337343 | ||||||
| chr2:28337483
|
G | A | 1 | a0001c0001t0002g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1089-967G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28337483 | ||||||
| chr2:28337560
|
C | T | 132 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0014others(129): Show | 132 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(129): Show |
intron_variant | MODIFIER | c.1089-890C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28337560 | ||||||
| chr2:28337568
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1089-882C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28337568 | ||||||
| chr2:28337733
|
C | T | 124 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0017others(121): Show | 124 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(121): Show |
intron_variant | MODIFIER | c.1089-717C>T | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28337733 | ||||||
| chr2:28337790
|
G | A | 6 | a0001c0001t0002g0010a0001c0001t0002g0016a0001c0001t0002g0061others(3): Show | 6 | HG01496.hp1 HG02818.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1089-660G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28337790 | ||||||
| chr2:28337820
|
G | A | 151 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(148): Show | 151 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(148): Show |
intron_variant | MODIFIER | c.1089-630G>A | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28337820 | ||||||
| chr2:28338191
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1089-259A>G | BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | chr2 | 28338191 |