| geneid | 8853 |
|---|---|
| ensemblid | ENSG00000151693.11 |
| hgncid | 2721 |
| symbol | ASAP2 |
| name | ArfGAP with SH3 domain, ankyrin repeat and PH domain 2 |
| refseq_nuc | NM_003887.3 |
| refseq_prot | NP_003878.1 |
| ensembl_nuc | ENST00000281419.8 |
| ensembl_prot | ENSP00000281419.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 9206812 |
| end | 9405678 |
| strand | + |
| ver | v1.2 |
| region | chr2:9206812-9405678 |
| region5000 | chr2:9201812-9410678 |
| regionname0 | ASAP2_chr2_9206812_9405678 |
| regionname5000 | ASAP2_chr2_9201812_9410678 |
| 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 | 0/0 | 1006 | 127 | 70 | 28 | 14 | 6 | 9 | 5 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0002 | 0/0 | 1006 | 81 | 10 | 24 | 29 | 2 | 16 | 15 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0003 | 0/0 | 1006 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0004 | 0/0 | 1006 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| 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 | 0/0 | 3021 | 67 | 8 | 18 | 27 | 2 | 12 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| c0002 | 0/0 | 3021 | 59 | 20 | 20 | 5 | 6 | 8 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| c0003 | 0/0 | 3021 | 32 | 21 | 1 | 9 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| c0004 | 0/0 | 3021 | 18 | 15 | 3 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| c0005 | 0/0 | 3021 | 12 | 2 | 6 | 0 | 0 | 4 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| c0006 | 0/0 | 3021 | 7 | 6 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| c0007 | 0/0 | 3021 | 6 | 4 | 2 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| c0008 | 0/0 | 3021 | 2 | 0 | 0 | 2 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| c0009 | 0/0 | 3021 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| c0010 | 0/0 | 3021 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| c0011 | 0/0 | 3021 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| c0012 | 0/0 | 3021 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| c0013 | 0/0 | 3021 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| c0014 | 0/0 | 3021 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| c0015 | 0/0 | 3021 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| 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 | 0/0 | 2645 | 95 | 24 | 31 | 23 | 2 | 15 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| t0002 | 0/0 | 2645 | 22 | 3 | 9 | 2 | 4 | 4 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| t0003 | 0/0 | 2644 | 22 | 8 | 5 | 3 | 2 | 4 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| t0004 | 0/0 | 2643 | 20 | 18 | 2 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| t0005 | 0/0 | 2644 | 18 | 15 | 3 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| t0006 | 0/0 | 2645 | 12 | 0 | 1 | 9 | 0 | 2 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| t0007 | 0/0 | 2644 | 2 | 2 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| t0008 | 0/0 | 2645 | 2 | 2 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| t0009 | 0/0 | 2643 | 2 | 2 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| t0010 | 0/0 | 2645 | 2 | 0 | 0 | 2 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| t0011 | 0/0 | 2645 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| t0012 | 0/0 | 2645 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| t0013 | 0/0 | 2645 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| t0014 | 0/0 | 2645 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| t0015 | 0/0 | 2645 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| t0016 | 0/0 | 2644 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| t0017 | 0/0 | 2645 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| t0018 | 0/0 | 2645 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| t0019 | 0/0 | 2645 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| t0020 | 0/0 | 2645 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| t0021 | 0/0 | 2645 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| t0022 | 0/0 | 2645 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| t0023 | 0/0 | 2645 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| 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 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 3021 | 59 | 20 | 20 | 5 | 6 | 8 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0003 | 0/0 | 3021 | 32 | 21 | 1 | 9 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0004 | 0/0 | 3021 | 18 | 15 | 3 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0006 | 0/0 | 3021 | 7 | 6 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0007 | 0/0 | 3021 | 6 | 4 | 2 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0009 | 0/0 | 3021 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0010 | 0/0 | 3021 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0011 | 0/0 | 3021 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0012 | 0/0 | 3021 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0013 | 0/0 | 3021 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0002c0001 | 0/0 | 3021 | 67 | 8 | 18 | 27 | 2 | 12 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0002c0005 | 0/0 | 3021 | 12 | 2 | 6 | 0 | 0 | 4 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0002c0008 | 0/0 | 3021 | 2 | 0 | 0 | 2 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0003c0014 | 0/0 | 3021 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0004c0015 | 0/0 | 3021 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/0 | 5665 | 8 | 4 | 4 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0002t0002 | 0/0 | 5665 | 22 | 3 | 9 | 2 | 4 | 4 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0002t0003 | 0/0 | 5664 | 18 | 7 | 5 | 1 | 2 | 3 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0002t0006 | 0/0 | 5665 | 2 | 0 | 1 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0002t0008 | 0/0 | 5665 | 2 | 2 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0002t0009 | 0/0 | 5663 | 2 | 2 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0002t0012 | 0/0 | 5665 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0002t0013 | 0/0 | 5665 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0002t0019 | 0/0 | 5665 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0002t0022 | 0/0 | 5665 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0002t0023 | 0/0 | 5665 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0003t0001 | 0/0 | 5665 | 11 | 10 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0003t0004 | 0/0 | 5663 | 7 | 7 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0003t0006 | 0/0 | 5665 | 9 | 0 | 0 | 8 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0003t0007 | 0/0 | 5664 | 2 | 2 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0003t0011 | 0/0 | 5665 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0003t0016 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0003t0021 | 0/0 | 5665 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0004t0005 | 0/0 | 5664 | 18 | 15 | 3 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0006t0004 | 0/0 | 5663 | 7 | 6 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0007t0001 | 0/0 | 5665 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0007t0004 | 0/0 | 5663 | 5 | 4 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0009t0004 | 0/0 | 5663 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0010t0018 | 0/0 | 5665 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0011t0001 | 0/0 | 5665 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0012t0003 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0001c0013t0017 | 0/0 | 5665 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0002c0001t0001 | 0/0 | 5665 | 61 | 8 | 18 | 22 | 2 | 11 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0002c0001t0003 | 0/0 | 5664 | 2 | 0 | 0 | 1 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0002c0001t0010 | 0/0 | 5665 | 2 | 0 | 0 | 2 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0002c0001t0014 | 0/0 | 5665 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0002c0001t0020 | 0/0 | 5665 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0002c0005t0001 | 0/0 | 5665 | 12 | 2 | 6 | 0 | 0 | 4 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0002c0008t0001 | 0/0 | 5665 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0002c0008t0006 | 0/0 | 5665 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0003c0014t0003 | 0/0 | 5664 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| a0004c0015t0015 | 0/0 | 5665 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | copy fasta | chr2 | 9201812 | 9410678 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0006g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0006g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0008g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0008g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0009g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0009g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0012g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0013g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0019g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0022g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0002t0023g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0006g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0006g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0006g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0006g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0006g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0006g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0006g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0006g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0007g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0007g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0011g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0016g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0003t0021g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0004t0005g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0004t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0004t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0004t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0004t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0004t0005g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0004t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0004t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0004t0005g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0004t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0004t0005g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0004t0005g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0004t0005g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0004t0005g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0004t0005g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0004t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0004t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0004t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0006t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0006t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0006t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0006t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0006t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0006t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0006t0004g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0007t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0007t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0007t0004g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0007t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0007t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0007t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0009t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0010t0018g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0011t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0012t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0001c0013t0017g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0010g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0010g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0014g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0001t0020g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0005t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0005t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0005t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0005t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0005t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0005t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0005t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0005t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0005t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0005t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0005t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0005t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0008t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0002c0008t0006g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0003c0014t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| a0004c0015t0015g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0096 | EUR | FIN | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0075 | EUR | FIN | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG00323 | hp1 | a0002 | c0001 | t0001 | g0207 | EUR | FIN | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG00323 | hp2 | a0001 | c0002 | t0003 | g0152 | EUR | FIN | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG00408 | hp1 | a0002 | c0001 | t0001 | g0067 | EAS | CHS | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG00408 | hp2 | a0001 | c0003 | t0006 | g0102 | EAS | CHS | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG00438 | hp1 | a0001 | c0003 | t0006 | g0065 | EAS | CHS | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG00438 | hp2 | a0002 | c0001 | t0001 | g0085 | EAS | CHS | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG00597 | hp1 | a0002 | c0001 | t0001 | g0160 | EAS | CHS | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG00597 | hp2 | a0001 | c0003 | t0006 | g0158 | EAS | CHS | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG00609 | hp1 | a0001 | c0003 | t0006 | g0135 | EAS | CHS | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG00609 | hp2 | a0002 | c0001 | t0001 | g0111 | EAS | CHS | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG00639 | hp1 | a0001 | c0004 | t0005 | g0041 | AMR | PUR | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG00639 | hp2 | a0002 | c0001 | t0001 | g0005 | AMR | PUR | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG00642 | hp1 | a0002 | c0005 | t0001 | g0009 | AMR | PUR | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG00642 | hp2 | a0001 | c0002 | t0003 | g0059 | AMR | PUR | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG00673 | hp1 | a0002 | c0001 | t0001 | g0163 | EAS | CHS | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG00673 | hp2 | a0001 | c0003 | t0011 | g0068 | EAS | CHS | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG00735 | hp1 | a0002 | c0001 | t0001 | g0012 | AMR | PUR | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG00735 | hp2 | a0002 | c0001 | t0001 | g0042 | AMR | PUR | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG00738 | hp1 | a0001 | c0004 | t0005 | g0195 | AMR | PUR | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG00738 | hp2 | a0001 | c0002 | t0003 | g0151 | AMR | PUR | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG00741 | hp1 | a0002 | c0001 | t0001 | g0159 | AMR | PUR | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG00741 | hp2 | a0001 | c0002 | t0006 | g0183 | AMR | PUR | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01070 | hp1 | a0001 | c0006 | t0004 | g0204 | AMR | PUR | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0056 | AMR | PUR | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01071 | hp1 | a0002 | c0001 | t0001 | g0049 | AMR | PUR | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0058 | AMR | PUR | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0073 | AMR | PUR | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01074 | hp2 | a0002 | c0005 | t0001 | g0054 | AMR | PUR | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0016 | AMR | PUR | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01099 | hp2 | a0002 | c0005 | t0001 | g0002 | AMR | PUR | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01106 | hp1 | a0002 | c0005 | t0001 | g0132 | AMR | PUR | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0126 | AMR | PUR | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01109 | hp1 | a0001 | c0007 | t0004 | g0019 | AMR | PUR | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01109 | hp2 | a0001 | c0004 | t0005 | g0193 | AMR | PUR | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01167 | hp1 | a0002 | c0001 | t0001 | g0157 | AMR | PUR | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0060 | AMR | PUR | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01168 | hp1 | a0002 | c0001 | t0001 | g0113 | AMR | PUR | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0162 | AMR | PUR | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01175 | hp2 | a0001 | c0007 | t0001 | g0030 | AMR | PUR | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01255 | hp1 | a0002 | c0001 | t0001 | g0168 | AMR | CLM | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01255 | hp2 | a0002 | c0005 | t0001 | g0180 | AMR | CLM | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0177 | AMR | CLM | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0115 | AMR | CLM | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01257 | hp1 | a0002 | c0001 | t0001 | g0086 | AMR | CLM | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01257 | hp2 | a0001 | c0002 | t0012 | g0143 | AMR | CLM | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0057 | AMR | CLM | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01261 | hp2 | a0001 | c0002 | t0003 | g0026 | AMR | CLM | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01346 | hp1 | a0002 | c0001 | t0001 | g0090 | AMR | CLM | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01346 | hp2 | a0001 | c0002 | t0003 | g0141 | AMR | CLM | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01358 | hp1 | a0002 | c0005 | t0001 | g0119 | AMR | CLM | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01358 | hp2 | a0002 | c0001 | t0001 | g0089 | AMR | CLM | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01361 | hp1 | a0002 | c0001 | t0001 | g0004 | AMR | CLM | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01361 | hp2 | a0002 | c0001 | t0001 | g0023 | AMR | CLM | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0181 | AMR | CLM | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01496 | hp2 | a0001 | c0011 | t0001 | g0178 | AMR | CLM | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0139 | EUR | IBS | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01515 | hp2 | a0001 | c0002 | t0003 | g0050 | EUR | IBS | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01884 | hp1 | a0001 | c0006 | t0004 | g0197 | AFR | ACB | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01884 | hp2 | a0001 | c0004 | t0005 | g0192 | AFR | ACB | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01891 | hp1 | a0002 | c0001 | t0001 | g0122 | AFR | ACB | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01891 | hp2 | a0001 | c0006 | t0004 | g0032 | AFR | ACB | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0116 | AMR | PEL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01934 | hp2 | a0001 | c0003 | t0001 | g0039 | AMR | PEL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01975 | hp1 | a0001 | c0002 | t0003 | g0149 | AMR | PEL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01975 | hp2 | a0002 | c0001 | t0001 | g0088 | AMR | PEL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01981 | hp1 | a0002 | c0001 | t0001 | g0093 | AMR | PEL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG01981 | hp2 | a0002 | c0001 | t0001 | g0179 | AMR | PEL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02004 | hp1 | a0002 | c0001 | t0001 | g0112 | AMR | PEL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02004 | hp2 | a0002 | c0001 | t0001 | g0092 | AMR | PEL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02080 | hp1 | a0002 | c0001 | t0020 | g0079 | EAS | KHV | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02080 | hp2 | a0002 | c0001 | t0001 | g0118 | EAS | KHV | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02083 | hp1 | a0002 | c0001 | t0003 | g0099 | EAS | KHV | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02083 | hp2 | a0001 | c0002 | t0003 | g0052 | EAS | KHV | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0069 | EAS | KHV | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02135 | hp2 | a0002 | c0001 | t0001 | g0077 | EAS | KHV | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02145 | hp1 | a0001 | c0003 | t0016 | g0174 | AFR | ACB | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02145 | hp2 | a0001 | c0006 | t0004 | g0063 | AFR | ACB | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02155 | hp1 | a0002 | c0001 | t0001 | g0109 | EAS | CDX | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02155 | hp2 | a0002 | c0001 | t0001 | g0081 | EAS | CDX | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02165 | hp1 | a0002 | c0001 | t0001 | g0076 | EAS | CDX | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02165 | hp2 | a0003 | c0014 | t0003 | g0051 | EAS | CDX | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0198 | AFR | ACB | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02257 | hp2 | a0001 | c0003 | t0004 | g0011 | AFR | ACB | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02258 | hp1 | a0001 | c0006 | t0004 | g0018 | AFR | ACB | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02258 | hp2 | a0001 | c0002 | t0003 | g0150 | AFR | ACB | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0134 | AFR | ACB | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02280 | hp2 | a0002 | c0001 | t0001 | g0146 | AFR | ACB | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02451 | hp1 | a0001 | c0006 | t0004 | g0189 | AFR | ACB | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02451 | hp2 | a0001 | c0004 | t0005 | g0010 | AFR | ACB | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02523 | hp1 | a0001 | c0002 | t0023 | g0008 | EAS | KHV | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02523 | hp2 | a0002 | c0001 | t0010 | g0125 | EAS | KHV | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02622 | hp1 | a0002 | c0001 | t0001 | g0121 | AFR | GWD | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02622 | hp2 | a0001 | c0002 | t0003 | g0124 | AFR | GWD | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | GWD | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02630 | hp2 | a0001 | c0006 | t0004 | g0014 | AFR | GWD | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02647 | hp1 | a0002 | c0005 | t0001 | g0098 | AFR | GWD | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02647 | hp2 | a0001 | c0002 | t0019 | g0164 | AFR | GWD | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0137 | SAS | PJL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02698 | hp2 | a0002 | c0001 | t0001 | g0087 | SAS | PJL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02717 | hp1 | a0001 | c0003 | t0001 | g0169 | AFR | GWD | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02717 | hp2 | a0001 | c0004 | t0005 | g0194 | AFR | GWD | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02723 | hp1 | a0001 | c0003 | t0004 | g0043 | AFR | GWD | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02723 | hp2 | a0001 | c0002 | t0003 | g0062 | AFR | GWD | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02735 | hp1 | a0002 | c0001 | t0001 | g0070 | SAS | PJL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02735 | hp2 | a0001 | c0003 | t0006 | g0006 | SAS | PJL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02738 | hp1 | a0002 | c0001 | t0001 | g0072 | SAS | PJL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02738 | hp2 | a0002 | c0001 | t0001 | g0053 | SAS | PJL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02809 | hp1 | a0002 | c0001 | t0001 | g0167 | AFR | GWD | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0202 | AFR | GWD | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02818 | hp1 | a0001 | c0003 | t0001 | g0029 | AFR | GWD | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02818 | hp2 | a0001 | c0002 | t0003 | g0166 | AFR | GWD | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02886 | hp1 | a0001 | c0004 | t0005 | g0176 | AFR | GWD | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02886 | hp2 | a0001 | c0002 | t0009 | g0208 | AFR | GWD | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02895 | hp1 | a0001 | c0009 | t0004 | g0047 | AFR | GWD | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02895 | hp2 | a0001 | c0002 | t0009 | g0031 | AFR | GWD | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02922 | hp1 | a0001 | c0007 | t0004 | g0015 | AFR | ESN | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02922 | hp2 | a0002 | c0001 | t0001 | g0186 | AFR | ESN | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02965 | hp1 | a0001 | c0002 | t0013 | g0001 | AFR | ESN | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02965 | hp2 | a0001 | c0002 | t0003 | g0209 | AFR | ESN | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02976 | hp1 | a0001 | c0002 | t0008 | g0048 | AFR | ESN | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02976 | hp2 | a0001 | c0004 | t0005 | g0185 | AFR | ESN | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03041 | hp1 | a0002 | c0001 | t0001 | g0061 | AFR | GWD | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0165 | AFR | GWD | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0171 | AFR | MSL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03098 | hp2 | a0001 | c0002 | t0003 | g0148 | AFR | MSL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03130 | hp1 | a0001 | c0004 | t0005 | g0034 | AFR | ESN | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03130 | hp2 | a0001 | c0004 | t0005 | g0196 | AFR | ESN | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03139 | hp1 | a0001 | c0002 | t0003 | g0188 | AFR | ESN | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03139 | hp2 | a0001 | c0010 | t0018 | g0173 | AFR | ESN | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03225 | hp1 | a0001 | c0003 | t0001 | g0190 | AFR | MSL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03225 | hp2 | a0001 | c0007 | t0004 | g0203 | AFR | MSL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03239 | hp1 | a0002 | c0005 | t0001 | g0130 | SAS | PJL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03239 | hp2 | a0002 | c0001 | t0001 | g0140 | SAS | PJL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0097 | AFR | MSL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03453 | hp2 | a0002 | c0001 | t0001 | g0022 | AFR | MSL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03486 | hp1 | a0001 | c0002 | t0008 | g0206 | AFR | MSL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03486 | hp2 | a0001 | c0004 | t0005 | g0028 | AFR | MSL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03491 | hp1 | a0002 | c0001 | t0001 | g0106 | SAS | PJL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03491 | hp2 | a0001 | c0002 | t0003 | g0142 | SAS | PJL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03516 | hp1 | a0001 | c0003 | t0004 | g0020 | AFR | ESN | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03516 | hp2 | a0001 | c0003 | t0007 | g0199 | AFR | ESN | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03540 | hp1 | a0001 | c0004 | t0005 | g0205 | AFR | GWD | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03540 | hp2 | a0001 | c0003 | t0004 | g0038 | AFR | GWD | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03579 | hp1 | a0001 | c0003 | t0004 | g0175 | AFR | MSL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03579 | hp2 | a0001 | c0003 | t0004 | g0200 | AFR | MSL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03654 | hp1 | a0002 | c0005 | t0001 | g0131 | SAS | PJL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03654 | hp2 | a0002 | c0001 | t0001 | g0128 | SAS | PJL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03831 | hp1 | a0002 | c0001 | t0001 | g0100 | SAS | BEB | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03831 | hp2 | a0001 | c0002 | t0003 | g0094 | SAS | BEB | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03834 | hp1 | a0002 | c0005 | t0001 | g0101 | SAS | BEB | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03834 | hp2 | a0002 | c0001 | t0001 | g0161 | SAS | BEB | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03927 | hp1 | a0002 | c0001 | t0001 | g0074 | SAS | BEB | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03927 | hp2 | a0004 | c0015 | t0015 | g0123 | SAS | BEB | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03942 | hp1 | a0001 | c0002 | t0003 | g0147 | SAS | BEB | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03942 | hp2 | a0001 | c0002 | t0006 | g0184 | SAS | BEB | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG04115 | hp1 | a0002 | c0005 | t0001 | g0025 | SAS | STU | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0055 | SAS | STU | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0027 | SAS | STU | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG04199 | hp2 | a0002 | c0001 | t0003 | g0136 | SAS | STU | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA18522 | hp1 | a0001 | c0004 | t0005 | g0138 | AFR | YRI | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA18522 | hp2 | a0001 | c0003 | t0001 | g0172 | AFR | YRI | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA18612 | hp1 | a0002 | c0001 | t0001 | g0117 | EAS | CHB | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA18612 | hp2 | a0001 | c0003 | t0006 | g0064 | EAS | CHB | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA18906 | hp1 | a0001 | c0007 | t0004 | g0037 | AFR | YRI | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA18906 | hp2 | a0001 | c0004 | t0005 | g0021 | AFR | YRI | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA18946 | hp1 | a0002 | c0001 | t0001 | g0071 | EAS | JPT | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA18946 | hp2 | a0002 | c0001 | t0014 | g0091 | EAS | JPT | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA18953 | hp1 | a0002 | c0001 | t0001 | g0082 | EAS | JPT | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA18953 | hp2 | a0002 | c0008 | t0001 | g0108 | EAS | JPT | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA18964 | hp1 | a0001 | c0003 | t0006 | g0080 | EAS | JPT | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA18964 | hp2 | a0002 | c0001 | t0001 | g0114 | EAS | JPT | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA19009 | hp1 | a0002 | c0001 | t0001 | g0095 | EAS | JPT | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA19009 | hp2 | a0002 | c0008 | t0006 | g0103 | EAS | JPT | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA19011 | hp1 | a0002 | c0001 | t0001 | g0084 | EAS | JPT | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA19011 | hp2 | a0001 | c0003 | t0006 | g0104 | EAS | JPT | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA19030 | hp1 | a0001 | c0004 | t0005 | g0191 | AFR | LWK | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0153 | AFR | LWK | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0046 | AFR | LWK | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA19043 | hp2 | a0001 | c0013 | t0017 | g0045 | AFR | LWK | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA19065 | hp1 | a0001 | c0003 | t0006 | g0105 | EAS | JPT | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA19065 | hp2 | a0002 | c0001 | t0001 | g0110 | EAS | JPT | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA19070 | hp1 | a0002 | c0001 | t0001 | g0156 | EAS | JPT | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA19070 | hp2 | a0001 | c0002 | t0022 | g0120 | EAS | JPT | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA19079 | hp1 | a0002 | c0001 | t0001 | g0078 | EAS | JPT | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA19079 | hp2 | a0002 | c0001 | t0001 | g0127 | EAS | JPT | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA19090 | hp1 | a0002 | c0001 | t0001 | g0155 | EAS | JPT | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA19090 | hp2 | a0002 | c0001 | t0001 | g0036 | EAS | JPT | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA19091 | hp1 | a0002 | c0001 | t0010 | g0066 | EAS | JPT | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0187 | EAS | JPT | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0133 | AFR | YRI | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA19240 | hp2 | a0001 | c0003 | t0007 | g0170 | AFR | YRI | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0210 | AFR | ASW | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA20129 | hp2 | a0002 | c0001 | t0001 | g0013 | AFR | ASW | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0107 | EUR | TSI | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA20752 | hp2 | a0002 | c0001 | t0001 | g0145 | EUR | TSI | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA20905 | hp1 | a0002 | c0001 | t0001 | g0083 | SAS | GIH | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0129 | SAS | GIH | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02486 | hp1 | a0001 | c0004 | t0005 | g0201 | AFR | ACB | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG02486 | hp2 | a0001 | c0007 | t0004 | g0154 | AFR | ACB | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03471 | hp1 | a0001 | c0004 | t0005 | g0144 | AFR | MSL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG03471 | hp2 | a0001 | c0003 | t0004 | g0044 | AFR | MSL | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG06807 | hp1 | a0001 | c0003 | t0001 | g0017 | AFR | USA | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| HG06807 | hp2 | a0001 | c0003 | t0021 | g0040 | AFR | USA | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA20300 | hp1 | a0001 | c0012 | t0003 | g0033 | AFR | USA | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0182 | AFR | USA | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA21309 | hp1 | a0002 | c0005 | t0001 | g0003 | AFR | LWK | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| NA21309 | hp2 | a0001 | c0004 | t0005 | g0035 | AFR | LWK | ASAP2_chr2_9201812_9410678 | ASAP2 | chr2 | 9201812 | 9410678 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:9388407
|
G | C | 2 | a0001a0003 | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(125): Show |
missense_variant | MODERATE | c.2244G>C | p.Glu748Asp | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 22/28 | 2537/5665 | 2244/3021 | 748/1006 | chr2 | 9388407 | ||
| chr2:9393566
|
C | T | 1 | a0004 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.2603C>T | p.Pro868Leu | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/28 | 2896/5665 | 2603/3021 | 868/1006 | chr2 | 9393566 | ||
| chr2:9400772
|
C | T | 1 | a0003 | 1 | HG02165.hp2 | missense_variant | MODERATE | c.2765C>T | p.Pro922Leu | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 26/28 | 3058/5665 | 2765/3021 | 922/1006 | chr2 | 9400772 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:9279325
|
C | T | 1 | a0001c0006 | 7 | HG01070.hp1 HG01884.hp1 HG01891.hp2 others(4): Show |
synonymous_variant | LOW | c.135C>T | p.Asp45Asp | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/28 | 428/5665 | 135/3021 | 45/1006 | chr2 | 9279325 | ||
| chr2:9350888
|
C | T | 8 | a0001c0002a0001c0004a0001c0012others(5): Show | 160 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(157): Show |
synonymous_variant | LOW | c.1104C>T | p.Leu368Leu | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/28 | 1397/5665 | 1104/3021 | 368/1006 | chr2 | 9350888 | ||
| chr2:9356320
|
C | T | 2 | a0001c0006a0001c0007 | 13 | HG01070.hp1 HG01109.hp1 HG01175.hp2 others(10): Show |
synonymous_variant | LOW | c.1302C>T | p.Asp434Asp | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 14/28 | 1595/5665 | 1302/3021 | 434/1006 | chr2 | 9356320 | ||
| chr2:9374788
|
C | T | 2 | a0002c0005a0004c0015 | 13 | HG00642.hp1 HG01074.hp2 HG01099.hp2 others(10): Show |
synonymous_variant | LOW | c.1590C>T | p.Tyr530Tyr | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 17/28 | 1883/5665 | 1590/3021 | 530/1006 | chr2 | 9374788 | ||
| chr2:9374830
|
G | A | 1 | a0001c0009 | 1 | HG02895.hp1 | synonymous_variant | LOW | c.1632G>A | p.Ala544Ala | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 17/28 | 1925/5665 | 1632/3021 | 544/1006 | chr2 | 9374830 | ||
| chr2:9378983
|
C | G | 1 | a0001c0011 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.1872C>G | p.Ala624Ala | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 19/28 | 2165/5665 | 1872/3021 | 624/1006 | chr2 | 9378983 | ||
| chr2:9380745
|
C | T | 2 | a0001c0004a0001c0010 | 19 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(16): Show |
synonymous_variant | LOW | c.1953C>T | p.Asn651Asn | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/28 | 2246/5665 | 1953/3021 | 651/1006 | chr2 | 9380745 | ||
| chr2:9393645
|
G | A | 2 | a0001c0004a0001c0012 | 19 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(16): Show |
splice_region_variant&synonymous_variant | LOW | c.2682G>A | p.Pro894Pro | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/28 | 2975/5665 | 2682/3021 | 894/1006 | chr2 | 9393645 | ||
| chr2:9403318
|
C | T | 1 | a0001c0013 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.3012C>T | p.Ile1004Ile | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 28/28 | 3305/5665 | 3012/3021 | 1004/1006 | chr2 | 9403318 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:9206818
|
C | T | 1 | a0001c0002t0023 | 1 | HG02523.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-287C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/28 | chr2 | 9206818 | ||||||
| chr2:9206819
|
G | A | 1 | a0001c0002t0023 | 1 | HG02523.hp1 | 5_prime_UTR_variant | MODIFIER | c.-286G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/28 | 286 | chr2 | 9206819 | |||||
| chr2:9207059
|
C | A | 1 | a0001c0003t0011 | 1 | HG00673.hp2 | 5_prime_UTR_variant | MODIFIER | c.-46C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/28 | 46 | chr2 | 9207059 | |||||
| chr2:9403407
|
C | T | 1 | a0001c0002t0022 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*80C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 28/28 | 80 | chr2 | 9403407 | |||||
| chr2:9403458
|
T | C | 1 | a0001c0002t0012 | 1 | HG01257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*131T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 28/28 | 131 | chr2 | 9403458 | |||||
| chr2:9403502
|
A | T | 4 | a0001c0002t0006a0001c0003t0006a0001c0003t0011others(1): Show | 13 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*175A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 28/28 | 175 | chr2 | 9403502 | |||||
| chr2:9403649
|
A | G | 1 | a0001c0003t0021 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*322A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 28/28 | 322 | chr2 | 9403649 | |||||
| chr2:9403722
|
C | T | 1 | a0002c0001t0020 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*395C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 28/28 | 395 | chr2 | 9403722 | |||||
| chr2:9403723
|
G | A | 5 | a0001c0002t0002a0001c0002t0012a0001c0002t0013others(2): Show | 26 | HG00280.hp1 HG00280.hp2 HG01070.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*396G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 28/28 | 396 | chr2 | 9403723 | |||||
| chr2:9404171
|
C | T | 1 | a0002c0001t0010 | 2 | HG02523.hp2 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*844C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 28/28 | 844 | chr2 | 9404171 | |||||
| chr2:9404240
|
C | G | 1 | a0001c0002t0019 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*913C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 28/28 | 913 | chr2 | 9404240 | |||||
| chr2:9404260
|
G | A | 1 | a0001c0003t0007 | 2 | HG03516.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*933G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 28/28 | 933 | chr2 | 9404260 | |||||
| chr2:9404410
|
C | G | 1 | a0001c0002t0009 | 2 | HG02886.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1083C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 28/28 | 1083 | chr2 | 9404410 | |||||
| chr2:9404623
|
G | A | 1 | a0002c0001t0014 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1296G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 28/28 | 1296 | chr2 | 9404623 | |||||
| chr2:9404643
|
C | T | 1 | a0001c0004t0005 | 18 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1316C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 28/28 | 1316 | chr2 | 9404643 | |||||
| chr2:9404659
|
G | A | 1 | a0004c0015t0015 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1332G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 28/28 | 1332 | chr2 | 9404659 | |||||
| chr2:9404686
|
A | G | 1 | a0001c0010t0018 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1359A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 28/28 | 1359 | chr2 | 9404686 | |||||
| chr2:9404737
|
GT | G | 7 | a0001c0002t0003a0001c0003t0007a0001c0003t0016others(4): Show | 43 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1424delT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 28/28 | 1424 | INFO_REALIGN_3_PRIME | chr2 | 9404737 | ||||
| chr2:9404737
|
GTT | G | 5 | a0001c0002t0009a0001c0003t0004a0001c0006t0004others(2): Show | 22 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1423_*1424delTT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 28/28 | 1423 | INFO_REALIGN_3_PRIME | chr2 | 9404737 | ||||
| chr2:9404745
|
T | C | 4 | a0001c0002t0003a0001c0012t0003a0002c0001t0003others(1): Show | 22 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1418T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 28/28 | 1418 | chr2 | 9404745 | |||||
| chr2:9404805
|
T | A | 1 | a0001c0002t0013 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1478T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 28/28 | 1478 | chr2 | 9404805 | |||||
| chr2:9405090
|
T | C | 1 | a0001c0002t0008 | 2 | HG02976.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1763T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 28/28 | 1763 | chr2 | 9405090 | |||||
| chr2:9405225
|
A | G | 1 | a0001c0013t0017 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1898A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 28/28 | 1898 | chr2 | 9405225 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:9207278
|
A | C | 3 | a0001c0002t0003g0209a0001c0002t0009g0208a0001c0003t0001g0210 | 3 | HG02886.hp2 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.126+48A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9207278 | ||||||
| chr2:9207289
|
C | T | 1 | a0002c0001t0001g0207 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.126+59C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9207289 | ||||||
| chr2:9207296
|
C | T | 1 | a0001c0002t0008g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.126+66C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9207296 | ||||||
| chr2:9207549
|
C | A | 1 | a0001c0002t0013g0001 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.126+319C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9207549 | ||||||
| chr2:9207564
|
C | T | 1 | a0001c0004t0005g0205 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.126+334C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9207564 | ||||||
| chr2:9207568
|
G | C | 1 | a0002c0005t0001g0002 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.126+338G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9207568 | ||||||
| chr2:9207628
|
G | A | 3 | a0002c0001t0001g0004a0002c0001t0001g0005a0002c0005t0001g0003 | 3 | HG00639.hp2 HG01361.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.126+398G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9207628 | ||||||
| chr2:9207813
|
G | T | 3 | a0002c0001t0001g0004a0002c0001t0001g0005a0002c0005t0001g0003 | 3 | HG00639.hp2 HG01361.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.126+583G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9207813 | ||||||
| chr2:9207955
|
C | A | 1 | a0001c0002t0008g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.126+725C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9207955 | ||||||
| chr2:9208001
|
C | G | 1 | a0001c0006t0004g0204 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.126+771C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9208001 | ||||||
| chr2:9208017
|
A | G | 21 | a0001c0002t0002g0187a0001c0002t0002g0198a0001c0002t0002g0202others(18): Show | 21 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.126+787A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9208017 | ||||||
| chr2:9208077
|
C | T | 1 | a0001c0002t0006g0184 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.126+847C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9208077 | ||||||
| chr2:9208132
|
T | C | 32 | a0001c0002t0001g0024a0001c0002t0002g0007a0001c0002t0002g0016others(29): Show | 32 | HG00642.hp1 HG00735.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.126+902T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9208132 | ||||||
| chr2:9208173
|
T | A | 1 | a0002c0001t0001g0036 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.126+943T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9208173 | ||||||
| chr2:9208275
|
G | A | 1 | a0001c0007t0004g0037 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.126+1045G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9208275 | ||||||
| chr2:9208336
|
A | AGT | 7 | a0001c0002t0001g0181a0001c0002t0001g0182a0001c0002t0002g0177others(4): Show | 7 | HG00741.hp2 HG01255.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+1116_126+1117d others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9208336 | |||||
| chr2:9208351
|
G | T | 12 | a0001c0002t0003g0166a0001c0003t0001g0165a0001c0003t0001g0169others(9): Show | 12 | HG01255.hp1 HG02145.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.126+1121G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9208351 | ||||||
| chr2:9208411
|
G | GT | 14 | a0001c0002t0002g0202a0001c0002t0006g0183a0001c0002t0008g0206others(11): Show | 14 | HG00597.hp1 HG00597.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.126+1196dupT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9208411 | |||||
| chr2:9208411
|
G | T | 4 | a0001c0002t0002g0162a0001c0002t0019g0164a0002c0001t0001g0161others(1): Show | 4 | HG00673.hp1 HG01175.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+1181G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9208411 | ||||||
| chr2:9208411
|
GT | G | 8 | a0001c0003t0001g0039a0001c0003t0001g0165a0001c0003t0004g0038others(5): Show | 8 | HG00639.hp1 HG00735.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.126+1196delT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9208411 | |||||
| chr2:9208412
|
T | G | 1 | a0001c0004t0005g0205 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.126+1182T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9208412 | ||||||
| chr2:9208495
|
G | C | 1 | a0002c0001t0001g0161 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.126+1265G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9208495 | ||||||
| chr2:9208538
|
G | A | 32 | a0001c0002t0001g0024a0001c0002t0002g0007a0001c0002t0002g0016others(29): Show | 32 | HG00642.hp1 HG00735.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.126+1308G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9208538 | ||||||
| chr2:9209000
|
A | AC | 32 | a0001c0002t0001g0024a0001c0002t0002g0007a0001c0002t0002g0016others(29): Show | 32 | HG00642.hp1 HG00735.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.126+1772dupC | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9209000 | |||||
| chr2:9209236
|
A | T | 1 | a0002c0001t0001g0157 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.126+2006A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9209236 | ||||||
| chr2:9209253
|
G | A | 1 | a0001c0003t0004g0200 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.126+2023G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9209253 | ||||||
| chr2:9209256
|
A | C | 3 | a0001c0003t0004g0175a0001c0003t0016g0174a0001c0010t0018g0173 | 3 | HG02145.hp1 HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.126+2026A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9209256 | ||||||
| chr2:9209315
|
A | G | 1 | a0002c0001t0001g0156 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.126+2085A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9209315 | ||||||
| chr2:9209399
|
A | C | 1 | a0001c0002t0019g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.126+2169A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9209399 | ||||||
| chr2:9209502
|
A | C | 1 | a0002c0001t0001g0163 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.126+2272A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9209502 | ||||||
| chr2:9209599
|
T | C | 210 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(207): Show | 210 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.126+2369T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9209599 | ||||||
| chr2:9209675
|
T | G | 1 | a0001c0002t0003g0166 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.126+2445T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9209675 | ||||||
| chr2:9209735
|
A | T | 12 | a0001c0002t0003g0166a0001c0003t0001g0165a0001c0003t0001g0169others(9): Show | 12 | HG01255.hp1 HG02145.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.126+2505A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9209735 | ||||||
| chr2:9210143
|
G | A | 1 | a0001c0007t0004g0037 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.126+2913G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9210143 | ||||||
| chr2:9210151
|
C | T | 12 | a0001c0002t0003g0166a0001c0003t0001g0165a0001c0003t0001g0169others(9): Show | 12 | HG01255.hp1 HG02145.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.126+2921C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9210151 | ||||||
| chr2:9210202
|
G | A | 1 | a0001c0013t0017g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126+2972G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9210202 | ||||||
| chr2:9210422
|
ATAGT | A | 63 | a0001c0002t0001g0024a0001c0002t0002g0007a0001c0002t0002g0016others(60): Show | 63 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.126+3197_126+3200d others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9210422 | |||||
| chr2:9210577
|
T | C | 31 | a0001c0002t0001g0024a0001c0002t0002g0007a0001c0002t0002g0016others(28): Show | 31 | HG00642.hp1 HG00735.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.126+3347T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9210577 | ||||||
| chr2:9210628
|
C | T | 31 | a0001c0002t0001g0024a0001c0002t0002g0007a0001c0002t0002g0016others(28): Show | 31 | HG00642.hp1 HG00735.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.126+3398C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9210628 | ||||||
| chr2:9210632
|
G | A | 31 | a0001c0002t0001g0024a0001c0002t0002g0007a0001c0002t0002g0016others(28): Show | 31 | HG00642.hp1 HG00735.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.126+3402G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9210632 | ||||||
| chr2:9210695
|
C | A | 1 | a0001c0003t0004g0200 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.126+3465C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9210695 | ||||||
| chr2:9210778
|
G | A | 15 | a0001c0002t0003g0166a0001c0003t0001g0165a0001c0003t0001g0169others(12): Show | 15 | HG01255.hp1 HG02145.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.126+3548G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9210778 | ||||||
| chr2:9210791
|
G | C | 1 | a0001c0002t0019g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.126+3561G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9210791 | ||||||
| chr2:9210812
|
T | G | 14 | a0001c0002t0003g0166a0001c0003t0001g0165a0001c0003t0001g0169others(11): Show | 14 | HG01255.hp1 HG02145.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.126+3582T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9210812 | ||||||
| chr2:9210930
|
C | G | 2 | a0001c0002t0009g0031a0001c0007t0001g0030 | 2 | HG01175.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.126+3700C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9210930 | ||||||
| chr2:9210930
|
C | T | 1 | a0001c0006t0004g0032 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.126+3700C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9210930 | ||||||
| chr2:9210931
|
A | G | 31 | a0001c0002t0001g0024a0001c0002t0002g0007a0001c0002t0002g0016others(28): Show | 31 | HG00642.hp1 HG00735.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.126+3701A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9210931 | ||||||
| chr2:9211155
|
CA | C | 14 | a0001c0002t0003g0050a0001c0002t0003g0052a0001c0002t0008g0048others(11): Show | 14 | HG00639.hp1 HG01071.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.126+3941delA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9211155 | |||||
| chr2:9211155
|
CAA | C | 28 | a0001c0002t0001g0024a0001c0002t0002g0016a0001c0002t0002g0027others(25): Show | 28 | HG00642.hp1 HG00735.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.126+3940_126+3941d others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9211155 | |||||
| chr2:9212188
|
A | G | 1 | a0001c0006t0004g0204 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.126+4958A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9212188 | ||||||
| chr2:9212253
|
C | G | 14 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0166others(11): Show | 14 | HG01175.hp2 HG02257.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.126+5023C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9212253 | ||||||
| chr2:9212363
|
G | A | 20 | a0001c0002t0002g0055a0001c0002t0002g0056a0001c0002t0002g0057others(17): Show | 20 | HG00639.hp1 HG00642.hp1 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.126+5133G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9212363 | ||||||
| chr2:9212366
|
G | A | 1 | a0001c0003t0001g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.126+5136G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9212366 | ||||||
| chr2:9212388
|
G | A | 27 | a0001c0002t0002g0060a0001c0002t0003g0062a0001c0002t0008g0048others(24): Show | 27 | HG00642.hp1 HG00735.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.126+5158G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9212388 | ||||||
| chr2:9212455
|
C | A | 93 | a0001c0002t0001g0097a0001c0002t0002g0016a0001c0002t0002g0055others(90): Show | 93 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.126+5225C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9212455 | ||||||
| chr2:9212519
|
G | A | 135 | a0001c0002t0001g0024a0001c0002t0001g0115a0001c0002t0001g0116others(132): Show | 135 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.126+5289G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9212519 | ||||||
| chr2:9212526
|
G | A | 1 | a0002c0005t0001g0054 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.126+5296G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9212526 | ||||||
| chr2:9212589
|
GTGA | G | 20 | a0001c0003t0001g0029a0001c0003t0001g0039a0001c0003t0004g0038others(17): Show | 20 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.126+5361_126+5363d others(5): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9212589 | |||||
| chr2:9212603
|
T | C | 1 | a0001c0004t0005g0176 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.126+5373T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9212603 | ||||||
| chr2:9212612
|
A | C | 1 | a0001c0003t0004g0200 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.126+5382A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9212612 | ||||||
| chr2:9212887
|
G | A | 1 | a0002c0005t0001g0025 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.126+5657G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9212887 | ||||||
| chr2:9212899
|
G | T | 39 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(36): Show | 39 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.126+5669G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9212899 | ||||||
| chr2:9212912
|
G | A | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.126+5682G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9212912 | ||||||
| chr2:9212955
|
C | A | 5 | a0001c0002t0003g0166a0001c0003t0001g0153a0001c0007t0004g0015others(2): Show | 5 | HG02486.hp2 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+5725C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9212955 | ||||||
| chr2:9213126
|
G | T | 33 | a0001c0002t0002g0129a0001c0002t0002g0162a0001c0002t0002g0198others(30): Show | 33 | HG00642.hp1 HG00738.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.126+5896G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9213126 | ||||||
| chr2:9213183
|
A | G | 1 | a0001c0002t0019g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.126+5953A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9213183 | ||||||
| chr2:9213366
|
G | T | 2 | a0001c0002t0008g0048a0001c0003t0004g0011 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.126+6136G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9213366 | ||||||
| chr2:9213620
|
G | T | 1 | a0002c0001t0001g0128 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.126+6390G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9213620 | ||||||
| chr2:9213913
|
A | G | 1 | a0001c0003t0021g0040 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.126+6683A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9213913 | ||||||
| chr2:9213943
|
G | T | 1 | a0002c0001t0001g0128 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.126+6713G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9213943 | ||||||
| chr2:9213996
|
A | G | 1 | a0002c0001t0001g0160 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.126+6766A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9213996 | ||||||
| chr2:9214134
|
C | T | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+6904C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9214134 | ||||||
| chr2:9214135
|
G | A | 30 | a0001c0002t0002g0129a0001c0002t0002g0162a0001c0002t0002g0198others(27): Show | 30 | HG00642.hp1 HG00738.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.126+6905G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9214135 | ||||||
| chr2:9214184
|
G | A | 1 | a0001c0002t0009g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.126+6954G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9214184 | ||||||
| chr2:9214205
|
A | G | 4 | a0001c0003t0004g0043a0001c0003t0004g0044a0001c0003t0004g0175others(1): Show | 4 | HG02723.hp1 HG02895.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+6975A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9214205 | ||||||
| chr2:9214515
|
TAGGCGTG others(74): Show |
T | 1 | a0001c0009t0004g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.126+7287_126+7367d others(83): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9214515 | |||||
| chr2:9214540
|
G | A | 18 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(15): Show | 18 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.126+7310G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9214540 | ||||||
| chr2:9214777
|
T | TA | 11 | a0001c0003t0001g0017a0001c0003t0004g0200a0001c0006t0004g0014others(8): Show | 11 | HG01070.hp1 HG01074.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.126+7568dupA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9214777 | |||||
| chr2:9214777
|
TA | T | 27 | a0001c0002t0003g0094a0001c0002t0008g0048a0001c0002t0009g0208others(24): Show | 27 | HG00639.hp2 HG00735.hp2 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.126+7568delA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9214777 | |||||
| chr2:9214777
|
TAA | T | 28 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(25): Show | 28 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.126+7567_126+7568d others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9214777 | |||||
| chr2:9214806
|
G | A | 1 | a0001c0002t0019g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.126+7576G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9214806 | ||||||
| chr2:9215189
|
G | A | 143 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(140): Show | 143 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.126+7959G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9215189 | ||||||
| chr2:9215566
|
A | G | 1 | a0002c0001t0001g0087 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.126+8336A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9215566 | ||||||
| chr2:9215611
|
C | A | 1 | a0001c0002t0009g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.126+8381C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9215611 | ||||||
| chr2:9215614
|
C | T | 36 | a0001c0002t0002g0129a0001c0002t0002g0162a0001c0002t0002g0198others(33): Show | 36 | HG00642.hp1 HG00738.hp1 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.126+8384C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9215614 | ||||||
| chr2:9215639
|
G | A | 1 | a0002c0001t0001g0070 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.126+8409G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9215639 | ||||||
| chr2:9215665
|
G | GT | 145 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(142): Show | 145 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.126+8451dupT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9215665 | |||||
| chr2:9215941
|
G | A | 14 | a0001c0002t0002g0007a0001c0002t0002g0129a0001c0002t0002g0162others(11): Show | 14 | HG00642.hp1 HG01099.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.126+8711G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9215941 | ||||||
| chr2:9215988
|
C | A | 207 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(204): Show | 207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.126+8758C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9215988 | ||||||
| chr2:9216109
|
G | A | 1 | a0001c0002t0002g0177 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.126+8879G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9216109 | ||||||
| chr2:9216282
|
A | AT | 8 | a0001c0002t0001g0126a0001c0002t0003g0094a0001c0002t0008g0206others(5): Show | 8 | HG00597.hp2 HG01074.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.126+9072dupT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9216282 | |||||
| chr2:9216282
|
AT | A | 8 | a0001c0002t0019g0164a0001c0003t0001g0169a0001c0003t0001g0171others(5): Show | 8 | HG01496.hp2 HG01975.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+9072delT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9216282 | |||||
| chr2:9216282
|
ATTTTTTT | A | 18 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(15): Show | 18 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.126+9066_126+9072d others(9): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9216282 | |||||
| chr2:9216453
|
A | AT | 35 | a0001c0002t0001g0126a0001c0002t0002g0162a0001c0002t0003g0026others(32): Show | 35 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.126+9248dupT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9216453 | |||||
| chr2:9216453
|
A | ATT | 6 | a0001c0002t0003g0124a0001c0003t0001g0017a0001c0013t0017g0045others(3): Show | 6 | HG00735.hp2 HG02622.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+9247_126+9248d others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9216453 | |||||
| chr2:9216453
|
AT | A | 5 | a0001c0002t0003g0188a0001c0002t0009g0031a0001c0004t0005g0176others(2): Show | 5 | HG01070.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+9248delT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9216453 | |||||
| chr2:9216693
|
T | G | 1 | a0004c0015t0015g0123 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.126+9463T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9216693 | ||||||
| chr2:9216756
|
C | T | 1 | a0001c0002t0009g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.126+9526C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9216756 | ||||||
| chr2:9216888
|
C | T | 11 | a0001c0002t0002g0202a0001c0002t0003g0188a0001c0003t0001g0165others(8): Show | 11 | HG01074.hp2 HG01361.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.126+9658C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9216888 | ||||||
| chr2:9217240
|
G | A | 1 | a0001c0002t0003g0149 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.126+10010G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9217240 | ||||||
| chr2:9217261
|
G | C | 1 | a0001c0002t0009g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.126+10031G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9217261 | ||||||
| chr2:9217271
|
G | A | 9 | a0001c0002t0003g0094a0002c0001t0001g0042a0002c0001t0001g0088others(6): Show | 9 | HG00735.hp2 HG01346.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+10041G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9217271 | ||||||
| chr2:9217326
|
T | C | 1 | a0002c0001t0001g0004 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.126+10096T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9217326 | ||||||
| chr2:9217331
|
A | G | 9 | a0001c0002t0003g0094a0002c0001t0001g0042a0002c0001t0001g0088others(6): Show | 9 | HG00735.hp2 HG01346.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+10101A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9217331 | ||||||
| chr2:9217404
|
T | C | 37 | a0001c0002t0002g0129a0001c0002t0002g0162a0001c0002t0002g0198others(34): Show | 37 | HG00642.hp1 HG00738.hp1 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.126+10174T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9217404 | ||||||
| chr2:9217620
|
G | GT | 11 | a0001c0002t0002g0129a0001c0002t0002g0198a0001c0002t0013g0001others(8): Show | 11 | HG00642.hp1 HG01099.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.126+10401dupT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9217620 | |||||
| chr2:9217620
|
G | GTT | 81 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(78): Show | 81 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.126+10400_126+1040 others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9217620 | |||||
| chr2:9217709
|
G | A | 3 | a0001c0003t0006g0064a0001c0003t0006g0065a0001c0003t0006g0102 | 3 | HG00408.hp2 HG00438.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.126+10479G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9217709 | ||||||
| chr2:9217739
|
C | T | 43 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(40): Show | 43 | HG00280.hp1 HG00639.hp1 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.126+10509C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9217739 | ||||||
| chr2:9217793
|
T | G | 1 | a0001c0002t0002g0129 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.126+10563T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9217793 | ||||||
| chr2:9217830
|
G | A | 1 | a0001c0002t0009g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.126+10600G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9217830 | ||||||
| chr2:9217912
|
CT | C | 121 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(118): Show | 121 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.126+10696delT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9217912 | |||||
| chr2:9217926
|
T | C | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.126+10696T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9217926 | ||||||
| chr2:9218273
|
A | G | 132 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(129): Show | 132 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.126+11043A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9218273 | ||||||
| chr2:9218286
|
G | A | 1 | a0001c0009t0004g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.126+11056G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9218286 | ||||||
| chr2:9218483
|
A | G | 27 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(24): Show | 27 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.126+11253A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9218483 | ||||||
| chr2:9218593
|
G | A | 3 | a0001c0003t0004g0043a0001c0003t0004g0044a0001c0003t0004g0175 | 3 | HG02723.hp1 HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.126+11363G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9218593 | ||||||
| chr2:9218611
|
CT | C | 9 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(6): Show | 9 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+11382delT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9218611 | ||||||
| chr2:9218764
|
A | T | 1 | a0001c0002t0002g0162 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.126+11534A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9218764 | ||||||
| chr2:9219198
|
A | G | 1 | a0001c0003t0006g0006 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.126+11968A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9219198 | ||||||
| chr2:9219206
|
C | T | 129 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(126): Show | 129 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.126+11976C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9219206 | ||||||
| chr2:9219302
|
G | A | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+12072G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9219302 | ||||||
| chr2:9219353
|
C | T | 1 | a0001c0004t0005g0041 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.126+12123C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9219353 | ||||||
| chr2:9219408
|
A | T | 1 | a0001c0002t0002g0162 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.126+12178A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9219408 | ||||||
| chr2:9219575
|
G | GT | 27 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(24): Show | 27 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.126+12345_126+1234 others(5): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9219575 | ||||||
| chr2:9219680
|
A | T | 2 | a0001c0002t0003g0052a0001c0013t0017g0045 | 2 | HG02083.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.126+12450A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9219680 | ||||||
| chr2:9219721
|
T | A | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+12491T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9219721 | ||||||
| chr2:9219781
|
G | C | 1 | a0001c0002t0009g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.126+12551G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9219781 | ||||||
| chr2:9219858
|
T | C | 1 | a0001c0013t0017g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126+12628T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9219858 | ||||||
| chr2:9219880
|
G | A | 1 | a0001c0003t0001g0190 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.126+12650G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9219880 | ||||||
| chr2:9219900
|
T | C | 1 | a0001c0009t0004g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.126+12670T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9219900 | ||||||
| chr2:9220015
|
C | T | 9 | a0001c0002t0003g0094a0002c0001t0001g0042a0002c0001t0001g0088others(6): Show | 9 | HG00735.hp2 HG01346.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+12785C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9220015 | ||||||
| chr2:9220322
|
C | T | 1 | a0001c0003t0006g0102 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.126+13092C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9220322 | ||||||
| chr2:9220849
|
G | A | 3 | a0001c0002t0002g0137a0001c0002t0023g0008a0002c0001t0003g0136 | 3 | HG02523.hp1 HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.126+13619G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9220849 | ||||||
| chr2:9221258
|
T | A | 1 | a0001c0002t0002g0129 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.126+14028T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9221258 | ||||||
| chr2:9221264
|
ATCTATCA others(8): Show |
A | 1 | a0001c0002t0002g0129 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.126+14041_126+1405 others(19): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9221264 | |||||
| chr2:9221270
|
C | T | 9 | a0001c0002t0003g0094a0002c0001t0001g0042a0002c0001t0001g0088others(6): Show | 9 | HG00735.hp2 HG01346.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+14040C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9221270 | ||||||
| chr2:9221323
|
C | CT | 6 | a0001c0002t0002g0202a0001c0002t0003g0188a0001c0003t0004g0020others(3): Show | 6 | HG01358.hp1 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+14109dupT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9221323 | |||||
| chr2:9221323
|
CT | C | 36 | a0001c0002t0002g0007a0001c0002t0002g0198a0001c0002t0003g0124others(33): Show | 36 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.126+14109delT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9221323 | |||||
| chr2:9221707
|
G | A | 6 | a0002c0005t0001g0002a0002c0005t0001g0009a0002c0005t0001g0025others(3): Show | 6 | HG00642.hp1 HG01099.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+14477G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9221707 | ||||||
| chr2:9221920
|
A | C | 12 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0027others(9): Show | 12 | HG01167.hp2 HG01168.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.126+14690A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9221920 | ||||||
| chr2:9221927
|
G | A | 1 | a0001c0003t0001g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.126+14697G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9221927 | ||||||
| chr2:9221960
|
AT | A | 6 | a0001c0002t0009g0031a0001c0003t0001g0169a0001c0003t0001g0171others(3): Show | 6 | HG01496.hp2 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+14743delT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9221960 | |||||
| chr2:9222002
|
A | G | 1 | a0001c0002t0003g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.126+14772A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9222002 | ||||||
| chr2:9222433
|
C | T | 10 | a0001c0002t0008g0206a0001c0006t0004g0014a0001c0006t0004g0018others(7): Show | 10 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+15203C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9222433 | ||||||
| chr2:9222584
|
T | C | 1 | a0002c0001t0001g0072 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.126+15354T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9222584 | ||||||
| chr2:9222789
|
G | C | 132 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(129): Show | 132 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.126+15559G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9222789 | ||||||
| chr2:9222853
|
G | A | 9 | a0001c0002t0003g0094a0002c0001t0001g0042a0002c0001t0001g0088others(6): Show | 9 | HG00735.hp2 HG01346.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+15623G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9222853 | ||||||
| chr2:9222856
|
T | C | 132 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(129): Show | 132 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.126+15626T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9222856 | ||||||
| chr2:9222857
|
G | A | 1 | a0001c0007t0004g0203 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.126+15627G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9222857 | ||||||
| chr2:9222979
|
G | T | 25 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(22): Show | 25 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.126+15749G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9222979 | ||||||
| chr2:9223006
|
G | C | 9 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(6): Show | 9 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+15776G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9223006 | ||||||
| chr2:9223195
|
G | A | 1 | a0001c0002t0009g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.126+15965G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9223195 | ||||||
| chr2:9223329
|
A | G | 27 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(24): Show | 27 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.126+16099A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9223329 | ||||||
| chr2:9223797
|
G | A | 1 | a0001c0002t0008g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.126+16567G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9223797 | ||||||
| chr2:9223949
|
C | T | 1 | a0001c0003t0004g0011 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.126+16719C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9223949 | ||||||
| chr2:9224178
|
A | T | 3 | a0001c0002t0002g0202a0001c0002t0003g0188a0001c0003t0004g0020 | 3 | HG02809.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.126+16948A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9224178 | ||||||
| chr2:9224248
|
C | T | 1 | a0002c0001t0001g0118 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.126+17018C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9224248 | ||||||
| chr2:9224249
|
G | A | 2 | a0001c0003t0016g0174a0001c0010t0018g0173 | 2 | HG02145.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.126+17019G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9224249 | ||||||
| chr2:9224478
|
T | G | 2 | a0001c0003t0016g0174a0001c0010t0018g0173 | 2 | HG02145.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.126+17248T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9224478 | ||||||
| chr2:9224538
|
C | T | 1 | a0001c0003t0001g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.126+17308C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9224538 | ||||||
| chr2:9224822
|
G | T | 1 | a0001c0002t0003g0147 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.126+17592G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9224822 | ||||||
| chr2:9224969
|
G | T | 1 | a0001c0002t0009g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.126+17739G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9224969 | ||||||
| chr2:9224994
|
T | A | 37 | a0001c0002t0002g0129a0001c0002t0002g0162a0001c0002t0002g0198others(34): Show | 37 | HG00642.hp1 HG00738.hp1 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.126+17764T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9224994 | ||||||
| chr2:9225754
|
C | T | 39 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(36): Show | 39 | HG00280.hp1 HG00639.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.126+18524C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9225754 | ||||||
| chr2:9225784
|
G | A | 1 | a0002c0008t0006g0103 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.126+18554G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9225784 | ||||||
| chr2:9226058
|
C | T | 2 | a0001c0003t0016g0174a0001c0010t0018g0173 | 2 | HG02145.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.126+18828C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9226058 | ||||||
| chr2:9226087
|
G | T | 25 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(22): Show | 25 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.126+18857G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9226087 | ||||||
| chr2:9226197
|
A | G | 132 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(129): Show | 132 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.126+18967A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9226197 | ||||||
| chr2:9226201
|
T | C | 10 | a0001c0002t0008g0206a0001c0006t0004g0014a0001c0006t0004g0018others(7): Show | 10 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+18971T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9226201 | ||||||
| chr2:9226673
|
C | T | 1 | a0001c0002t0009g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.126+19443C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9226673 | ||||||
| chr2:9226779
|
G | A | 1 | a0001c0010t0018g0173 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.126+19549G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9226779 | ||||||
| chr2:9226792
|
C | T | 1 | a0002c0001t0001g0012 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.126+19562C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9226792 | ||||||
| chr2:9226966
|
G | A | 2 | a0001c0002t0002g0198a0001c0002t0013g0001 | 2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.126+19736G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9226966 | ||||||
| chr2:9227038
|
C | T | 6 | a0001c0004t0005g0192a0001c0004t0005g0193a0001c0004t0005g0194others(3): Show | 6 | HG00738.hp1 HG01109.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+19808C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9227038 | ||||||
| chr2:9227203
|
T | C | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+19973T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9227203 | ||||||
| chr2:9227267
|
G | C | 2 | a0001c0002t0008g0048a0001c0003t0004g0011 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.126+20037G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9227267 | ||||||
| chr2:9227273
|
T | A | 127 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(124): Show | 127 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.126+20043T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9227273 | ||||||
| chr2:9227317
|
C | T | 127 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(124): Show | 127 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.126+20087C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9227317 | ||||||
| chr2:9227327
|
T | C | 39 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(36): Show | 39 | HG00280.hp1 HG00639.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.126+20097T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9227327 | ||||||
| chr2:9227492
|
C | T | 10 | a0001c0002t0003g0094a0001c0009t0004g0047a0002c0001t0001g0042others(7): Show | 10 | HG00735.hp2 HG01346.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.126+20262C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9227492 | ||||||
| chr2:9227621
|
A | G | 1 | a0002c0001t0001g0117 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.126+20391A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9227621 | ||||||
| chr2:9227661
|
A | G | 25 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(22): Show | 25 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.126+20431A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9227661 | ||||||
| chr2:9227844
|
T | C | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+20614T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9227844 | ||||||
| chr2:9228002
|
A | G | 1 | a0002c0001t0001g0155 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.126+20772A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9228002 | ||||||
| chr2:9228091
|
G | A | 36 | a0001c0002t0002g0162a0001c0002t0002g0198a0001c0002t0003g0148others(33): Show | 36 | HG00642.hp1 HG00738.hp1 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.126+20861G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9228091 | ||||||
| chr2:9228169
|
G | A | 1 | a0001c0002t0001g0097 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.126+20939G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9228169 | ||||||
| chr2:9228274
|
A | G | 6 | a0001c0002t0003g0209a0001c0002t0009g0208a0001c0004t0005g0191others(3): Show | 6 | HG02886.hp2 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+21044A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9228274 | ||||||
| chr2:9228321
|
A | G | 1 | a0001c0002t0002g0069 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.126+21091A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9228321 | ||||||
| chr2:9228358
|
G | A | 1 | a0001c0003t0001g0153 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.126+21128G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9228358 | ||||||
| chr2:9228610
|
T | C | 1 | a0004c0015t0015g0123 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.126+21380T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9228610 | ||||||
| chr2:9228619
|
T | C | 39 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(36): Show | 39 | HG00280.hp1 HG00639.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.126+21389T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9228619 | ||||||
| chr2:9228781
|
G | A | 9 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(6): Show | 9 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+21551G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9228781 | ||||||
| chr2:9228969
|
C | T | 1 | a0001c0009t0004g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.126+21739C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9228969 | ||||||
| chr2:9229063
|
G | C | 1 | a0002c0001t0001g0061 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.126+21833G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9229063 | ||||||
| chr2:9229068
|
T | C | 1 | a0001c0002t0002g0055 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.126+21838T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9229068 | ||||||
| chr2:9229333
|
G | T | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+22103G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9229333 | ||||||
| chr2:9229346
|
CCACCTCT others(8): Show |
C | 1 | a0001c0003t0007g0199 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.126+22121_126+2213 others(19): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9229346 | |||||
| chr2:9229416
|
A | G | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+22186A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9229416 | ||||||
| chr2:9229492
|
C | T | 3 | a0001c0003t0004g0043a0001c0003t0004g0044a0001c0003t0004g0175 | 3 | HG02723.hp1 HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.126+22262C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9229492 | ||||||
| chr2:9229590
|
G | A | 1 | a0002c0001t0001g0109 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.126+22360G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9229590 | ||||||
| chr2:9229651
|
C | A | 34 | a0001c0002t0002g0162a0001c0002t0002g0198a0001c0002t0003g0148others(31): Show | 34 | HG00642.hp1 HG00738.hp1 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.126+22421C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9229651 | ||||||
| chr2:9229741
|
G | C | 1 | a0001c0002t0009g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.126+22511G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9229741 | ||||||
| chr2:9229883
|
G | T | 52 | a0001c0002t0002g0162a0001c0002t0002g0198a0001c0002t0003g0094others(49): Show | 52 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.126+22653G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9229883 | ||||||
| chr2:9230247
|
A | T | 1 | a0002c0001t0001g0084 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.126+23017A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9230247 | ||||||
| chr2:9230331
|
G | A | 1 | a0001c0003t0006g0158 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.126+23101G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9230331 | ||||||
| chr2:9230334
|
T | C | 131 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(128): Show | 131 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.126+23104T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9230334 | ||||||
| chr2:9230538
|
A | G | 1 | a0001c0002t0019g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.126+23308A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9230538 | ||||||
| chr2:9230625
|
A | T | 2 | a0001c0002t0008g0048a0001c0003t0004g0011 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.126+23395A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9230625 | ||||||
| chr2:9230721
|
T | C | 1 | a0001c0003t0007g0170 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.126+23491T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9230721 | ||||||
| chr2:9230920
|
T | G | 130 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(127): Show | 130 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.126+23690T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9230920 | ||||||
| chr2:9230984
|
C | T | 1 | a0001c0002t0008g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.126+23754C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9230984 | ||||||
| chr2:9231147
|
G | A | 1 | a0001c0013t0017g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126+23917G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9231147 | ||||||
| chr2:9231388
|
C | T | 25 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(22): Show | 25 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.126+24158C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9231388 | ||||||
| chr2:9231476
|
C | A | 1 | a0001c0002t0009g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.126+24246C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9231476 | ||||||
| chr2:9231580
|
C | T | 4 | a0001c0002t0002g0007a0001c0002t0002g0027a0001c0002t0012g0143others(1): Show | 4 | HG01168.hp2 HG01257.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+24350C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9231580 | ||||||
| chr2:9231602
|
G | C | 10 | a0001c0002t0003g0094a0001c0009t0004g0047a0002c0001t0001g0042others(7): Show | 10 | HG00735.hp2 HG01346.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.126+24372G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9231602 | ||||||
| chr2:9231784
|
G | A | 2 | a0001c0003t0001g0171a0001c0003t0001g0172 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.126+24554G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9231784 | ||||||
| chr2:9231868
|
C | T | 1 | a0001c0003t0001g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.126+24638C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9231868 | ||||||
| chr2:9231912
|
A | G | 1 | a0002c0008t0006g0103 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.126+24682A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9231912 | ||||||
| chr2:9232264
|
CCGAT | C | 9 | a0001c0002t0003g0094a0002c0001t0001g0042a0002c0001t0001g0088others(6): Show | 9 | HG00735.hp2 HG01346.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+25036_126+2503 others(8): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9232264 | |||||
| chr2:9232265
|
C | T | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+25035C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9232265 | ||||||
| chr2:9232270
|
C | T | 9 | a0001c0002t0003g0094a0002c0001t0001g0042a0002c0001t0001g0088others(6): Show | 9 | HG00735.hp2 HG01346.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+25040C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9232270 | ||||||
| chr2:9232280
|
G | A | 7 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(4): Show | 7 | HG02280.hp1 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+25050G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9232280 | ||||||
| chr2:9232299
|
G | A | 1 | a0002c0001t0001g0089 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.126+25069G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9232299 | ||||||
| chr2:9232341
|
T | G | 5 | a0001c0002t0008g0206a0001c0003t0001g0169a0001c0003t0001g0171others(2): Show | 5 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+25111T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9232341 | ||||||
| chr2:9232418
|
G | A | 12 | a0001c0002t0002g0202a0001c0002t0003g0188a0001c0003t0001g0165others(9): Show | 12 | HG01074.hp2 HG01361.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.126+25188G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9232418 | ||||||
| chr2:9232601
|
G | A | 2 | a0001c0003t0004g0038a0001c0003t0021g0040 | 2 | HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.126+25371G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9232601 | ||||||
| chr2:9232713
|
C | T | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+25483C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9232713 | ||||||
| chr2:9232908
|
C | A | 1 | a0001c0002t0003g0124 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.126+25678C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9232908 | ||||||
| chr2:9232931
|
C | T | 1 | a0002c0001t0001g0140 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.126+25701C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9232931 | ||||||
| chr2:9232961
|
T | C | 1 | a0001c0002t0003g0188 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.126+25731T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9232961 | ||||||
| chr2:9233121
|
G | A | 119 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(116): Show | 119 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.126+25891G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9233121 | ||||||
| chr2:9233192
|
T | C | 3 | a0001c0002t0008g0048a0001c0003t0004g0011a0001c0004t0005g0185 | 3 | HG02257.hp2 HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.126+25962T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9233192 | ||||||
| chr2:9233633
|
T | C | 1 | a0001c0002t0009g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.126+26403T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9233633 | ||||||
| chr2:9233928
|
C | T | 1 | a0002c0001t0001g0083 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.126+26698C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9233928 | ||||||
| chr2:9234004
|
G | A | 1 | a0002c0001t0001g0070 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.126+26774G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9234004 | ||||||
| chr2:9234098
|
G | A | 1 | a0001c0002t0008g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.126+26868G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9234098 | ||||||
| chr2:9234110
|
C | CA | 8 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(5): Show | 8 | HG00597.hp1 HG01071.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.126+26901dupA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9234110 | |||||
| chr2:9234110
|
CA | C | 97 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0007others(94): Show | 97 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.126+26901delA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9234110 | |||||
| chr2:9234110
|
CAAA | C | 9 | a0001c0002t0003g0094a0002c0001t0001g0042a0002c0001t0001g0088others(6): Show | 9 | HG00735.hp2 HG01346.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+26899_126+2690 others(7): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9234110 | |||||
| chr2:9234112
|
A | G | 1 | a0002c0001t0010g0066 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.126+26882A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9234112 | ||||||
| chr2:9234256
|
CAGCTTCC others(8): Show |
C | 1 | a0002c0001t0003g0099 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.126+27037_126+2705 others(19): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9234256 | |||||
| chr2:9234370
|
C | T | 1 | a0001c0002t0009g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.126+27140C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9234370 | ||||||
| chr2:9234456
|
G | C | 1 | a0002c0001t0001g0100 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.126+27226G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9234456 | ||||||
| chr2:9234524
|
G | T | 1 | a0001c0002t0002g0060 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.126+27294G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9234524 | ||||||
| chr2:9234640
|
T | C | 1 | a0001c0002t0009g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.126+27410T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9234640 | ||||||
| chr2:9234909
|
T | C | 1 | a0001c0002t0019g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.126+27679T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9234909 | ||||||
| chr2:9235016
|
C | T | 1 | a0002c0001t0001g0161 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.126+27786C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9235016 | ||||||
| chr2:9235035
|
C | T | 40 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(37): Show | 40 | HG00642.hp1 HG00738.hp1 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.126+27805C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9235035 | ||||||
| chr2:9235109
|
A | G | 1 | a0001c0004t0005g0205 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.126+27879A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9235109 | ||||||
| chr2:9235188
|
C | T | 24 | a0001c0002t0003g0166a0001c0003t0001g0029a0001c0003t0001g0153others(21): Show | 24 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.126+27958C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9235188 | ||||||
| chr2:9235262
|
G | A | 1 | a0002c0001t0001g0023 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.126+28032G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9235262 | ||||||
| chr2:9235319
|
GTTTTCT | G | 10 | a0001c0002t0003g0094a0001c0002t0008g0206a0002c0001t0001g0042others(7): Show | 10 | HG00735.hp2 HG01346.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.126+28094_126+2809 others(10): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9235319 | |||||
| chr2:9235444
|
A | G | 9 | a0001c0002t0003g0094a0002c0001t0001g0042a0002c0001t0001g0088others(6): Show | 9 | HG00735.hp2 HG01346.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+28214A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9235444 | ||||||
| chr2:9235496
|
C | CAGCA | 4 | a0001c0002t0008g0048a0001c0002t0008g0206a0001c0003t0004g0011others(1): Show | 4 | HG02257.hp2 HG02976.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+28267_126+2827 others(8): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9235496 | |||||
| chr2:9235518
|
C | T | 1 | a0001c0004t0005g0035 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.126+28288C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9235518 | ||||||
| chr2:9235627
|
T | C | 121 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(118): Show | 121 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.126+28397T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9235627 | ||||||
| chr2:9235882
|
G | A | 130 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(127): Show | 130 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.126+28652G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9235882 | ||||||
| chr2:9235933
|
C | T | 26 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(23): Show | 26 | HG00280.hp1 HG00639.hp1 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.126+28703C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9235933 | ||||||
| chr2:9236231
|
A | G | 5 | a0001c0002t0001g0115a0001c0002t0001g0116a0001c0002t0001g0126others(2): Show | 5 | HG01106.hp2 HG01256.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+29001A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9236231 | ||||||
| chr2:9236308
|
G | A | 2 | a0001c0002t0019g0164a0001c0003t0004g0200 | 2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.126+29078G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9236308 | ||||||
| chr2:9236706
|
A | C | 38 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(35): Show | 38 | HG00280.hp1 HG00639.hp1 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.126+29476A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9236706 | ||||||
| chr2:9236993
|
G | C | 1 | a0002c0001t0001g0090 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.126+29763G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9236993 | ||||||
| chr2:9237144
|
G | C | 1 | a0001c0003t0021g0040 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.126+29914G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9237144 | ||||||
| chr2:9237177
|
TA | T | 11 | a0001c0002t0003g0094a0002c0001t0001g0042a0002c0001t0001g0085others(8): Show | 11 | HG00438.hp2 HG00735.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.126+29957delA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9237177 | |||||
| chr2:9237414
|
C | CT | 68 | a0001c0002t0001g0097a0001c0002t0001g0126a0001c0002t0002g0007others(65): Show | 68 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.126+30201dupT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9237414 | |||||
| chr2:9237414
|
C | CTT | 5 | a0001c0002t0023g0008a0001c0003t0001g0029a0001c0004t0005g0010others(2): Show | 5 | HG02451.hp2 HG02523.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+30200_126+3020 others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9237414 | |||||
| chr2:9237748
|
G | A | 22 | a0001c0002t0003g0166a0001c0003t0001g0153a0001c0003t0006g0006others(19): Show | 22 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(19): Show |
intron_variant | MODIFIER | c.126+30518G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9237748 | ||||||
| chr2:9237855
|
A | G | 1 | a0001c0002t0008g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.126+30625A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9237855 | ||||||
| chr2:9237891
|
G | A | 1 | a0001c0003t0006g0135 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.126+30661G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9237891 | ||||||
| chr2:9238069
|
ATGGCTC | A | 9 | a0001c0002t0003g0094a0002c0001t0001g0042a0002c0001t0001g0088others(6): Show | 9 | HG00735.hp2 HG01346.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+30844_126+3084 others(10): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9238069 | |||||
| chr2:9238079
|
C | G | 1 | a0001c0004t0005g0041 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.126+30849C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9238079 | ||||||
| chr2:9238152
|
T | C | 1 | a0002c0001t0001g0023 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.126+30922T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9238152 | ||||||
| chr2:9238357
|
G | A | 1 | a0002c0001t0001g0157 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.126+31127G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9238357 | ||||||
| chr2:9238522
|
G | C | 8 | a0001c0003t0007g0170a0001c0003t0007g0199a0001c0004t0005g0192others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.126+31292G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9238522 | ||||||
| chr2:9238547
|
C | G | 1 | a0001c0004t0005g0205 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.126+31317C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9238547 | ||||||
| chr2:9238800
|
G | A | 8 | a0002c0001t0001g0042a0002c0001t0001g0088a0002c0001t0001g0089others(5): Show | 8 | HG00735.hp2 HG01346.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.126+31570G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9238800 | ||||||
| chr2:9238873
|
A | G | 1 | a0004c0015t0015g0123 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.126+31643A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9238873 | ||||||
| chr2:9238956
|
A | G | 1 | a0002c0001t0001g0049 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.126+31726A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9238956 | ||||||
| chr2:9239015
|
A | G | 3 | a0001c0002t0008g0048a0001c0003t0004g0011a0001c0004t0005g0185 | 3 | HG02257.hp2 HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.126+31785A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9239015 | ||||||
| chr2:9239152
|
C | T | 4 | a0001c0002t0002g0069a0001c0002t0002g0187a0001c0002t0022g0120others(1): Show | 4 | HG00673.hp2 HG02135.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+31922C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9239152 | ||||||
| chr2:9239219
|
A | G | 1 | a0001c0003t0001g0190 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.126+31989A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9239219 | ||||||
| chr2:9239420
|
A | G | 4 | a0001c0003t0006g0104a0001c0003t0006g0105a0001c0003t0006g0158others(1): Show | 4 | HG00597.hp2 NA19009.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+32190A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9239420 | ||||||
| chr2:9239444
|
CAT | C | 40 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(37): Show | 40 | HG00642.hp1 HG00738.hp1 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.126+32215_126+3221 others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9239444 | ||||||
| chr2:9239516
|
C | G | 124 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(121): Show | 124 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.126+32286C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9239516 | ||||||
| chr2:9239642
|
T | C | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+32412T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9239642 | ||||||
| chr2:9239647
|
C | T | 1 | a0001c0002t0009g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.126+32417C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9239647 | ||||||
| chr2:9239648
|
G | A | 2 | a0001c0002t0008g0048a0001c0003t0004g0011 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.126+32418G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9239648 | ||||||
| chr2:9239739
|
T | G | 63 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(60): Show | 63 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.126+32509T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9239739 | ||||||
| chr2:9239882
|
A | G | 1 | a0001c0002t0006g0183 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.126+32652A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9239882 | ||||||
| chr2:9239912
|
T | G | 124 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(121): Show | 124 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.126+32682T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9239912 | ||||||
| chr2:9240042
|
G | A | 124 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(121): Show | 124 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.126+32812G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9240042 | ||||||
| chr2:9240159
|
C | T | 1 | a0001c0002t0008g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.126+32929C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9240159 | ||||||
| chr2:9240178
|
G | A | 24 | a0001c0002t0003g0166a0001c0003t0001g0029a0001c0003t0001g0153others(21): Show | 24 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.126+32948G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9240178 | ||||||
| chr2:9240208
|
C | T | 1 | a0001c0012t0003g0033 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.126+32978C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9240208 | ||||||
| chr2:9240209
|
G | A | 28 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(25): Show | 28 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.126+32979G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9240209 | ||||||
| chr2:9240245
|
A | T | 1 | a0002c0001t0001g0087 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.126+33015A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9240245 | ||||||
| chr2:9240245
|
AT | A | 43 | a0001c0002t0001g0024a0001c0002t0001g0115a0001c0002t0001g0133others(40): Show | 43 | HG00642.hp1 HG00738.hp1 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.126+33037delT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9240245 | |||||
| chr2:9240245
|
ATTTTTTT | A | 9 | a0001c0002t0003g0094a0002c0001t0001g0042a0002c0001t0001g0088others(6): Show | 9 | HG00735.hp2 HG01346.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+33031_126+3303 others(11): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9240245 | |||||
| chr2:9240259
|
T | A | 1 | a0001c0013t0017g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126+33029T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9240259 | ||||||
| chr2:9240509
|
G | T | 1 | a0001c0004t0005g0176 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.126+33279G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9240509 | ||||||
| chr2:9240553
|
A | C | 125 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(122): Show | 125 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.126+33323A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9240553 | ||||||
| chr2:9240592
|
C | A | 2 | a0001c0003t0016g0174a0001c0010t0018g0173 | 2 | HG02145.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.126+33362C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9240592 | ||||||
| chr2:9240717
|
C | T | 9 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(6): Show | 9 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+33487C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9240717 | ||||||
| chr2:9240782
|
C | T | 2 | a0001c0004t0005g0176a0001c0007t0001g0030 | 2 | HG01175.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.126+33552C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9240782 | ||||||
| chr2:9240925
|
T | C | 10 | a0001c0002t0003g0094a0001c0002t0019g0164a0002c0001t0001g0042others(7): Show | 10 | HG00735.hp2 HG01346.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.126+33695T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9240925 | ||||||
| chr2:9241098
|
G | C | 36 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(33): Show | 36 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.126+33868G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9241098 | ||||||
| chr2:9241137
|
G | A | 124 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(121): Show | 124 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.126+33907G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9241137 | ||||||
| chr2:9241414
|
A | AT | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+34185dupT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9241414 | |||||
| chr2:9241483
|
A | T | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+34253A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9241483 | ||||||
| chr2:9241538
|
T | C | 10 | a0001c0002t0002g0202a0001c0002t0003g0188a0001c0003t0004g0020others(7): Show | 10 | HG01074.hp2 HG01361.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+34308T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9241538 | ||||||
| chr2:9241602
|
C | G | 1 | a0001c0002t0009g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.126+34372C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9241602 | ||||||
| chr2:9241698
|
T | C | 26 | a0001c0002t0003g0166a0001c0002t0008g0048a0001c0003t0001g0029others(23): Show | 26 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.126+34468T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9241698 | ||||||
| chr2:9241806
|
G | A | 1 | a0001c0002t0003g0147 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.126+34576G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9241806 | ||||||
| chr2:9241964
|
CAT | C | 7 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0027others(4): Show | 7 | HG01167.hp2 HG01168.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+34735_126+3473 others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9241964 | ||||||
| chr2:9242214
|
G | A | 29 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(26): Show | 29 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.126+34984G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9242214 | ||||||
| chr2:9242226
|
G | A | 1 | a0001c0003t0001g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.126+34996G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9242226 | ||||||
| chr2:9242653
|
C | G | 36 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(33): Show | 36 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.126+35423C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9242653 | ||||||
| chr2:9242795
|
A | G | 9 | a0001c0002t0003g0094a0002c0001t0001g0042a0002c0001t0001g0088others(6): Show | 9 | HG00735.hp2 HG01346.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+35565A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9242795 | ||||||
| chr2:9242846
|
A | G | 3 | a0001c0002t0002g0202a0001c0002t0003g0188a0001c0003t0004g0020 | 3 | HG02809.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.126+35616A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9242846 | ||||||
| chr2:9242967
|
T | C | 2 | a0001c0002t0002g0198a0001c0002t0013g0001 | 2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.126+35737T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9242967 | ||||||
| chr2:9243120
|
T | C | 2 | a0001c0004t0005g0176a0001c0007t0001g0030 | 2 | HG01175.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.126+35890T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9243120 | ||||||
| chr2:9243132
|
G | A | 2 | a0001c0003t0001g0210a0001c0004t0005g0205 | 2 | HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.126+35902G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9243132 | ||||||
| chr2:9243148
|
G | A | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.126+35918G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9243148 | ||||||
| chr2:9243234
|
A | G | 1 | a0001c0002t0019g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.126+36004A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9243234 | ||||||
| chr2:9243329
|
C | T | 1 | a0002c0005t0001g0098 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.127-35988C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9243329 | ||||||
| chr2:9243343
|
C | T | 120 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(117): Show | 120 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.127-35974C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9243343 | ||||||
| chr2:9243365
|
C | T | 1 | a0002c0001t0001g0036 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.127-35952C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9243365 | ||||||
| chr2:9243442
|
T | G | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127-35875T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9243442 | ||||||
| chr2:9243475
|
C | T | 1 | a0001c0003t0004g0044 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.127-35842C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9243475 | ||||||
| chr2:9243515
|
C | A | 1 | a0002c0001t0001g0140 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.127-35802C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9243515 | ||||||
| chr2:9243563
|
T | C | 2 | a0001c0002t0008g0048a0001c0003t0004g0011 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.127-35754T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9243563 | ||||||
| chr2:9243587
|
T | C | 9 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(6): Show | 9 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-35730T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9243587 | ||||||
| chr2:9243673
|
T | C | 38 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(35): Show | 38 | HG00280.hp1 HG00639.hp1 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.127-35644T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9243673 | ||||||
| chr2:9243725
|
G | A | 1 | a0001c0003t0001g0171 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.127-35592G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9243725 | ||||||
| chr2:9244032
|
G | A | 1 | a0001c0002t0003g0094 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.127-35285G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9244032 | ||||||
| chr2:9244247
|
G | A | 64 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(61): Show | 64 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.127-35070G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9244247 | ||||||
| chr2:9244580
|
C | T | 1 | a0002c0001t0001g0095 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.127-34737C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9244580 | ||||||
| chr2:9244679
|
A | G | 1 | a0001c0009t0004g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.127-34638A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9244679 | ||||||
| chr2:9244833
|
T | C | 124 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(121): Show | 124 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.127-34484T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9244833 | ||||||
| chr2:9244923
|
G | T | 1 | a0001c0011t0001g0178 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.127-34394G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9244923 | ||||||
| chr2:9244953
|
C | T | 1 | a0002c0001t0001g0036 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.127-34364C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9244953 | ||||||
| chr2:9245010
|
ATAAAAGG | A | 2 | a0001c0002t0008g0048a0001c0003t0004g0011 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.127-34300_127-3429 others(11): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9245010 | |||||
| chr2:9245070
|
C | T | 1 | a0001c0002t0019g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.127-34247C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9245070 | ||||||
| chr2:9245108
|
C | G | 2 | a0001c0002t0008g0048a0001c0003t0004g0011 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.127-34209C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9245108 | ||||||
| chr2:9245247
|
T | G | 1 | a0001c0004t0005g0028 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.127-34070T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9245247 | ||||||
| chr2:9245283
|
G | A | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-34034G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9245283 | ||||||
| chr2:9245299
|
C | T | 6 | a0001c0002t0003g0209a0001c0002t0009g0208a0001c0004t0005g0191others(3): Show | 6 | HG02886.hp2 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-34018C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9245299 | ||||||
| chr2:9245425
|
T | A | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-33892T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9245425 | ||||||
| chr2:9245500
|
C | CA | 129 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(126): Show | 129 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.127-33817_127-3381 others(5): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9245500 | ||||||
| chr2:9245746
|
G | C | 2 | a0001c0002t0002g0073a0002c0001t0001g0157 | 2 | HG01074.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.127-33571G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9245746 | ||||||
| chr2:9245812
|
A | G | 1 | a0002c0001t0001g0163 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.127-33505A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9245812 | ||||||
| chr2:9245839
|
T | C | 38 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(35): Show | 38 | HG00280.hp1 HG00639.hp1 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.127-33478T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9245839 | ||||||
| chr2:9245931
|
GC | G | 4 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(1): Show | 4 | HG02280.hp1 HG02630.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-33382delC | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9245931 | |||||
| chr2:9245977
|
A | G | 1 | a0001c0002t0008g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.127-33340A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9245977 | ||||||
| chr2:9246422
|
AGCTACAG others(6): Show |
A | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127-32890_127-3287 others(17): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9246422 | |||||
| chr2:9246442
|
A | T | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127-32875A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9246442 | ||||||
| chr2:9246445
|
C | G | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127-32872C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9246445 | ||||||
| chr2:9246486
|
A | G | 1 | a0002c0001t0003g0099 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.127-32831A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9246486 | ||||||
| chr2:9246581
|
A | T | 26 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(23): Show | 26 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.127-32736A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9246581 | ||||||
| chr2:9247016
|
G | A | 2 | a0001c0002t0002g0198a0001c0002t0013g0001 | 2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.127-32301G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9247016 | ||||||
| chr2:9247164
|
A | G | 1 | a0001c0002t0006g0183 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.127-32153A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9247164 | ||||||
| chr2:9247208
|
C | T | 1 | a0002c0001t0001g0161 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.127-32109C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9247208 | ||||||
| chr2:9247367
|
C | T | 1 | a0002c0001t0001g0093 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.127-31950C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9247367 | ||||||
| chr2:9247928
|
A | G | 23 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(20): Show | 23 | HG00323.hp2 HG00597.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.127-31389A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9247928 | ||||||
| chr2:9247953
|
A | G | 1 | a0002c0001t0001g0089 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.127-31364A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9247953 | ||||||
| chr2:9248087
|
G | T | 2 | a0001c0002t0019g0164a0001c0003t0004g0200 | 2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.127-31230G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9248087 | ||||||
| chr2:9248208
|
C | T | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-31109C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9248208 | ||||||
| chr2:9248267
|
G | T | 1 | a0002c0001t0001g0082 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.127-31050G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9248267 | ||||||
| chr2:9248358
|
T | C | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127-30959T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9248358 | ||||||
| chr2:9248404
|
T | C | 1 | a0001c0002t0003g0150 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.127-30913T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9248404 | ||||||
| chr2:9248543
|
G | A | 1 | a0001c0003t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.127-30774G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9248543 | ||||||
| chr2:9248652
|
G | A | 1 | a0001c0003t0001g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.127-30665G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9248652 | ||||||
| chr2:9248995
|
G | A | 1 | a0001c0002t0009g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.127-30322G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9248995 | ||||||
| chr2:9249012
|
G | A | 1 | a0001c0004t0005g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.127-30305G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9249012 | ||||||
| chr2:9249110
|
G | T | 4 | a0001c0003t0001g0029a0001c0004t0005g0010a0001c0004t0005g0021others(1): Show | 4 | HG02451.hp2 HG02818.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-30207G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9249110 | ||||||
| chr2:9249202
|
A | G | 2 | a0001c0004t0005g0034a0001c0004t0005g0144 | 2 | HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.127-30115A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9249202 | ||||||
| chr2:9249310
|
C | A | 1 | a0002c0001t0001g0111 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.127-30007C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9249310 | ||||||
| chr2:9249337
|
C | T | 107 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(104): Show | 107 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.127-29980C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9249337 | ||||||
| chr2:9249365
|
C | T | 1 | a0001c0004t0005g0205 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.127-29952C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9249365 | ||||||
| chr2:9249683
|
G | T | 102 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(99): Show | 102 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.127-29634G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9249683 | ||||||
| chr2:9249684
|
C | T | 1 | a0001c0002t0003g0166 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.127-29633C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9249684 | ||||||
| chr2:9249728
|
AGGCATGC others(44): Show |
A | 1 | a0002c0005t0001g0132 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.127-29584_127-2953 others(55): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9249728 | |||||
| chr2:9249763
|
T | C | 12 | a0001c0002t0003g0094a0001c0002t0008g0206a0001c0002t0009g0031others(9): Show | 12 | HG00735.hp2 HG01346.hp1 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.127-29554T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9249763 | ||||||
| chr2:9249775
|
A | G | 1 | a0001c0009t0004g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.127-29542A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9249775 | ||||||
| chr2:9249986
|
T | C | 1 | a0002c0001t0001g0074 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.127-29331T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9249986 | ||||||
| chr2:9250263
|
A | G | 41 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(38): Show | 41 | HG00642.hp1 HG00738.hp1 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.127-29054A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9250263 | ||||||
| chr2:9250300
|
A | G | 129 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(126): Show | 129 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.127-29017A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9250300 | ||||||
| chr2:9250437
|
T | C | 1 | a0001c0003t0021g0040 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.127-28880T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9250437 | ||||||
| chr2:9250457
|
G | A | 18 | a0001c0002t0003g0094a0001c0002t0008g0048a0001c0002t0008g0206others(15): Show | 18 | HG00735.hp2 HG01346.hp1 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.127-28860G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9250457 | ||||||
| chr2:9250525
|
C | T | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127-28792C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9250525 | ||||||
| chr2:9250591
|
GGT | G | 108 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(105): Show | 108 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.127-28722_127-2872 others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9250591 | |||||
| chr2:9250930
|
A | G | 2 | a0001c0002t0003g0062a0001c0002t0003g0124 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.127-28387A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9250930 | ||||||
| chr2:9251004
|
G | A | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127-28313G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9251004 | ||||||
| chr2:9251130
|
G | A | 2 | a0001c0002t0008g0206a0001c0002t0009g0031 | 2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.127-28187G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9251130 | ||||||
| chr2:9251155
|
C | T | 8 | a0001c0003t0006g0064a0001c0003t0006g0065a0001c0003t0006g0102others(5): Show | 8 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(5): Show |
intron_variant | MODIFIER | c.127-28162C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9251155 | ||||||
| chr2:9251172
|
G | A | 6 | a0001c0002t0008g0206a0001c0002t0009g0031a0001c0003t0001g0169others(3): Show | 6 | HG01496.hp2 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-28145G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9251172 | ||||||
| chr2:9251490
|
C | T | 121 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(118): Show | 121 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.127-27827C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9251490 | ||||||
| chr2:9251499
|
G | A | 83 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0129others(80): Show | 83 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.127-27818G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9251499 | ||||||
| chr2:9251501
|
C | T | 1 | a0001c0004t0005g0035 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.127-27816C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9251501 | ||||||
| chr2:9251536
|
C | T | 1 | a0001c0004t0005g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.127-27781C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9251536 | ||||||
| chr2:9251562
|
C | T | 37 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(34): Show | 37 | HG00280.hp1 HG00639.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.127-27755C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9251562 | ||||||
| chr2:9251698
|
G | A | 1 | a0001c0002t0002g0027 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.127-27619G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9251698 | ||||||
| chr2:9251836
|
T | C | 133 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(130): Show | 133 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.127-27481T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9251836 | ||||||
| chr2:9251851
|
T | C | 93 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0129others(90): Show | 93 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.127-27466T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9251851 | ||||||
| chr2:9252065
|
C | G | 39 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0129others(36): Show | 39 | HG00642.hp1 HG00738.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.127-27252C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9252065 | ||||||
| chr2:9252165
|
C | A | 1 | a0001c0003t0001g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.127-27152C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9252165 | ||||||
| chr2:9252401
|
C | A | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127-26916C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9252401 | ||||||
| chr2:9252412
|
C | G | 1 | a0001c0003t0001g0172 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.127-26905C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9252412 | ||||||
| chr2:9252585
|
C | T | 1 | a0003c0014t0003g0051 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.127-26732C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9252585 | ||||||
| chr2:9252592
|
C | A | 5 | a0001c0002t0008g0206a0001c0003t0001g0169a0001c0003t0001g0171others(2): Show | 5 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-26725C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9252592 | ||||||
| chr2:9252686
|
C | T | 1 | a0002c0001t0001g0084 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.127-26631C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9252686 | ||||||
| chr2:9252733
|
G | A | 1 | a0001c0002t0008g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.127-26584G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9252733 | ||||||
| chr2:9252894
|
G | C | 1 | a0001c0002t0006g0183 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.127-26423G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9252894 | ||||||
| chr2:9252901
|
C | T | 37 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(34): Show | 37 | HG00642.hp1 HG00738.hp1 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.127-26416C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9252901 | ||||||
| chr2:9252914
|
C | CA | 103 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(100): Show | 103 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.127-26386dupA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9252914 | |||||
| chr2:9252914
|
C | CAA | 13 | a0001c0002t0003g0094a0001c0004t0005g0034a0001c0004t0005g0176others(10): Show | 13 | HG00408.hp1 HG00735.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.127-26387_127-2638 others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9252914 | |||||
| chr2:9253118
|
G | C | 9 | a0001c0002t0003g0094a0002c0001t0001g0042a0002c0001t0001g0088others(6): Show | 9 | HG00735.hp2 HG01346.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-26199G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9253118 | ||||||
| chr2:9253174
|
C | T | 119 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(116): Show | 119 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.127-26143C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9253174 | ||||||
| chr2:9253225
|
G | A | 1 | a0002c0001t0001g0140 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.127-26092G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9253225 | ||||||
| chr2:9253357
|
A | G | 3 | a0001c0003t0006g0080a0002c0001t0001g0117a0002c0001t0020g0079 | 3 | HG02080.hp1 NA18612.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.127-25960A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9253357 | ||||||
| chr2:9253413
|
G | A | 1 | a0001c0003t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.127-25904G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9253413 | ||||||
| chr2:9253423
|
CA | C | 38 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(35): Show | 38 | HG00642.hp1 HG00738.hp1 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.127-25891delA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9253423 | |||||
| chr2:9253432
|
A | G | 152 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(149): Show | 152 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.127-25885A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9253432 | ||||||
| chr2:9253718
|
T | A | 1 | a0002c0001t0001g0140 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.127-25599T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9253718 | ||||||
| chr2:9253889
|
G | A | 4 | a0001c0003t0001g0029a0001c0004t0005g0010a0001c0004t0005g0021others(1): Show | 4 | HG02451.hp2 HG02818.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-25428G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9253889 | ||||||
| chr2:9253895
|
A | G | 1 | a0001c0002t0012g0143 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.127-25422A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9253895 | ||||||
| chr2:9254077
|
G | A | 1 | a0002c0001t0001g0106 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.127-25240G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254077 | ||||||
| chr2:9254119
|
T | C | 2 | a0002c0005t0001g0119a0004c0015t0015g0123 | 2 | HG01358.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.127-25198T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254119 | ||||||
| chr2:9254208
|
C | CAAAA | 9 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0137others(6): Show | 9 | HG00639.hp1 HG00673.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-25083_127-2508 others(8): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254208 | |||||
| chr2:9254208
|
C | CAAAAA | 7 | a0001c0002t0002g0107a0001c0002t0002g0139a0001c0002t0002g0187others(4): Show | 7 | HG00735.hp1 HG01515.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-25084_127-2508 others(9): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254208 | |||||
| chr2:9254208
|
CA | C | 6 | a0001c0002t0006g0183a0001c0003t0001g0171a0002c0001t0001g0036others(3): Show | 6 | HG00438.hp2 HG00741.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-25080delA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254208 | |||||
| chr2:9254208
|
CAA | C | 10 | a0001c0002t0006g0184a0001c0003t0001g0172a0001c0006t0004g0063others(7): Show | 10 | HG00609.hp2 HG02145.hp2 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.127-25081_127-2508 others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254208 | |||||
| chr2:9254208
|
CAAA | C | 9 | a0001c0002t0003g0052a0001c0006t0004g0014a0001c0006t0004g0018others(6): Show | 9 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-25082_127-2508 others(7): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254208 | |||||
| chr2:9254208
|
CAAAAAAA others(3): Show |
C | 9 | a0001c0003t0006g0006a0001c0003t0006g0064a0001c0003t0006g0065others(6): Show | 9 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-25089_127-2508 others(14): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254208 | |||||
| chr2:9254208
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0003t0006g0135 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.127-25090_127-2508 others(15): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254208 | |||||
| chr2:9254226
|
A | T | 1 | a0001c0002t0009g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.127-25091A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254226 | ||||||
| chr2:9254228
|
A | ATATATAT others(12): Show |
1 | a0001c0010t0018g0173 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.127-25089_127-2508 others(23): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254228 | ||||||
| chr2:9254228
|
A | ATATATAT others(14): Show |
1 | a0001c0003t0016g0174 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.127-25089_127-2508 others(25): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254228 | ||||||
| chr2:9254228
|
A | T | 1 | a0001c0002t0009g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.127-25089A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254228 | ||||||
| chr2:9254228
|
AAAAAAAA others(3): Show |
A | 1 | a0002c0001t0001g0067 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.127-25087_127-2507 others(14): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254228 | |||||
| chr2:9254230
|
A | T | 3 | a0001c0002t0009g0031a0001c0003t0016g0174a0001c0010t0018g0173 | 3 | HG02145.hp1 HG02895.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.127-25087A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254230 | ||||||
| chr2:9254232
|
A | T | 4 | a0001c0002t0009g0031a0001c0003t0016g0174a0001c0004t0005g0176others(1): Show | 4 | HG02145.hp1 HG02886.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-25085A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254232 | ||||||
| chr2:9254234
|
A | T | 13 | a0001c0002t0009g0031a0001c0003t0016g0174a0001c0004t0005g0176others(10): Show | 13 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.127-25083A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254234 | ||||||
| chr2:9254235
|
AAAT | A | 14 | a0001c0002t0001g0116a0001c0002t0001g0126a0001c0002t0003g0026others(11): Show | 14 | HG00323.hp2 HG00738.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.127-25080_127-2507 others(7): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254235 | |||||
| chr2:9254236
|
A | AAAAAAAA others(20): Show |
1 | a0001c0004t0005g0028 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.127-25080_127-2507 others(31): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAA others(16): Show |
1 | a0001c0004t0005g0205 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.127-25080_127-2507 others(27): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAA others(27): Show |
1 | a0002c0001t0001g0168 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.127-25080_127-2507 others(38): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAA others(8): Show |
2 | a0001c0002t0003g0141a0001c0004t0005g0138 | 2 | HG01346.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.127-25080_127-2507 others(19): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAA others(20): Show |
1 | a0002c0001t0001g0090 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.127-25080_127-2507 others(31): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAA others(26): Show |
1 | a0001c0003t0004g0200 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.127-25080_127-2507 others(37): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAA others(32): Show |
1 | a0001c0002t0002g0129 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.127-25080_127-2507 others(43): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAA others(9): Show |
1 | a0001c0003t0004g0043 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.127-25080_127-2507 others(20): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAA others(29): Show |
1 | a0002c0005t0001g0009 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.127-25080_127-2507 others(40): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAA others(33): Show |
1 | a0002c0005t0001g0101 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.127-25080_127-2507 others(44): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAA others(8): Show |
1 | a0001c0003t0004g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.127-25080_127-2507 others(19): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAA others(10): Show |
3 | a0001c0002t0002g0069a0001c0002t0012g0143a0002c0005t0001g0098 | 3 | HG01257.hp2 HG02135.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.127-25080_127-2507 others(21): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAA others(12): Show |
2 | a0002c0005t0001g0003a0002c0005t0001g0054 | 2 | HG01074.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.127-25080_127-2507 others(23): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAA others(18): Show |
1 | a0001c0003t0007g0199 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.127-25080_127-2507 others(29): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAA others(24): Show |
2 | a0001c0002t0001g0133a0001c0003t0007g0170 | 2 | NA19240.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.127-25080_127-2507 others(35): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAA others(28): Show |
1 | a0002c0005t0001g0130 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.127-25080_127-2507 others(39): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAA others(32): Show |
2 | a0001c0004t0005g0192a0001c0004t0005g0193 | 2 | HG01109.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.127-25080_127-2507 others(43): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAA others(34): Show |
1 | a0001c0004t0005g0201 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.127-25080_127-2507 others(45): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAA others(5): Show |
1 | a0001c0003t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.127-25080_127-2507 others(16): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAA others(9): Show |
1 | a0001c0002t0022g0120 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.127-25080_127-2507 others(20): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAA others(11): Show |
3 | a0001c0002t0002g0016a0001c0002t0002g0177a0002c0001t0001g0140 | 3 | HG01099.hp1 HG01256.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.127-25080_127-2507 others(22): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAA others(13): Show |
1 | a0002c0001t0001g0093 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.127-25080_127-2507 others(24): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAA others(19): Show |
1 | a0001c0004t0005g0194 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.127-25080_127-2507 others(30): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAA others(23): Show |
1 | a0002c0001t0001g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.127-25080_127-2507 others(34): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAA others(29): Show |
2 | a0001c0004t0005g0195a0002c0001t0001g0042 | 2 | HG00735.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.127-25080_127-2507 others(40): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAT others(8): Show |
1 | a0002c0001t0001g0022 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.127-25080_127-2507 others(19): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAT others(10): Show |
1 | a0001c0002t0003g0142 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.127-25080_127-2507 others(21): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAT others(16): Show |
1 | a0001c0002t0019g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.127-25080_127-2507 others(27): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAT others(18): Show |
1 | a0002c0001t0001g0088 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.127-25080_127-2507 others(29): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAT others(22): Show |
1 | a0001c0002t0002g0162 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.127-25080_127-2507 others(33): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAT others(24): Show |
1 | a0002c0005t0001g0131 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.127-25080_127-2507 others(35): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAT others(26): Show |
2 | a0002c0001t0001g0081a0002c0005t0001g0132 | 2 | HG01106.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.127-25080_127-2507 others(37): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAT others(28): Show |
1 | a0001c0003t0001g0017 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.127-25080_127-2507 others(39): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAAAT others(30): Show |
2 | a0002c0001t0001g0092a0002c0001t0014g0091 | 2 | HG02004.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.127-25080_127-2507 others(41): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAATA others(3): Show |
1 | a0001c0003t0001g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.127-25080_127-2507 others(14): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAATA others(7): Show |
3 | a0001c0002t0008g0048a0001c0003t0004g0011a0001c0007t0001g0030 | 3 | HG01175.hp2 HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.127-25080_127-2507 others(18): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAATA others(21): Show |
1 | a0002c0005t0001g0025 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.127-25080_127-2507 others(32): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAATA others(25): Show |
3 | a0001c0002t0002g0198a0001c0004t0005g0196a0002c0001t0001g0089 | 3 | HG01358.hp2 HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.127-25080_127-2507 others(36): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAATA others(27): Show |
2 | a0001c0002t0003g0148a0001c0002t0013g0001 | 2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.127-25080_127-2507 others(38): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAATA others(29): Show |
1 | a0001c0002t0003g0094 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.127-25080_127-2507 others(40): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAAATA others(31): Show |
1 | a0002c0001t0001g0127 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.127-25080_127-2507 others(42): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAATAT others(20): Show |
1 | a0001c0002t0002g0134 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.127-25080_127-2507 others(31): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAAATAT others(26): Show |
1 | a0001c0002t0001g0024 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.127-25080_127-2507 others(37): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAAATATA others(21): Show |
1 | a0001c0013t0017g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127-25080_127-2507 others(32): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAATATAT others(8): Show |
1 | a0001c0003t0001g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.127-25080_127-2507 others(19): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AAATATAT others(22): Show |
1 | a0001c0004t0005g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.127-25080_127-2507 others(33): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254236
|
A | AT | 3 | a0001c0003t0001g0190a0001c0004t0005g0035a0001c0004t0005g0185 | 3 | HG02976.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.127-25081_127-2508 others(5): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254236 | ||||||
| chr2:9254236
|
A | T | 23 | a0001c0002t0003g0188a0001c0002t0008g0206a0001c0002t0009g0031others(20): Show | 23 | HG00323.hp1 HG01070.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.127-25081A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254236 | ||||||
| chr2:9254236
|
AAT | A | 27 | a0001c0002t0002g0056a0001c0002t0002g0057a0001c0002t0002g0058others(24): Show | 27 | HG00639.hp2 HG00642.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.127-25063_127-2506 others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254236 | |||||
| chr2:9254237
|
AT | A | 18 | a0001c0002t0002g0055a0001c0002t0002g0075a0001c0002t0003g0147others(15): Show | 18 | HG00280.hp2 HG00741.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.127-25079delT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254237 | ||||||
| chr2:9254238
|
T | A | 3 | a0001c0003t0001g0039a0002c0001t0001g0121a0002c0001t0001g0160 | 3 | HG00597.hp1 HG01934.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.127-25079T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254238 | ||||||
| chr2:9254240
|
T | A | 1 | a0002c0001t0001g0155 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.127-25077T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254240 | ||||||
| chr2:9254240
|
T | G | 1 | a0002c0001t0001g0157 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.127-25077T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254240 | ||||||
| chr2:9254242
|
T | C | 1 | a0001c0002t0003g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.127-25075T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254242 | ||||||
| chr2:9254252
|
T | C | 2 | a0002c0001t0001g0081a0002c0005t0001g0130 | 2 | HG02155.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.127-25065T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254252 | ||||||
| chr2:9254254
|
T | C | 58 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0129others(55): Show | 58 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.127-25063T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254254 | ||||||
| chr2:9254254
|
T | TACACAC | 4 | a0001c0002t0008g0206a0001c0002t0009g0031a0001c0003t0001g0165others(1): Show | 4 | HG01074.hp2 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-25059_127-2505 others(10): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254254 | |||||
| chr2:9254254
|
T | TACACACA others(1): Show |
11 | a0001c0002t0002g0016a0001c0002t0002g0069a0001c0002t0002g0177others(8): Show | 11 | HG01099.hp1 HG01256.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-25059_127-2505 others(12): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254254 | |||||
| chr2:9254254
|
T | TATATATA others(15): Show |
12 | a0001c0002t0001g0097a0001c0002t0002g0060a0001c0002t0002g0107others(9): Show | 12 | HG00639.hp1 HG00673.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.127-25062_127-2506 others(26): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254254 | |||||
| chr2:9254254
|
T | TATATATA others(17): Show |
1 | a0001c0002t0002g0027 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.127-25062_127-2506 others(28): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254254 | |||||
| chr2:9254254
|
T | TATATATA others(15): Show |
3 | a0001c0004t0005g0034a0001c0004t0005g0035a0001c0004t0005g0144 | 3 | HG03130.hp1 HG03471.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.127-25062_127-2506 others(26): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254254 | |||||
| chr2:9254254
|
T | TATATATA others(17): Show |
1 | a0001c0002t0002g0007 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.127-25062_127-2506 others(28): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254254 | |||||
| chr2:9254254
|
T | TATATATA others(19): Show |
1 | a0001c0002t0002g0096 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.127-25062_127-2506 others(30): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254254 | |||||
| chr2:9254254
|
T | TATATATA others(25): Show |
1 | a0001c0003t0001g0190 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.127-25062_127-2506 others(36): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254254 | |||||
| chr2:9254254
|
T | TATATATA others(19): Show |
1 | a0002c0001t0001g0122 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.127-25062_127-2506 others(30): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254254 | |||||
| chr2:9254254
|
T | TATATATA others(21): Show |
1 | a0001c0003t0004g0038 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.127-25062_127-2506 others(32): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254254 | |||||
| chr2:9254254
|
T | TATATATA others(23): Show |
1 | a0001c0002t0003g0188 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.127-25062_127-2506 others(34): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254254 | |||||
| chr2:9254254
|
T | TATATATA others(27): Show |
1 | a0001c0003t0001g0039 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.127-25062_127-2506 others(38): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254254 | |||||
| chr2:9254254
|
T | TATATATA others(17): Show |
1 | a0001c0003t0001g0029 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.127-25062_127-2506 others(28): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254254 | |||||
| chr2:9254254
|
T | TATATATA others(21): Show |
1 | a0002c0001t0001g0121 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.127-25062_127-2506 others(32): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254254 | |||||
| chr2:9254254
|
T | TATATATA others(27): Show |
1 | a0001c0002t0002g0202 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.127-25062_127-2506 others(38): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254254 | |||||
| chr2:9254254
|
T | TATATATA others(14): Show |
2 | a0001c0003t0004g0020a0001c0003t0004g0044 | 2 | HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.127-25062_127-2506 others(25): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254254 | |||||
| chr2:9254254
|
T | TTATATAT others(2): Show |
2 | a0001c0003t0004g0043a0001c0003t0004g0175 | 2 | HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.127-25063_127-2506 others(13): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254254 | ||||||
| chr2:9254256
|
C | T | 5 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(2): Show | 5 | HG01496.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-25061C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254256 | ||||||
| chr2:9254259
|
G | A | 2 | a0001c0003t0001g0210a0001c0004t0005g0185 | 2 | HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.127-25058G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254259 | ||||||
| chr2:9254260
|
T | C | 2 | a0001c0003t0001g0210a0001c0004t0005g0185 | 2 | HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.127-25057T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254260 | ||||||
| chr2:9254298
|
A | G | 120 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(117): Show | 120 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.127-25019A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254298 | ||||||
| chr2:9254353
|
C | CT | 42 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(39): Show | 42 | HG00280.hp1 HG00597.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.127-24948dupT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254353 | |||||
| chr2:9254401
|
G | A | 1 | a0001c0002t0008g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.127-24916G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254401 | ||||||
| chr2:9254445
|
C | T | 36 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(33): Show | 36 | HG00280.hp1 HG00639.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.127-24872C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254445 | ||||||
| chr2:9254502
|
A | T | 120 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(117): Show | 120 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.127-24815A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254502 | ||||||
| chr2:9254525
|
GGATTTTT others(3): Show |
G | 37 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(34): Show | 37 | HG00280.hp1 HG00639.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.127-24791_127-2478 others(14): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254525 | ||||||
| chr2:9254526
|
G | T | 172 | a0001c0002t0001g0024a0001c0002t0001g0115a0001c0002t0001g0116others(169): Show | 172 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.127-24791G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254526 | ||||||
| chr2:9254527
|
A | AT | 40 | a0001c0002t0001g0115a0001c0002t0001g0116a0001c0002t0001g0133others(37): Show | 40 | HG00438.hp2 HG00639.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.127-24764dupT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254527 | |||||
| chr2:9254527
|
A | ATT | 11 | a0001c0002t0001g0126a0001c0002t0001g0182a0001c0002t0008g0206others(8): Show | 11 | HG00673.hp1 HG00735.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.127-24765_127-2476 others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254527 | |||||
| chr2:9254527
|
A | ATTTTT | 12 | a0001c0003t0001g0029a0001c0003t0004g0200a0001c0003t0006g0006others(9): Show | 12 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(9): Show |
intron_variant | MODIFIER | c.127-24768_127-2476 others(9): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254527 | |||||
| chr2:9254527
|
A | ATTTTTT | 10 | a0001c0002t0008g0048a0001c0003t0001g0046a0001c0003t0004g0011others(7): Show | 10 | HG00438.hp1 HG02155.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.127-24769_127-2476 others(10): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254527 | |||||
| chr2:9254527
|
A | ATTTTTTT | 7 | a0001c0002t0003g0166a0001c0003t0001g0153a0001c0003t0006g0104others(4): Show | 7 | HG00597.hp2 HG01175.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-24770_127-2476 others(11): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9254527 | |||||
| chr2:9254536
|
T | A | 1 | a0001c0002t0009g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.127-24781T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254536 | ||||||
| chr2:9254537
|
T | A | 37 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(34): Show | 37 | HG00280.hp1 HG00639.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.127-24780T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254537 | ||||||
| chr2:9254557
|
A | G | 4 | a0001c0003t0004g0020a0001c0003t0004g0043a0001c0003t0004g0044others(1): Show | 4 | HG02723.hp1 HG03471.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-24760A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254557 | ||||||
| chr2:9254676
|
T | C | 4 | a0001c0002t0008g0048a0001c0003t0001g0046a0001c0003t0004g0011others(1): Show | 4 | HG02257.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-24641T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254676 | ||||||
| chr2:9254731
|
C | T | 120 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(117): Show | 120 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.127-24586C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254731 | ||||||
| chr2:9254800
|
G | A | 1 | a0001c0009t0004g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.127-24517G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254800 | ||||||
| chr2:9254990
|
A | C | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-24327A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9254990 | ||||||
| chr2:9255218
|
T | C | 1 | a0001c0002t0009g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.127-24099T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9255218 | ||||||
| chr2:9255254
|
C | T | 2 | a0001c0003t0001g0171a0001c0003t0001g0172 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.127-24063C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9255254 | ||||||
| chr2:9255310
|
T | G | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127-24007T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9255310 | ||||||
| chr2:9255463
|
T | C | 1 | a0002c0001t0001g0023 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.127-23854T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9255463 | ||||||
| chr2:9255521
|
A | G | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-23796A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9255521 | ||||||
| chr2:9255694
|
C | T | 9 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(6): Show | 9 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-23623C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9255694 | ||||||
| chr2:9256162
|
C | CA | 67 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0129others(64): Show | 67 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.127-23136dupA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9256162 | |||||
| chr2:9256162
|
C | CAA | 7 | a0001c0002t0003g0148a0001c0002t0003g0166a0001c0003t0001g0153others(4): Show | 7 | HG02145.hp1 HG02486.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-23137_127-2313 others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9256162 | |||||
| chr2:9256178
|
AAAAG | A | 9 | a0001c0002t0003g0094a0002c0001t0001g0042a0002c0001t0001g0088others(6): Show | 9 | HG00735.hp2 HG01346.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-23134_127-2313 others(8): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9256178 | |||||
| chr2:9256385
|
A | G | 126 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(123): Show | 126 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.127-22932A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9256385 | ||||||
| chr2:9256387
|
A | T | 2 | a0002c0001t0001g0121a0002c0001t0001g0122 | 2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.127-22930A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9256387 | ||||||
| chr2:9256417
|
CA | C | 126 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(123): Show | 126 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.127-22898delA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9256417 | |||||
| chr2:9256590
|
G | T | 1 | a0001c0003t0001g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.127-22727G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9256590 | ||||||
| chr2:9256819
|
G | A | 2 | a0001c0002t0002g0073a0002c0001t0001g0157 | 2 | HG01074.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.127-22498G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9256819 | ||||||
| chr2:9256874
|
G | A | 126 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(123): Show | 126 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.127-22443G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9256874 | ||||||
| chr2:9257126
|
C | A | 1 | a0001c0002t0008g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.127-22191C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9257126 | ||||||
| chr2:9257140
|
T | C | 1 | a0001c0003t0001g0169 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.127-22177T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9257140 | ||||||
| chr2:9257255
|
A | G | 126 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(123): Show | 126 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.127-22062A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9257255 | ||||||
| chr2:9257293
|
A | AGGG | 70 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(67): Show | 70 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.127-22023_127-2202 others(7): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9257293 | |||||
| chr2:9257326
|
A | G | 1 | a0001c0009t0004g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.127-21991A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9257326 | ||||||
| chr2:9257404
|
C | T | 1 | a0001c0002t0008g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.127-21913C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9257404 | ||||||
| chr2:9257466
|
T | C | 1 | a0001c0002t0003g0052 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.127-21851T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9257466 | ||||||
| chr2:9257484
|
C | T | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-21833C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9257484 | ||||||
| chr2:9257559
|
C | T | 1 | a0002c0001t0001g0074 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.127-21758C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9257559 | ||||||
| chr2:9257717
|
C | G | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127-21600C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9257717 | ||||||
| chr2:9257723
|
G | A | 126 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(123): Show | 126 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.127-21594G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9257723 | ||||||
| chr2:9257741
|
G | C | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127-21576G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9257741 | ||||||
| chr2:9257776
|
G | A | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127-21541G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9257776 | ||||||
| chr2:9258111
|
A | G | 41 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(38): Show | 41 | HG00280.hp1 HG00639.hp1 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.127-21206A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9258111 | ||||||
| chr2:9258233
|
A | C | 41 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(38): Show | 41 | HG00280.hp1 HG00639.hp1 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.127-21084A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9258233 | ||||||
| chr2:9258244
|
C | CA | 94 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(91): Show | 94 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.127-21058dupA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9258244 | |||||
| chr2:9258244
|
C | CAA | 25 | a0001c0002t0003g0166a0001c0002t0008g0206a0001c0002t0009g0031others(22): Show | 25 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.127-21059_127-2105 others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9258244 | |||||
| chr2:9258244
|
C | CAAA | 9 | a0001c0002t0008g0048a0001c0003t0001g0029a0001c0003t0001g0046others(6): Show | 9 | HG01175.hp2 HG02155.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-21060_127-2105 others(7): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9258244 | |||||
| chr2:9258322
|
G | A | 1 | a0002c0001t0001g0113 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.127-20995G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9258322 | ||||||
| chr2:9258332
|
G | GT | 13 | a0001c0002t0002g0055a0001c0002t0002g0056a0001c0002t0002g0057others(10): Show | 13 | HG00609.hp1 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.127-20983dupT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9258332 | |||||
| chr2:9258332
|
G | GTT | 25 | a0001c0002t0003g0166a0001c0003t0001g0029a0001c0003t0001g0169others(22): Show | 25 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.127-20984_127-2098 others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9258332 | |||||
| chr2:9258333
|
TTG | T | 39 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(36): Show | 39 | HG00642.hp1 HG00738.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.127-20982_127-2098 others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9258333 | |||||
| chr2:9258334
|
TG | T | 6 | a0001c0002t0002g0007a0001c0002t0002g0137a0001c0002t0012g0143others(3): Show | 6 | HG01168.hp2 HG01257.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-20982delG | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9258334 | ||||||
| chr2:9258335
|
G | T | 82 | a0001c0002t0001g0097a0001c0002t0002g0016a0001c0002t0002g0027others(79): Show | 82 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.127-20982G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9258335 | ||||||
| chr2:9258458
|
G | A | 126 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(123): Show | 126 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.127-20859G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9258458 | ||||||
| chr2:9258567
|
G | A | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127-20750G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9258567 | ||||||
| chr2:9258715
|
A | G | 135 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(132): Show | 135 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.127-20602A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9258715 | ||||||
| chr2:9258819
|
C | G | 1 | a0001c0002t0008g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.127-20498C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9258819 | ||||||
| chr2:9258894
|
G | A | 1 | a0001c0004t0005g0035 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.127-20423G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9258894 | ||||||
| chr2:9258897
|
T | A | 1 | a0002c0001t0001g0036 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.127-20420T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9258897 | ||||||
| chr2:9258987
|
A | G | 126 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(123): Show | 126 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.127-20330A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9258987 | ||||||
| chr2:9259075
|
T | C | 1 | a0001c0002t0003g0094 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.127-20242T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9259075 | ||||||
| chr2:9259268
|
C | T | 1 | a0001c0009t0004g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.127-20049C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9259268 | ||||||
| chr2:9259286
|
T | C | 93 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(90): Show | 93 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.127-20031T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9259286 | ||||||
| chr2:9259294
|
C | A | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127-20023C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9259294 | ||||||
| chr2:9259538
|
A | G | 1 | a0001c0003t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.127-19779A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9259538 | ||||||
| chr2:9259553
|
CAGCCCAA others(6): Show |
C | 71 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(68): Show | 71 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.127-19762_127-1975 others(17): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9259553 | |||||
| chr2:9259562
|
A | C | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127-19755A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9259562 | ||||||
| chr2:9259564
|
C | G | 1 | a0001c0003t0001g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.127-19753C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9259564 | ||||||
| chr2:9259637
|
C | G | 70 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(67): Show | 70 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.127-19680C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9259637 | ||||||
| chr2:9259657
|
C | T | 4 | a0001c0003t0004g0020a0001c0003t0004g0043a0001c0003t0004g0044others(1): Show | 4 | HG02723.hp1 HG03471.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-19660C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9259657 | ||||||
| chr2:9259795
|
C | T | 3 | a0001c0003t0006g0064a0001c0003t0006g0065a0001c0003t0006g0102 | 3 | HG00408.hp2 HG00438.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.127-19522C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9259795 | ||||||
| chr2:9259883
|
G | A | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127-19434G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9259883 | ||||||
| chr2:9259939
|
T | C | 1 | a0001c0002t0009g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.127-19378T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9259939 | ||||||
| chr2:9259999
|
T | G | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-19318T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9259999 | ||||||
| chr2:9260044
|
C | CCA | 135 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(132): Show | 135 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.127-19273_127-1927 others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9260044 | ||||||
| chr2:9260081
|
T | C | 1 | a0001c0004t0005g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.127-19236T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9260081 | ||||||
| chr2:9260303
|
T | C | 154 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(151): Show | 154 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.127-19014T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9260303 | ||||||
| chr2:9260418
|
G | GA | 70 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(67): Show | 70 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.127-18894dupA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9260418 | |||||
| chr2:9260563
|
C | T | 1 | a0001c0003t0016g0174 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.127-18754C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9260563 | ||||||
| chr2:9260879
|
A | C | 1 | a0002c0001t0001g0005 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.127-18438A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9260879 | ||||||
| chr2:9260939
|
G | A | 3 | a0001c0002t0003g0149a0001c0002t0003g0151a0001c0002t0003g0152 | 3 | HG00323.hp2 HG00738.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.127-18378G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9260939 | ||||||
| chr2:9261002
|
C | G | 1 | a0001c0002t0009g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.127-18315C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9261002 | ||||||
| chr2:9261110
|
C | A | 1 | a0002c0001t0001g0070 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.127-18207C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9261110 | ||||||
| chr2:9261133
|
C | T | 41 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(38): Show | 41 | HG00642.hp1 HG00738.hp1 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.127-18184C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9261133 | ||||||
| chr2:9261363
|
T | C | 1 | a0002c0008t0001g0108 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.127-17954T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9261363 | ||||||
| chr2:9261379
|
TAA | T | 29 | a0001c0002t0003g0166a0001c0002t0008g0048a0001c0002t0009g0031others(26): Show | 29 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.127-17936_127-1793 others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9261379 | |||||
| chr2:9261380
|
A | T | 1 | a0001c0002t0002g0069 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.127-17937A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9261380 | ||||||
| chr2:9261526
|
A | G | 1 | a0001c0002t0008g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.127-17791A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9261526 | ||||||
| chr2:9261528
|
G | A | 1 | a0001c0004t0005g0138 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.127-17789G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9261528 | ||||||
| chr2:9261642
|
T | C | 40 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(37): Show | 40 | HG00280.hp1 HG00639.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.127-17675T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9261642 | ||||||
| chr2:9261865
|
G | A | 1 | a0002c0001t0001g0159 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.127-17452G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9261865 | ||||||
| chr2:9261940
|
C | T | 1 | a0002c0001t0001g0087 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.127-17377C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9261940 | ||||||
| chr2:9262193
|
T | C | 1 | a0001c0003t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.127-17124T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9262193 | ||||||
| chr2:9262528
|
C | T | 6 | a0001c0002t0003g0209a0001c0002t0009g0208a0001c0004t0005g0191others(3): Show | 6 | HG02886.hp2 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-16789C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9262528 | ||||||
| chr2:9262607
|
C | T | 1 | a0002c0001t0001g0074 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.127-16710C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9262607 | ||||||
| chr2:9262711
|
A | G | 28 | a0001c0002t0003g0166a0001c0002t0008g0048a0001c0003t0001g0029others(25): Show | 28 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-16606A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9262711 | ||||||
| chr2:9262777
|
C | T | 1 | a0001c0002t0019g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.127-16540C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9262777 | ||||||
| chr2:9262848
|
T | C | 1 | a0001c0003t0006g0105 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.127-16469T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9262848 | ||||||
| chr2:9262859
|
A | G | 81 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(78): Show | 81 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.127-16458A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9262859 | ||||||
| chr2:9262976
|
C | A | 2 | a0001c0002t0002g0016a0001c0002t0002g0096 | 2 | HG00280.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.127-16341C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9262976 | ||||||
| chr2:9263135
|
A | G | 2 | a0002c0001t0001g0092a0002c0001t0001g0093 | 2 | HG01981.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.127-16182A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9263135 | ||||||
| chr2:9263212
|
C | T | 30 | a0001c0002t0003g0166a0001c0002t0008g0048a0001c0002t0009g0031others(27): Show | 30 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.127-16105C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9263212 | ||||||
| chr2:9263426
|
T | A | 1 | a0002c0001t0001g0023 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.127-15891T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9263426 | ||||||
| chr2:9263476
|
G | A | 1 | a0001c0004t0005g0035 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.127-15841G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9263476 | ||||||
| chr2:9263579
|
C | T | 29 | a0001c0002t0003g0166a0001c0002t0008g0048a0001c0002t0009g0031others(26): Show | 29 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.127-15738C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9263579 | ||||||
| chr2:9263607
|
C | T | 1 | a0001c0004t0005g0205 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.127-15710C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9263607 | ||||||
| chr2:9263679
|
A | C | 1 | a0001c0002t0019g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.127-15638A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9263679 | ||||||
| chr2:9263693
|
C | T | 79 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(76): Show | 79 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.127-15624C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9263693 | ||||||
| chr2:9263697
|
G | T | 1 | a0002c0001t0001g0159 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.127-15620G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9263697 | ||||||
| chr2:9263796
|
A | G | 3 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0059 | 3 | HG00642.hp2 HG01261.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.127-15521A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9263796 | ||||||
| chr2:9263920
|
C | G | 125 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(122): Show | 125 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.127-15397C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9263920 | ||||||
| chr2:9264139
|
C | G | 1 | a0001c0004t0005g0205 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.127-15178C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9264139 | ||||||
| chr2:9264190
|
C | CAAAAAA | 31 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(28): Show | 31 | HG00642.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.127-15125_127-1512 others(10): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9264190 | |||||
| chr2:9264195
|
A | AAAT | 3 | a0001c0002t0008g0206a0001c0009t0004g0047a0002c0001t0001g0049 | 3 | HG01071.hp1 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.127-15095_127-1509 others(7): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9264195 | |||||
| chr2:9264195
|
A | AAATAAT | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-15098_127-1509 others(10): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9264195 | |||||
| chr2:9264195
|
AAAT | A | 73 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(70): Show | 73 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.127-15095_127-1509 others(7): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9264195 | |||||
| chr2:9264198
|
T | A | 40 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(37): Show | 40 | HG00642.hp1 HG00738.hp1 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.127-15119T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9264198 | ||||||
| chr2:9264199
|
A | AAAAAAT | 4 | a0001c0003t0004g0020a0001c0003t0004g0043a0001c0003t0004g0044others(1): Show | 4 | HG02723.hp1 HG03471.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-15117_127-1511 others(10): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9264199 | |||||
| chr2:9264201
|
T | A | 50 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(47): Show | 50 | HG00735.hp2 HG00738.hp1 HG01099.hp2 others(47): Show |
intron_variant | MODIFIER | c.127-15116T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9264201 | ||||||
| chr2:9264204
|
T | A | 44 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(41): Show | 44 | HG00735.hp2 HG00738.hp1 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.127-15113T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9264204 | ||||||
| chr2:9264207
|
T | A | 21 | a0001c0002t0002g0162a0001c0002t0003g0094a0001c0003t0007g0170others(18): Show | 21 | HG00735.hp2 HG00738.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.127-15110T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9264207 | ||||||
| chr2:9264210
|
T | A | 1 | a0001c0004t0005g0028 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.127-15107T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9264210 | ||||||
| chr2:9264352
|
G | A | 18 | a0001c0002t0001g0024a0001c0002t0002g0134a0001c0002t0002g0162others(15): Show | 18 | HG00642.hp1 HG01099.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.127-14965G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9264352 | ||||||
| chr2:9264359
|
C | T | 2 | a0001c0004t0005g0185a0002c0001t0001g0155 | 2 | HG02976.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.127-14958C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9264359 | ||||||
| chr2:9264835
|
C | A | 1 | a0001c0009t0004g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.127-14482C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9264835 | ||||||
| chr2:9264851
|
A | C | 1 | a0001c0009t0004g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.127-14466A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9264851 | ||||||
| chr2:9264993
|
G | A | 1 | a0001c0003t0001g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.127-14324G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9264993 | ||||||
| chr2:9264998
|
T | C | 1 | a0001c0002t0009g0031 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.127-14319T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9264998 | ||||||
| chr2:9265037
|
G | C | 1 | a0001c0003t0001g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.127-14280G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9265037 | ||||||
| chr2:9265084
|
C | T | 1 | a0001c0002t0006g0183 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.127-14233C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9265084 | ||||||
| chr2:9265187
|
C | A | 1 | a0001c0004t0005g0195 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127-14130C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9265187 | ||||||
| chr2:9265391
|
T | C | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127-13926T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9265391 | ||||||
| chr2:9265458
|
T | C | 1 | a0002c0005t0001g0002 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.127-13859T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9265458 | ||||||
| chr2:9265483
|
A | T | 4 | a0001c0002t0008g0048a0001c0003t0001g0046a0001c0003t0004g0011others(1): Show | 4 | HG02257.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-13834A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9265483 | ||||||
| chr2:9265521
|
C | A | 129 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(126): Show | 129 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.127-13796C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9265521 | ||||||
| chr2:9265627
|
T | A | 4 | a0001c0002t0008g0048a0001c0003t0001g0046a0001c0003t0004g0011others(1): Show | 4 | HG02257.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-13690T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9265627 | ||||||
| chr2:9265641
|
G | A | 1 | a0002c0005t0001g0180 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.127-13676G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9265641 | ||||||
| chr2:9265819
|
C | G | 1 | a0002c0005t0001g0025 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.127-13498C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9265819 | ||||||
| chr2:9265879
|
T | G | 47 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(44): Show | 47 | HG00280.hp1 HG00639.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.127-13438T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9265879 | ||||||
| chr2:9266010
|
G | A | 1 | a0001c0003t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.127-13307G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9266010 | ||||||
| chr2:9266017
|
AC | A | 31 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(28): Show | 31 | HG00280.hp1 HG00639.hp1 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.127-13293delC | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9266017 | |||||
| chr2:9266022
|
C | T | 1 | a0001c0003t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.127-13295C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9266022 | ||||||
| chr2:9266073
|
C | T | 1 | a0001c0002t0008g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.127-13244C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9266073 | ||||||
| chr2:9266133
|
G | A | 1 | a0002c0001t0001g0207 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.127-13184G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9266133 | ||||||
| chr2:9266147
|
C | CTT | 53 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0129others(50): Show | 53 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.127-13155_127-1315 others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9266147 | |||||
| chr2:9266147
|
C | CTTT | 42 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(39): Show | 42 | HG00280.hp1 HG00639.hp1 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.127-13156_127-1315 others(7): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9266147 | |||||
| chr2:9266147
|
C | CTTTT | 30 | a0001c0002t0003g0166a0001c0002t0008g0048a0001c0002t0009g0031others(27): Show | 30 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.127-13157_127-1315 others(8): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9266147 | |||||
| chr2:9266147
|
C | CTTTTTT | 7 | a0002c0001t0001g0042a0002c0001t0001g0088a0002c0001t0001g0089others(4): Show | 7 | HG00735.hp2 HG01346.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-13159_127-1315 others(10): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9266147 | |||||
| chr2:9266181
|
C | T | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127-13136C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9266181 | ||||||
| chr2:9266182
|
T | A | 1 | a0002c0008t0001g0108 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.127-13135T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9266182 | ||||||
| chr2:9266222
|
C | T | 1 | a0001c0004t0005g0028 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.127-13095C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9266222 | ||||||
| chr2:9266224
|
G | T | 1 | a0001c0009t0004g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.127-13093G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9266224 | ||||||
| chr2:9266231
|
C | T | 1 | a0001c0002t0008g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.127-13086C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9266231 | ||||||
| chr2:9266425
|
G | A | 1 | a0002c0001t0001g0106 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.127-12892G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9266425 | ||||||
| chr2:9266491
|
A | C | 1 | a0001c0003t0001g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.127-12826A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9266491 | ||||||
| chr2:9266792
|
G | T | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127-12525G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9266792 | ||||||
| chr2:9266801
|
C | T | 1 | a0001c0003t0001g0190 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.127-12516C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9266801 | ||||||
| chr2:9266848
|
C | T | 1 | a0001c0002t0008g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.127-12469C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9266848 | ||||||
| chr2:9266876
|
A | T | 1 | a0001c0003t0001g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.127-12441A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9266876 | ||||||
| chr2:9267068
|
T | G | 2 | a0001c0003t0004g0038a0001c0003t0021g0040 | 2 | HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.127-12249T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9267068 | ||||||
| chr2:9267087
|
T | A | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127-12230T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9267087 | ||||||
| chr2:9267142
|
T | A | 2 | a0002c0001t0001g0121a0002c0001t0001g0122 | 2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.127-12175T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9267142 | ||||||
| chr2:9267217
|
G | A | 53 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(50): Show | 53 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.127-12100G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9267217 | ||||||
| chr2:9267227
|
G | A | 1 | a0001c0003t0001g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.127-12090G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9267227 | ||||||
| chr2:9267621
|
G | C | 3 | a0002c0001t0001g0118a0002c0001t0001g0155a0002c0005t0001g0180 | 3 | HG01255.hp2 HG02080.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.127-11696G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9267621 | ||||||
| chr2:9267643
|
T | C | 54 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0129others(51): Show | 54 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.127-11674T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9267643 | ||||||
| chr2:9267897
|
C | CA | 27 | a0001c0002t0002g0027a0001c0002t0002g0055a0001c0002t0022g0120others(24): Show | 27 | HG01070.hp1 HG01106.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.127-11395dupA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9267897 | |||||
| chr2:9267897
|
C | CAA | 15 | a0001c0002t0002g0202a0001c0002t0003g0094a0001c0002t0003g0148others(12): Show | 15 | HG00735.hp2 HG01074.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.127-11396_127-1139 others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9267897 | |||||
| chr2:9267897
|
C | CAAAA | 27 | a0001c0002t0003g0166a0001c0003t0001g0046a0001c0003t0001g0153others(24): Show | 27 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.127-11398_127-1139 others(8): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9267897 | |||||
| chr2:9267897
|
CA | C | 59 | a0001c0002t0001g0115a0001c0002t0001g0116a0001c0002t0001g0126others(56): Show | 59 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.127-11395delA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9267897 | |||||
| chr2:9267897
|
CAA | C | 6 | a0001c0002t0001g0181a0002c0001t0001g0070a0002c0001t0001g0074others(3): Show | 6 | HG01496.hp1 HG02735.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-11396_127-1139 others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9267897 | |||||
| chr2:9267897
|
CAAAAAAA others(6): Show |
C | 1 | a0002c0001t0001g0113 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.127-11407_127-1139 others(17): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9267897 | |||||
| chr2:9267969
|
G | A | 4 | a0001c0002t0003g0209a0001c0007t0004g0037a0002c0001t0001g0061others(1): Show | 4 | HG02922.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-11348G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9267969 | ||||||
| chr2:9267987
|
A | G | 2 | a0002c0001t0001g0121a0002c0001t0001g0122 | 2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.127-11330A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9267987 | ||||||
| chr2:9268003
|
T | G | 135 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(132): Show | 135 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.127-11314T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9268003 | ||||||
| chr2:9268207
|
C | T | 1 | a0001c0004t0005g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.127-11110C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9268207 | ||||||
| chr2:9268479
|
C | A | 30 | a0001c0002t0003g0166a0001c0002t0008g0048a0001c0002t0009g0031others(27): Show | 30 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.127-10838C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9268479 | ||||||
| chr2:9268789
|
A | G | 9 | a0001c0002t0003g0094a0002c0001t0001g0042a0002c0001t0001g0088others(6): Show | 9 | HG00735.hp2 HG01346.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-10528A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9268789 | ||||||
| chr2:9268800
|
G | A | 1 | a0002c0001t0001g0155 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.127-10517G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9268800 | ||||||
| chr2:9268861
|
C | T | 9 | a0001c0002t0003g0094a0002c0001t0001g0042a0002c0001t0001g0088others(6): Show | 9 | HG00735.hp2 HG01346.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-10456C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9268861 | ||||||
| chr2:9268888
|
T | C | 49 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0129others(46): Show | 49 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.127-10429T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9268888 | ||||||
| chr2:9268921
|
G | T | 5 | a0001c0002t0002g0202a0001c0002t0003g0188a0001c0004t0005g0034others(2): Show | 5 | HG01074.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-10396G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9268921 | ||||||
| chr2:9268937
|
C | T | 1 | a0001c0009t0004g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.127-10380C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9268937 | ||||||
| chr2:9268938
|
G | A | 1 | a0001c0004t0005g0138 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.127-10379G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9268938 | ||||||
| chr2:9269009
|
T | C | 1 | a0001c0004t0005g0028 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.127-10308T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9269009 | ||||||
| chr2:9269101
|
C | T | 1 | a0001c0003t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.127-10216C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9269101 | ||||||
| chr2:9269113
|
C | T | 46 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0129others(43): Show | 46 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.127-10204C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9269113 | ||||||
| chr2:9269414
|
G | A | 47 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(44): Show | 47 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.127-9903G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9269414 | ||||||
| chr2:9269447
|
C | T | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-9870C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9269447 | ||||||
| chr2:9269531
|
T | A | 12 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(9): Show | 12 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.127-9786T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9269531 | ||||||
| chr2:9269621
|
C | T | 2 | a0001c0002t0002g0198a0001c0002t0013g0001 | 2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.127-9696C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9269621 | ||||||
| chr2:9269622
|
G | T | 1 | a0001c0003t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.127-9695G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9269622 | ||||||
| chr2:9269885
|
C | T | 1 | a0001c0002t0003g0142 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.127-9432C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9269885 | ||||||
| chr2:9269914
|
G | A | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127-9403G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9269914 | ||||||
| chr2:9269964
|
C | T | 9 | a0001c0002t0003g0094a0002c0001t0001g0042a0002c0001t0001g0088others(6): Show | 9 | HG00735.hp2 HG01346.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-9353C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9269964 | ||||||
| chr2:9270185
|
T | C | 2 | a0001c0003t0001g0165a0001c0003t0001g0210 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.127-9132T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9270185 | ||||||
| chr2:9270250
|
A | AGTTCCC | 3 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0011t0001g0178 | 3 | HG01496.hp2 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.127-9064_127-9059d others(8): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9270250 | |||||
| chr2:9270273
|
C | A | 1 | a0001c0002t0001g0116 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.127-9044C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9270273 | ||||||
| chr2:9270431
|
A | T | 178 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(175): Show | 178 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.127-8886A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9270431 | ||||||
| chr2:9270482
|
G | A | 13 | a0001c0003t0004g0020a0001c0003t0004g0043a0001c0003t0004g0044others(10): Show | 13 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.127-8835G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9270482 | ||||||
| chr2:9270500
|
T | C | 54 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(51): Show | 54 | HG00280.hp1 HG00639.hp1 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.127-8817T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9270500 | ||||||
| chr2:9270581
|
A | G | 3 | a0001c0004t0005g0176a0001c0004t0005g0205a0001c0006t0004g0063 | 3 | HG02145.hp2 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.127-8736A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9270581 | ||||||
| chr2:9270604
|
A | G | 15 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0007others(12): Show | 15 | HG01099.hp2 HG01106.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.127-8713A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9270604 | ||||||
| chr2:9270652
|
A | C | 41 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(38): Show | 41 | HG00280.hp1 HG00639.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.127-8665A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9270652 | ||||||
| chr2:9270773
|
T | C | 2 | a0001c0003t0001g0165a0001c0003t0004g0200 | 2 | HG03041.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.127-8544T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9270773 | ||||||
| chr2:9270785
|
A | AT | 42 | a0001c0002t0002g0202a0001c0002t0003g0026a0001c0002t0003g0050others(39): Show | 42 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.127-8507dupT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9270785 | |||||
| chr2:9270785
|
A | ATT | 5 | a0001c0002t0003g0094a0001c0003t0001g0046a0001c0004t0005g0196others(2): Show | 5 | HG03130.hp2 HG03453.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-8508_127-8507d others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9270785 | |||||
| chr2:9270785
|
A | ATTTTTTT others(3): Show |
1 | a0001c0002t0002g0007 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.127-8516_127-8507d others(12): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9270785 | |||||
| chr2:9270785
|
A | ATTTTTTT others(6): Show |
3 | a0001c0002t0023g0008a0001c0004t0005g0021a0001c0004t0005g0034 | 3 | HG02523.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.127-8519_127-8507d others(15): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9270785 | |||||
| chr2:9270785
|
A | ATTTTTTT others(7): Show |
11 | a0001c0002t0002g0056a0001c0002t0002g0107a0001c0002t0002g0137others(8): Show | 11 | HG00639.hp1 HG01070.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-8520_127-8507d others(16): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9270785 | |||||
| chr2:9270785
|
A | ATTTTTTT others(8): Show |
10 | a0001c0002t0002g0027a0001c0002t0002g0055a0001c0002t0002g0060others(7): Show | 10 | HG00735.hp1 HG01074.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.127-8521_127-8507d others(17): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9270785 | |||||
| chr2:9270785
|
A | ATTTTTTT others(9): Show |
6 | a0001c0002t0001g0097a0001c0002t0002g0057a0001c0002t0002g0058others(3): Show | 6 | HG00280.hp1 HG01071.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-8522_127-8507d others(18): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9270785 | |||||
| chr2:9270785
|
A | ATTTTTTT others(11): Show |
1 | a0001c0003t0011g0068 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.127-8524_127-8507d others(20): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9270785 | |||||
| chr2:9270785
|
A | ATTTTTTT others(12): Show |
1 | a0002c0005t0001g0025 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.127-8525_127-8507d others(21): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9270785 | |||||
| chr2:9270785
|
A | ATTTTTTT others(17): Show |
1 | a0002c0001t0001g0122 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.127-8530_127-8507d others(26): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9270785 | |||||
| chr2:9270785
|
A | ATTTTTTT others(18): Show |
1 | a0001c0002t0002g0129 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.127-8531_127-8507d others(27): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9270785 | |||||
| chr2:9270785
|
A | ATTTTTTT others(19): Show |
1 | a0002c0001t0001g0121 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.127-8507_127-8506i others(28): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9270785 | |||||
| chr2:9270785
|
A | ATTTTTTT others(23): Show |
1 | a0001c0002t0002g0016 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.127-8507_127-8506i others(32): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9270785 | |||||
| chr2:9270785
|
AT | A | 75 | a0001c0002t0001g0024a0001c0002t0001g0115a0001c0002t0001g0126others(72): Show | 75 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.127-8507delT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9270785 | |||||
| chr2:9270785
|
ATT | A | 20 | a0001c0002t0002g0073a0001c0002t0009g0031a0001c0002t0019g0164others(17): Show | 20 | HG01070.hp1 HG01074.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.127-8508_127-8507d others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9270785 | |||||
| chr2:9270785
|
ATTTTTTT others(4): Show |
A | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-8517_127-8507d others(13): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9270785 | |||||
| chr2:9270823
|
C | G | 48 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(45): Show | 48 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.127-8494C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9270823 | ||||||
| chr2:9270828
|
C | T | 96 | a0001c0002t0001g0024a0001c0002t0001g0115a0001c0002t0001g0116others(93): Show | 96 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.127-8489C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9270828 | ||||||
| chr2:9270829
|
G | C | 1 | a0001c0009t0004g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.127-8488G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9270829 | ||||||
| chr2:9270832
|
G | A | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-8485G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9270832 | ||||||
| chr2:9270850
|
T | C | 187 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(184): Show | 187 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.127-8467T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9270850 | ||||||
| chr2:9270857
|
A | C | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127-8460A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9270857 | ||||||
| chr2:9270861
|
C | T | 1 | a0001c0004t0005g0028 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.127-8456C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9270861 | ||||||
| chr2:9270874
|
G | C | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127-8443G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9270874 | ||||||
| chr2:9270876
|
C | T | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127-8441C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9270876 | ||||||
| chr2:9270937
|
T | C | 1 | a0001c0003t0004g0200 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.127-8380T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9270937 | ||||||
| chr2:9270947
|
T | C | 83 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(80): Show | 83 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.127-8370T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9270947 | ||||||
| chr2:9270950
|
G | A | 2 | a0001c0002t0002g0198a0001c0002t0013g0001 | 2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.127-8367G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9270950 | ||||||
| chr2:9270956
|
C | T | 35 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(32): Show | 35 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.127-8361C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9270956 | ||||||
| chr2:9270983
|
C | T | 1 | a0001c0004t0005g0205 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.127-8334C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9270983 | ||||||
| chr2:9271039
|
T | C | 151 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(148): Show | 151 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.127-8278T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9271039 | ||||||
| chr2:9271054
|
A | G | 1 | a0004c0015t0015g0123 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.127-8263A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9271054 | ||||||
| chr2:9271090
|
G | A | 103 | a0001c0002t0001g0024a0001c0002t0001g0115a0001c0002t0001g0116others(100): Show | 103 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.127-8227G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9271090 | ||||||
| chr2:9271101
|
A | AT | 44 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(41): Show | 44 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.127-8207dupT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9271101 | |||||
| chr2:9271312
|
G | A | 28 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(25): Show | 28 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-8005G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9271312 | ||||||
| chr2:9271457
|
T | C | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.127-7860T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9271457 | ||||||
| chr2:9271603
|
T | G | 41 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(38): Show | 41 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.127-7714T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9271603 | ||||||
| chr2:9271630
|
C | T | 13 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(10): Show | 13 | HG01099.hp2 HG01106.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.127-7687C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9271630 | ||||||
| chr2:9271650
|
G | A | 1 | a0001c0003t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.127-7667G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9271650 | ||||||
| chr2:9271802
|
A | G | 1 | a0001c0002t0022g0120 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.127-7515A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9271802 | ||||||
| chr2:9272308
|
A | T | 1 | a0001c0003t0001g0039 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.127-7009A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9272308 | ||||||
| chr2:9272421
|
T | G | 1 | a0002c0005t0001g0002 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.127-6896T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9272421 | ||||||
| chr2:9272852
|
G | A | 1 | a0001c0002t0003g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.127-6465G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9272852 | ||||||
| chr2:9272982
|
G | A | 30 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(27): Show | 30 | HG00323.hp2 HG00642.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.127-6335G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9272982 | ||||||
| chr2:9273084
|
A | G | 38 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(35): Show | 38 | HG00323.hp2 HG00642.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.127-6233A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9273084 | ||||||
| chr2:9273178
|
A | G | 1 | a0002c0008t0001g0108 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.127-6139A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9273178 | ||||||
| chr2:9273194
|
A | AT | 4 | a0001c0003t0001g0165a0001c0003t0001g0210a0001c0004t0005g0185others(1): Show | 4 | HG02895.hp1 HG02976.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-6115dupT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9273194 | |||||
| chr2:9273228
|
A | G | 1 | a0002c0001t0001g0163 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.127-6089A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9273228 | ||||||
| chr2:9273231
|
G | T | 2 | a0001c0003t0004g0038a0001c0003t0021g0040 | 2 | HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.127-6086G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9273231 | ||||||
| chr2:9273506
|
G | A | 31 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(28): Show | 31 | HG00323.hp2 HG00642.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.127-5811G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9273506 | ||||||
| chr2:9273511
|
G | C | 1 | a0001c0002t0002g0055 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.127-5806G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9273511 | ||||||
| chr2:9273568
|
G | C | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-5749G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9273568 | ||||||
| chr2:9273913
|
C | T | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.127-5404C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9273913 | ||||||
| chr2:9274024
|
A | G | 1 | a0002c0001t0001g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.127-5293A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9274024 | ||||||
| chr2:9274108
|
G | A | 1 | a0002c0001t0001g0067 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.127-5209G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9274108 | ||||||
| chr2:9274122
|
T | A | 30 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(27): Show | 30 | HG00323.hp2 HG00642.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.127-5195T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9274122 | ||||||
| chr2:9274141
|
A | T | 30 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(27): Show | 30 | HG00323.hp2 HG00642.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.127-5176A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9274141 | ||||||
| chr2:9274317
|
ATCTTTTT others(5): Show |
A | 1 | a0002c0001t0001g0042 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.127-4998_127-4987d others(14): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9274317 | |||||
| chr2:9274319
|
C | CT | 149 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(146): Show | 149 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.127-4977dupT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9274319 | |||||
| chr2:9274319
|
C | CTTT | 5 | a0001c0003t0004g0011a0001c0003t0004g0020a0001c0003t0004g0043others(2): Show | 5 | HG02257.hp2 HG02723.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-4979_127-4977d others(5): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9274319 | |||||
| chr2:9274319
|
CTTT | C | 28 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(25): Show | 28 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.127-4979_127-4977d others(5): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9274319 | |||||
| chr2:9274392
|
C | T | 2 | a0001c0002t0002g0198a0001c0002t0013g0001 | 2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.127-4925C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9274392 | ||||||
| chr2:9274525
|
G | A | 1 | a0001c0002t0002g0027 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.127-4792G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9274525 | ||||||
| chr2:9274619
|
A | G | 104 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(101): Show | 104 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.127-4698A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9274619 | ||||||
| chr2:9274630
|
CAATCTT | C | 3 | a0001c0004t0005g0021a0001c0004t0005g0034a0001c0004t0005g0144 | 3 | HG03130.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.127-4684_127-4679d others(8): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9274630 | |||||
| chr2:9274943
|
C | G | 104 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(101): Show | 104 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.127-4374C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9274943 | ||||||
| chr2:9275082
|
G | GT | 18 | a0001c0002t0002g0075a0001c0002t0003g0148a0001c0003t0001g0169others(15): Show | 18 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.127-4219dupT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9275082 | |||||
| chr2:9275082
|
G | GTTTT | 33 | a0001c0002t0002g0007a0001c0002t0002g0016a0001c0002t0002g0027others(30): Show | 33 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.127-4222_127-4219d others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9275082 | |||||
| chr2:9275082
|
G | GTTTTT | 6 | a0001c0002t0001g0097a0001c0003t0001g0165a0001c0003t0004g0200others(3): Show | 6 | HG02895.hp1 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-4223_127-4219d others(7): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9275082 | |||||
| chr2:9275082
|
G | GTTTTTT | 8 | a0001c0003t0004g0038a0001c0003t0006g0104a0001c0003t0006g0105others(5): Show | 8 | HG00597.hp2 HG02451.hp2 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.127-4224_127-4219d others(8): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9275082 | |||||
| chr2:9275082
|
G | GTTTTTTT | 13 | a0001c0002t0008g0048a0001c0003t0001g0029a0001c0003t0001g0046others(10): Show | 13 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(10): Show |
intron_variant | MODIFIER | c.127-4225_127-4219d others(9): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9275082 | |||||
| chr2:9275084
|
T | TTTTTG | 31 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(28): Show | 31 | HG00323.hp2 HG00642.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.127-4229_127-4228i others(7): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9275084 | |||||
| chr2:9275141
|
C | T | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127-4176C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9275141 | ||||||
| chr2:9275223
|
C | G | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.127-4094C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9275223 | ||||||
| chr2:9275319
|
C | G | 11 | a0001c0002t0003g0148a0001c0002t0003g0166a0001c0003t0001g0039others(8): Show | 11 | HG00738.hp1 HG01934.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-3998C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9275319 | ||||||
| chr2:9275436
|
T | C | 1 | a0001c0003t0001g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.127-3881T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9275436 | ||||||
| chr2:9275528
|
G | C | 13 | a0001c0003t0004g0011a0001c0003t0004g0020a0001c0003t0004g0043others(10): Show | 13 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.127-3789G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9275528 | ||||||
| chr2:9275559
|
G | A | 22 | a0001c0002t0008g0048a0001c0003t0001g0029a0001c0003t0001g0046others(19): Show | 22 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(19): Show |
intron_variant | MODIFIER | c.127-3758G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9275559 | ||||||
| chr2:9275568
|
A | G | 1 | a0001c0002t0001g0182 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.127-3749A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9275568 | ||||||
| chr2:9275797
|
A | C | 2 | a0001c0003t0001g0210a0001c0009t0004g0047 | 2 | HG02895.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.127-3520A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9275797 | ||||||
| chr2:9275912
|
G | A | 4 | a0001c0002t0002g0055a0001c0002t0002g0056a0001c0002t0002g0057others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-3405G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9275912 | ||||||
| chr2:9275915
|
G | A | 22 | a0001c0002t0008g0048a0001c0003t0001g0029a0001c0003t0001g0046others(19): Show | 22 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(19): Show |
intron_variant | MODIFIER | c.127-3402G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9275915 | ||||||
| chr2:9275927
|
A | G | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.127-3390A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9275927 | ||||||
| chr2:9275961
|
G | A | 113 | a0001c0002t0001g0024a0001c0002t0001g0115a0001c0002t0001g0116others(110): Show | 113 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.127-3356G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9275961 | ||||||
| chr2:9275973
|
G | A | 113 | a0001c0002t0001g0024a0001c0002t0001g0115a0001c0002t0001g0116others(110): Show | 113 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.127-3344G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9275973 | ||||||
| chr2:9276253
|
G | T | 1 | a0002c0001t0001g0089 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.127-3064G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9276253 | ||||||
| chr2:9276263
|
C | G | 210 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(207): Show | 210 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.127-3054C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9276263 | ||||||
| chr2:9276528
|
A | G | 188 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(185): Show | 188 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.127-2789A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9276528 | ||||||
| chr2:9276673
|
G | A | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-2644G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9276673 | ||||||
| chr2:9277172
|
A | T | 1 | a0002c0001t0001g0145 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.127-2145A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9277172 | ||||||
| chr2:9277205
|
C | T | 33 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(30): Show | 33 | HG00323.hp2 HG00642.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.127-2112C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9277205 | ||||||
| chr2:9277377
|
G | T | 2 | a0001c0002t0002g0137a0001c0002t0023g0008 | 2 | HG02523.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.127-1940G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9277377 | ||||||
| chr2:9277662
|
C | T | 33 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(30): Show | 33 | HG00323.hp2 HG00642.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.127-1655C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9277662 | ||||||
| chr2:9277907
|
T | C | 1 | a0002c0005t0001g0009 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.127-1410T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9277907 | ||||||
| chr2:9277938
|
G | A | 2 | a0002c0001t0001g0092a0002c0001t0001g0093 | 2 | HG01981.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.127-1379G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9277938 | ||||||
| chr2:9278111
|
A | G | 1 | a0001c0004t0005g0144 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.127-1206A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9278111 | ||||||
| chr2:9278145
|
C | G | 144 | a0001c0002t0001g0024a0001c0002t0001g0115a0001c0002t0001g0116others(141): Show | 144 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.127-1172C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9278145 | ||||||
| chr2:9278293
|
C | A | 33 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(30): Show | 33 | HG00323.hp2 HG00642.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.127-1024C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9278293 | ||||||
| chr2:9278406
|
G | C | 1 | a0002c0001t0020g0079 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.127-911G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9278406 | ||||||
| chr2:9278512
|
CA | C | 47 | a0001c0002t0001g0181a0001c0002t0003g0026a0001c0002t0003g0050others(44): Show | 47 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.127-789delA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9278512 | |||||
| chr2:9278512
|
CAA | C | 42 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(39): Show | 42 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.127-790_127-789del others(2): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9278512 | |||||
| chr2:9278552
|
C | G | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-765C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9278552 | ||||||
| chr2:9278676
|
G | A | 21 | a0001c0003t0001g0029a0001c0003t0001g0046a0001c0003t0001g0153others(18): Show | 21 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.127-641G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9278676 | ||||||
| chr2:9278715
|
T | G | 21 | a0001c0003t0001g0029a0001c0003t0001g0046a0001c0003t0001g0153others(18): Show | 21 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.127-602T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9278715 | ||||||
| chr2:9278755
|
G | T | 31 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(28): Show | 31 | HG00323.hp2 HG00642.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.127-562G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9278755 | ||||||
| chr2:9278790
|
A | G | 1 | a0001c0003t0006g0080 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.127-527A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9278790 | ||||||
| chr2:9278969
|
AG | A | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-346delG | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9278969 | |||||
| chr2:9278976
|
C | T | 1 | a0001c0004t0005g0176 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.127-341C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9278976 | ||||||
| chr2:9278977
|
G | T | 32 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(29): Show | 32 | HG00323.hp2 HG00642.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.127-340G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9278977 | ||||||
| chr2:9279005
|
G | A | 29 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(26): Show | 29 | HG00323.hp2 HG00642.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.127-312G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9279005 | ||||||
| chr2:9279061
|
CAGG | C | 34 | a0001c0002t0002g0198a0001c0002t0003g0026a0001c0002t0003g0050others(31): Show | 34 | HG00323.hp2 HG00642.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.127-247_127-245del others(3): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9279061 | |||||
| chr2:9279167
|
G | A | 1 | a0002c0001t0001g0127 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.127-150G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9279167 | ||||||
| chr2:9279170
|
GAGGGACC others(36): Show |
G | 1 | a0002c0001t0001g0081 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.127-130_127-88delA others(42): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | 9279170 | |||||
| chr2:9279282
|
G | A | 117 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(114): Show | 117 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.127-35G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9279282 | ||||||
| chr2:9279286
|
C | T | 85 | a0001c0002t0002g0073a0001c0002t0002g0075a0001c0002t0002g0162others(82): Show | 85 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.127-31C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | chr2 | 9279286 | ||||||
| chr2:9279434
|
G | A | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.199+45G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9279434 | ||||||
| chr2:9279453
|
C | T | 2 | a0001c0003t0001g0210a0001c0009t0004g0047 | 2 | HG02895.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.199+64C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9279453 | ||||||
| chr2:9279454
|
G | A | 29 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0026others(26): Show | 29 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.199+65G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9279454 | ||||||
| chr2:9279479
|
G | A | 28 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0026others(25): Show | 28 | HG00323.hp2 HG00642.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.199+90G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9279479 | ||||||
| chr2:9279880
|
A | ATTT | 6 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0003t0001g0169others(3): Show | 6 | HG01496.hp2 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.199+492_199+494dup others(3): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 9279880 | |||||
| chr2:9279880
|
A | ATTTACAC others(10): Show |
125 | a0001c0002t0001g0024a0001c0002t0001g0115a0001c0002t0001g0116others(122): Show | 125 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.199+501_199+502ins others(17): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 9279880 | |||||
| chr2:9279880
|
A | ATTTACAC others(10): Show |
3 | a0001c0003t0001g0210a0001c0004t0005g0185a0001c0009t0004g0047 | 3 | HG02895.hp1 HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.199+496_199+512dup others(17): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 9279880 | |||||
| chr2:9280003
|
G | A | 150 | a0001c0002t0001g0024a0001c0002t0001g0115a0001c0002t0001g0116others(147): Show | 150 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.199+614G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9280003 | ||||||
| chr2:9280235
|
C | T | 14 | a0001c0003t0004g0011a0001c0003t0004g0020a0001c0003t0004g0038others(11): Show | 14 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.199+846C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9280235 | ||||||
| chr2:9280299
|
C | T | 84 | a0001c0002t0001g0024a0001c0002t0001g0115a0001c0002t0001g0116others(81): Show | 84 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.199+910C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9280299 | ||||||
| chr2:9280986
|
T | A | 44 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0026others(41): Show | 44 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.199+1597T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9280986 | ||||||
| chr2:9281089
|
C | T | 1 | a0001c0004t0005g0028 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.199+1700C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9281089 | ||||||
| chr2:9281137
|
A | ATT | 36 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(33): Show | 36 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.199+1761_199+1762d others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 9281137 | |||||
| chr2:9281348
|
G | C | 1 | a0001c0002t0003g0142 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.199+1959G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9281348 | ||||||
| chr2:9281365
|
G | C | 23 | a0001c0002t0001g0133a0001c0002t0003g0148a0001c0003t0001g0029others(20): Show | 23 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(20): Show |
intron_variant | MODIFIER | c.199+1976G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9281365 | ||||||
| chr2:9281419
|
G | T | 1 | a0001c0003t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.199+2030G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9281419 | ||||||
| chr2:9281714
|
C | T | 22 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(19): Show | 22 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(19): Show |
intron_variant | MODIFIER | c.199+2325C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9281714 | ||||||
| chr2:9281768
|
G | A | 2 | a0001c0003t0001g0017a0001c0003t0001g0046 | 2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.199+2379G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9281768 | ||||||
| chr2:9281792
|
C | T | 163 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(160): Show | 163 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.199+2403C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9281792 | ||||||
| chr2:9281890
|
A | G | 40 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(37): Show | 40 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.199+2501A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9281890 | ||||||
| chr2:9282170
|
A | G | 4 | a0001c0002t0002g0069a0001c0002t0002g0187a0001c0002t0022g0120others(1): Show | 4 | HG00673.hp2 HG02135.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+2781A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9282170 | ||||||
| chr2:9282335
|
C | G | 1 | a0001c0002t0003g0142 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.199+2946C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9282335 | ||||||
| chr2:9282336
|
A | G | 8 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(5): Show | 8 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.199+2947A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9282336 | ||||||
| chr2:9282397
|
A | C | 85 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(82): Show | 85 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.199+3008A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9282397 | ||||||
| chr2:9282512
|
G | T | 2 | a0001c0004t0005g0041a0001c0004t0005g0138 | 2 | HG00639.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.199+3123G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9282512 | ||||||
| chr2:9282572
|
C | T | 1 | a0001c0004t0005g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.199+3183C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9282572 | ||||||
| chr2:9282659
|
A | G | 128 | a0001c0002t0001g0024a0001c0002t0001g0115a0001c0002t0001g0116others(125): Show | 128 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.199+3270A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9282659 | ||||||
| chr2:9282688
|
G | A | 22 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0026others(19): Show | 22 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.199+3299G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9282688 | ||||||
| chr2:9282837
|
A | C | 46 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0026others(43): Show | 46 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.199+3448A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9282837 | ||||||
| chr2:9283014
|
C | T | 29 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(26): Show | 29 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.199+3625C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9283014 | ||||||
| chr2:9283037
|
C | T | 1 | a0001c0004t0005g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.199+3648C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9283037 | ||||||
| chr2:9283072
|
CT | C | 46 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0026others(43): Show | 46 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.199+3693delT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 9283072 | |||||
| chr2:9283074
|
T | C | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.199+3685T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9283074 | ||||||
| chr2:9283102
|
G | A | 46 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0026others(43): Show | 46 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.199+3713G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9283102 | ||||||
| chr2:9283164
|
G | A | 1 | a0002c0001t0001g0160 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.199+3775G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9283164 | ||||||
| chr2:9283549
|
C | T | 13 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(10): Show | 13 | HG01099.hp2 HG01106.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.199+4160C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9283549 | ||||||
| chr2:9283673
|
G | A | 22 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(19): Show | 22 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(19): Show |
intron_variant | MODIFIER | c.199+4284G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9283673 | ||||||
| chr2:9283791
|
T | C | 13 | a0001c0003t0001g0153a0001c0003t0006g0006a0001c0003t0006g0064others(10): Show | 13 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(10): Show |
intron_variant | MODIFIER | c.199+4402T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9283791 | ||||||
| chr2:9283802
|
A | G | 36 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(33): Show | 36 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.199+4413A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9283802 | ||||||
| chr2:9283913
|
G | A | 151 | a0001c0002t0001g0024a0001c0002t0001g0115a0001c0002t0001g0116others(148): Show | 151 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.199+4524G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9283913 | ||||||
| chr2:9283918
|
C | A | 22 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(19): Show | 22 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(19): Show |
intron_variant | MODIFIER | c.199+4529C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9283918 | ||||||
| chr2:9284393
|
G | A | 1 | a0002c0005t0001g0054 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.199+5004G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9284393 | ||||||
| chr2:9284523
|
C | A | 1 | a0001c0003t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.199+5134C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9284523 | ||||||
| chr2:9284523
|
C | T | 24 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0026others(21): Show | 24 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.199+5134C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9284523 | ||||||
| chr2:9284718
|
C | T | 83 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(80): Show | 83 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.199+5329C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9284718 | ||||||
| chr2:9285044
|
T | C | 1 | a0001c0003t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.199+5655T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9285044 | ||||||
| chr2:9285179
|
A | G | 1 | a0002c0001t0001g0159 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.199+5790A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9285179 | ||||||
| chr2:9285268
|
T | A | 83 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(80): Show | 83 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.199+5879T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9285268 | ||||||
| chr2:9285501
|
G | T | 1 | a0002c0005t0001g0025 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.199+6112G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9285501 | ||||||
| chr2:9285977
|
T | C | 30 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(27): Show | 30 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.199+6588T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9285977 | ||||||
| chr2:9286319
|
A | C | 21 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(18): Show | 21 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.199+6930A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9286319 | ||||||
| chr2:9286429
|
T | A | 21 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(18): Show | 21 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.199+7040T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9286429 | ||||||
| chr2:9286437
|
GA | G | 35 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0026others(32): Show | 35 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.199+7059delA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 9286437 | |||||
| chr2:9286445
|
A | AAT | 30 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(27): Show | 30 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.199+7057_199+7058i others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 9286445 | |||||
| chr2:9286445
|
A | ATATATAT others(12): Show |
1 | a0001c0003t0001g0153 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.199+7056_199+7057i others(21): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9286445 | ||||||
| chr2:9286445
|
A | T | 6 | a0001c0002t0002g0073a0001c0002t0006g0183a0001c0007t0001g0030others(3): Show | 6 | HG00741.hp2 HG01074.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.199+7056A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9286445 | ||||||
| chr2:9286447
|
A | AAAAAAAT others(22): Show |
1 | a0001c0003t0001g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.199+7059_199+7060i others(31): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 9286447 | |||||
| chr2:9286447
|
A | AAAAATAT others(6): Show |
2 | a0001c0003t0006g0135a0001c0003t0006g0158 | 2 | HG00597.hp2 HG00609.hp1 |
intron_variant | MODIFIER | c.199+7059_199+7060i others(15): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 9286447 | |||||
| chr2:9286447
|
A | AAAAATAT others(8): Show |
1 | a0002c0001t0001g0067 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.199+7059_199+7060i others(17): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 9286447 | |||||
| chr2:9286447
|
A | AAAATATA others(5): Show |
1 | a0002c0008t0001g0108 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.199+7059_199+7060i others(14): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 9286447 | |||||
| chr2:9286447
|
A | AAAATATA others(7): Show |
4 | a0001c0002t0003g0148a0001c0003t0001g0039a0001c0003t0001g0190others(1): Show | 4 | HG01934.hp2 HG02735.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+7059_199+7060i others(16): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 9286447 | |||||
| chr2:9286447
|
A | AAATATAT others(6): Show |
5 | a0001c0003t0006g0064a0001c0003t0006g0065a0001c0003t0006g0104others(2): Show | 5 | HG00438.hp1 HG02083.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.199+7059_199+7060i others(15): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 9286447 | |||||
| chr2:9286447
|
A | AAATATAT others(8): Show |
1 | a0001c0003t0006g0105 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.199+7059_199+7060i others(17): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 9286447 | |||||
| chr2:9286447
|
A | AATATATA others(7): Show |
1 | a0001c0003t0006g0102 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.199+7060_199+7073d others(16): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 9286447 | |||||
| chr2:9286447
|
A | AT | 10 | a0001c0002t0003g0166a0001c0003t0004g0200a0001c0003t0007g0199others(7): Show | 10 | HG00738.hp1 HG02486.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.199+7058_199+7059i others(3): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9286447 | ||||||
| chr2:9286447
|
A | ATATATAT others(8): Show |
1 | a0001c0004t0005g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.199+7058_199+7059i others(17): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9286447 | ||||||
| chr2:9286447
|
A | ATATATAT others(14): Show |
1 | a0001c0003t0001g0029 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.199+7058_199+7059i others(23): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9286447 | ||||||
| chr2:9286447
|
A | T | 109 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(106): Show | 109 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.199+7058A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9286447 | ||||||
| chr2:9286505
|
C | G | 1 | a0002c0001t0001g0023 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.199+7116C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9286505 | ||||||
| chr2:9286665
|
G | T | 3 | a0001c0003t0001g0046a0001c0004t0005g0035a0002c0001t0001g0022 | 3 | HG03453.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.199+7276G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9286665 | ||||||
| chr2:9287015
|
G | A | 6 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0003t0001g0169others(3): Show | 6 | HG01496.hp2 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.199+7626G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9287015 | ||||||
| chr2:9287060
|
G | A | 1 | a0001c0004t0005g0194 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.199+7671G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9287060 | ||||||
| chr2:9287128
|
C | T | 21 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(18): Show | 21 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.199+7739C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9287128 | ||||||
| chr2:9287188
|
C | T | 1 | a0002c0005t0001g0025 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.199+7799C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9287188 | ||||||
| chr2:9287205
|
A | G | 82 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(79): Show | 82 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.199+7816A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9287205 | ||||||
| chr2:9287218
|
A | G | 82 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(79): Show | 82 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.199+7829A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9287218 | ||||||
| chr2:9287271
|
G | A | 30 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(27): Show | 30 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.199+7882G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9287271 | ||||||
| chr2:9287462
|
A | G | 45 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0026others(42): Show | 45 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.199+8073A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9287462 | ||||||
| chr2:9287564
|
T | C | 1 | a0002c0001t0001g0095 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.199+8175T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9287564 | ||||||
| chr2:9287602
|
A | T | 6 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0003t0001g0169others(3): Show | 6 | HG01496.hp2 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.199+8213A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9287602 | ||||||
| chr2:9287677
|
C | T | 3 | a0001c0002t0003g0149a0001c0002t0003g0151a0001c0002t0003g0152 | 3 | HG00323.hp2 HG00738.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.199+8288C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9287677 | ||||||
| chr2:9287718
|
G | A | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.199+8329G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9287718 | ||||||
| chr2:9287725
|
C | T | 45 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0026others(42): Show | 45 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.199+8336C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9287725 | ||||||
| chr2:9287780
|
CG | C | 31 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(28): Show | 31 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.199+8392delG | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9287780 | ||||||
| chr2:9287837
|
G | A | 2 | a0001c0007t0001g0030a0002c0001t0001g0036 | 2 | HG01175.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.199+8448G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9287837 | ||||||
| chr2:9288003
|
C | G | 81 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(78): Show | 81 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.199+8614C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9288003 | ||||||
| chr2:9288110
|
C | A | 1 | a0001c0002t0006g0184 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.199+8721C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9288110 | ||||||
| chr2:9288205
|
A | G | 18 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(15): Show | 18 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.199+8816A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9288205 | ||||||
| chr2:9288227
|
A | C | 3 | a0001c0003t0001g0165a0001c0003t0001g0210a0001c0009t0004g0047 | 3 | HG02895.hp1 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.199+8838A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9288227 | ||||||
| chr2:9288250
|
A | T | 1 | a0002c0005t0001g0003 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.199+8861A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9288250 | ||||||
| chr2:9288419
|
C | T | 24 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0026others(21): Show | 24 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.200-8881C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9288419 | ||||||
| chr2:9288532
|
T | A | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.200-8768T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9288532 | ||||||
| chr2:9288570
|
T | C | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.200-8730T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9288570 | ||||||
| chr2:9288830
|
T | G | 1 | a0001c0003t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.200-8470T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9288830 | ||||||
| chr2:9288876
|
A | G | 22 | a0001c0002t0003g0148a0001c0002t0006g0184a0001c0003t0001g0029others(19): Show | 22 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(19): Show |
intron_variant | MODIFIER | c.200-8424A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9288876 | ||||||
| chr2:9289073
|
G | A | 21 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(18): Show | 21 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.200-8227G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9289073 | ||||||
| chr2:9289199
|
C | T | 1 | a0001c0010t0018g0173 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.200-8101C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9289199 | ||||||
| chr2:9289404
|
T | C | 3 | a0001c0004t0005g0041a0001c0004t0005g0138a0001c0007t0001g0030 | 3 | HG00639.hp1 HG01175.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.200-7896T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9289404 | ||||||
| chr2:9289489
|
A | G | 79 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(76): Show | 79 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.200-7811A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9289489 | ||||||
| chr2:9289571
|
C | G | 30 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(27): Show | 30 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.200-7729C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9289571 | ||||||
| chr2:9289643
|
T | C | 6 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0003t0001g0169others(3): Show | 6 | HG01496.hp2 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.200-7657T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9289643 | ||||||
| chr2:9289706
|
G | A | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.200-7594G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9289706 | ||||||
| chr2:9289989
|
C | CGGT | 79 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(76): Show | 79 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.200-7309_200-7307d others(5): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 9289989 | |||||
| chr2:9290193
|
GTTAT | G | 7 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(4): Show | 7 | HG00639.hp1 HG01175.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.200-7084_200-7081d others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 9290193 | |||||
| chr2:9290242
|
G | C | 89 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(86): Show | 89 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.200-7058G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9290242 | ||||||
| chr2:9290407
|
G | A | 2 | a0001c0004t0005g0041a0001c0004t0005g0138 | 2 | HG00639.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.200-6893G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9290407 | ||||||
| chr2:9290451
|
C | G | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.200-6849C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9290451 | ||||||
| chr2:9290467
|
C | T | 3 | a0001c0004t0005g0041a0001c0004t0005g0138a0001c0007t0001g0030 | 3 | HG00639.hp1 HG01175.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.200-6833C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9290467 | ||||||
| chr2:9290492
|
G | T | 16 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(13): Show | 16 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.200-6808G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9290492 | ||||||
| chr2:9290581
|
T | A | 36 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(33): Show | 36 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.200-6719T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9290581 | ||||||
| chr2:9290602
|
C | T | 88 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(85): Show | 88 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.200-6698C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9290602 | ||||||
| chr2:9290649
|
G | A | 88 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(85): Show | 88 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.200-6651G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9290649 | ||||||
| chr2:9290794
|
A | G | 1 | a0001c0003t0004g0200 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.200-6506A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9290794 | ||||||
| chr2:9290812
|
C | T | 21 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(18): Show | 21 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.200-6488C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9290812 | ||||||
| chr2:9291228
|
TC | T | 28 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0026others(25): Show | 28 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.200-6070delC | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 9291228 | |||||
| chr2:9291491
|
G | A | 1 | a0002c0001t0001g0100 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.200-5809G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9291491 | ||||||
| chr2:9291507
|
A | G | 89 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(86): Show | 89 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.200-5793A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9291507 | ||||||
| chr2:9291799
|
A | G | 210 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(207): Show | 210 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.200-5501A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9291799 | ||||||
| chr2:9291810
|
A | T | 1 | a0001c0002t0003g0150 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.200-5490A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9291810 | ||||||
| chr2:9291839
|
C | A | 1 | a0002c0001t0001g0146 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.200-5461C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9291839 | ||||||
| chr2:9291865
|
A | C | 8 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(5): Show | 8 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.200-5435A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9291865 | ||||||
| chr2:9291972
|
G | A | 6 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0003t0001g0169others(3): Show | 6 | HG01496.hp2 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.200-5328G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9291972 | ||||||
| chr2:9292163
|
C | G | 1 | a0001c0002t0019g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.200-5137C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9292163 | ||||||
| chr2:9292274
|
C | T | 1 | a0002c0001t0014g0091 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.200-5026C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9292274 | ||||||
| chr2:9292290
|
A | T | 2 | a0001c0003t0001g0165a0001c0009t0004g0047 | 2 | HG02895.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.200-5010A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9292290 | ||||||
| chr2:9292294
|
T | C | 63 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(60): Show | 63 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.200-5006T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9292294 | ||||||
| chr2:9292295
|
G | A | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.200-5005G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9292295 | ||||||
| chr2:9292375
|
A | G | 63 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(60): Show | 63 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.200-4925A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9292375 | ||||||
| chr2:9292391
|
G | A | 1 | a0001c0004t0005g0028 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.200-4909G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9292391 | ||||||
| chr2:9292397
|
A | G | 16 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(13): Show | 16 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.200-4903A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9292397 | ||||||
| chr2:9292445
|
G | A | 18 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(15): Show | 18 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.200-4855G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9292445 | ||||||
| chr2:9292636
|
A | G | 21 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(18): Show | 21 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.200-4664A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9292636 | ||||||
| chr2:9292640
|
G | A | 12 | a0001c0003t0006g0006a0001c0003t0006g0064a0001c0003t0006g0065others(9): Show | 12 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(9): Show |
intron_variant | MODIFIER | c.200-4660G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9292640 | ||||||
| chr2:9292680
|
C | T | 26 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0026others(23): Show | 26 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.200-4620C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9292680 | ||||||
| chr2:9292767
|
A | G | 3 | a0001c0004t0005g0041a0001c0004t0005g0138a0001c0007t0001g0030 | 3 | HG00639.hp1 HG01175.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.200-4533A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9292767 | ||||||
| chr2:9293126
|
G | A | 3 | a0001c0004t0005g0041a0001c0004t0005g0138a0001c0007t0001g0030 | 3 | HG00639.hp1 HG01175.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.200-4174G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9293126 | ||||||
| chr2:9293411
|
C | A | 1 | a0001c0002t0013g0001 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.200-3889C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9293411 | ||||||
| chr2:9293516
|
C | G | 21 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(18): Show | 21 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.200-3784C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9293516 | ||||||
| chr2:9293638
|
C | T | 8 | a0001c0004t0005g0176a0001c0004t0005g0191a0001c0004t0005g0192others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.200-3662C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9293638 | ||||||
| chr2:9293700
|
C | T | 3 | a0001c0004t0005g0041a0001c0004t0005g0138a0001c0007t0001g0030 | 3 | HG00639.hp1 HG01175.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.200-3600C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9293700 | ||||||
| chr2:9293800
|
G | A | 86 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(83): Show | 86 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.200-3500G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9293800 | ||||||
| chr2:9293830
|
A | G | 2 | a0002c0001t0001g0121a0002c0001t0001g0122 | 2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.200-3470A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9293830 | ||||||
| chr2:9293838
|
A | G | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.200-3462A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9293838 | ||||||
| chr2:9293949
|
G | C | 1 | a0001c0004t0005g0205 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.200-3351G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9293949 | ||||||
| chr2:9293996
|
A | AT | 14 | a0001c0002t0003g0148a0001c0002t0003g0188a0001c0002t0008g0206others(11): Show | 14 | HG01074.hp2 HG01891.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.200-3285dupT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 9293996 | |||||
| chr2:9293996
|
AT | A | 14 | a0001c0003t0001g0210a0001c0004t0005g0041a0001c0004t0005g0138others(11): Show | 14 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.200-3285delT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 9293996 | |||||
| chr2:9293996
|
ATT | A | 58 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(55): Show | 58 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.200-3286_200-3285d others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 9293996 | |||||
| chr2:9294124
|
G | A | 1 | a0001c0004t0005g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.200-3176G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9294124 | ||||||
| chr2:9294378
|
G | A | 23 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0026others(20): Show | 23 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.200-2922G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9294378 | ||||||
| chr2:9294433
|
G | A | 21 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(18): Show | 21 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.200-2867G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9294433 | ||||||
| chr2:9294437
|
C | G | 21 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(18): Show | 21 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.200-2863C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9294437 | ||||||
| chr2:9294510
|
C | T | 1 | a0001c0002t0002g0187 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.200-2790C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9294510 | ||||||
| chr2:9294513
|
A | G | 3 | a0001c0004t0005g0041a0001c0004t0005g0138a0001c0007t0001g0030 | 3 | HG00639.hp1 HG01175.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.200-2787A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9294513 | ||||||
| chr2:9294541
|
A | G | 36 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(33): Show | 36 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.200-2759A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9294541 | ||||||
| chr2:9294647
|
C | T | 1 | a0002c0008t0001g0108 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.200-2653C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9294647 | ||||||
| chr2:9294682
|
G | A | 83 | a0001c0002t0001g0024a0001c0002t0001g0115a0001c0002t0001g0116others(80): Show | 83 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.200-2618G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9294682 | ||||||
| chr2:9294727
|
G | A | 86 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(83): Show | 86 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.200-2573G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9294727 | ||||||
| chr2:9294828
|
C | T | 1 | a0002c0001t0001g0179 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.200-2472C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9294828 | ||||||
| chr2:9294902
|
G | A | 6 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0003t0001g0169others(3): Show | 6 | HG01496.hp2 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.200-2398G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9294902 | ||||||
| chr2:9295012
|
A | G | 36 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(33): Show | 36 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.200-2288A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9295012 | ||||||
| chr2:9295233
|
A | G | 1 | a0002c0001t0001g0118 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.200-2067A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9295233 | ||||||
| chr2:9295256
|
C | G | 30 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(27): Show | 30 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.200-2044C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9295256 | ||||||
| chr2:9295400
|
C | T | 3 | a0001c0004t0005g0041a0001c0004t0005g0138a0001c0007t0001g0030 | 3 | HG00639.hp1 HG01175.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.200-1900C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9295400 | ||||||
| chr2:9295443
|
G | A | 30 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(27): Show | 30 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.200-1857G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9295443 | ||||||
| chr2:9295556
|
G | A | 21 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(18): Show | 21 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.200-1744G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9295556 | ||||||
| chr2:9295643
|
C | T | 2 | a0002c0001t0001g0082a0002c0001t0001g0114 | 2 | NA18953.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.200-1657C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9295643 | ||||||
| chr2:9295706
|
C | T | 1 | a0001c0007t0004g0019 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.200-1594C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9295706 | ||||||
| chr2:9295718
|
T | C | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.200-1582T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9295718 | ||||||
| chr2:9295967
|
A | T | 86 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(83): Show | 86 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.200-1333A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9295967 | ||||||
| chr2:9296093
|
GC | G | 3 | a0001c0004t0005g0041a0001c0004t0005g0138a0001c0007t0001g0030 | 3 | HG00639.hp1 HG01175.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.200-1206delC | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9296093 | ||||||
| chr2:9296133
|
G | A | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.200-1167G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9296133 | ||||||
| chr2:9296151
|
G | A | 26 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0026others(23): Show | 26 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.200-1149G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9296151 | ||||||
| chr2:9296179
|
G | A | 65 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(62): Show | 65 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.200-1121G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9296179 | ||||||
| chr2:9296185
|
C | G | 28 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(25): Show | 28 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.200-1115C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9296185 | ||||||
| chr2:9296410
|
A | T | 3 | a0001c0004t0005g0041a0001c0004t0005g0138a0001c0007t0001g0030 | 3 | HG00639.hp1 HG01175.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.200-890A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9296410 | ||||||
| chr2:9296530
|
G | C | 26 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0026others(23): Show | 26 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.200-770G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9296530 | ||||||
| chr2:9296589
|
C | T | 3 | a0001c0004t0005g0041a0001c0004t0005g0138a0001c0007t0001g0030 | 3 | HG00639.hp1 HG01175.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.200-711C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9296589 | ||||||
| chr2:9296770
|
A | T | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.200-530A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9296770 | ||||||
| chr2:9296850
|
G | A | 1 | a0001c0002t0002g0069 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.200-450G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9296850 | ||||||
| chr2:9296975
|
G | C | 86 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(83): Show | 86 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.200-325G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9296975 | ||||||
| chr2:9297022
|
G | T | 26 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0026others(23): Show | 26 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.200-278G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9297022 | ||||||
| chr2:9297210
|
T | C | 1 | a0002c0001t0001g0159 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.200-90T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9297210 | ||||||
| chr2:9297284
|
C | T | 26 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0026others(23): Show | 26 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.200-16C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 2/27 | chr2 | 9297284 | ||||||
| chr2:9297515
|
T | C | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.345+70T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9297515 | ||||||
| chr2:9297701
|
C | T | 1 | a0002c0001t0014g0091 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.345+256C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9297701 | ||||||
| chr2:9297728
|
T | G | 56 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(53): Show | 56 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.345+283T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9297728 | ||||||
| chr2:9297850
|
C | A | 3 | a0001c0003t0006g0104a0001c0003t0006g0105a0001c0003t0006g0158 | 3 | HG00597.hp2 NA19011.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.345+405C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9297850 | ||||||
| chr2:9298016
|
T | C | 1 | a0001c0004t0005g0035 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.345+571T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9298016 | ||||||
| chr2:9298019
|
C | A | 1 | a0001c0004t0005g0035 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.345+574C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9298019 | ||||||
| chr2:9298161
|
C | T | 13 | a0001c0003t0001g0153a0001c0003t0006g0006a0001c0003t0006g0064others(10): Show | 13 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(10): Show |
intron_variant | MODIFIER | c.345+716C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9298161 | ||||||
| chr2:9298304
|
G | A | 23 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0026others(20): Show | 23 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.345+859G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9298304 | ||||||
| chr2:9298703
|
G | A | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.345+1258G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9298703 | ||||||
| chr2:9298785
|
G | C | 1 | a0002c0001t0001g0179 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.345+1340G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9298785 | ||||||
| chr2:9298834
|
C | T | 6 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0003t0001g0169others(3): Show | 6 | HG01496.hp2 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.345+1389C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9298834 | ||||||
| chr2:9299059
|
C | T | 26 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0026others(23): Show | 26 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.345+1614C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9299059 | ||||||
| chr2:9299303
|
T | C | 88 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(85): Show | 88 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.345+1858T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9299303 | ||||||
| chr2:9299836
|
T | TA | 21 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(18): Show | 21 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.345+2392dupA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9299836 | |||||
| chr2:9299866
|
C | G | 3 | a0001c0003t0004g0038a0001c0003t0004g0043a0001c0003t0004g0175 | 3 | HG02723.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.345+2421C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9299866 | ||||||
| chr2:9299886
|
A | G | 57 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(54): Show | 57 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.345+2441A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9299886 | ||||||
| chr2:9299914
|
A | G | 1 | a0002c0001t0001g0004 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.345+2469A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9299914 | ||||||
| chr2:9300007
|
G | C | 21 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(18): Show | 21 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.345+2562G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9300007 | ||||||
| chr2:9300008
|
G | T | 1 | a0001c0004t0005g0034 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.345+2563G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9300008 | ||||||
| chr2:9300108
|
C | T | 3 | a0001c0004t0005g0041a0001c0004t0005g0138a0001c0007t0001g0030 | 3 | HG00639.hp1 HG01175.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.345+2663C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9300108 | ||||||
| chr2:9300265
|
C | G | 57 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(54): Show | 57 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.345+2820C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9300265 | ||||||
| chr2:9300392
|
CCTT | C | 15 | a0001c0002t0003g0166a0001c0003t0016g0174a0001c0004t0005g0176others(12): Show | 15 | HG00738.hp1 HG01109.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.345+2950_345+2952d others(5): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9300392 | |||||
| chr2:9300460
|
A | G | 30 | a0001c0002t0003g0148a0001c0002t0009g0031a0001c0002t0009g0208others(27): Show | 30 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.345+3015A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9300460 | ||||||
| chr2:9300485
|
C | T | 1 | a0002c0001t0001g0155 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.345+3040C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9300485 | ||||||
| chr2:9300486
|
A | G | 23 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0026others(20): Show | 23 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.345+3041A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9300486 | ||||||
| chr2:9300597
|
G | A | 3 | a0001c0004t0005g0041a0001c0004t0005g0138a0001c0007t0001g0030 | 3 | HG00639.hp1 HG01175.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.345+3152G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9300597 | ||||||
| chr2:9300773
|
A | T | 87 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(84): Show | 87 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.345+3328A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9300773 | ||||||
| chr2:9301005
|
G | T | 3 | a0001c0004t0005g0041a0001c0004t0005g0138a0001c0007t0001g0030 | 3 | HG00639.hp1 HG01175.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.345+3560G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9301005 | ||||||
| chr2:9301256
|
GT | G | 8 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(5): Show | 8 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+3814delT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9301256 | |||||
| chr2:9301366
|
C | T | 1 | a0002c0005t0001g0054 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.345+3921C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9301366 | ||||||
| chr2:9301414
|
A | G | 1 | a0002c0005t0001g0132 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.345+3969A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9301414 | ||||||
| chr2:9301478
|
T | A | 6 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0003t0001g0169others(3): Show | 6 | HG01496.hp2 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.345+4033T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9301478 | ||||||
| chr2:9301549
|
G | T | 1 | a0002c0001t0010g0066 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.345+4104G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9301549 | ||||||
| chr2:9301660
|
A | C | 1 | a0002c0001t0001g0042 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.345+4215A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9301660 | ||||||
| chr2:9301790
|
G | T | 1 | a0001c0009t0004g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.345+4345G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9301790 | ||||||
| chr2:9301819
|
TC | T | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.345+4375delC | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9301819 | ||||||
| chr2:9301820
|
C | CT | 12 | a0001c0002t0002g0016a0001c0002t0008g0206a0001c0002t0019g0164others(9): Show | 12 | HG01099.hp1 HG01099.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.345+4396dupT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9301820 | |||||
| chr2:9301820
|
C | CTT | 46 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0027others(43): Show | 46 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.345+4395_345+4396d others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9301820 | |||||
| chr2:9301820
|
C | CTTT | 5 | a0001c0002t0003g0094a0001c0002t0003g0147a0001c0003t0001g0165others(2): Show | 5 | HG02738.hp2 HG02895.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.345+4394_345+4396d others(5): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9301820 | |||||
| chr2:9301820
|
C | CTTTTTTT others(8): Show |
1 | a0001c0002t0013g0001 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.345+4382_345+4396d others(17): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9301820 | |||||
| chr2:9301820
|
C | CTTTTTTT others(9): Show |
2 | a0001c0002t0002g0198a0001c0002t0002g0202 | 2 | HG02257.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.345+4381_345+4396d others(18): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9301820 | |||||
| chr2:9301820
|
C | CTTTTTTT others(12): Show |
1 | a0001c0002t0003g0124 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.345+4378_345+4396d others(21): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9301820 | |||||
| chr2:9301820
|
C | CTTTTTTT others(13): Show |
1 | a0001c0002t0003g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.345+4377_345+4396d others(22): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9301820 | |||||
| chr2:9301820
|
CT | C | 37 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(34): Show | 37 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.345+4396delT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9301820 | |||||
| chr2:9301846
|
C | T | 3 | a0001c0004t0005g0041a0001c0004t0005g0138a0001c0007t0001g0030 | 3 | HG00639.hp1 HG01175.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.345+4401C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9301846 | ||||||
| chr2:9301856
|
T | C | 90 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(87): Show | 90 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.345+4411T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9301856 | ||||||
| chr2:9302003
|
T | G | 5 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0062others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.345+4558T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9302003 | ||||||
| chr2:9302027
|
G | A | 1 | a0001c0004t0005g0176 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.345+4582G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9302027 | ||||||
| chr2:9302037
|
A | C | 1 | a0002c0005t0001g0119 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.345+4592A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9302037 | ||||||
| chr2:9302060
|
TGATCCAC others(208): Show |
T | 1 | a0002c0001t0001g0081 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.345+4621_345+4835d others(2): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9302060 | |||||
| chr2:9302069
|
C | T | 6 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0003t0001g0169others(3): Show | 6 | HG01496.hp2 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.345+4624C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9302069 | ||||||
| chr2:9302122
|
C | CT | 37 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(34): Show | 37 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.345+4694dupT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9302122 | |||||
| chr2:9302122
|
C | CTT | 28 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0026others(25): Show | 28 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.345+4693_345+4694d others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9302122 | |||||
| chr2:9302122
|
C | CTTT | 29 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(26): Show | 29 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.345+4692_345+4694d others(5): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9302122 | |||||
| chr2:9302158
|
G | A | 60 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(57): Show | 60 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.345+4713G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9302158 | ||||||
| chr2:9302169
|
C | CT | 35 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0027others(32): Show | 35 | HG00280.hp1 HG00735.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.345+4745dupT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9302169 | |||||
| chr2:9302169
|
C | CTT | 25 | a0001c0002t0002g0016a0001c0002t0009g0031a0001c0002t0009g0208others(22): Show | 25 | HG00408.hp1 HG00438.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.345+4744_345+4745d others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9302169 | |||||
| chr2:9302169
|
CT | C | 25 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0050others(22): Show | 25 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.345+4745delT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9302169 | |||||
| chr2:9302266
|
G | A | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.345+4821G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9302266 | ||||||
| chr2:9302268
|
G | T | 1 | a0002c0001t0001g0160 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.345+4823G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9302268 | ||||||
| chr2:9302290
|
A | G | 4 | a0002c0001t0001g0071a0002c0001t0001g0110a0002c0001t0001g0160others(1): Show | 4 | HG00597.hp1 HG02523.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.345+4845A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9302290 | ||||||
| chr2:9302477
|
TTTTG | T | 3 | a0001c0004t0005g0041a0001c0004t0005g0138a0001c0007t0001g0030 | 3 | HG00639.hp1 HG01175.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.345+5045_345+5048d others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9302477 | |||||
| chr2:9302503
|
C | T | 3 | a0001c0004t0005g0041a0001c0004t0005g0138a0001c0007t0001g0030 | 3 | HG00639.hp1 HG01175.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.345+5058C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9302503 | ||||||
| chr2:9302639
|
T | C | 3 | a0001c0004t0005g0041a0001c0004t0005g0138a0001c0007t0001g0030 | 3 | HG00639.hp1 HG01175.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.345+5194T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9302639 | ||||||
| chr2:9302721
|
C | T | 1 | a0002c0001t0001g0022 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.345+5276C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9302721 | ||||||
| chr2:9302905
|
C | T | 31 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(28): Show | 31 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.345+5460C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9302905 | ||||||
| chr2:9303019
|
C | G | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.345+5574C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9303019 | ||||||
| chr2:9303038
|
A | T | 27 | a0001c0002t0003g0148a0001c0002t0009g0031a0001c0002t0009g0208others(24): Show | 27 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.345+5593A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9303038 | ||||||
| chr2:9303042
|
T | C | 55 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(52): Show | 55 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.345+5597T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9303042 | ||||||
| chr2:9303169
|
C | T | 1 | a0001c0002t0012g0143 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.345+5724C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9303169 | ||||||
| chr2:9303253
|
T | A | 1 | a0002c0001t0001g0078 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.345+5808T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9303253 | ||||||
| chr2:9303261
|
C | A | 1 | a0002c0001t0001g0078 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.345+5816C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9303261 | ||||||
| chr2:9303386
|
G | T | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.345+5941G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9303386 | ||||||
| chr2:9303429
|
A | G | 2 | a0001c0002t0002g0073a0002c0001t0001g0157 | 2 | HG01074.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.345+5984A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9303429 | ||||||
| chr2:9303448
|
A | T | 1 | a0001c0002t0008g0048 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.345+6003A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9303448 | ||||||
| chr2:9303714
|
A | G | 91 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(88): Show | 91 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.345+6269A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9303714 | ||||||
| chr2:9303739
|
A | T | 6 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0003t0001g0169others(3): Show | 6 | HG01496.hp2 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.345+6294A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9303739 | ||||||
| chr2:9303742
|
T | C | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.345+6297T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9303742 | ||||||
| chr2:9303885
|
A | G | 64 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(61): Show | 64 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.345+6440A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9303885 | ||||||
| chr2:9303895
|
C | T | 1 | a0002c0001t0001g0087 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.345+6450C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9303895 | ||||||
| chr2:9303906
|
G | A | 6 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0003t0001g0169others(3): Show | 6 | HG01496.hp2 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.345+6461G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9303906 | ||||||
| chr2:9304491
|
G | C | 11 | a0001c0004t0005g0176a0001c0004t0005g0191a0001c0004t0005g0192others(8): Show | 11 | HG00738.hp1 HG01109.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.345+7046G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9304491 | ||||||
| chr2:9304549
|
C | T | 210 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(207): Show | 210 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.345+7104C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9304549 | ||||||
| chr2:9304590
|
T | C | 1 | a0001c0002t0002g0075 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.345+7145T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9304590 | ||||||
| chr2:9304732
|
G | A | 27 | a0001c0002t0003g0148a0001c0002t0009g0031a0001c0002t0009g0208others(24): Show | 27 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.345+7287G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9304732 | ||||||
| chr2:9304735
|
T | C | 5 | a0001c0003t0016g0174a0001c0007t0004g0015a0001c0007t0004g0154others(2): Show | 5 | HG02145.hp1 HG02486.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.345+7290T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9304735 | ||||||
| chr2:9304738
|
G | A | 5 | a0001c0003t0016g0174a0001c0007t0004g0015a0001c0007t0004g0154others(2): Show | 5 | HG02145.hp1 HG02486.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.345+7293G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9304738 | ||||||
| chr2:9304887
|
C | G | 1 | a0002c0005t0001g0009 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.345+7442C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9304887 | ||||||
| chr2:9304912
|
G | A | 63 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(60): Show | 63 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.345+7467G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9304912 | ||||||
| chr2:9304952
|
G | A | 5 | a0001c0002t0019g0164a0001c0003t0021g0040a0001c0004t0005g0041others(2): Show | 5 | HG00639.hp1 HG01175.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.345+7507G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9304952 | ||||||
| chr2:9305025
|
G | A | 6 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0003t0001g0169others(3): Show | 6 | HG01496.hp2 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.345+7580G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9305025 | ||||||
| chr2:9305130
|
T | TTGTAATA others(95): Show |
3 | a0001c0004t0005g0041a0001c0004t0005g0138a0001c0007t0001g0030 | 3 | HG00639.hp1 HG01175.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.345+7744_345+7745i others(104): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9305130 | |||||
| chr2:9305257
|
G | T | 3 | a0001c0004t0005g0041a0001c0004t0005g0138a0001c0007t0001g0030 | 3 | HG00639.hp1 HG01175.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.345+7812G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9305257 | ||||||
| chr2:9305260
|
G | A | 3 | a0001c0004t0005g0041a0001c0004t0005g0138a0001c0007t0001g0030 | 3 | HG00639.hp1 HG01175.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.345+7815G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9305260 | ||||||
| chr2:9305274
|
G | A | 2 | a0002c0001t0001g0083a0002c0001t0001g0128 | 2 | HG03654.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.345+7829G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9305274 | ||||||
| chr2:9305318
|
G | A | 63 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(60): Show | 63 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.345+7873G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9305318 | ||||||
| chr2:9305342
|
G | A | 63 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(60): Show | 63 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.345+7897G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9305342 | ||||||
| chr2:9305390
|
G | A | 1 | a0001c0003t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.345+7945G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9305390 | ||||||
| chr2:9305399
|
T | C | 60 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(57): Show | 60 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.345+7954T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9305399 | ||||||
| chr2:9305401
|
A | G | 63 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(60): Show | 63 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.345+7956A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9305401 | ||||||
| chr2:9305424
|
G | GAGAGGCT others(331): Show |
1 | a0002c0001t0001g0077 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.345+8012_345+8013i others(340): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9305424 | |||||
| chr2:9305435
|
G | GTAGTGGG others(251): Show |
59 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(56): Show | 59 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.345+8027_345+8028i others(260): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9305435 | |||||
| chr2:9305458
|
T | G | 1 | a0002c0001t0001g0077 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.345+8013T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9305458 | ||||||
| chr2:9305458
|
T | TAGAGGCT others(365): Show |
1 | a0002c0005t0001g0119 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.345+8083_345+8084i others(374): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9305458 | |||||
| chr2:9305458
|
T | TAGAGGCT others(399): Show |
4 | a0001c0004t0005g0021a0001c0004t0005g0034a0001c0004t0005g0144others(1): Show | 4 | HG01074.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.345+8083_345+8084i others(408): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9305458 | |||||
| chr2:9305458
|
T | TAGAGGCT others(399): Show |
2 | a0001c0004t0005g0185a0002c0001t0001g0118 | 2 | HG02080.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.345+8083_345+8084i others(408): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9305458 | |||||
| chr2:9305458
|
T | TAGAGGCT others(365): Show |
2 | a0002c0001t0001g0121a0002c0001t0001g0122 | 2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.345+8083_345+8084i others(374): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9305458 | |||||
| chr2:9305458
|
T | TAGAGGCT others(365): Show |
2 | a0002c0001t0001g0074a0002c0001t0001g0161 | 2 | HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.345+8083_345+8084i others(374): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9305458 | |||||
| chr2:9305458
|
T | TAGAGGCT others(365): Show |
93 | a0001c0002t0001g0115a0001c0002t0001g0116a0001c0002t0001g0126others(90): Show | 93 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.345+8083_345+8084i others(374): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9305458 | |||||
| chr2:9305458
|
T | TAGAGGCT others(634): Show |
2 | a0001c0002t0008g0048a0001c0002t0008g0206 | 2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.345+8083_345+8084i others(643): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9305458 | |||||
| chr2:9305491
|
G | T | 59 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(56): Show | 59 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.345+8046G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9305491 | ||||||
| chr2:9305494
|
G | C | 59 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(56): Show | 59 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.345+8049G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9305494 | ||||||
| chr2:9305501
|
T | G | 59 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(56): Show | 59 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.345+8056T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9305501 | ||||||
| chr2:9305501
|
T | TAGTAGTG others(630): Show |
1 | a0002c0001t0001g0067 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.345+8083_345+8084i others(639): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9305501 | |||||
| chr2:9305501
|
T | TAGTAGTG others(630): Show |
2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.345+8083_345+8084i others(639): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9305501 | |||||
| chr2:9305501
|
T | TAGTAGTG others(630): Show |
2 | a0001c0003t0001g0029a0001c0004t0005g0010 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.345+8083_345+8084i others(639): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9305501 | |||||
| chr2:9305501
|
T | TAGTAGTG others(630): Show |
18 | a0001c0002t0003g0148a0001c0003t0001g0039a0001c0003t0001g0046others(15): Show | 18 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.345+8083_345+8084i others(639): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9305501 | |||||
| chr2:9305501
|
T | TAGTAGTG others(630): Show |
4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.345+8083_345+8084i others(639): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9305501 | |||||
| chr2:9305501
|
T | TAGTAGTG others(429): Show |
2 | a0001c0004t0005g0041a0001c0004t0005g0138 | 2 | HG00639.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.345+8083_345+8084i others(438): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9305501 | |||||
| chr2:9305501
|
T | TAGTAGTG others(463): Show |
1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.345+8083_345+8084i others(472): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9305501 | |||||
| chr2:9305501
|
T | TAGTAGTG others(535): Show |
8 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(5): Show | 8 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+8083_345+8084i others(544): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9305501 | |||||
| chr2:9305503
|
G | GTAGTGGG others(96): Show |
4 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(1): Show | 4 | HG02280.hp1 HG02630.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.345+8083_345+8084i others(105): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9305503 | |||||
| chr2:9305509
|
G | A | 1 | a0001c0002t0003g0147 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.345+8064G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9305509 | ||||||
| chr2:9305514
|
T | TAGATATT others(433): Show |
1 | a0001c0002t0003g0188 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.345+8083_345+8084i others(442): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9305514 | |||||
| chr2:9305523
|
G | GAGGGGCT others(252): Show |
1 | a0001c0002t0003g0147 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.345+8078_345+8079i others(261): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9305523 | ||||||
| chr2:9305529
|
G | A | 4 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(1): Show | 4 | HG02280.hp1 HG02630.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.345+8084G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9305529 | ||||||
| chr2:9305537
|
A | G | 4 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(1): Show | 4 | HG02280.hp1 HG02630.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.345+8092A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9305537 | ||||||
| chr2:9305548
|
C | T | 4 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(1): Show | 4 | HG02280.hp1 HG02630.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.345+8103C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9305548 | ||||||
| chr2:9305569
|
T | G | 210 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(207): Show | 210 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.345+8124T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9305569 | ||||||
| chr2:9305624
|
G | T | 210 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(207): Show | 210 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.345+8179G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9305624 | ||||||
| chr2:9305686
|
A | G | 210 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(207): Show | 210 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.345+8241A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9305686 | ||||||
| chr2:9305693
|
G | T | 210 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(207): Show | 210 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.345+8248G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9305693 | ||||||
| chr2:9305715
|
T | C | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.345+8270T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9305715 | ||||||
| chr2:9305810
|
C | G | 1 | a0001c0003t0004g0200 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.345+8365C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9305810 | ||||||
| chr2:9305844
|
G | T | 11 | a0001c0004t0005g0041a0001c0004t0005g0138a0001c0006t0004g0014others(8): Show | 11 | HG00639.hp1 HG01070.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.345+8399G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9305844 | ||||||
| chr2:9305971
|
T | G | 11 | a0001c0004t0005g0041a0001c0004t0005g0138a0001c0006t0004g0014others(8): Show | 11 | HG00639.hp1 HG01070.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.345+8526T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9305971 | ||||||
| chr2:9306038
|
C | A | 60 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(57): Show | 60 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.345+8593C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9306038 | ||||||
| chr2:9306076
|
G | A | 115 | a0001c0002t0001g0024a0001c0002t0001g0115a0001c0002t0001g0116others(112): Show | 115 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.345+8631G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9306076 | ||||||
| chr2:9306174
|
G | A | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.345+8729G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9306174 | ||||||
| chr2:9306219
|
G | A | 57 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(54): Show | 57 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.345+8774G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9306219 | ||||||
| chr2:9306243
|
G | A | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.345+8798G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9306243 | ||||||
| chr2:9306269
|
G | A | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.345+8824G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9306269 | ||||||
| chr2:9306495
|
G | A | 1 | a0002c0001t0001g0140 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.345+9050G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9306495 | ||||||
| chr2:9306554
|
G | T | 14 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(11): Show | 14 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.345+9109G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9306554 | ||||||
| chr2:9306623
|
T | C | 90 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(87): Show | 90 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.345+9178T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9306623 | ||||||
| chr2:9306670
|
G | A | 27 | a0001c0002t0003g0148a0001c0002t0009g0031a0001c0002t0009g0208others(24): Show | 27 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.345+9225G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9306670 | ||||||
| chr2:9306765
|
C | T | 1 | a0001c0003t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.345+9320C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9306765 | ||||||
| chr2:9306844
|
G | A | 3 | a0001c0003t0001g0046a0001c0004t0005g0035a0002c0001t0001g0022 | 3 | HG03453.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.345+9399G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9306844 | ||||||
| chr2:9306881
|
G | A | 6 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0003t0001g0169others(3): Show | 6 | HG01496.hp2 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.345+9436G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9306881 | ||||||
| chr2:9306946
|
C | T | 54 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(51): Show | 54 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.345+9501C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9306946 | ||||||
| chr2:9307031
|
A | G | 3 | a0001c0002t0002g0129a0001c0002t0003g0141a0002c0005t0001g0025 | 3 | HG01346.hp2 HG04115.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.345+9586A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9307031 | ||||||
| chr2:9307106
|
C | T | 60 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(57): Show | 60 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.345+9661C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9307106 | ||||||
| chr2:9307532
|
T | C | 30 | a0001c0002t0003g0148a0001c0002t0009g0031a0001c0002t0009g0208others(27): Show | 30 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.345+10087T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9307532 | ||||||
| chr2:9307810
|
C | G | 2 | a0001c0002t0019g0164a0001c0003t0021g0040 | 2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.345+10365C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9307810 | ||||||
| chr2:9307870
|
G | A | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.345+10425G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9307870 | ||||||
| chr2:9307937
|
C | T | 1 | a0002c0001t0003g0099 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.345+10492C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9307937 | ||||||
| chr2:9308290
|
G | A | 21 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(18): Show | 21 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.346-10234G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9308290 | ||||||
| chr2:9308315
|
G | A | 2 | a0001c0002t0002g0075a0002c0001t0001g0146 | 2 | HG00280.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.346-10209G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9308315 | ||||||
| chr2:9308502
|
T | C | 1 | a0001c0003t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.346-10022T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9308502 | ||||||
| chr2:9308674
|
C | T | 1 | a0001c0003t0001g0153 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.346-9850C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9308674 | ||||||
| chr2:9308895
|
T | C | 6 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0003t0001g0169others(3): Show | 6 | HG01496.hp2 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.346-9629T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9308895 | ||||||
| chr2:9309066
|
C | T | 60 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(57): Show | 60 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.346-9458C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9309066 | ||||||
| chr2:9309087
|
C | G | 1 | a0002c0001t0001g0092 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.346-9437C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9309087 | ||||||
| chr2:9309103
|
C | T | 1 | a0002c0001t0003g0099 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.346-9421C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9309103 | ||||||
| chr2:9309238
|
G | A | 1 | a0001c0002t0019g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.346-9286G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9309238 | ||||||
| chr2:9309305
|
A | G | 1 | a0002c0001t0001g0100 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.346-9219A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9309305 | ||||||
| chr2:9309354
|
A | G | 8 | a0001c0002t0003g0188a0001c0004t0005g0021a0001c0004t0005g0034others(5): Show | 8 | HG01074.hp2 HG01891.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.346-9170A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9309354 | ||||||
| chr2:9309395
|
G | T | 24 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(21): Show | 24 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.346-9129G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9309395 | ||||||
| chr2:9309427
|
G | A | 24 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(21): Show | 24 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.346-9097G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9309427 | ||||||
| chr2:9309617
|
ATG | A | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.346-8900_346-8899d others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9309617 | |||||
| chr2:9309621
|
G | A | 24 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(21): Show | 24 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.346-8903G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9309621 | ||||||
| chr2:9309761
|
G | T | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.346-8763G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9309761 | ||||||
| chr2:9309771
|
A | G | 21 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(18): Show | 21 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.346-8753A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9309771 | ||||||
| chr2:9310016
|
C | A | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.346-8508C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9310016 | ||||||
| chr2:9310052
|
A | G | 6 | a0001c0003t0004g0011a0001c0003t0004g0020a0001c0003t0004g0038others(3): Show | 6 | HG02257.hp2 HG02723.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.346-8472A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9310052 | ||||||
| chr2:9310236
|
G | T | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.346-8288G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9310236 | ||||||
| chr2:9310319
|
C | T | 1 | a0002c0001t0001g0070 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.346-8205C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9310319 | ||||||
| chr2:9310325
|
C | T | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.346-8199C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9310325 | ||||||
| chr2:9310328
|
T | C | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.346-8196T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9310328 | ||||||
| chr2:9310383
|
C | G | 54 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(51): Show | 54 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.346-8141C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9310383 | ||||||
| chr2:9311041
|
C | CG | 66 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(63): Show | 66 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.346-7477dupG | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9311041 | |||||
| chr2:9311357
|
CA | C | 90 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(87): Show | 90 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.346-7156delA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9311357 | |||||
| chr2:9311390
|
T | G | 21 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(18): Show | 21 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.346-7134T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9311390 | ||||||
| chr2:9311400
|
A | G | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.346-7124A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9311400 | ||||||
| chr2:9311503
|
T | G | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.346-7021T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9311503 | ||||||
| chr2:9311737
|
G | A | 54 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(51): Show | 54 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.346-6787G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9311737 | ||||||
| chr2:9311921
|
G | A | 2 | a0001c0002t0001g0097a0001c0002t0002g0060 | 2 | HG01167.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.346-6603G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9311921 | ||||||
| chr2:9312109
|
A | G | 1 | a0001c0002t0003g0052 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.346-6415A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9312109 | ||||||
| chr2:9312125
|
C | T | 2 | a0002c0001t0001g0121a0002c0001t0001g0122 | 2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.346-6399C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9312125 | ||||||
| chr2:9312143
|
T | A | 24 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(21): Show | 24 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.346-6381T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9312143 | ||||||
| chr2:9312310
|
C | T | 23 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(20): Show | 23 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(20): Show |
intron_variant | MODIFIER | c.346-6214C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9312310 | ||||||
| chr2:9312339
|
A | G | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.346-6185A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9312339 | ||||||
| chr2:9312386
|
C | G | 2 | a0001c0004t0005g0041a0001c0004t0005g0138 | 2 | HG00639.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.346-6138C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9312386 | ||||||
| chr2:9312389
|
C | T | 1 | a0002c0005t0001g0025 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.346-6135C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9312389 | ||||||
| chr2:9312425
|
C | T | 4 | a0001c0002t0008g0048a0001c0002t0008g0206a0001c0004t0005g0041others(1): Show | 4 | HG00639.hp1 HG02976.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.346-6099C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9312425 | ||||||
| chr2:9312479
|
G | A | 8 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(5): Show | 8 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.346-6045G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9312479 | ||||||
| chr2:9312678
|
G | A | 8 | a0001c0002t0003g0188a0001c0004t0005g0021a0001c0004t0005g0034others(5): Show | 8 | HG01074.hp2 HG01891.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.346-5846G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9312678 | ||||||
| chr2:9312690
|
C | T | 5 | a0002c0001t0001g0042a0002c0001t0001g0088a0002c0001t0001g0089others(2): Show | 5 | HG00735.hp2 HG01358.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.346-5834C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9312690 | ||||||
| chr2:9312779
|
T | C | 81 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(78): Show | 81 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.346-5745T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9312779 | ||||||
| chr2:9312812
|
C | T | 1 | a0002c0001t0001g0118 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.346-5712C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9312812 | ||||||
| chr2:9312927
|
C | T | 1 | a0001c0009t0004g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.346-5597C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9312927 | ||||||
| chr2:9312946
|
C | T | 2 | a0001c0006t0004g0189a0001c0006t0004g0204 | 2 | HG01070.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.346-5578C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9312946 | ||||||
| chr2:9313082
|
A | C | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.346-5442A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9313082 | ||||||
| chr2:9313117
|
C | T | 85 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(82): Show | 85 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.346-5407C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9313117 | ||||||
| chr2:9313172
|
C | T | 1 | a0002c0005t0001g0119 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.346-5352C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9313172 | ||||||
| chr2:9313325
|
G | A | 6 | a0001c0003t0004g0011a0001c0003t0004g0020a0001c0003t0004g0038others(3): Show | 6 | HG02257.hp2 HG02723.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.346-5199G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9313325 | ||||||
| chr2:9313417
|
ATTCATG | A | 2 | a0001c0002t0019g0164a0001c0003t0021g0040 | 2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.346-5099_346-5094d others(8): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9313417 | |||||
| chr2:9313433
|
G | A | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.346-5091G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9313433 | ||||||
| chr2:9313441
|
G | C | 2 | a0001c0002t0019g0164a0001c0003t0021g0040 | 2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.346-5083G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9313441 | ||||||
| chr2:9313569
|
T | C | 108 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(105): Show | 108 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.346-4955T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9313569 | ||||||
| chr2:9313587
|
A | G | 10 | a0001c0002t0003g0188a0001c0004t0005g0021a0001c0004t0005g0034others(7): Show | 10 | HG00639.hp1 HG01074.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.346-4937A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9313587 | ||||||
| chr2:9313686
|
G | A | 1 | a0002c0001t0001g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.346-4838G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9313686 | ||||||
| chr2:9313689
|
G | A | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.346-4835G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9313689 | ||||||
| chr2:9313887
|
C | T | 2 | a0001c0002t0019g0164a0001c0003t0021g0040 | 2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.346-4637C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9313887 | ||||||
| chr2:9314015
|
G | T | 1 | a0001c0002t0002g0069 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.346-4509G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9314015 | ||||||
| chr2:9314204
|
G | A | 2 | a0001c0003t0016g0174a0001c0010t0018g0173 | 2 | HG02145.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.346-4320G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9314204 | ||||||
| chr2:9314281
|
G | T | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.346-4243G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9314281 | ||||||
| chr2:9314454
|
C | T | 2 | a0001c0002t0019g0164a0001c0003t0021g0040 | 2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.346-4070C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9314454 | ||||||
| chr2:9314762
|
C | T | 1 | a0001c0002t0012g0143 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.346-3762C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9314762 | ||||||
| chr2:9314922
|
CA | C | 16 | a0001c0003t0001g0169a0001c0004t0005g0176a0001c0004t0005g0191others(13): Show | 16 | HG00738.hp1 HG01109.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.346-3581delA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9314922 | |||||
| chr2:9314922
|
CAA | C | 122 | a0001c0002t0001g0024a0001c0002t0001g0115a0001c0002t0001g0116others(119): Show | 122 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.346-3582_346-3581d others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9314922 | |||||
| chr2:9314922
|
CAAA | C | 38 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(35): Show | 38 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.346-3583_346-3581d others(5): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9314922 | |||||
| chr2:9314922
|
CAAAA | C | 27 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0026others(24): Show | 27 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.346-3584_346-3581d others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9314922 | |||||
| chr2:9315020
|
G | A | 1 | a0002c0001t0001g0100 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.346-3504G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9315020 | ||||||
| chr2:9315150
|
A | G | 5 | a0001c0002t0001g0115a0001c0002t0001g0116a0001c0002t0001g0126others(2): Show | 5 | HG01106.hp2 HG01256.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.346-3374A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9315150 | ||||||
| chr2:9315212
|
A | C | 64 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(61): Show | 64 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.346-3312A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9315212 | ||||||
| chr2:9315222
|
A | G | 1 | a0002c0001t0001g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.346-3302A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9315222 | ||||||
| chr2:9315244
|
C | T | 3 | a0001c0002t0003g0166a0001c0002t0003g0209a0001c0012t0003g0033 | 3 | HG02818.hp2 HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.346-3280C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9315244 | ||||||
| chr2:9315339
|
A | G | 6 | a0001c0003t0004g0011a0001c0003t0004g0020a0001c0003t0004g0038others(3): Show | 6 | HG02257.hp2 HG02723.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.346-3185A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9315339 | ||||||
| chr2:9315347
|
G | A | 1 | a0001c0003t0021g0040 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.346-3177G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9315347 | ||||||
| chr2:9315519
|
G | A | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.346-3005G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9315519 | ||||||
| chr2:9315526
|
TAGG | T | 4 | a0001c0003t0004g0011a0001c0003t0004g0038a0001c0003t0004g0043others(1): Show | 4 | HG02257.hp2 HG02723.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.346-2996_346-2994d others(5): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9315526 | |||||
| chr2:9315539
|
C | A | 39 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(36): Show | 39 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.346-2985C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9315539 | ||||||
| chr2:9315622
|
G | A | 1 | a0001c0003t0001g0029 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.346-2902G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9315622 | ||||||
| chr2:9315646
|
G | C | 1 | a0001c0003t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.346-2878G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9315646 | ||||||
| chr2:9315784
|
C | T | 1 | a0001c0004t0005g0205 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.346-2740C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9315784 | ||||||
| chr2:9315971
|
T | G | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.346-2553T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9315971 | ||||||
| chr2:9316066
|
C | G | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.346-2458C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9316066 | ||||||
| chr2:9316068
|
C | T | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.346-2456C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9316068 | ||||||
| chr2:9316087
|
G | T | 2 | a0001c0002t0003g0141a0002c0005t0001g0025 | 2 | HG01346.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.346-2437G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9316087 | ||||||
| chr2:9316094
|
A | G | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.346-2430A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9316094 | ||||||
| chr2:9316189
|
G | A | 54 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(51): Show | 54 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.346-2335G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9316189 | ||||||
| chr2:9316230
|
G | A | 3 | a0001c0002t0002g0137a0001c0002t0023g0008a0002c0001t0003g0136 | 3 | HG02523.hp1 HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.346-2294G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9316230 | ||||||
| chr2:9316696
|
G | A | 4 | a0001c0002t0003g0147a0001c0002t0003g0149a0001c0002t0003g0151others(1): Show | 4 | HG00323.hp2 HG00738.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.346-1828G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9316696 | ||||||
| chr2:9316846
|
G | T | 1 | a0002c0001t0001g0109 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.346-1678G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9316846 | ||||||
| chr2:9316892
|
C | G | 3 | a0001c0002t0003g0166a0001c0002t0003g0209a0001c0012t0003g0033 | 3 | HG02818.hp2 HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.346-1632C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9316892 | ||||||
| chr2:9316896
|
G | C | 74 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(71): Show | 74 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.346-1628G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9316896 | ||||||
| chr2:9316943
|
A | C | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.346-1581A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9316943 | ||||||
| chr2:9316969
|
C | A | 1 | a0001c0002t0003g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.346-1555C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9316969 | ||||||
| chr2:9316969
|
C | CCA | 77 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(74): Show | 77 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.346-1555_346-1554i others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9316969 | ||||||
| chr2:9316989
|
A | G | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.346-1535A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9316989 | ||||||
| chr2:9317022
|
A | G | 1 | a0001c0002t0006g0183 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.346-1502A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9317022 | ||||||
| chr2:9317036
|
CCAAT | C | 62 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(59): Show | 62 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.346-1485_346-1482d others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9317036 | |||||
| chr2:9317039
|
A | G | 10 | a0001c0002t0003g0188a0001c0002t0019g0164a0001c0003t0021g0040others(7): Show | 10 | HG00639.hp1 HG01074.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.346-1485A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9317039 | ||||||
| chr2:9317093
|
T | C | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.346-1431T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9317093 | ||||||
| chr2:9317117
|
A | ATCAC | 11 | a0001c0002t0003g0188a0001c0002t0019g0164a0001c0003t0021g0040others(8): Show | 11 | HG00639.hp1 HG01074.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.346-1406_346-1403d others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9317117 | |||||
| chr2:9317117
|
A | ATCACATC others(13): Show |
5 | a0001c0003t0016g0174a0001c0007t0004g0015a0001c0007t0004g0154others(2): Show | 5 | HG02145.hp1 HG02486.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.346-1402_346-1401i others(22): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9317117 | |||||
| chr2:9317117
|
A | ATCACTCA others(17): Show |
58 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(55): Show | 58 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.346-1403_346-1402i others(26): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9317117 | |||||
| chr2:9317119
|
CACA | C | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.346-1402_346-1400d others(5): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9317119 | |||||
| chr2:9317133
|
A | ACACT | 63 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(60): Show | 63 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.346-1388_346-1387i others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9317133 | |||||
| chr2:9317133
|
A | ACT | 147 | a0001c0002t0001g0024a0001c0002t0001g0115a0001c0002t0001g0116others(144): Show | 147 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.346-1390_346-1389i others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9317133 | |||||
| chr2:9317166
|
T | A | 2 | a0001c0003t0001g0029a0001c0004t0005g0010 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.346-1358T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9317166 | ||||||
| chr2:9317168
|
TCACCACA others(4): Show |
T | 8 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(5): Show | 8 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.346-1355_346-1345d others(13): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9317168 | ||||||
| chr2:9317175
|
ACT | A | 21 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(18): Show | 21 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.346-1347_346-1346d others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9317175 | |||||
| chr2:9317177
|
TCAA | T | 10 | a0001c0002t0003g0188a0001c0002t0019g0164a0001c0003t0021g0040others(7): Show | 10 | HG00639.hp1 HG01074.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.346-1344_346-1342d others(5): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9317177 | |||||
| chr2:9317213
|
CCACACTC others(1): Show |
C | 6 | a0001c0003t0004g0011a0001c0003t0004g0020a0001c0003t0004g0038others(3): Show | 6 | HG02257.hp2 HG02723.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.346-1306_346-1299d others(10): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9317213 | |||||
| chr2:9317215
|
ACACT | A | 63 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(60): Show | 63 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.346-1305_346-1302d others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9317215 | |||||
| chr2:9317259
|
TCA | T | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.346-1257_346-1256d others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9317259 | |||||
| chr2:9317270
|
CAT | C | 2 | a0001c0002t0008g0048a0001c0002t0008g0206 | 2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.346-1251_346-1250d others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9317270 | |||||
| chr2:9317336
|
C | CTCAA | 205 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(202): Show | 205 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.346-1185_346-1184i others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9317336 | |||||
| chr2:9317384
|
CCA | C | 63 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(60): Show | 63 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.346-1130_346-1129d others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9317384 | |||||
| chr2:9317434
|
A | T | 2 | a0002c0001t0001g0071a0002c0001t0010g0125 | 2 | HG02523.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.346-1090A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9317434 | ||||||
| chr2:9317442
|
T | TCA | 210 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(207): Show | 210 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.346-1081_346-1080i others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9317442 | |||||
| chr2:9317452
|
A | ACACT | 63 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(60): Show | 63 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.346-1070_346-1069i others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9317452 | |||||
| chr2:9317452
|
A | ACT | 147 | a0001c0002t0001g0024a0001c0002t0001g0115a0001c0002t0001g0116others(144): Show | 147 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.346-1071_346-1070i others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9317452 | |||||
| chr2:9317527
|
CTCAA | C | 2 | a0001c0002t0002g0007a0001c0002t0002g0177 | 2 | HG01168.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.346-996_346-993del others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9317527 | ||||||
| chr2:9317531
|
A | C | 62 | a0001c0002t0001g0097a0001c0002t0002g0016a0001c0002t0002g0027others(59): Show | 62 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.346-993A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9317531 | ||||||
| chr2:9317534
|
C | G | 18 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(15): Show | 18 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.346-990C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9317534 | ||||||
| chr2:9317541
|
ATC | A | 7 | a0001c0003t0001g0029a0001c0003t0001g0169a0001c0003t0001g0171others(4): Show | 7 | HG01175.hp2 HG01496.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.346-978_346-977del others(2): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9317541 | |||||
| chr2:9317550
|
A | C | 63 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(60): Show | 63 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.346-974A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9317550 | ||||||
| chr2:9317551
|
T | G | 1 | a0001c0003t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.346-973T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9317551 | ||||||
| chr2:9317552
|
C | T | 2 | a0001c0003t0001g0165a0001c0009t0004g0047 | 2 | HG02895.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.346-972C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9317552 | ||||||
| chr2:9317562
|
ACT | A | 90 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(87): Show | 90 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.346-958_346-957del others(2): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9317562 | |||||
| chr2:9317562
|
ACTCT | A | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.346-960_346-957del others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9317562 | |||||
| chr2:9317585
|
TACAC | T | 13 | a0001c0003t0001g0153a0001c0003t0006g0006a0001c0003t0006g0064others(10): Show | 13 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(10): Show |
intron_variant | MODIFIER | c.346-937_346-934del others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9317585 | |||||
| chr2:9317675
|
T | C | 63 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(60): Show | 63 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.346-849T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9317675 | ||||||
| chr2:9317719
|
C | T | 1 | a0002c0001t0001g0118 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.346-805C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9317719 | ||||||
| chr2:9317737
|
C | T | 1 | a0002c0001t0001g0004 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.346-787C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9317737 | ||||||
| chr2:9317785
|
C | G | 3 | a0001c0002t0003g0166a0001c0002t0003g0209a0001c0012t0003g0033 | 3 | HG02818.hp2 HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.346-739C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9317785 | ||||||
| chr2:9317786
|
A | G | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.346-738A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9317786 | ||||||
| chr2:9317789
|
C | T | 6 | a0001c0003t0001g0210a0001c0003t0016g0174a0001c0007t0004g0015others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.346-735C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9317789 | ||||||
| chr2:9317796
|
G | A | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.346-728G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9317796 | ||||||
| chr2:9317812
|
A | ACAAT | 63 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(60): Show | 63 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.346-709_346-706dup others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9317812 | |||||
| chr2:9317935
|
A | T | 6 | a0001c0003t0001g0210a0001c0003t0016g0174a0001c0007t0004g0015others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.346-589A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9317935 | ||||||
| chr2:9317948
|
A | C | 8 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(5): Show | 8 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.346-576A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9317948 | ||||||
| chr2:9317995
|
A | AAC | 54 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(51): Show | 54 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.346-520_346-519dup others(2): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr2 | 9317995 | |||||
| chr2:9318008
|
C | G | 3 | a0001c0003t0001g0046a0001c0004t0005g0035a0002c0001t0001g0022 | 3 | HG03453.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.346-516C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9318008 | ||||||
| chr2:9318052
|
A | G | 63 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(60): Show | 63 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.346-472A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9318052 | ||||||
| chr2:9318159
|
G | A | 2 | a0001c0002t0019g0164a0001c0003t0021g0040 | 2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.346-365G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9318159 | ||||||
| chr2:9318221
|
T | G | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.346-303T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9318221 | ||||||
| chr2:9318243
|
C | G | 1 | a0001c0003t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.346-281C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9318243 | ||||||
| chr2:9318245
|
T | C | 3 | a0001c0002t0003g0166a0001c0002t0003g0209a0001c0012t0003g0033 | 3 | HG02818.hp2 HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.346-279T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9318245 | ||||||
| chr2:9318246
|
C | T | 3 | a0001c0002t0003g0166a0001c0002t0003g0209a0001c0012t0003g0033 | 3 | HG02818.hp2 HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.346-278C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9318246 | ||||||
| chr2:9318325
|
C | T | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.346-199C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9318325 | ||||||
| chr2:9318331
|
A | G | 63 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(60): Show | 63 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.346-193A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9318331 | ||||||
| chr2:9318337
|
C | T | 8 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(5): Show | 8 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.346-187C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9318337 | ||||||
| chr2:9318399
|
A | G | 1 | a0001c0002t0003g0094 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.346-125A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 3/27 | chr2 | 9318399 | ||||||
| chr2:9318669
|
G | A | 24 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0026others(21): Show | 24 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.420+71G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 4/27 | chr2 | 9318669 | ||||||
| chr2:9318682
|
G | A | 1 | a0002c0001t0001g0093 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.420+84G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 4/27 | chr2 | 9318682 | ||||||
| chr2:9318881
|
G | C | 1 | a0002c0005t0001g0132 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.420+283G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 4/27 | chr2 | 9318881 | ||||||
| chr2:9318973
|
G | GGTGT | 8 | a0001c0004t0005g0176a0001c0004t0005g0191a0001c0004t0005g0192others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.420+376_420+379dup others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr2 | 9318973 | |||||
| chr2:9318992
|
A | G | 1 | a0002c0001t0001g0049 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.420+394A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 4/27 | chr2 | 9318992 | ||||||
| chr2:9319125
|
G | A | 2 | a0001c0002t0019g0164a0001c0003t0021g0040 | 2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.420+527G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 4/27 | chr2 | 9319125 | ||||||
| chr2:9319224
|
G | A | 1 | a0002c0001t0001g0113 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.420+626G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 4/27 | chr2 | 9319224 | ||||||
| chr2:9319239
|
C | T | 1 | a0001c0003t0021g0040 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.420+641C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 4/27 | chr2 | 9319239 | ||||||
| chr2:9319277
|
C | T | 63 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(60): Show | 63 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.420+679C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 4/27 | chr2 | 9319277 | ||||||
| chr2:9319379
|
C | T | 2 | a0001c0002t0019g0164a0001c0003t0021g0040 | 2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.420+781C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 4/27 | chr2 | 9319379 | ||||||
| chr2:9319417
|
G | A | 2 | a0001c0002t0019g0164a0001c0003t0021g0040 | 2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.420+819G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 4/27 | chr2 | 9319417 | ||||||
| chr2:9319440
|
C | A | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.420+842C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 4/27 | chr2 | 9319440 | ||||||
| chr2:9319569
|
T | C | 63 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(60): Show | 63 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.421-719T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 4/27 | chr2 | 9319569 | ||||||
| chr2:9319753
|
C | G | 6 | a0001c0003t0004g0011a0001c0003t0004g0020a0001c0003t0004g0038others(3): Show | 6 | HG02257.hp2 HG02723.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.421-535C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 4/27 | chr2 | 9319753 | ||||||
| chr2:9319857
|
T | G | 63 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(60): Show | 63 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.421-431T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 4/27 | chr2 | 9319857 | ||||||
| chr2:9320105
|
G | A | 28 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(25): Show | 28 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.421-183G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 4/27 | chr2 | 9320105 | ||||||
| chr2:9320225
|
T | G | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.421-63T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 4/27 | chr2 | 9320225 | ||||||
| chr2:9320431
|
C | A | 4 | a0001c0002t0003g0147a0001c0002t0003g0149a0001c0002t0003g0151others(1): Show | 4 | HG00323.hp2 HG00738.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.470+94C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 5/27 | chr2 | 9320431 | ||||||
| chr2:9320570
|
G | A | 1 | a0002c0001t0001g0061 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.470+233G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 5/27 | chr2 | 9320570 | ||||||
| chr2:9320590
|
T | C | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.470+253T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 5/27 | chr2 | 9320590 | ||||||
| chr2:9320658
|
C | T | 1 | a0001c0004t0005g0192 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.470+321C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 5/27 | chr2 | 9320658 | ||||||
| chr2:9320861
|
C | T | 8 | a0002c0001t0001g0168a0002c0005t0001g0002a0002c0005t0001g0101others(5): Show | 8 | HG01099.hp2 HG01106.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.470+524C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 5/27 | chr2 | 9320861 | ||||||
| chr2:9320875
|
A | G | 1 | a0001c0003t0001g0017 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.470+538A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 5/27 | chr2 | 9320875 | ||||||
| chr2:9320885
|
T | A | 1 | a0001c0009t0004g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.470+548T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 5/27 | chr2 | 9320885 | ||||||
| chr2:9321052
|
A | C | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.470+715A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 5/27 | chr2 | 9321052 | ||||||
| chr2:9321157
|
A | G | 1 | a0002c0005t0001g0098 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.470+820A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 5/27 | chr2 | 9321157 | ||||||
| chr2:9321431
|
C | T | 54 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(51): Show | 54 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.470+1094C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 5/27 | chr2 | 9321431 | ||||||
| chr2:9321472
|
C | A | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.470+1135C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 5/27 | chr2 | 9321472 | ||||||
| chr2:9321566
|
T | G | 20 | a0001c0002t0003g0188a0001c0002t0019g0164a0001c0003t0001g0210others(17): Show | 20 | HG00639.hp1 HG01074.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.470+1229T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 5/27 | chr2 | 9321566 | ||||||
| chr2:9321695
|
G | C | 1 | a0002c0001t0001g0078 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.470+1358G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 5/27 | chr2 | 9321695 | ||||||
| chr2:9321798
|
G | C | 2 | a0001c0002t0003g0062a0001c0002t0003g0124 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.471-1323G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 5/27 | chr2 | 9321798 | ||||||
| chr2:9321891
|
A | G | 9 | a0001c0003t0001g0210a0001c0003t0004g0200a0001c0003t0007g0170others(6): Show | 9 | HG02145.hp1 HG02486.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.471-1230A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 5/27 | chr2 | 9321891 | ||||||
| chr2:9322107
|
A | G | 2 | a0001c0002t0019g0164a0001c0003t0021g0040 | 2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.471-1014A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 5/27 | chr2 | 9322107 | ||||||
| chr2:9322219
|
G | A | 1 | a0001c0002t0003g0142 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.471-902G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 5/27 | chr2 | 9322219 | ||||||
| chr2:9322291
|
G | A | 1 | a0001c0003t0021g0040 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.471-830G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 5/27 | chr2 | 9322291 | ||||||
| chr2:9322487
|
C | T | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.471-634C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 5/27 | chr2 | 9322487 | ||||||
| chr2:9322513
|
C | A | 10 | a0001c0003t0001g0210a0001c0003t0004g0200a0001c0003t0007g0170others(7): Show | 10 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.471-608C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 5/27 | chr2 | 9322513 | ||||||
| chr2:9322516
|
C | T | 10 | a0001c0003t0001g0210a0001c0003t0004g0200a0001c0003t0007g0170others(7): Show | 10 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.471-605C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 5/27 | chr2 | 9322516 | ||||||
| chr2:9322518
|
A | ATTTTGTG others(8): Show |
10 | a0001c0003t0001g0210a0001c0003t0004g0200a0001c0003t0007g0170others(7): Show | 10 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.471-601_471-600ins others(15): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr2 | 9322518 | |||||
| chr2:9322622
|
A | G | 10 | a0001c0003t0001g0210a0001c0003t0004g0200a0001c0003t0007g0170others(7): Show | 10 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.471-499A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 5/27 | chr2 | 9322622 | ||||||
| chr2:9322763
|
G | A | 10 | a0001c0003t0001g0210a0001c0003t0004g0200a0001c0003t0007g0170others(7): Show | 10 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.471-358G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 5/27 | chr2 | 9322763 | ||||||
| chr2:9322820
|
A | C | 116 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(113): Show | 116 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.471-301A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 5/27 | chr2 | 9322820 | ||||||
| chr2:9322864
|
C | A | 10 | a0001c0002t0003g0188a0001c0002t0019g0164a0001c0003t0021g0040others(7): Show | 10 | HG00639.hp1 HG01074.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.471-257C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 5/27 | chr2 | 9322864 | ||||||
| chr2:9322957
|
C | T | 6 | a0001c0003t0001g0210a0001c0003t0016g0174a0001c0007t0004g0015others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.471-164C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 5/27 | chr2 | 9322957 | ||||||
| chr2:9323012
|
G | A | 2 | a0002c0001t0001g0121a0002c0001t0001g0122 | 2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.471-109G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 5/27 | chr2 | 9323012 | ||||||
| chr2:9323023
|
G | A | 1 | a0001c0003t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.471-98G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 5/27 | chr2 | 9323023 | ||||||
| chr2:9323078
|
T | C | 20 | a0001c0002t0003g0188a0001c0002t0019g0164a0001c0003t0001g0210others(17): Show | 20 | HG00639.hp1 HG01074.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.471-43T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 5/27 | chr2 | 9323078 | ||||||
| chr2:9323275
|
C | G | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.600+25C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9323275 | ||||||
| chr2:9323325
|
C | T | 94 | a0001c0002t0001g0024a0001c0002t0001g0115a0001c0002t0001g0116others(91): Show | 94 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.600+75C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9323325 | ||||||
| chr2:9323472
|
A | G | 1 | a0001c0004t0005g0138 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.600+222A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9323472 | ||||||
| chr2:9323476
|
C | T | 10 | a0001c0002t0003g0188a0001c0002t0019g0164a0001c0003t0021g0040others(7): Show | 10 | HG00639.hp1 HG01074.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.600+226C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9323476 | ||||||
| chr2:9323506
|
T | C | 116 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(113): Show | 116 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.600+256T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9323506 | ||||||
| chr2:9323510
|
C | T | 22 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(19): Show | 22 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(19): Show |
intron_variant | MODIFIER | c.600+260C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9323510 | ||||||
| chr2:9323511
|
G | A | 10 | a0001c0003t0001g0210a0001c0003t0004g0200a0001c0003t0007g0170others(7): Show | 10 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.600+261G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9323511 | ||||||
| chr2:9323522
|
T | G | 10 | a0001c0002t0003g0188a0001c0002t0019g0164a0001c0003t0021g0040others(7): Show | 10 | HG00639.hp1 HG01074.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.600+272T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9323522 | ||||||
| chr2:9323695
|
TG | T | 6 | a0001c0003t0004g0011a0001c0003t0004g0020a0001c0003t0004g0038others(3): Show | 6 | HG02257.hp2 HG02723.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.600+446delG | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9323695 | ||||||
| chr2:9323727
|
A | G | 1 | a0004c0015t0015g0123 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.600+477A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9323727 | ||||||
| chr2:9323774
|
G | A | 10 | a0001c0003t0001g0210a0001c0003t0004g0200a0001c0003t0007g0170others(7): Show | 10 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.600+524G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9323774 | ||||||
| chr2:9323794
|
T | C | 20 | a0001c0002t0003g0188a0001c0002t0019g0164a0001c0003t0001g0210others(17): Show | 20 | HG00639.hp1 HG01074.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.600+544T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9323794 | ||||||
| chr2:9323811
|
C | A | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.600+561C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9323811 | ||||||
| chr2:9323821
|
A | G | 10 | a0001c0002t0003g0188a0001c0002t0019g0164a0001c0003t0021g0040others(7): Show | 10 | HG00639.hp1 HG01074.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.600+571A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9323821 | ||||||
| chr2:9324016
|
C | T | 2 | a0001c0002t0002g0073a0002c0001t0001g0157 | 2 | HG01074.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.600+766C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9324016 | ||||||
| chr2:9324168
|
A | G | 1 | a0002c0001t0001g0083 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.600+918A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9324168 | ||||||
| chr2:9324514
|
C | T | 6 | a0001c0003t0001g0210a0001c0003t0016g0174a0001c0007t0004g0015others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.600+1264C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9324514 | ||||||
| chr2:9324515
|
G | A | 1 | a0001c0002t0019g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.600+1265G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9324515 | ||||||
| chr2:9324600
|
A | G | 6 | a0001c0003t0001g0210a0001c0003t0016g0174a0001c0007t0004g0015others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.600+1350A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9324600 | ||||||
| chr2:9324660
|
G | A | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.600+1410G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9324660 | ||||||
| chr2:9324838
|
A | G | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+1588A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9324838 | ||||||
| chr2:9324914
|
G | A | 1 | a0001c0002t0002g0129 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.600+1664G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9324914 | ||||||
| chr2:9325181
|
C | T | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.600+1931C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9325181 | ||||||
| chr2:9325196
|
G | A | 12 | a0001c0002t0019g0164a0001c0003t0001g0210a0001c0003t0004g0200others(9): Show | 12 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.600+1946G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9325196 | ||||||
| chr2:9325283
|
C | T | 2 | a0001c0002t0019g0164a0001c0003t0021g0040 | 2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.600+2033C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9325283 | ||||||
| chr2:9325423
|
A | C | 6 | a0001c0003t0004g0011a0001c0003t0004g0020a0001c0003t0004g0038others(3): Show | 6 | HG02257.hp2 HG02723.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.600+2173A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9325423 | ||||||
| chr2:9325558
|
G | T | 107 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(104): Show | 107 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.601-2268G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9325558 | ||||||
| chr2:9325619
|
G | C | 3 | a0001c0002t0003g0148a0001c0003t0001g0039a0001c0003t0001g0190 | 3 | HG01934.hp2 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.601-2207G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9325619 | ||||||
| chr2:9325640
|
G | A | 1 | a0001c0002t0001g0097 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.601-2186G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9325640 | ||||||
| chr2:9325913
|
T | C | 3 | a0001c0003t0006g0064a0001c0003t0006g0065a0001c0003t0006g0102 | 3 | HG00408.hp2 HG00438.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.601-1913T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9325913 | ||||||
| chr2:9326392
|
G | A | 24 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0026others(21): Show | 24 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.601-1434G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9326392 | ||||||
| chr2:9326476
|
GA | G | 99 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(96): Show | 99 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.601-1348delA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 9326476 | |||||
| chr2:9326723
|
A | G | 1 | a0001c0003t0006g0065 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.601-1103A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9326723 | ||||||
| chr2:9326872
|
C | T | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.601-954C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9326872 | ||||||
| chr2:9326921
|
T | G | 2 | a0001c0002t0019g0164a0001c0003t0021g0040 | 2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.601-905T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9326921 | ||||||
| chr2:9326923
|
G | T | 1 | a0001c0002t0002g0057 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.601-903G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9326923 | ||||||
| chr2:9326971
|
C | T | 8 | a0002c0001t0001g0042a0002c0001t0001g0088a0002c0001t0001g0089others(5): Show | 8 | HG00735.hp2 HG01346.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.601-855C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9326971 | ||||||
| chr2:9327092
|
A | G | 8 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(5): Show | 8 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.601-734A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9327092 | ||||||
| chr2:9327128
|
AC | A | 60 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(57): Show | 60 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.601-694delC | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 9327128 | |||||
| chr2:9327139
|
G | A | 6 | a0001c0003t0004g0011a0001c0003t0004g0020a0001c0003t0004g0038others(3): Show | 6 | HG02257.hp2 HG02723.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.601-687G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9327139 | ||||||
| chr2:9327224
|
G | A | 2 | a0001c0002t0019g0164a0001c0003t0021g0040 | 2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.601-602G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9327224 | ||||||
| chr2:9327388
|
C | A | 2 | a0001c0002t0019g0164a0001c0003t0021g0040 | 2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.601-438C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9327388 | ||||||
| chr2:9327465
|
C | G | 8 | a0002c0001t0001g0042a0002c0001t0001g0088a0002c0001t0001g0089others(5): Show | 8 | HG00735.hp2 HG01346.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.601-361C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9327465 | ||||||
| chr2:9327598
|
A | G | 62 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(59): Show | 62 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.601-228A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9327598 | ||||||
| chr2:9327676
|
G | C | 8 | a0002c0001t0001g0042a0002c0001t0001g0088a0002c0001t0001g0089others(5): Show | 8 | HG00735.hp2 HG01346.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.601-150G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9327676 | ||||||
| chr2:9327686
|
C | T | 54 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(51): Show | 54 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.601-140C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9327686 | ||||||
| chr2:9327805
|
T | A | 10 | a0001c0003t0001g0210a0001c0003t0004g0200a0001c0003t0007g0170others(7): Show | 10 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.601-21T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 6/27 | chr2 | 9327805 | ||||||
| chr2:9328261
|
A | G | 12 | a0001c0002t0019g0164a0001c0003t0001g0210a0001c0003t0004g0200others(9): Show | 12 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.686+350A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9328261 | ||||||
| chr2:9328366
|
A | G | 10 | a0001c0003t0001g0210a0001c0003t0004g0200a0001c0003t0007g0170others(7): Show | 10 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.686+455A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9328366 | ||||||
| chr2:9328463
|
C | T | 2 | a0002c0001t0001g0121a0002c0001t0001g0122 | 2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.686+552C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9328463 | ||||||
| chr2:9328757
|
C | T | 10 | a0001c0003t0001g0210a0001c0003t0004g0200a0001c0003t0007g0170others(7): Show | 10 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.686+846C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9328757 | ||||||
| chr2:9328795
|
T | G | 1 | a0001c0003t0001g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.686+884T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9328795 | ||||||
| chr2:9328818
|
A | G | 20 | a0001c0002t0003g0188a0001c0002t0019g0164a0001c0003t0001g0210others(17): Show | 20 | HG00639.hp1 HG01074.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.686+907A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9328818 | ||||||
| chr2:9328868
|
T | G | 10 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0006t0004g0014others(7): Show | 10 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.686+957T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9328868 | ||||||
| chr2:9329022
|
G | A | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.686+1111G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9329022 | ||||||
| chr2:9329040
|
G | A | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.686+1129G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9329040 | ||||||
| chr2:9329123
|
G | A | 1 | a0002c0001t0001g0113 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.686+1212G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9329123 | ||||||
| chr2:9329247
|
G | A | 2 | a0001c0002t0019g0164a0001c0003t0021g0040 | 2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.686+1336G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9329247 | ||||||
| chr2:9329363
|
C | T | 1 | a0001c0003t0001g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.686+1452C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9329363 | ||||||
| chr2:9329502
|
G | A | 1 | a0001c0003t0001g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.686+1591G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9329502 | ||||||
| chr2:9329512
|
C | G | 3 | a0001c0002t0002g0056a0001c0002t0002g0057a0001c0002t0002g0058 | 3 | HG01070.hp2 HG01071.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.686+1601C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9329512 | ||||||
| chr2:9329550
|
G | A | 1 | a0002c0005t0001g0131 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.686+1639G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9329550 | ||||||
| chr2:9329610
|
G | A | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.686+1699G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9329610 | ||||||
| chr2:9329672
|
C | G | 116 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(113): Show | 116 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.686+1761C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9329672 | ||||||
| chr2:9329741
|
G | A | 6 | a0001c0003t0004g0011a0001c0003t0004g0020a0001c0003t0004g0038others(3): Show | 6 | HG02257.hp2 HG02723.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.686+1830G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9329741 | ||||||
| chr2:9329755
|
C | T | 4 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199others(1): Show | 4 | HG01175.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.686+1844C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9329755 | ||||||
| chr2:9329891
|
C | T | 1 | a0001c0003t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.686+1980C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9329891 | ||||||
| chr2:9329937
|
A | G | 12 | a0001c0002t0019g0164a0001c0003t0001g0210a0001c0003t0004g0200others(9): Show | 12 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.686+2026A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9329937 | ||||||
| chr2:9329962
|
A | G | 10 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0006t0004g0014others(7): Show | 10 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.686+2051A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9329962 | ||||||
| chr2:9330315
|
C | T | 6 | a0001c0003t0001g0210a0001c0003t0016g0174a0001c0007t0004g0015others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.686+2404C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9330315 | ||||||
| chr2:9330732
|
A | G | 4 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0002g0134others(1): Show | 4 | HG02280.hp1 HG02630.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.686+2821A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9330732 | ||||||
| chr2:9330775
|
G | A | 3 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0059 | 3 | HG00642.hp2 HG01261.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.686+2864G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9330775 | ||||||
| chr2:9330824
|
G | A | 8 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(5): Show | 8 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.686+2913G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9330824 | ||||||
| chr2:9330863
|
C | T | 107 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(104): Show | 107 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.686+2952C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9330863 | ||||||
| chr2:9330899
|
C | T | 2 | a0002c0001t0001g0117a0002c0001t0020g0079 | 2 | HG02080.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.686+2988C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9330899 | ||||||
| chr2:9331031
|
G | A | 13 | a0001c0003t0001g0153a0001c0003t0006g0006a0001c0003t0006g0064others(10): Show | 13 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(10): Show |
intron_variant | MODIFIER | c.686+3120G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9331031 | ||||||
| chr2:9331038
|
T | G | 1 | a0001c0003t0001g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.686+3127T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9331038 | ||||||
| chr2:9331150
|
T | C | 210 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(207): Show | 210 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.686+3239T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9331150 | ||||||
| chr2:9331224
|
C | T | 2 | a0001c0002t0019g0164a0001c0003t0021g0040 | 2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.686+3313C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9331224 | ||||||
| chr2:9331263
|
G | A | 4 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199others(1): Show | 4 | HG01175.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.686+3352G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9331263 | ||||||
| chr2:9331310
|
C | G | 1 | a0001c0004t0005g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.686+3399C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9331310 | ||||||
| chr2:9331640
|
C | T | 6 | a0002c0001t0001g0042a0002c0001t0001g0088a0002c0001t0001g0089others(3): Show | 6 | HG00735.hp2 HG01346.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.687-3098C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9331640 | ||||||
| chr2:9331653
|
G | A | 1 | a0001c0003t0001g0039 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.687-3085G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9331653 | ||||||
| chr2:9331755
|
G | A | 6 | a0001c0003t0004g0011a0001c0003t0004g0020a0001c0003t0004g0038others(3): Show | 6 | HG02257.hp2 HG02723.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.687-2983G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9331755 | ||||||
| chr2:9331756
|
A | AT | 24 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0026others(21): Show | 24 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.687-2971dupT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 9331756 | |||||
| chr2:9331768
|
C | T | 1 | a0001c0004t0005g0205 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.687-2970C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9331768 | ||||||
| chr2:9331933
|
G | A | 1 | a0001c0002t0003g0188 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.687-2805G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9331933 | ||||||
| chr2:9331955
|
A | G | 107 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(104): Show | 107 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.687-2783A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9331955 | ||||||
| chr2:9331960
|
C | A | 10 | a0001c0003t0001g0210a0001c0003t0004g0200a0001c0003t0007g0170others(7): Show | 10 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.687-2778C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9331960 | ||||||
| chr2:9332169
|
G | A | 8 | a0002c0001t0001g0168a0002c0005t0001g0002a0002c0005t0001g0101others(5): Show | 8 | HG01099.hp2 HG01106.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.687-2569G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9332169 | ||||||
| chr2:9332388
|
C | T | 6 | a0001c0003t0001g0029a0001c0003t0001g0169a0001c0003t0001g0171others(3): Show | 6 | HG01496.hp2 HG02451.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.687-2350C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9332388 | ||||||
| chr2:9332528
|
G | A | 3 | a0001c0004t0005g0021a0001c0004t0005g0034a0001c0004t0005g0144 | 3 | HG03130.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.687-2210G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9332528 | ||||||
| chr2:9332532
|
T | C | 10 | a0001c0002t0003g0188a0001c0002t0019g0164a0001c0003t0021g0040others(7): Show | 10 | HG00639.hp1 HG01074.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.687-2206T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9332532 | ||||||
| chr2:9332563
|
T | G | 1 | a0001c0003t0001g0017 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.687-2175T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9332563 | ||||||
| chr2:9332689
|
T | C | 8 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(5): Show | 8 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.687-2049T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9332689 | ||||||
| chr2:9332803
|
TAAAG | T | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.687-1931_687-1928d others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 9332803 | |||||
| chr2:9333001
|
G | A | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.687-1737G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9333001 | ||||||
| chr2:9333051
|
C | T | 1 | a0002c0001t0001g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.687-1687C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9333051 | ||||||
| chr2:9333433
|
T | C | 1 | a0002c0001t0001g0140 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.687-1305T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9333433 | ||||||
| chr2:9333536
|
A | G | 1 | a0002c0001t0001g0053 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.687-1202A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9333536 | ||||||
| chr2:9334018
|
C | CTCTCTG | 10 | a0001c0002t0003g0188a0001c0002t0019g0164a0001c0003t0021g0040others(7): Show | 10 | HG00639.hp1 HG01074.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.687-710_687-705dup others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 9334018 | |||||
| chr2:9334024
|
G | C | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.687-714G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9334024 | ||||||
| chr2:9334039
|
C | CTT | 12 | a0001c0002t0003g0188a0001c0002t0019g0164a0001c0003t0004g0200others(9): Show | 12 | HG00639.hp1 HG01074.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.687-674_687-673dup others(2): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 9334039 | |||||
| chr2:9334039
|
CT | C | 158 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(155): Show | 158 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.687-673delT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 9334039 | |||||
| chr2:9334067
|
G | A | 22 | a0001c0002t0003g0188a0001c0002t0009g0031a0001c0002t0009g0208others(19): Show | 22 | HG00639.hp1 HG01074.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.687-671G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9334067 | ||||||
| chr2:9334086
|
C | T | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.687-652C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9334086 | ||||||
| chr2:9334096
|
G | A | 12 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0003t0001g0210others(9): Show | 12 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.687-642G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9334096 | ||||||
| chr2:9334200
|
T | TG | 6 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0003t0004g0200others(3): Show | 6 | HG01175.hp2 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.687-537dupG | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 9334200 | |||||
| chr2:9334201
|
G | GGTT | 9 | a0001c0002t0003g0188a0001c0003t0021g0040a0001c0004t0005g0021others(6): Show | 9 | HG00639.hp1 HG01074.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.687-537_687-536ins others(3): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9334201 | ||||||
| chr2:9334201
|
G | GT | 56 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(53): Show | 56 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.687-523dupT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 9334201 | |||||
| chr2:9334201
|
G | GTT | 29 | a0001c0002t0002g0107a0001c0002t0002g0139a0001c0002t0002g0198others(26): Show | 29 | HG00323.hp2 HG00642.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.687-524_687-523dup others(2): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 9334201 | |||||
| chr2:9334202
|
T | G | 1 | a0001c0003t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.687-536T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9334202 | ||||||
| chr2:9334278
|
G | C | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.687-460G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9334278 | ||||||
| chr2:9334345
|
A | C | 16 | a0001c0002t0003g0188a0001c0002t0019g0164a0001c0003t0001g0210others(13): Show | 16 | HG00639.hp1 HG01074.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.687-393A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9334345 | ||||||
| chr2:9334345
|
A | T | 6 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0003t0004g0200others(3): Show | 6 | HG01175.hp2 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.687-393A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9334345 | ||||||
| chr2:9334349
|
C | T | 1 | a0002c0005t0001g0130 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.687-389C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9334349 | ||||||
| chr2:9334374
|
TC | T | 10 | a0001c0002t0003g0188a0001c0002t0019g0164a0001c0003t0021g0040others(7): Show | 10 | HG00639.hp1 HG01074.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.687-362delC | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr2 | 9334374 | |||||
| chr2:9334385
|
G | A | 6 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0003t0004g0200others(3): Show | 6 | HG01175.hp2 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.687-353G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9334385 | ||||||
| chr2:9334397
|
G | A | 10 | a0001c0003t0001g0210a0001c0003t0004g0200a0001c0003t0007g0170others(7): Show | 10 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.687-341G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 7/27 | chr2 | 9334397 | ||||||
| chr2:9334898
|
G | A | 8 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(5): Show | 8 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.762+85G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 8/27 | chr2 | 9334898 | ||||||
| chr2:9335071
|
T | TTG | 22 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(19): Show | 22 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(19): Show |
splice_region_variant&intron_variant | LOW | c.763-10_763-9dupGT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr2 | 9335071 | |||||
| chr2:9335208
|
A | G | 30 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(27): Show | 30 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.849+29A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9335208 | ||||||
| chr2:9335676
|
C | T | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+497C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9335676 | ||||||
| chr2:9335739
|
G | A | 1 | a0001c0004t0005g0144 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.849+560G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9335739 | ||||||
| chr2:9336095
|
G | A | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.849+916G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9336095 | ||||||
| chr2:9336188
|
A | G | 1 | a0002c0001t0001g0087 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.849+1009A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9336188 | ||||||
| chr2:9336215
|
G | A | 4 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199others(1): Show | 4 | HG01175.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+1036G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9336215 | ||||||
| chr2:9336414
|
C | T | 1 | a0002c0001t0001g0118 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.849+1235C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9336414 | ||||||
| chr2:9336657
|
G | T | 12 | a0001c0002t0019g0164a0001c0003t0001g0210a0001c0003t0004g0200others(9): Show | 12 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.849+1478G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9336657 | ||||||
| chr2:9336781
|
C | T | 1 | a0001c0002t0003g0188 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.849+1602C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9336781 | ||||||
| chr2:9336797
|
C | T | 1 | a0001c0002t0001g0097 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.849+1618C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9336797 | ||||||
| chr2:9336818
|
C | T | 2 | a0001c0002t0019g0164a0001c0003t0021g0040 | 2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.849+1639C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9336818 | ||||||
| chr2:9336948
|
G | A | 12 | a0001c0002t0019g0164a0001c0003t0001g0210a0001c0003t0004g0200others(9): Show | 12 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.849+1769G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9336948 | ||||||
| chr2:9337050
|
C | T | 2 | a0001c0002t0019g0164a0001c0003t0021g0040 | 2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.849+1871C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9337050 | ||||||
| chr2:9337168
|
A | G | 12 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0003t0001g0210others(9): Show | 12 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.849+1989A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9337168 | ||||||
| chr2:9337221
|
A | G | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+2042A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9337221 | ||||||
| chr2:9337240
|
CG | C | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.849+2062delG | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9337240 | ||||||
| chr2:9337310
|
T | C | 4 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199others(1): Show | 4 | HG01175.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+2131T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9337310 | ||||||
| chr2:9337422
|
T | C | 70 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(67): Show | 70 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.849+2243T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9337422 | ||||||
| chr2:9337428
|
T | C | 2 | a0001c0002t0019g0164a0001c0003t0021g0040 | 2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.849+2249T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9337428 | ||||||
| chr2:9337541
|
C | A | 12 | a0001c0002t0019g0164a0001c0003t0001g0210a0001c0003t0004g0200others(9): Show | 12 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.849+2362C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9337541 | ||||||
| chr2:9337547
|
G | GT | 10 | a0001c0003t0001g0210a0001c0003t0004g0200a0001c0003t0007g0170others(7): Show | 10 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.849+2369dupT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 9337547 | |||||
| chr2:9337743
|
T | C | 12 | a0001c0002t0019g0164a0001c0003t0001g0210a0001c0003t0004g0200others(9): Show | 12 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.849+2564T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9337743 | ||||||
| chr2:9337810
|
A | G | 1 | a0001c0007t0004g0154 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.849+2631A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9337810 | ||||||
| chr2:9337854
|
A | G | 1 | a0001c0003t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.849+2675A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9337854 | ||||||
| chr2:9337986
|
A | G | 5 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(2): Show | 5 | HG01934.hp2 HG02451.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+2807A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9337986 | ||||||
| chr2:9338123
|
G | A | 1 | a0001c0002t0002g0027 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.849+2944G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9338123 | ||||||
| chr2:9338290
|
GCTCT | G | 12 | a0001c0002t0019g0164a0001c0003t0001g0210a0001c0003t0004g0200others(9): Show | 12 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.849+3126_849+3129d others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 9338290 | |||||
| chr2:9338309
|
G | C | 1 | a0002c0005t0001g0054 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.849+3130G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9338309 | ||||||
| chr2:9338347
|
A | ATCTCTC | 12 | a0001c0002t0019g0164a0001c0003t0001g0210a0001c0003t0004g0200others(9): Show | 12 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.849+3180_849+3185d others(8): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 9338347 | |||||
| chr2:9338356
|
TC | T | 8 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(5): Show | 8 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.849+3178delC | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9338356 | ||||||
| chr2:9338471
|
T | C | 2 | a0001c0002t0019g0164a0001c0003t0021g0040 | 2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.849+3292T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9338471 | ||||||
| chr2:9338715
|
A | C | 12 | a0001c0002t0019g0164a0001c0003t0001g0210a0001c0003t0004g0200others(9): Show | 12 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.849+3536A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9338715 | ||||||
| chr2:9338761
|
A | G | 37 | a0001c0002t0003g0148a0001c0002t0019g0164a0001c0003t0001g0029others(34): Show | 37 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.849+3582A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9338761 | ||||||
| chr2:9338782
|
C | T | 1 | a0002c0001t0001g0081 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.849+3603C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9338782 | ||||||
| chr2:9338804
|
C | T | 2 | a0001c0003t0016g0174a0001c0010t0018g0173 | 2 | HG02145.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.849+3625C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9338804 | ||||||
| chr2:9338941
|
G | A | 1 | a0002c0001t0001g0081 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.849+3762G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9338941 | ||||||
| chr2:9339054
|
G | A | 1 | a0001c0003t0004g0200 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.849+3875G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9339054 | ||||||
| chr2:9339191
|
A | G | 10 | a0001c0003t0001g0210a0001c0003t0004g0200a0001c0003t0007g0170others(7): Show | 10 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.849+4012A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9339191 | ||||||
| chr2:9339401
|
C | T | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+4222C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9339401 | ||||||
| chr2:9339545
|
A | G | 1 | a0002c0001t0001g0163 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.849+4366A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9339545 | ||||||
| chr2:9339662
|
C | T | 10 | a0001c0003t0001g0210a0001c0003t0004g0200a0001c0003t0007g0170others(7): Show | 10 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.849+4483C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9339662 | ||||||
| chr2:9339701
|
G | A | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+4522G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9339701 | ||||||
| chr2:9339744
|
C | T | 1 | a0001c0003t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.849+4565C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9339744 | ||||||
| chr2:9339859
|
G | A | 1 | a0002c0005t0001g0119 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.850-4673G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9339859 | ||||||
| chr2:9339883
|
G | A | 1 | a0002c0001t0001g0118 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.850-4649G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9339883 | ||||||
| chr2:9340021
|
A | G | 22 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(19): Show | 22 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(19): Show |
intron_variant | MODIFIER | c.850-4511A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9340021 | ||||||
| chr2:9340111
|
C | T | 3 | a0001c0002t0003g0166a0001c0002t0003g0209a0001c0012t0003g0033 | 3 | HG02818.hp2 HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.850-4421C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9340111 | ||||||
| chr2:9340171
|
C | T | 30 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(27): Show | 30 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.850-4361C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9340171 | ||||||
| chr2:9340179
|
C | T | 1 | a0001c0002t0003g0188 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.850-4353C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9340179 | ||||||
| chr2:9340210
|
A | G | 24 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0026others(21): Show | 24 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.850-4322A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9340210 | ||||||
| chr2:9340212
|
G | A | 21 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(18): Show | 21 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.850-4320G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9340212 | ||||||
| chr2:9340233
|
G | A | 1 | a0001c0003t0004g0200 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.850-4299G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9340233 | ||||||
| chr2:9340286
|
G | T | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-4246G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9340286 | ||||||
| chr2:9340318
|
G | A | 30 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(27): Show | 30 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.850-4214G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9340318 | ||||||
| chr2:9340325
|
A | T | 2 | a0001c0002t0019g0164a0001c0003t0021g0040 | 2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.850-4207A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9340325 | ||||||
| chr2:9340438
|
C | T | 58 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(55): Show | 58 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.850-4094C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9340438 | ||||||
| chr2:9340570
|
G | C | 10 | a0001c0003t0001g0210a0001c0003t0004g0200a0001c0003t0007g0170others(7): Show | 10 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.850-3962G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9340570 | ||||||
| chr2:9340734
|
T | C | 1 | a0001c0002t0002g0187 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.850-3798T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9340734 | ||||||
| chr2:9340859
|
G | T | 1 | a0001c0002t0003g0124 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.850-3673G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9340859 | ||||||
| chr2:9340885
|
G | T | 1 | a0001c0002t0002g0075 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.850-3647G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9340885 | ||||||
| chr2:9340937
|
G | C | 3 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0059 | 3 | HG00642.hp2 HG01261.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.850-3595G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9340937 | ||||||
| chr2:9341081
|
T | C | 2 | a0002c0001t0001g0074a0002c0001t0001g0161 | 2 | HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.850-3451T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9341081 | ||||||
| chr2:9341192
|
T | C | 1 | a0001c0002t0008g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.850-3340T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9341192 | ||||||
| chr2:9341232
|
C | T | 24 | a0001c0002t0002g0198a0001c0002t0002g0202a0001c0002t0003g0026others(21): Show | 24 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.850-3300C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9341232 | ||||||
| chr2:9341283
|
G | A | 1 | a0002c0001t0020g0079 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.850-3249G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9341283 | ||||||
| chr2:9341297
|
A | G | 107 | a0001c0002t0001g0097a0001c0002t0002g0007a0001c0002t0002g0016others(104): Show | 107 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.850-3235A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9341297 | ||||||
| chr2:9341312
|
A | G | 12 | a0001c0002t0019g0164a0001c0003t0001g0210a0001c0003t0004g0200others(9): Show | 12 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.850-3220A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9341312 | ||||||
| chr2:9341453
|
G | A | 10 | a0001c0003t0001g0210a0001c0003t0004g0200a0001c0003t0007g0170others(7): Show | 10 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.850-3079G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9341453 | ||||||
| chr2:9341458
|
CT | C | 2 | a0001c0002t0019g0164a0001c0003t0021g0040 | 2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.850-3072delT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 9341458 | |||||
| chr2:9341486
|
G | A | 1 | a0002c0001t0001g0159 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.850-3046G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9341486 | ||||||
| chr2:9341525
|
G | A | 6 | a0001c0003t0001g0210a0001c0003t0016g0174a0001c0007t0004g0015others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.850-3007G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9341525 | ||||||
| chr2:9341548
|
G | A | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-2984G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9341548 | ||||||
| chr2:9341560
|
C | T | 1 | a0002c0001t0001g0078 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.850-2972C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9341560 | ||||||
| chr2:9341659
|
C | T | 1 | a0001c0002t0002g0069 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.850-2873C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9341659 | ||||||
| chr2:9341693
|
A | G | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-2839A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9341693 | ||||||
| chr2:9341727
|
A | G | 10 | a0001c0003t0001g0210a0001c0003t0004g0200a0001c0003t0007g0170others(7): Show | 10 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.850-2805A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9341727 | ||||||
| chr2:9341746
|
T | C | 2 | a0001c0002t0019g0164a0001c0003t0021g0040 | 2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.850-2786T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9341746 | ||||||
| chr2:9341837
|
G | A | 6 | a0001c0003t0001g0210a0001c0003t0016g0174a0001c0007t0004g0015others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.850-2695G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9341837 | ||||||
| chr2:9341910
|
C | T | 10 | a0001c0003t0001g0210a0001c0003t0004g0200a0001c0003t0007g0170others(7): Show | 10 | HG01175.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.850-2622C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9341910 | ||||||
| chr2:9342089
|
C | T | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-2443C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9342089 | ||||||
| chr2:9342227
|
C | T | 1 | a0001c0002t0001g0097 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.850-2305C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9342227 | ||||||
| chr2:9342231
|
G | A | 5 | a0001c0003t0016g0174a0001c0007t0004g0015a0001c0007t0004g0154others(2): Show | 5 | HG02145.hp1 HG02486.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.850-2301G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9342231 | ||||||
| chr2:9342681
|
T | C | 1 | a0001c0002t0002g0177 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.850-1851T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9342681 | ||||||
| chr2:9342721
|
G | A | 6 | a0001c0003t0004g0011a0001c0003t0004g0020a0001c0003t0004g0038others(3): Show | 6 | HG02257.hp2 HG02723.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.850-1811G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9342721 | ||||||
| chr2:9342746
|
C | T | 6 | a0001c0003t0001g0210a0001c0003t0016g0174a0001c0007t0004g0015others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.850-1786C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9342746 | ||||||
| chr2:9342765
|
C | T | 26 | a0001c0002t0003g0148a0001c0003t0001g0029a0001c0003t0001g0039others(23): Show | 26 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.850-1767C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9342765 | ||||||
| chr2:9342848
|
C | T | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.850-1684C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9342848 | ||||||
| chr2:9342932
|
C | T | 1 | a0002c0001t0010g0066 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.850-1600C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9342932 | ||||||
| chr2:9342963
|
C | G | 1 | a0002c0005t0001g0025 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.850-1569C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9342963 | ||||||
| chr2:9342977
|
T | G | 1 | a0001c0002t0003g0188 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.850-1555T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9342977 | ||||||
| chr2:9343030
|
C | T | 1 | a0001c0002t0002g0137 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.850-1502C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9343030 | ||||||
| chr2:9343047
|
C | T | 6 | a0001c0003t0001g0210a0001c0003t0016g0174a0001c0007t0004g0015others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.850-1485C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9343047 | ||||||
| chr2:9343353
|
T | A | 1 | a0001c0002t0012g0143 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.850-1179T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9343353 | ||||||
| chr2:9343405
|
C | CCT | 182 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(179): Show | 182 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.850-1125_850-1124d others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 9343405 | |||||
| chr2:9343458
|
T | C | 112 | a0001c0002t0001g0097a0001c0002t0001g0115a0001c0002t0001g0116others(109): Show | 112 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.850-1074T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9343458 | ||||||
| chr2:9343531
|
C | T | 5 | a0001c0007t0004g0037a0002c0001t0001g0004a0002c0001t0001g0013others(2): Show | 5 | HG01361.hp1 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.850-1001C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9343531 | ||||||
| chr2:9343539
|
C | G | 1 | a0002c0001t0001g0067 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.850-993C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9343539 | ||||||
| chr2:9343579
|
T | C | 1 | a0001c0003t0004g0044 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.850-953T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9343579 | ||||||
| chr2:9343602
|
A | G | 3 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0003t0001g0210 | 3 | HG02886.hp2 HG02895.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.850-930A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9343602 | ||||||
| chr2:9343883
|
A | T | 3 | a0001c0002t0003g0209a0001c0003t0001g0153a0001c0012t0003g0033 | 3 | HG02965.hp2 NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.850-649A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9343883 | ||||||
| chr2:9344167
|
T | A | 1 | a0001c0002t0001g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.850-365T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9344167 | ||||||
| chr2:9344212
|
G | A | 21 | a0001c0003t0001g0029a0001c0003t0001g0153a0001c0003t0001g0165others(18): Show | 21 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.850-320G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9344212 | ||||||
| chr2:9344232
|
C | T | 183 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(180): Show | 183 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.850-300C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9344232 | ||||||
| chr2:9344312
|
G | C | 13 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(10): Show | 13 | HG01070.hp1 HG01109.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.850-220G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9344312 | ||||||
| chr2:9344341
|
A | T | 1 | a0001c0003t0007g0199 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.850-191A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9344341 | ||||||
| chr2:9344413
|
C | T | 156 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(153): Show | 156 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.850-119C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9344413 | ||||||
| chr2:9344432
|
TAAAA | T | 156 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(153): Show | 156 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.850-93_850-90delAA others(2): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 9344432 | |||||
| chr2:9344442
|
A | G | 1 | a0001c0013t0017g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.850-90A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 9/27 | chr2 | 9344442 | ||||||
| chr2:9344893
|
C | T | 3 | a0002c0001t0001g0013a0002c0001t0001g0061a0002c0001t0001g0186 | 3 | HG02922.hp2 HG03041.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1023+93C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9344893 | ||||||
| chr2:9344990
|
GT | G | 152 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(149): Show | 152 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.1023+203delT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr2 | 9344990 | |||||
| chr2:9344990
|
GTT | G | 5 | a0001c0002t0002g0134a0001c0002t0002g0198a0001c0002t0002g0202others(2): Show | 5 | HG01257.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1023+202_1023+203d others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr2 | 9344990 | |||||
| chr2:9345016
|
A | T | 28 | a0001c0002t0002g0007a0001c0002t0002g0016a0001c0002t0002g0027others(25): Show | 28 | HG00280.hp1 HG00280.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.1023+216A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9345016 | ||||||
| chr2:9345022
|
T | A | 3 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0004t0005g0028 | 3 | HG02886.hp2 HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1023+222T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9345022 | ||||||
| chr2:9345108
|
C | A | 4 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1023+308C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9345108 | ||||||
| chr2:9345281
|
G | A | 181 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(178): Show | 181 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.1023+481G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9345281 | ||||||
| chr2:9345402
|
G | A | 1 | a0001c0010t0018g0173 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1023+602G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9345402 | ||||||
| chr2:9345478
|
A | G | 1 | a0001c0010t0018g0173 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1023+678A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9345478 | ||||||
| chr2:9345496
|
G | A | 1 | a0002c0005t0001g0119 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1023+696G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9345496 | ||||||
| chr2:9345506
|
T | TA | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1023+707dupA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr2 | 9345506 | |||||
| chr2:9345667
|
T | C | 12 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(9): Show | 12 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1023+867T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9345667 | ||||||
| chr2:9345672
|
G | T | 155 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(152): Show | 155 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1023+872G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9345672 | ||||||
| chr2:9345703
|
A | G | 155 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(152): Show | 155 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1023+903A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9345703 | ||||||
| chr2:9345890
|
T | G | 12 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(9): Show | 12 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1023+1090T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9345890 | ||||||
| chr2:9346104
|
C | T | 24 | a0001c0002t0006g0184a0001c0003t0001g0017a0001c0003t0001g0029others(21): Show | 24 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.1023+1304C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9346104 | ||||||
| chr2:9346193
|
C | A | 4 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1023+1393C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9346193 | ||||||
| chr2:9346198
|
C | T | 2 | a0001c0002t0008g0048a0001c0002t0008g0206 | 2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1023+1398C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9346198 | ||||||
| chr2:9346223
|
C | T | 24 | a0001c0002t0006g0184a0001c0003t0001g0017a0001c0003t0001g0029others(21): Show | 24 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.1023+1423C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9346223 | ||||||
| chr2:9346383
|
C | T | 4 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1023+1583C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9346383 | ||||||
| chr2:9346392
|
C | T | 2 | a0002c0001t0001g0093a0002c0001t0001g0112 | 2 | HG01981.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1023+1592C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9346392 | ||||||
| chr2:9346401
|
A | G | 4 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1023+1601A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9346401 | ||||||
| chr2:9346435
|
CA | C | 25 | a0001c0002t0006g0184a0001c0003t0001g0017a0001c0003t0001g0029others(22): Show | 25 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.1023+1651delA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr2 | 9346435 | |||||
| chr2:9346453
|
C | A | 174 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(171): Show | 174 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.1023+1653C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9346453 | ||||||
| chr2:9346550
|
AT | A | 3 | a0001c0002t0003g0094a0001c0002t0003g0142a0002c0001t0003g0136 | 3 | HG03491.hp2 HG03831.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1023+1752delT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr2 | 9346550 | |||||
| chr2:9346654
|
C | T | 3 | a0001c0003t0001g0017a0001c0003t0001g0046a0001c0007t0001g0030 | 3 | HG01175.hp2 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1023+1854C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9346654 | ||||||
| chr2:9346703
|
A | G | 1 | a0001c0010t0018g0173 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1023+1903A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9346703 | ||||||
| chr2:9346940
|
C | T | 169 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(166): Show | 169 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.1023+2140C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9346940 | ||||||
| chr2:9347043
|
C | G | 1 | a0001c0002t0019g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1023+2243C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9347043 | ||||||
| chr2:9347071
|
TCTC | T | 83 | a0001c0002t0001g0097a0001c0002t0002g0073a0001c0002t0003g0148others(80): Show | 83 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.1023+2277_1023+227 others(7): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr2 | 9347071 | |||||
| chr2:9347120
|
T | C | 173 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(170): Show | 173 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.1023+2320T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9347120 | ||||||
| chr2:9347148
|
C | T | 4 | a0001c0002t0003g0147a0001c0002t0003g0149a0001c0002t0003g0151others(1): Show | 4 | HG00323.hp2 HG00738.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1023+2348C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9347148 | ||||||
| chr2:9347364
|
T | A | 1 | a0001c0010t0018g0173 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1023+2564T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9347364 | ||||||
| chr2:9347507
|
C | T | 156 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(153): Show | 156 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1023+2707C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9347507 | ||||||
| chr2:9347738
|
A | G | 4 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1023+2938A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9347738 | ||||||
| chr2:9347875
|
C | G | 156 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(153): Show | 156 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1024-2933C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9347875 | ||||||
| chr2:9347930
|
G | A | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1024-2878G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9347930 | ||||||
| chr2:9347957
|
A | T | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1024-2851A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9347957 | ||||||
| chr2:9348085
|
G | A | 202 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(199): Show | 202 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.1024-2723G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9348085 | ||||||
| chr2:9348110
|
T | TTTTG | 12 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(9): Show | 12 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1024-2696_1024-269 others(8): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr2 | 9348110 | |||||
| chr2:9348110
|
TTTTGTCT others(5): Show |
T | 2 | a0001c0002t0003g0050a0002c0001t0001g0111 | 2 | HG00609.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.1024-2692_1024-268 others(16): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr2 | 9348110 | |||||
| chr2:9348112
|
TTGTC | T | 4 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0004t0005g0185others(1): Show | 4 | HG02886.hp2 HG02895.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024-2692_1024-268 others(8): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr2 | 9348112 | |||||
| chr2:9348116
|
C | T | 168 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(165): Show | 168 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.1024-2692C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9348116 | ||||||
| chr2:9348116
|
CTGTT | C | 24 | a0001c0002t0006g0184a0001c0003t0001g0017a0001c0003t0001g0029others(21): Show | 24 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.1024-2670_1024-266 others(8): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr2 | 9348116 | |||||
| chr2:9348142
|
T | G | 1 | a0001c0002t0003g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1024-2666T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9348142 | ||||||
| chr2:9348226
|
C | T | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1024-2582C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9348226 | ||||||
| chr2:9348265
|
T | C | 4 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024-2543T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9348265 | ||||||
| chr2:9348305
|
CTA | C | 4 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024-2502_1024-250 others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9348305 | ||||||
| chr2:9348309
|
A | G | 4 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024-2499A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9348309 | ||||||
| chr2:9348310
|
A | G | 4 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024-2498A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9348310 | ||||||
| chr2:9348311
|
A | G | 4 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024-2497A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9348311 | ||||||
| chr2:9348313
|
C | T | 4 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024-2495C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9348313 | ||||||
| chr2:9348315
|
CT | C | 4 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024-2492delT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9348315 | ||||||
| chr2:9348319
|
T | C | 4 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024-2489T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9348319 | ||||||
| chr2:9348321
|
A | T | 4 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024-2487A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9348321 | ||||||
| chr2:9348323
|
TCAGCC | T | 4 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024-2484_1024-248 others(9): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9348323 | ||||||
| chr2:9348329
|
A | T | 4 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024-2479A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9348329 | ||||||
| chr2:9348345
|
G | A | 2 | a0001c0002t0002g0073a0002c0001t0001g0157 | 2 | HG01074.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.1024-2463G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9348345 | ||||||
| chr2:9348527
|
A | G | 174 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(171): Show | 174 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.1024-2281A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9348527 | ||||||
| chr2:9348757
|
A | G | 4 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024-2051A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9348757 | ||||||
| chr2:9348784
|
G | A | 1 | a0002c0001t0001g0023 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1024-2024G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9348784 | ||||||
| chr2:9348893
|
A | G | 174 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(171): Show | 174 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.1024-1915A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9348893 | ||||||
| chr2:9349149
|
A | G | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1024-1659A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9349149 | ||||||
| chr2:9349236
|
A | G | 4 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024-1572A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9349236 | ||||||
| chr2:9349266
|
A | G | 3 | a0001c0003t0006g0064a0001c0003t0006g0065a0001c0003t0006g0102 | 3 | HG00408.hp2 HG00438.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1024-1542A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9349266 | ||||||
| chr2:9349310
|
G | A | 202 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(199): Show | 202 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.1024-1498G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9349310 | ||||||
| chr2:9349332
|
G | A | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1024-1476G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9349332 | ||||||
| chr2:9349439
|
G | T | 1 | a0001c0010t0018g0173 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1024-1369G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9349439 | ||||||
| chr2:9349659
|
G | A | 1 | a0002c0005t0001g0119 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1024-1149G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9349659 | ||||||
| chr2:9349886
|
G | T | 24 | a0001c0003t0001g0017a0001c0003t0001g0029a0001c0003t0001g0039others(21): Show | 24 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.1024-922G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9349886 | ||||||
| chr2:9349914
|
C | G | 83 | a0001c0002t0001g0097a0001c0002t0002g0073a0001c0002t0003g0148others(80): Show | 83 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.1024-894C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9349914 | ||||||
| chr2:9350042
|
G | T | 4 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024-766G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9350042 | ||||||
| chr2:9350196
|
C | T | 1 | a0001c0002t0019g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1024-612C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9350196 | ||||||
| chr2:9350397
|
G | A | 1 | a0002c0001t0001g0067 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1024-411G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9350397 | ||||||
| chr2:9350450
|
A | T | 4 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024-358A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9350450 | ||||||
| chr2:9350496
|
A | G | 4 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024-312A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9350496 | ||||||
| chr2:9350598
|
T | G | 1 | a0001c0003t0021g0040 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1024-210T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9350598 | ||||||
| chr2:9350681
|
T | G | 1 | a0001c0002t0019g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1024-127T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 11/27 | chr2 | 9350681 | ||||||
| chr2:9350930
|
C | T | 1 | a0002c0001t0001g0159 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1111+35C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9350930 | ||||||
| chr2:9351013
|
T | A | 4 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111+118T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9351013 | ||||||
| chr2:9351289
|
T | C | 1 | a0001c0002t0008g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1111+394T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9351289 | ||||||
| chr2:9351311
|
T | G | 4 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111+416T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9351311 | ||||||
| chr2:9351374
|
T | G | 4 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111+479T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9351374 | ||||||
| chr2:9351455
|
C | G | 1 | a0002c0001t0001g0077 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1111+560C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9351455 | ||||||
| chr2:9351457
|
C | T | 169 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(166): Show | 169 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.1111+562C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9351457 | ||||||
| chr2:9351535
|
G | C | 3 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164 | 3 | HG02647.hp2 HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1111+640G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9351535 | ||||||
| chr2:9351540
|
T | C | 170 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(167): Show | 170 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.1111+645T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9351540 | ||||||
| chr2:9351626
|
G | A | 13 | a0001c0003t0001g0029a0001c0003t0001g0153a0001c0003t0006g0006others(10): Show | 13 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(10): Show |
intron_variant | MODIFIER | c.1111+731G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9351626 | ||||||
| chr2:9351773
|
C | T | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1111+878C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9351773 | ||||||
| chr2:9351783
|
T | C | 4 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111+888T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9351783 | ||||||
| chr2:9351797
|
C | T | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1111+902C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9351797 | ||||||
| chr2:9351833
|
C | G | 1 | a0002c0001t0001g0109 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1111+938C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9351833 | ||||||
| chr2:9351835
|
C | T | 1 | a0002c0001t0001g0085 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1111+940C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9351835 | ||||||
| chr2:9351863
|
G | A | 4 | a0001c0004t0005g0192a0001c0004t0005g0193a0001c0004t0005g0196others(1): Show | 4 | HG01109.hp2 HG01884.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111+968G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9351863 | ||||||
| chr2:9352092
|
G | C | 24 | a0001c0003t0001g0017a0001c0003t0001g0029a0001c0003t0001g0039others(21): Show | 24 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.1111+1197G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9352092 | ||||||
| chr2:9352212
|
A | AAC | 3 | a0001c0003t0004g0044a0001c0003t0021g0040a0002c0008t0001g0108 | 3 | HG03471.hp2 HG06807.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.1111+1351_1111+135 others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | 9352212 | |||||
| chr2:9352212
|
A | AACAC | 11 | a0001c0003t0001g0039a0001c0003t0001g0169a0001c0003t0001g0171others(8): Show | 11 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(8): Show |
intron_variant | MODIFIER | c.1111+1349_1111+135 others(8): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | 9352212 | |||||
| chr2:9352212
|
A | AACACAC | 7 | a0001c0003t0001g0017a0001c0003t0001g0029a0001c0003t0001g0046others(4): Show | 7 | HG02818.hp1 HG06807.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.1111+1347_1111+135 others(10): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | 9352212 | |||||
| chr2:9352212
|
A | AACACACA others(1): Show |
3 | a0001c0003t0001g0165a0001c0003t0001g0190a0001c0003t0006g0102 | 3 | HG00408.hp2 HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1111+1345_1111+135 others(12): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | 9352212 | |||||
| chr2:9352212
|
A | C | 3 | a0001c0002t0009g0031a0001c0002t0019g0164a0001c0013t0017g0045 | 3 | HG02647.hp2 HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1111+1317A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9352212 | ||||||
| chr2:9352212
|
AACAC | A | 4 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199others(1): Show | 4 | HG03139.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111+1349_1111+135 others(8): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | 9352212 | |||||
| chr2:9352212
|
AACACACA others(3): Show |
A | 2 | a0001c0004t0005g0041a0001c0004t0005g0138 | 2 | HG00639.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1111+1343_1111+135 others(14): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | 9352212 | |||||
| chr2:9352212
|
AACACACA others(5): Show |
A | 98 | a0001c0002t0001g0097a0001c0002t0002g0073a0001c0002t0003g0148others(95): Show | 98 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1111+1341_1111+135 others(16): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | 9352212 | |||||
| chr2:9352212
|
AACACACA others(7): Show |
A | 69 | a0001c0002t0001g0024a0001c0002t0001g0115a0001c0002t0001g0116others(66): Show | 69 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.1111+1339_1111+135 others(18): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | 9352212 | |||||
| chr2:9352248
|
A | C | 4 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111+1353A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9352248 | ||||||
| chr2:9352302
|
T | C | 2 | a0001c0002t0019g0164a0001c0013t0017g0045 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1111+1407T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9352302 | ||||||
| chr2:9352375
|
CCTTT | C | 4 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111+1483_1111+148 others(8): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | 9352375 | |||||
| chr2:9352533
|
C | T | 12 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(9): Show | 12 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1111+1638C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9352533 | ||||||
| chr2:9352599
|
A | G | 4 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111+1704A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9352599 | ||||||
| chr2:9352717
|
A | C | 1 | a0001c0010t0018g0173 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1111+1822A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9352717 | ||||||
| chr2:9352809
|
G | C | 1 | a0002c0001t0001g0081 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1111+1914G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9352809 | ||||||
| chr2:9352915
|
C | T | 155 | a0001c0002t0001g0097a0001c0002t0001g0115a0001c0002t0001g0116others(152): Show | 155 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1111+2020C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9352915 | ||||||
| chr2:9353168
|
G | C | 43 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0009g0031others(40): Show | 43 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.1111+2273G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9353168 | ||||||
| chr2:9353239
|
C | CCAAGATG others(12): Show |
2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1111+2362_1111+238 others(23): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | 9353239 | |||||
| chr2:9353414
|
C | T | 4 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111+2519C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9353414 | ||||||
| chr2:9353417
|
T | C | 44 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0006g0184others(41): Show | 44 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.1111+2522T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9353417 | ||||||
| chr2:9353532
|
G | C | 1 | a0001c0010t0018g0173 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1112-2515G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9353532 | ||||||
| chr2:9353553
|
TA | T | 125 | a0001c0002t0001g0024a0001c0002t0001g0115a0001c0002t0001g0116others(122): Show | 125 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.1112-2481delA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | 9353553 | |||||
| chr2:9353566
|
AG | A | 2 | a0002c0001t0001g0076a0002c0001t0001g0081 | 2 | HG02155.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1112-2480delG | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9353566 | ||||||
| chr2:9353788
|
C | T | 1 | a0001c0003t0021g0040 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1112-2259C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9353788 | ||||||
| chr2:9353832
|
A | G | 57 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0006g0184others(54): Show | 57 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.1112-2215A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9353832 | ||||||
| chr2:9353901
|
G | A | 2 | a0001c0002t0019g0164a0001c0013t0017g0045 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1112-2146G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9353901 | ||||||
| chr2:9354013
|
T | C | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1112-2034T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9354013 | ||||||
| chr2:9354061
|
T | C | 44 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0006g0184others(41): Show | 44 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.1112-1986T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9354061 | ||||||
| chr2:9354080
|
C | G | 1 | a0001c0010t0018g0173 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1112-1967C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9354080 | ||||||
| chr2:9354237
|
A | C | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1112-1810A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9354237 | ||||||
| chr2:9354353
|
G | A | 2 | a0001c0002t0019g0164a0001c0013t0017g0045 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1112-1694G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9354353 | ||||||
| chr2:9354375
|
C | T | 2 | a0001c0002t0019g0164a0001c0013t0017g0045 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1112-1672C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9354375 | ||||||
| chr2:9354473
|
G | A | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1112-1574G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9354473 | ||||||
| chr2:9354621
|
G | A | 2 | a0001c0002t0003g0062a0001c0002t0003g0124 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1112-1426G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9354621 | ||||||
| chr2:9354645
|
C | CA | 45 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0006g0184others(42): Show | 45 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.1112-1386dupA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | 9354645 | |||||
| chr2:9354865
|
A | G | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1112-1182A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9354865 | ||||||
| chr2:9355055
|
T | C | 2 | a0002c0001t0001g0074a0002c0001t0001g0161 | 2 | HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1112-992T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9355055 | ||||||
| chr2:9355064
|
C | T | 25 | a0001c0002t0006g0184a0001c0003t0001g0017a0001c0003t0001g0029others(22): Show | 25 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.1112-983C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9355064 | ||||||
| chr2:9355073
|
A | G | 3 | a0001c0002t0003g0149a0001c0002t0003g0151a0001c0002t0003g0152 | 3 | HG00323.hp2 HG00738.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1112-974A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9355073 | ||||||
| chr2:9355207
|
T | C | 2 | a0001c0002t0019g0164a0001c0013t0017g0045 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1112-840T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9355207 | ||||||
| chr2:9355260
|
A | T | 1 | a0001c0002t0001g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1112-787A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9355260 | ||||||
| chr2:9355323
|
A | G | 1 | a0001c0003t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1112-724A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9355323 | ||||||
| chr2:9355425
|
A | G | 1 | a0001c0002t0003g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1112-622A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9355425 | ||||||
| chr2:9355433
|
A | C | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1112-614A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9355433 | ||||||
| chr2:9355504
|
G | A | 2 | a0001c0003t0006g0135a0001c0003t0011g0068 | 2 | HG00609.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.1112-543G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9355504 | ||||||
| chr2:9355520
|
A | G | 110 | a0001c0002t0001g0024a0001c0002t0001g0115a0001c0002t0001g0116others(107): Show | 110 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1112-527A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9355520 | ||||||
| chr2:9355530
|
T | C | 2 | a0001c0003t0001g0039a0001c0003t0001g0190 | 2 | HG01934.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1112-517T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9355530 | ||||||
| chr2:9355536
|
T | A | 53 | a0001c0002t0001g0115a0001c0002t0001g0116a0001c0002t0001g0126others(50): Show | 53 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.1112-511T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9355536 | ||||||
| chr2:9355552
|
C | T | 1 | a0002c0005t0001g0054 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1112-495C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9355552 | ||||||
| chr2:9355844
|
G | T | 2 | a0002c0001t0001g0110a0002c0001t0001g0140 | 2 | HG03239.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1112-203G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9355844 | ||||||
| chr2:9355859
|
A | G | 2 | a0001c0002t0019g0164a0001c0013t0017g0045 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1112-188A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 12/27 | chr2 | 9355859 | ||||||
| chr2:9356152
|
A | G | 1 | a0001c0013t0017g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1161-27A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 13/27 | chr2 | 9356152 | ||||||
| chr2:9356158
|
G | A | 2 | a0001c0002t0019g0164a0001c0013t0017g0045 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1161-21G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 13/27 | chr2 | 9356158 | ||||||
| chr2:9356160
|
G | A | 3 | a0001c0004t0005g0021a0001c0004t0005g0034a0001c0004t0005g0144 | 3 | HG03130.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1161-19G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 13/27 | chr2 | 9356160 | ||||||
| chr2:9356162
|
T | C | 143 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(140): Show | 143 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.1161-17T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 13/27 | chr2 | 9356162 | ||||||
| chr2:9356386
|
T | A | 2 | a0001c0002t0019g0164a0001c0013t0017g0045 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1327+41T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 14/27 | chr2 | 9356386 | ||||||
| chr2:9356731
|
G | T | 2 | a0001c0002t0003g0062a0001c0002t0003g0124 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1327+386G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 14/27 | chr2 | 9356731 | ||||||
| chr2:9357015
|
A | G | 2 | a0001c0003t0001g0039a0001c0003t0001g0190 | 2 | HG01934.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1327+670A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 14/27 | chr2 | 9357015 | ||||||
| chr2:9357105
|
TA | T | 2 | a0001c0002t0019g0164a0001c0013t0017g0045 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1327+762delA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr2 | 9357105 | |||||
| chr2:9357176
|
T | TA | 55 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0006g0184others(52): Show | 55 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.1327+844dupA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr2 | 9357176 | |||||
| chr2:9357370
|
A | G | 4 | a0002c0005t0001g0025a0002c0005t0001g0101a0002c0005t0001g0130others(1): Show | 4 | HG03239.hp1 HG03654.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1327+1025A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 14/27 | chr2 | 9357370 | ||||||
| chr2:9357525
|
A | T | 1 | a0001c0002t0003g0059 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1327+1180A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 14/27 | chr2 | 9357525 | ||||||
| chr2:9357659
|
G | A | 1 | a0001c0004t0005g0028 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1328-1097G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 14/27 | chr2 | 9357659 | ||||||
| chr2:9357861
|
C | T | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1328-895C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 14/27 | chr2 | 9357861 | ||||||
| chr2:9357882
|
A | T | 1 | a0001c0004t0005g0194 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1328-874A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 14/27 | chr2 | 9357882 | ||||||
| chr2:9358014
|
T | C | 2 | a0001c0002t0019g0164a0001c0013t0017g0045 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1328-742T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 14/27 | chr2 | 9358014 | ||||||
| chr2:9358060
|
C | T | 12 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(9): Show | 12 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1328-696C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 14/27 | chr2 | 9358060 | ||||||
| chr2:9358264
|
C | T | 2 | a0001c0002t0019g0164a0001c0013t0017g0045 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1328-492C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 14/27 | chr2 | 9358264 | ||||||
| chr2:9358269
|
A | G | 52 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0006g0184others(49): Show | 52 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.1328-487A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 14/27 | chr2 | 9358269 | ||||||
| chr2:9358352
|
C | T | 1 | a0002c0001t0001g0012 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1328-404C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 14/27 | chr2 | 9358352 | ||||||
| chr2:9358392
|
C | T | 1 | a0002c0001t0001g0023 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1328-364C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 14/27 | chr2 | 9358392 | ||||||
| chr2:9358493
|
T | G | 1 | a0002c0001t0001g0160 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1328-263T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 14/27 | chr2 | 9358493 | ||||||
| chr2:9358637
|
A | C | 52 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0006g0184others(49): Show | 52 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.1328-119A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 14/27 | chr2 | 9358637 | ||||||
| chr2:9358734
|
T | C | 8 | a0002c0001t0001g0036a0002c0001t0001g0085a0002c0001t0001g0095others(5): Show | 8 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(5): Show |
intron_variant | MODIFIER | c.1328-22T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 14/27 | chr2 | 9358734 | ||||||
| chr2:9359004
|
T | G | 2 | a0001c0002t0019g0164a0001c0013t0017g0045 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1461+115T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9359004 | ||||||
| chr2:9359248
|
T | C | 110 | a0001c0002t0001g0024a0001c0002t0001g0115a0001c0002t0001g0116others(107): Show | 110 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1461+359T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9359248 | ||||||
| chr2:9359523
|
A | G | 1 | a0002c0001t0001g0086 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1461+634A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9359523 | ||||||
| chr2:9359652
|
A | G | 2 | a0001c0002t0008g0048a0001c0002t0008g0206 | 2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1461+763A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9359652 | ||||||
| chr2:9359667
|
C | T | 43 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0009g0031others(40): Show | 43 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.1461+778C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9359667 | ||||||
| chr2:9359730
|
A | G | 14 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0003t0001g0210others(11): Show | 14 | HG02145.hp1 HG02257.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1461+841A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9359730 | ||||||
| chr2:9360417
|
G | A | 2 | a0001c0002t0019g0164a0001c0013t0017g0045 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1461+1528G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9360417 | ||||||
| chr2:9360539
|
G | A | 39 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0006g0184others(36): Show | 39 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1461+1650G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9360539 | ||||||
| chr2:9360551
|
A | G | 2 | a0001c0002t0019g0164a0001c0013t0017g0045 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1461+1662A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9360551 | ||||||
| chr2:9360616
|
T | C | 1 | a0001c0003t0021g0040 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1461+1727T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9360616 | ||||||
| chr2:9360833
|
G | A | 1 | a0002c0001t0001g0186 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1461+1944G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9360833 | ||||||
| chr2:9360888
|
A | T | 2 | a0001c0002t0019g0164a0001c0013t0017g0045 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1461+1999A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9360888 | ||||||
| chr2:9361062
|
G | A | 10 | a0001c0004t0005g0010a0001c0004t0005g0035a0001c0004t0005g0176others(7): Show | 10 | HG00738.hp1 HG01109.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1461+2173G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9361062 | ||||||
| chr2:9361204
|
C | T | 8 | a0001c0003t0004g0011a0001c0003t0004g0020a0001c0003t0004g0038others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1461+2315C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9361204 | ||||||
| chr2:9361354
|
G | A | 1 | a0001c0003t0001g0190 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1461+2465G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9361354 | ||||||
| chr2:9361440
|
C | T | 2 | a0001c0002t0019g0164a0001c0013t0017g0045 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1461+2551C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9361440 | ||||||
| chr2:9361546
|
T | TTTCC | 13 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(10): Show | 13 | HG01070.hp1 HG01109.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.1461+2664_1461+266 others(8): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 9361546 | |||||
| chr2:9361606
|
G | A | 38 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0003t0001g0017others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.1461+2717G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9361606 | ||||||
| chr2:9361711
|
G | A | 1 | a0002c0005t0001g0002 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1461+2822G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9361711 | ||||||
| chr2:9361712
|
C | T | 1 | a0002c0005t0001g0002 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1461+2823C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9361712 | ||||||
| chr2:9361862
|
G | C | 2 | a0001c0002t0019g0164a0001c0013t0017g0045 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1461+2973G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9361862 | ||||||
| chr2:9361862
|
G | T | 1 | a0001c0003t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1461+2973G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9361862 | ||||||
| chr2:9361896
|
A | G | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1461+3007A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9361896 | ||||||
| chr2:9361974
|
C | CGT | 27 | a0001c0002t0003g0148a0001c0002t0003g0150a0001c0003t0004g0175others(24): Show | 27 | HG00735.hp2 HG01074.hp2 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.1461+3122_1461+312 others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 9361974 | |||||
| chr2:9361974
|
C | CGTGT | 14 | a0001c0002t0003g0052a0001c0002t0008g0048a0001c0002t0008g0206others(11): Show | 14 | HG01099.hp2 HG01106.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.1461+3120_1461+312 others(8): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 9361974 | |||||
| chr2:9361974
|
C | CGTGTGT | 13 | a0001c0002t0001g0097a0001c0002t0002g0055a0001c0002t0002g0060others(10): Show | 13 | HG00738.hp1 HG01167.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1461+3118_1461+312 others(10): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 9361974 | |||||
| chr2:9361974
|
C | CGTGTGTG others(1): Show |
16 | a0001c0002t0002g0016a0001c0002t0002g0027a0001c0002t0002g0134others(13): Show | 16 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.1461+3116_1461+312 others(12): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 9361974 | |||||
| chr2:9361974
|
C | CGTGTGTG others(3): Show |
18 | a0001c0002t0001g0182a0001c0002t0002g0007a0001c0002t0002g0056others(15): Show | 18 | HG00280.hp2 HG01070.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.1461+3114_1461+312 others(14): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 9361974 | |||||
| chr2:9361974
|
C | CGTGTGTG others(5): Show |
7 | a0001c0002t0001g0116a0001c0002t0001g0126a0001c0002t0001g0181others(4): Show | 7 | HG00280.hp1 HG01106.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1461+3112_1461+312 others(16): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 9361974 | |||||
| chr2:9361974
|
C | CGTGTGTG others(7): Show |
2 | a0001c0002t0001g0115a0001c0002t0002g0177 | 2 | HG01256.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.1461+3110_1461+312 others(18): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 9361974 | |||||
| chr2:9361974
|
C | CGTGTGTG others(9): Show |
1 | a0001c0002t0023g0008 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1461+3108_1461+312 others(20): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 9361974 | |||||
| chr2:9361974
|
CGT | C | 6 | a0001c0004t0005g0035a0001c0006t0004g0018a0001c0007t0004g0019others(3): Show | 6 | HG01109.hp1 HG02004.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1461+3122_1461+312 others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 9361974 | |||||
| chr2:9361974
|
CGTGT | C | 18 | a0001c0002t0019g0164a0001c0003t0001g0039a0001c0003t0001g0190others(15): Show | 18 | HG01070.hp1 HG01109.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1461+3120_1461+312 others(8): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 9361974 | |||||
| chr2:9361974
|
CGTGTGT | C | 3 | a0001c0003t0001g0210a0001c0010t0018g0173a0001c0013t0017g0045 | 3 | HG03139.hp2 NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1461+3118_1461+312 others(10): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 9361974 | |||||
| chr2:9361974
|
CGTGTGTG others(1): Show |
C | 2 | a0001c0002t0001g0133a0001c0007t0001g0030 | 2 | HG01175.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1461+3116_1461+312 others(12): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 9361974 | |||||
| chr2:9361974
|
CGTGTGTG others(3): Show |
C | 1 | a0001c0003t0001g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1461+3114_1461+312 others(14): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 9361974 | |||||
| chr2:9361974
|
CGTGTGTG others(5): Show |
C | 21 | a0001c0003t0001g0017a0001c0003t0001g0029a0001c0003t0001g0046others(18): Show | 21 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.1461+3112_1461+312 others(16): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 9361974 | |||||
| chr2:9362034
|
A | G | 53 | a0001c0002t0001g0115a0001c0002t0001g0116a0001c0002t0001g0126others(50): Show | 53 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.1461+3145A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9362034 | ||||||
| chr2:9362551
|
C | G | 2 | a0001c0003t0001g0017a0001c0003t0001g0046 | 2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1461+3662C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9362551 | ||||||
| chr2:9362821
|
G | C | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1461+3932G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9362821 | ||||||
| chr2:9363036
|
G | A | 53 | a0001c0002t0001g0115a0001c0002t0001g0116a0001c0002t0001g0126others(50): Show | 53 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.1461+4147G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9363036 | ||||||
| chr2:9363197
|
T | C | 54 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0019g0164others(51): Show | 54 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.1461+4308T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9363197 | ||||||
| chr2:9363495
|
A | T | 14 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0003t0001g0210others(11): Show | 14 | HG02145.hp1 HG02257.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1461+4606A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9363495 | ||||||
| chr2:9363498
|
G | A | 1 | a0001c0010t0018g0173 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1461+4609G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9363498 | ||||||
| chr2:9363545
|
G | A | 1 | a0001c0003t0021g0040 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1461+4656G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9363545 | ||||||
| chr2:9363608
|
G | A | 2 | a0001c0002t0019g0164a0001c0013t0017g0045 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1461+4719G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9363608 | ||||||
| chr2:9363651
|
T | C | 2 | a0001c0002t0019g0164a0001c0013t0017g0045 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1461+4762T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9363651 | ||||||
| chr2:9363687
|
A | G | 55 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0006g0184others(52): Show | 55 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.1462-4738A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9363687 | ||||||
| chr2:9363695
|
T | A | 1 | a0001c0003t0001g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1462-4730T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9363695 | ||||||
| chr2:9363825
|
C | T | 22 | a0001c0003t0001g0017a0001c0003t0001g0029a0001c0003t0001g0046others(19): Show | 22 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.1462-4600C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9363825 | ||||||
| chr2:9363890
|
A | G | 1 | a0001c0013t0017g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1462-4535A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9363890 | ||||||
| chr2:9363932
|
G | T | 1 | a0002c0005t0001g0009 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1462-4493G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9363932 | ||||||
| chr2:9364109
|
A | G | 1 | a0001c0003t0001g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1462-4316A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9364109 | ||||||
| chr2:9364110
|
T | G | 1 | a0001c0002t0001g0024 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1462-4315T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9364110 | ||||||
| chr2:9364233
|
C | T | 2 | a0001c0002t0019g0164a0001c0013t0017g0045 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1462-4192C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9364233 | ||||||
| chr2:9364324
|
A | G | 2 | a0001c0002t0019g0164a0001c0013t0017g0045 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1462-4101A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9364324 | ||||||
| chr2:9364413
|
G | A | 1 | a0001c0013t0017g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1462-4012G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9364413 | ||||||
| chr2:9364800
|
A | C | 13 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(10): Show | 13 | HG01070.hp1 HG01109.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.1462-3625A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9364800 | ||||||
| chr2:9365058
|
G | A | 54 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0019g0164others(51): Show | 54 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.1462-3367G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9365058 | ||||||
| chr2:9365101
|
A | G | 1 | a0002c0001t0001g0012 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1462-3324A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9365101 | ||||||
| chr2:9365106
|
T | A | 1 | a0001c0004t0005g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1462-3319T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9365106 | ||||||
| chr2:9365182
|
A | G | 13 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(10): Show | 13 | HG01070.hp1 HG01109.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.1462-3243A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9365182 | ||||||
| chr2:9365310
|
C | T | 13 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(10): Show | 13 | HG01070.hp1 HG01109.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.1462-3115C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9365310 | ||||||
| chr2:9365365
|
C | T | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1462-3060C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9365365 | ||||||
| chr2:9365494
|
C | G | 1 | a0001c0004t0005g0205 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1462-2931C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9365494 | ||||||
| chr2:9365684
|
C | T | 2 | a0001c0002t0019g0164a0001c0013t0017g0045 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1462-2741C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9365684 | ||||||
| chr2:9365883
|
G | A | 13 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(10): Show | 13 | HG01070.hp1 HG01109.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.1462-2542G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9365883 | ||||||
| chr2:9365890
|
G | A | 31 | a0001c0002t0001g0115a0001c0002t0001g0116a0001c0002t0001g0126others(28): Show | 31 | HG00280.hp1 HG00280.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.1462-2535G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9365890 | ||||||
| chr2:9365893
|
T | G | 1 | a0001c0004t0005g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1462-2532T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9365893 | ||||||
| chr2:9365919
|
GAACTTA | G | 2 | a0001c0002t0019g0164a0001c0013t0017g0045 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1462-2502_1462-249 others(10): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 9365919 | |||||
| chr2:9366038
|
G | C | 54 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0019g0164others(51): Show | 54 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.1462-2387G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9366038 | ||||||
| chr2:9366154
|
G | A | 1 | a0001c0003t0016g0174 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1462-2271G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9366154 | ||||||
| chr2:9366189
|
G | A | 1 | a0001c0013t0017g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1462-2236G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9366189 | ||||||
| chr2:9366293
|
C | T | 2 | a0002c0001t0001g0093a0002c0001t0001g0112 | 2 | HG01981.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1462-2132C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9366293 | ||||||
| chr2:9366319
|
C | A | 1 | a0001c0010t0018g0173 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1462-2106C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9366319 | ||||||
| chr2:9366445
|
A | C | 2 | a0002c0001t0001g0076a0002c0001t0001g0081 | 2 | HG02155.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1462-1980A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9366445 | ||||||
| chr2:9366469
|
C | A | 2 | a0001c0002t0019g0164a0001c0013t0017g0045 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1462-1956C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9366469 | ||||||
| chr2:9366490
|
G | A | 3 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0019g0164 | 3 | HG02630.hp1 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1462-1935G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9366490 | ||||||
| chr2:9366569
|
A | T | 1 | a0002c0001t0001g0086 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1462-1856A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9366569 | ||||||
| chr2:9366635
|
G | A | 1 | a0002c0001t0001g0070 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1462-1790G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9366635 | ||||||
| chr2:9366761
|
A | G | 22 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(19): Show | 22 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1462-1664A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9366761 | ||||||
| chr2:9367004
|
T | C | 43 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0009g0031others(40): Show | 43 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.1462-1421T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9367004 | ||||||
| chr2:9367027
|
A | ATTTTTTT others(1): Show |
24 | a0001c0003t0001g0029a0001c0003t0001g0039a0001c0003t0001g0165others(21): Show | 24 | HG00408.hp2 HG00609.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.1462-1387_1462-138 others(12): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 9367027 | |||||
| chr2:9367027
|
A | ATTTTTTT others(2): Show |
13 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0003t0001g0017others(10): Show | 13 | HG00438.hp1 HG00597.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1462-1388_1462-138 others(13): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 9367027 | |||||
| chr2:9367027
|
A | ATTTTTTT others(7): Show |
1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1462-1393_1462-138 others(18): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 9367027 | |||||
| chr2:9367027
|
A | ATTTTTTT others(9): Show |
6 | a0001c0002t0019g0164a0001c0006t0004g0014a0001c0006t0004g0189others(3): Show | 6 | HG01884.hp1 HG02451.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1462-1395_1462-138 others(20): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 9367027 | |||||
| chr2:9367027
|
A | ATTTTTTT others(10): Show |
6 | a0001c0006t0004g0018a0001c0006t0004g0063a0001c0006t0004g0204others(3): Show | 6 | HG01070.hp1 HG01109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1462-1396_1462-138 others(21): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 9367027 | |||||
| chr2:9367027
|
A | ATTTTTTT others(11): Show |
2 | a0001c0006t0004g0032a0001c0013t0017g0045 | 2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1462-1397_1462-138 others(22): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 9367027 | |||||
| chr2:9367111
|
A | G | 1 | a0001c0010t0018g0173 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1462-1314A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9367111 | ||||||
| chr2:9367151
|
C | T | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1462-1274C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9367151 | ||||||
| chr2:9367183
|
G | A | 1 | a0001c0013t0017g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1462-1242G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9367183 | ||||||
| chr2:9367263
|
G | A | 2 | a0001c0002t0019g0164a0001c0013t0017g0045 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1462-1162G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9367263 | ||||||
| chr2:9367284
|
C | T | 43 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0009g0031others(40): Show | 43 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.1462-1141C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9367284 | ||||||
| chr2:9367363
|
T | G | 3 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0059 | 3 | HG00642.hp2 HG01261.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.1462-1062T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9367363 | ||||||
| chr2:9367568
|
C | G | 1 | a0002c0001t0001g0160 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1462-857C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9367568 | ||||||
| chr2:9367789
|
T | G | 8 | a0001c0003t0004g0011a0001c0003t0004g0020a0001c0003t0004g0038others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1462-636T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9367789 | ||||||
| chr2:9367926
|
T | A | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1462-499T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9367926 | ||||||
| chr2:9368020
|
C | T | 8 | a0001c0003t0004g0011a0001c0003t0004g0020a0001c0003t0004g0038others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1462-405C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9368020 | ||||||
| chr2:9368033
|
C | G | 1 | a0001c0010t0018g0173 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1462-392C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9368033 | ||||||
| chr2:9368352
|
T | A | 2 | a0001c0003t0007g0170a0001c0003t0007g0199 | 2 | HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1462-73T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 15/27 | chr2 | 9368352 | ||||||
| chr2:9368694
|
A | G | 2 | a0001c0002t0019g0164a0001c0013t0017g0045 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1556+175A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9368694 | ||||||
| chr2:9368779
|
A | T | 38 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0003t0001g0017others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.1556+260A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9368779 | ||||||
| chr2:9369001
|
C | A | 109 | a0001c0002t0001g0024a0001c0002t0001g0115a0001c0002t0001g0116others(106): Show | 109 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.1556+482C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9369001 | ||||||
| chr2:9369017
|
CT | C | 40 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0019g0164others(37): Show | 40 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.1556+512delT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr2 | 9369017 | |||||
| chr2:9369030
|
T | C | 52 | a0001c0002t0001g0115a0001c0002t0001g0116a0001c0002t0001g0126others(49): Show | 52 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1556+511T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9369030 | ||||||
| chr2:9369081
|
C | T | 1 | a0001c0006t0004g0197 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1556+562C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9369081 | ||||||
| chr2:9369165
|
C | T | 24 | a0001c0003t0001g0017a0001c0003t0001g0029a0001c0003t0001g0039others(21): Show | 24 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.1556+646C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9369165 | ||||||
| chr2:9369207
|
CAG | C | 2 | a0001c0002t0019g0164a0001c0013t0017g0045 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1556+691_1556+692d others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr2 | 9369207 | |||||
| chr2:9369469
|
G | A | 1 | a0001c0003t0001g0029 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1556+950G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9369469 | ||||||
| chr2:9369635
|
C | T | 1 | a0001c0013t0017g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1556+1116C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9369635 | ||||||
| chr2:9369717
|
C | T | 1 | a0001c0002t0001g0097 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1556+1198C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9369717 | ||||||
| chr2:9369750
|
C | T | 2 | a0001c0002t0019g0164a0001c0013t0017g0045 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1556+1231C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9369750 | ||||||
| chr2:9369910
|
C | A | 8 | a0001c0003t0004g0011a0001c0003t0004g0020a0001c0003t0004g0038others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1556+1391C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9369910 | ||||||
| chr2:9369941
|
G | A | 1 | a0001c0002t0002g0075 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1556+1422G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9369941 | ||||||
| chr2:9370016
|
C | G | 1 | a0001c0003t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1556+1497C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9370016 | ||||||
| chr2:9370077
|
A | G | 1 | a0001c0004t0005g0205 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1556+1558A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9370077 | ||||||
| chr2:9370085
|
A | C | 81 | a0001c0002t0001g0115a0001c0002t0001g0116a0001c0002t0001g0126others(78): Show | 81 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1556+1566A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9370085 | ||||||
| chr2:9370152
|
C | T | 1 | a0001c0004t0005g0035 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1556+1633C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9370152 | ||||||
| chr2:9370317
|
G | A | 1 | a0001c0013t0017g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1556+1798G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9370317 | ||||||
| chr2:9370382
|
G | A | 2 | a0001c0004t0005g0041a0001c0004t0005g0138 | 2 | HG00639.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1556+1863G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9370382 | ||||||
| chr2:9370405
|
C | T | 16 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(13): Show | 16 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1556+1886C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9370405 | ||||||
| chr2:9370552
|
C | T | 1 | a0001c0004t0005g0035 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1556+2033C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9370552 | ||||||
| chr2:9370634
|
G | C | 1 | a0001c0003t0004g0011 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1556+2115G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9370634 | ||||||
| chr2:9370640
|
G | T | 14 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0003t0001g0210others(11): Show | 14 | HG02145.hp1 HG02257.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1556+2121G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9370640 | ||||||
| chr2:9370654
|
T | C | 38 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.1556+2135T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9370654 | ||||||
| chr2:9370665
|
G | A | 1 | a0002c0001t0001g0076 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1556+2146G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9370665 | ||||||
| chr2:9370744
|
C | T | 4 | a0001c0002t0001g0133a0001c0003t0004g0200a0001c0003t0007g0170others(1): Show | 4 | HG03516.hp2 HG03579.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1556+2225C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9370744 | ||||||
| chr2:9370851
|
C | T | 1 | a0002c0001t0001g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1556+2332C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9370851 | ||||||
| chr2:9371105
|
A | G | 2 | a0001c0002t0001g0024a0001c0002t0001g0133 | 2 | HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1556+2586A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9371105 | ||||||
| chr2:9371109
|
T | A | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1556+2590T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9371109 | ||||||
| chr2:9371167
|
T | C | 1 | a0002c0001t0001g0127 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1556+2648T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9371167 | ||||||
| chr2:9371175
|
C | T | 1 | a0002c0001t0001g0087 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1556+2656C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9371175 | ||||||
| chr2:9371288
|
G | C | 12 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(9): Show | 12 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1556+2769G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9371288 | ||||||
| chr2:9371387
|
T | C | 16 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(13): Show | 16 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1556+2868T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9371387 | ||||||
| chr2:9371409
|
C | A | 16 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(13): Show | 16 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1556+2890C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9371409 | ||||||
| chr2:9371692
|
A | G | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1557-3063A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9371692 | ||||||
| chr2:9371842
|
C | T | 1 | a0001c0002t0002g0027 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1557-2913C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9371842 | ||||||
| chr2:9371883
|
G | A | 3 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0003t0001g0210 | 3 | HG02630.hp1 NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1557-2872G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9371883 | ||||||
| chr2:9371912
|
C | T | 1 | a0002c0001t0001g0086 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1557-2843C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9371912 | ||||||
| chr2:9371933
|
G | A | 1 | a0002c0001t0001g0049 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1557-2822G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9371933 | ||||||
| chr2:9372132
|
G | A | 1 | a0001c0002t0003g0147 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1557-2623G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9372132 | ||||||
| chr2:9372304
|
C | G | 1 | a0002c0001t0001g0118 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1557-2451C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9372304 | ||||||
| chr2:9372319
|
C | A | 24 | a0001c0002t0001g0097a0001c0003t0001g0017a0001c0003t0001g0029others(21): Show | 24 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.1557-2436C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9372319 | ||||||
| chr2:9372683
|
A | C | 4 | a0001c0003t0006g0080a0001c0003t0006g0104a0001c0003t0006g0105others(1): Show | 4 | HG00597.hp2 NA18964.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.1557-2072A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9372683 | ||||||
| chr2:9372685
|
T | C | 2 | a0001c0002t0001g0024a0001c0002t0001g0133 | 2 | HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1557-2070T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9372685 | ||||||
| chr2:9372985
|
C | T | 1 | a0001c0002t0001g0126 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1557-1770C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9372985 | ||||||
| chr2:9373108
|
C | T | 13 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(10): Show | 13 | HG01070.hp1 HG01109.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1557-1647C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9373108 | ||||||
| chr2:9373120
|
G | A | 5 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0003t0004g0200others(2): Show | 5 | HG02630.hp1 HG03516.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1557-1635G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9373120 | ||||||
| chr2:9373134
|
G | A | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1557-1621G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9373134 | ||||||
| chr2:9373167
|
C | A | 21 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(18): Show | 21 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1557-1588C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9373167 | ||||||
| chr2:9373217
|
A | G | 5 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0003t0004g0200others(2): Show | 5 | HG02630.hp1 HG03516.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1557-1538A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9373217 | ||||||
| chr2:9373225
|
C | T | 16 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(13): Show | 16 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1557-1530C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9373225 | ||||||
| chr2:9373250
|
CT | C | 14 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0003t0001g0210others(11): Show | 14 | HG02145.hp1 HG02257.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1557-1504delT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9373250 | ||||||
| chr2:9373439
|
C | T | 12 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(9): Show | 12 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1557-1316C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9373439 | ||||||
| chr2:9373685
|
G | A | 1 | a0001c0002t0002g0073 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1557-1070G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9373685 | ||||||
| chr2:9373716
|
C | T | 16 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(13): Show | 16 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1557-1039C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9373716 | ||||||
| chr2:9373721
|
T | G | 56 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(53): Show | 56 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.1557-1034T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9373721 | ||||||
| chr2:9373843
|
T | C | 6 | a0001c0004t0005g0021a0001c0004t0005g0034a0001c0004t0005g0041others(3): Show | 6 | HG00639.hp1 HG02976.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1557-912T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9373843 | ||||||
| chr2:9373875
|
A | G | 5 | a0001c0004t0005g0191a0001c0004t0005g0192a0001c0004t0005g0193others(2): Show | 5 | HG01109.hp2 HG01884.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1557-880A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9373875 | ||||||
| chr2:9373931
|
G | A | 38 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(35): Show | 38 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.1557-824G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9373931 | ||||||
| chr2:9373964
|
G | A | 15 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0002t0019g0164others(12): Show | 15 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1557-791G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9373964 | ||||||
| chr2:9374013
|
G | A | 1 | a0001c0002t0003g0142 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1557-742G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9374013 | ||||||
| chr2:9374083
|
G | T | 12 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(9): Show | 12 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1557-672G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9374083 | ||||||
| chr2:9374108
|
G | A | 1 | a0001c0003t0004g0044 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1557-647G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9374108 | ||||||
| chr2:9374400
|
G | A | 2 | a0001c0004t0005g0041a0001c0004t0005g0138 | 2 | HG00639.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1557-355G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9374400 | ||||||
| chr2:9374444
|
T | C | 96 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(93): Show | 96 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.1557-311T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9374444 | ||||||
| chr2:9374445
|
G | A | 1 | a0001c0007t0004g0015 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1557-310G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9374445 | ||||||
| chr2:9374683
|
C | T | 1 | a0001c0003t0001g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1557-72C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 16/27 | chr2 | 9374683 | ||||||
| chr2:9374970
|
T | TA | 57 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(54): Show | 57 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1746+40dupA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr2 | 9374970 | |||||
| chr2:9374987
|
C | T | 5 | a0001c0002t0001g0133a0001c0002t0003g0148a0001c0003t0004g0200others(2): Show | 5 | HG03098.hp2 HG03516.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1746+43C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 17/27 | chr2 | 9374987 | ||||||
| chr2:9374988
|
C | T | 1 | a0001c0002t0003g0052 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1746+44C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 17/27 | chr2 | 9374988 | ||||||
| chr2:9375028
|
C | T | 96 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(93): Show | 96 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.1746+84C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 17/27 | chr2 | 9375028 | ||||||
| chr2:9375086
|
A | G | 13 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(10): Show | 13 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1746+142A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 17/27 | chr2 | 9375086 | ||||||
| chr2:9375101
|
C | A | 1 | a0001c0002t0019g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1746+157C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 17/27 | chr2 | 9375101 | ||||||
| chr2:9375106
|
CA | C | 89 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1746+182delA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr2 | 9375106 | |||||
| chr2:9375282
|
C | CA | 45 | a0001c0002t0002g0134a0001c0002t0002g0198a0001c0002t0002g0202others(42): Show | 45 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.1746+347dupA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr2 | 9375282 | |||||
| chr2:9375331
|
G | A | 3 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0003t0001g0210 | 3 | HG02886.hp2 HG02895.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1746+387G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 17/27 | chr2 | 9375331 | ||||||
| chr2:9375376
|
G | T | 1 | a0001c0013t0017g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1746+432G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 17/27 | chr2 | 9375376 | ||||||
| chr2:9375405
|
T | G | 142 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(139): Show | 142 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.1746+461T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 17/27 | chr2 | 9375405 | ||||||
| chr2:9375422
|
G | A | 52 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(49): Show | 52 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.1746+478G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 17/27 | chr2 | 9375422 | ||||||
| chr2:9375481
|
T | C | 9 | a0001c0002t0001g0024a0001c0003t0004g0011a0001c0003t0004g0020others(6): Show | 9 | HG02145.hp1 HG02257.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1746+537T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 17/27 | chr2 | 9375481 | ||||||
| chr2:9375528
|
G | T | 13 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(10): Show | 13 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1746+584G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 17/27 | chr2 | 9375528 | ||||||
| chr2:9375539
|
T | C | 28 | a0001c0002t0001g0097a0001c0002t0006g0184a0001c0002t0009g0031others(25): Show | 28 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.1746+595T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 17/27 | chr2 | 9375539 | ||||||
| chr2:9375980
|
G | A | 1 | a0002c0001t0001g0109 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1747-928G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 17/27 | chr2 | 9375980 | ||||||
| chr2:9376131
|
G | A | 67 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0003g0026others(64): Show | 67 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.1747-777G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 17/27 | chr2 | 9376131 | ||||||
| chr2:9376156
|
C | T | 1 | a0001c0003t0016g0174 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1747-752C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 17/27 | chr2 | 9376156 | ||||||
| chr2:9376263
|
G | A | 25 | a0001c0002t0001g0097a0001c0002t0006g0184a0001c0003t0001g0017others(22): Show | 25 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.1747-645G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 17/27 | chr2 | 9376263 | ||||||
| chr2:9376464
|
G | A | 26 | a0001c0002t0001g0097a0001c0002t0006g0184a0001c0003t0001g0017others(23): Show | 26 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.1747-444G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 17/27 | chr2 | 9376464 | ||||||
| chr2:9376641
|
A | G | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1747-267A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 17/27 | chr2 | 9376641 | ||||||
| chr2:9376693
|
C | T | 8 | a0001c0003t0004g0011a0001c0003t0004g0020a0001c0003t0004g0038others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1747-215C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 17/27 | chr2 | 9376693 | ||||||
| chr2:9376787
|
T | G | 25 | a0001c0002t0001g0097a0001c0002t0006g0184a0001c0003t0001g0017others(22): Show | 25 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.1747-121T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 17/27 | chr2 | 9376787 | ||||||
| chr2:9376995
|
T | G | 1 | a0002c0001t0001g0100 | 1 | HG03831.hp1 | splice_donor_variant&intron_variant | HIGH | c.1832+2T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 18/27 | chr2 | 9376995 | ||||||
| chr2:9377209
|
C | T | 18 | a0001c0004t0005g0010a0001c0004t0005g0021a0001c0004t0005g0028others(15): Show | 18 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1832+216C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 18/27 | chr2 | 9377209 | ||||||
| chr2:9377306
|
G | A | 1 | a0002c0001t0001g0113 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1832+313G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 18/27 | chr2 | 9377306 | ||||||
| chr2:9377324
|
G | A | 3 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0003g0148 | 3 | HG02630.hp1 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1832+331G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 18/27 | chr2 | 9377324 | ||||||
| chr2:9377337
|
C | T | 1 | a0001c0003t0021g0040 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1832+344C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 18/27 | chr2 | 9377337 | ||||||
| chr2:9377427
|
C | T | 30 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(27): Show | 30 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1832+434C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 18/27 | chr2 | 9377427 | ||||||
| chr2:9377518
|
A | G | 96 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(93): Show | 96 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.1832+525A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 18/27 | chr2 | 9377518 | ||||||
| chr2:9377535
|
C | T | 1 | a0002c0001t0001g0109 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1832+542C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 18/27 | chr2 | 9377535 | ||||||
| chr2:9377632
|
G | A | 20 | a0001c0002t0006g0184a0001c0003t0001g0029a0001c0003t0001g0153others(17): Show | 20 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.1832+639G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 18/27 | chr2 | 9377632 | ||||||
| chr2:9377920
|
G | A | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1832+927G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 18/27 | chr2 | 9377920 | ||||||
| chr2:9377984
|
C | T | 1 | a0002c0001t0003g0099 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1833-960C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 18/27 | chr2 | 9377984 | ||||||
| chr2:9377997
|
C | T | 25 | a0001c0002t0001g0097a0001c0002t0006g0184a0001c0003t0001g0017others(22): Show | 25 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.1833-947C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 18/27 | chr2 | 9377997 | ||||||
| chr2:9378005
|
A | G | 2 | a0001c0003t0001g0039a0001c0003t0001g0190 | 2 | HG01934.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1833-939A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 18/27 | chr2 | 9378005 | ||||||
| chr2:9378264
|
A | C | 49 | a0001c0002t0001g0097a0001c0002t0006g0184a0001c0002t0009g0031others(46): Show | 49 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1833-680A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 18/27 | chr2 | 9378264 | ||||||
| chr2:9378514
|
C | T | 44 | a0001c0002t0001g0097a0001c0002t0006g0184a0001c0003t0001g0017others(41): Show | 44 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.1833-430C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 18/27 | chr2 | 9378514 | ||||||
| chr2:9378566
|
A | C | 1 | a0002c0001t0001g0109 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1833-378A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 18/27 | chr2 | 9378566 | ||||||
| chr2:9378643
|
C | T | 1 | a0002c0008t0001g0108 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1833-301C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 18/27 | chr2 | 9378643 | ||||||
| chr2:9378663
|
T | G | 18 | a0001c0004t0005g0010a0001c0004t0005g0021a0001c0004t0005g0028others(15): Show | 18 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1833-281T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 18/27 | chr2 | 9378663 | ||||||
| chr2:9378678
|
C | A | 8 | a0001c0003t0004g0011a0001c0003t0004g0020a0001c0003t0004g0038others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1833-266C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 18/27 | chr2 | 9378678 | ||||||
| chr2:9378764
|
C | A | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1833-180C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 18/27 | chr2 | 9378764 | ||||||
| chr2:9378926
|
G | C | 25 | a0001c0002t0001g0097a0001c0003t0001g0017a0001c0003t0001g0029others(22): Show | 25 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.1833-18G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 18/27 | chr2 | 9378926 | ||||||
| chr2:9379072
|
G | A | 26 | a0001c0002t0001g0097a0001c0002t0006g0184a0001c0003t0001g0017others(23): Show | 26 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.1948+13G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 19/27 | chr2 | 9379072 | ||||||
| chr2:9379124
|
T | G | 1 | a0003c0014t0003g0051 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1948+65T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 19/27 | chr2 | 9379124 | ||||||
| chr2:9379130
|
C | T | 3 | a0001c0003t0004g0038a0001c0003t0004g0043a0001c0003t0004g0175 | 3 | HG02723.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1948+71C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 19/27 | chr2 | 9379130 | ||||||
| chr2:9379144
|
A | G | 14 | a0001c0003t0001g0165a0001c0006t0004g0014a0001c0006t0004g0018others(11): Show | 14 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1948+85A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 19/27 | chr2 | 9379144 | ||||||
| chr2:9379153
|
A | G | 21 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1948+94A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 19/27 | chr2 | 9379153 | ||||||
| chr2:9379232
|
G | A | 1 | a0002c0001t0001g0159 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1948+173G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 19/27 | chr2 | 9379232 | ||||||
| chr2:9379533
|
C | T | 3 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0003g0148 | 3 | HG02630.hp1 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1948+474C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 19/27 | chr2 | 9379533 | ||||||
| chr2:9379791
|
G | A | 1 | a0002c0001t0001g0109 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1948+732G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 19/27 | chr2 | 9379791 | ||||||
| chr2:9379828
|
C | T | 1 | a0002c0001t0001g0161 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1948+769C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 19/27 | chr2 | 9379828 | ||||||
| chr2:9379890
|
G | C | 1 | a0001c0004t0005g0205 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1948+831G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 19/27 | chr2 | 9379890 | ||||||
| chr2:9379916
|
C | T | 1 | a0001c0009t0004g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1949-825C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 19/27 | chr2 | 9379916 | ||||||
| chr2:9379924
|
G | A | 1 | a0002c0001t0001g0168 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1949-817G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 19/27 | chr2 | 9379924 | ||||||
| chr2:9380003
|
AT | A | 19 | a0001c0002t0002g0162a0001c0004t0005g0010a0001c0004t0005g0021others(16): Show | 19 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1949-737delT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 19/27 | chr2 | 9380003 | ||||||
| chr2:9380004
|
T | A | 179 | a0001c0002t0001g0097a0001c0002t0001g0115a0001c0002t0001g0116others(176): Show | 179 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.1949-737T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 19/27 | chr2 | 9380004 | ||||||
| chr2:9380005
|
A | T | 17 | a0001c0002t0003g0062a0001c0002t0003g0124a0001c0003t0001g0165others(14): Show | 17 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1949-736A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 19/27 | chr2 | 9380005 | ||||||
| chr2:9380134
|
A | G | 20 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0003g0148others(17): Show | 20 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1949-607A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 19/27 | chr2 | 9380134 | ||||||
| chr2:9380181
|
A | AGTTTTT | 6 | a0001c0004t0005g0021a0001c0004t0005g0034a0001c0004t0005g0041others(3): Show | 6 | HG00639.hp1 HG02976.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1949-541_1949-536d others(8): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr2 | 9380181 | |||||
| chr2:9380417
|
C | T | 25 | a0001c0002t0001g0097a0001c0003t0001g0017a0001c0003t0001g0029others(22): Show | 25 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.1949-324C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 19/27 | chr2 | 9380417 | ||||||
| chr2:9380464
|
C | T | 1 | a0002c0001t0014g0091 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1949-277C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 19/27 | chr2 | 9380464 | ||||||
| chr2:9380475
|
G | A | 3 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0003g0148 | 3 | HG02630.hp1 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1949-266G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 19/27 | chr2 | 9380475 | ||||||
| chr2:9380533
|
T | G | 1 | a0002c0001t0001g0072 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1949-208T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 19/27 | chr2 | 9380533 | ||||||
| chr2:9380696
|
C | T | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1949-45C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 19/27 | chr2 | 9380696 | ||||||
| chr2:9380820
|
A | C | 17 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0003g0148others(14): Show | 17 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.2016+12A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9380820 | ||||||
| chr2:9380830
|
C | T | 21 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(18): Show | 21 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.2016+22C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9380830 | ||||||
| chr2:9380983
|
G | A | 3 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0003g0148 | 3 | HG02630.hp1 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2016+175G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9380983 | ||||||
| chr2:9381005
|
C | G | 1 | a0001c0003t0004g0200 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2016+197C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9381005 | ||||||
| chr2:9381082
|
A | G | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2016+274A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9381082 | ||||||
| chr2:9381202
|
A | T | 2 | a0001c0002t0008g0048a0001c0002t0008g0206 | 2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2016+394A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9381202 | ||||||
| chr2:9381434
|
G | A | 21 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(18): Show | 21 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.2016+626G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9381434 | ||||||
| chr2:9381626
|
C | T | 8 | a0001c0003t0004g0011a0001c0003t0004g0020a0001c0003t0004g0038others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.2016+818C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9381626 | ||||||
| chr2:9381638
|
A | G | 2 | a0002c0001t0001g0110a0002c0001t0001g0140 | 2 | HG03239.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.2016+830A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9381638 | ||||||
| chr2:9381980
|
CT | C | 57 | a0001c0002t0001g0024a0001c0002t0001g0115a0001c0002t0001g0133others(54): Show | 57 | HG00642.hp2 HG00738.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.2016+1193delT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 9381980 | |||||
| chr2:9381980
|
CTT | C | 40 | a0001c0002t0001g0097a0001c0002t0003g0150a0001c0002t0003g0152others(37): Show | 40 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.2016+1192_2016+119 others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 9381980 | |||||
| chr2:9382173
|
G | A | 1 | a0002c0001t0001g0128 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2016+1365G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9382173 | ||||||
| chr2:9382181
|
A | G | 2 | a0002c0001t0001g0074a0002c0001t0001g0161 | 2 | HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2016+1373A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9382181 | ||||||
| chr2:9382263
|
C | A | 2 | a0001c0002t0002g0137a0001c0002t0023g0008 | 2 | HG02523.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.2016+1455C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9382263 | ||||||
| chr2:9382276
|
A | G | 1 | a0001c0003t0001g0153 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2016+1468A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9382276 | ||||||
| chr2:9382294
|
A | G | 10 | a0001c0004t0005g0010a0001c0004t0005g0035a0001c0004t0005g0176others(7): Show | 10 | HG00738.hp1 HG01109.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.2016+1486A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9382294 | ||||||
| chr2:9382335
|
C | G | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2016+1527C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9382335 | ||||||
| chr2:9382337
|
C | T | 1 | a0002c0001t0001g0100 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2016+1529C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9382337 | ||||||
| chr2:9382488
|
G | A | 1 | a0002c0001t0001g0146 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2016+1680G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9382488 | ||||||
| chr2:9382495
|
G | T | 1 | a0001c0004t0005g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2016+1687G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9382495 | ||||||
| chr2:9382523
|
A | G | 26 | a0001c0002t0001g0097a0001c0002t0006g0184a0001c0003t0001g0017others(23): Show | 26 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.2016+1715A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9382523 | ||||||
| chr2:9382683
|
A | G | 1 | a0001c0002t0006g0183 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2016+1875A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9382683 | ||||||
| chr2:9382821
|
T | G | 96 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(93): Show | 96 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.2016+2013T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9382821 | ||||||
| chr2:9382894
|
C | T | 17 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0003g0148others(14): Show | 17 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.2016+2086C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9382894 | ||||||
| chr2:9382929
|
C | T | 1 | a0001c0003t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2016+2121C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9382929 | ||||||
| chr2:9383066
|
A | G | 66 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(63): Show | 66 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.2017-2179A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9383066 | ||||||
| chr2:9383103
|
G | A | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2017-2142G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9383103 | ||||||
| chr2:9383233
|
A | G | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2017-2012A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9383233 | ||||||
| chr2:9383275
|
T | A | 29 | a0001c0002t0001g0097a0001c0002t0006g0184a0001c0003t0001g0017others(26): Show | 29 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.2017-1970T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9383275 | ||||||
| chr2:9383276
|
A | T | 17 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0003g0148others(14): Show | 17 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.2017-1969A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9383276 | ||||||
| chr2:9383380
|
G | A | 1 | a0002c0001t0001g0111 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2017-1865G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9383380 | ||||||
| chr2:9383543
|
G | A | 1 | a0003c0014t0003g0051 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2017-1702G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9383543 | ||||||
| chr2:9383549
|
C | G | 4 | a0001c0004t0005g0021a0001c0004t0005g0034a0001c0004t0005g0144others(1): Show | 4 | HG02976.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2017-1696C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9383549 | ||||||
| chr2:9383616
|
C | A | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2017-1629C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9383616 | ||||||
| chr2:9383619
|
T | C | 96 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(93): Show | 96 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.2017-1626T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9383619 | ||||||
| chr2:9383711
|
C | T | 7 | a0002c0001t0001g0071a0002c0001t0001g0078a0002c0001t0001g0088others(4): Show | 7 | HG01346.hp1 HG01358.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.2017-1534C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9383711 | ||||||
| chr2:9383776
|
G | A | 66 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(63): Show | 66 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.2017-1469G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9383776 | ||||||
| chr2:9383815
|
G | A | 1 | a0002c0001t0001g0117 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2017-1430G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9383815 | ||||||
| chr2:9383819
|
A | G | 2 | a0002c0001t0001g0127a0002c0001t0020g0079 | 2 | HG02080.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2017-1426A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9383819 | ||||||
| chr2:9383834
|
T | TA | 8 | a0001c0003t0004g0011a0001c0003t0004g0020a0001c0003t0004g0038others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.2017-1405dupA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 9383834 | |||||
| chr2:9383933
|
C | T | 64 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(61): Show | 64 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.2017-1312C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9383933 | ||||||
| chr2:9384094
|
A | G | 20 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0003g0148others(17): Show | 20 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.2017-1151A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9384094 | ||||||
| chr2:9384171
|
A | T | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2017-1074A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9384171 | ||||||
| chr2:9384376
|
C | T | 43 | a0001c0002t0001g0097a0001c0002t0006g0184a0001c0003t0001g0017others(40): Show | 43 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.2017-869C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9384376 | ||||||
| chr2:9384810
|
G | A | 61 | a0001c0002t0001g0097a0001c0002t0006g0184a0001c0003t0001g0017others(58): Show | 61 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.2017-435G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9384810 | ||||||
| chr2:9384836
|
C | T | 96 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(93): Show | 96 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.2017-409C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9384836 | ||||||
| chr2:9384893
|
C | A | 66 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(63): Show | 66 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.2017-352C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9384893 | ||||||
| chr2:9384990
|
T | G | 2 | a0002c0005t0001g0003a0002c0005t0001g0009 | 2 | HG00642.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2017-255T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9384990 | ||||||
| chr2:9385052
|
G | A | 1 | a0001c0013t0017g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2017-193G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 20/27 | chr2 | 9385052 | ||||||
| chr2:9385465
|
T | C | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2130+107T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9385465 | ||||||
| chr2:9385581
|
T | C | 46 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(43): Show | 46 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.2130+223T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9385581 | ||||||
| chr2:9385624
|
C | T | 1 | a0002c0001t0001g0086 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2130+266C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9385624 | ||||||
| chr2:9385625
|
G | C | 4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2130+267G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9385625 | ||||||
| chr2:9385694
|
T | C | 1 | a0001c0003t0007g0199 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2130+336T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9385694 | ||||||
| chr2:9385762
|
G | A | 1 | a0001c0003t0021g0040 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2130+404G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9385762 | ||||||
| chr2:9386158
|
G | A | 3 | a0001c0004t0005g0021a0001c0004t0005g0034a0001c0004t0005g0144 | 3 | HG03130.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2130+800G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9386158 | ||||||
| chr2:9386212
|
A | G | 1 | a0002c0001t0001g0012 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2130+854A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9386212 | ||||||
| chr2:9386386
|
TA | T | 16 | a0001c0002t0003g0166a0001c0002t0003g0188a0001c0002t0003g0209others(13): Show | 16 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.2130+1039delA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 9386386 | |||||
| chr2:9386567
|
C | G | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2130+1209C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9386567 | ||||||
| chr2:9386579
|
G | T | 1 | a0001c0002t0006g0184 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2130+1221G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9386579 | ||||||
| chr2:9386950
|
A | G | 17 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0003g0148others(14): Show | 17 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.2131-1344A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9386950 | ||||||
| chr2:9387070
|
G | A | 1 | a0002c0005t0001g0098 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2131-1224G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9387070 | ||||||
| chr2:9387072
|
G | T | 1 | a0001c0003t0001g0169 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2131-1222G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9387072 | ||||||
| chr2:9387073
|
G | T | 1 | a0001c0003t0001g0169 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2131-1221G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9387073 | ||||||
| chr2:9387074
|
T | G | 4 | a0001c0003t0001g0169a0001c0003t0004g0200a0001c0003t0007g0170others(1): Show | 4 | HG02717.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2131-1220T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9387074 | ||||||
| chr2:9387074
|
T | TG | 44 | a0001c0002t0001g0024a0001c0002t0001g0115a0001c0002t0001g0116others(41): Show | 44 | HG00280.hp1 HG00280.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.2131-1217dupG | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 9387074 | |||||
| chr2:9387074
|
T | TGG | 12 | a0001c0002t0001g0126a0001c0002t0001g0182a0001c0002t0003g0124others(9): Show | 12 | HG01070.hp1 HG01106.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2131-1218_2131-121 others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 9387074 | |||||
| chr2:9387074
|
T | TGGG | 5 | a0001c0004t0005g0021a0001c0006t0004g0018a0001c0006t0004g0063others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.2131-1219_2131-121 others(7): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 9387074 | |||||
| chr2:9387074
|
TG | T | 22 | a0001c0002t0003g0094a0001c0002t0003g0142a0001c0002t0008g0048others(19): Show | 22 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.2131-1217delG | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 9387074 | |||||
| chr2:9387077
|
G | C | 1 | a0001c0002t0022g0120 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2131-1217G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9387077 | ||||||
| chr2:9387077
|
GT | G | 2 | a0001c0003t0001g0017a0001c0003t0001g0046 | 2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2131-1216delT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9387077 | ||||||
| chr2:9387078
|
T | C | 11 | a0001c0002t0001g0024a0001c0002t0003g0148a0001c0007t0001g0030others(8): Show | 11 | HG00639.hp2 HG01167.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.2131-1216T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9387078 | ||||||
| chr2:9387078
|
T | G | 120 | a0001c0002t0001g0097a0001c0002t0001g0115a0001c0002t0001g0116others(117): Show | 120 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.2131-1216T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9387078 | ||||||
| chr2:9387079
|
G | C | 1 | a0001c0002t0001g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2131-1215G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9387079 | ||||||
| chr2:9387080
|
G | C | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2131-1214G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9387080 | ||||||
| chr2:9387080
|
G | T | 1 | a0002c0001t0001g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2131-1214G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9387080 | ||||||
| chr2:9387138
|
C | T | 1 | a0002c0001t0014g0091 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2131-1156C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9387138 | ||||||
| chr2:9387180
|
T | C | 1 | a0002c0001t0001g0113 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2131-1114T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9387180 | ||||||
| chr2:9387195
|
C | A | 47 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(44): Show | 47 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.2131-1099C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9387195 | ||||||
| chr2:9387196
|
A | G | 1 | a0001c0004t0005g0205 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2131-1098A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9387196 | ||||||
| chr2:9387213
|
C | CAAAAAAA | 14 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0003g0148others(11): Show | 14 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.2131-1073_2131-106 others(11): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 9387213 | |||||
| chr2:9387213
|
C | CAAAAAAA others(1): Show |
8 | a0001c0002t0003g0150a0001c0003t0001g0046a0001c0003t0001g0169others(5): Show | 8 | HG01496.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.2131-1074_2131-106 others(12): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 9387213 | |||||
| chr2:9387213
|
C | CAAAAAAA others(2): Show |
31 | a0001c0002t0001g0097a0001c0002t0003g0026a0001c0002t0003g0050others(28): Show | 31 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.2131-1075_2131-106 others(13): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 9387213 | |||||
| chr2:9387213
|
C | CAAAAAAA others(3): Show |
18 | a0001c0002t0003g0059a0001c0002t0003g0124a0001c0002t0003g0166others(15): Show | 18 | HG00438.hp1 HG00597.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.2131-1076_2131-106 others(14): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 9387213 | |||||
| chr2:9387213
|
C | CAAAAAAA others(4): Show |
3 | a0001c0003t0004g0038a0001c0003t0004g0175a0001c0003t0016g0174 | 3 | HG02145.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2131-1077_2131-106 others(15): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 9387213 | |||||
| chr2:9387213
|
C | CAAAAAAA others(5): Show |
13 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0004t0005g0010others(10): Show | 13 | HG00639.hp1 HG00738.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.2131-1078_2131-106 others(16): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 9387213 | |||||
| chr2:9387213
|
C | CAAAAAAA others(6): Show |
7 | a0001c0003t0007g0199a0001c0004t0005g0028a0001c0004t0005g0035others(4): Show | 7 | HG01109.hp2 HG02886.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.2131-1079_2131-106 others(17): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 9387213 | |||||
| chr2:9387228
|
C | A | 1 | a0002c0001t0001g0159 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2131-1066C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9387228 | ||||||
| chr2:9387240
|
CA | C | 3 | a0001c0003t0004g0038a0001c0003t0004g0043a0001c0003t0004g0175 | 3 | HG02723.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2131-1053delA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9387240 | ||||||
| chr2:9387244
|
G | A | 21 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(18): Show | 21 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.2131-1050G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9387244 | ||||||
| chr2:9387248
|
A | G | 8 | a0001c0003t0004g0011a0001c0003t0004g0020a0001c0003t0004g0038others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.2131-1046A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9387248 | ||||||
| chr2:9387486
|
C | CTCCT | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2131-807_2131-804d others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 9387486 | |||||
| chr2:9387557
|
G | A | 1 | a0001c0002t0001g0116 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2131-737G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9387557 | ||||||
| chr2:9387589
|
T | C | 1 | a0002c0001t0001g0022 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2131-705T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9387589 | ||||||
| chr2:9388043
|
G | A | 65 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(62): Show | 65 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.2131-251G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9388043 | ||||||
| chr2:9388097
|
C | T | 7 | a0001c0002t0002g0007a0001c0002t0002g0027a0001c0002t0002g0073others(4): Show | 7 | HG00280.hp1 HG01074.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.2131-197C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9388097 | ||||||
| chr2:9388198
|
T | C | 1 | a0002c0005t0001g0009 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2131-96T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 21/27 | chr2 | 9388198 | ||||||
| chr2:9388672
|
T | C | 40 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0003g0026others(37): Show | 40 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.2383+126T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 22/27 | chr2 | 9388672 | ||||||
| chr2:9388944
|
G | A | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2383+398G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 22/27 | chr2 | 9388944 | ||||||
| chr2:9388964
|
C | T | 26 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(23): Show | 26 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.2383+418C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 22/27 | chr2 | 9388964 | ||||||
| chr2:9388988
|
C | T | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2383+442C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 22/27 | chr2 | 9388988 | ||||||
| chr2:9388990
|
T | C | 3 | a0001c0004t0005g0021a0001c0004t0005g0034a0001c0004t0005g0144 | 3 | HG03130.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2383+444T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 22/27 | chr2 | 9388990 | ||||||
| chr2:9389165
|
G | A | 63 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(60): Show | 63 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2383+619G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 22/27 | chr2 | 9389165 | ||||||
| chr2:9389315
|
CTT | C | 22 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(19): Show | 22 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.2383+771_2383+772d others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr2 | 9389315 | |||||
| chr2:9389324
|
G | A | 1 | a0002c0001t0001g0084 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2383+778G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 22/27 | chr2 | 9389324 | ||||||
| chr2:9389498
|
G | A | 12 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(9): Show | 12 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.2383+952G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 22/27 | chr2 | 9389498 | ||||||
| chr2:9389588
|
C | G | 1 | a0001c0010t0018g0173 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2383+1042C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 22/27 | chr2 | 9389588 | ||||||
| chr2:9389603
|
A | C | 4 | a0001c0003t0004g0011a0001c0003t0004g0038a0001c0003t0004g0043others(1): Show | 4 | HG02257.hp2 HG02723.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2383+1057A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 22/27 | chr2 | 9389603 | ||||||
| chr2:9389686
|
C | CCCGAAGA others(23): Show |
1 | a0001c0002t0003g0026 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2383+1141_2383+117 others(34): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr2 | 9389686 | |||||
| chr2:9389847
|
C | T | 15 | a0001c0003t0001g0165a0001c0006t0004g0014a0001c0006t0004g0018others(12): Show | 15 | HG01070.hp1 HG01109.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.2384-1215C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 22/27 | chr2 | 9389847 | ||||||
| chr2:9389915
|
G | A | 31 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(28): Show | 31 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.2384-1147G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 22/27 | chr2 | 9389915 | ||||||
| chr2:9390032
|
G | A | 22 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(19): Show | 22 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.2384-1030G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 22/27 | chr2 | 9390032 | ||||||
| chr2:9390139
|
C | T | 2 | a0001c0002t0003g0141a0001c0003t0016g0174 | 2 | HG01346.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.2384-923C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 22/27 | chr2 | 9390139 | ||||||
| chr2:9390301
|
C | T | 8 | a0001c0003t0004g0011a0001c0003t0004g0020a0001c0003t0004g0038others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.2384-761C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 22/27 | chr2 | 9390301 | ||||||
| chr2:9390390
|
C | T | 1 | a0001c0002t0002g0055 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2384-672C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 22/27 | chr2 | 9390390 | ||||||
| chr2:9390392
|
G | A | 63 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(60): Show | 63 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2384-670G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 22/27 | chr2 | 9390392 | ||||||
| chr2:9390407
|
C | T | 1 | a0001c0003t0006g0006 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2384-655C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 22/27 | chr2 | 9390407 | ||||||
| chr2:9390441
|
C | T | 1 | a0001c0003t0006g0135 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2384-621C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 22/27 | chr2 | 9390441 | ||||||
| chr2:9390574
|
A | G | 18 | a0001c0004t0005g0010a0001c0004t0005g0021a0001c0004t0005g0028others(15): Show | 18 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.2384-488A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 22/27 | chr2 | 9390574 | ||||||
| chr2:9390671
|
A | G | 95 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(92): Show | 95 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.2384-391A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 22/27 | chr2 | 9390671 | ||||||
| chr2:9390827
|
T | C | 2 | a0001c0002t0001g0024a0001c0002t0001g0133 | 2 | HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2384-235T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 22/27 | chr2 | 9390827 | ||||||
| chr2:9391518
|
A | G | 1 | a0001c0003t0007g0170 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2518+322A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 23/27 | chr2 | 9391518 | ||||||
| chr2:9391529
|
A | G | 27 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(24): Show | 27 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.2518+333A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 23/27 | chr2 | 9391529 | ||||||
| chr2:9391576
|
CT | C | 45 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(42): Show | 45 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.2518+397delT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr2 | 9391576 | |||||
| chr2:9391655
|
A | G | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2518+459A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 23/27 | chr2 | 9391655 | ||||||
| chr2:9391740
|
A | AT | 19 | a0001c0002t0006g0183a0001c0004t0005g0010a0001c0004t0005g0021others(16): Show | 19 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.2518+560dupT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr2 | 9391740 | |||||
| chr2:9391740
|
A | ATT | 35 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0003t0001g0017others(32): Show | 35 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.2518+559_2518+560d others(4): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr2 | 9391740 | |||||
| chr2:9391740
|
AT | A | 10 | a0001c0002t0001g0115a0001c0002t0001g0116a0001c0002t0001g0126others(7): Show | 10 | HG01106.hp2 HG01256.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.2518+560delT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr2 | 9391740 | |||||
| chr2:9392423
|
A | T | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2519-1059A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 23/27 | chr2 | 9392423 | ||||||
| chr2:9392668
|
T | A | 14 | a0001c0003t0001g0165a0001c0006t0004g0014a0001c0006t0004g0018others(11): Show | 14 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.2519-814T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 23/27 | chr2 | 9392668 | ||||||
| chr2:9392722
|
G | A | 2 | a0002c0001t0010g0066a0002c0001t0010g0125 | 2 | HG02523.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.2519-760G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 23/27 | chr2 | 9392722 | ||||||
| chr2:9392728
|
C | G | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2519-754C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 23/27 | chr2 | 9392728 | ||||||
| chr2:9392767
|
C | T | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2519-715C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 23/27 | chr2 | 9392767 | ||||||
| chr2:9392909
|
T | A | 1 | a0001c0003t0001g0017 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2519-573T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 23/27 | chr2 | 9392909 | ||||||
| chr2:9392966
|
A | G | 1 | a0002c0001t0001g0036 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2519-516A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 23/27 | chr2 | 9392966 | ||||||
| chr2:9393156
|
C | T | 1 | a0002c0001t0001g0070 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2519-326C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 23/27 | chr2 | 9393156 | ||||||
| chr2:9393229
|
TACTC | T | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2519-246_2519-243d others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr2 | 9393229 | |||||
| chr2:9393777
|
C | T | 18 | a0001c0004t0005g0010a0001c0004t0005g0021a0001c0004t0005g0028others(15): Show | 18 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.2684+130C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9393777 | ||||||
| chr2:9393839
|
G | A | 1 | a0001c0002t0023g0008 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2684+192G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9393839 | ||||||
| chr2:9393900
|
G | T | 2 | a0001c0002t0002g0198a0001c0002t0013g0001 | 2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2684+253G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9393900 | ||||||
| chr2:9393922
|
C | T | 1 | a0001c0003t0001g0029 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2684+275C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9393922 | ||||||
| chr2:9394132
|
C | A | 1 | a0001c0003t0004g0200 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2684+485C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9394132 | ||||||
| chr2:9394159
|
C | CT | 35 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(32): Show | 35 | HG00323.hp2 HG00408.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.2684+535dupT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9394159 | |||||
| chr2:9394159
|
CT | C | 78 | a0001c0002t0001g0115a0001c0002t0001g0116a0001c0002t0001g0126others(75): Show | 78 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.2684+535delT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9394159 | |||||
| chr2:9394238
|
C | T | 1 | a0002c0001t0020g0079 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2684+591C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9394238 | ||||||
| chr2:9394269
|
A | G | 22 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(19): Show | 22 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.2684+622A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9394269 | ||||||
| chr2:9394300
|
G | A | 1 | a0002c0001t0001g0157 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2684+653G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9394300 | ||||||
| chr2:9394399
|
C | G | 2 | a0001c0002t0002g0075a0001c0002t0002g0129 | 2 | HG00280.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2684+752C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9394399 | ||||||
| chr2:9394416
|
G | A | 1 | a0001c0010t0018g0173 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2684+769G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9394416 | ||||||
| chr2:9394444
|
G | C | 1 | a0002c0008t0001g0108 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2684+797G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9394444 | ||||||
| chr2:9394726
|
C | T | 1 | a0001c0002t0001g0115 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2684+1079C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9394726 | ||||||
| chr2:9394838
|
C | T | 1 | a0002c0001t0001g0022 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2684+1191C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9394838 | ||||||
| chr2:9394944
|
C | T | 31 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(28): Show | 31 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.2684+1297C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9394944 | ||||||
| chr2:9395085
|
C | T | 1 | a0001c0006t0004g0014 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2684+1438C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9395085 | ||||||
| chr2:9395111
|
G | A | 2 | a0002c0001t0001g0093a0002c0001t0001g0112 | 2 | HG01981.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.2684+1464G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9395111 | ||||||
| chr2:9395136
|
G | A | 1 | a0001c0013t0017g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2684+1489G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9395136 | ||||||
| chr2:9395301
|
C | T | 2 | a0001c0002t0001g0024a0001c0002t0001g0133 | 2 | HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2684+1654C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9395301 | ||||||
| chr2:9395345
|
T | C | 65 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(62): Show | 65 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.2684+1698T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9395345 | ||||||
| chr2:9395439
|
T | C | 104 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(101): Show | 104 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.2684+1792T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9395439 | ||||||
| chr2:9395440
|
A | C | 1 | a0001c0002t0002g0075 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2684+1793A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9395440 | ||||||
| chr2:9395489
|
T | A | 18 | a0001c0004t0005g0010a0001c0004t0005g0021a0001c0004t0005g0028others(15): Show | 18 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.2684+1842T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9395489 | ||||||
| chr2:9395503
|
A | G | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2684+1856A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9395503 | ||||||
| chr2:9395594
|
C | CT | 28 | a0001c0002t0001g0126a0001c0002t0002g0069a0001c0003t0007g0199others(25): Show | 28 | HG00438.hp2 HG00673.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.2684+1978dupT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9395594 | |||||
| chr2:9395594
|
C | CTT | 8 | a0002c0001t0001g0042a0002c0001t0001g0077a0002c0001t0001g0078others(5): Show | 8 | HG00597.hp1 HG00735.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.2684+1977_2684+197 others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9395594 | |||||
| chr2:9395594
|
C | CTTTTTCT others(6): Show |
1 | a0001c0013t0017g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2684+1952_2684+195 others(17): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9395594 | |||||
| chr2:9395594
|
CT | C | 24 | a0001c0002t0002g0007a0001c0002t0002g0027a0001c0002t0002g0055others(21): Show | 24 | HG00280.hp1 HG01070.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.2684+1978delT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9395594 | |||||
| chr2:9395594
|
CTTTTT | C | 21 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(18): Show | 21 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.2684+1974_2684+197 others(9): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9395594 | |||||
| chr2:9395594
|
CTTTTTT | C | 23 | a0001c0002t0003g0149a0001c0003t0004g0011a0001c0003t0004g0038others(20): Show | 23 | HG00639.hp1 HG01109.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.2684+1973_2684+197 others(10): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9395594 | |||||
| chr2:9395594
|
CTTTTTTT others(2): Show |
C | 10 | a0001c0003t0001g0165a0001c0006t0004g0014a0001c0006t0004g0018others(7): Show | 10 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.2684+1970_2684+197 others(13): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9395594 | |||||
| chr2:9395594
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0006t0004g0204a0001c0007t0004g0203 | 2 | HG01070.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2684+1969_2684+197 others(14): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9395594 | |||||
| chr2:9395594
|
CTTTTTTT others(9): Show |
C | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2684+1963_2684+197 others(20): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9395594 | |||||
| chr2:9395594
|
CTTTTTTT others(10): Show |
C | 28 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(25): Show | 28 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.2684+1962_2684+197 others(21): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9395594 | |||||
| chr2:9395599
|
T | C | 1 | a0002c0001t0020g0079 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2684+1952T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9395599 | ||||||
| chr2:9395604
|
T | C | 1 | a0001c0002t0003g0094 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2684+1957T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9395604 | ||||||
| chr2:9395605
|
T | C | 20 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(17): Show | 20 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.2684+1958T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9395605 | ||||||
| chr2:9395606
|
T | C | 1 | a0001c0002t0003g0149 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2684+1959T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9395606 | ||||||
| chr2:9395662
|
C | T | 22 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(19): Show | 22 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.2684+2015C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9395662 | ||||||
| chr2:9395701
|
A | G | 93 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(90): Show | 93 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.2684+2054A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9395701 | ||||||
| chr2:9395783
|
A | T | 27 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(24): Show | 27 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.2684+2136A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9395783 | ||||||
| chr2:9395811
|
G | C | 31 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(28): Show | 31 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.2684+2164G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9395811 | ||||||
| chr2:9395842
|
C | T | 1 | a0001c0003t0006g0065 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2684+2195C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9395842 | ||||||
| chr2:9396021
|
G | C | 14 | a0001c0003t0001g0165a0001c0006t0004g0014a0001c0006t0004g0018others(11): Show | 14 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.2684+2374G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9396021 | ||||||
| chr2:9396292
|
G | T | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2684+2645G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9396292 | ||||||
| chr2:9396372
|
C | T | 93 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(90): Show | 93 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.2684+2725C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9396372 | ||||||
| chr2:9396450
|
ATATTTTG others(25): Show |
A | 1 | a0001c0004t0005g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2684+2804_2684+283 others(36): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9396450 | ||||||
| chr2:9396538
|
G | C | 1 | a0001c0010t0018g0173 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2684+2891G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9396538 | ||||||
| chr2:9396566
|
T | C | 93 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(90): Show | 93 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.2684+2919T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9396566 | ||||||
| chr2:9396747
|
A | G | 12 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(9): Show | 12 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.2684+3100A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9396747 | ||||||
| chr2:9396826
|
A | C | 1 | a0002c0001t0001g0078 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2684+3179A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9396826 | ||||||
| chr2:9396831
|
A | G | 49 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(46): Show | 49 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.2684+3184A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9396831 | ||||||
| chr2:9396840
|
A | T | 1 | a0001c0010t0018g0173 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2685-3183A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9396840 | ||||||
| chr2:9396859
|
G | A | 1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2685-3164G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9396859 | ||||||
| chr2:9396963
|
C | T | 57 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(54): Show | 57 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.2685-3060C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9396963 | ||||||
| chr2:9397135
|
C | G | 1 | a0001c0002t0019g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2685-2888C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9397135 | ||||||
| chr2:9397448
|
G | A | 1 | a0002c0001t0001g0078 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2685-2575G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9397448 | ||||||
| chr2:9397651
|
T | C | 1 | a0002c0001t0001g0087 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2685-2372T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9397651 | ||||||
| chr2:9397689
|
T | C | 2 | a0001c0003t0001g0017a0001c0003t0001g0046 | 2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2685-2334T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9397689 | ||||||
| chr2:9397727
|
G | GAGATATA others(5): Show |
1 | a0001c0004t0005g0028 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2685-2295_2685-229 others(16): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397727 | |||||
| chr2:9397727
|
G | GAGATATA others(25): Show |
1 | a0001c0004t0005g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2685-2295_2685-229 others(36): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397727 | |||||
| chr2:9397727
|
G | GAGATATA others(29): Show |
1 | a0001c0004t0005g0138 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2685-2295_2685-229 others(40): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397727 | |||||
| chr2:9397727
|
G | GAT | 8 | a0001c0002t0023g0008a0002c0001t0001g0082a0002c0001t0001g0085others(5): Show | 8 | HG00438.hp2 HG01099.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2685-2273_2685-227 others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397727 | |||||
| chr2:9397727
|
GAT | G | 15 | a0001c0002t0003g0026a0001c0002t0003g0052a0001c0002t0003g0059others(12): Show | 15 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.2685-2273_2685-227 others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397727 | |||||
| chr2:9397729
|
T | G | 14 | a0001c0004t0005g0035a0001c0004t0005g0041a0001c0004t0005g0176others(11): Show | 14 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.2685-2294T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9397729 | ||||||
| chr2:9397731
|
T | G | 3 | a0001c0004t0005g0021a0001c0004t0005g0034a0001c0004t0005g0144 | 3 | HG03130.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2685-2292T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9397731 | ||||||
| chr2:9397742
|
ATATATAT others(3): Show |
A | 9 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(6): Show | 9 | HG01070.hp1 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.2685-2279_2685-227 others(14): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397742 | |||||
| chr2:9397742
|
ATATATAT others(4): Show |
A | 3 | a0001c0003t0001g0046a0001c0007t0004g0015a0001c0007t0004g0154 | 3 | HG02486.hp2 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2685-2279_2685-226 others(15): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397742 | |||||
| chr2:9397744
|
ATATATAT others(3): Show |
A | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2685-2277_2685-226 others(14): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397744 | |||||
| chr2:9397744
|
ATATATAT others(4): Show |
A | 1 | a0001c0003t0001g0017 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2685-2277_2685-226 others(15): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397744 | |||||
| chr2:9397745
|
TA | T | 2 | a0001c0012t0003g0033a0002c0001t0003g0136 | 2 | HG04199.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2685-2277delA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9397745 | ||||||
| chr2:9397745
|
TATA | T | 3 | a0001c0002t0003g0050a0001c0002t0003g0062a0001c0002t0003g0150 | 3 | HG01515.hp2 HG02258.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2685-2277_2685-227 others(7): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9397745 | ||||||
| chr2:9397746
|
A | AT | 2 | a0001c0002t0003g0094a0002c0001t0001g0042 | 2 | HG00735.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2685-2276dupT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397746 | |||||
| chr2:9397746
|
A | T | 5 | a0001c0002t0003g0141a0001c0002t0003g0148a0001c0002t0003g0166others(2): Show | 5 | HG01346.hp2 HG02165.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2685-2277A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9397746 | ||||||
| chr2:9397746
|
ATATATTT others(3): Show |
A | 18 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(15): Show | 18 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(15): Show |
intron_variant | MODIFIER | c.2685-2275_2685-226 others(14): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397746 | |||||
| chr2:9397746
|
ATATATTT others(4): Show |
A | 2 | a0001c0003t0006g0006a0001c0003t0021g0040 | 2 | HG02735.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2685-2275_2685-226 others(15): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397746 | |||||
| chr2:9397748
|
A | AT | 12 | a0001c0002t0002g0016a0001c0002t0002g0027a0001c0002t0002g0069others(9): Show | 12 | HG00280.hp1 HG01099.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.2685-2274dupT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397748 | |||||
| chr2:9397748
|
A | ATT | 6 | a0001c0002t0002g0134a0001c0002t0002g0139a0001c0002t0002g0198others(3): Show | 6 | HG01515.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2685-2274_2685-227 others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397748 | |||||
| chr2:9397748
|
A | T | 23 | a0001c0002t0002g0007a0001c0002t0003g0026a0001c0002t0003g0059others(20): Show | 23 | HG00642.hp2 HG00735.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.2685-2275A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9397748 | ||||||
| chr2:9397750
|
A | AT | 10 | a0001c0002t0002g0056a0001c0007t0001g0030a0002c0001t0001g0053others(7): Show | 10 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(7): Show |
intron_variant | MODIFIER | c.2685-2247dupT | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397750 | |||||
| chr2:9397750
|
A | ATATATAT others(22): Show |
1 | a0001c0004t0005g0041 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2685-2272_2685-227 others(33): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397750 | |||||
| chr2:9397750
|
A | ATATATAT others(34): Show |
1 | a0001c0004t0005g0195 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2685-2272_2685-227 others(45): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397750 | |||||
| chr2:9397750
|
A | ATATATAT others(32): Show |
1 | a0001c0004t0005g0035 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2685-2272_2685-227 others(43): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397750 | |||||
| chr2:9397750
|
A | ATATATAT others(27): Show |
1 | a0001c0004t0005g0194 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2685-2272_2685-227 others(38): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397750 | |||||
| chr2:9397750
|
A | ATATATAT others(28): Show |
1 | a0001c0003t0004g0038 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2685-2272_2685-227 others(39): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397750 | |||||
| chr2:9397750
|
A | ATATATAT others(30): Show |
1 | a0001c0003t0016g0174 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2685-2272_2685-227 others(41): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397750 | |||||
| chr2:9397750
|
A | ATATATAT others(22): Show |
1 | a0001c0013t0017g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2685-2272_2685-227 others(33): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397750 | |||||
| chr2:9397750
|
A | ATATATAT others(26): Show |
1 | a0001c0003t0004g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2685-2272_2685-227 others(37): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397750 | |||||
| chr2:9397750
|
A | ATATATAT others(23): Show |
1 | a0001c0009t0004g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2685-2272_2685-227 others(34): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397750 | |||||
| chr2:9397750
|
A | ATATATAT others(24): Show |
1 | a0001c0003t0004g0011 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2685-2272_2685-227 others(35): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397750 | |||||
| chr2:9397750
|
A | ATATATAT others(26): Show |
1 | a0001c0003t0004g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2685-2272_2685-227 others(37): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397750 | |||||
| chr2:9397750
|
A | ATATATAT others(11): Show |
1 | a0001c0004t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2685-2272_2685-227 others(22): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397750 | |||||
| chr2:9397750
|
A | ATATATAT others(17): Show |
1 | a0001c0003t0004g0044 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2685-2272_2685-227 others(28): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397750 | |||||
| chr2:9397750
|
A | ATATATAT others(10): Show |
1 | a0001c0004t0005g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2685-2272_2685-227 others(21): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397750 | |||||
| chr2:9397750
|
A | ATATATAT others(5): Show |
1 | a0001c0004t0005g0176 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2685-2272_2685-227 others(16): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397750 | |||||
| chr2:9397750
|
A | ATATATAT others(4): Show |
4 | a0001c0004t0005g0192a0001c0004t0005g0193a0001c0004t0005g0196others(1): Show | 4 | HG01109.hp2 HG01884.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2685-2272_2685-227 others(15): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397750 | |||||
| chr2:9397750
|
A | ATATATTT others(9): Show |
1 | a0001c0003t0004g0043 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2685-2272_2685-227 others(20): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397750 | |||||
| chr2:9397750
|
A | T | 60 | a0001c0002t0002g0007a0001c0002t0002g0016a0001c0002t0002g0027others(57): Show | 60 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.2685-2273A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9397750 | ||||||
| chr2:9397750
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0010t0018g0173 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2685-2256_2685-224 others(14): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9397750 | |||||
| chr2:9397751
|
T | TA | 5 | a0001c0002t0002g0137a0002c0001t0001g0074a0002c0001t0001g0161others(2): Show | 5 | HG00323.hp1 HG02698.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.2685-2272_2685-227 others(5): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9397751 | ||||||
| chr2:9397752
|
T | A | 10 | a0001c0002t0001g0126a0001c0002t0019g0164a0001c0004t0005g0010others(7): Show | 10 | HG00741.hp1 HG01099.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.2685-2271T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9397752 | ||||||
| chr2:9397753
|
T | A | 3 | a0001c0003t0001g0210a0001c0003t0004g0200a0002c0001t0001g0207 | 3 | HG00323.hp1 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2685-2270T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9397753 | ||||||
| chr2:9397754
|
T | A | 1 | a0001c0004t0005g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2685-2269T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9397754 | ||||||
| chr2:9397781
|
C | T | 2 | a0001c0004t0005g0194a0001c0004t0005g0195 | 2 | HG00738.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2685-2242C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9397781 | ||||||
| chr2:9397790
|
G | A | 3 | a0001c0002t0003g0094a0001c0002t0003g0142a0002c0001t0003g0136 | 3 | HG03491.hp2 HG03831.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2685-2233G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9397790 | ||||||
| chr2:9397844
|
C | T | 60 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(57): Show | 60 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.2685-2179C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9397844 | ||||||
| chr2:9397852
|
G | A | 49 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(46): Show | 49 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.2685-2171G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9397852 | ||||||
| chr2:9397854
|
G | A | 31 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(28): Show | 31 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.2685-2169G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9397854 | ||||||
| chr2:9397908
|
G | A | 91 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(88): Show | 91 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.2685-2115G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9397908 | ||||||
| chr2:9398025
|
T | C | 18 | a0001c0004t0005g0010a0001c0004t0005g0021a0001c0004t0005g0028others(15): Show | 18 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.2685-1998T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9398025 | ||||||
| chr2:9398044
|
C | T | 11 | a0001c0004t0005g0010a0001c0004t0005g0028a0001c0004t0005g0035others(8): Show | 11 | HG00738.hp1 HG01109.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.2685-1979C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9398044 | ||||||
| chr2:9398355
|
T | G | 1 | a0002c0001t0001g0022 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2685-1668T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9398355 | ||||||
| chr2:9398408
|
G | A | 1 | a0001c0002t0019g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2685-1615G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9398408 | ||||||
| chr2:9398452
|
C | T | 3 | a0001c0003t0004g0200a0001c0003t0007g0170a0001c0003t0007g0199 | 3 | HG03516.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2685-1571C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9398452 | ||||||
| chr2:9398461
|
G | T | 12 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(9): Show | 12 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.2685-1562G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9398461 | ||||||
| chr2:9398637
|
G | A | 4 | a0001c0002t0003g0166a0001c0002t0003g0188a0001c0002t0003g0209others(1): Show | 4 | HG02818.hp2 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2685-1386G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9398637 | ||||||
| chr2:9398676
|
G | T | 1 | a0002c0001t0001g0023 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2685-1347G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9398676 | ||||||
| chr2:9398808
|
C | CA | 52 | a0001c0002t0001g0116a0001c0002t0002g0069a0001c0002t0002g0107others(49): Show | 52 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.2685-1197dupA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9398808 | |||||
| chr2:9398808
|
C | CAA | 6 | a0001c0003t0004g0011a0001c0003t0004g0175a0001c0004t0005g0041others(3): Show | 6 | HG00639.hp1 HG02257.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.2685-1198_2685-119 others(6): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9398808 | |||||
| chr2:9398808
|
CA | C | 5 | a0001c0002t0003g0141a0001c0002t0003g0148a0001c0003t0006g0006others(2): Show | 5 | HG00408.hp1 HG01346.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.2685-1197delA | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 9398808 | |||||
| chr2:9399167
|
C | T | 44 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(41): Show | 44 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.2685-856C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9399167 | ||||||
| chr2:9399199
|
C | T | 3 | a0001c0004t0005g0021a0001c0004t0005g0034a0001c0004t0005g0144 | 3 | HG03130.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2685-824C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9399199 | ||||||
| chr2:9399361
|
C | T | 14 | a0001c0003t0001g0165a0001c0006t0004g0014a0001c0006t0004g0018others(11): Show | 14 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.2685-662C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9399361 | ||||||
| chr2:9399534
|
T | C | 170 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(167): Show | 170 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.2685-489T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9399534 | ||||||
| chr2:9399555
|
C | T | 1 | a0001c0004t0005g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2685-468C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9399555 | ||||||
| chr2:9399631
|
G | A | 26 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(23): Show | 26 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.2685-392G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 24/27 | chr2 | 9399631 | ||||||
| chr2:9400154
|
G | GTTATTTA others(3): Show |
1 | a0001c0003t0016g0174 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2734+82_2734+83ins others(10): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400154 | ||||||
| chr2:9400160
|
A | G | 1 | a0001c0003t0016g0174 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2734+88A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400160 | ||||||
| chr2:9400163
|
G | GCCTCCTG others(3): Show |
1 | a0001c0003t0016g0174 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2734+91_2734+92ins others(10): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400163 | ||||||
| chr2:9400167
|
G | A | 1 | a0001c0003t0016g0174 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2734+95G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400167 | ||||||
| chr2:9400169
|
C | T | 1 | a0001c0003t0016g0174 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2734+97C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400169 | ||||||
| chr2:9400190
|
G | GCCCTCCT others(23): Show |
1 | a0002c0001t0001g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2734+148_2734+177d others(32): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400190 | |||||
| chr2:9400190
|
G | GCCCTCCT others(352): Show |
1 | a0002c0001t0001g0140 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2734+177_2734+178i others(361): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400190 | |||||
| chr2:9400197
|
T | G | 10 | a0001c0003t0001g0017a0001c0003t0001g0046a0001c0003t0001g0169others(7): Show | 10 | HG01175.hp2 HG01496.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.2734+125T>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400197 | ||||||
| chr2:9400203
|
C | CCTCGCCC others(655): Show |
1 | a0001c0004t0005g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2734+131_2734+132i others(664): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400203 | ||||||
| chr2:9400205
|
C | G | 1 | a0001c0004t0005g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2734+133C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400205 | ||||||
| chr2:9400231
|
C | CCCCTCCC others(1067): Show |
1 | a0001c0002t0002g0129 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2734+161_2734+162i others(1076): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400231 | |||||
| chr2:9400231
|
C | CCCTCCCC others(919): Show |
1 | a0001c0003t0004g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2734+174_2734+175i others(928): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400231 | |||||
| chr2:9400231
|
C | CCCTCCCC others(918): Show |
6 | a0001c0003t0004g0011a0001c0003t0004g0020a0001c0003t0004g0038others(3): Show | 6 | HG02257.hp2 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2734+174_2734+175i others(927): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400231 | |||||
| chr2:9400231
|
C | CCCTCCCC others(995): Show |
5 | a0001c0002t0003g0141a0001c0002t0003g0147a0001c0002t0003g0149others(2): Show | 5 | HG00323.hp2 HG00738.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.2734+174_2734+175i others(1004): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400231 | |||||
| chr2:9400231
|
C | CCCTCCCC others(1043): Show |
1 | a0001c0002t0003g0026 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2734+174_2734+175i others(1052): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400231 | |||||
| chr2:9400231
|
C | CCCTCCCC others(1043): Show |
1 | a0001c0002t0003g0150 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2734+174_2734+175i others(1052): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400231 | |||||
| chr2:9400231
|
C | CCCTCCCC others(1033): Show |
1 | a0001c0002t0003g0052 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2734+174_2734+175i others(1042): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400231 | |||||
| chr2:9400231
|
C | CCCTCCCC others(1042): Show |
1 | a0001c0002t0003g0059 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2734+174_2734+175i others(1051): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400231 | |||||
| chr2:9400231
|
C | CCCTCCCC others(1041): Show |
2 | a0001c0002t0003g0050a0002c0001t0003g0099 | 2 | HG01515.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.2734+174_2734+175i others(1050): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400231 | |||||
| chr2:9400231
|
C | CCCTCCCC others(816): Show |
1 | a0003c0014t0003g0051 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2734+174_2734+175i others(825): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400231 | |||||
| chr2:9400231
|
C | CTCCTCCC others(723): Show |
1 | a0001c0003t0016g0174 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2734+159_2734+160i others(732): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400231 | ||||||
| chr2:9400233
|
C | CCCTCCCC others(4): Show |
1 | a0001c0004t0005g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2734+161_2734+162i others(13): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400233 | ||||||
| chr2:9400233
|
C | CTCCCCTC others(24): Show |
2 | a0001c0003t0001g0017a0001c0003t0001g0046 | 2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2734+177_2734+178i others(33): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400233 | |||||
| chr2:9400234
|
T | C | 1 | a0001c0004t0005g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2734+162T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400234 | ||||||
| chr2:9400249
|
T | C | 23 | a0001c0002t0001g0182a0001c0002t0002g0129a0001c0002t0003g0026others(20): Show | 23 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.2734+177T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(1126): Show |
1 | a0001c0003t0001g0153 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2734+177_2734+178i others(1135): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(1213): Show |
2 | a0001c0002t0001g0024a0001c0002t0001g0133 | 2 | HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2734+177_2734+178i others(1222): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(984): Show |
1 | a0001c0002t0002g0096 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2734+177_2734+178i others(993): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(882): Show |
1 | a0001c0002t0002g0075 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2734+177_2734+178i others(891): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(1476): Show |
1 | a0001c0003t0011g0068 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2734+177_2734+178i others(1485): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(1107): Show |
1 | a0002c0008t0006g0103 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2734+177_2734+178i others(1116): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(1392): Show |
1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2734+177_2734+178i others(1401): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(1133): Show |
1 | a0001c0003t0001g0029 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2734+177_2734+178i others(1142): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(1114): Show |
1 | a0001c0003t0006g0104 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2734+177_2734+178i others(1123): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(1702): Show |
1 | a0001c0002t0006g0183 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2734+177_2734+178i others(1711): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(889): Show |
1 | a0001c0003t0001g0190 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2734+177_2734+178i others(898): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(1129): Show |
1 | a0001c0003t0006g0080 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2734+177_2734+178i others(1138): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(1831): Show |
1 | a0001c0003t0006g0135 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2734+177_2734+178i others(1840): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(897): Show |
1 | a0001c0003t0001g0039 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2734+177_2734+178i others(906): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(1092): Show |
1 | a0001c0003t0006g0158 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2734+177_2734+178i others(1101): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(1091): Show |
1 | a0001c0003t0006g0105 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2734+177_2734+178i others(1100): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(1115): Show |
1 | a0001c0003t0006g0006 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2734+177_2734+178i others(1124): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(1114): Show |
1 | a0001c0002t0001g0097 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2734+177_2734+178i others(1123): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(1123): Show |
2 | a0001c0003t0006g0064a0001c0003t0006g0102 | 2 | HG00408.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.2734+177_2734+178i others(1132): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(1177): Show |
1 | a0001c0003t0006g0065 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2734+177_2734+178i others(1186): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(429): Show |
1 | a0001c0010t0018g0173 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2734+177_2734+178i others(438): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(946): Show |
1 | a0001c0004t0005g0034 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2734+177_2734+178i others(955): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(649): Show |
1 | a0001c0004t0005g0028 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2734+177_2734+178i others(658): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(542): Show |
1 | a0001c0004t0005g0192 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2734+177_2734+178i others(551): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(510): Show |
1 | a0001c0004t0005g0205 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2734+177_2734+178i others(519): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(816): Show |
2 | a0001c0004t0005g0021a0001c0004t0005g0144 | 2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2734+177_2734+178i others(825): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(565): Show |
3 | a0001c0004t0005g0041a0001c0004t0005g0138a0001c0004t0005g0185 | 3 | HG00639.hp1 HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2734+177_2734+178i others(574): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(541): Show |
6 | a0001c0004t0005g0010a0001c0004t0005g0176a0001c0004t0005g0193others(3): Show | 6 | HG00738.hp1 HG01109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2734+177_2734+178i others(550): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(540): Show |
1 | a0001c0004t0005g0201 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2734+177_2734+178i others(549): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(1155): Show |
1 | a0001c0003t0021g0040 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2734+177_2734+178i others(1164): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(1034): Show |
1 | a0001c0002t0003g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2734+177_2734+178i others(1043): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(1071): Show |
4 | a0001c0002t0003g0062a0001c0002t0003g0124a0001c0002t0003g0166others(1): Show | 4 | HG02622.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2734+177_2734+178i others(1080): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(1057): Show |
1 | a0001c0002t0003g0094 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2734+177_2734+178i others(1066): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(1056): Show |
2 | a0001c0002t0003g0142a0002c0001t0003g0136 | 2 | HG03491.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2734+177_2734+178i others(1065): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TCCCCTCC others(1056): Show |
2 | a0001c0002t0003g0188a0001c0012t0003g0033 | 2 | HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2734+177_2734+178i others(1065): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400249 | ||||||
| chr2:9400249
|
T | TTCCCCCT others(893): Show |
1 | a0001c0002t0002g0139 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2734+182_2734+183i others(902): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(950): Show |
1 | a0002c0005t0001g0132 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2734+190_2734+191i others(959): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(935): Show |
1 | a0002c0005t0001g0180 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2734+190_2734+191i others(944): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(1060): Show |
1 | a0002c0005t0001g0002 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2734+190_2734+191i others(1069): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(1051): Show |
1 | a0002c0005t0001g0119 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2734+190_2734+191i others(1060): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(991): Show |
1 | a0002c0005t0001g0003 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2734+190_2734+191i others(1000): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(989): Show |
3 | a0002c0005t0001g0009a0002c0005t0001g0054a0002c0005t0001g0098 | 3 | HG00642.hp1 HG01074.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2734+190_2734+191i others(998): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(1114): Show |
1 | a0004c0015t0015g0123 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2734+190_2734+191i others(1123): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(1169): Show |
1 | a0002c0005t0001g0025 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2734+190_2734+191i others(1178): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(1279): Show |
2 | a0002c0005t0001g0101a0002c0005t0001g0130 | 2 | HG03239.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.2734+190_2734+191i others(1288): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(1208): Show |
1 | a0002c0005t0001g0131 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2734+190_2734+191i others(1217): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(1199): Show |
1 | a0001c0002t0022g0120 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2734+190_2734+191i others(1208): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(812): Show |
2 | a0001c0002t0002g0027a0001c0002t0002g0073 | 2 | HG01074.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.2734+190_2734+191i others(821): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(1190): Show |
1 | a0001c0002t0002g0187 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2734+190_2734+191i others(1199): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(1010): Show |
1 | a0001c0002t0002g0177 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2734+190_2734+191i others(1019): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(1587): Show |
1 | a0001c0002t0002g0137 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2734+190_2734+191i others(1596): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(1026): Show |
1 | a0001c0002t0002g0134 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2734+190_2734+191i others(1035): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(994): Show |
1 | a0001c0002t0002g0202 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2734+190_2734+191i others(1003): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(884): Show |
1 | a0001c0002t0002g0162 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2734+190_2734+191i others(893): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(883): Show |
3 | a0001c0002t0002g0007a0001c0002t0002g0107a0001c0002t0012g0143 | 3 | HG01168.hp2 HG01257.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2734+190_2734+191i others(892): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(883): Show |
1 | a0001c0002t0002g0016 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2734+190_2734+191i others(892): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(843): Show |
3 | a0001c0002t0002g0056a0001c0002t0002g0057a0001c0002t0002g0058 | 3 | HG01070.hp2 HG01071.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.2734+190_2734+191i others(852): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(867): Show |
1 | a0001c0002t0002g0055 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2734+190_2734+191i others(876): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(1095): Show |
1 | a0001c0002t0002g0069 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2734+190_2734+191i others(1104): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(2095): Show |
1 | a0001c0002t0023g0008 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2734+190_2734+191i others(2104): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(614): Show |
1 | a0001c0002t0008g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2734+190_2734+191i others(623): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(978): Show |
1 | a0001c0002t0013g0001 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2734+190_2734+191i others(987): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(962): Show |
1 | a0001c0002t0002g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2734+190_2734+191i others(971): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(2411): Show |
1 | a0001c0002t0019g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2734+190_2734+191i others(2420): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(2136): Show |
1 | a0001c0003t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2734+190_2734+191i others(2145): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(875): Show |
1 | a0001c0003t0001g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2734+190_2734+191i others(884): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(684): Show |
1 | a0001c0002t0002g0060 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2734+190_2734+191i others(693): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(1643): Show |
1 | a0001c0006t0004g0204 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2734+190_2734+191i others(1652): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(1439): Show |
2 | a0001c0006t0004g0189a0001c0007t0004g0037 | 2 | HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2734+190_2734+191i others(1448): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(1567): Show |
1 | a0001c0006t0004g0014 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2734+190_2734+191i others(1576): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(1119): Show |
1 | a0001c0007t0004g0203 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2734+190_2734+191i others(1128): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(1118): Show |
2 | a0001c0007t0004g0015a0001c0007t0004g0154 | 2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2734+190_2734+191i others(1127): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(1027): Show |
1 | a0001c0006t0004g0063 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2734+190_2734+191i others(1036): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(1028): Show |
1 | a0001c0007t0004g0019 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2734+190_2734+191i others(1037): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(1025): Show |
3 | a0001c0006t0004g0018a0001c0006t0004g0032a0001c0006t0004g0197 | 3 | HG01884.hp1 HG01891.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.2734+190_2734+191i others(1034): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(786): Show |
1 | a0001c0013t0017g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2734+192_2734+193i others(795): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(526): Show |
1 | a0001c0004t0005g0035 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2734+192_2734+193i others(535): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(688): Show |
2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2734+192_2734+193i others(697): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(3689): Show |
1 | a0001c0003t0001g0017 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2734+192_2734+193i others(3698): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(794): Show |
1 | a0001c0002t0008g0048 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2734+192_2734+193i others(803): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCCTC others(4930): Show |
1 | a0001c0003t0001g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2734+192_2734+193i others(4939): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCTCC others(1320): Show |
1 | a0001c0003t0007g0170 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2734+181_2734+182i others(1329): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCTCC others(1217): Show |
1 | a0001c0003t0004g0200 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2734+181_2734+182i others(1226): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCTCC others(1307): Show |
1 | a0001c0003t0007g0199 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2734+181_2734+182i others(1316): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400249
|
T | TTCCCTCC others(1372): Show |
4 | a0001c0003t0001g0169a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG01496.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2734+181_2734+182i others(1381): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 9400249 | |||||
| chr2:9400269
|
T | C | 126 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(123): Show | 126 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.2734+197T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400269 | ||||||
| chr2:9400317
|
T | C | 1 | a0001c0004t0005g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2734+245T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400317 | ||||||
| chr2:9400372
|
C | G | 1 | a0001c0004t0005g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2734+300C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400372 | ||||||
| chr2:9400373
|
G | C | 1 | a0001c0004t0005g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2734+301G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400373 | ||||||
| chr2:9400493
|
C | A | 1 | a0001c0004t0005g0205 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2735-249C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400493 | ||||||
| chr2:9400720
|
C | T | 57 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(54): Show | 57 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.2735-22C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 25/27 | chr2 | 9400720 | ||||||
| chr2:9400873
|
G | C | 1 | a0002c0001t0001g0036 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2823+43G>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 26/27 | chr2 | 9400873 | ||||||
| chr2:9401252
|
G | T | 49 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0133others(46): Show | 49 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.2824-22G>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 26/27 | chr2 | 9401252 | ||||||
| chr2:9401468
|
G | A | 1 | a0002c0001t0014g0091 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2946+72G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 27/27 | chr2 | 9401468 | ||||||
| chr2:9401568
|
C | G | 1 | a0001c0007t0001g0030 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2946+172C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 27/27 | chr2 | 9401568 | ||||||
| chr2:9401796
|
C | G | 30 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(27): Show | 30 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.2946+400C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 27/27 | chr2 | 9401796 | ||||||
| chr2:9401909
|
T | A | 2 | a0001c0002t0009g0031a0001c0002t0009g0208 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2946+513T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 27/27 | chr2 | 9401909 | ||||||
| chr2:9402003
|
G | A | 3 | a0002c0005t0001g0101a0002c0005t0001g0130a0002c0005t0001g0131 | 3 | HG03239.hp1 HG03654.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.2946+607G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 27/27 | chr2 | 9402003 | ||||||
| chr2:9402030
|
T | C | 196 | a0001c0002t0001g0024a0001c0002t0001g0097a0001c0002t0001g0115others(193): Show | 196 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.2946+634T>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 27/27 | chr2 | 9402030 | ||||||
| chr2:9402086
|
C | T | 30 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(27): Show | 30 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.2946+690C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 27/27 | chr2 | 9402086 | ||||||
| chr2:9402090
|
A | G | 48 | a0001c0002t0003g0026a0001c0002t0003g0050a0001c0002t0003g0052others(45): Show | 48 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.2946+694A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 27/27 | chr2 | 9402090 | ||||||
| chr2:9402157
|
G | A | 73 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0003g0026others(70): Show | 73 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.2946+761G>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 27/27 | chr2 | 9402157 | ||||||
| chr2:9402323
|
C | T | 2 | a0001c0002t0001g0024a0001c0002t0001g0133 | 2 | HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2946+927C>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 27/27 | chr2 | 9402323 | ||||||
| chr2:9402395
|
C | G | 1 | a0002c0001t0001g0077 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2947-858C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 27/27 | chr2 | 9402395 | ||||||
| chr2:9402610
|
T | A | 2 | a0001c0002t0001g0024a0001c0002t0001g0133 | 2 | HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2947-643T>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 27/27 | chr2 | 9402610 | ||||||
| chr2:9402676
|
C | A | 1 | a0002c0001t0001g0168 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2947-577C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 27/27 | chr2 | 9402676 | ||||||
| chr2:9403092
|
C | A | 92 | a0001c0002t0001g0024a0001c0002t0001g0133a0001c0002t0003g0026others(89): Show | 92 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.2947-161C>A | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 27/27 | chr2 | 9403092 | ||||||
| chr2:9403110
|
A | T | 12 | a0001c0006t0004g0014a0001c0006t0004g0018a0001c0006t0004g0032others(9): Show | 12 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.2947-143A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 27/27 | chr2 | 9403110 | ||||||
| chr2:9403192
|
C | G | 1 | a0001c0004t0005g0028 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2947-61C>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 27/27 | chr2 | 9403192 | ||||||
| chr2:9403224
|
A | G | 1 | a0002c0001t0001g0163 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2947-29A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 27/27 | chr2 | 9403224 | ||||||
| chr2:9403227
|
A | C | 1 | a0001c0002t0012g0143 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2947-26A>C | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 27/27 | chr2 | 9403227 | ||||||
| chr2:9403229
|
A | T | 1 | a0001c0002t0012g0143 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2947-24A>T | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 27/27 | chr2 | 9403229 | ||||||
| chr2:9403236
|
A | G | 19 | a0001c0002t0009g0031a0001c0002t0009g0208a0001c0003t0001g0165others(16): Show | 19 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.2947-17A>G | ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 27/27 | chr2 | 9403236 |