Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 51071 |
|---|---|
| ensemblid | ENSG00000023697.13 |
| hgncid | 24269 |
| symbol | DERA |
| name | deoxyribose-phosphate aldolase |
| refseq_nuc | NM_015954.4 |
| refseq_prot | NP_057038.2 |
| ensembl_nuc | ENST00000428559.7 |
| ensembl_prot | ENSP00000416583.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 15911332 |
| end | 16037381 |
| strand | + |
| ver | v1.2 |
| region | chr12:15911332-16037381 |
| region5000 | chr12:15906332-16042381 |
| regionname0 | DERA_chr12_15911332_16037381 |
| regionname5000 | DERA_chr12_15906332_16042381 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 318 | 255 | 80 | 52 | 92 | 4 | 25 | 66 | DERA_chr12_15906332_16042381 | DERA | copy fasta | chr12 | 15906332 | 16042381 |
| a0002 | 0/0 | 318 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | copy fasta | chr12 | 15906332 | 16042381 |
| a0003 | 0/0 | 318 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DERA_chr12_15906332_16042381 | DERA | copy fasta | chr12 | 15906332 | 16042381 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 957 | 253 | 78 | 52 | 92 | 4 | 25 | DERA_chr12_15906332_16042381 | DERA | copy fasta | chr12 | 15906332 | 16042381 |
| c0002 | 0/0 | 957 | 2 | 2 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | copy fasta | chr12 | 15906332 | 16042381 |
| c0003 | 0/0 | 957 | 2 | 2 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | copy fasta | chr12 | 15906332 | 16042381 |
| c0004 | 0/0 | 957 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | copy fasta | chr12 | 15906332 | 16042381 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 688 | 206 | 58 | 49 | 67 | 4 | 26 | DERA_chr12_15906332_16042381 | DERA | copy fasta | chr12 | 15906332 | 16042381 |
| t0002 | 0/0 | 688 | 27 | 1 | 1 | 25 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | copy fasta | chr12 | 15906332 | 16042381 |
| t0003 | 0/0 | 688 | 15 | 14 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | copy fasta | chr12 | 15906332 | 16042381 |
| t0004 | 0/0 | 688 | 5 | 5 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | copy fasta | chr12 | 15906332 | 16042381 |
| t0005 | 0/0 | 688 | 4 | 3 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | copy fasta | chr12 | 15906332 | 16042381 |
| t0006 | 0/0 | 688 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | copy fasta | chr12 | 15906332 | 16042381 |
| 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 | 2 | 0 | 2 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0086 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0192 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 957 | 253 | 78 | 52 | 92 | 4 | 25 | DERA_chr12_15906332_16042381 | DERA | copy fasta | chr12 | 15906332 | 16042381 |
| a0001c0003 | 0/0 | 957 | 2 | 2 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | copy fasta | chr12 | 15906332 | 16042381 |
| a0002c0002 | 0/0 | 957 | 2 | 2 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | copy fasta | chr12 | 15906332 | 16042381 |
| a0003c0004 | 0/0 | 957 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | copy fasta | chr12 | 15906332 | 16042381 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1644 | 204 | 57 | 49 | 67 | 4 | 25 | DERA_chr12_15906332_16042381 | DERA | copy fasta | chr12 | 15906332 | 16042381 |
| a0001c0001t0002 | 0/0 | 1644 | 27 | 1 | 1 | 25 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | copy fasta | chr12 | 15906332 | 16042381 |
| a0001c0001t0003 | 0/0 | 1644 | 13 | 12 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | copy fasta | chr12 | 15906332 | 16042381 |
| a0001c0001t0004 | 0/0 | 1644 | 4 | 4 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | copy fasta | chr12 | 15906332 | 16042381 |
| a0001c0001t0005 | 0/0 | 1644 | 4 | 3 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | copy fasta | chr12 | 15906332 | 16042381 |
| a0001c0001t0006 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | copy fasta | chr12 | 15906332 | 16042381 |
| a0001c0003t0001 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | copy fasta | chr12 | 15906332 | 16042381 |
| a0001c0003t0004 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | copy fasta | chr12 | 15906332 | 16042381 |
| a0002c0002t0003 | 0/0 | 1644 | 2 | 2 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | copy fasta | chr12 | 15906332 | 16042381 |
| a0003c0004t0001 | 0/0 | 1644 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | copy fasta | chr12 | 15906332 | 16042381 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0086 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0192 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0003g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0003g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0005g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0001t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0003t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0001c0003t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0002c0002t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0002c0002t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| a0003c0004t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | FIN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0133 | EUR | FIN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | CHS | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | CHS | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0044 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0226 | EUR | IBS | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0155 | EUR | IBS | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | KHV | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0043 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | KHV | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | KHV | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | KHV | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | CDX | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CDX | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | PEL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02630 | hp2 | a0002 | c0002 | t0003 | g0020 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0058 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0010 | AFR | ESN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0089 | AFR | ESN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03098 | hp1 | a0002 | c0002 | t0003 | g0018 | AFR | MSL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | ESN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0116 | AFR | ESN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | MSL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ESN | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0213 | AFR | GWD | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | MSL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | STU | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | STU | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03834 | hp2 | a0003 | c0004 | t0001 | g0225 | SAS | BEB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | STU | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | STU | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | STU | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | STU | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0073 | AFR | YRI | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | YRI | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | CHB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0041 | AFR | YRI | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | YRI | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | LWK | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | LWK | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | LWK | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | LWK | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0042 | AFR | YRI | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | YRI | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | GIH | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | GIH | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG06807 | hp1 | a0001 | c0003 | t0004 | g0072 | AFR | USA | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | USA | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | USA | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | USA | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | LWK | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | LWK | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0192 | REF | REF | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0086 | REF | REF | DERA_chr12_15906332_16042381 | DERA | chr12 | 15906332 | 16042381 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:15958297
|
G | A | 1 | a0002 | 2 | HG02630.hp2 HG03098.hp1 |
missense_variant | MODERATE | c.239G>A | p.Arg80Gln | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 3/9 | 291/1644 | 239/957 | 80/318 | chr12 | 15958297 | ||
| chr12:15982416
|
G | A | 1 | a0003 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.617G>A | p.Ser206Asn | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/9 | 669/1644 | 617/957 | 206/318 | chr12 | 15982416 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:15959842
|
C | T | 1 | a0001c0003 | 2 | HG06807.hp1 NA18522.hp1 |
synonymous_variant | LOW | c.291C>T | p.Ala97Ala | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/9 | 343/1644 | 291/957 | 97/318 | chr12 | 15959842 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:15911332
|
G | A | 1 | a0001c0001t0005 | 4 | HG01109.hp1 HG02055.hp2 NA18906.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-52G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/9 | 52 | chr12 | 15911332 | |||||
| chr12:15911377
|
C | T | 3 | a0001c0001t0003a0001c0001t0006a0002c0002t0003 | 16 | HG01934.hp1 HG02055.hp1 HG02109.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-7C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/9 | 7 | chr12 | 15911377 | |||||
| chr12:16036760
|
T | A | 1 | a0001c0001t0002 | 27 | HG00438.hp1 HG00621.hp1 HG02027.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*14T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 9/9 | 14 | chr12 | 16036760 | |||||
| chr12:16037283
|
T | A | 3 | a0001c0001t0004a0001c0001t0006a0001c0003t0004 | 6 | HG02897.hp2 HG02965.hp1 HG02976.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*537T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 9/9 | 537 | chr12 | 16037283 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:15912020
|
CT | C | 39 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(36): Show | 39 | HG00733.hp1 HG01070.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.31+622delT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15912020 | |||||
| chr12:15912112
|
T | A | 42 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(39): Show | 42 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.31+698T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15912112 | ||||||
| chr12:15912114
|
A | G | 5 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.31+700A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15912114 | ||||||
| chr12:15912251
|
T | G | 1 | a0001c0001t0001g0045 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.31+837T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15912251 | ||||||
| chr12:15912713
|
G | T | 5 | a0001c0001t0001g0034a0001c0001t0005g0041a0001c0001t0005g0042others(2): Show | 5 | HG00733.hp1 HG01109.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.31+1299G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15912713 | ||||||
| chr12:15912747
|
G | T | 9 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(6): Show | 9 | HG01109.hp2 HG01891.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.31+1333G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15912747 | ||||||
| chr12:15912827
|
C | T | 1 | a0001c0001t0002g0257 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.31+1413C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15912827 | ||||||
| chr12:15912982
|
T | C | 24 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(21): Show | 24 | HG00733.hp1 HG01109.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.31+1568T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15912982 | ||||||
| chr12:15913112
|
A | G | 42 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(39): Show | 42 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.31+1698A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15913112 | ||||||
| chr12:15913153
|
T | C | 1 | a0001c0001t0001g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.31+1739T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15913153 | ||||||
| chr12:15913492
|
G | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG01261.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.31+2078G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15913492 | ||||||
| chr12:15913677
|
A | AGG | 4 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(1): Show | 4 | HG01934.hp1 HG02559.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.31+2263_31+2264ins others(2): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15913677 | ||||||
| chr12:15913680
|
G | T | 4 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(1): Show | 4 | HG01934.hp1 HG02559.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.31+2266G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15913680 | ||||||
| chr12:15913939
|
T | A | 5 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.31+2525T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15913939 | ||||||
| chr12:15913979
|
A | T | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG00544.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.31+2565A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15913979 | ||||||
| chr12:15914123
|
A | G | 1 | a0001c0001t0002g0254 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.31+2709A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15914123 | ||||||
| chr12:15914137
|
T | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG01884.hp2 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.31+2723T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15914137 | ||||||
| chr12:15914335
|
T | C | 23 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0025others(20): Show | 23 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.31+2921T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15914335 | ||||||
| chr12:15914387
|
A | G | 1 | a0001c0001t0001g0253 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.31+2973A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15914387 | ||||||
| chr12:15914392
|
A | AT | 7 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(4): Show | 7 | HG01884.hp2 HG01934.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.31+2979dupT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15914392 | |||||
| chr12:15914393
|
T | TA | 9 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0051others(6): Show | 9 | HG00438.hp1 HG00558.hp2 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.31+2998dupA | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15914393 | |||||
| chr12:15914393
|
TA | T | 7 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(4): Show | 7 | HG00438.hp2 HG00544.hp2 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.31+2998delA | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15914393 | |||||
| chr12:15914394
|
A | T | 35 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0025others(32): Show | 35 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.31+2980A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15914394 | ||||||
| chr12:15914793
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG01884.hp2 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.31+3379C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15914793 | ||||||
| chr12:15914922
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.31+3508C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15914922 | ||||||
| chr12:15915024
|
A | G | 1 | a0001c0001t0001g0246 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.31+3610A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15915024 | ||||||
| chr12:15915480
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.31+4066A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15915480 | ||||||
| chr12:15915510
|
T | G | 44 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(41): Show | 44 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.31+4096T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15915510 | ||||||
| chr12:15915582
|
A | T | 2 | a0001c0001t0001g0057a0001c0001t0004g0058 | 2 | HG02897.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.31+4168A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15915582 | ||||||
| chr12:15915886
|
T | C | 6 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(3): Show | 6 | HG01109.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.31+4472T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15915886 | ||||||
| chr12:15916446
|
C | CT | 12 | a0001c0001t0001g0055a0001c0001t0001g0236a0001c0001t0001g0237others(9): Show | 12 | HG00621.hp2 HG01361.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.31+5054dupT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15916446 | |||||
| chr12:15916446
|
CT | C | 41 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0026others(38): Show | 41 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.31+5054delT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15916446 | |||||
| chr12:15916450
|
T | C | 2 | a0001c0001t0002g0022a0001c0001t0002g0023 | 2 | NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.31+5036T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15916450 | ||||||
| chr12:15916451
|
T | C | 32 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0026others(29): Show | 32 | HG01109.hp2 HG01243.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.31+5037T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15916451 | ||||||
| chr12:15916452
|
T | C | 1 | a0001c0001t0001g0024 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.31+5038T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15916452 | ||||||
| chr12:15916519
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG01884.hp2 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.31+5105C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15916519 | ||||||
| chr12:15916557
|
C | T | 28 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0045others(25): Show | 29 | HG00558.hp1 HG00621.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.31+5143C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15916557 | ||||||
| chr12:15916650
|
A | T | 36 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0025others(33): Show | 36 | HG01109.hp2 HG01243.hp1 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.31+5236A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15916650 | ||||||
| chr12:15917005
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31+5591G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15917005 | ||||||
| chr12:15917166
|
ATTTTGCC others(6): Show |
A | 1 | a0001c0001t0001g0035 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.31+5755_31+5767del others(13): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15917166 | |||||
| chr12:15917202
|
A | G | 5 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0216others(2): Show | 5 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.31+5788A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15917202 | ||||||
| chr12:15917445
|
C | G | 1 | a0001c0001t0001g0212 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.31+6031C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15917445 | ||||||
| chr12:15917497
|
C | G | 1 | a0001c0001t0001g0211 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.31+6083C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15917497 | ||||||
| chr12:15917688
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.31+6274C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15917688 | ||||||
| chr12:15917771
|
A | G | 9 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(6): Show | 9 | HG01109.hp2 HG01891.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.31+6357A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15917771 | ||||||
| chr12:15917787
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.31+6373A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15917787 | ||||||
| chr12:15917793
|
T | TA | 4 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(1): Show | 4 | HG01934.hp1 HG02559.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.31+6381dupA | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15917793 | |||||
| chr12:15917795
|
A | C | 1 | a0001c0001t0001g0209 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.31+6381A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15917795 | ||||||
| chr12:15917818
|
T | G | 1 | a0001c0001t0004g0213 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.31+6404T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15917818 | ||||||
| chr12:15917835
|
C | T | 4 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208others(1): Show | 4 | HG02258.hp2 HG02615.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.31+6421C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15917835 | ||||||
| chr12:15917857
|
C | T | 5 | a0001c0001t0001g0034a0001c0001t0005g0041a0001c0001t0005g0042others(2): Show | 5 | HG00733.hp1 HG01109.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.31+6443C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15917857 | ||||||
| chr12:15917997
|
T | C | 45 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0025others(42): Show | 45 | HG01109.hp2 HG01243.hp1 HG01891.hp2 others(42): Show |
intron_variant | MODIFIER | c.31+6583T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15917997 | ||||||
| chr12:15918049
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.31+6635G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918049 | ||||||
| chr12:15918176
|
C | G | 9 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(6): Show | 9 | HG02109.hp1 HG02257.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.31+6762C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918176 | ||||||
| chr12:15918186
|
T | G | 54 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(51): Show | 54 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.31+6772T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918186 | ||||||
| chr12:15918203
|
G | A | 3 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004 | 3 | HG02559.hp2 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.31+6789G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918203 | ||||||
| chr12:15918243
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.31+6829A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918243 | ||||||
| chr12:15918399
|
T | C | 1 | a0001c0001t0002g0049 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.31+6985T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918399 | ||||||
| chr12:15918435
|
T | C | 1 | a0001c0001t0001g0075 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.31+7021T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918435 | ||||||
| chr12:15918457
|
C | T | 6 | a0001c0001t0001g0034a0001c0001t0003g0005a0001c0001t0005g0041others(3): Show | 6 | HG00733.hp1 HG01109.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.31+7043C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918457 | ||||||
| chr12:15918459
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.31+7045G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918459 | ||||||
| chr12:15918520
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.31+7106C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918520 | ||||||
| chr12:15918582
|
A | T | 1 | a0001c0001t0001g0216 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.31+7168A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918582 | ||||||
| chr12:15918642
|
C | T | 44 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0026others(41): Show | 44 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(41): Show |
intron_variant | MODIFIER | c.31+7228C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918642 | ||||||
| chr12:15918748
|
G | A | 24 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(21): Show | 24 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.31+7334G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918748 | ||||||
| chr12:15918810
|
A | G | 54 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(51): Show | 54 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.31+7396A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918810 | ||||||
| chr12:15918930
|
G | A | 45 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0025others(42): Show | 45 | HG01109.hp2 HG01243.hp1 HG01891.hp2 others(42): Show |
intron_variant | MODIFIER | c.31+7516G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918930 | ||||||
| chr12:15918940
|
C | T | 9 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(6): Show | 9 | HG01109.hp2 HG01891.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.31+7526C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918940 | ||||||
| chr12:15918949
|
A | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG01884.hp2 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.31+7535A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918949 | ||||||
| chr12:15918990
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.31+7576A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15918990 | ||||||
| chr12:15919028
|
C | G | 4 | a0001c0001t0001g0200a0001c0001t0001g0202a0001c0001t0001g0246others(1): Show | 4 | NA18942.hp2 NA18950.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.31+7614C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15919028 | ||||||
| chr12:15919199
|
G | T | 1 | a0001c0001t0001g0235 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.31+7785G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15919199 | ||||||
| chr12:15919273
|
A | T | 2 | a0001c0001t0001g0057a0001c0001t0004g0058 | 2 | HG02897.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.31+7859A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15919273 | ||||||
| chr12:15919686
|
A | C | 33 | a0001c0001t0001g0053a0001c0001t0001g0061a0001c0001t0001g0074others(30): Show | 33 | HG00735.hp2 HG01070.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.31+8272A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15919686 | ||||||
| chr12:15919970
|
A | ATG | 186 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0026others(183): Show | 186 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.31+8578_31+8579dup others(2): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15919970 | |||||
| chr12:15919970
|
A | ATGTG | 15 | a0001c0001t0001g0024a0001c0001t0001g0034a0001c0001t0001g0065others(12): Show | 15 | HG00733.hp1 HG01934.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.31+8576_31+8579dup others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15919970 | |||||
| chr12:15919994
|
C | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG01884.hp2 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.31+8580C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15919994 | ||||||
| chr12:15919998
|
G | GTC | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG01884.hp2 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.31+8585_31+8586ins others(2): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15919998 | |||||
| chr12:15920007
|
A | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG01884.hp2 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.31+8593A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15920007 | ||||||
| chr12:15920009
|
A | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG01884.hp2 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.31+8595A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15920009 | ||||||
| chr12:15920014
|
A | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG01884.hp2 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.31+8600A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15920014 | ||||||
| chr12:15920018
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG01884.hp2 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.31+8604G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15920018 | ||||||
| chr12:15920110
|
TATAG | T | 149 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(146): Show | 149 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.31+8702_31+8705del others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15920110 | |||||
| chr12:15920527
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.31+9113A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15920527 | ||||||
| chr12:15920561
|
G | T | 1 | a0001c0001t0001g0234 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.31+9147G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15920561 | ||||||
| chr12:15920639
|
C | A | 3 | a0001c0001t0001g0024a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | NA18964.hp1 NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.31+9225C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15920639 | ||||||
| chr12:15920783
|
C | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0170 | 2 | HG01358.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.31+9369C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15920783 | ||||||
| chr12:15920834
|
C | T | 3 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004 | 3 | HG02559.hp2 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.31+9420C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15920834 | ||||||
| chr12:15921127
|
T | G | 1 | a0001c0001t0001g0205 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.31+9713T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15921127 | ||||||
| chr12:15921130
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG01884.hp2 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.31+9716G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15921130 | ||||||
| chr12:15921473
|
A | G | 48 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0025others(45): Show | 48 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.31+10059A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15921473 | ||||||
| chr12:15921595
|
A | G | 8 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(5): Show | 8 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.31+10181A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15921595 | ||||||
| chr12:15921813
|
C | G | 1 | a0001c0001t0001g0212 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.31+10399C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15921813 | ||||||
| chr12:15921819
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.31+10405G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15921819 | ||||||
| chr12:15921894
|
C | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG00733.hp1 HG01884.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.31+10480C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15921894 | ||||||
| chr12:15921926
|
GATA | G | 206 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(203): Show | 206 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.31+10529_31+10531d others(5): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15921926 | |||||
| chr12:15922195
|
C | T | 54 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(51): Show | 54 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.31+10781C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15922195 | ||||||
| chr12:15922217
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.31+10803C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15922217 | ||||||
| chr12:15922265
|
C | G | 2 | a0001c0001t0001g0034a0001c0001t0003g0005 | 2 | HG00733.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.31+10851C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15922265 | ||||||
| chr12:15922375
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.31+10961T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15922375 | ||||||
| chr12:15922557
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG01884.hp2 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.31+11143G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15922557 | ||||||
| chr12:15922720
|
GAT | G | 10 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(7): Show | 10 | HG01109.hp2 HG01891.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.31+11308_31+11309d others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15922720 | |||||
| chr12:15922731
|
G | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG00733.hp1 HG01884.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.31+11317G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15922731 | ||||||
| chr12:15922756
|
C | T | 54 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(51): Show | 54 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.31+11342C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15922756 | ||||||
| chr12:15922876
|
A | G | 206 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(203): Show | 206 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.31+11462A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15922876 | ||||||
| chr12:15923017
|
C | CT | 62 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0035others(59): Show | 62 | HG00438.hp2 HG00642.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.31+11626dupT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15923017 | |||||
| chr12:15923017
|
CTTTTTTT | C | 12 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(9): Show | 12 | HG02109.hp1 HG02257.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.31+11620_31+11626d others(9): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15923017 | |||||
| chr12:15923017
|
CTTTTTTT others(3): Show |
C | 10 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(7): Show | 10 | HG01109.hp2 HG01891.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.31+11617_31+11626d others(12): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15923017 | |||||
| chr12:15923085
|
C | G | 49 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0025others(46): Show | 49 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.31+11671C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15923085 | ||||||
| chr12:15923086
|
G | T | 1 | a0001c0001t0001g0211 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.31+11672G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15923086 | ||||||
| chr12:15923108
|
C | T | 49 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0025others(46): Show | 49 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.31+11694C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15923108 | ||||||
| chr12:15923148
|
A | G | 2 | a0001c0001t0001g0060a0001c0001t0001g0156 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.31+11734A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15923148 | ||||||
| chr12:15923297
|
C | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.31+11883C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15923297 | ||||||
| chr12:15923320
|
C | T | 24 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(21): Show | 24 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.31+11906C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15923320 | ||||||
| chr12:15923461
|
AC | A | 9 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(6): Show | 9 | HG02109.hp1 HG02257.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.31+12049delC | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15923461 | |||||
| chr12:15923464
|
T | A | 9 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(6): Show | 9 | HG02109.hp1 HG02257.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.31+12050T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15923464 | ||||||
| chr12:15923578
|
C | A | 1 | a0001c0001t0001g0157 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.31+12164C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15923578 | ||||||
| chr12:15923578
|
C | T | 49 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0025others(46): Show | 49 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.31+12164C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15923578 | ||||||
| chr12:15923701
|
C | CT | 109 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0046others(106): Show | 109 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(106): Show |
intron_variant | MODIFIER | c.31+12300dupT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15923701 | |||||
| chr12:15923701
|
C | CTT | 43 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0055others(40): Show | 43 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.31+12299_31+12300d others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15923701 | |||||
| chr12:15923701
|
CTT | C | 49 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0025others(46): Show | 49 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.31+12299_31+12300d others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15923701 | |||||
| chr12:15923908
|
C | A | 1 | a0001c0001t0001g0026 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.31+12494C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15923908 | ||||||
| chr12:15924176
|
C | T | 49 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0025others(46): Show | 49 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.31+12762C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15924176 | ||||||
| chr12:15924238
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0003g0005 | 2 | HG00733.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.31+12824G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15924238 | ||||||
| chr12:15924475
|
A | G | 9 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(6): Show | 9 | HG02109.hp1 HG02257.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.31+13061A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15924475 | ||||||
| chr12:15924529
|
T | C | 3 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004 | 3 | HG02559.hp2 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.31+13115T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15924529 | ||||||
| chr12:15924543
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.31+13129A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15924543 | ||||||
| chr12:15924644
|
A | G | 2 | a0001c0001t0001g0215a0001c0001t0001g0252 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.31+13230A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15924644 | ||||||
| chr12:15924741
|
T | G | 10 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(7): Show | 10 | HG01109.hp2 HG01891.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.31+13327T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15924741 | ||||||
| chr12:15924955
|
A | G | 12 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0012others(9): Show | 12 | HG02055.hp1 HG02109.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.31+13541A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15924955 | ||||||
| chr12:15925044
|
G | A | 49 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0025others(46): Show | 49 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.31+13630G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15925044 | ||||||
| chr12:15925160
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.31+13746G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15925160 | ||||||
| chr12:15925163
|
G | C | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG00733.hp1 HG01884.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.31+13749G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15925163 | ||||||
| chr12:15925274
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.31+13860C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15925274 | ||||||
| chr12:15925316
|
T | G | 49 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0025others(46): Show | 49 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.31+13902T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15925316 | ||||||
| chr12:15925374
|
T | G | 6 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(3): Show | 6 | HG00733.hp2 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.31+13960T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15925374 | ||||||
| chr12:15925409
|
C | T | 2 | a0001c0001t0001g0057a0001c0001t0004g0058 | 2 | HG02897.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.31+13995C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15925409 | ||||||
| chr12:15925429
|
A | T | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.31+14015A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15925429 | ||||||
| chr12:15925452
|
C | T | 48 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0025others(45): Show | 48 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.31+14038C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15925452 | ||||||
| chr12:15925594
|
C | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(1): Show | 4 | HG01109.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.31+14180C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15925594 | ||||||
| chr12:15925822
|
C | CT | 26 | a0001c0001t0001g0051a0001c0001t0001g0055a0001c0001t0001g0077others(23): Show | 26 | HG00558.hp2 HG00621.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.31+14431dupT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15925822 | |||||
| chr12:15925822
|
CT | C | 19 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(16): Show | 19 | HG01109.hp2 HG01261.hp1 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.31+14431delT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15925822 | |||||
| chr12:15925822
|
CTTT | C | 20 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0039others(17): Show | 20 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.31+14429_31+14431d others(5): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15925822 | |||||
| chr12:15925822
|
CTTTT | C | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0035others(15): Show | 18 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.31+14428_31+14431d others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15925822 | |||||
| chr12:15925954
|
T | TG | 54 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(51): Show | 54 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.31+14542dupG | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15925954 | |||||
| chr12:15926188
|
G | T | 42 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(39): Show | 42 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.31+14774G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926188 | ||||||
| chr12:15926433
|
G | A | 9 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(6): Show | 9 | HG02109.hp1 HG02257.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.31+15019G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926433 | ||||||
| chr12:15926458
|
C | T | 1 | a0001c0001t0001g0249 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.31+15044C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926458 | ||||||
| chr12:15926472
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.31+15058C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926472 | ||||||
| chr12:15926532
|
C | T | 1 | a0002c0002t0003g0018 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.31+15118C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926532 | ||||||
| chr12:15926561
|
A | C | 16 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(13): Show | 16 | HG01109.hp2 HG01243.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.31+15147A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926561 | ||||||
| chr12:15926563
|
C | G | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0004g0089 | 3 | HG02809.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.31+15149C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926563 | ||||||
| chr12:15926566
|
C | G | 40 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(37): Show | 40 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.31+15152C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926566 | ||||||
| chr12:15926598
|
T | C | 3 | a0001c0001t0005g0042a0001c0001t0005g0043a0001c0001t0005g0044 | 3 | HG01109.hp1 HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.31+15184T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926598 | ||||||
| chr12:15926599
|
G | A | 14 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(11): Show | 14 | HG00733.hp1 HG01109.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.31+15185G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926599 | ||||||
| chr12:15926626
|
C | A | 7 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.31+15212C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926626 | ||||||
| chr12:15926645
|
G | A | 7 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.31+15231G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926645 | ||||||
| chr12:15926691
|
C | G | 1 | a0001c0001t0002g0187 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.31+15277C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926691 | ||||||
| chr12:15926693
|
A | C | 7 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.31+15279A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926693 | ||||||
| chr12:15926693
|
A | G | 1 | a0001c0001t0002g0187 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.31+15279A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926693 | ||||||
| chr12:15926706
|
C | A | 1 | a0001c0001t0002g0187 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.31+15292C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926706 | ||||||
| chr12:15926742
|
G | GA | 165 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0046others(162): Show | 165 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.31+15347dupA | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15926742 | |||||
| chr12:15926742
|
G | GAA | 13 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0160others(10): Show | 13 | HG01109.hp1 HG02027.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.31+15346_31+15347d others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15926742 | |||||
| chr12:15926930
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0091 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.31+15516C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15926930 | ||||||
| chr12:15927018
|
T | G | 2 | a0001c0001t0001g0059a0001c0001t0001g0091 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.31+15604T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15927018 | ||||||
| chr12:15927193
|
A | G | 24 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(21): Show | 24 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.31+15779A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15927193 | ||||||
| chr12:15927413
|
C | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0226 | 2 | HG01071.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.31+15999C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15927413 | ||||||
| chr12:15927414
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0027others(52): Show | 56 | HG00733.hp2 HG01071.hp2 HG01123.hp2 others(53): Show |
intron_variant | MODIFIER | c.31+16000G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15927414 | ||||||
| chr12:15927490
|
T | C | 1 | a0001c0001t0002g0217 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.31+16076T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15927490 | ||||||
| chr12:15927715
|
T | C | 69 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(66): Show | 69 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.31+16301T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15927715 | ||||||
| chr12:15927753
|
T | G | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.31+16339T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15927753 | ||||||
| chr12:15927781
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.31+16367A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15927781 | ||||||
| chr12:15927828
|
T | A | 7 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(4): Show | 7 | HG02109.hp1 HG02257.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.31+16414T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15927828 | ||||||
| chr12:15927899
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.31+16485G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15927899 | ||||||
| chr12:15927934
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.31+16520C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15927934 | ||||||
| chr12:15927966
|
A | G | 1 | a0001c0001t0001g0001 | 2 | HG01123.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.31+16552A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15927966 | ||||||
| chr12:15928030
|
T | TTG | 63 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(60): Show | 63 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.31+16617_31+16618i others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15928030 | |||||
| chr12:15928041
|
G | T | 63 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(60): Show | 63 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.31+16627G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15928041 | ||||||
| chr12:15928093
|
C | A | 1 | a0001c0001t0002g0217 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.31+16679C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15928093 | ||||||
| chr12:15928101
|
G | T | 75 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(72): Show | 75 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.31+16687G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15928101 | ||||||
| chr12:15928166
|
G | A | 2 | a0001c0001t0002g0022a0001c0001t0002g0023 | 2 | NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.31+16752G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15928166 | ||||||
| chr12:15928360
|
T | C | 8 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0012others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.31+16946T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15928360 | ||||||
| chr12:15928375
|
C | T | 47 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(44): Show | 47 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.31+16961C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15928375 | ||||||
| chr12:15928689
|
GAGA | G | 8 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0012others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.31+17280_31+17282d others(5): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15928689 | |||||
| chr12:15928707
|
G | A | 63 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(60): Show | 63 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.31+17293G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15928707 | ||||||
| chr12:15928826
|
G | T | 1 | a0001c0001t0002g0257 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.31+17412G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15928826 | ||||||
| chr12:15928979
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.31+17565C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15928979 | ||||||
| chr12:15929259
|
G | C | 1 | a0001c0001t0001g0107 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.31+17845G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15929259 | ||||||
| chr12:15929342
|
G | C | 63 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(60): Show | 63 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.31+17928G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15929342 | ||||||
| chr12:15929388
|
C | T | 1 | a0001c0001t0004g0089 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.31+17974C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15929388 | ||||||
| chr12:15929516
|
GTCA | G | 7 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(4): Show | 7 | HG02257.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.31+18103_31+18105d others(5): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15929516 | ||||||
| chr12:15929532
|
A | C | 7 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(4): Show | 7 | HG02109.hp1 HG02257.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.31+18118A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15929532 | ||||||
| chr12:15929583
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0003g0017 | 2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.31+18169C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15929583 | ||||||
| chr12:15929637
|
G | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0207a0001c0001t0001g0208others(1): Show | 4 | HG02258.hp2 HG02615.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.31+18223G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15929637 | ||||||
| chr12:15929652
|
T | A | 75 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(72): Show | 75 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.31+18238T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15929652 | ||||||
| chr12:15929809
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0003g0017 | 2 | HG02647.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.31+18395G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15929809 | ||||||
| chr12:15929842
|
G | A | 2 | a0002c0002t0003g0018a0002c0002t0003g0020 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.31+18428G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15929842 | ||||||
| chr12:15929999
|
T | G | 1 | a0001c0001t0001g0227 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.31+18585T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15929999 | ||||||
| chr12:15930040
|
T | C | 5 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0087others(2): Show | 5 | HG02559.hp1 HG02809.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.31+18626T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15930040 | ||||||
| chr12:15930581
|
G | A | 25 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(22): Show | 25 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.31+19167G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15930581 | ||||||
| chr12:15930762
|
T | G | 2 | a0002c0002t0003g0018a0002c0002t0003g0020 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.31+19348T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15930762 | ||||||
| chr12:15931179
|
G | A | 1 | a0001c0001t0002g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.31+19765G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15931179 | ||||||
| chr12:15931261
|
CAG | C | 4 | a0001c0001t0001g0125a0001c0001t0001g0130a0001c0001t0001g0163others(1): Show | 4 | HG00642.hp2 HG00738.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.31+19850_31+19851d others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15931261 | |||||
| chr12:15931535
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0064 | 2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.31+20121G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15931535 | ||||||
| chr12:15931870
|
C | G | 1 | a0001c0001t0001g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.31+20456C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15931870 | ||||||
| chr12:15932121
|
C | T | 7 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(4): Show | 7 | HG02109.hp1 HG02257.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.31+20707C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15932121 | ||||||
| chr12:15932320
|
T | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG03491.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.31+20906T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15932320 | ||||||
| chr12:15932355
|
C | A | 5 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(2): Show | 5 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.31+20941C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15932355 | ||||||
| chr12:15932434
|
G | A | 1 | a0001c0001t0001g0177 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.31+21020G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15932434 | ||||||
| chr12:15932438
|
C | T | 4 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(1): Show | 4 | HG02647.hp1 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.31+21024C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15932438 | ||||||
| chr12:15932444
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.31+21030G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15932444 | ||||||
| chr12:15932507
|
G | A | 2 | a0001c0001t0002g0022a0001c0001t0002g0023 | 2 | NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.31+21093G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15932507 | ||||||
| chr12:15932523
|
G | C | 11 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(8): Show | 11 | HG02257.hp2 HG02559.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.31+21109G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15932523 | ||||||
| chr12:15932640
|
TA | T | 7 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(4): Show | 7 | HG02257.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.31+21238delA | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15932640 | |||||
| chr12:15932641
|
A | T | 8 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.31+21227A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15932641 | ||||||
| chr12:15932659
|
C | G | 19 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(16): Show | 19 | HG02055.hp1 HG02109.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.31+21245C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15932659 | ||||||
| chr12:15932727
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.31+21313C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15932727 | ||||||
| chr12:15932847
|
G | T | 1 | a0001c0001t0001g0234 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.31+21433G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15932847 | ||||||
| chr12:15932881
|
A | ACT | 67 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(64): Show | 67 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.31+21470_31+21471d others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15932881 | |||||
| chr12:15933061
|
A | G | 8 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0012others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.31+21647A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15933061 | ||||||
| chr12:15933246
|
T | C | 4 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(1): Show | 4 | HG02647.hp1 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.31+21832T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15933246 | ||||||
| chr12:15933273
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.31+21859C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15933273 | ||||||
| chr12:15933615
|
G | A | 66 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 66 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.31+22201G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15933615 | ||||||
| chr12:15933667
|
T | C | 1 | a0001c0001t0001g0242 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.31+22253T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15933667 | ||||||
| chr12:15933671
|
G | A | 8 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.31+22257G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15933671 | ||||||
| chr12:15933939
|
G | A | 15 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0098others(12): Show | 15 | HG01358.hp2 HG02738.hp2 HG03834.hp1 others(12): Show |
intron_variant | MODIFIER | c.31+22525G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15933939 | ||||||
| chr12:15934000
|
G | T | 1 | a0001c0001t0001g0093 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.31+22586G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15934000 | ||||||
| chr12:15934260
|
C | A | 1 | a0001c0001t0001g0021 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.32-22676C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15934260 | ||||||
| chr12:15934381
|
T | A | 43 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0031others(40): Show | 43 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.32-22555T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15934381 | ||||||
| chr12:15934638
|
A | C | 5 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(2): Show | 5 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.32-22298A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15934638 | ||||||
| chr12:15934957
|
A | C | 11 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(8): Show | 11 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.32-21979A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15934957 | ||||||
| chr12:15935162
|
A | G | 7 | a0001c0001t0001g0053a0001c0001t0001g0157a0001c0001t0001g0178others(4): Show | 7 | NA18942.hp1 NA18950.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.32-21774A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15935162 | ||||||
| chr12:15935169
|
T | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(1): Show | 4 | HG02647.hp1 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.32-21767T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15935169 | ||||||
| chr12:15935229
|
G | C | 6 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0202others(3): Show | 6 | HG02080.hp1 HG02135.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.32-21707G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15935229 | ||||||
| chr12:15935540
|
A | G | 48 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(45): Show | 48 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.32-21396A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15935540 | ||||||
| chr12:15935547
|
G | A | 7 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(4): Show | 7 | HG02257.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.32-21389G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15935547 | ||||||
| chr12:15935606
|
G | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(1): Show | 4 | HG02647.hp1 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.32-21330G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15935606 | ||||||
| chr12:15935870
|
T | G | 1 | a0001c0001t0001g0129 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.32-21066T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15935870 | ||||||
| chr12:15935874
|
A | T | 1 | a0001c0001t0001g0211 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.32-21062A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15935874 | ||||||
| chr12:15935988
|
A | G | 4 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(1): Show | 4 | HG02647.hp1 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.32-20948A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15935988 | ||||||
| chr12:15936130
|
G | A | 4 | a0001c0001t0002g0147a0001c0001t0002g0148a0001c0001t0002g0154others(1): Show | 4 | HG00621.hp1 HG02165.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-20806G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936130 | ||||||
| chr12:15936456
|
G | T | 1 | a0001c0001t0002g0201 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.32-20480G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936456 | ||||||
| chr12:15936761
|
A | G | 4 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(1): Show | 4 | HG02647.hp1 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.32-20175A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936761 | ||||||
| chr12:15936850
|
G | GTTGTC | 80 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0034others(77): Show | 80 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.32-20050_32-20046d others(7): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936850 | |||||
| chr12:15936850
|
G | GTTGTCTT others(3): Show |
9 | a0001c0001t0001g0052a0001c0001t0001g0061a0001c0001t0001g0062others(6): Show | 9 | HG02027.hp2 HG02074.hp2 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.32-20055_32-20046d others(12): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936850 | |||||
| chr12:15936850
|
G | GTTGTCTT others(8): Show |
3 | a0001c0001t0001g0135a0001c0001t0001g0146a0001c0001t0001g0227 | 3 | HG01168.hp1 HG01169.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.32-20060_32-20046d others(17): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936850 | |||||
| chr12:15936850
|
G | GTTGTCTT others(13): Show |
1 | a0001c0001t0001g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.32-20065_32-20046d others(22): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936850 | |||||
| chr12:15936850
|
GTTGTC | G | 9 | a0001c0001t0001g0096a0001c0001t0003g0009a0001c0001t0003g0011others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.32-20050_32-20046d others(7): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936850 | |||||
| chr12:15936855
|
C | CTTGTG | 2 | a0001c0003t0001g0073a0001c0003t0004g0072 | 2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.32-20077_32-20076i others(7): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936855 | |||||
| chr12:15936861
|
T | C | 2 | a0001c0001t0002g0022a0001c0001t0002g0023 | 2 | NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.32-20075T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936861 | ||||||
| chr12:15936865
|
C | G | 2 | a0001c0001t0002g0022a0001c0001t0002g0023 | 2 | NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.32-20071C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936865 | ||||||
| chr12:15936871
|
TTGTCTTG others(18): Show |
T | 4 | a0001c0001t0002g0022a0001c0001t0002g0023a0002c0002t0003g0018others(1): Show | 4 | HG02630.hp2 HG03098.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-20060_32-20036d others(27): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936871 | |||||
| chr12:15936876
|
TTGTCTTG others(23): Show |
T | 3 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004 | 3 | HG02559.hp2 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.32-20055_32-20026d others(32): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936876 | |||||
| chr12:15936876
|
TTGTCTTG others(28): Show |
T | 3 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0236 | 3 | HG02257.hp2 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.32-20055_32-20021d others(37): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936876 | |||||
| chr12:15936876
|
TTGTCTTG others(33): Show |
T | 1 | a0001c0001t0001g0174 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.32-20055_32-20016d others(42): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936876 | |||||
| chr12:15936881
|
T | TTGTCCTG others(13): Show |
1 | a0001c0001t0001g0129 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.32-20051_32-20050i others(22): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936881 | |||||
| chr12:15936881
|
T | TTGTCCTG others(18): Show |
6 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.32-20051_32-20050i others(27): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936881 | |||||
| chr12:15936881
|
T | TTGTCCTG others(23): Show |
1 | a0001c0001t0001g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.32-20051_32-20050i others(32): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936881 | |||||
| chr12:15936886
|
T | C | 9 | a0001c0001t0001g0033a0001c0001t0001g0065a0001c0001t0001g0066others(6): Show | 9 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.32-20050T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936886 | ||||||
| chr12:15936886
|
T | TTGTCC | 2 | a0001c0001t0001g0219a0001c0001t0002g0257 | 2 | NA19003.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.32-20005_32-20001d others(7): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936886 | |||||
| chr12:15936886
|
T | TTGTCCTG others(13): Show |
1 | a0001c0001t0001g0083 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.32-20020_32-20001d others(22): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936886 | |||||
| chr12:15936886
|
T | TTGTCCTG others(18): Show |
1 | a0001c0001t0001g0180 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.32-20025_32-20001d others(27): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936886 | |||||
| chr12:15936886
|
T | TTGTCTTG others(3): Show |
8 | a0001c0001t0001g0123a0001c0001t0001g0178a0001c0001t0001g0198others(5): Show | 8 | HG02080.hp1 HG02135.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.32-20046_32-20045i others(12): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936886 | |||||
| chr12:15936886
|
T | TTGTCTTG others(8): Show |
3 | a0001c0001t0001g0092a0001c0001t0001g0122a0001c0001t0001g0218 | 3 | HG02300.hp1 HG02602.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.32-20046_32-20045i others(17): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936886 | |||||
| chr12:15936886
|
T | TTGTCTTG others(8): Show |
2 | a0001c0001t0001g0130a0001c0001t0001g0211 | 2 | HG01496.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.32-20046_32-20045i others(17): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936886 | |||||
| chr12:15936886
|
T | TTGTCTTG others(18): Show |
2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.32-20046_32-20045i others(27): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936886 | |||||
| chr12:15936886
|
TTGTCC | T | 7 | a0001c0001t0001g0036a0001c0001t0001g0081a0001c0001t0004g0058others(4): Show | 7 | HG01109.hp1 HG02055.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.32-20005_32-20001d others(7): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936886 | |||||
| chr12:15936887
|
T | TGTCCCGT others(53): Show |
1 | a0001c0001t0001g0033 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.32-20045_32-20044i others(62): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936887 | |||||
| chr12:15936891
|
C | T | 55 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(52): Show | 55 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.32-20045C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936891 | ||||||
| chr12:15936892
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.32-20044T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936892 | ||||||
| chr12:15936896
|
C | T | 52 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(49): Show | 52 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.32-20040C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936896 | ||||||
| chr12:15936897
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.32-20039T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936897 | ||||||
| chr12:15936901
|
C | T | 42 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(39): Show | 42 | HG00280.hp1 HG00280.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.32-20035C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936901 | ||||||
| chr12:15936902
|
T | C | 9 | a0001c0001t0001g0033a0001c0001t0001g0192a0001c0001t0001g0210others(6): Show | 9 | HG00621.hp1 HG01891.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.32-20034T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936902 | ||||||
| chr12:15936906
|
C | T | 38 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(35): Show | 38 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.32-20030C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936906 | ||||||
| chr12:15936907
|
T | C | 12 | a0001c0001t0001g0033a0001c0001t0001g0102a0001c0001t0001g0132others(9): Show | 12 | HG00280.hp1 HG00621.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.32-20029T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936907 | ||||||
| chr12:15936911
|
C | T | 6 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(3): Show | 6 | HG01516.hp2 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.32-20025C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936911 | ||||||
| chr12:15936911
|
CTGTCCTG others(18): Show |
C | 1 | a0001c0001t0001g0031 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.32-20014_32-19990d others(27): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936911 | |||||
| chr12:15936912
|
T | C | 46 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0060others(43): Show | 46 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.32-20024T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936912 | ||||||
| chr12:15936916
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0032 | 3 | HG01884.hp2 HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.32-20020C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936916 | ||||||
| chr12:15936916
|
CTGTCCTG others(13): Show |
C | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.32-20009_32-19990d others(22): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936916 | |||||
| chr12:15936917
|
T | C | 59 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0040others(56): Show | 59 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.32-20019T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936917 | ||||||
| chr12:15936921
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0032 | 3 | HG01884.hp2 HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.32-20015C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936921 | ||||||
| chr12:15936922
|
T | C | 60 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0040others(57): Show | 60 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.32-20014T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936922 | ||||||
| chr12:15936926
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0032 | 3 | HG01884.hp2 HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.32-20010C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936926 | ||||||
| chr12:15936926
|
CTGTCCTG others(3): Show |
C | 2 | a0001c0001t0001g0192a0001c0001t0001g0210 | 2 | HG02572.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.32-20000_32-19991d others(12): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936926 | |||||
| chr12:15936927
|
T | C | 60 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0040others(57): Show | 60 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.32-20009T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936927 | ||||||
| chr12:15936931
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0032 | 3 | HG01884.hp2 HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.32-20005C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936931 | ||||||
| chr12:15936931
|
CTGTCT | C | 8 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0001g0208others(5): Show | 8 | HG00280.hp1 HG00621.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.32-20000_32-19996d others(7): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936931 | |||||
| chr12:15936932
|
T | C | 52 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0040others(49): Show | 52 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.32-20004T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936932 | ||||||
| chr12:15936936
|
T | C | 60 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026others(57): Show | 60 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.32-20000T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936936 | ||||||
| chr12:15936937
|
T | C | 64 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0033others(61): Show | 64 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.32-19999T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936937 | ||||||
| chr12:15936937
|
T | TGTCCCGT others(28): Show |
1 | a0001c0001t0001g0006 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.32-19995_32-19994i others(37): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936937 | |||||
| chr12:15936937
|
T | TGTCTTGT others(43): Show |
1 | a0001c0001t0001g0032 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.32-19996_32-19995i others(52): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936937 | |||||
| chr12:15936937
|
T | TGTCTTGT others(53): Show |
1 | a0001c0001t0001g0007 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.32-19996_32-19995i others(62): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936937 | |||||
| chr12:15936942
|
T | C | 67 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(64): Show | 67 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.32-19994T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936942 | ||||||
| chr12:15936947
|
C | T | 8 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(5): Show | 8 | HG01109.hp2 HG02486.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.32-19989C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936947 | ||||||
| chr12:15936952
|
T | C | 71 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(68): Show | 71 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.32-19984T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936952 | ||||||
| chr12:15936953
|
G | A | 4 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(1): Show | 4 | HG02257.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-19983G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936953 | ||||||
| chr12:15936957
|
T | C | 20 | a0001c0001t0001g0033a0001c0001t0001g0172a0001c0001t0001g0173others(17): Show | 20 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.32-19979T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936957 | ||||||
| chr12:15936957
|
T | TGTCCTGT others(38): Show |
2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.32-19978_32-19977i others(47): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936957 | |||||
| chr12:15936957
|
T | TGTCCTGT others(33): Show |
1 | a0001c0001t0001g0026 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.32-19978_32-19977i others(42): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936957 | |||||
| chr12:15936957
|
T | TGTCCTGT others(28): Show |
1 | a0001c0001t0001g0025 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.32-19978_32-19977i others(37): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15936957 | |||||
| chr12:15936959
|
C | T | 21 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(18): Show | 21 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.32-19977C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936959 | ||||||
| chr12:15936969
|
C | T | 7 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(4): Show | 7 | HG02257.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.32-19967C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936969 | ||||||
| chr12:15936971
|
C | T | 7 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(4): Show | 7 | HG02257.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.32-19965C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15936971 | ||||||
| chr12:15937020
|
C | T | 2 | a0002c0002t0003g0018a0002c0002t0003g0020 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.32-19916C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15937020 | ||||||
| chr12:15937103
|
C | T | 5 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(2): Show | 5 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.32-19833C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15937103 | ||||||
| chr12:15937105
|
C | A | 1 | a0001c0001t0005g0041 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.32-19831C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15937105 | ||||||
| chr12:15937152
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.32-19784C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15937152 | ||||||
| chr12:15937459
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.32-19477A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15937459 | ||||||
| chr12:15937462
|
G | C | 5 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0191others(2): Show | 5 | HG01070.hp2 HG01074.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.32-19474G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15937462 | ||||||
| chr12:15937677
|
G | T | 1 | a0001c0001t0003g0017 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.32-19259G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15937677 | ||||||
| chr12:15937796
|
G | A | 2 | a0001c0001t0002g0022a0001c0001t0002g0023 | 2 | NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.32-19140G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15937796 | ||||||
| chr12:15937966
|
A | T | 5 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(2): Show | 5 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.32-18970A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15937966 | ||||||
| chr12:15938039
|
C | T | 3 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0236 | 3 | HG02257.hp2 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.32-18897C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15938039 | ||||||
| chr12:15938393
|
C | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0207a0001c0001t0001g0208others(1): Show | 4 | HG02258.hp2 HG02615.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-18543C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15938393 | ||||||
| chr12:15938488
|
A | T | 67 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(64): Show | 67 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.32-18448A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15938488 | ||||||
| chr12:15938698
|
T | C | 1 | a0001c0001t0001g0103 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.32-18238T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15938698 | ||||||
| chr12:15938699
|
G | A | 2 | a0001c0001t0002g0022a0001c0001t0002g0023 | 2 | NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.32-18237G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15938699 | ||||||
| chr12:15939034
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.32-17902A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15939034 | ||||||
| chr12:15939624
|
T | A | 1 | a0001c0001t0001g0133 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.32-17312T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15939624 | ||||||
| chr12:15940063
|
C | T | 2 | a0001c0001t0001g0215a0001c0001t0001g0252 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.32-16873C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15940063 | ||||||
| chr12:15940149
|
C | T | 8 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0012others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.32-16787C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15940149 | ||||||
| chr12:15940264
|
C | G | 1 | a0001c0001t0001g0211 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.32-16672C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15940264 | ||||||
| chr12:15940341
|
T | A | 2 | a0001c0001t0001g0206a0001c0001t0005g0041 | 2 | HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.32-16595T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15940341 | ||||||
| chr12:15940444
|
C | T | 1 | a0001c0001t0002g0097 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.32-16492C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15940444 | ||||||
| chr12:15940497
|
G | A | 7 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(4): Show | 7 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.32-16439G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15940497 | ||||||
| chr12:15940512
|
T | C | 84 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(81): Show | 84 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.32-16424T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15940512 | ||||||
| chr12:15940513
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0064 | 2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.32-16423G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15940513 | ||||||
| chr12:15940537
|
G | A | 2 | a0001c0001t0002g0022a0001c0001t0002g0023 | 2 | NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.32-16399G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15940537 | ||||||
| chr12:15940568
|
G | C | 1 | a0001c0001t0001g0031 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.32-16368G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15940568 | ||||||
| chr12:15940641
|
G | A | 7 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(4): Show | 7 | HG02257.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.32-16295G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15940641 | ||||||
| chr12:15941196
|
G | A | 5 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(2): Show | 5 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.32-15740G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15941196 | ||||||
| chr12:15941227
|
G | A | 84 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(81): Show | 84 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.32-15709G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15941227 | ||||||
| chr12:15941242
|
C | G | 2 | a0001c0001t0002g0022a0001c0001t0002g0023 | 2 | NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.32-15694C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15941242 | ||||||
| chr12:15941448
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.32-15488A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15941448 | ||||||
| chr12:15941565
|
C | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0207a0001c0001t0001g0208others(1): Show | 4 | HG02258.hp2 HG02615.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-15371C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15941565 | ||||||
| chr12:15941625
|
G | A | 2 | a0002c0002t0003g0018a0002c0002t0003g0020 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.32-15311G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15941625 | ||||||
| chr12:15941661
|
C | T | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(5): Show | 8 | HG02630.hp2 HG02647.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.32-15275C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15941661 | ||||||
| chr12:15941683
|
A | G | 2 | a0002c0002t0003g0018a0002c0002t0003g0020 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.32-15253A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15941683 | ||||||
| chr12:15941707
|
G | A | 1 | a0001c0001t0001g0192 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.32-15229G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15941707 | ||||||
| chr12:15941793
|
T | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0032 | 3 | HG01884.hp2 HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.32-15143T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15941793 | ||||||
| chr12:15941795
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.32-15141C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15941795 | ||||||
| chr12:15941890
|
A | G | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(5): Show | 8 | HG02630.hp2 HG02647.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.32-15046A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15941890 | ||||||
| chr12:15942014
|
A | G | 2 | a0002c0002t0003g0018a0002c0002t0003g0020 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.32-14922A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15942014 | ||||||
| chr12:15942159
|
C | G | 1 | a0001c0001t0001g0001 | 2 | HG01123.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.32-14777C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15942159 | ||||||
| chr12:15942470
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.32-14466T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15942470 | ||||||
| chr12:15942614
|
A | G | 6 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(3): Show | 6 | HG02647.hp1 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.32-14322A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15942614 | ||||||
| chr12:15942676
|
T | G | 7 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(4): Show | 7 | HG02257.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.32-14260T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15942676 | ||||||
| chr12:15942771
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.32-14165G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15942771 | ||||||
| chr12:15942783
|
G | C | 1 | a0001c0001t0001g0120 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.32-14153G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15942783 | ||||||
| chr12:15942820
|
G | C | 2 | a0001c0001t0002g0022a0001c0001t0002g0023 | 2 | NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.32-14116G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15942820 | ||||||
| chr12:15942938
|
C | A | 1 | a0001c0001t0001g0118 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.32-13998C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15942938 | ||||||
| chr12:15943059
|
C | T | 69 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(66): Show | 69 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.32-13877C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15943059 | ||||||
| chr12:15943276
|
C | G | 1 | a0001c0001t0001g0136 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.32-13660C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15943276 | ||||||
| chr12:15943294
|
T | G | 3 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004 | 3 | HG02559.hp2 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.32-13642T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15943294 | ||||||
| chr12:15943492
|
A | T | 6 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(3): Show | 6 | HG02647.hp1 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.32-13444A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15943492 | ||||||
| chr12:15943561
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0003g0005 | 2 | HG00733.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.32-13375C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15943561 | ||||||
| chr12:15943563
|
T | G | 84 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(81): Show | 84 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.32-13373T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15943563 | ||||||
| chr12:15943576
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.32-13360T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15943576 | ||||||
| chr12:15943701
|
T | A | 1 | a0001c0001t0001g0218 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.32-13235T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15943701 | ||||||
| chr12:15943703
|
A | T | 1 | a0001c0001t0001g0218 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.32-13233A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15943703 | ||||||
| chr12:15943705
|
T | TTTATTTA others(4): Show |
1 | a0001c0001t0001g0218 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.32-13229_32-13228i others(13): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15943705 | |||||
| chr12:15943705
|
T | TTTTA | 73 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(70): Show | 73 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.32-13199_32-13196d others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15943705 | |||||
| chr12:15943705
|
T | TTTTATTT others(1): Show |
31 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0029others(28): Show | 31 | HG00735.hp2 HG01070.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.32-13203_32-13196d others(10): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15943705 | |||||
| chr12:15943705
|
T | TTTTATTT others(5): Show |
2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG01081.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.32-13207_32-13196d others(14): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15943705 | |||||
| chr12:15943705
|
T | TTTTATTT others(9): Show |
1 | a0001c0001t0001g0120 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.32-13211_32-13196d others(18): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15943705 | |||||
| chr12:15943705
|
TTTTA | T | 15 | a0001c0001t0001g0107a0001c0001t0001g0128a0001c0001t0001g0172others(12): Show | 15 | HG02015.hp1 HG02257.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.32-13199_32-13196d others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15943705 | |||||
| chr12:15943705
|
TTTTATTT others(5): Show |
T | 2 | a0002c0002t0003g0018a0002c0002t0003g0020 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.32-13207_32-13196d others(14): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15943705 | |||||
| chr12:15943835
|
C | T | 3 | a0001c0001t0005g0042a0001c0001t0005g0043a0001c0001t0005g0044 | 3 | HG01109.hp1 HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.32-13101C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15943835 | ||||||
| chr12:15943877
|
C | G | 2 | a0002c0002t0003g0018a0002c0002t0003g0020 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.32-13059C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15943877 | ||||||
| chr12:15943920
|
T | G | 50 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0031others(47): Show | 50 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.32-13016T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15943920 | ||||||
| chr12:15943942
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.32-12994T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15943942 | ||||||
| chr12:15944036
|
T | C | 12 | a0001c0001t0001g0075a0001c0001t0001g0107a0001c0001t0001g0113others(9): Show | 12 | HG00621.hp2 HG02015.hp1 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.32-12900T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15944036 | ||||||
| chr12:15944074
|
C | G | 1 | a0001c0001t0001g0183 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.32-12862C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15944074 | ||||||
| chr12:15944078
|
T | A | 1 | a0001c0001t0006g0010 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.32-12858T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15944078 | ||||||
| chr12:15944141
|
G | A | 43 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0031others(40): Show | 43 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.32-12795G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15944141 | ||||||
| chr12:15944197
|
A | C | 4 | a0001c0001t0001g0008a0001c0001t0001g0207a0001c0001t0001g0208others(1): Show | 4 | HG02258.hp2 HG02615.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-12739A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15944197 | ||||||
| chr12:15944299
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.32-12637G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15944299 | ||||||
| chr12:15944377
|
C | T | 8 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0012others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.32-12559C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15944377 | ||||||
| chr12:15944416
|
C | A | 1 | a0001c0001t0003g0017 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.32-12520C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15944416 | ||||||
| chr12:15944556
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.32-12380G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15944556 | ||||||
| chr12:15944791
|
T | G | 8 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0012others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.32-12145T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15944791 | ||||||
| chr12:15945335
|
C | G | 7 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(4): Show | 7 | HG02257.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.32-11601C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15945335 | ||||||
| chr12:15945462
|
A | T | 1 | a0001c0001t0001g0210 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.32-11474A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15945462 | ||||||
| chr12:15945492
|
A | G | 1 | a0001c0001t0002g0254 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.32-11444A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15945492 | ||||||
| chr12:15945595
|
G | T | 5 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(2): Show | 5 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.32-11341G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15945595 | ||||||
| chr12:15945659
|
G | A | 4 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(1): Show | 4 | HG02257.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-11277G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15945659 | ||||||
| chr12:15945746
|
G | A | 1 | a0001c0001t0003g0017 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.32-11190G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15945746 | ||||||
| chr12:15946191
|
C | T | 3 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004 | 3 | HG02559.hp2 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.32-10745C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15946191 | ||||||
| chr12:15946291
|
T | A | 5 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(2): Show | 5 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.32-10645T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15946291 | ||||||
| chr12:15946569
|
G | T | 8 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0012others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.32-10367G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15946569 | ||||||
| chr12:15946580
|
T | C | 12 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(9): Show | 12 | HG02257.hp2 HG02559.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.32-10356T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15946580 | ||||||
| chr12:15946612
|
C | G | 1 | a0001c0001t0001g0211 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.32-10324C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15946612 | ||||||
| chr12:15946777
|
G | A | 1 | a0001c0001t0002g0168 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.32-10159G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15946777 | ||||||
| chr12:15946782
|
C | T | 6 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(3): Show | 6 | HG02647.hp1 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.32-10154C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15946782 | ||||||
| chr12:15946954
|
T | A | 2 | a0002c0002t0003g0018a0002c0002t0003g0020 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.32-9982T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15946954 | ||||||
| chr12:15947294
|
G | A | 69 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(66): Show | 69 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.32-9642G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15947294 | ||||||
| chr12:15947403
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.32-9533C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15947403 | ||||||
| chr12:15947436
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.32-9500G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15947436 | ||||||
| chr12:15947542
|
A | T | 85 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(82): Show | 85 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.32-9394A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15947542 | ||||||
| chr12:15947566
|
T | C | 1 | a0001c0001t0001g0253 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.32-9370T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15947566 | ||||||
| chr12:15947615
|
A | G | 6 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0202others(3): Show | 6 | HG02080.hp1 HG02135.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.32-9321A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15947615 | ||||||
| chr12:15947623
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.32-9313C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15947623 | ||||||
| chr12:15947649
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.32-9287T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15947649 | ||||||
| chr12:15947737
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.32-9199T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15947737 | ||||||
| chr12:15947744
|
C | T | 8 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0012others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.32-9192C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15947744 | ||||||
| chr12:15947811
|
C | G | 1 | a0001c0001t0001g0088 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.32-9125C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15947811 | ||||||
| chr12:15947862
|
A | G | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0247 | 3 | HG02258.hp2 HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.32-9074A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15947862 | ||||||
| chr12:15947945
|
A | T | 2 | a0001c0003t0001g0073a0001c0003t0004g0072 | 2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.32-8991A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15947945 | ||||||
| chr12:15948035
|
T | G | 2 | a0001c0001t0001g0151a0001c0001t0001g0165 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.32-8901T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15948035 | ||||||
| chr12:15948198
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.32-8738G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15948198 | ||||||
| chr12:15948240
|
A | G | 1 | a0001c0001t0003g0004 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.32-8696A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15948240 | ||||||
| chr12:15948285
|
T | A | 2 | a0001c0001t0001g0034a0001c0001t0003g0005 | 2 | HG00733.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.32-8651T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15948285 | ||||||
| chr12:15948365
|
C | T | 11 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(8): Show | 11 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.32-8571C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15948365 | ||||||
| chr12:15948686
|
T | G | 1 | a0001c0001t0001g0001 | 2 | HG01123.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.32-8250T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15948686 | ||||||
| chr12:15948708
|
C | G | 5 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(2): Show | 5 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.32-8228C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15948708 | ||||||
| chr12:15948712
|
C | G | 1 | a0001c0001t0001g0250 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.32-8224C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15948712 | ||||||
| chr12:15948719
|
C | T | 2 | a0002c0002t0003g0018a0002c0002t0003g0020 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.32-8217C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15948719 | ||||||
| chr12:15948784
|
A | T | 1 | a0001c0001t0001g0205 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.32-8152A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15948784 | ||||||
| chr12:15949012
|
C | T | 5 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(2): Show | 5 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.32-7924C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15949012 | ||||||
| chr12:15949353
|
C | T | 6 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(3): Show | 6 | HG02647.hp1 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.32-7583C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15949353 | ||||||
| chr12:15949458
|
A | AGGCTCCG others(2): Show |
54 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(51): Show | 54 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.32-7477_32-7476ins others(9): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15949458 | |||||
| chr12:15949460
|
C | G | 54 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(51): Show | 54 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.32-7476C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15949460 | ||||||
| chr12:15949461
|
A | C | 54 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(51): Show | 54 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.32-7475A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15949461 | ||||||
| chr12:15949462
|
A | G | 54 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(51): Show | 54 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.32-7474A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15949462 | ||||||
| chr12:15949482
|
G | A | 8 | a0001c0001t0001g0085a0001c0001t0001g0172a0001c0001t0001g0173others(5): Show | 8 | HG02257.hp2 HG02559.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.32-7454G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15949482 | ||||||
| chr12:15949493
|
T | C | 84 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(81): Show | 84 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.32-7443T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15949493 | ||||||
| chr12:15949540
|
G | A | 3 | a0001c0001t0001g0036a0001c0001t0001g0215a0001c0001t0001g0252 | 3 | HG02647.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.32-7396G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15949540 | ||||||
| chr12:15949674
|
C | T | 5 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(2): Show | 5 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.32-7262C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15949674 | ||||||
| chr12:15949739
|
G | A | 1 | a0003c0004t0001g0225 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.32-7197G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15949739 | ||||||
| chr12:15949815
|
C | T | 1 | a0001c0001t0004g0116 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.32-7121C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15949815 | ||||||
| chr12:15949872
|
C | T | 69 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(66): Show | 69 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.32-7064C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15949872 | ||||||
| chr12:15949894
|
T | G | 6 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(3): Show | 6 | HG02647.hp1 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.32-7042T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15949894 | ||||||
| chr12:15949983
|
G | A | 12 | a0001c0001t0001g0075a0001c0001t0001g0107a0001c0001t0001g0113others(9): Show | 12 | HG00621.hp2 HG02015.hp1 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.32-6953G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15949983 | ||||||
| chr12:15950270
|
A | G | 1 | a0001c0001t0003g0017 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.32-6666A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15950270 | ||||||
| chr12:15950281
|
A | G | 84 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(81): Show | 84 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.32-6655A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15950281 | ||||||
| chr12:15950407
|
C | G | 2 | a0001c0001t0002g0022a0001c0001t0002g0023 | 2 | NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.32-6529C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15950407 | ||||||
| chr12:15950478
|
A | G | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG00544.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.32-6458A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15950478 | ||||||
| chr12:15950723
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.32-6213C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15950723 | ||||||
| chr12:15950795
|
A | T | 4 | a0001c0001t0002g0147a0001c0001t0002g0148a0001c0001t0002g0154others(1): Show | 4 | HG00621.hp1 HG02165.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-6141A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15950795 | ||||||
| chr12:15950876
|
A | T | 13 | a0001c0001t0001g0075a0001c0001t0001g0107a0001c0001t0001g0113others(10): Show | 13 | HG00621.hp2 HG02015.hp1 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.32-6060A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15950876 | ||||||
| chr12:15950878
|
C | T | 13 | a0001c0001t0001g0075a0001c0001t0001g0107a0001c0001t0001g0113others(10): Show | 13 | HG00621.hp2 HG02015.hp1 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.32-6058C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15950878 | ||||||
| chr12:15951017
|
T | A | 1 | a0001c0001t0001g0256 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.32-5919T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15951017 | ||||||
| chr12:15951137
|
A | C | 1 | a0001c0001t0001g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.32-5799A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15951137 | ||||||
| chr12:15951226
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.32-5710C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15951226 | ||||||
| chr12:15951256
|
T | G | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110 | 3 | HG02818.hp1 HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.32-5680T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15951256 | ||||||
| chr12:15951257
|
G | C | 4 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(1): Show | 4 | HG02257.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-5679G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15951257 | ||||||
| chr12:15951357
|
T | G | 10 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0099others(7): Show | 10 | HG00642.hp2 HG00738.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.32-5579T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15951357 | ||||||
| chr12:15951514
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.32-5422C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15951514 | ||||||
| chr12:15951518
|
T | G | 1 | a0001c0001t0001g0234 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.32-5418T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15951518 | ||||||
| chr12:15951737
|
T | C | 5 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(2): Show | 5 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.32-5199T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15951737 | ||||||
| chr12:15951938
|
G | C | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.32-4998G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15951938 | ||||||
| chr12:15951972
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.32-4964G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15951972 | ||||||
| chr12:15951995
|
A | C | 1 | a0001c0001t0001g0129 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.32-4941A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15951995 | ||||||
| chr12:15952024
|
C | T | 5 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(2): Show | 5 | HG03130.hp2 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.32-4912C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15952024 | ||||||
| chr12:15952118
|
C | G | 4 | a0001c0001t0002g0147a0001c0001t0002g0148a0001c0001t0002g0154others(1): Show | 4 | HG00621.hp1 HG02165.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-4818C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15952118 | ||||||
| chr12:15952134
|
C | T | 54 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(51): Show | 54 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.32-4802C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15952134 | ||||||
| chr12:15952255
|
A | G | 2 | a0002c0002t0003g0018a0002c0002t0003g0020 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.32-4681A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15952255 | ||||||
| chr12:15952311
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.32-4625G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15952311 | ||||||
| chr12:15952433
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.32-4503C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15952433 | ||||||
| chr12:15952610
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.32-4326T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15952610 | ||||||
| chr12:15952635
|
C | A | 3 | a0001c0001t0002g0139a0001c0001t0002g0152a0001c0001t0002g0217 | 3 | NA19000.hp1 NA19070.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.32-4301C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15952635 | ||||||
| chr12:15952636
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.32-4300G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15952636 | ||||||
| chr12:15952816
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.32-4120A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15952816 | ||||||
| chr12:15953168
|
T | G | 2 | a0001c0003t0001g0073a0001c0003t0004g0072 | 2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.32-3768T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15953168 | ||||||
| chr12:15953296
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0177a0001c0001t0001g0183 | 3 | HG01074.hp1 HG01081.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.32-3640G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15953296 | ||||||
| chr12:15953589
|
A | G | 54 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(51): Show | 54 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.32-3347A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15953589 | ||||||
| chr12:15953614
|
A | C | 5 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(2): Show | 5 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.32-3322A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15953614 | ||||||
| chr12:15953813
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.32-3123A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15953813 | ||||||
| chr12:15953942
|
T | C | 7 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(4): Show | 7 | HG02257.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.32-2994T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15953942 | ||||||
| chr12:15954034
|
T | C | 2 | a0001c0001t0001g0084a0001c0001t0001g0214 | 2 | HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.32-2902T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15954034 | ||||||
| chr12:15954038
|
T | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0170 | 2 | HG01358.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.32-2898T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15954038 | ||||||
| chr12:15954279
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.32-2657A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15954279 | ||||||
| chr12:15954280
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.32-2656T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15954280 | ||||||
| chr12:15954412
|
C | G | 7 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(4): Show | 7 | HG02257.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.32-2524C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15954412 | ||||||
| chr12:15954772
|
G | A | 6 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(3): Show | 6 | HG02647.hp1 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.32-2164G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15954772 | ||||||
| chr12:15954801
|
G | T | 1 | a0001c0001t0001g0193 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.32-2135G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15954801 | ||||||
| chr12:15954866
|
C | T | 1 | a0001c0001t0003g0013 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.32-2070C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15954866 | ||||||
| chr12:15955078
|
T | C | 2 | a0001c0001t0001g0083a0001c0001t0001g0129 | 2 | HG02486.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.32-1858T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15955078 | ||||||
| chr12:15955089
|
C | T | 2 | a0002c0002t0003g0018a0002c0002t0003g0020 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.32-1847C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15955089 | ||||||
| chr12:15955117
|
T | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0064 | 2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.32-1819T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15955117 | ||||||
| chr12:15955166
|
G | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0177a0001c0001t0001g0183 | 3 | HG01074.hp1 HG01081.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.32-1770G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15955166 | ||||||
| chr12:15955170
|
C | T | 4 | a0001c0001t0001g0085a0001c0001t0001g0087a0001c0001t0001g0088others(1): Show | 4 | HG02809.hp2 HG02965.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-1766C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15955170 | ||||||
| chr12:15955254
|
G | T | 1 | a0001c0001t0001g0036 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.32-1682G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15955254 | ||||||
| chr12:15955261
|
T | G | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.32-1675T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15955261 | ||||||
| chr12:15955296
|
GA | G | 6 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(3): Show | 6 | HG01261.hp1 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.32-1626delA | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 15955296 | |||||
| chr12:15955795
|
A | G | 4 | a0001c0001t0002g0147a0001c0001t0002g0148a0001c0001t0002g0154others(1): Show | 4 | HG00621.hp1 HG02165.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-1141A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15955795 | ||||||
| chr12:15956013
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.32-923T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15956013 | ||||||
| chr12:15956070
|
A | G | 2 | a0002c0002t0003g0018a0002c0002t0003g0020 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.32-866A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15956070 | ||||||
| chr12:15956416
|
A | T | 1 | a0001c0001t0001g0176 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.32-520A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15956416 | ||||||
| chr12:15956483
|
G | A | 2 | a0001c0001t0001g0143a0001c0001t0001g0167 | 2 | HG02273.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.32-453G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15956483 | ||||||
| chr12:15956525
|
A | G | 6 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0099others(3): Show | 6 | NA18747.hp1 NA18943.hp2 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.32-411A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15956525 | ||||||
| chr12:15956739
|
T | G | 21 | a0001c0001t0001g0021a0001c0001t0001g0048a0001c0001t0001g0074others(18): Show | 21 | HG00735.hp2 HG01070.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.32-197T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 1/8 | chr12 | 15956739 | ||||||
| chr12:15957240
|
T | A | 50 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0031others(47): Show | 50 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.129+207T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 2/8 | chr12 | 15957240 | ||||||
| chr12:15957324
|
G | A | 5 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0099others(2): Show | 5 | NA18943.hp2 NA18975.hp2 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+291G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 2/8 | chr12 | 15957324 | ||||||
| chr12:15957516
|
G | A | 2 | a0001c0001t0002g0022a0001c0001t0002g0023 | 2 | NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.129+483G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 2/8 | chr12 | 15957516 | ||||||
| chr12:15957551
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.129+518C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 2/8 | chr12 | 15957551 | ||||||
| chr12:15957675
|
G | A | 8 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0012others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.130-513G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 2/8 | chr12 | 15957675 | ||||||
| chr12:15957918
|
G | A | 5 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(2): Show | 5 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.130-270G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 2/8 | chr12 | 15957918 | ||||||
| chr12:15958514
|
CT | C | 166 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(163): Show | 166 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.277+198delT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 15958514 | |||||
| chr12:15958663
|
C | T | 1 | a0001c0001t0003g0017 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.277+328C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 3/8 | chr12 | 15958663 | ||||||
| chr12:15959131
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.278-698G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 3/8 | chr12 | 15959131 | ||||||
| chr12:15959426
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.278-403T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 3/8 | chr12 | 15959426 | ||||||
| chr12:15959820
|
T | C | 2 | a0002c0002t0003g0018a0002c0002t0003g0020 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.278-9T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 3/8 | chr12 | 15959820 | ||||||
| chr12:15959958
|
T | A | 1 | a0001c0001t0002g0161 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.373+34T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15959958 | ||||||
| chr12:15959964
|
T | C | 7 | a0001c0001t0001g0057a0001c0001t0001g0084a0001c0001t0001g0085others(4): Show | 7 | HG02559.hp1 HG02809.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.373+40T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15959964 | ||||||
| chr12:15960020
|
A | G | 2 | a0001c0001t0001g0095a0001c0001t0001g0230 | 2 | HG00735.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.373+96A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15960020 | ||||||
| chr12:15960207
|
T | C | 79 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0021others(76): Show | 79 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.373+283T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15960207 | ||||||
| chr12:15960273
|
T | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0170 | 2 | HG01358.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.373+349T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15960273 | ||||||
| chr12:15960362
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.373+438G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15960362 | ||||||
| chr12:15960597
|
C | A | 256 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(253): Show | 257 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(254): Show |
intron_variant | MODIFIER | c.373+673C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15960597 | ||||||
| chr12:15960636
|
C | CA | 52 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0039others(49): Show | 52 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.373+739dupA | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 15960636 | |||||
| chr12:15960636
|
C | CAA | 19 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0037others(16): Show | 19 | HG01168.hp1 HG01516.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.373+738_373+739dup others(2): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 15960636 | |||||
| chr12:15960636
|
C | CAAA | 20 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0066others(17): Show | 20 | HG00280.hp1 HG00280.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.373+737_373+739dup others(3): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 15960636 | |||||
| chr12:15960636
|
C | CAAAA | 23 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0031others(20): Show | 23 | HG00738.hp2 HG01361.hp2 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.373+736_373+739dup others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 15960636 | |||||
| chr12:15960636
|
C | CAAAAA | 7 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0001g0130others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.373+735_373+739dup others(5): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 15960636 | |||||
| chr12:15960636
|
CA | C | 14 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0026others(11): Show | 15 | HG00642.hp1 HG01071.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.373+739delA | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 15960636 | |||||
| chr12:15960636
|
CAAAAAAA others(4): Show |
C | 6 | a0001c0001t0001g0206a0001c0001t0002g0147a0001c0001t0002g0148others(3): Show | 6 | HG00621.hp1 HG02165.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.373+729_373+739del others(11): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 15960636 | |||||
| chr12:15960691
|
C | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0207a0001c0001t0001g0208others(1): Show | 4 | HG02258.hp2 HG02615.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.373+767C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15960691 | ||||||
| chr12:15960849
|
C | T | 4 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(1): Show | 4 | HG02257.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.373+925C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15960849 | ||||||
| chr12:15960887
|
G | T | 1 | a0001c0001t0002g0023 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.373+963G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15960887 | ||||||
| chr12:15961293
|
A | G | 15 | a0001c0001t0001g0008a0001c0001t0001g0053a0001c0001t0001g0157others(12): Show | 15 | HG02080.hp1 HG02135.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.373+1369A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15961293 | ||||||
| chr12:15961393
|
G | C | 1 | a0001c0001t0001g0081 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.374-1420G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15961393 | ||||||
| chr12:15961446
|
C | T | 5 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0082others(2): Show | 5 | HG00733.hp2 HG01081.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.374-1367C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15961446 | ||||||
| chr12:15961506
|
AAAAAT | A | 11 | a0001c0001t0001g0085a0001c0001t0001g0115a0001c0001t0003g0009others(8): Show | 11 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.374-1299_374-1295d others(7): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 15961506 | |||||
| chr12:15961596
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.374-1217A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15961596 | ||||||
| chr12:15961664
|
A | G | 55 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0040others(52): Show | 55 | HG00280.hp1 HG00280.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.374-1149A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15961664 | ||||||
| chr12:15961962
|
T | G | 1 | a0001c0001t0001g0081 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.374-851T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15961962 | ||||||
| chr12:15962430
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.374-383G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15962430 | ||||||
| chr12:15962617
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.374-196C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15962617 | ||||||
| chr12:15962808
|
A | C | 5 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0191others(2): Show | 5 | HG01070.hp2 HG01074.hp2 HG01243.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.374-5A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 4/8 | chr12 | 15962808 | ||||||
| chr12:15963022
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.508+75A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15963022 | ||||||
| chr12:15963243
|
C | A | 7 | a0001c0001t0001g0053a0001c0001t0001g0157a0001c0001t0001g0178others(4): Show | 7 | NA18942.hp1 NA18950.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.508+296C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15963243 | ||||||
| chr12:15963257
|
A | T | 9 | a0001c0001t0001g0085a0001c0001t0003g0009a0001c0001t0003g0011others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.508+310A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15963257 | ||||||
| chr12:15963270
|
C | G | 3 | a0001c0001t0005g0042a0001c0001t0005g0043a0001c0001t0005g0044 | 3 | HG01109.hp1 HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.508+323C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15963270 | ||||||
| chr12:15963444
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.508+497G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15963444 | ||||||
| chr12:15963685
|
C | T | 102 | a0001c0001t0001g0024a0001c0001t0001g0034a0001c0001t0001g0035others(99): Show | 102 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.508+738C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15963685 | ||||||
| chr12:15963722
|
A | G | 14 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(11): Show | 14 | HG01109.hp2 HG01891.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.508+775A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15963722 | ||||||
| chr12:15963876
|
TCTGTATC others(8): Show |
T | 5 | a0001c0001t0001g0008a0001c0001t0001g0083a0001c0001t0003g0002others(2): Show | 5 | HG02559.hp2 HG02886.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.508+932_508+946del others(15): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 15963876 | |||||
| chr12:15963976
|
G | C | 1 | a0001c0001t0001g0032 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.508+1029G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15963976 | ||||||
| chr12:15964053
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.508+1106G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15964053 | ||||||
| chr12:15964177
|
A | T | 254 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(251): Show | 255 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(252): Show |
intron_variant | MODIFIER | c.508+1230A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15964177 | ||||||
| chr12:15964205
|
A | G | 1 | a0001c0001t0001g0219 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.508+1258A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15964205 | ||||||
| chr12:15964246
|
C | T | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0145 | 3 | HG03491.hp1 HG03669.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.508+1299C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15964246 | ||||||
| chr12:15964367
|
T | C | 207 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(204): Show | 207 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(204): Show |
intron_variant | MODIFIER | c.508+1420T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15964367 | ||||||
| chr12:15964502
|
T | G | 1 | a0001c0001t0001g0143 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.508+1555T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15964502 | ||||||
| chr12:15964624
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.508+1677A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15964624 | ||||||
| chr12:15964700
|
A | G | 4 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(1): Show | 4 | HG02257.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.508+1753A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15964700 | ||||||
| chr12:15964874
|
T | A | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0065others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.508+1927T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15964874 | ||||||
| chr12:15965048
|
C | A | 1 | a0001c0001t0002g0188 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.508+2101C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15965048 | ||||||
| chr12:15965211
|
C | T | 3 | a0001c0001t0001g0129a0001c0003t0001g0073a0001c0003t0004g0072 | 3 | HG02486.hp2 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.508+2264C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15965211 | ||||||
| chr12:15965259
|
G | A | 5 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.508+2312G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15965259 | ||||||
| chr12:15965355
|
A | G | 4 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(1): Show | 4 | HG02257.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.508+2408A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15965355 | ||||||
| chr12:15965370
|
G | T | 1 | a0001c0001t0001g0062 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.508+2423G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15965370 | ||||||
| chr12:15965604
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.508+2657C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15965604 | ||||||
| chr12:15965605
|
G | C | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0065others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.508+2658G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15965605 | ||||||
| chr12:15965625
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.508+2678G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15965625 | ||||||
| chr12:15965820
|
C | T | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0247 | 3 | HG02258.hp2 HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.508+2873C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15965820 | ||||||
| chr12:15965876
|
C | G | 1 | a0001c0001t0001g0032 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.508+2929C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15965876 | ||||||
| chr12:15965936
|
G | A | 5 | a0001c0001t0001g0024a0001c0001t0002g0124a0001c0001t0002g0139others(2): Show | 5 | NA18964.hp1 NA19000.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.508+2989G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15965936 | ||||||
| chr12:15965989
|
A | G | 10 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0003g0009others(7): Show | 10 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.508+3042A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15965989 | ||||||
| chr12:15965996
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0064 | 2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.508+3049C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15965996 | ||||||
| chr12:15966063
|
T | G | 5 | a0001c0001t0001g0008a0001c0001t0001g0083a0001c0001t0003g0002others(2): Show | 5 | HG02559.hp2 HG02886.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.508+3116T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15966063 | ||||||
| chr12:15966110
|
C | T | 2 | a0002c0002t0003g0018a0002c0002t0003g0020 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.508+3163C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15966110 | ||||||
| chr12:15966280
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.508+3333A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15966280 | ||||||
| chr12:15966317
|
C | T | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110 | 3 | HG02818.hp1 HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.508+3370C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15966317 | ||||||
| chr12:15966318
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.508+3371G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15966318 | ||||||
| chr12:15966337
|
G | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0230 | 2 | HG00735.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.508+3390G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15966337 | ||||||
| chr12:15966421
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.508+3474G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15966421 | ||||||
| chr12:15966438
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.508+3491T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15966438 | ||||||
| chr12:15966613
|
GC | G | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0004g0089 | 3 | HG02809.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.508+3667delC | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15966613 | ||||||
| chr12:15966670
|
C | T | 14 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(11): Show | 14 | HG01109.hp2 HG01891.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.508+3723C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15966670 | ||||||
| chr12:15966840
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.508+3893C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15966840 | ||||||
| chr12:15966916
|
G | C | 1 | a0001c0001t0001g0177 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.508+3969G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15966916 | ||||||
| chr12:15966950
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.508+4003G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15966950 | ||||||
| chr12:15967071
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.508+4124C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15967071 | ||||||
| chr12:15967202
|
T | A | 1 | a0001c0001t0001g0170 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.508+4255T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15967202 | ||||||
| chr12:15967208
|
A | C | 10 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0003g0009others(7): Show | 10 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.508+4261A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15967208 | ||||||
| chr12:15967464
|
C | T | 102 | a0001c0001t0001g0024a0001c0001t0001g0034a0001c0001t0001g0035others(99): Show | 102 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.508+4517C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15967464 | ||||||
| chr12:15967723
|
C | T | 1 | a0001c0001t0002g0222 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.508+4776C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15967723 | ||||||
| chr12:15967728
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.508+4781C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15967728 | ||||||
| chr12:15967788
|
G | A | 4 | a0001c0001t0001g0008a0001c0001t0003g0002a0001c0001t0003g0003others(1): Show | 4 | HG02559.hp2 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.508+4841G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15967788 | ||||||
| chr12:15967886
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.508+4939T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15967886 | ||||||
| chr12:15968086
|
C | CT | 54 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0031others(51): Show | 54 | HG00280.hp1 HG00280.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.508+5153dupT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 15968086 | |||||
| chr12:15968372
|
A | C | 3 | a0001c0001t0001g0193a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | NA18967.hp2 NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.508+5425A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15968372 | ||||||
| chr12:15968799
|
C | G | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0247 | 3 | HG02258.hp2 HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.508+5852C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15968799 | ||||||
| chr12:15968909
|
T | C | 5 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0191others(2): Show | 5 | HG01070.hp2 HG01074.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.508+5962T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15968909 | ||||||
| chr12:15969024
|
C | T | 3 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004 | 3 | HG02559.hp2 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.508+6077C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15969024 | ||||||
| chr12:15969102
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.508+6155G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15969102 | ||||||
| chr12:15969244
|
T | A | 175 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(172): Show | 175 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.508+6297T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15969244 | ||||||
| chr12:15969480
|
G | A | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110 | 3 | HG02818.hp1 HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.508+6533G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15969480 | ||||||
| chr12:15969512
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.508+6565C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15969512 | ||||||
| chr12:15969684
|
C | T | 187 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(184): Show | 187 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.508+6737C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15969684 | ||||||
| chr12:15969780
|
A | G | 3 | a0001c0001t0001g0193a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | NA18967.hp2 NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.508+6833A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15969780 | ||||||
| chr12:15969809
|
G | T | 10 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0003g0009others(7): Show | 10 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.508+6862G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15969809 | ||||||
| chr12:15969920
|
CAG | C | 4 | a0001c0001t0001g0008a0001c0001t0003g0002a0001c0001t0003g0003others(1): Show | 4 | HG02559.hp2 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.508+6975_508+6976d others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 15969920 | |||||
| chr12:15969937
|
C | G | 106 | a0001c0001t0001g0024a0001c0001t0001g0034a0001c0001t0001g0035others(103): Show | 106 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.508+6990C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15969937 | ||||||
| chr12:15970048
|
G | T | 4 | a0001c0001t0001g0008a0001c0001t0003g0002a0001c0001t0003g0003others(1): Show | 4 | HG02559.hp2 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.508+7101G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15970048 | ||||||
| chr12:15970138
|
T | G | 3 | a0001c0001t0001g0129a0001c0003t0001g0073a0001c0003t0004g0072 | 3 | HG02486.hp2 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.508+7191T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15970138 | ||||||
| chr12:15970277
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.508+7330G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15970277 | ||||||
| chr12:15970359
|
C | G | 1 | a0001c0001t0001g0191 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.508+7412C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15970359 | ||||||
| chr12:15970366
|
C | T | 1 | a0001c0001t0003g0009 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.508+7419C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15970366 | ||||||
| chr12:15970421
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.508+7474T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15970421 | ||||||
| chr12:15970540
|
T | A | 176 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(173): Show | 176 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.508+7593T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15970540 | ||||||
| chr12:15970732
|
G | C | 1 | a0001c0001t0001g0032 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.508+7785G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15970732 | ||||||
| chr12:15970732
|
G | T | 188 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(185): Show | 188 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.508+7785G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15970732 | ||||||
| chr12:15971119
|
G | C | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.508+8172G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971119 | ||||||
| chr12:15971120
|
G | A | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.508+8173G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971120 | ||||||
| chr12:15971201
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.508+8254A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971201 | ||||||
| chr12:15971208
|
G | A | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.508+8261G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971208 | ||||||
| chr12:15971275
|
A | G | 158 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0024others(155): Show | 158 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.508+8328A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971275 | ||||||
| chr12:15971346
|
A | G | 3 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0236 | 3 | HG02257.hp2 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.508+8399A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971346 | ||||||
| chr12:15971476
|
G | A | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.508+8529G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971476 | ||||||
| chr12:15971491
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.508+8544A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971491 | ||||||
| chr12:15971498
|
T | G | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.508+8551T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971498 | ||||||
| chr12:15971508
|
CT | C | 28 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0028others(25): Show | 29 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.508+8586delT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 15971508 | |||||
| chr12:15971508
|
CTTTT | C | 102 | a0001c0001t0001g0024a0001c0001t0001g0034a0001c0001t0001g0035others(99): Show | 102 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.508+8583_508+8586d others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 15971508 | |||||
| chr12:15971508
|
CTTTTT | C | 11 | a0001c0001t0001g0038a0001c0001t0001g0065a0001c0001t0001g0066others(8): Show | 11 | HG02074.hp2 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.508+8582_508+8586d others(7): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 15971508 | |||||
| chr12:15971508
|
CTTTTTT | C | 70 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(67): Show | 70 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.508+8581_508+8586d others(8): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 15971508 | |||||
| chr12:15971527
|
T | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0045a0001c0001t0001g0126others(7): Show | 11 | HG00642.hp1 HG01071.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.508+8580T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971527 | ||||||
| chr12:15971529
|
T | G | 3 | a0001c0001t0001g0193a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | NA18967.hp2 NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.508+8582T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971529 | ||||||
| chr12:15971530
|
T | A | 3 | a0001c0001t0001g0193a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | NA18967.hp2 NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.508+8583T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971530 | ||||||
| chr12:15971531
|
T | G | 3 | a0001c0001t0001g0193a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | NA18967.hp2 NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.508+8584T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971531 | ||||||
| chr12:15971532
|
T | A | 3 | a0001c0001t0001g0193a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | NA18967.hp2 NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.508+8585T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971532 | ||||||
| chr12:15971533
|
TGA | T | 3 | a0001c0001t0001g0193a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | NA18967.hp2 NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.508+8589_508+8590d others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 15971533 | |||||
| chr12:15971551
|
T | C | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.508+8604T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971551 | ||||||
| chr12:15971723
|
G | A | 4 | a0001c0001t0001g0008a0001c0001t0003g0002a0001c0001t0003g0003others(1): Show | 4 | HG02559.hp2 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.508+8776G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971723 | ||||||
| chr12:15971758
|
C | T | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.508+8811C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971758 | ||||||
| chr12:15971859
|
G | A | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.508+8912G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15971859 | ||||||
| chr12:15972014
|
C | T | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.508+9067C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15972014 | ||||||
| chr12:15972017
|
G | C | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.508+9070G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15972017 | ||||||
| chr12:15972140
|
G | A | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.508+9193G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15972140 | ||||||
| chr12:15972340
|
C | T | 4 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(1): Show | 4 | HG02257.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.508+9393C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15972340 | ||||||
| chr12:15972436
|
C | T | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.508+9489C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15972436 | ||||||
| chr12:15972488
|
T | C | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.508+9541T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15972488 | ||||||
| chr12:15972506
|
A | AG | 9 | a0001c0001t0001g0085a0001c0001t0003g0009a0001c0001t0003g0011others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.508+9561dupG | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 15972506 | |||||
| chr12:15972638
|
T | C | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.509-9670T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15972638 | ||||||
| chr12:15972662
|
C | T | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.509-9646C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15972662 | ||||||
| chr12:15972711
|
G | A | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.509-9597G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15972711 | ||||||
| chr12:15972718
|
C | T | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.509-9590C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15972718 | ||||||
| chr12:15972836
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.509-9472A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15972836 | ||||||
| chr12:15972886
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.509-9422G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15972886 | ||||||
| chr12:15972987
|
G | A | 1 | a0001c0001t0001g0249 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.509-9321G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15972987 | ||||||
| chr12:15973199
|
T | C | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0247 | 3 | HG02258.hp2 HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.509-9109T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15973199 | ||||||
| chr12:15973215
|
CT | C | 9 | a0001c0001t0001g0085a0001c0001t0003g0009a0001c0001t0003g0011others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.509-9092delT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15973215 | ||||||
| chr12:15973428
|
A | ATAATAGC others(20): Show |
189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.509-8875_509-8874i others(29): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 15973428 | |||||
| chr12:15973444
|
A | G | 3 | a0001c0001t0005g0042a0001c0001t0005g0043a0001c0001t0005g0044 | 3 | HG01109.hp1 HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.509-8864A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15973444 | ||||||
| chr12:15973541
|
G | A | 6 | a0001c0001t0001g0040a0001c0001t0001g0117a0001c0001t0001g0232others(3): Show | 6 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.509-8767G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15973541 | ||||||
| chr12:15973564
|
C | T | 1 | a0001c0001t0003g0013 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.509-8744C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15973564 | ||||||
| chr12:15973683
|
C | G | 1 | a0001c0001t0002g0090 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.509-8625C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15973683 | ||||||
| chr12:15973916
|
T | G | 1 | a0003c0004t0001g0225 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.509-8392T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15973916 | ||||||
| chr12:15973973
|
C | T | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.509-8335C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15973973 | ||||||
| chr12:15974104
|
G | A | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.509-8204G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15974104 | ||||||
| chr12:15974230
|
A | G | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.509-8078A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15974230 | ||||||
| chr12:15974247
|
G | A | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.509-8061G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15974247 | ||||||
| chr12:15974254
|
C | T | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.509-8054C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15974254 | ||||||
| chr12:15974318
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0232 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.509-7990G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15974318 | ||||||
| chr12:15974398
|
T | G | 14 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(11): Show | 14 | HG01109.hp2 HG01891.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.509-7910T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15974398 | ||||||
| chr12:15974417
|
G | A | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.509-7891G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15974417 | ||||||
| chr12:15974516
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0214 | 2 | HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.509-7792C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15974516 | ||||||
| chr12:15974717
|
A | T | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.509-7591A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15974717 | ||||||
| chr12:15974920
|
CCCTT | C | 3 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004 | 3 | HG02559.hp2 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.509-7376_509-7373d others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 15974920 | |||||
| chr12:15974968
|
C | G | 9 | a0001c0001t0001g0085a0001c0001t0003g0009a0001c0001t0003g0011others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.509-7340C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15974968 | ||||||
| chr12:15975035
|
G | A | 5 | a0001c0001t0001g0048a0001c0001t0001g0120a0001c0001t0001g0169others(2): Show | 5 | HG00735.hp2 HG01168.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.509-7273G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15975035 | ||||||
| chr12:15975202
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.509-7106A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15975202 | ||||||
| chr12:15975229
|
G | A | 1 | a0001c0001t0001g0237 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.509-7079G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15975229 | ||||||
| chr12:15975291
|
ATTAT | A | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.509-7014_509-7011d others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 15975291 | |||||
| chr12:15975365
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.509-6943G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15975365 | ||||||
| chr12:15975425
|
A | G | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.509-6883A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15975425 | ||||||
| chr12:15975488
|
G | A | 2 | a0001c0001t0001g0200a0001c0001t0001g0245 | 2 | NA18950.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.509-6820G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15975488 | ||||||
| chr12:15975524
|
C | T | 14 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(11): Show | 14 | HG01109.hp2 HG01891.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.509-6784C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15975524 | ||||||
| chr12:15975743
|
C | T | 10 | a0001c0001t0001g0001a0001c0001t0001g0045a0001c0001t0001g0126others(7): Show | 11 | HG00642.hp1 HG01071.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.509-6565C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15975743 | ||||||
| chr12:15975771
|
T | G | 10 | a0001c0001t0001g0001a0001c0001t0001g0045a0001c0001t0001g0126others(7): Show | 11 | HG00642.hp1 HG01071.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.509-6537T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15975771 | ||||||
| chr12:15975834
|
C | T | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.509-6474C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15975834 | ||||||
| chr12:15975851
|
C | G | 52 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0040others(49): Show | 52 | HG00280.hp1 HG00280.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.509-6457C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15975851 | ||||||
| chr12:15975856
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.509-6452C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15975856 | ||||||
| chr12:15975865
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.509-6443G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15975865 | ||||||
| chr12:15975911
|
CTG | C | 8 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(5): Show | 8 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.509-6395_509-6394d others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 15975911 | |||||
| chr12:15976185
|
C | T | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.509-6123C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15976185 | ||||||
| chr12:15976265
|
A | G | 2 | a0001c0001t0001g0169a0001c0001t0001g0189 | 2 | HG00735.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.509-6043A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15976265 | ||||||
| chr12:15976343
|
G | T | 33 | a0001c0001t0001g0024a0001c0001t0001g0052a0001c0001t0001g0092others(30): Show | 33 | HG02027.hp1 HG02080.hp1 HG02080.hp2 others(30): Show |
intron_variant | MODIFIER | c.509-5965G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15976343 | ||||||
| chr12:15976424
|
T | C | 6 | a0001c0001t0001g0040a0001c0001t0001g0117a0001c0001t0001g0232others(3): Show | 6 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.509-5884T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15976424 | ||||||
| chr12:15976808
|
GA | G | 4 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(1): Show | 4 | HG03130.hp2 HG03471.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.509-5495delA | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 15976808 | |||||
| chr12:15976946
|
G | C | 2 | a0001c0001t0001g0186a0001c0001t0001g0219 | 2 | NA19012.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.509-5362G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15976946 | ||||||
| chr12:15977088
|
C | A | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.509-5220C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15977088 | ||||||
| chr12:15977231
|
G | A | 54 | a0001c0001t0001g0034a0001c0001t0001g0047a0001c0001t0001g0050others(51): Show | 54 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.509-5077G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15977231 | ||||||
| chr12:15977268
|
G | T | 2 | a0002c0002t0003g0018a0002c0002t0003g0020 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.509-5040G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15977268 | ||||||
| chr12:15977299
|
G | A | 119 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(116): Show | 119 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.509-5009G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15977299 | ||||||
| chr12:15977315
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.509-4993G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15977315 | ||||||
| chr12:15977375
|
C | T | 2 | a0002c0002t0003g0018a0002c0002t0003g0020 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.509-4933C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15977375 | ||||||
| chr12:15977646
|
C | T | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.509-4662C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15977646 | ||||||
| chr12:15977826
|
G | A | 3 | a0001c0001t0001g0193a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | NA18967.hp2 NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.509-4482G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15977826 | ||||||
| chr12:15977887
|
A | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0177a0001c0001t0001g0183 | 3 | HG01074.hp1 HG01081.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.509-4421A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15977887 | ||||||
| chr12:15977917
|
A | T | 28 | a0001c0001t0001g0024a0001c0001t0001g0052a0001c0001t0001g0122others(25): Show | 28 | HG02027.hp1 HG02080.hp1 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.509-4391A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15977917 | ||||||
| chr12:15977918
|
T | G | 10 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0003g0009others(7): Show | 10 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.509-4390T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15977918 | ||||||
| chr12:15977947
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.509-4361T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15977947 | ||||||
| chr12:15978008
|
C | T | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.509-4300C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15978008 | ||||||
| chr12:15978023
|
TCCTACCA others(9): Show |
T | 1 | a0001c0001t0001g0025 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.509-4284_509-4269d others(18): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15978023 | ||||||
| chr12:15978040
|
A | T | 1 | a0001c0001t0001g0025 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.509-4268A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15978040 | ||||||
| chr12:15978096
|
T | C | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.509-4212T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15978096 | ||||||
| chr12:15978151
|
A | G | 4 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(1): Show | 4 | HG03130.hp2 HG03471.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.509-4157A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15978151 | ||||||
| chr12:15978194
|
A | G | 1 | a0001c0001t0004g0213 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.509-4114A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15978194 | ||||||
| chr12:15978228
|
A | G | 5 | a0001c0001t0001g0008a0001c0001t0001g0083a0001c0001t0003g0002others(2): Show | 5 | HG02559.hp2 HG02886.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.509-4080A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15978228 | ||||||
| chr12:15978358
|
C | T | 10 | a0001c0001t0001g0001a0001c0001t0001g0045a0001c0001t0001g0126others(7): Show | 11 | HG00642.hp1 HG01071.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.509-3950C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15978358 | ||||||
| chr12:15978370
|
C | T | 7 | a0001c0001t0001g0053a0001c0001t0001g0157a0001c0001t0001g0178others(4): Show | 7 | NA18942.hp1 NA18950.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.509-3938C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15978370 | ||||||
| chr12:15978371
|
G | A | 4 | a0001c0001t0001g0008a0001c0001t0003g0002a0001c0001t0003g0003others(1): Show | 4 | HG02559.hp2 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.509-3937G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15978371 | ||||||
| chr12:15978545
|
C | A | 9 | a0001c0001t0001g0085a0001c0001t0003g0009a0001c0001t0003g0011others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.509-3763C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15978545 | ||||||
| chr12:15978552
|
T | A | 9 | a0001c0001t0001g0085a0001c0001t0003g0009a0001c0001t0003g0011others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.509-3756T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15978552 | ||||||
| chr12:15978792
|
C | G | 7 | a0001c0001t0001g0053a0001c0001t0001g0157a0001c0001t0001g0178others(4): Show | 7 | NA18942.hp1 NA18950.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.509-3516C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15978792 | ||||||
| chr12:15978824
|
C | T | 52 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0040others(49): Show | 52 | HG00280.hp1 HG00280.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.509-3484C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15978824 | ||||||
| chr12:15979077
|
C | T | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.509-3231C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15979077 | ||||||
| chr12:15979196
|
A | G | 3 | a0001c0001t0001g0193a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | NA18967.hp2 NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.509-3112A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15979196 | ||||||
| chr12:15979232
|
G | A | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.509-3076G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15979232 | ||||||
| chr12:15979252
|
C | T | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.509-3056C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15979252 | ||||||
| chr12:15979457
|
G | A | 3 | a0001c0001t0001g0159a0001c0001t0001g0218a0001c0001t0001g0228 | 3 | NA18949.hp1 NA19062.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.509-2851G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15979457 | ||||||
| chr12:15979457
|
G | T | 1 | a0001c0001t0001g0253 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.509-2851G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15979457 | ||||||
| chr12:15979614
|
A | G | 10 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0003g0009others(7): Show | 10 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.509-2694A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15979614 | ||||||
| chr12:15979680
|
G | T | 3 | a0001c0001t0001g0129a0001c0003t0001g0073a0001c0003t0004g0072 | 3 | HG02486.hp2 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.509-2628G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15979680 | ||||||
| chr12:15980100
|
A | G | 8 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(5): Show | 8 | HG01109.hp2 HG01891.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.509-2208A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15980100 | ||||||
| chr12:15980225
|
A | G | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110 | 3 | HG02818.hp1 HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.509-2083A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15980225 | ||||||
| chr12:15980409
|
G | A | 175 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(172): Show | 175 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.509-1899G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15980409 | ||||||
| chr12:15980441
|
T | G | 3 | a0001c0001t0001g0193a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | NA18967.hp2 NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.509-1867T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15980441 | ||||||
| chr12:15980555
|
T | C | 3 | a0001c0001t0001g0193a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | NA18967.hp2 NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.509-1753T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15980555 | ||||||
| chr12:15980577
|
T | A | 7 | a0001c0001t0001g0053a0001c0001t0001g0157a0001c0001t0001g0178others(4): Show | 7 | NA18942.hp1 NA18950.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.509-1731T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15980577 | ||||||
| chr12:15980682
|
A | G | 10 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0003g0009others(7): Show | 10 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.509-1626A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15980682 | ||||||
| chr12:15980706
|
A | G | 10 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0003g0009others(7): Show | 10 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.509-1602A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15980706 | ||||||
| chr12:15980821
|
C | A | 1 | a0001c0001t0002g0138 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.509-1487C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15980821 | ||||||
| chr12:15981086
|
C | T | 10 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0003g0009others(7): Show | 10 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.509-1222C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15981086 | ||||||
| chr12:15981123
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG01123.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.509-1185C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15981123 | ||||||
| chr12:15981158
|
T | C | 2 | a0001c0001t0001g0132a0001c0001t0001g0238 | 2 | HG00280.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.509-1150T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15981158 | ||||||
| chr12:15981396
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.509-912C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15981396 | ||||||
| chr12:15981471
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.509-837C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15981471 | ||||||
| chr12:15981728
|
T | G | 2 | a0002c0002t0003g0018a0002c0002t0003g0020 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.509-580T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15981728 | ||||||
| chr12:15981866
|
C | T | 176 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(173): Show | 176 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.509-442C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15981866 | ||||||
| chr12:15981872
|
A | AT | 256 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(253): Show | 257 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(254): Show |
intron_variant | MODIFIER | c.509-435dupT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 15981872 | |||||
| chr12:15981974
|
C | T | 9 | a0001c0001t0001g0085a0001c0001t0003g0009a0001c0001t0003g0011others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.509-334C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15981974 | ||||||
| chr12:15981983
|
T | G | 9 | a0001c0001t0001g0085a0001c0001t0003g0009a0001c0001t0003g0011others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.509-325T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 5/8 | chr12 | 15981983 | ||||||
| chr12:15982492
|
A | G | 8 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.637+56A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15982492 | ||||||
| chr12:15982565
|
A | G | 9 | a0001c0001t0001g0085a0001c0001t0003g0009a0001c0001t0003g0011others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.637+129A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15982565 | ||||||
| chr12:15982660
|
C | T | 9 | a0001c0001t0001g0085a0001c0001t0003g0009a0001c0001t0003g0011others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.637+224C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15982660 | ||||||
| chr12:15982767
|
A | T | 1 | a0001c0001t0001g0092 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.637+331A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15982767 | ||||||
| chr12:15982770
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.637+334C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15982770 | ||||||
| chr12:15982798
|
C | G | 14 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(11): Show | 14 | HG01109.hp2 HG01891.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.637+362C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15982798 | ||||||
| chr12:15982956
|
A | G | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(5): Show | 8 | HG02257.hp2 HG02630.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.637+520A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15982956 | ||||||
| chr12:15983018
|
G | C | 206 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(203): Show | 206 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.637+582G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15983018 | ||||||
| chr12:15983170
|
T | A | 1 | a0001c0001t0002g0254 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.637+734T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15983170 | ||||||
| chr12:15983443
|
C | T | 4 | a0001c0001t0002g0147a0001c0001t0002g0148a0001c0001t0002g0154others(1): Show | 4 | HG00621.hp1 HG02165.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+1007C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15983443 | ||||||
| chr12:15983516
|
C | T | 3 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004 | 3 | HG02559.hp2 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.637+1080C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15983516 | ||||||
| chr12:15983539
|
G | A | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.637+1103G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15983539 | ||||||
| chr12:15983771
|
T | G | 1 | a0001c0001t0001g0033 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.637+1335T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15983771 | ||||||
| chr12:15983817
|
C | T | 4 | a0001c0001t0001g0202a0001c0001t0001g0223a0001c0001t0001g0231others(1): Show | 4 | NA18971.hp1 NA18978.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+1381C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15983817 | ||||||
| chr12:15983848
|
T | C | 109 | a0001c0001t0001g0024a0001c0001t0001g0034a0001c0001t0001g0035others(106): Show | 109 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.637+1412T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15983848 | ||||||
| chr12:15983903
|
C | T | 4 | a0001c0001t0001g0060a0001c0001t0001g0135a0001c0001t0001g0146others(1): Show | 4 | HG01168.hp1 HG01169.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+1467C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15983903 | ||||||
| chr12:15984023
|
C | G | 1 | a0001c0001t0001g0045 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.637+1587C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15984023 | ||||||
| chr12:15984123
|
T | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0091 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.637+1687T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15984123 | ||||||
| chr12:15984147
|
T | C | 3 | a0001c0001t0001g0193a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | NA18967.hp2 NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.637+1711T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15984147 | ||||||
| chr12:15984277
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0002g0257 | 2 | NA18950.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.637+1841C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15984277 | ||||||
| chr12:15984530
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.637+2094C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15984530 | ||||||
| chr12:15984633
|
T | A | 8 | a0001c0001t0001g0085a0001c0001t0003g0009a0001c0001t0003g0011others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.637+2197T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15984633 | ||||||
| chr12:15984962
|
T | C | 57 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(54): Show | 57 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.637+2526T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15984962 | ||||||
| chr12:15985364
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0174 | 2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.637+2928T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15985364 | ||||||
| chr12:15985575
|
T | C | 2 | a0001c0001t0001g0121a0002c0002t0003g0020 | 2 | HG01934.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.637+3139T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15985575 | ||||||
| chr12:15985581
|
CTTTTCAG others(3): Show |
C | 131 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(128): Show | 131 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.637+3146_637+3155d others(12): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15985581 | ||||||
| chr12:15985595
|
T | A | 1 | a0001c0001t0001g0032 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.637+3159T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15985595 | ||||||
| chr12:15985853
|
G | C | 109 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0026others(106): Show | 109 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.637+3417G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15985853 | ||||||
| chr12:15985869
|
G | A | 2 | a0001c0001t0001g0203a0001c0001t0001g0220 | 2 | HG02015.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.637+3433G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15985869 | ||||||
| chr12:15985872
|
T | C | 31 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0067others(28): Show | 31 | HG00280.hp2 HG00558.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.637+3436T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15985872 | ||||||
| chr12:15985992
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.637+3556C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15985992 | ||||||
| chr12:15986054
|
G | T | 15 | a0001c0001t0001g0051a0001c0001t0001g0060a0001c0001t0001g0081others(12): Show | 15 | HG00558.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.637+3618G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15986054 | ||||||
| chr12:15986386
|
G | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0174others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+3950G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15986386 | ||||||
| chr12:15986453
|
A | G | 3 | a0001c0001t0001g0065a0001c0001t0001g0079a0001c0001t0001g0080 | 3 | HG01884.hp1 HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.637+4017A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15986453 | ||||||
| chr12:15986480
|
C | T | 1 | a0001c0001t0001g0237 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.637+4044C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15986480 | ||||||
| chr12:15986650
|
A | C | 1 | a0001c0001t0002g0185 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.637+4214A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15986650 | ||||||
| chr12:15986668
|
T | A | 5 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(2): Show | 5 | HG03130.hp2 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+4232T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15986668 | ||||||
| chr12:15986704
|
CTT | C | 28 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(25): Show | 28 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+4271_637+4272d others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15986704 | |||||
| chr12:15986782
|
T | C | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | NA18942.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.637+4346T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15986782 | ||||||
| chr12:15986840
|
T | C | 28 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(25): Show | 28 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+4404T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15986840 | ||||||
| chr12:15986869
|
A | C | 5 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0174others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+4433A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15986869 | ||||||
| chr12:15987042
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.637+4606A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15987042 | ||||||
| chr12:15987055
|
C | G | 1 | a0001c0001t0001g0099 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.637+4619C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15987055 | ||||||
| chr12:15987229
|
A | C | 1 | a0001c0001t0003g0004 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.637+4793A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15987229 | ||||||
| chr12:15987230
|
C | CT | 16 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0037others(13): Show | 16 | HG00642.hp2 HG01243.hp1 HG02717.hp2 others(13): Show |
intron_variant | MODIFIER | c.637+4818dupT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15987230 | |||||
| chr12:15987230
|
CT | C | 12 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0047others(9): Show | 12 | HG01071.hp2 HG01358.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.637+4818delT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15987230 | |||||
| chr12:15987230
|
CTTT | C | 10 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(7): Show | 10 | HG01109.hp2 HG02109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.637+4816_637+4818d others(5): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15987230 | |||||
| chr12:15987230
|
CTTTT | C | 18 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0032others(15): Show | 18 | HG01884.hp2 HG02165.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.637+4815_637+4818d others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15987230 | |||||
| chr12:15987384
|
A | G | 28 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(25): Show | 28 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+4948A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15987384 | ||||||
| chr12:15987446
|
G | A | 28 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(25): Show | 28 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+5010G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15987446 | ||||||
| chr12:15987479
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.637+5043C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15987479 | ||||||
| chr12:15987480
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.637+5044G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15987480 | ||||||
| chr12:15987695
|
T | C | 1 | a0001c0001t0003g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.637+5259T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15987695 | ||||||
| chr12:15987829
|
G | A | 8 | a0001c0001t0001g0062a0001c0001t0001g0099a0001c0001t0001g0114others(5): Show | 8 | HG02165.hp2 NA18949.hp2 NA18967.hp1 others(5): Show |
intron_variant | MODIFIER | c.637+5393G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15987829 | ||||||
| chr12:15987865
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.637+5429C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15987865 | ||||||
| chr12:15987921
|
G | T | 28 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(25): Show | 28 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+5485G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15987921 | ||||||
| chr12:15987946
|
C | G | 22 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(19): Show | 22 | HG00621.hp2 HG02027.hp1 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.637+5510C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15987946 | ||||||
| chr12:15987979
|
G | A | 5 | a0001c0001t0001g0034a0001c0001t0001g0214a0001c0001t0003g0005others(2): Show | 5 | HG00733.hp1 HG01934.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+5543G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15987979 | ||||||
| chr12:15988022
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.637+5586G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15988022 | ||||||
| chr12:15988134
|
A | C | 18 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0085others(15): Show | 18 | HG00642.hp1 HG01167.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.637+5698A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15988134 | ||||||
| chr12:15988340
|
G | A | 80 | a0001c0001t0001g0034a0001c0001t0001g0045a0001c0001t0001g0047others(77): Show | 80 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.637+5904G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15988340 | ||||||
| chr12:15988461
|
A | T | 10 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(7): Show | 10 | HG01109.hp2 HG02109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.637+6025A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15988461 | ||||||
| chr12:15988500
|
C | T | 28 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(25): Show | 28 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+6064C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15988500 | ||||||
| chr12:15988505
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.637+6069A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15988505 | ||||||
| chr12:15988508
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.637+6072G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15988508 | ||||||
| chr12:15988615
|
C | T | 73 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(70): Show | 73 | HG00558.hp2 HG00642.hp1 HG01109.hp2 others(70): Show |
intron_variant | MODIFIER | c.637+6179C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15988615 | ||||||
| chr12:15988655
|
T | C | 256 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(253): Show | 257 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(254): Show |
intron_variant | MODIFIER | c.637+6219T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15988655 | ||||||
| chr12:15988656
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0173 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.637+6220G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15988656 | ||||||
| chr12:15988809
|
C | T | 28 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(25): Show | 28 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+6373C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15988809 | ||||||
| chr12:15988868
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.637+6432A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15988868 | ||||||
| chr12:15988927
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.637+6491C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15988927 | ||||||
| chr12:15988941
|
T | C | 28 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(25): Show | 28 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+6505T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15988941 | ||||||
| chr12:15989174
|
G | C | 1 | a0001c0001t0003g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.637+6738G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15989174 | ||||||
| chr12:15989220
|
G | A | 8 | a0001c0001t0001g0136a0001c0001t0001g0143a0001c0001t0001g0167others(5): Show | 8 | HG00544.hp1 HG01496.hp1 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.637+6784G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15989220 | ||||||
| chr12:15989228
|
C | T | 5 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(2): Show | 5 | HG03130.hp2 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+6792C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15989228 | ||||||
| chr12:15989296
|
T | C | 28 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(25): Show | 28 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+6860T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15989296 | ||||||
| chr12:15989316
|
T | A | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(5): Show | 8 | HG02615.hp1 HG02886.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.637+6880T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15989316 | ||||||
| chr12:15989462
|
T | G | 1 | a0001c0001t0001g0129 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.637+7026T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15989462 | ||||||
| chr12:15989633
|
T | C | 28 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(25): Show | 28 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+7197T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15989633 | ||||||
| chr12:15989694
|
A | G | 28 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(25): Show | 28 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+7258A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15989694 | ||||||
| chr12:15989915
|
A | G | 28 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(25): Show | 28 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+7479A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15989915 | ||||||
| chr12:15989982
|
C | T | 28 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(25): Show | 28 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+7546C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15989982 | ||||||
| chr12:15990032
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.637+7596G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15990032 | ||||||
| chr12:15990187
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.637+7751C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15990187 | ||||||
| chr12:15990409
|
C | T | 2 | a0001c0001t0001g0211a0001c0001t0003g0017 | 2 | HG02647.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.637+7973C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15990409 | ||||||
| chr12:15990410
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.637+7974G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15990410 | ||||||
| chr12:15990425
|
C | T | 28 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(25): Show | 28 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+7989C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15990425 | ||||||
| chr12:15990427
|
T | G | 1 | a0001c0001t0005g0041 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.637+7991T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15990427 | ||||||
| chr12:15990635
|
T | C | 3 | a0001c0001t0001g0118a0001c0001t0001g0132a0001c0001t0001g0218 | 3 | HG00280.hp1 NA18949.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.637+8199T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15990635 | ||||||
| chr12:15990779
|
A | T | 4 | a0001c0001t0001g0024a0001c0001t0001g0113a0001c0001t0001g0127others(1): Show | 4 | NA18964.hp1 NA18989.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+8343A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15990779 | ||||||
| chr12:15990802
|
G | A | 1 | a0001c0001t0001g0024 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.637+8366G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15990802 | ||||||
| chr12:15990871
|
C | G | 72 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(69): Show | 72 | HG00642.hp1 HG01109.hp2 HG01167.hp1 others(69): Show |
intron_variant | MODIFIER | c.637+8435C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15990871 | ||||||
| chr12:15990892
|
G | A | 30 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(27): Show | 30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+8456G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15990892 | ||||||
| chr12:15991159
|
G | A | 2 | a0001c0001t0001g0120a0001c0001t0001g0140 | 2 | HG01168.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.637+8723G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15991159 | ||||||
| chr12:15991191
|
C | T | 30 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(27): Show | 30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+8755C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15991191 | ||||||
| chr12:15991214
|
T | A | 1 | a0001c0001t0004g0213 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.637+8778T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15991214 | ||||||
| chr12:15991703
|
T | C | 24 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026others(21): Show | 24 | HG01109.hp2 HG02109.hp1 HG02165.hp2 others(21): Show |
intron_variant | MODIFIER | c.637+9267T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15991703 | ||||||
| chr12:15991704
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.637+9268C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15991704 | ||||||
| chr12:15991899
|
C | T | 1 | a0001c0001t0003g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.637+9463C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15991899 | ||||||
| chr12:15991949
|
A | AATTTTAT others(20): Show |
1 | a0001c0001t0001g0118 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.637+9514_637+9515i others(29): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15991949 | |||||
| chr12:15991951
|
C | A | 1 | a0001c0001t0001g0118 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.637+9515C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15991951 | ||||||
| chr12:15992061
|
C | T | 29 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(26): Show | 29 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.637+9625C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15992061 | ||||||
| chr12:15992069
|
A | AT | 46 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026others(43): Show | 46 | HG00558.hp2 HG01109.hp2 HG01168.hp1 others(43): Show |
intron_variant | MODIFIER | c.637+9647dupT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15992069 | |||||
| chr12:15992318
|
T | A | 4 | a0001c0001t0001g0107a0001c0001t0001g0128a0001c0001t0001g0160others(1): Show | 4 | NA18943.hp1 NA18954.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+9882T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15992318 | ||||||
| chr12:15992322
|
A | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0229 | 2 | NA18943.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.637+9886A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15992322 | ||||||
| chr12:15992330
|
G | A | 29 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(26): Show | 29 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.637+9894G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15992330 | ||||||
| chr12:15992586
|
A | C | 1 | a0001c0001t0001g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.637+10150A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15992586 | ||||||
| chr12:15993060
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.637+10624C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15993060 | ||||||
| chr12:15993256
|
T | TA | 30 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(27): Show | 30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+10827dupA | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15993256 | |||||
| chr12:15993264
|
T | A | 1 | a0001c0001t0001g0111 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.637+10828T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15993264 | ||||||
| chr12:15993444
|
C | G | 1 | a0001c0001t0001g0219 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.637+11008C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15993444 | ||||||
| chr12:15993480
|
C | CT | 17 | a0001c0001t0001g0060a0001c0001t0001g0081a0001c0001t0001g0094others(14): Show | 17 | HG01168.hp1 HG01169.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.637+11059dupT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15993480 | |||||
| chr12:15993480
|
CT | C | 10 | a0001c0001t0001g0085a0001c0001t0001g0099a0001c0001t0001g0103others(7): Show | 10 | HG01516.hp2 HG02273.hp1 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.637+11059delT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15993480 | |||||
| chr12:15993480
|
CTT | C | 5 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(2): Show | 5 | HG03130.hp2 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+11058_637+1105 others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15993480 | |||||
| chr12:15993492
|
T | A | 1 | a0001c0001t0001g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.637+11056T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15993492 | ||||||
| chr12:15993493
|
T | A | 26 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026others(23): Show | 26 | HG01109.hp2 HG02109.hp1 HG02165.hp2 others(23): Show |
intron_variant | MODIFIER | c.637+11057T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15993493 | ||||||
| chr12:15993494
|
T | A | 29 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(26): Show | 29 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.637+11058T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15993494 | ||||||
| chr12:15993495
|
T | A | 42 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(39): Show | 42 | HG01109.hp2 HG01358.hp2 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.637+11059T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15993495 | ||||||
| chr12:15993496
|
A | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0190 | 2 | HG02300.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.637+11060A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15993496 | ||||||
| chr12:15993634
|
C | A | 30 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(27): Show | 30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+11198C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15993634 | ||||||
| chr12:15993710
|
C | T | 5 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(2): Show | 5 | HG03130.hp2 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+11274C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15993710 | ||||||
| chr12:15993745
|
C | A | 1 | a0001c0001t0001g0033 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.637+11309C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15993745 | ||||||
| chr12:15993822
|
G | A | 15 | a0001c0001t0001g0051a0001c0001t0001g0060a0001c0001t0001g0081others(12): Show | 15 | HG00558.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.637+11386G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15993822 | ||||||
| chr12:15993978
|
A | G | 1 | a0001c0001t0004g0116 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.637+11542A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15993978 | ||||||
| chr12:15994202
|
A | G | 33 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(30): Show | 33 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.637+11766A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15994202 | ||||||
| chr12:15994204
|
A | C | 29 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(26): Show | 29 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.637+11768A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15994204 | ||||||
| chr12:15994438
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.637+12002G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15994438 | ||||||
| chr12:15994499
|
G | A | 29 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(26): Show | 29 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.637+12063G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15994499 | ||||||
| chr12:15994614
|
T | C | 48 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(45): Show | 48 | HG00558.hp2 HG01109.hp2 HG01168.hp1 others(45): Show |
intron_variant | MODIFIER | c.637+12178T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15994614 | ||||||
| chr12:15994692
|
A | C | 5 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(2): Show | 5 | HG03130.hp2 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+12256A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15994692 | ||||||
| chr12:15994705
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.637+12269G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15994705 | ||||||
| chr12:15994819
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.637+12383A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15994819 | ||||||
| chr12:15994821
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.637+12385A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15994821 | ||||||
| chr12:15994926
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.637+12490G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15994926 | ||||||
| chr12:15995379
|
G | A | 10 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(7): Show | 10 | HG01109.hp2 HG02109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.637+12943G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15995379 | ||||||
| chr12:15995416
|
T | C | 30 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(27): Show | 30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+12980T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15995416 | ||||||
| chr12:15995517
|
G | A | 5 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(2): Show | 5 | HG03130.hp2 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+13081G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15995517 | ||||||
| chr12:15995871
|
C | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(208): Show | 212 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.637+13435C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15995871 | ||||||
| chr12:15996013
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.637+13577C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15996013 | ||||||
| chr12:15996087
|
T | A | 30 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(27): Show | 30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+13651T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15996087 | ||||||
| chr12:15996105
|
T | C | 30 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(27): Show | 30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+13669T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15996105 | ||||||
| chr12:15996106
|
A | G | 1 | a0001c0001t0001g0233 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.637+13670A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15996106 | ||||||
| chr12:15996157
|
A | ATG | 37 | a0001c0001t0001g0045a0001c0001t0001g0059a0001c0001t0001g0064others(34): Show | 37 | HG00438.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.637+13755_637+1375 others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15996157 | |||||
| chr12:15996157
|
A | ATGTG | 10 | a0001c0001t0001g0094a0001c0001t0001g0126a0001c0001t0001g0190others(7): Show | 10 | HG00438.hp2 HG01071.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.637+13753_637+1375 others(8): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15996157 | |||||
| chr12:15996157
|
ATG | A | 92 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0024others(89): Show | 92 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.637+13755_637+1375 others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15996157 | |||||
| chr12:15996157
|
ATGTG | A | 4 | a0001c0001t0001g0083a0001c0001t0001g0208a0001c0001t0001g0247others(1): Show | 4 | HG02615.hp1 HG02886.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+13753_637+1375 others(8): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15996157 | |||||
| chr12:15996157
|
ATGTGTGT others(1): Show |
A | 14 | a0001c0001t0001g0060a0001c0001t0001g0081a0001c0001t0001g0098others(11): Show | 14 | HG01168.hp1 HG01169.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.637+13749_637+1375 others(12): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15996157 | |||||
| chr12:15996157
|
ATGTGTGT others(5): Show |
A | 2 | a0001c0001t0001g0008a0001c0001t0001g0108 | 2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.637+13745_637+1375 others(16): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15996157 | |||||
| chr12:15996157
|
ATGTGTGT others(7): Show |
A | 28 | a0001c0001t0001g0006a0001c0001t0001g0025a0001c0001t0001g0026others(25): Show | 28 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.637+13743_637+1375 others(18): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15996157 | |||||
| chr12:15996330
|
G | A | 30 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(27): Show | 30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+13894G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15996330 | ||||||
| chr12:15996355
|
G | A | 1 | a0002c0002t0003g0020 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.637+13919G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15996355 | ||||||
| chr12:15996401
|
T | C | 79 | a0001c0001t0001g0034a0001c0001t0001g0045a0001c0001t0001g0047others(76): Show | 79 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.637+13965T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15996401 | ||||||
| chr12:15996676
|
C | A | 14 | a0001c0001t0001g0060a0001c0001t0001g0081a0001c0001t0001g0098others(11): Show | 14 | HG01168.hp1 HG01169.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.637+14240C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15996676 | ||||||
| chr12:15996685
|
G | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0075 | 2 | NA18939.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.637+14249G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15996685 | ||||||
| chr12:15996737
|
A | T | 14 | a0001c0001t0001g0060a0001c0001t0001g0081a0001c0001t0001g0098others(11): Show | 14 | HG01168.hp1 HG01169.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.637+14301A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15996737 | ||||||
| chr12:15996805
|
T | G | 30 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(27): Show | 30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+14369T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15996805 | ||||||
| chr12:15996845
|
A | G | 30 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(27): Show | 30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+14409A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15996845 | ||||||
| chr12:15996935
|
A | G | 30 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(27): Show | 30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+14499A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15996935 | ||||||
| chr12:15997229
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.637+14793A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15997229 | ||||||
| chr12:15997298
|
ATTTC | A | 10 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(7): Show | 10 | HG01109.hp2 HG02109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.637+14866_637+1486 others(8): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15997298 | |||||
| chr12:15997360
|
A | T | 1 | a0001c0001t0001g0174 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.637+14924A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15997360 | ||||||
| chr12:15997386
|
T | A | 30 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(27): Show | 30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+14950T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15997386 | ||||||
| chr12:15997504
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.637+15068C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15997504 | ||||||
| chr12:15997555
|
G | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0031 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.637+15119G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15997555 | ||||||
| chr12:15997578
|
G | A | 14 | a0001c0001t0001g0060a0001c0001t0001g0081a0001c0001t0001g0098others(11): Show | 14 | HG01168.hp1 HG01169.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.637+15142G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15997578 | ||||||
| chr12:15997588
|
G | A | 30 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(27): Show | 30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+15152G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15997588 | ||||||
| chr12:15997592
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.637+15156C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15997592 | ||||||
| chr12:15997653
|
C | CTCT | 29 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(26): Show | 29 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.637+15219_637+1522 others(7): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15997653 | |||||
| chr12:15997661
|
A | T | 29 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(26): Show | 29 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.637+15225A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15997661 | ||||||
| chr12:15997662
|
A | T | 29 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(26): Show | 29 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.637+15226A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15997662 | ||||||
| chr12:15997715
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.637+15279C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15997715 | ||||||
| chr12:15997974
|
C | T | 29 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(26): Show | 29 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.637+15538C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15997974 | ||||||
| chr12:15998083
|
C | T | 1 | a0002c0002t0003g0020 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.637+15647C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998083 | ||||||
| chr12:15998112
|
G | A | 30 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(27): Show | 30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+15676G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998112 | ||||||
| chr12:15998311
|
CTTTATTT others(1): Show |
C | 30 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(27): Show | 30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+15892_637+1589 others(12): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 15998311 | |||||
| chr12:15998394
|
G | A | 30 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(27): Show | 30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+15958G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998394 | ||||||
| chr12:15998403
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.637+15967C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998403 | ||||||
| chr12:15998422
|
G | A | 30 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(27): Show | 30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+15986G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998422 | ||||||
| chr12:15998429
|
C | T | 30 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(27): Show | 30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+15993C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998429 | ||||||
| chr12:15998474
|
T | C | 30 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(27): Show | 30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+16038T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998474 | ||||||
| chr12:15998478
|
C | T | 4 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(1): Show | 4 | HG03130.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+16042C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998478 | ||||||
| chr12:15998523
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.637+16087G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998523 | ||||||
| chr12:15998566
|
C | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0174others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+16130C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998566 | ||||||
| chr12:15998579
|
T | A | 30 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(27): Show | 30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+16143T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998579 | ||||||
| chr12:15998675
|
G | A | 30 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(27): Show | 30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+16239G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998675 | ||||||
| chr12:15998696
|
T | G | 30 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(27): Show | 30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+16260T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998696 | ||||||
| chr12:15998754
|
A | G | 42 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0028others(39): Show | 42 | HG00642.hp1 HG01167.hp1 HG01168.hp1 others(39): Show |
intron_variant | MODIFIER | c.637+16318A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998754 | ||||||
| chr12:15998780
|
T | G | 1 | a0001c0001t0001g0048 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.637+16344T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998780 | ||||||
| chr12:15998807
|
A | C | 1 | a0001c0001t0001g0219 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.637+16371A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998807 | ||||||
| chr12:15998872
|
T | G | 1 | a0001c0001t0001g0033 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.637+16436T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998872 | ||||||
| chr12:15998898
|
C | T | 1 | a0001c0001t0001g0223 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.637+16462C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998898 | ||||||
| chr12:15998938
|
T | C | 30 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(27): Show | 30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+16502T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15998938 | ||||||
| chr12:15999080
|
G | A | 2 | a0001c0001t0001g0207a0001c0001t0003g0012 | 2 | HG02258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.637+16644G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15999080 | ||||||
| chr12:15999235
|
T | G | 30 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(27): Show | 30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+16799T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15999235 | ||||||
| chr12:15999244
|
C | T | 1 | a0001c0001t0001g0179 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.637+16808C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15999244 | ||||||
| chr12:15999288
|
G | C | 1 | a0001c0001t0002g0254 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.637+16852G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15999288 | ||||||
| chr12:15999475
|
A | T | 4 | a0001c0001t0001g0036a0001c0001t0001g0057a0001c0001t0001g0115others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+17039A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15999475 | ||||||
| chr12:15999548
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.637+17112G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15999548 | ||||||
| chr12:15999722
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.637+17286C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 15999722 | ||||||
| chr12:16000025
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.637+17589T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16000025 | ||||||
| chr12:16000172
|
C | T | 29 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(26): Show | 29 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.637+17736C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16000172 | ||||||
| chr12:16000191
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.637+17755C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16000191 | ||||||
| chr12:16000269
|
C | T | 30 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(27): Show | 30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+17833C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16000269 | ||||||
| chr12:16000434
|
C | T | 30 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(27): Show | 30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+17998C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16000434 | ||||||
| chr12:16000535
|
G | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0164 | 2 | HG02698.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.637+18099G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16000535 | ||||||
| chr12:16000598
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.637+18162C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16000598 | ||||||
| chr12:16000624
|
G | A | 30 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(27): Show | 30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+18188G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16000624 | ||||||
| chr12:16000632
|
A | C | 30 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(27): Show | 30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+18196A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16000632 | ||||||
| chr12:16000708
|
C | T | 30 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0025others(27): Show | 30 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.637+18272C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16000708 | ||||||
| chr12:16000852
|
GT | G | 19 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0055others(16): Show | 20 | HG00738.hp2 HG01070.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.637+18425delT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16000852 | |||||
| chr12:16000854
|
T | G | 19 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0055others(16): Show | 20 | HG00738.hp2 HG01070.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.637+18418T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16000854 | ||||||
| chr12:16000958
|
C | T | 24 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026others(21): Show | 24 | HG01109.hp2 HG02109.hp1 HG02165.hp2 others(21): Show |
intron_variant | MODIFIER | c.637+18522C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16000958 | ||||||
| chr12:16001161
|
C | T | 2 | a0001c0001t0001g0135a0001c0001t0001g0146 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.637+18725C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16001161 | ||||||
| chr12:16001200
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0005g0043 | 2 | HG02055.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.637+18764C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16001200 | ||||||
| chr12:16001304
|
G | T | 20 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0059others(17): Show | 20 | HG00642.hp1 HG01167.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.637+18868G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16001304 | ||||||
| chr12:16001417
|
G | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0174others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+18981G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16001417 | ||||||
| chr12:16001505
|
A | G | 1 | a0002c0002t0003g0020 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.637+19069A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16001505 | ||||||
| chr12:16001830
|
C | T | 1 | a0001c0001t0003g0004 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.637+19394C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16001830 | ||||||
| chr12:16002100
|
C | T | 18 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0093others(15): Show | 18 | HG00280.hp2 HG00558.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.637+19664C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16002100 | ||||||
| chr12:16002204
|
A | G | 4 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(1): Show | 4 | HG03130.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+19768A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16002204 | ||||||
| chr12:16002342
|
AC | A | 61 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0050others(58): Show | 61 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.637+19908delC | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16002342 | |||||
| chr12:16002349
|
G | A | 61 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0050others(58): Show | 61 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.637+19913G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16002349 | ||||||
| chr12:16002509
|
T | C | 39 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0021others(36): Show | 39 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.637+20073T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16002509 | ||||||
| chr12:16002682
|
T | A | 1 | a0001c0001t0001g0035 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.637+20246T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16002682 | ||||||
| chr12:16002687
|
T | C | 118 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0045others(115): Show | 118 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.637+20251T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16002687 | ||||||
| chr12:16002872
|
C | A | 1 | a0001c0001t0005g0043 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.637+20436C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16002872 | ||||||
| chr12:16002895
|
A | C | 1 | a0001c0001t0003g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.637+20459A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16002895 | ||||||
| chr12:16002983
|
C | A | 2 | a0001c0001t0002g0138a0001c0001t0002g0257 | 2 | NA18747.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.637+20547C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16002983 | ||||||
| chr12:16003105
|
A | G | 47 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0021others(44): Show | 47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.637+20669A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16003105 | ||||||
| chr12:16003114
|
GT | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0174 | 3 | HG01884.hp2 HG02258.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.637+20682delT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16003114 | |||||
| chr12:16003196
|
C | T | 1 | a0001c0001t0004g0089 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.637+20760C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16003196 | ||||||
| chr12:16003297
|
G | C | 47 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0021others(44): Show | 47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.637+20861G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16003297 | ||||||
| chr12:16003508
|
G | A | 1 | a0001c0001t0002g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.637+21072G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16003508 | ||||||
| chr12:16003518
|
C | T | 50 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0021others(47): Show | 50 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(47): Show |
intron_variant | MODIFIER | c.637+21082C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16003518 | ||||||
| chr12:16003538
|
CTG | C | 10 | a0001c0001t0001g0024a0001c0001t0001g0061a0001c0001t0001g0075others(7): Show | 10 | HG02015.hp1 HG02132.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.637+21105_637+2110 others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16003538 | |||||
| chr12:16003547
|
G | C | 1 | a0001c0001t0001g0035 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.637+21111G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16003547 | ||||||
| chr12:16003578
|
G | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0174 | 3 | HG01884.hp2 HG02258.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.637+21142G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16003578 | ||||||
| chr12:16003670
|
T | C | 163 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(160): Show | 163 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.637+21234T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16003670 | ||||||
| chr12:16003922
|
C | T | 9 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0084others(6): Show | 9 | HG01884.hp2 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.637+21486C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16003922 | ||||||
| chr12:16003933
|
C | G | 1 | a0001c0001t0001g0082 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.637+21497C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16003933 | ||||||
| chr12:16004114
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.637+21678T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16004114 | ||||||
| chr12:16004158
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.637+21722T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16004158 | ||||||
| chr12:16004363
|
A | AATCC | 47 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0021others(44): Show | 47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.637+21928_637+2192 others(8): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16004363 | |||||
| chr12:16004365
|
C | A | 47 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0021others(44): Show | 47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.637+21929C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16004365 | ||||||
| chr12:16004384
|
T | TC | 50 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0021others(47): Show | 50 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(47): Show |
intron_variant | MODIFIER | c.637+21948_637+2194 others(5): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16004384 | ||||||
| chr12:16004857
|
A | G | 4 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(1): Show | 4 | HG03130.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+22421A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16004857 | ||||||
| chr12:16005192
|
C | A | 10 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(7): Show | 10 | HG01109.hp2 HG02109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.637+22756C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16005192 | ||||||
| chr12:16005224
|
G | A | 1 | a0001c0001t0004g0116 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.637+22788G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16005224 | ||||||
| chr12:16005763
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0003g0012 | 2 | HG01891.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.637+23327G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16005763 | ||||||
| chr12:16005991
|
A | G | 2 | a0001c0001t0001g0223a0001c0001t0001g0231 | 2 | NA18971.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.637+23555A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16005991 | ||||||
| chr12:16006083
|
G | C | 1 | a0001c0001t0001g0077 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.637+23647G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16006083 | ||||||
| chr12:16006181
|
C | T | 4 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(1): Show | 4 | HG02818.hp1 HG02895.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+23745C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16006181 | ||||||
| chr12:16006227
|
T | C | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.637+23791T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16006227 | ||||||
| chr12:16006274
|
CCAG | C | 47 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0021others(44): Show | 47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.637+23839_637+2384 others(7): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16006274 | ||||||
| chr12:16006324
|
C | T | 1 | a0001c0001t0001g0186 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.637+23888C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16006324 | ||||||
| chr12:16006471
|
G | A | 2 | a0001c0001t0001g0205a0001c0001t0001g0226 | 2 | HG01358.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.637+24035G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16006471 | ||||||
| chr12:16006489
|
G | A | 2 | a0001c0001t0001g0211a0001c0001t0003g0017 | 2 | HG02647.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.637+24053G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16006489 | ||||||
| chr12:16006529
|
C | G | 1 | a0001c0001t0001g0131 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.637+24093C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16006529 | ||||||
| chr12:16006557
|
C | T | 10 | a0001c0001t0001g0024a0001c0001t0001g0061a0001c0001t0001g0075others(7): Show | 10 | HG02015.hp1 HG02132.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.637+24121C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16006557 | ||||||
| chr12:16006578
|
G | A | 3 | a0001c0001t0001g0083a0001c0001t0001g0208a0001c0001t0001g0247 | 3 | HG02615.hp1 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.637+24142G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16006578 | ||||||
| chr12:16006633
|
C | A | 47 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0021others(44): Show | 47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.637+24197C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16006633 | ||||||
| chr12:16006664
|
C | G | 48 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(45): Show | 48 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(45): Show |
intron_variant | MODIFIER | c.637+24228C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16006664 | ||||||
| chr12:16006763
|
G | T | 1 | a0001c0001t0002g0097 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.637+24327G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16006763 | ||||||
| chr12:16006963
|
G | T | 47 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0021others(44): Show | 47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.637+24527G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16006963 | ||||||
| chr12:16007027
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.637+24591C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16007027 | ||||||
| chr12:16007175
|
G | GT | 11 | a0001c0001t0001g0198a0001c0001t0001g0245a0001c0001t0002g0056others(8): Show | 11 | HG00621.hp1 HG02027.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.637+24752dupT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16007175 | |||||
| chr12:16007175
|
GT | G | 5 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(2): Show | 5 | HG02630.hp2 HG03130.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+24752delT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16007175 | |||||
| chr12:16007189
|
G | GT | 6 | a0001c0001t0001g0007a0001c0001t0001g0135a0001c0001t0001g0146others(3): Show | 6 | HG01123.hp1 HG01168.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.637+24765dupT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16007189 | |||||
| chr12:16007189
|
G | T | 7 | a0001c0001t0001g0083a0001c0001t0001g0087a0001c0001t0001g0088others(4): Show | 7 | HG02257.hp2 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.637+24753G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16007189 | ||||||
| chr12:16007189
|
GT | G | 46 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0021others(43): Show | 46 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(43): Show |
intron_variant | MODIFIER | c.637+24765delT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16007189 | |||||
| chr12:16007190
|
T | G | 7 | a0001c0001t0001g0083a0001c0001t0001g0087a0001c0001t0001g0088others(4): Show | 7 | HG02257.hp2 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.637+24754T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16007190 | ||||||
| chr12:16007255
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.637+24819C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16007255 | ||||||
| chr12:16007260
|
T | G | 19 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0032others(16): Show | 19 | HG01884.hp2 HG02015.hp1 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.637+24824T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16007260 | ||||||
| chr12:16007290
|
T | G | 1 | a0001c0001t0001g0170 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.637+24854T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16007290 | ||||||
| chr12:16007380
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.637+24944C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16007380 | ||||||
| chr12:16007702
|
G | A | 86 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0045others(83): Show | 86 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.638-24840G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16007702 | ||||||
| chr12:16007842
|
GTGTTT | G | 50 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(47): Show | 51 | HG00558.hp1 HG00733.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.638-24676_638-2467 others(9): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16007842 | |||||
| chr12:16008223
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.638-24319C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16008223 | ||||||
| chr12:16008305
|
C | G | 1 | a0001c0001t0001g0007 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.638-24237C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16008305 | ||||||
| chr12:16008319
|
A | G | 28 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0025others(25): Show | 28 | HG01109.hp2 HG01167.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.638-24223A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16008319 | ||||||
| chr12:16008402
|
G | T | 47 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0021others(44): Show | 47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.638-24140G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16008402 | ||||||
| chr12:16008520
|
C | G | 103 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0045others(100): Show | 103 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.638-24022C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16008520 | ||||||
| chr12:16008634
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.638-23908G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16008634 | ||||||
| chr12:16009365
|
T | A | 1 | a0001c0001t0001g0007 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.638-23177T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16009365 | ||||||
| chr12:16009440
|
A | C | 6 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(3): Show | 6 | HG02630.hp2 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.638-23102A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16009440 | ||||||
| chr12:16010093
|
A | G | 47 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0021others(44): Show | 47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.638-22449A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16010093 | ||||||
| chr12:16010140
|
T | G | 1 | a0001c0001t0001g0199 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.638-22402T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16010140 | ||||||
| chr12:16010268
|
T | A | 2 | a0001c0001t0003g0011a0002c0002t0003g0020 | 2 | HG02630.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.638-22274T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16010268 | ||||||
| chr12:16010356
|
T | A | 10 | a0001c0001t0001g0024a0001c0001t0001g0061a0001c0001t0001g0075others(7): Show | 10 | HG02015.hp1 HG02132.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.638-22186T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16010356 | ||||||
| chr12:16010449
|
C | T | 103 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0045others(100): Show | 103 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.638-22093C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16010449 | ||||||
| chr12:16010500
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.638-22042C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16010500 | ||||||
| chr12:16010527
|
C | T | 10 | a0001c0001t0001g0024a0001c0001t0001g0061a0001c0001t0001g0075others(7): Show | 10 | HG02015.hp1 HG02132.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.638-22015C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16010527 | ||||||
| chr12:16010570
|
G | A | 1 | a0001c0001t0003g0013 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.638-21972G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16010570 | ||||||
| chr12:16010705
|
A | G | 2 | a0001c0001t0001g0209a0001c0001t0002g0090 | 2 | HG02293.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.638-21837A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16010705 | ||||||
| chr12:16010711
|
T | C | 6 | a0001c0001t0001g0083a0001c0001t0001g0087a0001c0001t0001g0088others(3): Show | 6 | HG02257.hp2 HG02615.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.638-21831T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16010711 | ||||||
| chr12:16010754
|
T | C | 10 | a0001c0001t0001g0024a0001c0001t0001g0061a0001c0001t0001g0075others(7): Show | 10 | HG02015.hp1 HG02132.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.638-21788T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16010754 | ||||||
| chr12:16010885
|
CACTTATC others(27): Show |
C | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0236 | 3 | HG02257.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.638-21655_638-2162 others(38): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16010885 | |||||
| chr12:16011175
|
G | C | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0236 | 3 | HG02257.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.638-21367G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16011175 | ||||||
| chr12:16011176
|
T | C | 1 | a0001c0001t0001g0053 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.638-21366T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16011176 | ||||||
| chr12:16011182
|
T | G | 1 | a0001c0001t0001g0237 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.638-21360T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16011182 | ||||||
| chr12:16011266
|
T | C | 47 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0021others(44): Show | 47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.638-21276T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16011266 | ||||||
| chr12:16011696
|
A | G | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0236 | 3 | HG02257.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.638-20846A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16011696 | ||||||
| chr12:16012006
|
G | GA | 47 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0021others(44): Show | 47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.638-20530dupA | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16012006 | |||||
| chr12:16012086
|
G | C | 1 | a0001c0001t0001g0035 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.638-20456G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16012086 | ||||||
| chr12:16012213
|
A | G | 1 | a0001c0001t0004g0213 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.638-20329A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16012213 | ||||||
| chr12:16012280
|
A | G | 16 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0095others(13): Show | 16 | HG00558.hp1 HG00735.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.638-20262A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16012280 | ||||||
| chr12:16012331
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.638-20211C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16012331 | ||||||
| chr12:16012378
|
A | G | 4 | a0001c0001t0001g0084a0001c0001t0004g0089a0001c0001t0004g0116others(1): Show | 4 | HG02559.hp1 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-20164A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16012378 | ||||||
| chr12:16012559
|
G | A | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0236 | 3 | HG02257.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.638-19983G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16012559 | ||||||
| chr12:16012629
|
A | G | 1 | a0001c0001t0003g0004 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.638-19913A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16012629 | ||||||
| chr12:16013146
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.638-19396G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16013146 | ||||||
| chr12:16013334
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.638-19208A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16013334 | ||||||
| chr12:16013365
|
G | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0164 | 2 | HG02698.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.638-19177G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16013365 | ||||||
| chr12:16013431
|
T | C | 6 | a0001c0001t0001g0083a0001c0001t0001g0087a0001c0001t0001g0088others(3): Show | 6 | HG02257.hp2 HG02615.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.638-19111T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16013431 | ||||||
| chr12:16013482
|
A | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0081 | 2 | HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.638-19060A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16013482 | ||||||
| chr12:16013511
|
C | T | 47 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0021others(44): Show | 47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.638-19031C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16013511 | ||||||
| chr12:16013958
|
C | T | 53 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0021others(50): Show | 53 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(50): Show |
intron_variant | MODIFIER | c.638-18584C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16013958 | ||||||
| chr12:16013973
|
G | C | 1 | a0001c0001t0001g0175 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.638-18569G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16013973 | ||||||
| chr12:16014246
|
C | T | 9 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0084others(6): Show | 9 | HG01884.hp2 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.638-18296C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16014246 | ||||||
| chr12:16014258
|
T | C | 3 | a0001c0001t0001g0083a0001c0001t0001g0208a0001c0001t0001g0247 | 3 | HG02615.hp1 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.638-18284T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16014258 | ||||||
| chr12:16014428
|
T | C | 1 | a0001c0001t0001g0238 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.638-18114T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16014428 | ||||||
| chr12:16014480
|
G | C | 1 | a0001c0001t0001g0166 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.638-18062G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16014480 | ||||||
| chr12:16014545
|
G | A | 14 | a0001c0001t0001g0021a0001c0001t0001g0062a0001c0001t0001g0099others(11): Show | 14 | HG01167.hp2 HG02165.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.638-17997G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16014545 | ||||||
| chr12:16014560
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.638-17982C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16014560 | ||||||
| chr12:16014840
|
T | C | 47 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0021others(44): Show | 47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.638-17702T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16014840 | ||||||
| chr12:16014841
|
G | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0174others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.638-17701G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16014841 | ||||||
| chr12:16015414
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.638-17128G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16015414 | ||||||
| chr12:16015508
|
C | A | 2 | a0001c0001t0001g0118a0001c0001t0001g0246 | 2 | NA18968.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.638-17034C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16015508 | ||||||
| chr12:16015556
|
T | C | 1 | a0001c0001t0003g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.638-16986T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16015556 | ||||||
| chr12:16015582
|
C | A | 47 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0021others(44): Show | 47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.638-16960C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16015582 | ||||||
| chr12:16015687
|
T | A | 1 | a0001c0001t0001g0007 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.638-16855T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16015687 | ||||||
| chr12:16015794
|
C | G | 1 | a0001c0001t0002g0188 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.638-16748C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16015794 | ||||||
| chr12:16015795
|
A | G | 5 | a0001c0001t0001g0036a0001c0001t0001g0057a0001c0001t0001g0087others(2): Show | 5 | HG02647.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.638-16747A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16015795 | ||||||
| chr12:16015865
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.638-16677T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16015865 | ||||||
| chr12:16015899
|
T | G | 1 | a0002c0002t0003g0020 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.638-16643T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16015899 | ||||||
| chr12:16015934
|
T | A | 1 | a0001c0001t0001g0226 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.638-16608T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16015934 | ||||||
| chr12:16016097
|
A | T | 162 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(159): Show | 162 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.638-16445A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16016097 | ||||||
| chr12:16016353
|
T | C | 2 | a0001c0001t0001g0163a0001c0001t0001g0166 | 2 | HG00642.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.638-16189T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16016353 | ||||||
| chr12:16016569
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.638-15973G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16016569 | ||||||
| chr12:16016594
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.638-15948G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16016594 | ||||||
| chr12:16016791
|
C | CA | 80 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0024others(77): Show | 81 | HG00558.hp1 HG00621.hp2 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.638-15724dupA | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16016791 | |||||
| chr12:16016791
|
C | CAA | 21 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0036others(18): Show | 21 | HG01978.hp1 HG02109.hp1 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.638-15725_638-1572 others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16016791 | |||||
| chr12:16016791
|
C | CAAA | 8 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0030others(5): Show | 8 | HG01109.hp2 HG02486.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.638-15726_638-1572 others(7): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16016791 | |||||
| chr12:16016791
|
CA | C | 68 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0034others(65): Show | 68 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.638-15724delA | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16016791 | |||||
| chr12:16016791
|
CAA | C | 8 | a0001c0001t0001g0074a0001c0001t0001g0135a0001c0001t0001g0169others(5): Show | 8 | HG00738.hp1 HG01070.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.638-15725_638-1572 others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16016791 | |||||
| chr12:16016913
|
C | A | 1 | a0001c0001t0001g0021 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.638-15629C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16016913 | ||||||
| chr12:16016940
|
T | C | 6 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0159others(3): Show | 6 | HG00558.hp1 HG02074.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.638-15602T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16016940 | ||||||
| chr12:16017052
|
A | T | 6 | a0001c0001t0001g0040a0001c0001t0001g0117a0001c0001t0001g0194others(3): Show | 6 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.638-15490A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16017052 | ||||||
| chr12:16017539
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0174 | 3 | HG01884.hp2 HG02258.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.638-15003C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16017539 | ||||||
| chr12:16017545
|
G | C | 1 | a0001c0001t0001g0163 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.638-14997G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16017545 | ||||||
| chr12:16017589
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.638-14953C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16017589 | ||||||
| chr12:16017640
|
T | C | 28 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0103others(25): Show | 28 | HG00621.hp2 HG01081.hp2 HG02027.hp1 others(25): Show |
intron_variant | MODIFIER | c.638-14902T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16017640 | ||||||
| chr12:16017963
|
C | G | 10 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(7): Show | 10 | HG01109.hp2 HG02109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.638-14579C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16017963 | ||||||
| chr12:16018041
|
A | G | 1 | a0001c0001t0003g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.638-14501A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16018041 | ||||||
| chr12:16018044
|
A | C | 3 | a0001c0001t0001g0083a0001c0001t0001g0208a0001c0001t0001g0247 | 3 | HG02615.hp1 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.638-14498A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16018044 | ||||||
| chr12:16018044
|
A | T | 50 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0021others(47): Show | 50 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(47): Show |
intron_variant | MODIFIER | c.638-14498A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16018044 | ||||||
| chr12:16018120
|
T | A | 10 | a0001c0001t0001g0024a0001c0001t0001g0061a0001c0001t0001g0075others(7): Show | 10 | HG02015.hp1 HG02132.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.638-14422T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16018120 | ||||||
| chr12:16018122
|
C | T | 1 | a0001c0001t0002g0257 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.638-14420C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16018122 | ||||||
| chr12:16018146
|
C | A | 6 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(3): Show | 6 | HG02630.hp2 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.638-14396C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16018146 | ||||||
| chr12:16018147
|
T | A | 6 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(3): Show | 6 | HG02630.hp2 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.638-14395T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16018147 | ||||||
| chr12:16018170
|
T | A | 2 | a0001c0001t0001g0211a0001c0001t0003g0017 | 2 | HG02647.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.638-14372T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16018170 | ||||||
| chr12:16018192
|
G | A | 47 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0021others(44): Show | 47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.638-14350G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16018192 | ||||||
| chr12:16018294
|
C | G | 3 | a0001c0001t0001g0083a0001c0001t0001g0208a0001c0001t0001g0247 | 3 | HG02615.hp1 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.638-14248C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16018294 | ||||||
| chr12:16018359
|
A | C | 255 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(252): Show | 256 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(253): Show |
intron_variant | MODIFIER | c.638-14183A>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16018359 | ||||||
| chr12:16019062
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.638-13480T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16019062 | ||||||
| chr12:16019069
|
TGGTGTTG others(46): Show |
T | 1 | a0001c0001t0001g0051 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.638-13471_638-1341 others(57): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16019069 | |||||
| chr12:16019083
|
C | G | 1 | a0001c0001t0001g0189 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.638-13459C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16019083 | ||||||
| chr12:16019455
|
G | A | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0236 | 3 | HG02257.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.638-13087G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16019455 | ||||||
| chr12:16019639
|
T | C | 1 | a0001c0001t0005g0042 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.638-12903T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16019639 | ||||||
| chr12:16019705
|
T | TC | 9 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0085others(6): Show | 9 | HG01167.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.638-12835dupC | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16019705 | |||||
| chr12:16019978
|
G | T | 1 | a0001c0001t0001g0157 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.638-12564G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16019978 | ||||||
| chr12:16020044
|
C | G | 1 | a0001c0001t0001g0104 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.638-12498C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16020044 | ||||||
| chr12:16020357
|
G | C | 60 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(57): Show | 60 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(57): Show |
intron_variant | MODIFIER | c.638-12185G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16020357 | ||||||
| chr12:16020586
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.638-11956G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16020586 | ||||||
| chr12:16020921
|
G | A | 2 | a0001c0001t0001g0007a0003c0004t0001g0225 | 2 | HG03041.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.638-11621G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16020921 | ||||||
| chr12:16021154
|
T | A | 3 | a0001c0001t0001g0064a0001c0001t0003g0014a0001c0001t0003g0019 | 3 | HG02055.hp1 HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.638-11388T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16021154 | ||||||
| chr12:16021166
|
C | T | 1 | a0001c0001t0005g0043 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.638-11376C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16021166 | ||||||
| chr12:16021333
|
A | G | 163 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(160): Show | 163 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.638-11209A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16021333 | ||||||
| chr12:16021343
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.638-11199G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16021343 | ||||||
| chr12:16021362
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.638-11180A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16021362 | ||||||
| chr12:16021778
|
C | T | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0236 | 3 | HG02257.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.638-10764C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16021778 | ||||||
| chr12:16021803
|
A | G | 47 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0021others(44): Show | 47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.638-10739A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16021803 | ||||||
| chr12:16022040
|
A | G | 53 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0021others(50): Show | 53 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(50): Show |
intron_variant | MODIFIER | c.638-10502A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16022040 | ||||||
| chr12:16022155
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.638-10387A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16022155 | ||||||
| chr12:16022480
|
A | T | 163 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(160): Show | 163 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.638-10062A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16022480 | ||||||
| chr12:16022662
|
A | G | 2 | a0001c0001t0001g0008a0001c0001t0001g0081 | 2 | HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.638-9880A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16022662 | ||||||
| chr12:16022836
|
C | T | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0236 | 3 | HG02257.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.638-9706C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16022836 | ||||||
| chr12:16022939
|
C | T | 1 | a0001c0001t0001g0249 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.638-9603C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16022939 | ||||||
| chr12:16023061
|
C | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0087a0001c0001t0001g0088others(1): Show | 5 | HG01123.hp2 HG01256.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.638-9481C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16023061 | ||||||
| chr12:16023136
|
C | T | 47 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0021others(44): Show | 47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.638-9406C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16023136 | ||||||
| chr12:16023266
|
G | A | 3 | a0001c0001t0001g0083a0001c0001t0001g0208a0001c0001t0001g0247 | 3 | HG02615.hp1 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.638-9276G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16023266 | ||||||
| chr12:16023473
|
C | CT | 21 | a0001c0001t0001g0007a0001c0001t0001g0055a0001c0001t0001g0069others(18): Show | 21 | HG01109.hp1 HG01361.hp2 HG01516.hp1 others(18): Show |
intron_variant | MODIFIER | c.638-9047dupT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16023473 | |||||
| chr12:16023473
|
C | CTT | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(5): Show | 8 | HG02615.hp1 HG02886.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.638-9048_638-9047d others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16023473 | |||||
| chr12:16023473
|
C | CTTTT | 12 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0084others(9): Show | 12 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.638-9050_638-9047d others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16023473 | |||||
| chr12:16023473
|
CT | C | 18 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0029others(15): Show | 18 | HG01261.hp1 HG02015.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.638-9047delT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16023473 | |||||
| chr12:16023473
|
CTT | C | 21 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0026others(18): Show | 21 | HG01109.hp2 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.638-9048_638-9047d others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16023473 | |||||
| chr12:16023502
|
G | A | 1 | a0001c0001t0001g0177 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.638-9040G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16023502 | ||||||
| chr12:16023508
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.638-9034C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16023508 | ||||||
| chr12:16023540
|
G | C | 47 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0021others(44): Show | 47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.638-9002G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16023540 | ||||||
| chr12:16023547
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0003g0012 | 2 | HG01891.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.638-8995G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16023547 | ||||||
| chr12:16023578
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.638-8964C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16023578 | ||||||
| chr12:16023644
|
A | T | 6 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(3): Show | 6 | HG02630.hp2 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.638-8898A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16023644 | ||||||
| chr12:16023723
|
C | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0081 | 2 | HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.638-8819C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16023723 | ||||||
| chr12:16023784
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.638-8758G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16023784 | ||||||
| chr12:16023809
|
G | T | 1 | a0001c0001t0001g0132 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.638-8733G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16023809 | ||||||
| chr12:16024040
|
G | A | 47 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0021others(44): Show | 47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.638-8502G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16024040 | ||||||
| chr12:16024074
|
T | A | 47 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0021others(44): Show | 47 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.638-8468T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16024074 | ||||||
| chr12:16024172
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.638-8370G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16024172 | ||||||
| chr12:16024347
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.638-8195C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16024347 | ||||||
| chr12:16024354
|
T | C | 1 | a0001c0001t0001g0219 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.638-8188T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16024354 | ||||||
| chr12:16024497
|
G | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0246 | 2 | NA18968.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.638-8045G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16024497 | ||||||
| chr12:16024661
|
AGCTGTAA others(14): Show |
A | 2 | a0001c0001t0003g0002a0001c0001t0003g0003 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.638-7859_638-7839d others(23): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16024661 | |||||
| chr12:16024758
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.638-7784G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16024758 | ||||||
| chr12:16024784
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.638-7758C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16024784 | ||||||
| chr12:16025106
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.638-7436A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16025106 | ||||||
| chr12:16025163
|
A | T | 1 | a0001c0001t0001g0062 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.638-7379A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16025163 | ||||||
| chr12:16025390
|
A | T | 5 | a0001c0001t0001g0083a0001c0001t0001g0087a0001c0001t0001g0088others(2): Show | 5 | HG02615.hp1 HG02809.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.638-7152A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16025390 | ||||||
| chr12:16025422
|
C | T | 2 | a0001c0001t0002g0138a0001c0001t0002g0257 | 2 | NA18747.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.638-7120C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16025422 | ||||||
| chr12:16025827
|
A | G | 64 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0036others(61): Show | 65 | HG00558.hp1 HG00642.hp1 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.638-6715A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16025827 | ||||||
| chr12:16025869
|
T | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0027others(166): Show | 170 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.638-6673T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16025869 | ||||||
| chr12:16025941
|
C | A | 6 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0046others(3): Show | 6 | HG02630.hp2 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.638-6601C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16025941 | ||||||
| chr12:16025970
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.638-6572C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16025970 | ||||||
| chr12:16026261
|
T | C | 3 | a0001c0001t0001g0083a0001c0001t0001g0208a0001c0001t0001g0247 | 3 | HG02615.hp1 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.638-6281T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16026261 | ||||||
| chr12:16026295
|
G | A | 67 | a0001c0001t0001g0036a0001c0001t0001g0051a0001c0001t0001g0062others(64): Show | 67 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.638-6247G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16026295 | ||||||
| chr12:16026371
|
G | A | 49 | a0001c0001t0001g0036a0001c0001t0001g0057a0001c0001t0001g0062others(46): Show | 49 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.638-6171G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16026371 | ||||||
| chr12:16026386
|
T | A | 203 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0025others(200): Show | 204 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.638-6156T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16026386 | ||||||
| chr12:16026437
|
G | C | 6 | a0001c0001t0001g0040a0001c0001t0001g0117a0001c0001t0001g0194others(3): Show | 6 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.638-6105G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16026437 | ||||||
| chr12:16026448
|
A | G | 57 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(54): Show | 57 | HG00280.hp1 HG00558.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.638-6094A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16026448 | ||||||
| chr12:16026487
|
A | G | 1 | a0001c0001t0002g0161 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.638-6055A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16026487 | ||||||
| chr12:16026594
|
AC | A | 10 | a0001c0001t0001g0036a0001c0001t0001g0062a0001c0001t0001g0094others(7): Show | 10 | HG01167.hp2 HG02647.hp2 NA18943.hp2 others(7): Show |
intron_variant | MODIFIER | c.638-5947delC | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16026594 | ||||||
| chr12:16026613
|
A | G | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.638-5929A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16026613 | ||||||
| chr12:16026614
|
C | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(132): Show | 136 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.638-5928C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16026614 | ||||||
| chr12:16026983
|
G | A | 103 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0001g0045others(100): Show | 103 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.638-5559G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16026983 | ||||||
| chr12:16027045
|
A | G | 2 | a0001c0001t0001g0069a0001c0001t0001g0173 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.638-5497A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16027045 | ||||||
| chr12:16027239
|
A | G | 50 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(47): Show | 51 | HG00558.hp1 HG00735.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.638-5303A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16027239 | ||||||
| chr12:16027249
|
C | G | 10 | a0001c0001t0001g0036a0001c0001t0001g0062a0001c0001t0001g0094others(7): Show | 10 | HG01167.hp2 HG02647.hp2 NA18943.hp2 others(7): Show |
intron_variant | MODIFIER | c.638-5293C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16027249 | ||||||
| chr12:16027437
|
T | G | 1 | a0001c0001t0001g0145 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.638-5105T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16027437 | ||||||
| chr12:16027446
|
T | C | 4 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0212others(1): Show | 4 | HG01081.hp1 HG01884.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.638-5096T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16027446 | ||||||
| chr12:16027452
|
G | C | 1 | a0001c0001t0001g0234 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.638-5090G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16027452 | ||||||
| chr12:16027711
|
A | G | 1 | a0001c0003t0001g0073 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.638-4831A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16027711 | ||||||
| chr12:16027880
|
C | T | 4 | a0001c0001t0001g0053a0001c0001t0001g0159a0001c0001t0001g0218others(1): Show | 4 | NA18949.hp1 NA19055.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-4662C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16027880 | ||||||
| chr12:16027988
|
A | G | 38 | a0001c0001t0001g0036a0001c0001t0001g0062a0001c0001t0001g0094others(35): Show | 38 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.638-4554A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16027988 | ||||||
| chr12:16028050
|
C | A | 8 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0030others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.638-4492C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16028050 | ||||||
| chr12:16028364
|
A | T | 44 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0027others(41): Show | 45 | HG00558.hp1 HG00735.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.638-4178A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16028364 | ||||||
| chr12:16028448
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.638-4094C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16028448 | ||||||
| chr12:16028489
|
T | C | 109 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0001g0045others(106): Show | 109 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.638-4053T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16028489 | ||||||
| chr12:16028565
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.638-3977G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16028565 | ||||||
| chr12:16029054
|
T | G | 1 | a0001c0001t0002g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.638-3488T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16029054 | ||||||
| chr12:16029280
|
G | A | 67 | a0001c0001t0001g0031a0001c0001t0001g0045a0001c0001t0001g0047others(64): Show | 67 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.638-3262G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16029280 | ||||||
| chr12:16029315
|
C | T | 2 | a0001c0001t0002g0056a0001c0001t0002g0185 | 2 | NA18995.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.638-3227C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16029315 | ||||||
| chr12:16029427
|
A | AAAAT | 9 | a0001c0001t0001g0068a0001c0001t0001g0070a0001c0001t0001g0071others(6): Show | 9 | HG02257.hp1 HG02615.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.638-3087_638-3084d others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16029427 | |||||
| chr12:16029427
|
A | AAAATAAA others(5): Show |
1 | a0001c0001t0001g0006 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.638-3095_638-3084d others(14): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16029427 | |||||
| chr12:16029427
|
A | AAAATAAA others(9): Show |
1 | a0001c0001t0001g0174 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.638-3099_638-3084d others(18): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16029427 | |||||
| chr12:16029427
|
AAAAT | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(154): Show | 158 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.638-3087_638-3084d others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16029427 | |||||
| chr12:16029589
|
G | C | 2 | a0001c0001t0001g0094a0001c0001t0001g0229 | 2 | NA18943.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.638-2953G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16029589 | ||||||
| chr12:16029723
|
A | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(163): Show | 167 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.638-2819A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16029723 | ||||||
| chr12:16029913
|
C | CT | 35 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0029others(32): Show | 35 | HG00544.hp1 HG00621.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.638-2602dupT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16029913 | |||||
| chr12:16029913
|
C | CTT | 26 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0032others(23): Show | 26 | HG00438.hp1 HG02080.hp2 HG02132.hp2 others(23): Show |
intron_variant | MODIFIER | c.638-2603_638-2602d others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16029913 | |||||
| chr12:16029913
|
C | CTTT | 26 | a0001c0001t0001g0031a0001c0001t0001g0051a0001c0001t0001g0060others(23): Show | 26 | HG00280.hp1 HG00558.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.638-2604_638-2602d others(5): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16029913 | |||||
| chr12:16029913
|
C | CTTTT | 23 | a0001c0001t0001g0045a0001c0001t0001g0098a0001c0001t0001g0101others(20): Show | 23 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.638-2605_638-2602d others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16029913 | |||||
| chr12:16029913
|
C | CTTTTT | 22 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0054others(19): Show | 22 | HG00738.hp1 HG01256.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.638-2606_638-2602d others(7): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16029913 | |||||
| chr12:16029913
|
C | CTTTTTT | 8 | a0001c0001t0001g0063a0001c0001t0001g0133a0001c0001t0001g0175others(5): Show | 8 | HG00280.hp2 HG00544.hp2 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.638-2607_638-2602d others(8): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16029913 | |||||
| chr12:16029913
|
CT | C | 9 | a0001c0001t0001g0036a0001c0001t0001g0077a0001c0001t0001g0087others(6): Show | 9 | HG01978.hp2 HG02027.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.638-2602delT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16029913 | |||||
| chr12:16029913
|
CTT | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0027others(42): Show | 46 | HG00558.hp1 HG00735.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.638-2603_638-2602d others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16029913 | |||||
| chr12:16029913
|
CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0001g0193 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.638-2618_638-2602d others(19): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16029913 | |||||
| chr12:16030064
|
A | T | 2 | a0001c0001t0001g0223a0001c0001t0001g0231 | 2 | NA18971.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.638-2478A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16030064 | ||||||
| chr12:16030089
|
A | AT | 10 | a0001c0001t0001g0006a0001c0001t0001g0025a0001c0001t0001g0029others(7): Show | 10 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.638-2437dupT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16030089 | |||||
| chr12:16030089
|
AT | A | 7 | a0001c0001t0001g0051a0001c0001t0001g0060a0001c0001t0001g0156others(4): Show | 7 | HG00558.hp2 HG01981.hp2 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.638-2437delT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16030089 | |||||
| chr12:16030089
|
ATT | A | 150 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(147): Show | 151 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.638-2438_638-2437d others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16030089 | |||||
| chr12:16030092
|
T | TC | 5 | a0001c0001t0001g0120a0001c0001t0001g0149a0001c0001t0001g0150others(2): Show | 5 | HG01168.hp2 HG01358.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.638-2450_638-2449i others(3): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16030092 | ||||||
| chr12:16030105
|
T | G | 2 | a0001c0001t0001g0207a0001c0001t0001g0210 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.638-2437T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16030105 | ||||||
| chr12:16030130
|
C | A | 2 | a0001c0001t0001g0120a0001c0001t0001g0170 | 2 | HG01168.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.638-2412C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16030130 | ||||||
| chr12:16030148
|
G | T | 27 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0049others(24): Show | 27 | HG00438.hp1 HG00621.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.638-2394G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16030148 | ||||||
| chr12:16030221
|
C | T | 2 | a0001c0001t0003g0011a0002c0002t0003g0020 | 2 | HG02630.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.638-2321C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16030221 | ||||||
| chr12:16030224
|
G | A | 1 | a0001c0001t0001g0241 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.638-2318G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16030224 | ||||||
| chr12:16030394
|
T | C | 1 | a0001c0001t0003g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.638-2148T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16030394 | ||||||
| chr12:16030607
|
GATTA | G | 10 | a0001c0001t0001g0036a0001c0001t0001g0062a0001c0001t0001g0094others(7): Show | 10 | HG01167.hp2 HG02647.hp2 NA18943.hp2 others(7): Show |
intron_variant | MODIFIER | c.638-1930_638-1927d others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16030607 | |||||
| chr12:16030823
|
G | C | 11 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0032others(8): Show | 11 | HG01168.hp2 HG01358.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.638-1719G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16030823 | ||||||
| chr12:16030894
|
T | G | 1 | a0001c0001t0001g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.638-1648T>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16030894 | ||||||
| chr12:16030932
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0003g0005 | 2 | HG00733.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.638-1610C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16030932 | ||||||
| chr12:16031097
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.638-1445G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16031097 | ||||||
| chr12:16031218
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.638-1324G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16031218 | ||||||
| chr12:16031563
|
G | A | 247 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(244): Show | 248 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(245): Show |
intron_variant | MODIFIER | c.638-979G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16031563 | ||||||
| chr12:16031636
|
G | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(194): Show | 198 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.638-906G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16031636 | ||||||
| chr12:16031683
|
G | A | 1 | a0001c0001t0001g0239 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.638-859G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16031683 | ||||||
| chr12:16031703
|
C | G | 27 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0049others(24): Show | 27 | HG00438.hp1 HG00621.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.638-839C>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16031703 | ||||||
| chr12:16031850
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.638-692C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16031850 | ||||||
| chr12:16031905
|
G | T | 1 | a0001c0001t0001g0093 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.638-637G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16031905 | ||||||
| chr12:16032283
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.638-259C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | chr12 | 16032283 | ||||||
| chr12:16032529
|
CTT | C | 63 | a0001c0001t0001g0031a0001c0001t0001g0045a0001c0001t0001g0047others(60): Show | 63 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(60): Show |
splice_region_variant&intron_variant | LOW | c.638-9_638-8delTT | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 16032529 | |||||
| chr12:16032781
|
T | A | 1 | a0001c0001t0001g0182 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.750+127T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16032781 | ||||||
| chr12:16032998
|
T | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(194): Show | 198 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.750+344T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16032998 | ||||||
| chr12:16033057
|
T | A | 1 | a0001c0001t0001g0128 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.750+403T>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16033057 | ||||||
| chr12:16033187
|
C | A | 8 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0030others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.750+533C>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16033187 | ||||||
| chr12:16033213
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.750+559A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16033213 | ||||||
| chr12:16033333
|
A | G | 2 | a0001c0001t0003g0011a0002c0002t0003g0020 | 2 | HG02630.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.750+679A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16033333 | ||||||
| chr12:16033581
|
T | TTG | 41 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0035others(38): Show | 41 | HG00558.hp1 HG00735.hp1 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.750+969_750+970dup others(2): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 16033581 | |||||
| chr12:16033581
|
T | TTGTG | 50 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0001g0050others(47): Show | 50 | HG00280.hp1 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.750+967_750+970dup others(4): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 16033581 | |||||
| chr12:16033581
|
T | TTGTGTG | 55 | a0001c0001t0001g0006a0001c0001t0001g0025a0001c0001t0001g0029others(52): Show | 55 | HG00558.hp2 HG00738.hp1 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.750+965_750+970dup others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 16033581 | |||||
| chr12:16033581
|
T | TTGTGTGT others(1): Show |
22 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0069others(19): Show | 23 | HG00438.hp2 HG00642.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.750+963_750+970dup others(8): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 16033581 | |||||
| chr12:16033581
|
T | TTGTGTGT others(3): Show |
5 | a0001c0001t0001g0079a0001c0001t0001g0153a0001c0001t0001g0166others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.750+961_750+970dup others(10): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 16033581 | |||||
| chr12:16033581
|
T | TTGTGTGT others(5): Show |
3 | a0001c0001t0001g0032a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG00544.hp2 HG02135.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.750+959_750+970dup others(12): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 16033581 | |||||
| chr12:16033581
|
T | TTGTGTGT others(9): Show |
1 | a0001c0001t0001g0133 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.750+955_750+970dup others(16): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 16033581 | |||||
| chr12:16033581
|
TTG | T | 23 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0046others(20): Show | 23 | HG02015.hp1 HG02080.hp2 HG02132.hp1 others(20): Show |
intron_variant | MODIFIER | c.750+969_750+970del others(2): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 16033581 | |||||
| chr12:16033581
|
TTGTGTGT others(5): Show |
T | 1 | a0001c0001t0001g0219 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.750+959_750+970del others(12): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 16033581 | |||||
| chr12:16033624
|
T | TGTG | 3 | a0001c0001t0001g0194a0001c0001t0001g0239a0001c0001t0001g0246 | 3 | HG01243.hp2 NA18968.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.750+970_750+971ins others(3): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16033624 | ||||||
| chr12:16033624
|
T | TGTGTG | 3 | a0001c0001t0001g0122a0001c0001t0001g0130a0001c0001t0001g0164 | 3 | HG01496.hp2 HG02602.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.750+970_750+971ins others(5): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16033624 | ||||||
| chr12:16033624
|
T | TGTGTGTG others(4): Show |
1 | a0001c0001t0001g0063 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.750+970_750+971ins others(11): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16033624 | ||||||
| chr12:16033742
|
TGTAA | T | 6 | a0001c0001t0004g0058a0001c0001t0004g0089a0001c0001t0004g0116others(3): Show | 6 | HG02897.hp2 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.750+1091_750+1094d others(6): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 16033742 | |||||
| chr12:16033833
|
C | T | 1 | a0001c0001t0002g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.750+1179C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16033833 | ||||||
| chr12:16034294
|
G | A | 47 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0054others(44): Show | 47 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.750+1640G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16034294 | ||||||
| chr12:16034466
|
G | A | 27 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0049others(24): Show | 27 | HG00438.hp1 HG00621.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.751-1766G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16034466 | ||||||
| chr12:16034698
|
C | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(155): Show | 159 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.751-1534C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16034698 | ||||||
| chr12:16034757
|
TA | T | 98 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0024others(95): Show | 98 | HG00544.hp1 HG00621.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.751-1463delA | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 16034757 | |||||
| chr12:16034962
|
T | TATAGAGT others(1): Show |
27 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0049others(24): Show | 27 | HG00438.hp1 HG00621.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.751-1269_751-1268i others(10): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 16034962 | |||||
| chr12:16034964
|
C | CAGAGTCA others(1): Show |
228 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(225): Show | 229 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.751-1266_751-1265i others(10): Show |
DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 16034964 | |||||
| chr12:16034964
|
C | T | 27 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0049others(24): Show | 27 | HG00438.hp1 HG00621.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.751-1268C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16034964 | ||||||
| chr12:16035004
|
C | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0027others(42): Show | 46 | HG00558.hp1 HG00735.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.751-1228C>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16035004 | ||||||
| chr12:16035033
|
G | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(58): Show | 62 | HG00558.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.751-1199G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16035033 | ||||||
| chr12:16035156
|
G | C | 2 | a0001c0001t0001g0008a0001c0001t0001g0208 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.751-1076G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16035156 | ||||||
| chr12:16035459
|
G | T | 26 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0049others(23): Show | 26 | HG00438.hp1 HG00621.hp1 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.751-773G>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16035459 | ||||||
| chr12:16035855
|
G | A | 8 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0030others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.751-377G>A | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16035855 | ||||||
| chr12:16035969
|
A | G | 1 | a0001c0001t0002g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.751-263A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16035969 | ||||||
| chr12:16036047
|
A | G | 1 | a0001c0001t0002g0168 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.751-185A>G | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16036047 | ||||||
| chr12:16036080
|
A | T | 1 | a0001c0001t0001g0193 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.751-152A>T | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 7/8 | chr12 | 16036080 | ||||||
| chr12:16036393
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.900+12T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 8/8 | chr12 | 16036393 | ||||||
| chr12:16036459
|
T | C | 1 | a0001c0001t0001g0208 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.900+78T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 8/8 | chr12 | 16036459 | ||||||
| chr12:16036544
|
G | C | 4 | a0001c0001t0001g0068a0001c0001t0001g0070a0001c0001t0001g0071others(1): Show | 4 | HG02257.hp1 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.901-146G>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 8/8 | chr12 | 16036544 | ||||||
| chr12:16036608
|
T | C | 66 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 67 | HG00558.hp1 HG00733.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.901-82T>C | DERA | ENSG00000023697.13 | transcript | ENST00000428559.7 | protein_coding | 8/8 | chr12 | 16036608 |