| geneid | 84873 |
|---|---|
| ensemblid | ENSG00000144820.8 |
| hgncid | 19241 |
| symbol | ADGRG7 |
| name | adhesion G protein-coupled receptor G7 |
| refseq_nuc | NM_032787.3 |
| refseq_prot | NP_116176.2 |
| ensembl_nuc | ENST00000273352.8 |
| ensembl_prot | ENSP00000273352.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 100609601 |
| end | 100695479 |
| strand | + |
| ver | v1.2 |
| region | chr3:100609601-100695479 |
| region5000 | chr3:100604601-100700479 |
| regionname0 | ADGRG7_chr3_100609601_100695479 |
| regionname5000 | ADGRG7_chr3_100604601_100700479 |
| 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 | 797 | 212 | 58 | 34 | 91 | 12 | 15 | 66 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0002 | 0/0 | 797 | 74 | 9 | 11 | 50 | 2 | 2 | 42 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0003 | 0/0 | 797 | 35 | 8 | 14 | 4 | 2 | 7 | 2 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0004 | 0/0 | 797 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0005 | 0/0 | 797 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0006 | 0/0 | 797 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0007 | 0/0 | 797 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0008 | 0/0 | 797 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0009 | 0/0 | 797 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0010 | 0/0 | 797 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0011 | 0/0 | 797 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0012 | 0/0 | 797 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| 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 | 2394 | 204 | 51 | 34 | 91 | 11 | 15 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| c0002 | 0/0 | 2394 | 74 | 9 | 11 | 50 | 2 | 2 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| c0003 | 0/0 | 2394 | 35 | 8 | 14 | 4 | 2 | 7 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| c0004 | 0/0 | 2394 | 4 | 4 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| c0005 | 0/0 | 2394 | 4 | 3 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| c0006 | 0/0 | 2394 | 4 | 3 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| c0007 | 0/0 | 2394 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| c0008 | 0/0 | 2394 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| c0009 | 0/0 | 2394 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| c0010 | 0/0 | 2394 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| c0011 | 0/0 | 2394 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| c0012 | 0/0 | 2394 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| c0013 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| c0014 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| c0015 | 0/0 | 2394 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| c0016 | 0/0 | 2394 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| c0017 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| 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 | 735 | 317 | 68 | 61 | 148 | 14 | 24 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| t0002 | 0/0 | 735 | 8 | 7 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| t0003 | 0/0 | 735 | 7 | 7 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| t0004 | 0/0 | 735 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| t0005 | 0/0 | 735 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| t0006 | 0/0 | 735 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| t0007 | 0/0 | 735 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| t0008 | 0/0 | 735 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| t0009 | 0/0 | 735 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| 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 | 6 | 0 | 0 | 6 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0049 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0082 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| 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 | 2394 | 204 | 51 | 34 | 91 | 11 | 15 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0001c0005 | 0/0 | 2394 | 4 | 3 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0001c0008 | 0/0 | 2394 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0001c0010 | 0/0 | 2394 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0001c0011 | 0/0 | 2394 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0002c0002 | 0/0 | 2394 | 74 | 9 | 11 | 50 | 2 | 2 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0003c0003 | 0/0 | 2394 | 35 | 8 | 14 | 4 | 2 | 7 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0004c0004 | 0/0 | 2394 | 4 | 4 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0004c0009 | 0/0 | 2394 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0005c0006 | 0/0 | 2394 | 4 | 3 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0006c0007 | 0/0 | 2394 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0007c0017 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0008c0016 | 0/0 | 2394 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0009c0015 | 0/0 | 2394 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0010c0014 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0011c0012 | 0/0 | 2394 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0012c0013 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3128 | 193 | 41 | 34 | 91 | 10 | 15 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0001c0001t0002 | 0/0 | 3128 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0001c0001t0003 | 0/0 | 3128 | 6 | 6 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0001c0001t0005 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0001c0001t0006 | 0/0 | 3128 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0001c0001t0007 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0001c0005t0001 | 0/0 | 3128 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0001c0005t0008 | 0/0 | 3128 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0001c0008t0001 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0001c0008t0009 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0001c0010t0001 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0001c0011t0001 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0002c0002t0001 | 0/0 | 3128 | 74 | 9 | 11 | 50 | 2 | 2 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0003c0003t0001 | 0/0 | 3128 | 34 | 7 | 14 | 4 | 2 | 7 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0003c0003t0003 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0004c0004t0002 | 0/0 | 3128 | 4 | 4 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0004c0009t0002 | 0/0 | 3128 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0005c0006t0001 | 0/0 | 3128 | 4 | 3 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0006c0007t0004 | 0/0 | 3128 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0007c0017t0001 | 0/0 | 3128 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0008c0016t0001 | 0/0 | 3128 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0009c0015t0001 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0010c0014t0001 | 0/0 | 3128 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0011c0012t0001 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| a0012c0013t0001 | 0/0 | 3128 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | copy fasta | chr3 | 100604601 | 100700479 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0049 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0082 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0006g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0001t0007g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0005t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0005t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0005t0008g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0008t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0008t0009g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0010t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0001c0011t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0003c0003t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0004c0004t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0004c0004t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0004c0004t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0004c0004t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0004c0009t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0004c0009t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0005c0006t0001g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0005c0006t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0005c0006t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0006c0007t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0006c0007t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0006c0007t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0007c0017t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0008c0016t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0009c0015t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0010c0014t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0011c0012t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| a0012c0013t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | GBR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0138 | EUR | GBR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0174 | EUR | GBR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG00140 | hp2 | a0001 | c0001 | t0006 | g0161 | EUR | GBR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG00280 | hp1 | a0001 | c0005 | t0008 | g0071 | EUR | FIN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | FIN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0267 | EAS | CHS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | CHS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG00597 | hp1 | a0003 | c0003 | t0001 | g0230 | EAS | CHS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0296 | EAS | CHS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0280 | EAS | CHS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG00735 | hp2 | a0004 | c0009 | t0002 | g0047 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG00741 | hp2 | a0003 | c0003 | t0001 | g0199 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01071 | hp2 | a0003 | c0003 | t0001 | g0225 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01074 | hp1 | a0003 | c0003 | t0001 | g0226 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01081 | hp2 | a0003 | c0003 | t0001 | g0234 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0260 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01109 | hp2 | a0003 | c0003 | t0001 | g0241 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01167 | hp1 | a0003 | c0003 | t0001 | g0236 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0294 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01168 | hp1 | a0003 | c0003 | t0001 | g0240 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01243 | hp2 | a0003 | c0003 | t0001 | g0235 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0015 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01256 | hp2 | a0003 | c0003 | t0001 | g0018 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01257 | hp1 | a0003 | c0003 | t0001 | g0011 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01258 | hp2 | a0003 | c0003 | t0001 | g0017 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0256 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0304 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01433 | hp2 | a0003 | c0003 | t0001 | g0019 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0015 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01496 | hp2 | a0003 | c0003 | t0001 | g0237 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01515 | hp1 | a0003 | c0003 | t0001 | g0242 | EUR | IBS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0276 | EUR | IBS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | IBS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | IBS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | IBS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0275 | EUR | IBS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0311 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0271 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0278 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01943 | hp2 | a0003 | c0003 | t0001 | g0227 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01975 | hp2 | a0005 | c0006 | t0001 | g0005 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0297 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0270 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0258 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02055 | hp2 | a0003 | c0003 | t0001 | g0024 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02145 | hp2 | a0003 | c0003 | t0001 | g0200 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02165 | hp1 | a0003 | c0003 | t0001 | g0136 | EAS | CDX | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0307 | EAS | CDX | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02257 | hp1 | a0001 | c0008 | t0009 | g0034 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0091 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0259 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02280 | hp2 | a0003 | c0003 | t0001 | g0027 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02300 | hp1 | a0008 | c0016 | t0001 | g0238 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0286 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02451 | hp1 | a0001 | c0011 | t0001 | g0058 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0303 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02523 | hp2 | a0007 | c0017 | t0001 | g0232 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02602 | hp2 | a0003 | c0003 | t0001 | g0250 | SAS | PJL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02615 | hp1 | a0004 | c0009 | t0002 | g0067 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0315 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02630 | hp1 | a0006 | c0007 | t0004 | g0042 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02630 | hp2 | a0003 | c0003 | t0001 | g0011 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0069 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02683 | hp1 | a0003 | c0003 | t0001 | g0228 | SAS | PJL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02698 | hp2 | a0003 | c0003 | t0001 | g0251 | SAS | PJL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02723 | hp2 | a0009 | c0015 | t0001 | g0022 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02735 | hp1 | a0003 | c0003 | t0001 | g0233 | SAS | PJL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02886 | hp1 | a0001 | c0001 | t0007 | g0302 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02895 | hp2 | a0001 | c0005 | t0001 | g0006 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0202 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02897 | hp1 | a0001 | c0005 | t0001 | g0006 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02922 | hp1 | a0003 | c0003 | t0001 | g0198 | AFR | ESN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0092 | AFR | ESN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0309 | AFR | ESN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02970 | hp1 | a0005 | c0006 | t0001 | g0028 | AFR | ESN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | ESN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03041 | hp2 | a0004 | c0004 | t0002 | g0020 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03098 | hp2 | a0005 | c0006 | t0001 | g0005 | AFR | MSL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | ESN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03195 | hp2 | a0003 | c0003 | t0001 | g0224 | AFR | ESN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0310 | AFR | MSL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03225 | hp2 | a0001 | c0008 | t0001 | g0039 | AFR | MSL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03239 | hp2 | a0003 | c0003 | t0001 | g0223 | SAS | PJL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03453 | hp1 | a0001 | c0005 | t0001 | g0068 | AFR | MSL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03453 | hp2 | a0004 | c0004 | t0002 | g0036 | AFR | MSL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03486 | hp2 | a0003 | c0003 | t0003 | g0023 | AFR | MSL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03516 | hp2 | a0006 | c0007 | t0004 | g0040 | AFR | ESN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0314 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0220 | AFR | MSL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0070 | AFR | MSL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03654 | hp2 | a0003 | c0003 | t0001 | g0249 | SAS | PJL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | BEB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03834 | hp2 | a0003 | c0003 | t0001 | g0229 | SAS | BEB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0261 | SAS | BEB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0262 | SAS | STU | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | STU | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | STU | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | STU | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | YRI | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18522 | hp2 | a0005 | c0006 | t0001 | g0029 | AFR | YRI | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0274 | EAS | CHB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CHB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | YRI | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | YRI | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0290 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0289 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0283 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18970 | hp1 | a0012 | c0013 | t0001 | g0147 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0282 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0316 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18987 | hp2 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18995 | hp1 | a0010 | c0014 | t0001 | g0277 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0308 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0299 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0295 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0284 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | LWK | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | LWK | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19043 | hp1 | a0003 | c0003 | t0001 | g0026 | AFR | LWK | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | LWK | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19055 | hp2 | a0003 | c0003 | t0001 | g0231 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19077 | hp2 | a0003 | c0003 | t0001 | g0243 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0288 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0305 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0293 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0287 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19240 | hp1 | a0001 | c0010 | t0001 | g0037 | AFR | YRI | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0313 | AFR | YRI | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ASW | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ASW | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0171 | EUR | TSI | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0163 | EUR | TSI | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0167 | EUR | TSI | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA20805 | hp2 | a0003 | c0003 | t0001 | g0239 | EUR | TSI | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | GIH | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | GIH | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02109 | hp1 | a0006 | c0007 | t0004 | g0041 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02486 | hp2 | a0004 | c0004 | t0002 | g0038 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0090 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG02559 | hp2 | a0011 | c0012 | t0001 | g0065 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0312 | AFR | MSL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| HG03471 | hp2 | a0004 | c0004 | t0002 | g0035 | AFR | MSL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | USA | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | USA | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0082 | REF | REF | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0049 | REF | REF | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:100635680
|
A | G | 3 | a0003a0007a0008 | 37 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(34): Show |
missense_variant | MODERATE | c.451A>G | p.Lys151Glu | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/16 | 707/3128 | 451/2394 | 151/797 | chr3 | 100635680 | ||
| chr3:100635812
|
A | G | 1 | a0009 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.583A>G | p.Asn195Asp | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/16 | 839/3128 | 583/2394 | 195/797 | chr3 | 100635812 | ||
| chr3:100643628
|
C | T | 1 | a0010 | 1 | NA18995.hp1 | missense_variant | MODERATE | c.941C>T | p.Thr314Met | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/16 | 1197/3128 | 941/2394 | 314/797 | chr3 | 100643628 | ||
| chr3:100646070
|
G | A | 1 | a0008 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.1072G>A | p.Asp358Asn | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 9/16 | 1328/3128 | 1072/2394 | 358/797 | chr3 | 100646070 | ||
| chr3:100649702
|
A | G | 2 | a0002a0010 | 75 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(72): Show |
missense_variant | MODERATE | c.1274A>G | p.Lys425Arg | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/16 | 1530/3128 | 1274/2394 | 425/797 | chr3 | 100649702 | ||
| chr3:100654863
|
G | A | 1 | a0011 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.1408G>A | p.Val470Ile | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 12/16 | 1664/3128 | 1408/2394 | 470/797 | chr3 | 100654863 | ||
| chr3:100655922
|
A | G | 1 | a0007 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.1750A>G | p.Ile584Val | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/16 | 2006/3128 | 1750/2394 | 584/797 | chr3 | 100655922 | ||
| chr3:100659797
|
A | T | 1 | a0006 | 3 | HG02109.hp1 HG02630.hp1 HG03516.hp2 |
missense_variant | MODERATE | c.1933A>T | p.Thr645Ser | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/16 | 2189/3128 | 1933/2394 | 645/797 | chr3 | 100659797 | ||
| chr3:100659833
|
A | C | 1 | a0012 | 1 | NA18970.hp1 | missense_variant | MODERATE | c.1969A>C | p.Asn657His | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/16 | 2225/3128 | 1969/2394 | 657/797 | chr3 | 100659833 | ||
| chr3:100694874
|
G | A | 2 | a0004a0006 | 9 | HG00735.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
missense_variant | MODERATE | c.2267G>A | p.Arg756His | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 16/16 | 2523/3128 | 2267/2394 | 756/797 | chr3 | 100694874 | ||
| chr3:100694910
|
C | A | 1 | a0005 | 4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
missense_variant | MODERATE | c.2303C>A | p.Thr768Asn | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 16/16 | 2559/3128 | 2303/2394 | 768/797 | chr3 | 100694910 | ||
| chr3:100694916
|
A | G | 1 | a0005 | 4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
missense_variant | MODERATE | c.2309A>G | p.His770Arg | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 16/16 | 2565/3128 | 2309/2394 | 770/797 | chr3 | 100694916 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:100609889
|
G | C | 4 | a0001c0008a0001c0010a0004c0004others(1): Show | 10 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(7): Show |
synonymous_variant | LOW | c.33G>C | p.Val11Val | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/16 | 289/3128 | 33/2394 | 11/797 | chr3 | 100609889 | ||
| chr3:100643317
|
G | A | 1 | a0001c0010 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.750G>A | p.Val250Val | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 7/16 | 1006/3128 | 750/2394 | 250/797 | chr3 | 100643317 | ||
| chr3:100646628
|
G | A | 1 | a0001c0011 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.1170G>A | p.Ala390Ala | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/16 | 1426/3128 | 1170/2394 | 390/797 | chr3 | 100646628 | ||
| chr3:100655966
|
G | A | 1 | a0001c0005 | 4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
synonymous_variant | LOW | c.1794G>A | p.Gln598Gln | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/16 | 2050/3128 | 1794/2394 | 598/797 | chr3 | 100655966 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:100609682
|
A | G | 1 | a0001c0008t0009 | 1 | HG02257.hp1 | 5_prime_UTR_variant | MODIFIER | c.-175A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/16 | 175 | chr3 | 100609682 | |||||
| chr3:100609716
|
C | T | 1 | a0001c0005t0008 | 1 | HG00280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-141C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/16 | 141 | chr3 | 100609716 | |||||
| chr3:100609779
|
C | T | 1 | a0001c0005t0008 | 1 | HG00280.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-78C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/16 | chr3 | 100609779 | ||||||
| chr3:100609783
|
T | C | 1 | a0001c0001t0005 | 1 | HG03579.hp2 | 5_prime_UTR_variant | MODIFIER | c.-74T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/16 | 74 | chr3 | 100609783 | |||||
| chr3:100609797
|
C | G | 1 | a0001c0001t0007 | 1 | HG02886.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-60C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/16 | chr3 | 100609797 | ||||||
| chr3:100695137
|
G | C | 4 | a0001c0001t0002a0004c0004t0002a0004c0009t0002others(1): Show | 11 | HG00735.hp2 HG02109.hp1 HG02486.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*136G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 16/16 | 136 | chr3 | 100695137 | |||||
| chr3:100695199
|
C | G | 1 | a0001c0001t0006 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*198C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 16/16 | 198 | chr3 | 100695199 | |||||
| chr3:100695263
|
C | A | 2 | a0001c0001t0003a0003c0003t0003 | 7 | HG02258.hp1 HG02559.hp1 HG02896.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*262C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 16/16 | 262 | chr3 | 100695263 | |||||
| chr3:100695274
|
A | G | 1 | a0006c0007t0004 | 3 | HG02109.hp1 HG02630.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*273A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 16/16 | 273 | chr3 | 100695274 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:100610207
|
T | G | 3 | a0003c0003t0001g0017a0003c0003t0001g0018a0003c0003t0001g0019 | 3 | HG01256.hp2 HG01258.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.115+236T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100610207 | ||||||
| chr3:100610356
|
A | G | 268 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(265): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.115+385A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100610356 | ||||||
| chr3:100610408
|
A | G | 1 | a0001c0001t0001g0318 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.115+437A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100610408 | ||||||
| chr3:100610482
|
C | A | 3 | a0001c0005t0001g0006a0001c0005t0001g0068a0004c0009t0002g0067 | 4 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+511C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100610482 | ||||||
| chr3:100610501
|
C | A | 1 | a0002c0002t0001g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.115+530C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100610501 | ||||||
| chr3:100610593
|
G | C | 3 | a0001c0005t0001g0006a0001c0005t0001g0068a0004c0009t0002g0067 | 4 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+622G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100610593 | ||||||
| chr3:100610635
|
A | G | 1 | a0001c0001t0001g0317 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.115+664A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100610635 | ||||||
| chr3:100610646
|
C | T | 2 | a0002c0002t0001g0016a0002c0002t0001g0316 | 3 | NA18961.hp1 NA18966.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.115+675C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100610646 | ||||||
| chr3:100610915
|
G | C | 293 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(290): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.115+944G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100610915 | ||||||
| chr3:100610985
|
C | T | 3 | a0001c0001t0001g0064a0001c0001t0001g0066a0011c0012t0001g0065 | 3 | HG02559.hp2 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.115+1014C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100610985 | ||||||
| chr3:100611043
|
G | A | 1 | a0004c0004t0002g0020 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.115+1072G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611043 | ||||||
| chr3:100611171
|
T | C | 1 | a0001c0001t0005g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.115+1200T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611171 | ||||||
| chr3:100611243
|
T | TTTTCCTT others(1): Show |
25 | a0001c0001t0001g0007a0001c0001t0001g0085a0001c0001t0001g0086others(22): Show | 26 | HG00438.hp1 HG00544.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.115+1273_115+1280d others(10): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100611243 | |||||
| chr3:100611244
|
T | TTTCC | 7 | a0001c0001t0001g0004a0001c0001t0001g0044a0001c0001t0001g0045others(4): Show | 8 | HG00735.hp2 HG01106.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.115+1328_115+1331d others(6): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100611244 | |||||
| chr3:100611244
|
T | TTTCCTTC others(1): Show |
3 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0064 | 3 | HG01952.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.115+1324_115+1331d others(10): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100611244 | |||||
| chr3:100611244
|
T | TTTCCTTC others(5): Show |
7 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(4): Show | 7 | HG00423.hp1 HG01168.hp2 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+1280_115+1281i others(14): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100611244 | |||||
| chr3:100611244
|
TTTCC | T | 10 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0061others(7): Show | 13 | HG01884.hp1 HG01975.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.115+1328_115+1331d others(6): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100611244 | |||||
| chr3:100611244
|
TTTCCTTC others(5): Show |
T | 1 | a0001c0001t0001g0030 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.115+1320_115+1331d others(14): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100611244 | |||||
| chr3:100611244
|
TTTCCTTC others(9): Show |
T | 8 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0003g0031others(5): Show | 8 | HG02145.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.115+1316_115+1331d others(18): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100611244 | |||||
| chr3:100611244
|
TTTCCTTC others(13): Show |
T | 4 | a0001c0008t0001g0039a0006c0007t0004g0040a0006c0007t0004g0041others(1): Show | 4 | HG02109.hp1 HG02630.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.115+1312_115+1331d others(22): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100611244 | |||||
| chr3:100611248
|
C | CTTCT | 81 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0075others(78): Show | 85 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.115+1280_115+1281i others(6): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100611248 | |||||
| chr3:100611252
|
C | T | 151 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0076others(148): Show | 164 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.115+1281C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611252 | ||||||
| chr3:100611253
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.115+1282T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611253 | ||||||
| chr3:100611257
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.115+1286T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611257 | ||||||
| chr3:100611283
|
C | CCTTCCTT others(5): Show |
1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115+1323_115+1324i others(14): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100611283 | |||||
| chr3:100611283
|
C | T | 12 | a0002c0002t0001g0069a0002c0002t0001g0305a0002c0002t0001g0306others(9): Show | 12 | HG01891.hp1 HG02165.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.115+1312C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611283 | ||||||
| chr3:100611287
|
C | T | 49 | a0001c0001t0001g0272a0001c0001t0001g0298a0001c0001t0007g0302others(46): Show | 59 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.115+1316C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611287 | ||||||
| chr3:100611291
|
C | T | 15 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(12): Show | 15 | HG01099.hp1 HG01346.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.115+1320C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611291 | ||||||
| chr3:100611291
|
CCTTCCTT others(5): Show |
C | 12 | a0002c0002t0001g0069a0002c0002t0001g0305a0002c0002t0001g0306others(9): Show | 12 | HG01891.hp1 HG02165.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.115+1325_115+1336d others(14): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100611291 | |||||
| chr3:100611295
|
C | CCTTCCTT others(3): Show |
1 | a0001c0001t0001g0077 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.115+1331_115+1332i others(12): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100611295 | |||||
| chr3:100611295
|
C | T | 60 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0201others(57): Show | 62 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.115+1324C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611295 | ||||||
| chr3:100611295
|
CCTTCCTT others(1): Show |
C | 49 | a0001c0001t0001g0272a0001c0001t0001g0298a0001c0001t0007g0302others(46): Show | 59 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.115+1329_115+1336d others(10): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100611295 | |||||
| chr3:100611296
|
C | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115+1325C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611296 | ||||||
| chr3:100611299
|
CCTTT | C | 18 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(15): Show | 18 | HG01099.hp1 HG01346.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.115+1332_115+1335d others(6): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100611299 | |||||
| chr3:100611303
|
T | C | 64 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(61): Show | 66 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.115+1332T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611303 | ||||||
| chr3:100611303
|
T | TCTTCCTT others(1): Show |
125 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(122): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.115+1336_115+1337i others(10): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100611303 | |||||
| chr3:100611345
|
G | A | 165 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(162): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.115+1374G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611345 | ||||||
| chr3:100611358
|
T | C | 1 | a0001c0001t0005g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.115+1387T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611358 | ||||||
| chr3:100611734
|
G | A | 6 | a0001c0001t0001g0021a0001c0001t0001g0025a0003c0003t0001g0024others(3): Show | 6 | HG01952.hp1 HG02055.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.115+1763G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611734 | ||||||
| chr3:100611914
|
T | C | 1 | a0002c0002t0001g0263 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.115+1943T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611914 | ||||||
| chr3:100611936
|
T | A | 254 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(251): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.115+1965T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611936 | ||||||
| chr3:100612052
|
T | C | 7 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0111others(4): Show | 7 | HG00438.hp1 HG02080.hp2 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.115+2081T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100612052 | ||||||
| chr3:100612110
|
G | T | 58 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0030others(55): Show | 60 | HG00280.hp1 HG00597.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.115+2139G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100612110 | ||||||
| chr3:100612164
|
A | T | 1 | a0002c0002t0001g0304 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.115+2193A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100612164 | ||||||
| chr3:100612201
|
G | T | 1 | a0001c0001t0001g0197 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.115+2230G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100612201 | ||||||
| chr3:100612317
|
T | C | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115+2346T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100612317 | ||||||
| chr3:100612467
|
T | C | 3 | a0001c0005t0001g0006a0001c0005t0001g0068a0004c0009t0002g0067 | 4 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+2496T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100612467 | ||||||
| chr3:100612680
|
C | T | 3 | a0001c0005t0001g0006a0001c0005t0001g0068a0004c0009t0002g0067 | 4 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+2709C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100612680 | ||||||
| chr3:100612913
|
A | T | 291 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(288): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.115+2942A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100612913 | ||||||
| chr3:100612922
|
A | G | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115+2951A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100612922 | ||||||
| chr3:100612992
|
C | T | 11 | a0001c0005t0008g0071a0001c0008t0001g0039a0001c0008t0009g0034others(8): Show | 11 | HG00280.hp1 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.115+3021C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100612992 | ||||||
| chr3:100613060
|
G | A | 1 | a0002c0002t0001g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.115+3089G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100613060 | ||||||
| chr3:100613060
|
G | T | 61 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0030others(58): Show | 64 | HG00280.hp1 HG00597.hp1 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.115+3089G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100613060 | ||||||
| chr3:100613142
|
G | A | 3 | a0001c0005t0001g0006a0001c0005t0001g0068a0004c0009t0002g0067 | 4 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+3171G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100613142 | ||||||
| chr3:100613169
|
C | T | 2 | a0001c0001t0001g0075a0001c0001t0001g0076 | 2 | HG00280.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.115+3198C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100613169 | ||||||
| chr3:100613538
|
TA | T | 170 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(167): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.115+3580delA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100613538 | |||||
| chr3:100613539
|
A | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115+3568A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100613539 | ||||||
| chr3:100613588
|
T | A | 3 | a0001c0005t0001g0006a0001c0005t0001g0068a0004c0009t0002g0067 | 4 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+3617T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100613588 | ||||||
| chr3:100613697
|
G | A | 5 | a0001c0001t0001g0021a0001c0001t0001g0025a0003c0003t0001g0024others(2): Show | 5 | HG01952.hp1 HG02055.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+3726G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100613697 | ||||||
| chr3:100613747
|
AT | A | 3 | a0001c0005t0001g0006a0001c0005t0001g0068a0004c0009t0002g0067 | 4 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+3781delT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100613747 | |||||
| chr3:100613794
|
C | T | 7 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.115+3823C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100613794 | ||||||
| chr3:100614554
|
G | A | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115+4583G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100614554 | ||||||
| chr3:100614589
|
C | T | 1 | a0003c0003t0001g0243 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.115+4618C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100614589 | ||||||
| chr3:100614630
|
A | G | 1 | a0001c0001t0001g0222 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.115+4659A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100614630 | ||||||
| chr3:100614692
|
C | T | 161 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(158): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.115+4721C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100614692 | ||||||
| chr3:100614852
|
T | A | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.115+4881T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100614852 | ||||||
| chr3:100614870
|
G | A | 1 | a0002c0002t0001g0305 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.115+4899G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100614870 | ||||||
| chr3:100614969
|
T | C | 11 | a0002c0002t0001g0012a0002c0002t0001g0013a0002c0002t0001g0264others(8): Show | 13 | HG00423.hp2 HG01928.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.115+4998T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100614969 | ||||||
| chr3:100615011
|
C | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115+5040C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615011 | ||||||
| chr3:100615038
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.115+5067C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615038 | ||||||
| chr3:100615104
|
C | G | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.115+5133C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615104 | ||||||
| chr3:100615137
|
G | A | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.115+5166G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615137 | ||||||
| chr3:100615205
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.115+5234G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615205 | ||||||
| chr3:100615252
|
A | G | 1 | a0002c0002t0001g0303 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.115+5281A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615252 | ||||||
| chr3:100615252
|
A | T | 1 | a0001c0001t0001g0196 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.115+5281A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615252 | ||||||
| chr3:100615313
|
C | A | 1 | a0001c0001t0001g0114 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.115+5342C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615313 | ||||||
| chr3:100615369
|
G | T | 2 | a0001c0001t0001g0064a0011c0012t0001g0065 | 2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.115+5398G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615369 | ||||||
| chr3:100615378
|
G | T | 1 | a0002c0002t0001g0262 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.115+5407G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615378 | ||||||
| chr3:100615412
|
T | C | 58 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0030others(55): Show | 60 | HG00280.hp1 HG00597.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.115+5441T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615412 | ||||||
| chr3:100615635
|
G | A | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115+5664G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615635 | ||||||
| chr3:100615681
|
A | G | 162 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(159): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.115+5710A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615681 | ||||||
| chr3:100615688
|
T | C | 1 | a0001c0001t0005g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.115+5717T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615688 | ||||||
| chr3:100615690
|
G | A | 57 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0030others(54): Show | 59 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(56): Show |
intron_variant | MODIFIER | c.115+5719G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615690 | ||||||
| chr3:100615724
|
A | T | 162 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(159): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.115+5753A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615724 | ||||||
| chr3:100615736
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.115+5765T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615736 | ||||||
| chr3:100615799
|
C | G | 61 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0030others(58): Show | 64 | HG00280.hp1 HG00597.hp1 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.115+5828C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615799 | ||||||
| chr3:100615872
|
G | T | 1 | a0001c0001t0001g0195 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.115+5901G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615872 | ||||||
| chr3:100615967
|
G | A | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.115+5996G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615967 | ||||||
| chr3:100616019
|
C | T | 1 | a0002c0002t0001g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.115+6048C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100616019 | ||||||
| chr3:100616244
|
A | G | 31 | a0003c0003t0001g0011a0003c0003t0001g0017a0003c0003t0001g0018others(28): Show | 32 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.115+6273A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100616244 | ||||||
| chr3:100616332
|
C | A | 296 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(293): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.115+6361C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100616332 | ||||||
| chr3:100616335
|
C | T | 293 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(290): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.115+6364C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100616335 | ||||||
| chr3:100616406
|
A | T | 13 | a0003c0003t0001g0017a0003c0003t0001g0018a0003c0003t0001g0019others(10): Show | 13 | HG01109.hp2 HG01167.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.115+6435A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100616406 | ||||||
| chr3:100616675
|
A | G | 58 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0030others(55): Show | 60 | HG00280.hp1 HG00597.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.115+6704A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100616675 | ||||||
| chr3:100616721
|
T | C | 1 | a0003c0003t0001g0235 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.115+6750T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100616721 | ||||||
| chr3:100616753
|
G | A | 10 | a0001c0008t0001g0039a0001c0008t0009g0034a0001c0010t0001g0037others(7): Show | 10 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.115+6782G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100616753 | ||||||
| chr3:100616762
|
A | C | 12 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0054others(9): Show | 14 | HG00735.hp2 HG01884.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.115+6791A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100616762 | ||||||
| chr3:100616786
|
A | T | 1 | a0001c0001t0005g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.115+6815A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100616786 | ||||||
| chr3:100617012
|
A | G | 1 | a0012c0013t0001g0147 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.115+7041A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100617012 | ||||||
| chr3:100617083
|
T | C | 4 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(1): Show | 4 | HG02145.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+7112T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100617083 | ||||||
| chr3:100617121
|
A | C | 1 | a0001c0001t0001g0108 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.115+7150A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100617121 | ||||||
| chr3:100617371
|
C | T | 3 | a0001c0001t0001g0142a0001c0001t0001g0193a0001c0001t0001g0194 | 3 | HG00099.hp1 HG01192.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.115+7400C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100617371 | ||||||
| chr3:100617462
|
A | G | 54 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0030others(51): Show | 56 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(53): Show |
intron_variant | MODIFIER | c.115+7491A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100617462 | ||||||
| chr3:100617517
|
G | A | 4 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(1): Show | 4 | HG02145.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+7546G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100617517 | ||||||
| chr3:100617616
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.115+7645G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100617616 | ||||||
| chr3:100617651
|
T | G | 161 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(158): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.115+7680T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100617651 | ||||||
| chr3:100617696
|
G | A | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115+7725G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100617696 | ||||||
| chr3:100617747
|
G | C | 1 | a0001c0008t0009g0034 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.115+7776G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100617747 | ||||||
| chr3:100617894
|
C | A | 4 | a0001c0005t0001g0006a0001c0005t0001g0068a0001c0005t0008g0071others(1): Show | 5 | HG00280.hp1 HG02615.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.115+7923C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100617894 | ||||||
| chr3:100617900
|
C | T | 3 | a0001c0005t0001g0006a0001c0005t0001g0068a0004c0009t0002g0067 | 4 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+7929C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100617900 | ||||||
| chr3:100617920
|
GA | G | 3 | a0001c0005t0001g0006a0001c0005t0001g0068a0004c0009t0002g0067 | 4 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+7951delA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100617920 | |||||
| chr3:100617977
|
C | T | 1 | a0002c0002t0001g0271 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.115+8006C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100617977 | ||||||
| chr3:100617978
|
A | G | 68 | a0001c0001t0001g0272a0001c0001t0001g0298a0001c0001t0007g0302others(65): Show | 78 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.115+8007A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100617978 | ||||||
| chr3:100618042
|
C | T | 37 | a0001c0001t0001g0021a0001c0001t0001g0025a0003c0003t0001g0011others(34): Show | 38 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.115+8071C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618042 | ||||||
| chr3:100618045
|
T | C | 291 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(288): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.115+8074T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618045 | ||||||
| chr3:100618047
|
G | A | 68 | a0001c0001t0001g0272a0001c0001t0001g0298a0001c0001t0007g0302others(65): Show | 78 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.115+8076G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618047 | ||||||
| chr3:100618076
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.115+8105T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618076 | ||||||
| chr3:100618145
|
A | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0188a0001c0001t0001g0189others(3): Show | 7 | HG02129.hp1 NA18960.hp2 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+8174A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618145 | ||||||
| chr3:100618155
|
A | G | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.115+8184A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618155 | ||||||
| chr3:100618260
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.115+8289C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618260 | ||||||
| chr3:100618273
|
C | A | 54 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0030others(51): Show | 56 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(53): Show |
intron_variant | MODIFIER | c.115+8302C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618273 | ||||||
| chr3:100618274
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.115+8303G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618274 | ||||||
| chr3:100618339
|
T | TA | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.115+8369dupA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100618339 | |||||
| chr3:100618398
|
G | T | 8 | a0001c0001t0001g0007a0001c0001t0001g0103a0001c0001t0001g0104others(5): Show | 9 | NA18946.hp2 NA18960.hp1 NA18966.hp2 others(6): Show |
intron_variant | MODIFIER | c.115+8427G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618398 | ||||||
| chr3:100618414
|
T | C | 291 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(288): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.115+8443T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618414 | ||||||
| chr3:100618433
|
T | A | 2 | a0001c0001t0001g0197a0001c0005t0008g0071 | 2 | HG00280.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.115+8462T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618433 | ||||||
| chr3:100618434
|
C | T | 2 | a0001c0001t0001g0197a0001c0005t0008g0071 | 2 | HG00280.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.115+8463C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618434 | ||||||
| chr3:100618449
|
C | T | 1 | a0003c0003t0001g0243 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.115+8478C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618449 | ||||||
| chr3:100618534
|
A | C | 296 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(293): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.115+8563A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618534 | ||||||
| chr3:100618535
|
G | A | 3 | a0002c0002t0001g0305a0002c0002t0001g0307a0002c0002t0001g0308 | 3 | HG02165.hp2 NA18999.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.115+8564G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618535 | ||||||
| chr3:100618570
|
T | G | 7 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.115+8599T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618570 | ||||||
| chr3:100618612
|
T | G | 1 | a0001c0001t0001g0272 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.115+8641T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618612 | ||||||
| chr3:100618655
|
C | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(1): Show | 4 | HG02145.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+8684C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618655 | ||||||
| chr3:100618669
|
C | G | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115+8698C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618669 | ||||||
| chr3:100618694
|
A | G | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.115+8723A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618694 | ||||||
| chr3:100618765
|
G | C | 54 | a0001c0001t0001g0298a0002c0002t0001g0001a0002c0002t0001g0012others(51): Show | 64 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.115+8794G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618765 | ||||||
| chr3:100618787
|
G | GA | 58 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0030others(55): Show | 60 | HG00280.hp1 HG00597.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.115+8817dupA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100618787 | |||||
| chr3:100618909
|
G | A | 3 | a0005c0006t0001g0005a0005c0006t0001g0028a0005c0006t0001g0029 | 4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.115+8938G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618909 | ||||||
| chr3:100619084
|
G | C | 1 | a0001c0001t0001g0008 | 2 | NA18969.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.115+9113G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100619084 | ||||||
| chr3:100619299
|
G | A | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115+9328G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100619299 | ||||||
| chr3:100619315
|
A | C | 1 | a0002c0002t0001g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.115+9344A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100619315 | ||||||
| chr3:100619378
|
C | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115+9407C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100619378 | ||||||
| chr3:100619396
|
A | T | 1 | a0009c0015t0001g0022 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.115+9425A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100619396 | ||||||
| chr3:100619470
|
T | G | 12 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0054others(9): Show | 14 | HG00735.hp2 HG01884.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.115+9499T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100619470 | ||||||
| chr3:100619540
|
C | T | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.115+9569C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100619540 | ||||||
| chr3:100619592
|
C | A | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115+9621C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100619592 | ||||||
| chr3:100619622
|
G | T | 37 | a0001c0001t0001g0021a0001c0001t0001g0025a0003c0003t0001g0011others(34): Show | 38 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.115+9651G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100619622 | ||||||
| chr3:100619656
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0195 | 2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.115+9685G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100619656 | ||||||
| chr3:100619765
|
G | A | 12 | a0003c0003t0001g0017a0003c0003t0001g0018a0003c0003t0001g0019others(9): Show | 12 | HG01109.hp2 HG01167.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.115+9794G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100619765 | ||||||
| chr3:100619780
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.115+9809C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100619780 | ||||||
| chr3:100619828
|
G | A | 1 | a0001c0001t0001g0201 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.116-9770G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100619828 | ||||||
| chr3:100620022
|
A | T | 47 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0008t0001g0039others(44): Show | 48 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.116-9576A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620022 | ||||||
| chr3:100620024
|
T | C | 2 | a0001c0001t0001g0075a0001c0001t0001g0076 | 2 | HG00280.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.116-9574T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620024 | ||||||
| chr3:100620048
|
G | A | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.116-9550G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620048 | ||||||
| chr3:100620136
|
G | A | 7 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.116-9462G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620136 | ||||||
| chr3:100620358
|
G | A | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.116-9240G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620358 | ||||||
| chr3:100620392
|
A | G | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.116-9206A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620392 | ||||||
| chr3:100620445
|
T | C | 60 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0030others(57): Show | 63 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.116-9153T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620445 | ||||||
| chr3:100620537
|
T | C | 3 | a0001c0005t0001g0006a0001c0005t0001g0068a0004c0009t0002g0067 | 4 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-9061T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620537 | ||||||
| chr3:100620617
|
G | C | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.116-8981G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620617 | ||||||
| chr3:100620744
|
C | T | 32 | a0003c0003t0001g0011a0003c0003t0001g0017a0003c0003t0001g0018others(29): Show | 33 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.116-8854C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620744 | ||||||
| chr3:100620832
|
TG | T | 47 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0008t0001g0039others(44): Show | 48 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.116-8765delG | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620832 | ||||||
| chr3:100620864
|
G | A | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.116-8734G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620864 | ||||||
| chr3:100620912
|
G | T | 7 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.116-8686G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620912 | ||||||
| chr3:100620917
|
C | T | 2 | a0002c0002t0001g0300a0002c0002t0001g0301 | 2 | NA18950.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.116-8681C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620917 | ||||||
| chr3:100620923
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.116-8675A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620923 | ||||||
| chr3:100620992
|
G | C | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.116-8606G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620992 | ||||||
| chr3:100621097
|
G | T | 1 | a0001c0001t0001g0192 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.116-8501G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100621097 | ||||||
| chr3:100621184
|
G | A | 54 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0030others(51): Show | 56 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(53): Show |
intron_variant | MODIFIER | c.116-8414G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100621184 | ||||||
| chr3:100621279
|
A | C | 1 | a0001c0001t0001g0184 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.116-8319A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100621279 | ||||||
| chr3:100621301
|
A | G | 60 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0030others(57): Show | 63 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.116-8297A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100621301 | ||||||
| chr3:100621304
|
A | T | 9 | a0001c0001t0001g0077a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG02027.hp2 NA18747.hp2 NA18964.hp1 others(6): Show |
intron_variant | MODIFIER | c.116-8294A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100621304 | ||||||
| chr3:100621571
|
G | A | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.116-8027G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100621571 | ||||||
| chr3:100621612
|
T | C | 3 | a0002c0002t0001g0016a0002c0002t0001g0273a0002c0002t0001g0316 | 4 | NA18961.hp1 NA18966.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.116-7986T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100621612 | ||||||
| chr3:100621813
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.116-7785C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100621813 | ||||||
| chr3:100621869
|
T | G | 1 | a0002c0002t0001g0274 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.116-7729T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100621869 | ||||||
| chr3:100621887
|
C | A | 1 | a0001c0001t0001g0118 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.116-7711C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100621887 | ||||||
| chr3:100621952
|
C | T | 47 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0008t0001g0039others(44): Show | 48 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.116-7646C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100621952 | ||||||
| chr3:100621976
|
C | G | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02129.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.116-7622C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100621976 | ||||||
| chr3:100621983
|
C | T | 10 | a0001c0008t0001g0039a0001c0008t0009g0034a0001c0010t0001g0037others(7): Show | 10 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.116-7615C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100621983 | ||||||
| chr3:100622008
|
A | C | 1 | a0003c0003t0001g0234 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.116-7590A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100622008 | ||||||
| chr3:100622053
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.116-7545C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100622053 | ||||||
| chr3:100622264
|
A | AT | 30 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0050others(27): Show | 32 | HG00735.hp2 HG01099.hp1 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.116-7313dupT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100622264 | |||||
| chr3:100622264
|
A | ATT | 53 | a0001c0001t0001g0043a0001c0001t0001g0061a0001c0001t0001g0298others(50): Show | 63 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.116-7314_116-7313d others(4): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100622264 | |||||
| chr3:100622264
|
ATTTT | A | 9 | a0001c0001t0001g0021a0001c0001t0001g0072a0001c0001t0001g0073others(6): Show | 10 | HG01884.hp2 HG01891.hp2 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.116-7316_116-7313d others(6): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100622264 | |||||
| chr3:100622264
|
ATTTTT | A | 38 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0032others(35): Show | 40 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.116-7317_116-7313d others(7): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100622264 | |||||
| chr3:100622264
|
ATTTTTT | A | 16 | a0001c0001t0001g0087a0001c0001t0001g0137a0001c0001t0001g0180others(13): Show | 16 | HG01255.hp1 HG01496.hp2 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.116-7318_116-7313d others(8): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100622264 | |||||
| chr3:100622264
|
ATTTTTTT | A | 156 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(153): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.116-7319_116-7313d others(9): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100622264 | |||||
| chr3:100622291
|
T | C | 7 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.116-7307T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100622291 | ||||||
| chr3:100622353
|
C | T | 3 | a0001c0005t0001g0006a0001c0005t0001g0068a0004c0009t0002g0067 | 4 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-7245C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100622353 | ||||||
| chr3:100622355
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.116-7243T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100622355 | ||||||
| chr3:100622460
|
A | G | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.116-7138A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100622460 | ||||||
| chr3:100622539
|
A | G | 1 | a0001c0001t0003g0220 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.116-7059A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100622539 | ||||||
| chr3:100622637
|
C | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0089others(4): Show | 9 | HG00544.hp1 HG02080.hp1 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.116-6961C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100622637 | ||||||
| chr3:100622720
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0195 | 2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.116-6878G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100622720 | ||||||
| chr3:100622721
|
C | T | 1 | a0001c0005t0001g0068 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.116-6877C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100622721 | ||||||
| chr3:100622768
|
T | A | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.116-6830T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100622768 | ||||||
| chr3:100622808
|
C | T | 1 | a0001c0001t0001g0272 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.116-6790C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100622808 | ||||||
| chr3:100622899
|
G | A | 2 | a0001c0001t0001g0119a0001c0005t0008g0071 | 2 | HG00280.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.116-6699G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100622899 | ||||||
| chr3:100622928
|
G | GT | 34 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(31): Show | 38 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.116-6658dupT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100622928 | |||||
| chr3:100622960
|
G | A | 7 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.116-6638G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100622960 | ||||||
| chr3:100622994
|
C | A | 10 | a0001c0008t0001g0039a0001c0008t0009g0034a0001c0010t0001g0037others(7): Show | 10 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.116-6604C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100622994 | ||||||
| chr3:100623126
|
A | G | 3 | a0001c0001t0001g0064a0001c0001t0001g0066a0011c0012t0001g0065 | 3 | HG02559.hp2 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.116-6472A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100623126 | ||||||
| chr3:100623136
|
A | G | 61 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0030others(58): Show | 64 | HG00280.hp1 HG00597.hp1 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.116-6462A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100623136 | ||||||
| chr3:100623153
|
T | G | 1 | a0002c0002t0001g0310 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.116-6445T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100623153 | ||||||
| chr3:100623535
|
A | T | 13 | a0001c0001t0001g0083a0001c0008t0001g0039a0001c0008t0009g0034others(10): Show | 13 | HG01928.hp2 HG01993.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.116-6063A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100623535 | ||||||
| chr3:100623543
|
T | A | 1 | a0002c0002t0001g0305 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.116-6055T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100623543 | ||||||
| chr3:100623568
|
T | C | 4 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(1): Show | 4 | HG02145.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-6030T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100623568 | ||||||
| chr3:100623612
|
C | A | 3 | a0001c0001t0001g0043a0001c0001t0001g0055a0001c0001t0001g0056 | 3 | HG02109.hp2 HG02258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.116-5986C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100623612 | ||||||
| chr3:100623649
|
C | G | 292 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(289): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.116-5949C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100623649 | ||||||
| chr3:100623693
|
C | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.116-5905C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100623693 | ||||||
| chr3:100623723
|
C | A | 1 | a0001c0001t0001g0181 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.116-5875C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100623723 | ||||||
| chr3:100623751
|
T | G | 4 | a0002c0002t0001g0309a0002c0002t0001g0313a0002c0002t0001g0314others(1): Show | 4 | HG02615.hp2 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.116-5847T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100623751 | ||||||
| chr3:100623864
|
T | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0193 | 2 | HG00099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.116-5734T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100623864 | ||||||
| chr3:100623945
|
T | G | 3 | a0001c0001t0001g0142a0001c0001t0001g0193a0001c0001t0001g0194 | 3 | HG00099.hp1 HG01192.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.116-5653T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100623945 | ||||||
| chr3:100624255
|
T | C | 1 | a0001c0001t0001g0246 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.116-5343T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100624255 | ||||||
| chr3:100624447
|
A | G | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.116-5151A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100624447 | ||||||
| chr3:100624453
|
A | C | 44 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0030others(41): Show | 46 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.116-5145A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100624453 | ||||||
| chr3:100624554
|
T | C | 48 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0030others(45): Show | 50 | HG00280.hp1 HG00597.hp1 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.116-5044T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100624554 | ||||||
| chr3:100624640
|
G | A | 1 | a0003c0003t0001g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.116-4958G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100624640 | ||||||
| chr3:100624910
|
C | G | 1 | a0002c0002t0001g0299 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.116-4688C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100624910 | ||||||
| chr3:100625211
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.116-4387T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100625211 | ||||||
| chr3:100625237
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.116-4361G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100625237 | ||||||
| chr3:100625255
|
T | A | 3 | a0001c0001t0001g0120a0001c0001t0001g0152a0001c0001t0001g0196 | 3 | HG01123.hp2 HG01516.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.116-4343T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100625255 | ||||||
| chr3:100625359
|
T | C | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.116-4239T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100625359 | ||||||
| chr3:100625394
|
A | G | 161 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(158): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.116-4204A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100625394 | ||||||
| chr3:100625400
|
A | T | 290 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(287): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.116-4198A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100625400 | ||||||
| chr3:100625487
|
A | G | 44 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0030others(41): Show | 46 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.116-4111A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100625487 | ||||||
| chr3:100625502
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.116-4096A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100625502 | ||||||
| chr3:100625617
|
GAA | G | 37 | a0001c0001t0001g0021a0001c0001t0001g0025a0003c0003t0001g0011others(34): Show | 38 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.116-3979_116-3978d others(4): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100625617 | |||||
| chr3:100625879
|
C | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.116-3719C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100625879 | ||||||
| chr3:100625880
|
A | G | 315 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(312): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.116-3718A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100625880 | ||||||
| chr3:100625892
|
G | A | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.116-3706G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100625892 | ||||||
| chr3:100626161
|
G | A | 7 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.116-3437G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100626161 | ||||||
| chr3:100626181
|
A | G | 1 | a0001c0001t0001g0119 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.116-3417A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100626181 | ||||||
| chr3:100626193
|
G | A | 3 | a0001c0001t0001g0118a0001c0001t0001g0139a0001c0001t0001g0153 | 3 | NA18953.hp2 NA18974.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.116-3405G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100626193 | ||||||
| chr3:100626317
|
C | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.116-3281C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100626317 | ||||||
| chr3:100626357
|
G | A | 44 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0030others(41): Show | 46 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.116-3241G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100626357 | ||||||
| chr3:100626455
|
C | A | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.116-3143C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100626455 | ||||||
| chr3:100626779
|
C | T | 7 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.116-2819C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100626779 | ||||||
| chr3:100627074
|
G | A | 3 | a0001c0001t0001g0142a0001c0001t0001g0193a0001c0001t0001g0194 | 3 | HG00099.hp1 HG01192.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.116-2524G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100627074 | ||||||
| chr3:100627150
|
C | A | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.116-2448C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100627150 | ||||||
| chr3:100627291
|
T | C | 3 | a0001c0001t0001g0118a0001c0001t0001g0139a0001c0001t0001g0153 | 3 | NA18953.hp2 NA18974.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.116-2307T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100627291 | ||||||
| chr3:100627403
|
G | A | 9 | a0003c0003t0001g0011a0003c0003t0001g0198a0003c0003t0001g0223others(6): Show | 10 | HG01071.hp2 HG01074.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.116-2195G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100627403 | ||||||
| chr3:100627544
|
G | C | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.116-2054G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100627544 | ||||||
| chr3:100627568
|
G | C | 60 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0030others(57): Show | 63 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.116-2030G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100627568 | ||||||
| chr3:100627755
|
A | G | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.116-1843A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100627755 | ||||||
| chr3:100627813
|
C | G | 2 | a0002c0002t0001g0261a0002c0002t0001g0262 | 2 | HG03927.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.116-1785C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100627813 | ||||||
| chr3:100627891
|
C | G | 1 | a0001c0001t0001g0112 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.116-1707C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100627891 | ||||||
| chr3:100627892
|
C | T | 1 | a0003c0003t0001g0199 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.116-1706C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100627892 | ||||||
| chr3:100628110
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.116-1488A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100628110 | ||||||
| chr3:100628112
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.116-1486C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100628112 | ||||||
| chr3:100628159
|
C | T | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.116-1439C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100628159 | ||||||
| chr3:100628269
|
T | A | 40 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(37): Show | 42 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.116-1329T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100628269 | ||||||
| chr3:100628292
|
C | G | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.116-1306C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100628292 | ||||||
| chr3:100628374
|
G | GT | 56 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0044others(53): Show | 57 | HG00597.hp1 HG00735.hp1 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.116-1214dupT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100628374 | |||||
| chr3:100628374
|
G | GTT | 10 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(7): Show | 12 | HG01975.hp2 HG02145.hp1 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.116-1215_116-1214d others(4): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100628374 | |||||
| chr3:100628416
|
T | C | 1 | a0002c0002t0001g0265 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.116-1182T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100628416 | ||||||
| chr3:100628437
|
C | A | 7 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.116-1161C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100628437 | ||||||
| chr3:100628445
|
G | A | 228 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(225): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.116-1153G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100628445 | ||||||
| chr3:100628564
|
C | G | 7 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.116-1034C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100628564 | ||||||
| chr3:100628599
|
G | A | 67 | a0001c0001t0001g0298a0001c0001t0007g0302a0002c0002t0001g0001others(64): Show | 77 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.116-999G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100628599 | ||||||
| chr3:100628619
|
G | C | 1 | a0002c0002t0001g0309 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.116-979G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100628619 | ||||||
| chr3:100628793
|
C | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.116-805C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100628793 | ||||||
| chr3:100628812
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.116-786C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100628812 | ||||||
| chr3:100628874
|
C | T | 3 | a0001c0001t0001g0118a0001c0001t0001g0139a0001c0001t0001g0153 | 3 | NA18953.hp2 NA18974.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.116-724C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100628874 | ||||||
| chr3:100629092
|
T | C | 1 | a0001c0001t0001g0122 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.116-506T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100629092 | ||||||
| chr3:100629100
|
G | C | 61 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0030others(58): Show | 64 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.116-498G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100629100 | ||||||
| chr3:100629118
|
C | T | 1 | a0005c0006t0001g0029 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.116-480C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100629118 | ||||||
| chr3:100629251
|
T | C | 2 | a0001c0005t0001g0068a0004c0009t0002g0067 | 2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116-347T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100629251 | ||||||
| chr3:100629267
|
C | A | 1 | a0002c0002t0001g0278 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.116-331C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100629267 | ||||||
| chr3:100629267
|
C | CTCTA | 56 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0045others(53): Show | 57 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.116-290_116-287dup others(4): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100629267 | |||||
| chr3:100629267
|
C | CTCTATCT others(1): Show |
15 | a0001c0001t0001g0074a0001c0001t0001g0120a0001c0001t0001g0175others(12): Show | 15 | HG00609.hp1 HG00735.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.116-294_116-287dup others(8): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100629267 | |||||
| chr3:100629267
|
CTCTA | C | 42 | a0001c0001t0001g0007a0001c0001t0001g0046a0001c0001t0001g0057others(39): Show | 43 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.116-290_116-287del others(4): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100629267 | |||||
| chr3:100629267
|
CTCTATCT others(1): Show |
C | 36 | a0001c0001t0001g0025a0001c0001t0001g0085a0001c0001t0003g0090others(33): Show | 37 | HG00438.hp1 HG00597.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.116-294_116-287del others(8): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100629267 | |||||
| chr3:100629267
|
CTCTATCT others(5): Show |
C | 1 | a0001c0001t0001g0154 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.116-298_116-287del others(12): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100629267 | |||||
| chr3:100629277
|
C | G | 1 | a0001c0001t0001g0298 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.116-321C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100629277 | ||||||
| chr3:100629322
|
A | G | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.116-276A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100629322 | ||||||
| chr3:100629514
|
G | A | 1 | a0001c0001t0001g0153 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.116-84G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100629514 | ||||||
| chr3:100629547
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.116-51A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100629547 | ||||||
| chr3:100629957
|
C | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.229+246C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 2/15 | chr3 | 100629957 | ||||||
| chr3:100629958
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.229+247G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 2/15 | chr3 | 100629958 | ||||||
| chr3:100629999
|
C | T | 10 | a0001c0008t0001g0039a0001c0008t0009g0034a0001c0010t0001g0037others(7): Show | 10 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.229+288C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 2/15 | chr3 | 100629999 | ||||||
| chr3:100630044
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0062 | 4 | HG01884.hp1 HG02486.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.229+333C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 2/15 | chr3 | 100630044 | ||||||
| chr3:100630186
|
CAATT | C | 9 | a0001c0005t0008g0071a0001c0008t0001g0039a0004c0004t0002g0020others(6): Show | 9 | HG00280.hp1 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.229+476_229+479del others(4): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 2/15 | chr3 | 100630186 | ||||||
| chr3:100630274
|
G | A | 1 | a0002c0002t0001g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.230-431G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 2/15 | chr3 | 100630274 | ||||||
| chr3:100630340
|
T | G | 1 | a0003c0003t0001g0239 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.230-365T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 2/15 | chr3 | 100630340 | ||||||
| chr3:100630343
|
C | T | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.230-362C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 2/15 | chr3 | 100630343 | ||||||
| chr3:100630345
|
T | C | 2 | a0001c0001t0001g0204a0001c0001t0001g0212 | 2 | HG00609.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.230-360T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 2/15 | chr3 | 100630345 | ||||||
| chr3:100630530
|
C | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.230-175C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 2/15 | chr3 | 100630530 | ||||||
| chr3:100630647
|
T | A | 1 | a0001c0001t0001g0008 | 2 | NA18969.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.230-58T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 2/15 | chr3 | 100630647 | ||||||
| chr3:100630851
|
C | T | 1 | a0002c0002t0001g0013 | 2 | NA18988.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.334+42C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100630851 | ||||||
| chr3:100630997
|
A | C | 1 | a0001c0001t0005g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.334+188A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100630997 | ||||||
| chr3:100630999
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.334+190C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100630999 | ||||||
| chr3:100631123
|
TA | T | 61 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0030others(58): Show | 64 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.334+323delA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr3 | 100631123 | |||||
| chr3:100631124
|
A | T | 1 | a0001c0001t0001g0063 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.334+315A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100631124 | ||||||
| chr3:100631400
|
A | G | 33 | a0003c0003t0001g0011a0003c0003t0001g0017a0003c0003t0001g0018others(30): Show | 34 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.334+591A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100631400 | ||||||
| chr3:100631403
|
C | A | 10 | a0001c0008t0001g0039a0001c0008t0009g0034a0001c0010t0001g0037others(7): Show | 10 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.334+594C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100631403 | ||||||
| chr3:100631422
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.334+613G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100631422 | ||||||
| chr3:100631550
|
T | C | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.334+741T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100631550 | ||||||
| chr3:100631584
|
T | C | 1 | a0002c0002t0001g0257 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.334+775T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100631584 | ||||||
| chr3:100631663
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.334+854G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100631663 | ||||||
| chr3:100631700
|
A | G | 1 | a0002c0002t0001g0312 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.334+891A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100631700 | ||||||
| chr3:100631844
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.334+1035C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100631844 | ||||||
| chr3:100631901
|
C | T | 61 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0030others(58): Show | 64 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.334+1092C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100631901 | ||||||
| chr3:100632031
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.334+1222A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100632031 | ||||||
| chr3:100632551
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.335-714C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100632551 | ||||||
| chr3:100632662
|
C | T | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.335-603C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100632662 | ||||||
| chr3:100632668
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.335-597A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100632668 | ||||||
| chr3:100632852
|
T | C | 291 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(288): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.335-413T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100632852 | ||||||
| chr3:100632968
|
A | C | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.335-297A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100632968 | ||||||
| chr3:100633052
|
C | T | 45 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0030others(42): Show | 47 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.335-213C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100633052 | ||||||
| chr3:100633199
|
C | T | 32 | a0003c0003t0001g0011a0003c0003t0001g0017a0003c0003t0001g0018others(29): Show | 33 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.335-66C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100633199 | ||||||
| chr3:100633588
|
C | T | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.447+211C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100633588 | ||||||
| chr3:100633593
|
C | T | 4 | a0002c0002t0001g0279a0002c0002t0001g0280a0002c0002t0001g0281others(1): Show | 4 | HG00621.hp1 NA19063.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.447+216C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100633593 | ||||||
| chr3:100633652
|
G | T | 3 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210 | 3 | HG00597.hp2 NA18946.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.447+275G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100633652 | ||||||
| chr3:100633676
|
C | T | 45 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0030others(42): Show | 47 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.447+299C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100633676 | ||||||
| chr3:100633764
|
C | T | 7 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.447+387C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100633764 | ||||||
| chr3:100633802
|
G | A | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.447+425G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100633802 | ||||||
| chr3:100633850
|
T | C | 1 | a0003c0003t0001g0239 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.447+473T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100633850 | ||||||
| chr3:100633885
|
C | A | 2 | a0001c0001t0001g0094a0001c0001t0001g0121 | 2 | HG02083.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.447+508C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100633885 | ||||||
| chr3:100633899
|
T | C | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.447+522T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100633899 | ||||||
| chr3:100633942
|
G | C | 2 | a0002c0002t0001g0261a0002c0002t0001g0262 | 2 | HG03927.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.447+565G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100633942 | ||||||
| chr3:100634051
|
C | T | 7 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.447+674C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100634051 | ||||||
| chr3:100634086
|
G | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.447+709G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100634086 | ||||||
| chr3:100634506
|
A | G | 1 | a0003c0003t0001g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.447+1129A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100634506 | ||||||
| chr3:100634619
|
A | G | 289 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(286): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.448-1058A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100634619 | ||||||
| chr3:100634885
|
G | C | 3 | a0003c0003t0001g0024a0003c0003t0001g0026a0003c0003t0003g0023 | 3 | HG02055.hp2 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.448-792G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100634885 | ||||||
| chr3:100634965
|
T | C | 69 | a0001c0001t0001g0108a0001c0001t0001g0143a0001c0001t0001g0144others(66): Show | 79 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.448-712T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100634965 | ||||||
| chr3:100635000
|
G | GAC | 229 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(226): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.448-649_448-648dup others(2): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr3 | 100635000 | |||||
| chr3:100635000
|
G | GACAC | 20 | a0001c0001t0001g0075a0001c0001t0001g0088a0001c0001t0001g0095others(17): Show | 20 | HG00280.hp2 HG00621.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.448-651_448-648dup others(4): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr3 | 100635000 | |||||
| chr3:100635000
|
G | GACACAC | 14 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(11): Show | 15 | HG01106.hp1 HG01516.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.448-653_448-648dup others(6): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr3 | 100635000 | |||||
| chr3:100635000
|
G | GACACACA others(1): Show |
3 | a0003c0003t0001g0024a0003c0003t0001g0026a0003c0003t0003g0023 | 3 | HG02055.hp2 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.448-655_448-648dup others(8): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr3 | 100635000 | |||||
| chr3:100635030
|
T | C | 2 | a0001c0001t0001g0252a0001c0005t0008g0071 | 2 | HG00280.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.448-647T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100635030 | ||||||
| chr3:100635034
|
C | CACACACA others(3): Show |
1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.448-637_448-636ins others(10): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr3 | 100635034 | |||||
| chr3:100635047
|
G | A | 4 | a0001c0001t0001g0025a0001c0001t0001g0052a0001c0001t0001g0053others(1): Show | 4 | HG03209.hp1 HG03239.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.448-630G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100635047 | ||||||
| chr3:100635089
|
A | T | 1 | a0003c0003t0001g0242 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.448-588A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100635089 | ||||||
| chr3:100635188
|
CA | C | 3 | a0003c0003t0001g0024a0003c0003t0001g0026a0003c0003t0003g0023 | 3 | HG02055.hp2 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.448-483delA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr3 | 100635188 | |||||
| chr3:100635231
|
A | ACC | 246 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(243): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.448-446_448-445ins others(2): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100635231 | ||||||
| chr3:100635247
|
T | C | 1 | a0003c0003t0001g0242 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.448-430T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100635247 | ||||||
| chr3:100635326
|
A | G | 230 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(227): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.448-351A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100635326 | ||||||
| chr3:100635652
|
G | GT | 7 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.448-17dupT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr3 | 100635652 | |||||
| chr3:100635839
|
G | A | 252 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(249): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.597+13G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/15 | chr3 | 100635839 | ||||||
| chr3:100635853
|
AT | A | 7 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.597+37delT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 100635853 | |||||
| chr3:100635854
|
T | A | 275 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(272): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.597+28T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/15 | chr3 | 100635854 | ||||||
| chr3:100635855
|
T | A | 3 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0205 | 3 | HG01884.hp2 HG01891.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.597+29T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/15 | chr3 | 100635855 | ||||||
| chr3:100636013
|
G | T | 3 | a0003c0003t0001g0024a0003c0003t0001g0026a0003c0003t0003g0023 | 3 | HG02055.hp2 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.597+187G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/15 | chr3 | 100636013 | ||||||
| chr3:100636250
|
G | T | 161 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(158): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.597+424G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/15 | chr3 | 100636250 | ||||||
| chr3:100636260
|
G | A | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.597+434G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/15 | chr3 | 100636260 | ||||||
| chr3:100636494
|
A | G | 2 | a0001c0001t0001g0135a0001c0001t0001g0218 | 2 | HG01346.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.597+668A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/15 | chr3 | 100636494 | ||||||
| chr3:100636575
|
T | C | 246 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(243): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.598-727T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/15 | chr3 | 100636575 | ||||||
| chr3:100636645
|
G | GA | 241 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(238): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.598-647dupA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 100636645 | |||||
| chr3:100636750
|
G | T | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.598-552G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/15 | chr3 | 100636750 | ||||||
| chr3:100636871
|
A | G | 1 | a0002c0002t0001g0304 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.598-431A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/15 | chr3 | 100636871 | ||||||
| chr3:100637014
|
C | T | 253 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(250): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.598-288C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/15 | chr3 | 100637014 | ||||||
| chr3:100637180
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.598-122C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/15 | chr3 | 100637180 | ||||||
| chr3:100637183
|
C | G | 253 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(250): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.598-119C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/15 | chr3 | 100637183 | ||||||
| chr3:100637437
|
C | G | 1 | a0001c0001t0001g0214 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.698+35C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100637437 | ||||||
| chr3:100637541
|
G | A | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.698+139G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100637541 | ||||||
| chr3:100637738
|
A | C | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.698+336A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100637738 | ||||||
| chr3:100637808
|
C | G | 1 | a0001c0001t0001g0115 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.698+406C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100637808 | ||||||
| chr3:100637871
|
G | A | 2 | a0001c0001t0001g0094a0001c0001t0001g0121 | 2 | HG02083.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.698+469G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100637871 | ||||||
| chr3:100637908
|
C | G | 4 | a0001c0008t0001g0039a0006c0007t0004g0040a0006c0007t0004g0041others(1): Show | 4 | HG02109.hp1 HG02630.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.698+506C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100637908 | ||||||
| chr3:100637947
|
A | C | 1 | a0001c0001t0001g0114 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.698+545A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100637947 | ||||||
| chr3:100637968
|
A | T | 1 | a0001c0001t0001g0083 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.698+566A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100637968 | ||||||
| chr3:100637974
|
C | A | 1 | a0001c0008t0009g0034 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.698+572C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100637974 | ||||||
| chr3:100638125
|
T | G | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.698+723T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100638125 | ||||||
| chr3:100638263
|
T | A | 3 | a0002c0002t0001g0305a0002c0002t0001g0307a0002c0002t0001g0308 | 3 | HG02165.hp2 NA18999.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.698+861T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100638263 | ||||||
| chr3:100638425
|
A | G | 2 | a0001c0005t0001g0006a0001c0005t0001g0068 | 3 | HG02895.hp2 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.698+1023A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100638425 | ||||||
| chr3:100638538
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.698+1136G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100638538 | ||||||
| chr3:100638542
|
C | T | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.698+1140C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100638542 | ||||||
| chr3:100638560
|
A | C | 1 | a0001c0001t0001g0177 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.698+1158A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100638560 | ||||||
| chr3:100638577
|
G | A | 2 | a0002c0002t0001g0300a0002c0002t0001g0301 | 2 | NA18950.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.698+1175G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100638577 | ||||||
| chr3:100638731
|
A | G | 7 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.698+1329A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100638731 | ||||||
| chr3:100638827
|
C | A | 68 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(65): Show | 71 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.698+1425C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100638827 | ||||||
| chr3:100638862
|
C | T | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.698+1460C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100638862 | ||||||
| chr3:100639010
|
CTG | C | 5 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0051others(2): Show | 5 | HG02809.hp1 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.698+1654_698+1655d others(4): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 100639010 | |||||
| chr3:100639010
|
CTGTG | C | 17 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0021others(14): Show | 20 | HG01884.hp1 HG01952.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.698+1652_698+1655d others(6): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 100639010 | |||||
| chr3:100639010
|
CTGTGTG | C | 9 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0032others(6): Show | 10 | HG01975.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.698+1650_698+1655d others(8): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 100639010 | |||||
| chr3:100639010
|
CTGTGTGT others(1): Show |
C | 13 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0064others(10): Show | 14 | HG01081.hp2 HG01106.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.698+1648_698+1655d others(10): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 100639010 | |||||
| chr3:100639010
|
CTGTGTGT others(3): Show |
C | 29 | a0003c0003t0001g0017a0003c0003t0001g0019a0003c0003t0001g0027others(26): Show | 29 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.698+1646_698+1655d others(12): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 100639010 | |||||
| chr3:100639010
|
CTGTGTGT others(5): Show |
C | 3 | a0002c0002t0001g0275a0002c0002t0001g0276a0002c0002t0001g0307 | 3 | HG01515.hp2 HG01517.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.698+1644_698+1655d others(14): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 100639010 | |||||
| chr3:100639010
|
CTGTGTGT others(7): Show |
C | 56 | a0002c0002t0001g0001a0002c0002t0001g0012a0002c0002t0001g0013others(53): Show | 66 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.698+1642_698+1655d others(16): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 100639010 | |||||
| chr3:100639010
|
CTGTGTGT others(9): Show |
C | 15 | a0001c0001t0001g0099a0001c0001t0001g0114a0001c0001t0001g0124others(12): Show | 16 | HG00597.hp2 HG01256.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.698+1640_698+1655d others(18): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 100639010 | |||||
| chr3:100639010
|
CTGTGTGT others(11): Show |
C | 152 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(149): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.698+1638_698+1655d others(20): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 100639010 | |||||
| chr3:100639010
|
CTGTGTGT others(15): Show |
C | 4 | a0001c0001t0001g0120a0001c0001t0001g0152a0001c0001t0001g0196others(1): Show | 4 | HG01123.hp1 HG01123.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.698+1634_698+1655d others(24): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 100639010 | |||||
| chr3:100639030
|
GTGTGTGT others(21): Show |
G | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.698+1632_698+1659d others(30): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 100639030 | |||||
| chr3:100639032
|
GTGTGTGT others(19): Show |
G | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.698+1634_698+1659d others(28): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 100639032 | |||||
| chr3:100639196
|
T | C | 289 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(286): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.698+1794T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100639196 | ||||||
| chr3:100639197
|
G | A | 56 | a0002c0002t0001g0001a0002c0002t0001g0012a0002c0002t0001g0013others(53): Show | 66 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.698+1795G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100639197 | ||||||
| chr3:100639300
|
T | A | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.698+1898T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100639300 | ||||||
| chr3:100639534
|
G | T | 66 | a0001c0001t0001g0085a0002c0002t0001g0001a0002c0002t0001g0012others(63): Show | 76 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.698+2132G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100639534 | ||||||
| chr3:100639696
|
C | A | 65 | a0002c0002t0001g0001a0002c0002t0001g0012a0002c0002t0001g0013others(62): Show | 75 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.698+2294C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100639696 | ||||||
| chr3:100639696
|
C | T | 2 | a0001c0001t0001g0064a0011c0012t0001g0065 | 2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.698+2294C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100639696 | ||||||
| chr3:100639801
|
G | C | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.698+2399G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100639801 | ||||||
| chr3:100639938
|
G | T | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0207 | 3 | HG02135.hp1 NA18747.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.698+2536G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100639938 | ||||||
| chr3:100639947
|
C | A | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.698+2545C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100639947 | ||||||
| chr3:100639951
|
T | A | 12 | a0001c0008t0001g0039a0001c0008t0009g0034a0001c0010t0001g0037others(9): Show | 12 | HG00735.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.698+2549T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100639951 | ||||||
| chr3:100640018
|
C | T | 2 | a0001c0001t0001g0064a0011c0012t0001g0065 | 2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.698+2616C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100640018 | ||||||
| chr3:100640061
|
C | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.698+2659C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100640061 | ||||||
| chr3:100640178
|
G | A | 1 | a0003c0003t0001g0233 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.698+2776G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100640178 | ||||||
| chr3:100640285
|
C | A | 1 | a0001c0001t0001g0052 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.698+2883C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100640285 | ||||||
| chr3:100640489
|
T | C | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.699-2777T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100640489 | ||||||
| chr3:100640544
|
C | T | 17 | a0001c0001t0001g0007a0001c0001t0001g0078a0001c0001t0001g0081others(14): Show | 18 | HG00544.hp2 HG00558.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.699-2722C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100640544 | ||||||
| chr3:100640618
|
T | C | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.699-2648T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100640618 | ||||||
| chr3:100640665
|
G | A | 2 | a0001c0005t0001g0006a0001c0005t0001g0068 | 3 | HG02895.hp2 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.699-2601G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100640665 | ||||||
| chr3:100640760
|
G | T | 1 | a0001c0001t0001g0134 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.699-2506G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100640760 | ||||||
| chr3:100640788
|
T | C | 68 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(65): Show | 71 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.699-2478T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100640788 | ||||||
| chr3:100640832
|
T | G | 65 | a0002c0002t0001g0001a0002c0002t0001g0012a0002c0002t0001g0013others(62): Show | 75 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.699-2434T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100640832 | ||||||
| chr3:100640864
|
A | G | 2 | a0001c0005t0001g0006a0001c0005t0001g0068 | 3 | HG02895.hp2 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.699-2402A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100640864 | ||||||
| chr3:100641051
|
G | A | 5 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0172others(2): Show | 5 | HG01358.hp1 HG01943.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.699-2215G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100641051 | ||||||
| chr3:100641154
|
G | A | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.699-2112G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100641154 | ||||||
| chr3:100641234
|
G | A | 1 | a0002c0002t0001g0313 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.699-2032G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100641234 | ||||||
| chr3:100641287
|
G | A | 2 | a0001c0005t0001g0006a0001c0005t0001g0068 | 3 | HG02895.hp2 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.699-1979G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100641287 | ||||||
| chr3:100641302
|
G | A | 2 | a0001c0001t0001g0165a0001c0001t0001g0175 | 2 | HG02071.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.699-1964G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100641302 | ||||||
| chr3:100641425
|
A | T | 65 | a0002c0002t0001g0001a0002c0002t0001g0012a0002c0002t0001g0013others(62): Show | 75 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.699-1841A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100641425 | ||||||
| chr3:100641427
|
G | A | 2 | a0001c0001t0001g0064a0011c0012t0001g0065 | 2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.699-1839G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100641427 | ||||||
| chr3:100641504
|
C | T | 163 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(160): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.699-1762C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100641504 | ||||||
| chr3:100641543
|
A | C | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.699-1723A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100641543 | ||||||
| chr3:100641613
|
G | A | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.699-1653G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100641613 | ||||||
| chr3:100641648
|
A | G | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.699-1618A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100641648 | ||||||
| chr3:100641894
|
C | A | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.699-1372C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100641894 | ||||||
| chr3:100641906
|
C | T | 1 | a0003c0003t0001g0234 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.699-1360C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100641906 | ||||||
| chr3:100641949
|
G | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.699-1317G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100641949 | ||||||
| chr3:100641973
|
C | G | 2 | a0001c0001t0001g0098a0001c0001t0001g0133 | 2 | HG02015.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.699-1293C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100641973 | ||||||
| chr3:100642205
|
T | C | 1 | a0001c0001t0001g0126 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.699-1061T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100642205 | ||||||
| chr3:100642532
|
C | G | 1 | a0003c0003t0001g0249 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.699-734C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100642532 | ||||||
| chr3:100642818
|
C | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(1): Show | 4 | HG02145.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.699-448C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100642818 | ||||||
| chr3:100642847
|
C | T | 2 | a0001c0001t0001g0252a0001c0001t0001g0254 | 2 | NA18999.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.699-419C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100642847 | ||||||
| chr3:100642901
|
A | G | 1 | a0001c0001t0001g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.699-365A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100642901 | ||||||
| chr3:100642962
|
T | C | 33 | a0003c0003t0001g0011a0003c0003t0001g0017a0003c0003t0001g0018others(30): Show | 34 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.699-304T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100642962 | ||||||
| chr3:100643098
|
C | A | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.699-168C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100643098 | ||||||
| chr3:100643148
|
T | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0096 | 2 | HG00423.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.699-118T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100643148 | ||||||
| chr3:100643670
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.946+37C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100643670 | ||||||
| chr3:100643782
|
T | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | NA18965.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.946+149T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100643782 | ||||||
| chr3:100643923
|
G | C | 12 | a0001c0008t0001g0039a0001c0008t0009g0034a0001c0010t0001g0037others(9): Show | 12 | HG00735.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.946+290G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100643923 | ||||||
| chr3:100644061
|
C | T | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.946+428C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100644061 | ||||||
| chr3:100644109
|
A | G | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.946+476A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100644109 | ||||||
| chr3:100644155
|
C | T | 253 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(250): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.946+522C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100644155 | ||||||
| chr3:100644187
|
T | TA | 242 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(239): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.946+564dupA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr3 | 100644187 | |||||
| chr3:100644213
|
G | C | 253 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(250): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.946+580G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100644213 | ||||||
| chr3:100644214
|
A | G | 2 | a0001c0005t0001g0006a0001c0005t0001g0068 | 3 | HG02895.hp2 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.946+581A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100644214 | ||||||
| chr3:100644223
|
C | G | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.946+590C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100644223 | ||||||
| chr3:100644256
|
G | A | 65 | a0002c0002t0001g0001a0002c0002t0001g0012a0002c0002t0001g0013others(62): Show | 75 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.946+623G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100644256 | ||||||
| chr3:100644282
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.946+649A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100644282 | ||||||
| chr3:100644332
|
G | A | 12 | a0001c0008t0001g0039a0001c0008t0009g0034a0001c0010t0001g0037others(9): Show | 12 | HG00735.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.946+699G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100644332 | ||||||
| chr3:100644379
|
T | C | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.946+746T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100644379 | ||||||
| chr3:100644532
|
G | A | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.946+899G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100644532 | ||||||
| chr3:100644597
|
G | A | 37 | a0001c0001t0001g0118a0001c0001t0001g0139a0001c0001t0001g0153others(34): Show | 38 | HG00597.hp1 HG00735.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.946+964G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100644597 | ||||||
| chr3:100644697
|
A | C | 2 | a0001c0005t0001g0006a0001c0005t0001g0068 | 3 | HG02895.hp2 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.946+1064A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100644697 | ||||||
| chr3:100644728
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.946+1095G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100644728 | ||||||
| chr3:100645007
|
C | T | 2 | a0001c0005t0001g0006a0001c0005t0001g0068 | 3 | HG02895.hp2 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.947-938C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100645007 | ||||||
| chr3:100645014
|
G | A | 1 | a0001c0001t0005g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.947-931G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100645014 | ||||||
| chr3:100645258
|
A | G | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.947-687A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100645258 | ||||||
| chr3:100645408
|
G | C | 1 | a0001c0001t0001g0120 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.947-537G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100645408 | ||||||
| chr3:100645431
|
C | CAGA | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.947-511_947-509dup others(3): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr3 | 100645431 | |||||
| chr3:100645474
|
G | A | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.947-471G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100645474 | ||||||
| chr3:100645633
|
A | G | 1 | a0001c0001t0001g0171 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.947-312A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100645633 | ||||||
| chr3:100645636
|
C | T | 1 | a0001c0001t0003g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.947-309C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100645636 | ||||||
| chr3:100645667
|
C | T | 2 | a0001c0001t0001g0215a0001c0001t0001g0245 | 2 | HG03654.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.947-278C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100645667 | ||||||
| chr3:100645749
|
G | A | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.947-196G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100645749 | ||||||
| chr3:100646220
|
G | C | 1 | a0003c0003t0001g0227 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1110+112G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 9/15 | chr3 | 100646220 | ||||||
| chr3:100646220
|
G | T | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1110+112G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 9/15 | chr3 | 100646220 | ||||||
| chr3:100646229
|
T | A | 4 | a0004c0004t0002g0020a0004c0004t0002g0035a0004c0009t0002g0047others(1): Show | 4 | HG00735.hp2 HG02615.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1110+121T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 9/15 | chr3 | 100646229 | ||||||
| chr3:100646280
|
G | A | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1110+172G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 9/15 | chr3 | 100646280 | ||||||
| chr3:100646354
|
C | T | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111-215C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 9/15 | chr3 | 100646354 | ||||||
| chr3:100646488
|
G | C | 1 | a0001c0001t0001g0176 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1111-81G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 9/15 | chr3 | 100646488 | ||||||
| chr3:100646807
|
T | C | 2 | a0002c0002t0001g0069a0002c0002t0001g0312 | 2 | HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1266+83T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100646807 | ||||||
| chr3:100646881
|
C | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1266+157C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100646881 | ||||||
| chr3:100646912
|
A | C | 289 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(286): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.1266+188A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100646912 | ||||||
| chr3:100646955
|
C | T | 101 | a0002c0002t0001g0001a0002c0002t0001g0012a0002c0002t0001g0013others(98): Show | 112 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.1266+231C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100646955 | ||||||
| chr3:100647017
|
T | C | 286 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(283): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1266+293T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100647017 | ||||||
| chr3:100647018
|
G | A | 177 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(174): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.1266+294G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100647018 | ||||||
| chr3:100647020
|
A | G | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1266+296A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100647020 | ||||||
| chr3:100647031
|
C | T | 285 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(282): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.1266+307C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100647031 | ||||||
| chr3:100647060
|
G | A | 2 | a0003c0003t0001g0199a0003c0003t0001g0229 | 2 | HG00741.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1266+336G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100647060 | ||||||
| chr3:100647122
|
A | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1266+398A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100647122 | ||||||
| chr3:100647168
|
C | G | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1266+444C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100647168 | ||||||
| chr3:100647184
|
A | T | 1 | a0001c0005t0001g0068 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1266+460A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100647184 | ||||||
| chr3:100647370
|
T | C | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1266+646T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100647370 | ||||||
| chr3:100647380
|
C | T | 286 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(283): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1266+656C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100647380 | ||||||
| chr3:100647699
|
C | T | 1 | a0001c0008t0009g0034 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1266+975C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100647699 | ||||||
| chr3:100647707
|
C | CA | 284 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(281): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1266+991dupA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr3 | 100647707 | |||||
| chr3:100647759
|
A | C | 1 | a0001c0001t0001g0048 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1266+1035A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100647759 | ||||||
| chr3:100647829
|
G | A | 1 | a0001c0001t0001g0244 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1266+1105G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100647829 | ||||||
| chr3:100647988
|
G | T | 2 | a0001c0005t0001g0006a0001c0005t0001g0068 | 3 | HG02895.hp2 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1266+1264G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100647988 | ||||||
| chr3:100648019
|
C | T | 285 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(282): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.1266+1295C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648019 | ||||||
| chr3:100648028
|
T | C | 286 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(283): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1266+1304T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648028 | ||||||
| chr3:100648055
|
C | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1266+1331C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648055 | ||||||
| chr3:100648260
|
T | C | 286 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(283): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1267-1435T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648260 | ||||||
| chr3:100648266
|
A | G | 7 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1267-1429A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648266 | ||||||
| chr3:100648315
|
G | GTAA | 286 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(283): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1267-1380_1267-137 others(7): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648315 | ||||||
| chr3:100648317
|
T | G | 286 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(283): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1267-1378T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648317 | ||||||
| chr3:100648340
|
GA | G | 286 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(283): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1267-1350delA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr3 | 100648340 | |||||
| chr3:100648343
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1267-1352A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648343 | ||||||
| chr3:100648381
|
C | T | 286 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(283): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1267-1314C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648381 | ||||||
| chr3:100648383
|
A | G | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1267-1312A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648383 | ||||||
| chr3:100648411
|
C | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1267-1284C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648411 | ||||||
| chr3:100648413
|
T | C | 285 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(282): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.1267-1282T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648413 | ||||||
| chr3:100648427
|
T | A | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1267-1268T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648427 | ||||||
| chr3:100648495
|
G | A | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1267-1200G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648495 | ||||||
| chr3:100648519
|
G | A | 286 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(283): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1267-1176G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648519 | ||||||
| chr3:100648522
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1267-1173C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648522 | ||||||
| chr3:100648647
|
C | T | 163 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(160): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.1267-1048C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648647 | ||||||
| chr3:100648672
|
C | G | 5 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0073others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1267-1023C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648672 | ||||||
| chr3:100648721
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1267-974C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648721 | ||||||
| chr3:100648766
|
A | T | 285 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(282): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.1267-929A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648766 | ||||||
| chr3:100648795
|
TA | T | 36 | a0003c0003t0001g0011a0003c0003t0001g0017a0003c0003t0001g0018others(33): Show | 37 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1267-893delA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr3 | 100648795 | |||||
| chr3:100648801
|
A | T | 36 | a0003c0003t0001g0011a0003c0003t0001g0017a0003c0003t0001g0018others(33): Show | 37 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1267-894A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648801 | ||||||
| chr3:100648833
|
T | C | 4 | a0001c0001t0001g0102a0001c0001t0001g0141a0001c0001t0001g0183others(1): Show | 4 | HG02027.hp2 NA18747.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.1267-862T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648833 | ||||||
| chr3:100648929
|
C | T | 3 | a0003c0003t0001g0024a0003c0003t0001g0026a0003c0003t0003g0023 | 3 | HG02055.hp2 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1267-766C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648929 | ||||||
| chr3:100648945
|
G | C | 1 | a0001c0001t0001g0152 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1267-750G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648945 | ||||||
| chr3:100649288
|
G | A | 3 | a0003c0003t0001g0024a0003c0003t0001g0026a0003c0003t0003g0023 | 3 | HG02055.hp2 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1267-407G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100649288 | ||||||
| chr3:100649300
|
T | C | 3 | a0003c0003t0001g0024a0003c0003t0001g0026a0003c0003t0003g0023 | 3 | HG02055.hp2 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1267-395T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100649300 | ||||||
| chr3:100649403
|
C | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1267-292C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100649403 | ||||||
| chr3:100649431
|
C | G | 1 | a0001c0001t0001g0076 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1267-264C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100649431 | ||||||
| chr3:100649581
|
A | G | 177 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(174): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.1267-114A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100649581 | ||||||
| chr3:100649631
|
G | A | 43 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(40): Show | 45 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1267-64G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100649631 | ||||||
| chr3:100649848
|
A | G | 285 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(282): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.1379+41A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100649848 | ||||||
| chr3:100650096
|
T | C | 285 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(282): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.1379+289T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100650096 | ||||||
| chr3:100650115
|
G | T | 285 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(282): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.1379+308G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100650115 | ||||||
| chr3:100650302
|
C | G | 242 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(239): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.1379+495C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100650302 | ||||||
| chr3:100650340
|
T | A | 3 | a0005c0006t0001g0005a0005c0006t0001g0028a0005c0006t0001g0029 | 4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1379+533T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100650340 | ||||||
| chr3:100650388
|
G | A | 12 | a0001c0008t0001g0039a0001c0008t0009g0034a0001c0010t0001g0037others(9): Show | 12 | HG00735.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1379+581G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100650388 | ||||||
| chr3:100650424
|
C | T | 12 | a0001c0008t0001g0039a0001c0008t0009g0034a0001c0010t0001g0037others(9): Show | 12 | HG00735.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1379+617C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100650424 | ||||||
| chr3:100650496
|
C | G | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1379+689C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100650496 | ||||||
| chr3:100650625
|
A | G | 1 | a0003c0003t0001g0241 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1379+818A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100650625 | ||||||
| chr3:100650641
|
G | A | 36 | a0003c0003t0001g0011a0003c0003t0001g0017a0003c0003t0001g0018others(33): Show | 37 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1379+834G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100650641 | ||||||
| chr3:100650649
|
A | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1379+842A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100650649 | ||||||
| chr3:100650666
|
G | T | 2 | a0001c0001t0001g0057a0001c0001t0001g0063 | 2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1379+859G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100650666 | ||||||
| chr3:100650824
|
T | A | 1 | a0001c0001t0001g0083 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1379+1017T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100650824 | ||||||
| chr3:100650851
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1379+1044G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100650851 | ||||||
| chr3:100651094
|
C | G | 230 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(227): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1379+1287C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100651094 | ||||||
| chr3:100651179
|
A | G | 1 | a0001c0001t0001g0164 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1379+1372A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100651179 | ||||||
| chr3:100651296
|
G | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1379+1489G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100651296 | ||||||
| chr3:100651310
|
T | G | 1 | a0001c0001t0001g0107 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1379+1503T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100651310 | ||||||
| chr3:100651347
|
A | G | 7 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1379+1540A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100651347 | ||||||
| chr3:100651350
|
A | G | 1 | a0003c0003t0003g0023 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1379+1543A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100651350 | ||||||
| chr3:100651441
|
A | G | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1379+1634A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100651441 | ||||||
| chr3:100651450
|
C | A | 1 | a0001c0001t0001g0160 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1379+1643C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100651450 | ||||||
| chr3:100651476
|
T | C | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1379+1669T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100651476 | ||||||
| chr3:100651524
|
A | G | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1379+1717A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100651524 | ||||||
| chr3:100651571
|
T | C | 2 | a0001c0005t0001g0006a0001c0005t0001g0068 | 3 | HG02895.hp2 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1379+1764T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100651571 | ||||||
| chr3:100651684
|
AT | A | 6 | a0001c0001t0001g0046a0001c0011t0001g0058a0003c0003t0001g0199others(3): Show | 7 | HG00741.hp2 HG01975.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1379+1888delT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr3 | 100651684 | |||||
| chr3:100651695
|
T | A | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1379+1888T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100651695 | ||||||
| chr3:100651696
|
A | T | 1 | a0001c0001t0001g0054 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1379+1889A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100651696 | ||||||
| chr3:100651924
|
T | A | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1379+2117T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100651924 | ||||||
| chr3:100651929
|
C | T | 162 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(159): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.1379+2122C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100651929 | ||||||
| chr3:100652116
|
C | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1379+2309C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652116 | ||||||
| chr3:100652205
|
G | A | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1379+2398G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652205 | ||||||
| chr3:100652207
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1379+2400A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652207 | ||||||
| chr3:100652232
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1379+2425G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652232 | ||||||
| chr3:100652242
|
T | C | 1 | a0001c0001t0001g0188 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1379+2435T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652242 | ||||||
| chr3:100652245
|
A | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1379+2438A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652245 | ||||||
| chr3:100652302
|
C | T | 2 | a0001c0005t0001g0006a0001c0005t0001g0068 | 3 | HG02895.hp2 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1379+2495C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652302 | ||||||
| chr3:100652340
|
C | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1380-2495C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652340 | ||||||
| chr3:100652352
|
A | G | 227 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(224): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1380-2483A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652352 | ||||||
| chr3:100652372
|
A | G | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1380-2463A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652372 | ||||||
| chr3:100652518
|
C | G | 1 | a0001c0001t0001g0211 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1380-2317C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652518 | ||||||
| chr3:100652518
|
C | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1380-2317C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652518 | ||||||
| chr3:100652576
|
G | T | 2 | a0001c0001t0001g0064a0011c0012t0001g0065 | 2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1380-2259G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652576 | ||||||
| chr3:100652616
|
T | C | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1380-2219T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652616 | ||||||
| chr3:100652633
|
C | T | 1 | a0002c0002t0001g0301 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1380-2202C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652633 | ||||||
| chr3:100652634
|
AT | A | 12 | a0001c0008t0001g0039a0001c0008t0009g0034a0001c0010t0001g0037others(9): Show | 12 | HG00735.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1380-2197delT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr3 | 100652634 | |||||
| chr3:100652647
|
A | G | 242 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(239): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.1380-2188A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652647 | ||||||
| chr3:100652843
|
C | T | 1 | a0001c0001t0005g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1380-1992C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652843 | ||||||
| chr3:100652896
|
G | C | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1380-1939G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652896 | ||||||
| chr3:100652986
|
C | G | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1380-1849C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652986 | ||||||
| chr3:100652998
|
C | G | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1380-1837C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652998 | ||||||
| chr3:100653027
|
C | T | 43 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(40): Show | 45 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1380-1808C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100653027 | ||||||
| chr3:100653182
|
T | C | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1380-1653T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100653182 | ||||||
| chr3:100653295
|
G | C | 7 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1380-1540G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100653295 | ||||||
| chr3:100653380
|
G | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1380-1455G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100653380 | ||||||
| chr3:100653390
|
C | G | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1380-1445C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100653390 | ||||||
| chr3:100653404
|
T | C | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1380-1431T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100653404 | ||||||
| chr3:100653577
|
A | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1380-1258A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100653577 | ||||||
| chr3:100653809
|
C | T | 161 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(158): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.1380-1026C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100653809 | ||||||
| chr3:100654042
|
G | T | 1 | a0002c0002t0001g0306 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1380-793G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100654042 | ||||||
| chr3:100654093
|
G | A | 1 | a0003c0003t0001g0198 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1380-742G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100654093 | ||||||
| chr3:100654142
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1380-693C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100654142 | ||||||
| chr3:100654161
|
G | A | 21 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(18): Show | 23 | HG00735.hp2 HG01975.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1380-674G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100654161 | ||||||
| chr3:100654243
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1380-592G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100654243 | ||||||
| chr3:100654294
|
T | G | 2 | a0001c0001t0001g0080a0001c0001t0001g0126 | 2 | NA18994.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1380-541T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100654294 | ||||||
| chr3:100654396
|
A | G | 4 | a0002c0002t0001g0309a0002c0002t0001g0313a0002c0002t0001g0314others(1): Show | 4 | HG02615.hp2 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1380-439A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100654396 | ||||||
| chr3:100654456
|
C | T | 162 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(159): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.1380-379C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100654456 | ||||||
| chr3:100654499
|
T | C | 287 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(284): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1380-336T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100654499 | ||||||
| chr3:100654562
|
G | A | 1 | a0001c0001t0001g0166 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1380-273G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100654562 | ||||||
| chr3:100654681
|
C | T | 1 | a0002c0002t0001g0288 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1380-154C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100654681 | ||||||
| chr3:100654708
|
A | C | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1380-127A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100654708 | ||||||
| chr3:100654775
|
T | G | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1380-60T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100654775 | ||||||
| chr3:100655229
|
T | C | 66 | a0001c0001t0005g0070a0002c0002t0001g0001a0002c0002t0001g0012others(63): Show | 76 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.1726+48T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 12/15 | chr3 | 100655229 | ||||||
| chr3:100655277
|
C | T | 65 | a0002c0002t0001g0001a0002c0002t0001g0012a0002c0002t0001g0013others(62): Show | 75 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.1726+96C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 12/15 | chr3 | 100655277 | ||||||
| chr3:100655320
|
C | T | 1 | a0007c0017t0001g0232 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1726+139C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 12/15 | chr3 | 100655320 | ||||||
| chr3:100655362
|
C | T | 3 | a0001c0005t0001g0006a0001c0005t0001g0068a0001c0005t0008g0071 | 4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1726+181C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 12/15 | chr3 | 100655362 | ||||||
| chr3:100655415
|
A | G | 3 | a0001c0005t0001g0006a0001c0005t0001g0068a0001c0005t0008g0071 | 4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1726+234A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 12/15 | chr3 | 100655415 | ||||||
| chr3:100655527
|
C | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1726+346C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 12/15 | chr3 | 100655527 | ||||||
| chr3:100655896
|
T | C | 123 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(120): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
splice_region_variant&intron_variant | LOW | c.1727-3T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 12/15 | chr3 | 100655896 | ||||||
| chr3:100656232
|
C | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1823+237C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100656232 | ||||||
| chr3:100656245
|
T | G | 1 | a0001c0008t0001g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1823+250T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100656245 | ||||||
| chr3:100656401
|
A | C | 3 | a0001c0005t0001g0006a0001c0005t0001g0068a0001c0005t0008g0071 | 4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1823+406A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100656401 | ||||||
| chr3:100656623
|
C | A | 1 | a0001c0001t0001g0172 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1823+628C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100656623 | ||||||
| chr3:100656711
|
G | T | 248 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(245): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1823+716G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100656711 | ||||||
| chr3:100656728
|
G | A | 248 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(245): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1823+733G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100656728 | ||||||
| chr3:100656794
|
T | TCA | 297 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(294): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1823+800_1823+801i others(4): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr3 | 100656794 | |||||
| chr3:100656853
|
G | T | 3 | a0001c0005t0001g0006a0001c0005t0001g0068a0001c0005t0008g0071 | 4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1823+858G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100656853 | ||||||
| chr3:100656925
|
C | G | 3 | a0001c0005t0001g0006a0001c0005t0001g0068a0001c0005t0008g0071 | 4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1823+930C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100656925 | ||||||
| chr3:100657185
|
G | A | 3 | a0001c0005t0001g0006a0001c0005t0001g0068a0001c0005t0008g0071 | 4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1823+1190G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100657185 | ||||||
| chr3:100657238
|
C | G | 2 | a0002c0002t0001g0300a0002c0002t0001g0301 | 2 | NA18950.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1823+1243C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100657238 | ||||||
| chr3:100657578
|
G | A | 2 | a0001c0001t0001g0094a0001c0001t0001g0121 | 2 | HG02083.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1823+1583G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100657578 | ||||||
| chr3:100657596
|
T | C | 143 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(140): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.1823+1601T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100657596 | ||||||
| chr3:100657599
|
T | C | 3 | a0001c0005t0001g0006a0001c0005t0001g0068a0001c0005t0008g0071 | 4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1823+1604T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100657599 | ||||||
| chr3:100657606
|
A | G | 9 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(6): Show | 10 | HG01975.hp2 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1823+1611A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100657606 | ||||||
| chr3:100657626
|
T | C | 9 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(6): Show | 10 | HG01975.hp2 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1823+1631T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100657626 | ||||||
| chr3:100657702
|
C | T | 44 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0045others(41): Show | 45 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.1823+1707C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100657702 | ||||||
| chr3:100657951
|
G | A | 3 | a0001c0005t0001g0006a0001c0005t0001g0068a0001c0005t0008g0071 | 4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1824-1737G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100657951 | ||||||
| chr3:100657999
|
A | G | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1824-1689A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100657999 | ||||||
| chr3:100658077
|
C | T | 49 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0045others(46): Show | 50 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.1824-1611C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100658077 | ||||||
| chr3:100658191
|
T | C | 1 | a0003c0003t0001g0227 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1824-1497T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100658191 | ||||||
| chr3:100658279
|
A | G | 49 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0045others(46): Show | 50 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.1824-1409A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100658279 | ||||||
| chr3:100658291
|
G | T | 1 | a0002c0002t0001g0258 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1824-1397G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100658291 | ||||||
| chr3:100658300
|
T | G | 1 | a0001c0001t0001g0096 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1824-1388T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100658300 | ||||||
| chr3:100658440
|
G | A | 42 | a0001c0001t0001g0007a0001c0001t0001g0064a0001c0001t0001g0077others(39): Show | 43 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1824-1248G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100658440 | ||||||
| chr3:100658517
|
G | C | 232 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(229): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.1824-1171G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100658517 | ||||||
| chr3:100658729
|
G | A | 231 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(228): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1824-959G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100658729 | ||||||
| chr3:100658872
|
T | A | 3 | a0001c0005t0001g0006a0001c0005t0001g0068a0001c0005t0008g0071 | 4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1824-816T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100658872 | ||||||
| chr3:100658903
|
T | G | 1 | a0001c0001t0001g0052 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1824-785T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100658903 | ||||||
| chr3:100658906
|
C | T | 1 | a0003c0003t0001g0226 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1824-782C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100658906 | ||||||
| chr3:100658957
|
C | A | 1 | a0002c0002t0001g0310 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1824-731C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100658957 | ||||||
| chr3:100658979
|
G | T | 1 | a0002c0002t0001g0307 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1824-709G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100658979 | ||||||
| chr3:100659099
|
A | G | 122 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(119): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.1824-589A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100659099 | ||||||
| chr3:100659135
|
A | T | 3 | a0001c0005t0001g0006a0001c0005t0001g0068a0001c0005t0008g0071 | 4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1824-553A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100659135 | ||||||
| chr3:100659157
|
G | C | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1824-531G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100659157 | ||||||
| chr3:100659418
|
C | T | 9 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(6): Show | 10 | HG01975.hp2 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1824-270C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100659418 | ||||||
| chr3:100659439
|
C | CA | 113 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(110): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.1824-224dupA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr3 | 100659439 | |||||
| chr3:100659439
|
C | CAA | 23 | a0001c0001t0001g0066a0001c0001t0001g0076a0001c0001t0001g0096others(20): Show | 23 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.1824-225_1824-224d others(4): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr3 | 100659439 | |||||
| chr3:100659439
|
CA | C | 14 | a0001c0001t0001g0021a0001c0001t0001g0030a0001c0001t0001g0032others(11): Show | 15 | HG01952.hp1 HG01975.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1824-224delA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr3 | 100659439 | |||||
| chr3:100659439
|
CAAAAAAA others(2): Show |
C | 32 | a0003c0003t0001g0011a0003c0003t0001g0017a0003c0003t0001g0018others(29): Show | 33 | HG00741.hp2 HG01071.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.1824-232_1824-224d others(11): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr3 | 100659439 | |||||
| chr3:100659448
|
A | G | 9 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(6): Show | 10 | HG01975.hp2 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1824-240A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100659448 | ||||||
| chr3:100659465
|
G | A | 3 | a0001c0005t0001g0006a0001c0005t0001g0068a0001c0005t0008g0071 | 4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1824-223G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100659465 | ||||||
| chr3:100659638
|
T | C | 2 | a0001c0005t0001g0006a0001c0005t0001g0068 | 3 | HG02895.hp2 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1824-50T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100659638 | ||||||
| chr3:100659892
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1979+49C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100659892 | ||||||
| chr3:100659898
|
G | A | 3 | a0001c0005t0001g0006a0001c0005t0001g0068a0001c0005t0008g0071 | 4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1979+55G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100659898 | ||||||
| chr3:100659906
|
A | G | 12 | a0001c0008t0001g0039a0001c0008t0009g0034a0001c0010t0001g0037others(9): Show | 12 | HG00735.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1979+63A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100659906 | ||||||
| chr3:100660002
|
G | T | 2 | a0001c0005t0001g0006a0001c0005t0001g0068 | 3 | HG02895.hp2 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1979+159G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100660002 | ||||||
| chr3:100660028
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1979+185C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100660028 | ||||||
| chr3:100660086
|
A | G | 1 | a0003c0003t0001g0136 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1979+243A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100660086 | ||||||
| chr3:100660109
|
C | T | 3 | a0001c0005t0001g0006a0001c0005t0001g0068a0001c0005t0008g0071 | 4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1979+266C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100660109 | ||||||
| chr3:100660129
|
G | T | 3 | a0003c0003t0001g0024a0003c0003t0001g0026a0003c0003t0003g0023 | 3 | HG02055.hp2 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1979+286G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100660129 | ||||||
| chr3:100660167
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1979+324A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100660167 | ||||||
| chr3:100660309
|
T | C | 54 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(51): Show | 56 | HG00597.hp1 HG00735.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.1979+466T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100660309 | ||||||
| chr3:100660678
|
C | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1979+835C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100660678 | ||||||
| chr3:100660821
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1979+978A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100660821 | ||||||
| chr3:100660952
|
C | CA | 9 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0005g0070others(6): Show | 10 | HG00280.hp1 HG01884.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1979+1124dupA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 100660952 | |||||
| chr3:100660952
|
C | CAA | 9 | a0001c0008t0009g0034a0001c0010t0001g0037a0004c0004t0002g0020others(6): Show | 9 | HG00735.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1979+1123_1979+112 others(6): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 100660952 | |||||
| chr3:100660952
|
C | CAAA | 11 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(8): Show | 12 | HG01975.hp2 HG02145.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1979+1122_1979+112 others(7): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 100660952 | |||||
| chr3:100660952
|
CA | C | 49 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0045others(46): Show | 50 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.1979+1124delA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 100660952 | |||||
| chr3:100661010
|
C | G | 1 | a0002c0002t0001g0305 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1979+1167C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100661010 | ||||||
| chr3:100661012
|
A | G | 113 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(110): Show | 117 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1979+1169A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100661012 | ||||||
| chr3:100661029
|
G | A | 20 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(17): Show | 21 | HG00735.hp2 HG01975.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1979+1186G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100661029 | ||||||
| chr3:100661065
|
C | T | 4 | a0002c0002t0001g0001a0002c0002t0001g0274a0002c0002t0001g0283others(1): Show | 9 | NA18612.hp1 NA18953.hp1 NA18955.hp1 others(6): Show |
intron_variant | MODIFIER | c.1979+1222C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100661065 | ||||||
| chr3:100661098
|
G | T | 9 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(6): Show | 10 | HG01975.hp2 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1979+1255G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100661098 | ||||||
| chr3:100661197
|
C | T | 3 | a0001c0005t0001g0006a0001c0005t0001g0068a0001c0005t0008g0071 | 4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1979+1354C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100661197 | ||||||
| chr3:100661295
|
T | C | 3 | a0001c0005t0001g0006a0001c0005t0001g0068a0001c0005t0008g0071 | 4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1979+1452T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100661295 | ||||||
| chr3:100661373
|
A | G | 1 | a0002c0002t0001g0287 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1979+1530A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100661373 | ||||||
| chr3:100661897
|
T | C | 3 | a0001c0005t0001g0006a0001c0005t0001g0068a0001c0005t0008g0071 | 4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1979+2054T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100661897 | ||||||
| chr3:100661961
|
C | T | 8 | a0001c0001t0001g0190a0001c0001t0001g0205a0001c0001t0001g0208others(5): Show | 8 | HG00597.hp2 NA18941.hp1 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.1979+2118C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100661961 | ||||||
| chr3:100661967
|
A | G | 292 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(289): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1979+2124A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100661967 | ||||||
| chr3:100662157
|
A | G | 9 | a0004c0004t0002g0020a0004c0004t0002g0035a0004c0004t0002g0036others(6): Show | 9 | HG00735.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1979+2314A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100662157 | ||||||
| chr3:100662282
|
A | C | 3 | a0001c0005t0001g0006a0001c0005t0001g0068a0001c0005t0008g0071 | 4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1979+2439A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100662282 | ||||||
| chr3:100662287
|
G | A | 1 | a0003c0003t0001g0249 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1979+2444G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100662287 | ||||||
| chr3:100662359
|
G | T | 1 | a0002c0002t0001g0297 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1979+2516G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100662359 | ||||||
| chr3:100662471
|
G | C | 235 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(232): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.1979+2628G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100662471 | ||||||
| chr3:100662583
|
C | T | 2 | a0001c0008t0009g0034a0001c0010t0001g0037 | 2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1979+2740C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100662583 | ||||||
| chr3:100662599
|
A | T | 7 | a0001c0001t0001g0137a0001c0001t0001g0155a0001c0001t0001g0156others(4): Show | 7 | HG01192.hp2 HG01255.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.1979+2756A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100662599 | ||||||
| chr3:100662629
|
C | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1979+2786C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100662629 | ||||||
| chr3:100662870
|
G | GA | 148 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0073others(145): Show | 161 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.1979+3033dupA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 100662870 | |||||
| chr3:100663027
|
C | T | 3 | a0005c0006t0001g0005a0005c0006t0001g0028a0005c0006t0001g0029 | 4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1979+3184C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100663027 | ||||||
| chr3:100663063
|
T | C | 2 | a0001c0008t0009g0034a0001c0010t0001g0037 | 2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1979+3220T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100663063 | ||||||
| chr3:100663102
|
T | C | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1979+3259T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100663102 | ||||||
| chr3:100663113
|
A | C | 235 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(232): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1979+3270A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100663113 | ||||||
| chr3:100663133
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1979+3290G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100663133 | ||||||
| chr3:100663297
|
T | A | 249 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(246): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1979+3454T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100663297 | ||||||
| chr3:100663448
|
T | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG01106.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1979+3605T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100663448 | ||||||
| chr3:100663487
|
C | T | 2 | a0001c0008t0009g0034a0001c0010t0001g0037 | 2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1979+3644C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100663487 | ||||||
| chr3:100663607
|
A | G | 1 | a0001c0005t0001g0068 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1979+3764A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100663607 | ||||||
| chr3:100663664
|
C | G | 148 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0073others(145): Show | 161 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.1979+3821C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100663664 | ||||||
| chr3:100663699
|
G | C | 215 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(212): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1979+3856G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100663699 | ||||||
| chr3:100663793
|
T | A | 1 | a0001c0001t0001g0025 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1979+3950T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100663793 | ||||||
| chr3:100664018
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1979+4175A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100664018 | ||||||
| chr3:100664080
|
A | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1979+4237A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100664080 | ||||||
| chr3:100664091
|
T | A | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1979+4248T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100664091 | ||||||
| chr3:100664324
|
C | T | 1 | a0001c0001t0001g0181 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1979+4481C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100664324 | ||||||
| chr3:100664441
|
A | G | 1 | a0002c0002t0001g0311 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1980-4508A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100664441 | ||||||
| chr3:100664458
|
C | G | 36 | a0001c0001t0001g0213a0003c0003t0001g0011a0003c0003t0001g0017others(33): Show | 37 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1980-4491C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100664458 | ||||||
| chr3:100664507
|
A | G | 3 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0005t0008g0071 | 3 | HG00280.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1980-4442A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100664507 | ||||||
| chr3:100664545
|
C | T | 9 | a0004c0004t0002g0020a0004c0004t0002g0035a0004c0004t0002g0036others(6): Show | 9 | HG00735.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1980-4404C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100664545 | ||||||
| chr3:100664895
|
A | C | 249 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(246): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1980-4054A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100664895 | ||||||
| chr3:100664920
|
G | T | 1 | a0001c0001t0001g0146 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1980-4029G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100664920 | ||||||
| chr3:100664972
|
A | C | 1 | a0001c0008t0001g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1980-3977A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100664972 | ||||||
| chr3:100665014
|
C | T | 249 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(246): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1980-3935C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100665014 | ||||||
| chr3:100665102
|
G | A | 1 | a0001c0005t0001g0068 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1980-3847G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100665102 | ||||||
| chr3:100665300
|
T | C | 3 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0005t0008g0071 | 3 | HG00280.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1980-3649T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100665300 | ||||||
| chr3:100665488
|
C | T | 7 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(4): Show | 7 | HG02258.hp1 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1980-3461C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100665488 | ||||||
| chr3:100665602
|
T | C | 14 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0115others(11): Show | 16 | HG00099.hp1 HG00438.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.1980-3347T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100665602 | ||||||
| chr3:100665617
|
T | C | 249 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(246): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1980-3332T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100665617 | ||||||
| chr3:100666013
|
T | C | 1 | a0001c0001t0001g0081 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1980-2936T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666013 | ||||||
| chr3:100666017
|
C | T | 1 | a0001c0001t0001g0219 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1980-2932C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666017 | ||||||
| chr3:100666054
|
C | CT | 9 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(6): Show | 9 | HG00621.hp2 HG01515.hp2 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.1980-2880dupT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 100666054 | |||||
| chr3:100666124
|
C | T | 51 | a0001c0001t0001g0248a0002c0002t0001g0001a0002c0002t0001g0012others(48): Show | 61 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1980-2825C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666124 | ||||||
| chr3:100666157
|
C | G | 5 | a0001c0001t0001g0118a0001c0001t0001g0139a0001c0001t0001g0153others(2): Show | 5 | NA18953.hp2 NA18974.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.1980-2792C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666157 | ||||||
| chr3:100666182
|
G | T | 1 | a0001c0005t0001g0068 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1980-2767G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666182 | ||||||
| chr3:100666250
|
G | C | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1980-2699G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666250 | ||||||
| chr3:100666254
|
C | T | 13 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0043others(10): Show | 13 | HG01891.hp1 HG02258.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1980-2695C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666254 | ||||||
| chr3:100666367
|
T | C | 1 | a0001c0008t0001g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1980-2582T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666367 | ||||||
| chr3:100666447
|
T | C | 1 | a0003c0003t0001g0237 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1980-2502T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666447 | ||||||
| chr3:100666455
|
G | A | 212 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(209): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1980-2494G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666455 | ||||||
| chr3:100666579
|
G | C | 1 | a0001c0005t0001g0068 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1980-2370G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666579 | ||||||
| chr3:100666807
|
T | C | 1 | a0005c0006t0001g0005 | 2 | HG01975.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1980-2142T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666807 | ||||||
| chr3:100666901
|
G | C | 1 | a0002c0002t0001g0259 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1980-2048G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666901 | ||||||
| chr3:100666933
|
C | T | 148 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0073others(145): Show | 161 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.1980-2016C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666933 | ||||||
| chr3:100666967
|
G | C | 1 | a0004c0009t0002g0067 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1980-1982G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666967 | ||||||
| chr3:100666996
|
G | A | 61 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(58): Show | 64 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.1980-1953G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666996 | ||||||
| chr3:100667021
|
G | A | 3 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0005t0008g0071 | 3 | HG00280.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1980-1928G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100667021 | ||||||
| chr3:100667035
|
C | T | 9 | a0004c0004t0002g0020a0004c0004t0002g0035a0004c0004t0002g0036others(6): Show | 9 | HG00735.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1980-1914C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100667035 | ||||||
| chr3:100667055
|
T | C | 1 | a0001c0005t0001g0068 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1980-1894T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100667055 | ||||||
| chr3:100667138
|
G | A | 7 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(4): Show | 7 | HG02258.hp1 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1980-1811G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100667138 | ||||||
| chr3:100667188
|
T | A | 213 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(210): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1980-1761T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100667188 | ||||||
| chr3:100667227
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1980-1722A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100667227 | ||||||
| chr3:100667286
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1980-1663C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100667286 | ||||||
| chr3:100667591
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1980-1358G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100667591 | ||||||
| chr3:100667855
|
C | T | 1 | a0003c0003t0001g0200 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1980-1094C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100667855 | ||||||
| chr3:100667864
|
C | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1980-1085C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100667864 | ||||||
| chr3:100667884
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1980-1065G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100667884 | ||||||
| chr3:100667952
|
G | C | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1980-997G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100667952 | ||||||
| chr3:100667965
|
G | T | 5 | a0001c0001t0003g0090a0001c0001t0003g0091a0001c0001t0003g0092others(2): Show | 5 | HG02258.hp1 HG02559.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1980-984G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100667965 | ||||||
| chr3:100668073
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1980-876G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100668073 | ||||||
| chr3:100668645
|
C | G | 16 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(13): Show | 16 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1980-304C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100668645 | ||||||
| chr3:100668672
|
A | G | 1 | a0001c0001t0001g0009 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1980-277A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100668672 | ||||||
| chr3:100668785
|
A | G | 7 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(4): Show | 7 | HG02258.hp1 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1980-164A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100668785 | ||||||
| chr3:100668865
|
A | G | 234 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(231): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1980-84A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100668865 | ||||||
| chr3:100669193
|
T | A | 1 | a0001c0001t0001g0181 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2136+88T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100669193 | ||||||
| chr3:100669296
|
A | C | 235 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(232): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.2136+191A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100669296 | ||||||
| chr3:100669305
|
G | T | 248 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(245): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.2136+200G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100669305 | ||||||
| chr3:100669406
|
A | G | 9 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0054others(6): Show | 12 | HG01884.hp1 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2136+301A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100669406 | ||||||
| chr3:100669418
|
T | C | 1 | a0001c0001t0003g0031 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2136+313T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100669418 | ||||||
| chr3:100669488
|
C | G | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2136+383C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100669488 | ||||||
| chr3:100669514
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2136+409A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100669514 | ||||||
| chr3:100669527
|
C | A | 1 | a0001c0001t0001g0171 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2136+422C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100669527 | ||||||
| chr3:100669533
|
C | CA | 18 | a0001c0001t0001g0080a0001c0001t0001g0085a0001c0001t0001g0086others(15): Show | 18 | HG00438.hp1 HG02027.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.2136+457dupA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100669533 | |||||
| chr3:100669533
|
CA | C | 32 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0021others(29): Show | 36 | HG01884.hp1 HG01891.hp1 HG01952.hp1 others(33): Show |
intron_variant | MODIFIER | c.2136+457delA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100669533 | |||||
| chr3:100669533
|
CAAA | C | 18 | a0001c0001t0001g0045a0001c0001t0001g0142a0001c0001t0001g0145others(15): Show | 18 | HG00099.hp1 HG00735.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.2136+455_2136+457d others(5): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100669533 | |||||
| chr3:100669533
|
CAAAA | C | 62 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(59): Show | 66 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.2136+454_2136+457d others(6): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100669533 | |||||
| chr3:100669533
|
CAAAAA | C | 11 | a0001c0001t0001g0089a0001c0001t0001g0138a0001c0001t0001g0181others(8): Show | 11 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(8): Show |
intron_variant | MODIFIER | c.2136+453_2136+457d others(7): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100669533 | |||||
| chr3:100669533
|
CAAAAAA | C | 123 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0073others(120): Show | 135 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.2136+452_2136+457d others(8): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100669533 | |||||
| chr3:100669533
|
CAAAAAAA | C | 16 | a0001c0001t0001g0094a0001c0001t0001g0139a0001c0001t0001g0214others(13): Show | 17 | HG00609.hp1 HG01255.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.2136+451_2136+457d others(9): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100669533 | |||||
| chr3:100669597
|
G | A | 1 | a0003c0003t0001g0223 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2136+492G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100669597 | ||||||
| chr3:100669633
|
A | G | 1 | a0003c0003t0001g0017 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2136+528A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100669633 | ||||||
| chr3:100669678
|
T | C | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2136+573T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100669678 | ||||||
| chr3:100669687
|
T | A | 1 | a0003c0003t0001g0024 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2136+582T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100669687 | ||||||
| chr3:100669788
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2136+683C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100669788 | ||||||
| chr3:100669990
|
A | G | 2 | a0001c0001t0001g0097a0001c0001t0001g0099 | 2 | HG00741.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.2136+885A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100669990 | ||||||
| chr3:100670066
|
A | C | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2136+961A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670066 | ||||||
| chr3:100670113
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2136+1008T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670113 | ||||||
| chr3:100670125
|
A | G | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2136+1020A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670125 | ||||||
| chr3:100670145
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2136+1040G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670145 | ||||||
| chr3:100670188
|
T | A | 148 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0073others(145): Show | 161 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.2136+1083T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670188 | ||||||
| chr3:100670200
|
C | CT | 6 | a0001c0001t0001g0079a0001c0001t0001g0096a0001c0001t0001g0098others(3): Show | 6 | HG00423.hp1 HG02015.hp1 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.2136+1096dupT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100670200 | |||||
| chr3:100670412
|
T | C | 1 | a0001c0001t0003g0031 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2136+1307T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670412 | ||||||
| chr3:100670481
|
G | A | 1 | a0003c0003t0003g0023 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2136+1376G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670481 | ||||||
| chr3:100670490
|
T | C | 1 | a0001c0001t0001g0104 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2136+1385T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670490 | ||||||
| chr3:100670495
|
A | G | 215 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(212): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.2136+1390A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670495 | ||||||
| chr3:100670513
|
T | C | 16 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(13): Show | 16 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+1408T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670513 | ||||||
| chr3:100670567
|
T | C | 68 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(65): Show | 72 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.2136+1462T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670567 | ||||||
| chr3:100670572
|
A | G | 3 | a0001c0001t0003g0090a0001c0001t0003g0091a0001c0001t0003g0092 | 3 | HG02258.hp1 HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2136+1467A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670572 | ||||||
| chr3:100670601
|
G | A | 1 | a0003c0003t0001g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2136+1496G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670601 | ||||||
| chr3:100670636
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2136+1531C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670636 | ||||||
| chr3:100670751
|
C | G | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2136+1646C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670751 | ||||||
| chr3:100670845
|
A | G | 2 | a0001c0008t0009g0034a0001c0010t0001g0037 | 2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2136+1740A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670845 | ||||||
| chr3:100670869
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2136+1764T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670869 | ||||||
| chr3:100671120
|
C | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2136+2015C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100671120 | ||||||
| chr3:100671121
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2136+2016G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100671121 | ||||||
| chr3:100671338
|
C | T | 1 | a0003c0003t0001g0024 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2136+2233C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100671338 | ||||||
| chr3:100671366
|
G | A | 1 | a0001c0001t0003g0031 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2136+2261G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100671366 | ||||||
| chr3:100671393
|
A | G | 248 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(245): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.2136+2288A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100671393 | ||||||
| chr3:100671428
|
G | C | 18 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(15): Show | 18 | HG00735.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.2136+2323G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100671428 | ||||||
| chr3:100671448
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2136+2343A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100671448 | ||||||
| chr3:100671503
|
G | T | 1 | a0003c0003t0003g0023 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2136+2398G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100671503 | ||||||
| chr3:100671606
|
T | C | 14 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(11): Show | 14 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2136+2501T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100671606 | ||||||
| chr3:100671694
|
A | G | 1 | a0001c0001t0001g0209 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2136+2589A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100671694 | ||||||
| chr3:100671931
|
C | G | 18 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(15): Show | 18 | HG00735.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.2136+2826C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100671931 | ||||||
| chr3:100672036
|
T | C | 234 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(231): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.2136+2931T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100672036 | ||||||
| chr3:100672037
|
G | A | 17 | a0001c0001t0001g0156a0001c0001t0003g0031a0001c0001t0003g0090others(14): Show | 17 | HG00735.hp2 HG01934.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.2136+2932G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100672037 | ||||||
| chr3:100672422
|
A | G | 218 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(215): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.2136+3317A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100672422 | ||||||
| chr3:100672461
|
G | A | 3 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0005t0008g0071 | 3 | HG00280.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2136+3356G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100672461 | ||||||
| chr3:100672494
|
G | A | 16 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(13): Show | 16 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+3389G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100672494 | ||||||
| chr3:100672499
|
C | G | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2136+3394C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100672499 | ||||||
| chr3:100672611
|
A | G | 4 | a0002c0002t0001g0309a0002c0002t0001g0313a0002c0002t0001g0314others(1): Show | 4 | HG02615.hp2 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2136+3506A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100672611 | ||||||
| chr3:100672621
|
C | A | 1 | a0001c0001t0001g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2136+3516C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100672621 | ||||||
| chr3:100672627
|
C | G | 16 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(13): Show | 16 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+3522C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100672627 | ||||||
| chr3:100672753
|
A | G | 45 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0083others(42): Show | 47 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.2136+3648A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100672753 | ||||||
| chr3:100672798
|
A | G | 1 | a0002c0002t0001g0287 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2136+3693A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100672798 | ||||||
| chr3:100673020
|
T | G | 3 | a0005c0006t0001g0005a0005c0006t0001g0028a0005c0006t0001g0029 | 4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2136+3915T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100673020 | ||||||
| chr3:100673022
|
G | T | 123 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(120): Show | 135 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.2136+3917G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100673022 | ||||||
| chr3:100673034
|
G | C | 2 | a0001c0008t0009g0034a0001c0010t0001g0037 | 2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2136+3929G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100673034 | ||||||
| chr3:100673054
|
T | A | 2 | a0001c0008t0009g0034a0001c0010t0001g0037 | 2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2136+3949T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100673054 | ||||||
| chr3:100673151
|
T | G | 248 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(245): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.2136+4046T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100673151 | ||||||
| chr3:100673271
|
G | A | 16 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(13): Show | 16 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+4166G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100673271 | ||||||
| chr3:100673276
|
C | G | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2136+4171C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100673276 | ||||||
| chr3:100673347
|
T | C | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2136+4242T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100673347 | ||||||
| chr3:100673467
|
C | CT | 5 | a0001c0001t0001g0010a0001c0001t0001g0105a0005c0006t0001g0005others(2): Show | 7 | HG00738.hp1 HG01071.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.2136+4376dupT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100673467 | |||||
| chr3:100673467
|
CT | C | 173 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(170): Show | 187 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.2136+4376delT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100673467 | |||||
| chr3:100673502
|
T | C | 233 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(230): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.2136+4397T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100673502 | ||||||
| chr3:100673519
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2136+4414T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100673519 | ||||||
| chr3:100673524
|
T | C | 230 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(227): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.2136+4419T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100673524 | ||||||
| chr3:100673544
|
C | T | 212 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(209): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.2136+4439C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100673544 | ||||||
| chr3:100673720
|
G | A | 14 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(11): Show | 14 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2136+4615G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100673720 | ||||||
| chr3:100673818
|
T | C | 1 | a0001c0008t0009g0034 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2136+4713T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100673818 | ||||||
| chr3:100673977
|
T | A | 3 | a0005c0006t0001g0005a0005c0006t0001g0028a0005c0006t0001g0029 | 4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2136+4872T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100673977 | ||||||
| chr3:100674068
|
G | T | 16 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(13): Show | 16 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+4963G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100674068 | ||||||
| chr3:100674207
|
T | C | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2136+5102T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100674207 | ||||||
| chr3:100674467
|
A | G | 1 | a0001c0001t0001g0253 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2136+5362A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100674467 | ||||||
| chr3:100674479
|
T | C | 1 | a0003c0003t0003g0023 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2136+5374T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100674479 | ||||||
| chr3:100674487
|
G | A | 7 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(4): Show | 7 | HG02258.hp1 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2136+5382G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100674487 | ||||||
| chr3:100674533
|
T | A | 1 | a0002c0002t0001g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2136+5428T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100674533 | ||||||
| chr3:100674576
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2136+5471T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100674576 | ||||||
| chr3:100674579
|
C | CT | 6 | a0001c0001t0001g0112a0001c0001t0001g0141a0001c0001t0001g0193others(3): Show | 7 | HG01192.hp1 HG01975.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.2136+5490dupT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100674579 | |||||
| chr3:100674579
|
CT | C | 161 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(158): Show | 174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.2136+5490delT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100674579 | |||||
| chr3:100674735
|
C | G | 233 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(230): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.2136+5630C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100674735 | ||||||
| chr3:100674800
|
A | G | 1 | a0002c0002t0001g0311 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2136+5695A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100674800 | ||||||
| chr3:100674913
|
T | C | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2136+5808T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100674913 | ||||||
| chr3:100675126
|
G | A | 233 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(230): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.2136+6021G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100675126 | ||||||
| chr3:100675129
|
A | G | 2 | a0001c0001t0001g0252a0001c0001t0001g0254 | 2 | NA18999.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.2136+6024A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100675129 | ||||||
| chr3:100675163
|
T | G | 233 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(230): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.2136+6058T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100675163 | ||||||
| chr3:100675325
|
A | T | 16 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(13): Show | 16 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+6220A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100675325 | ||||||
| chr3:100675534
|
G | T | 1 | a0001c0001t0001g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2136+6429G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100675534 | ||||||
| chr3:100675656
|
T | G | 1 | a0001c0001t0001g0247 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2136+6551T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100675656 | ||||||
| chr3:100675788
|
G | C | 7 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(4): Show | 7 | HG02258.hp1 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2136+6683G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100675788 | ||||||
| chr3:100676052
|
A | T | 1 | a0003c0003t0003g0023 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2136+6947A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100676052 | ||||||
| chr3:100676361
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2136+7256C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100676361 | ||||||
| chr3:100676362
|
G | A | 16 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(13): Show | 16 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+7257G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100676362 | ||||||
| chr3:100676443
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2136+7338T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100676443 | ||||||
| chr3:100676447
|
G | A | 2 | a0001c0001t0001g0119a0001c0005t0008g0071 | 2 | HG00280.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.2136+7342G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100676447 | ||||||
| chr3:100676605
|
T | C | 1 | a0001c0001t0003g0031 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2136+7500T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100676605 | ||||||
| chr3:100676666
|
C | A | 13 | a0002c0002t0001g0015a0002c0002t0001g0256a0002c0002t0001g0278others(10): Show | 14 | HG00609.hp1 HG01255.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.2136+7561C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100676666 | ||||||
| chr3:100676791
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2136+7686C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100676791 | ||||||
| chr3:100676812
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2136+7707G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100676812 | ||||||
| chr3:100676885
|
T | C | 9 | a0004c0004t0002g0020a0004c0004t0002g0035a0004c0004t0002g0036others(6): Show | 9 | HG00735.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2136+7780T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100676885 | ||||||
| chr3:100676976
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2136+7871G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100676976 | ||||||
| chr3:100677006
|
G | A | 14 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(11): Show | 14 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2136+7901G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100677006 | ||||||
| chr3:100677115
|
A | G | 9 | a0004c0004t0002g0020a0004c0004t0002g0035a0004c0004t0002g0036others(6): Show | 9 | HG00735.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2136+8010A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100677115 | ||||||
| chr3:100677167
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2136+8062C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100677167 | ||||||
| chr3:100677295
|
C | T | 18 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(15): Show | 18 | HG00735.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.2136+8190C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100677295 | ||||||
| chr3:100677383
|
T | C | 4 | a0002c0002t0001g0292a0002c0002t0001g0293a0002c0002t0001g0295others(1): Show | 4 | HG00609.hp1 NA19005.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.2136+8278T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100677383 | ||||||
| chr3:100677539
|
A | G | 2 | a0002c0002t0001g0259a0002c0002t0001g0260 | 2 | HG01099.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2136+8434A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100677539 | ||||||
| chr3:100677610
|
G | T | 1 | a0001c0001t0001g0044 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2136+8505G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100677610 | ||||||
| chr3:100677752
|
T | C | 2 | a0001c0008t0009g0034a0001c0010t0001g0037 | 2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2136+8647T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100677752 | ||||||
| chr3:100677761
|
A | G | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2136+8656A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100677761 | ||||||
| chr3:100677763
|
A | C | 2 | a0003c0003t0001g0231a0007c0017t0001g0232 | 2 | HG02523.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.2136+8658A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100677763 | ||||||
| chr3:100677780
|
A | G | 234 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(231): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.2136+8675A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100677780 | ||||||
| chr3:100677883
|
A | G | 68 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(65): Show | 72 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.2136+8778A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100677883 | ||||||
| chr3:100677951
|
C | T | 3 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0005t0008g0071 | 3 | HG00280.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2136+8846C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100677951 | ||||||
| chr3:100678071
|
G | T | 62 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(59): Show | 65 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.2136+8966G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100678071 | ||||||
| chr3:100678113
|
AT | A | 7 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(4): Show | 7 | HG02258.hp1 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2136+9010delT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100678113 | |||||
| chr3:100678306
|
A | G | 14 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(11): Show | 14 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2136+9201A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100678306 | ||||||
| chr3:100678358
|
C | T | 16 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(13): Show | 16 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+9253C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100678358 | ||||||
| chr3:100678410
|
G | T | 3 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0005t0008g0071 | 3 | HG00280.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2136+9305G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100678410 | ||||||
| chr3:100678748
|
T | C | 18 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(15): Show | 18 | HG00735.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.2136+9643T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100678748 | ||||||
| chr3:100678938
|
G | C | 1 | a0001c0001t0001g0079 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2136+9833G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100678938 | ||||||
| chr3:100678978
|
C | G | 1 | a0001c0001t0001g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2136+9873C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100678978 | ||||||
| chr3:100679070
|
C | G | 243 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(240): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.2136+9965C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100679070 | ||||||
| chr3:100679243
|
C | T | 16 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(13): Show | 16 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+10138C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100679243 | ||||||
| chr3:100679383
|
C | A | 2 | a0001c0001t0001g0064a0011c0012t0001g0065 | 2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2136+10278C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100679383 | ||||||
| chr3:100679397
|
G | C | 1 | a0007c0017t0001g0232 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2136+10292G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100679397 | ||||||
| chr3:100679460
|
T | C | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2136+10355T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100679460 | ||||||
| chr3:100679561
|
C | T | 16 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(13): Show | 16 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+10456C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100679561 | ||||||
| chr3:100679678
|
A | C | 153 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(150): Show | 166 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.2136+10573A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100679678 | ||||||
| chr3:100680330
|
T | A | 5 | a0001c0001t0003g0090a0001c0001t0003g0091a0001c0001t0003g0092others(2): Show | 5 | HG02258.hp1 HG02559.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2136+11225T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100680330 | ||||||
| chr3:100680373
|
A | G | 1 | a0003c0003t0001g0241 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2136+11268A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100680373 | ||||||
| chr3:100680395
|
G | A | 1 | a0001c0001t0005g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2136+11290G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100680395 | ||||||
| chr3:100680466
|
T | A | 16 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(13): Show | 16 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+11361T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100680466 | ||||||
| chr3:100680607
|
G | A | 3 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0005t0008g0071 | 3 | HG00280.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2136+11502G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100680607 | ||||||
| chr3:100680608
|
C | A | 3 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0005t0008g0071 | 3 | HG00280.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2136+11503C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100680608 | ||||||
| chr3:100680613
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2136+11508C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100680613 | ||||||
| chr3:100680658
|
T | C | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2136+11553T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100680658 | ||||||
| chr3:100680668
|
G | A | 247 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(244): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.2136+11563G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100680668 | ||||||
| chr3:100680751
|
C | T | 1 | a0001c0001t0001g0317 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2136+11646C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100680751 | ||||||
| chr3:100680752
|
G | A | 16 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(13): Show | 16 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+11647G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100680752 | ||||||
| chr3:100680768
|
C | T | 64 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(61): Show | 67 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.2136+11663C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100680768 | ||||||
| chr3:100680769
|
G | A | 16 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(13): Show | 16 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+11664G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100680769 | ||||||
| chr3:100680792
|
A | G | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2136+11687A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100680792 | ||||||
| chr3:100681070
|
T | C | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2136+11965T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100681070 | ||||||
| chr3:100681190
|
T | C | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2136+12085T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100681190 | ||||||
| chr3:100681293
|
A | ATCTTT | 16 | a0001c0001t0001g0077a0001c0001t0001g0100a0001c0001t0001g0101others(13): Show | 16 | HG02027.hp2 HG02129.hp1 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.2136+12200_2136+12 others(11): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100681293 | |||||
| chr3:100681305
|
C | CT | 8 | a0001c0001t0001g0184a0001c0001t0001g0217a0001c0001t0005g0070others(5): Show | 9 | HG00438.hp2 HG00609.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.2136+12214dupT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100681305 | |||||
| chr3:100681321
|
T | C | 9 | a0004c0004t0002g0020a0004c0004t0002g0035a0004c0004t0002g0036others(6): Show | 9 | HG00735.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2136+12216T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100681321 | ||||||
| chr3:100681396
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2136+12291C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100681396 | ||||||
| chr3:100681410
|
A | G | 70 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(67): Show | 75 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.2136+12305A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100681410 | ||||||
| chr3:100681438
|
G | C | 1 | a0002c0002t0001g0258 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2136+12333G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100681438 | ||||||
| chr3:100681784
|
A | G | 3 | a0003c0003t0001g0223a0003c0003t0001g0226a0003c0003t0001g0227 | 3 | HG01074.hp1 HG01943.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.2136+12679A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100681784 | ||||||
| chr3:100681799
|
C | G | 1 | a0001c0001t0001g0096 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2136+12694C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100681799 | ||||||
| chr3:100681889
|
C | T | 152 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(149): Show | 165 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.2136+12784C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100681889 | ||||||
| chr3:100682295
|
G | A | 218 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(215): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.2137-12449G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100682295 | ||||||
| chr3:100682356
|
C | T | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2137-12388C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100682356 | ||||||
| chr3:100682357
|
G | C | 2 | a0002c0002t0001g0268a0002c0002t0001g0301 | 2 | NA18950.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.2137-12387G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100682357 | ||||||
| chr3:100682404
|
A | T | 9 | a0004c0004t0002g0020a0004c0004t0002g0035a0004c0004t0002g0036others(6): Show | 9 | HG00735.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2137-12340A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100682404 | ||||||
| chr3:100682499
|
C | A | 1 | a0001c0001t0001g0128 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2137-12245C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100682499 | ||||||
| chr3:100682661
|
G | T | 218 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(215): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.2137-12083G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100682661 | ||||||
| chr3:100682700
|
C | A | 3 | a0005c0006t0001g0005a0005c0006t0001g0028a0005c0006t0001g0029 | 4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2137-12044C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100682700 | ||||||
| chr3:100682824
|
G | T | 1 | a0002c0002t0001g0311 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2137-11920G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100682824 | ||||||
| chr3:100682955
|
T | C | 239 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(236): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.2137-11789T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100682955 | ||||||
| chr3:100682967
|
G | A | 1 | a0003c0003t0001g0230 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2137-11777G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100682967 | ||||||
| chr3:100683137
|
A | G | 8 | a0001c0008t0001g0039a0002c0002t0001g0069a0002c0002t0001g0309others(5): Show | 8 | HG01891.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2137-11607A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100683137 | ||||||
| chr3:100683183
|
C | T | 52 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0082others(49): Show | 54 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.2137-11561C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100683183 | ||||||
| chr3:100683336
|
C | A | 3 | a0005c0006t0001g0005a0005c0006t0001g0028a0005c0006t0001g0029 | 4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2137-11408C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100683336 | ||||||
| chr3:100683378
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2137-11366C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100683378 | ||||||
| chr3:100683528
|
C | A | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-11216C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100683528 | ||||||
| chr3:100683570
|
C | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-11174C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100683570 | ||||||
| chr3:100683641
|
G | A | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-11103G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100683641 | ||||||
| chr3:100683667
|
T | G | 2 | a0002c0002t0001g0268a0002c0002t0001g0301 | 2 | NA18950.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.2137-11077T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100683667 | ||||||
| chr3:100683676
|
G | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0115a0001c0001t0001g0184 | 4 | HG00438.hp2 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2137-11068G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100683676 | ||||||
| chr3:100683847
|
T | C | 9 | a0004c0004t0002g0020a0004c0004t0002g0035a0004c0004t0002g0036others(6): Show | 9 | HG00735.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2137-10897T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100683847 | ||||||
| chr3:100684187
|
C | G | 2 | a0001c0008t0009g0034a0001c0010t0001g0037 | 2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2137-10557C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100684187 | ||||||
| chr3:100684257
|
C | CTATCTAT others(5): Show |
2 | a0001c0001t0001g0064a0011c0012t0001g0065 | 2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2137-10484_2137-10 others(18): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100684257 | |||||
| chr3:100684257
|
C | CTATTTAT others(1): Show |
183 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0030others(180): Show | 196 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.2137-10470_2137-10 others(14): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100684257 | |||||
| chr3:100684257
|
C | CTATTTAT others(5): Show |
13 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0152others(10): Show | 14 | HG01109.hp2 HG01123.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.2137-10474_2137-10 others(18): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100684257 | |||||
| chr3:100684257
|
C | CTATTTAT others(9): Show |
5 | a0001c0001t0001g0089a0001c0001t0001g0197a0001c0001t0002g0059others(2): Show | 5 | HG02080.hp1 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2137-10478_2137-10 others(22): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100684257 | |||||
| chr3:100684257
|
C | CTATTTAT others(13): Show |
33 | a0001c0001t0001g0109a0001c0001t0001g0115a0001c0001t0001g0157others(30): Show | 34 | HG00735.hp2 HG01243.hp1 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.2137-10482_2137-10 others(26): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100684257 | |||||
| chr3:100684257
|
C | CTATTTAT others(17): Show |
56 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(53): Show | 59 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.2137-10486_2137-10 others(30): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100684257 | |||||
| chr3:100684257
|
C | CTATTTAT others(21): Show |
1 | a0001c0001t0001g0318 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2137-10463_2137-10 others(34): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100684257 | |||||
| chr3:100684266
|
T | TATTTATT others(6): Show |
1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-10477_2137-10 others(19): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100684266 | |||||
| chr3:100684364
|
A | G | 3 | a0005c0006t0001g0005a0005c0006t0001g0028a0005c0006t0001g0029 | 4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2137-10380A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100684364 | ||||||
| chr3:100684389
|
A | C | 18 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(15): Show | 18 | HG00735.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.2137-10355A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100684389 | ||||||
| chr3:100685033
|
T | C | 1 | a0004c0004t0002g0020 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2137-9711T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685033 | ||||||
| chr3:100685083
|
T | C | 115 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(112): Show | 127 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.2137-9661T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685083 | ||||||
| chr3:100685126
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2137-9618C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685126 | ||||||
| chr3:100685296
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0080 | 2 | HG03130.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.2137-9448C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685296 | ||||||
| chr3:100685354
|
T | A | 2 | a0001c0008t0009g0034a0001c0010t0001g0037 | 2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2137-9390T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685354 | ||||||
| chr3:100685422
|
C | T | 8 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(5): Show | 8 | HG00280.hp1 HG02258.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2137-9322C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685422 | ||||||
| chr3:100685482
|
G | A | 115 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(112): Show | 127 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.2137-9262G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685482 | ||||||
| chr3:100685494
|
T | G | 1 | a0001c0001t0001g0098 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2137-9250T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685494 | ||||||
| chr3:100685580
|
T | C | 1 | a0001c0001t0005g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2137-9164T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685580 | ||||||
| chr3:100685602
|
C | A | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2137-9142C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685602 | ||||||
| chr3:100685643
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2137-9101C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685643 | ||||||
| chr3:100685660
|
T | A | 3 | a0005c0006t0001g0005a0005c0006t0001g0028a0005c0006t0001g0029 | 4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2137-9084T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685660 | ||||||
| chr3:100685717
|
C | T | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2137-9027C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685717 | ||||||
| chr3:100685823
|
C | T | 4 | a0001c0001t0001g0079a0001c0001t0001g0096a0001c0001t0001g0165others(1): Show | 4 | HG00423.hp1 HG02027.hp1 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.2137-8921C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685823 | ||||||
| chr3:100685824
|
A | G | 4 | a0001c0001t0001g0079a0001c0001t0001g0096a0001c0001t0001g0165others(1): Show | 4 | HG00423.hp1 HG02027.hp1 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.2137-8920A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685824 | ||||||
| chr3:100685982
|
G | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-8762G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685982 | ||||||
| chr3:100686020
|
A | G | 18 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0003g0031others(15): Show | 18 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.2137-8724A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100686020 | ||||||
| chr3:100686061
|
G | A | 1 | a0001c0001t0003g0031 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2137-8683G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100686061 | ||||||
| chr3:100686067
|
G | C | 140 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(137): Show | 152 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.2137-8677G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100686067 | ||||||
| chr3:100686151
|
T | C | 2 | a0001c0008t0009g0034a0001c0010t0001g0037 | 2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2137-8593T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100686151 | ||||||
| chr3:100686293
|
A | G | 1 | a0003c0003t0001g0243 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2137-8451A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100686293 | ||||||
| chr3:100686324
|
T | C | 3 | a0006c0007t0004g0040a0006c0007t0004g0041a0006c0007t0004g0042 | 3 | HG02109.hp1 HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2137-8420T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100686324 | ||||||
| chr3:100686459
|
G | A | 211 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(208): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.2137-8285G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100686459 | ||||||
| chr3:100686475
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2137-8269C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100686475 | ||||||
| chr3:100686581
|
G | C | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-8163G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100686581 | ||||||
| chr3:100686644
|
A | G | 68 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(65): Show | 72 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.2137-8100A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100686644 | ||||||
| chr3:100686693
|
T | C | 315 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(312): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.2137-8051T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100686693 | ||||||
| chr3:100686828
|
C | A | 2 | a0001c0008t0009g0034a0001c0010t0001g0037 | 2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2137-7916C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100686828 | ||||||
| chr3:100686852
|
G | A | 141 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(138): Show | 153 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.2137-7892G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100686852 | ||||||
| chr3:100686857
|
G | A | 141 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(138): Show | 153 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.2137-7887G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100686857 | ||||||
| chr3:100687014
|
A | G | 3 | a0002c0002t0001g0305a0002c0002t0001g0307a0002c0002t0001g0308 | 3 | HG02165.hp2 NA18999.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2137-7730A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687014 | ||||||
| chr3:100687039
|
A | T | 1 | a0001c0001t0003g0031 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2137-7705A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687039 | ||||||
| chr3:100687172
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2137-7572C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687172 | ||||||
| chr3:100687242
|
G | T | 1 | a0001c0001t0001g0051 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2137-7502G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687242 | ||||||
| chr3:100687335
|
G | A | 122 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(119): Show | 134 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.2137-7409G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687335 | ||||||
| chr3:100687431
|
C | G | 18 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0003g0031others(15): Show | 18 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.2137-7313C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687431 | ||||||
| chr3:100687510
|
C | G | 1 | a0012c0013t0001g0147 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2137-7234C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687510 | ||||||
| chr3:100687511
|
G | A | 3 | a0001c0001t0002g0059a0001c0001t0002g0060a0002c0002t0001g0304 | 3 | HG01358.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2137-7233G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687511 | ||||||
| chr3:100687583
|
C | T | 211 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(208): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.2137-7161C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687583 | ||||||
| chr3:100687616
|
C | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-7128C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687616 | ||||||
| chr3:100687718
|
G | C | 1 | a0001c0001t0001g0175 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2137-7026G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687718 | ||||||
| chr3:100687743
|
G | T | 1 | a0001c0001t0001g0211 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2137-7001G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687743 | ||||||
| chr3:100687771
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2137-6973C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687771 | ||||||
| chr3:100687815
|
C | A | 2 | a0002c0002t0001g0259a0002c0002t0001g0260 | 2 | HG01099.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2137-6929C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687815 | ||||||
| chr3:100687896
|
T | C | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2137-6848T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687896 | ||||||
| chr3:100687903
|
G | T | 1 | a0001c0008t0001g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2137-6841G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687903 | ||||||
| chr3:100687934
|
A | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-6810A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687934 | ||||||
| chr3:100687950
|
T | A | 122 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(119): Show | 134 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.2137-6794T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687950 | ||||||
| chr3:100687999
|
T | C | 8 | a0001c0008t0001g0039a0002c0002t0001g0069a0002c0002t0001g0309others(5): Show | 8 | HG01891.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2137-6745T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687999 | ||||||
| chr3:100688005
|
A | C | 145 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(142): Show | 158 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.2137-6739A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688005 | ||||||
| chr3:100688046
|
T | A | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-6698T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688046 | ||||||
| chr3:100688109
|
A | G | 141 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(138): Show | 153 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.2137-6635A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688109 | ||||||
| chr3:100688141
|
C | G | 1 | a0002c0002t0001g0306 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2137-6603C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688141 | ||||||
| chr3:100688181
|
T | C | 1 | a0002c0002t0001g0257 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2137-6563T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688181 | ||||||
| chr3:100688187
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2137-6557G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688187 | ||||||
| chr3:100688191
|
C | G | 1 | a0002c0002t0001g0257 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2137-6553C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688191 | ||||||
| chr3:100688214
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2137-6530A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688214 | ||||||
| chr3:100688245
|
T | C | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2137-6499T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688245 | ||||||
| chr3:100688246
|
G | A | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2137-6498G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688246 | ||||||
| chr3:100688264
|
T | C | 1 | a0003c0003t0003g0023 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2137-6480T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688264 | ||||||
| chr3:100688291
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2137-6453T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688291 | ||||||
| chr3:100688292
|
G | T | 1 | a0001c0001t0001g0212 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2137-6452G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688292 | ||||||
| chr3:100688297
|
A | T | 1 | a0001c0001t0001g0212 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2137-6447A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688297 | ||||||
| chr3:100688431
|
T | A | 5 | a0001c0001t0001g0152a0001c0001t0001g0178a0001c0001t0001g0189others(2): Show | 5 | HG01123.hp2 HG01952.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.2137-6313T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688431 | ||||||
| chr3:100688477
|
C | A | 141 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(138): Show | 153 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.2137-6267C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688477 | ||||||
| chr3:100688576
|
G | C | 1 | a0001c0001t0001g0137 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2137-6168G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688576 | ||||||
| chr3:100688582
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2137-6162G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688582 | ||||||
| chr3:100688588
|
A | G | 50 | a0001c0001t0001g0118a0002c0002t0001g0001a0002c0002t0001g0012others(47): Show | 60 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.2137-6156A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688588 | ||||||
| chr3:100688593
|
C | T | 50 | a0001c0001t0001g0118a0002c0002t0001g0001a0002c0002t0001g0012others(47): Show | 60 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.2137-6151C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688593 | ||||||
| chr3:100688622
|
A | G | 1 | a0001c0008t0001g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2137-6122A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688622 | ||||||
| chr3:100688649
|
A | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-6095A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688649 | ||||||
| chr3:100688655
|
G | A | 140 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(137): Show | 152 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.2137-6089G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688655 | ||||||
| chr3:100688738
|
C | G | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-6006C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688738 | ||||||
| chr3:100688763
|
C | G | 2 | a0001c0001t0001g0064a0011c0012t0001g0065 | 2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2137-5981C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688763 | ||||||
| chr3:100688782
|
G | A | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-5962G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688782 | ||||||
| chr3:100688783
|
A | C | 122 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(119): Show | 134 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.2137-5961A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688783 | ||||||
| chr3:100688830
|
G | A | 1 | a0002c0002t0001g0286 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2137-5914G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688830 | ||||||
| chr3:100688862
|
G | C | 1 | a0001c0008t0009g0034 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2137-5882G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688862 | ||||||
| chr3:100688924
|
G | T | 8 | a0001c0008t0001g0039a0002c0002t0001g0069a0002c0002t0001g0309others(5): Show | 8 | HG01891.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2137-5820G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688924 | ||||||
| chr3:100688928
|
G | T | 141 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(138): Show | 153 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.2137-5816G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688928 | ||||||
| chr3:100688971
|
G | A | 3 | a0005c0006t0001g0005a0005c0006t0001g0028a0005c0006t0001g0029 | 4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2137-5773G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688971 | ||||||
| chr3:100688983
|
A | C | 114 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(111): Show | 126 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.2137-5761A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688983 | ||||||
| chr3:100688999
|
T | C | 3 | a0005c0006t0001g0005a0005c0006t0001g0028a0005c0006t0001g0029 | 4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2137-5745T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688999 | ||||||
| chr3:100689045
|
G | A | 122 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(119): Show | 134 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.2137-5699G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689045 | ||||||
| chr3:100689112
|
A | T | 9 | a0001c0001t0001g0007a0001c0001t0001g0103a0001c0001t0001g0104others(6): Show | 10 | NA18946.hp2 NA18957.hp2 NA18960.hp1 others(7): Show |
intron_variant | MODIFIER | c.2137-5632A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689112 | ||||||
| chr3:100689170
|
G | A | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2137-5574G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689170 | ||||||
| chr3:100689279
|
G | A | 15 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(12): Show | 15 | HG02109.hp1 HG02258.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.2137-5465G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689279 | ||||||
| chr3:100689397
|
C | T | 122 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(119): Show | 134 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.2137-5347C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689397 | ||||||
| chr3:100689403
|
A | T | 1 | a0003c0003t0001g0249 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2137-5341A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689403 | ||||||
| chr3:100689442
|
G | A | 16 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(13): Show | 16 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2137-5302G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689442 | ||||||
| chr3:100689444
|
T | C | 8 | a0001c0008t0001g0039a0002c0002t0001g0069a0002c0002t0001g0309others(5): Show | 8 | HG01891.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2137-5300T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689444 | ||||||
| chr3:100689447
|
T | C | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-5297T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689447 | ||||||
| chr3:100689453
|
C | T | 18 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0003g0031others(15): Show | 18 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.2137-5291C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689453 | ||||||
| chr3:100689514
|
G | A | 3 | a0001c0001t0002g0059a0001c0001t0002g0060a0002c0002t0001g0310 | 3 | HG02970.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2137-5230G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689514 | ||||||
| chr3:100689682
|
T | C | 1 | a0001c0001t0001g0009 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2137-5062T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689682 | ||||||
| chr3:100689703
|
C | A | 1 | a0004c0004t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2137-5041C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689703 | ||||||
| chr3:100689729
|
T | G | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2137-5015T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689729 | ||||||
| chr3:100689770
|
A | G | 143 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(140): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.2137-4974A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689770 | ||||||
| chr3:100689866
|
T | A | 9 | a0004c0004t0002g0020a0004c0004t0002g0035a0004c0004t0002g0036others(6): Show | 9 | HG00735.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2137-4878T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689866 | ||||||
| chr3:100689887
|
C | T | 140 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(137): Show | 152 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.2137-4857C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689887 | ||||||
| chr3:100689942
|
T | C | 8 | a0001c0008t0001g0039a0002c0002t0001g0069a0002c0002t0001g0309others(5): Show | 8 | HG01891.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2137-4802T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689942 | ||||||
| chr3:100689973
|
C | G | 3 | a0005c0006t0001g0005a0005c0006t0001g0028a0005c0006t0001g0029 | 4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2137-4771C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689973 | ||||||
| chr3:100690069
|
G | A | 9 | a0004c0004t0002g0020a0004c0004t0002g0035a0004c0004t0002g0036others(6): Show | 9 | HG00735.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2137-4675G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100690069 | ||||||
| chr3:100690102
|
G | A | 2 | a0001c0008t0009g0034a0001c0010t0001g0037 | 2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2137-4642G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100690102 | ||||||
| chr3:100690126
|
A | G | 1 | a0001c0001t0005g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2137-4618A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100690126 | ||||||
| chr3:100690136
|
G | A | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-4608G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100690136 | ||||||
| chr3:100690157
|
T | C | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2137-4587T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100690157 | ||||||
| chr3:100690445
|
T | A | 18 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0003g0031others(15): Show | 18 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.2137-4299T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100690445 | ||||||
| chr3:100690474
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2137-4270C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100690474 | ||||||
| chr3:100690551
|
G | A | 1 | a0001c0001t0001g0253 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2137-4193G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100690551 | ||||||
| chr3:100690628
|
G | A | 1 | a0003c0003t0001g0241 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2137-4116G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100690628 | ||||||
| chr3:100690844
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2137-3900G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100690844 | ||||||
| chr3:100690863
|
T | C | 143 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(140): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.2137-3881T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100690863 | ||||||
| chr3:100690925
|
G | T | 114 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(111): Show | 126 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.2137-3819G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100690925 | ||||||
| chr3:100691027
|
C | T | 3 | a0005c0006t0001g0005a0005c0006t0001g0028a0005c0006t0001g0029 | 4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2137-3717C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691027 | ||||||
| chr3:100691141
|
A | G | 2 | a0003c0003t0001g0024a0003c0003t0001g0026 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2137-3603A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691141 | ||||||
| chr3:100691152
|
A | C | 8 | a0001c0008t0001g0039a0002c0002t0001g0069a0002c0002t0001g0309others(5): Show | 8 | HG01891.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2137-3592A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691152 | ||||||
| chr3:100691159
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2137-3585G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691159 | ||||||
| chr3:100691169
|
C | T | 8 | a0001c0008t0001g0039a0002c0002t0001g0069a0002c0002t0001g0309others(5): Show | 8 | HG01891.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2137-3575C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691169 | ||||||
| chr3:100691230
|
G | A | 3 | a0001c0001t0001g0142a0001c0001t0001g0193a0001c0001t0001g0194 | 3 | HG00099.hp1 HG01192.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.2137-3514G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691230 | ||||||
| chr3:100691256
|
G | A | 9 | a0004c0004t0002g0020a0004c0004t0002g0035a0004c0004t0002g0036others(6): Show | 9 | HG00735.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2137-3488G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691256 | ||||||
| chr3:100691313
|
G | A | 1 | a0003c0003t0001g0224 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2137-3431G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691313 | ||||||
| chr3:100691441
|
A | G | 143 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(140): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.2137-3303A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691441 | ||||||
| chr3:100691523
|
A | G | 1 | a0002c0002t0001g0259 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2137-3221A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691523 | ||||||
| chr3:100691591
|
T | G | 1 | a0001c0001t0001g0179 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2137-3153T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691591 | ||||||
| chr3:100691608
|
C | T | 124 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(121): Show | 136 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.2137-3136C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691608 | ||||||
| chr3:100691609
|
A | G | 143 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(140): Show | 155 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.2137-3135A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691609 | ||||||
| chr3:100691649
|
T | G | 1 | a0001c0001t0001g0205 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2137-3095T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691649 | ||||||
| chr3:100691698
|
T | TGATGGGC others(320): Show |
4 | a0001c0001t0001g0075a0001c0001t0001g0135a0001c0001t0001g0149others(1): Show | 4 | HG00280.hp2 HG01943.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.2137-3028_2137-302 others(331): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100691698 | |||||
| chr3:100691698
|
T | TGATGGGC others(321): Show |
1 | a0001c0001t0001g0115 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2137-3028_2137-302 others(332): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100691698 | |||||
| chr3:100691698
|
T | TGATGGGC others(321): Show |
1 | a0001c0001t0001g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2137-3028_2137-302 others(332): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100691698 | |||||
| chr3:100691698
|
T | TGATGGGC others(321): Show |
50 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(47): Show | 53 | HG00140.hp2 HG00597.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.2137-3028_2137-302 others(332): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100691698 | |||||
| chr3:100691698
|
T | TGATGGGC others(321): Show |
5 | a0001c0008t0009g0034a0001c0010t0001g0037a0005c0006t0001g0005others(2): Show | 6 | HG01975.hp2 HG02257.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2137-3028_2137-302 others(332): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100691698 | |||||
| chr3:100691698
|
T | TGATGGGC others(322): Show |
7 | a0001c0001t0001g0142a0001c0001t0001g0184a0001c0001t0001g0187others(4): Show | 7 | HG00099.hp1 HG00438.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.2137-3028_2137-302 others(333): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100691698 | |||||
| chr3:100691698
|
T | TGATGGGC others(322): Show |
1 | a0001c0001t0005g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2137-3028_2137-302 others(333): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100691698 | |||||
| chr3:100691698
|
T | TGATGGGC others(323): Show |
1 | a0001c0001t0001g0193 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2137-3028_2137-302 others(334): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100691698 | |||||
| chr3:100691740
|
C | A | 1 | a0001c0001t0005g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2137-3004C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691740 | ||||||
| chr3:100691748
|
C | T | 122 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(119): Show | 134 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.2137-2996C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691748 | ||||||
| chr3:100691779
|
A | T | 114 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(111): Show | 126 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.2137-2965A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691779 | ||||||
| chr3:100691880
|
C | T | 114 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(111): Show | 126 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.2137-2864C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691880 | ||||||
| chr3:100692021
|
C | T | 1 | a0003c0003t0001g0228 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2137-2723C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100692021 | ||||||
| chr3:100692081
|
T | C | 9 | a0004c0004t0002g0020a0004c0004t0002g0035a0004c0004t0002g0036others(6): Show | 9 | HG00735.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2137-2663T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100692081 | ||||||
| chr3:100692112
|
A | C | 9 | a0004c0004t0002g0020a0004c0004t0002g0035a0004c0004t0002g0036others(6): Show | 9 | HG00735.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2137-2632A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100692112 | ||||||
| chr3:100692138
|
A | G | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-2606A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100692138 | ||||||
| chr3:100692456
|
A | C | 3 | a0005c0006t0001g0005a0005c0006t0001g0028a0005c0006t0001g0029 | 4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2137-2288A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100692456 | ||||||
| chr3:100692490
|
A | G | 79 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(76): Show | 83 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.2137-2254A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100692490 | ||||||
| chr3:100692508
|
C | T | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2137-2236C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100692508 | ||||||
| chr3:100692517
|
G | A | 211 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(208): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.2137-2227G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100692517 | ||||||
| chr3:100692589
|
C | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-2155C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100692589 | ||||||
| chr3:100692738
|
G | C | 2 | a0001c0001t0001g0204a0001c0001t0001g0212 | 2 | HG00609.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.2137-2006G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100692738 | ||||||
| chr3:100692794
|
T | G | 114 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(111): Show | 126 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.2137-1950T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100692794 | ||||||
| chr3:100692851
|
A | G | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-1893A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100692851 | ||||||
| chr3:100692892
|
G | A | 1 | a0001c0001t0001g0181 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2137-1852G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100692892 | ||||||
| chr3:100692949
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2137-1795C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100692949 | ||||||
| chr3:100693033
|
A | T | 211 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(208): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.2137-1711A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100693033 | ||||||
| chr3:100693050
|
G | A | 211 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(208): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.2137-1694G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100693050 | ||||||
| chr3:100693266
|
G | T | 1 | a0001c0001t0001g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2137-1478G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100693266 | ||||||
| chr3:100693320
|
A | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | NA18965.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2137-1424A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100693320 | ||||||
| chr3:100693320
|
A | G | 7 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(4): Show | 7 | HG02258.hp1 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2137-1424A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100693320 | ||||||
| chr3:100693397
|
A | G | 211 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(208): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.2137-1347A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100693397 | ||||||
| chr3:100693648
|
A | T | 19 | a0001c0001t0001g0007a0001c0001t0001g0078a0001c0001t0001g0081others(16): Show | 20 | HG00544.hp2 HG00558.hp2 HG02071.hp2 others(17): Show |
intron_variant | MODIFIER | c.2137-1096A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100693648 | ||||||
| chr3:100693685
|
A | T | 1 | a0001c0005t0008g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-1059A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100693685 | ||||||
| chr3:100693719
|
C | A | 1 | a0001c0001t0001g0248 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2137-1025C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100693719 | ||||||
| chr3:100693732
|
T | C | 1 | a0001c0001t0001g0087 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2137-1012T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100693732 | ||||||
| chr3:100693759
|
T | G | 5 | a0001c0001t0003g0090a0001c0001t0003g0091a0001c0001t0003g0092others(2): Show | 5 | HG02258.hp1 HG02559.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2137-985T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100693759 | ||||||
| chr3:100693841
|
C | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0120a0001c0001t0001g0162others(4): Show | 8 | HG00735.hp1 HG00738.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.2137-903C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100693841 | ||||||
| chr3:100693997
|
A | C | 1 | a0001c0001t0001g0222 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2137-747A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100693997 | ||||||
| chr3:100694088
|
C | A | 1 | a0002c0002t0001g0278 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2137-656C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100694088 | ||||||
| chr3:100694165
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2137-579G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100694165 | ||||||
| chr3:100694297
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2137-447A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100694297 | ||||||
| chr3:100694419
|
A | G | 7 | a0001c0001t0003g0031a0001c0001t0003g0090a0001c0001t0003g0091others(4): Show | 7 | HG02258.hp1 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2137-325A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100694419 | ||||||
| chr3:100694515
|
C | T | 8 | a0001c0008t0001g0039a0002c0002t0001g0069a0002c0002t0001g0309others(5): Show | 8 | HG01891.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2137-229C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100694515 | ||||||
| chr3:100694641
|
T | C | 1 | a0001c0001t0003g0031 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2137-103T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100694641 |