Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 575 |
|---|---|
| ensemblid | ENSG00000181790.13 |
| hgncid | 943 |
| symbol | ADGRB1 |
| name | adhesion G protein-coupled receptor B1 |
| refseq_nuc | NM_001702.3 |
| refseq_prot | NP_001693.2 |
| ensembl_nuc | ENST00000517894.6 |
| ensembl_prot | ENSP00000430945.1 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 142449649 |
| end | 142545007 |
| strand | + |
| ver | v1.2 |
| region | chr8:142449649-142545007 |
| region5000 | chr8:142444649-142550007 |
| regionname0 | ADGRB1_chr8_142449649_142545007 |
| regionname5000 | ADGRB1_chr8_142444649_142550007 |
| 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 | 1584 | 283 | 77 | 71 | 95 | 13 | 25 | 63 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0002 | 0/0 | 1584 | 10 | 0 | 0 | 10 | 0 | 0 | 5 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0003 | 0/0 | 1584 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0004 | 0/0 | 1584 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0005 | 0/0 | 1584 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0006 | 0/0 | 584 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0007 | 0/0 | 1584 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0008 | 0/0 | 1584 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0009 | 0/0 | 1584 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0010 | 0/0 | 1584 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0011 | 0/0 | 1584 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0012 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0013 | 0/0 | 1584 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 4755 | 165 | 24 | 62 | 54 | 10 | 14 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0002 | 0/0 | 4755 | 33 | 0 | 3 | 23 | 0 | 7 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0003 | 1/0 | 4755 | 18 | 12 | 1 | 1 | 1 | 2 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0004 | 0/0 | 4755 | 16 | 6 | 0 | 9 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0005 | 0/0 | 4755 | 8 | 0 | 0 | 8 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0006 | 0/0 | 4755 | 7 | 6 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0007 | 0/0 | 4755 | 7 | 7 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0008 | 0/0 | 4755 | 7 | 4 | 0 | 2 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0009 | 0/0 | 4755 | 6 | 6 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0010 | 0/0 | 4755 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0011 | 0/0 | 4755 | 3 | 2 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0012 | 0/0 | 4755 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0013 | 0/0 | 4755 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0014 | 0/0 | 4755 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0015 | 0/0 | 4755 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0016 | 0/0 | 4755 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0017 | 0/0 | 4755 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0018 | 0/0 | 4755 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0019 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0020 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0021 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0022 | 0/0 | 4742 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0023 | 0/0 | 4755 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0024 | 0/0 | 4755 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0025 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0026 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0027 | 0/0 | 4755 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0028 | 0/0 | 4755 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0029 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0030 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0031 | 0/0 | 4755 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0032 | 0/0 | 4755 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0033 | 0/0 | 4755 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0034 | 0/0 | 4755 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0035 | 0/0 | 4755 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0036 | 0/0 | 4755 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0037 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0038 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0039 | 0/0 | 4755 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0040 | 0/0 | 4755 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| c0041 | 0/0 | 4755 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| 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 | 1266 | 171 | 43 | 52 | 50 | 10 | 14 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| t0002 | 0/0 | 1266 | 100 | 14 | 17 | 55 | 2 | 12 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| t0003 | 0/0 | 1266 | 20 | 19 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| t0004 | 0/0 | 1266 | 4 | 4 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| t0005 | 0/0 | 1266 | 4 | 0 | 0 | 4 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| t0006 | 0/0 | 1266 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| t0007 | 0/0 | 1266 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| t0008 | 0/0 | 1266 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| t0009 | 0/0 | 1266 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| t0010 | 0/0 | 1266 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| t0011 | 0/0 | 1266 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| t0012 | 0/0 | 1266 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| t0013 | 0/0 | 1266 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| t0014 | 0/0 | 1266 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| t0015 | 0/0 | 1266 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| 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 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0175 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0196 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| 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 | 0/1 | 4755 | 165 | 24 | 62 | 54 | 10 | 14 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0002 | 0/0 | 4755 | 33 | 0 | 3 | 23 | 0 | 7 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0003 | 1/0 | 4755 | 18 | 12 | 1 | 1 | 1 | 2 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0004 | 0/0 | 4755 | 16 | 6 | 0 | 9 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0006 | 0/0 | 4755 | 7 | 6 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0007 | 0/0 | 4755 | 7 | 7 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0008 | 0/0 | 4755 | 7 | 4 | 0 | 2 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0010 | 0/0 | 4755 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0011 | 0/0 | 4755 | 3 | 2 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0013 | 0/0 | 4755 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0014 | 0/0 | 4755 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0015 | 0/0 | 4755 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0016 | 0/0 | 4755 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0017 | 0/0 | 4755 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0018 | 0/0 | 4755 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0024 | 0/0 | 4755 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0025 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0026 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0027 | 0/0 | 4755 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0028 | 0/0 | 4755 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0029 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0030 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0032 | 0/0 | 4755 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0033 | 0/0 | 4755 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0034 | 0/0 | 4755 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0035 | 0/0 | 4755 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0036 | 0/0 | 4755 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0002c0005 | 0/0 | 4755 | 8 | 0 | 0 | 8 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0002c0019 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0002c0020 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0003c0009 | 0/0 | 4755 | 6 | 6 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0004c0012 | 0/0 | 4755 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0005c0021 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0006c0022 | 0/0 | 4742 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0007c0038 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0008c0031 | 0/0 | 4755 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0009c0037 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0010c0023 | 0/0 | 4755 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0011c0041 | 0/0 | 4755 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0012c0039 | 0/0 | 4755 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0013c0040 | 0/0 | 4755 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 6020 | 108 | 13 | 50 | 28 | 7 | 9 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0001t0002 | 0/0 | 6020 | 42 | 3 | 10 | 23 | 2 | 4 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0001t0003 | 0/0 | 6020 | 6 | 6 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0001t0005 | 0/0 | 6020 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0001t0006 | 0/0 | 6020 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0001t0009 | 0/0 | 6020 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0001t0011 | 0/0 | 6020 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0001t0013 | 0/0 | 6020 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0001t0014 | 0/0 | 6020 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0002t0001 | 0/0 | 6020 | 5 | 0 | 1 | 3 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0002t0002 | 0/0 | 6020 | 27 | 0 | 2 | 19 | 0 | 6 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0002t0012 | 0/0 | 6020 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0003t0001 | 1/0 | 6020 | 12 | 8 | 0 | 0 | 1 | 2 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0003t0002 | 0/0 | 6020 | 2 | 1 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0003t0003 | 0/0 | 6020 | 4 | 3 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0004t0001 | 0/0 | 6020 | 14 | 4 | 0 | 9 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0004t0003 | 0/0 | 6020 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0004t0015 | 0/0 | 6020 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0006t0001 | 0/0 | 6020 | 5 | 4 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0006t0002 | 0/0 | 6020 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0006t0004 | 0/0 | 6020 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0007t0001 | 0/0 | 6020 | 5 | 5 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0007t0003 | 0/0 | 6020 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0007t0007 | 0/0 | 6020 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0008t0001 | 0/0 | 6020 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0008t0002 | 0/0 | 6020 | 3 | 1 | 0 | 2 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0008t0003 | 0/0 | 6020 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0008t0010 | 0/0 | 6020 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0010t0001 | 0/0 | 6020 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0010t0004 | 0/0 | 6020 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0011t0002 | 0/0 | 6020 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0011t0003 | 0/0 | 6020 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0013t0001 | 0/0 | 6020 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0013t0003 | 0/0 | 6020 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0014t0002 | 0/0 | 6020 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0015t0001 | 0/0 | 6020 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0015t0004 | 0/0 | 6020 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0016t0001 | 0/0 | 6020 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0017t0001 | 0/0 | 6020 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0018t0003 | 0/0 | 6020 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0024t0001 | 0/0 | 6020 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0025t0002 | 0/0 | 6020 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0026t0001 | 0/0 | 6020 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0027t0001 | 0/0 | 6020 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0028t0002 | 0/0 | 6020 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0029t0002 | 0/0 | 6020 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0030t0001 | 0/0 | 6020 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0032t0008 | 0/0 | 6020 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0033t0003 | 0/0 | 6020 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0034t0002 | 0/0 | 6020 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0035t0001 | 0/0 | 6020 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0001c0036t0002 | 0/0 | 6020 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0002c0005t0001 | 0/0 | 6020 | 4 | 0 | 0 | 4 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0002c0005t0002 | 0/0 | 6020 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0002c0005t0005 | 0/0 | 6020 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0002c0019t0002 | 0/0 | 6020 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0002c0020t0002 | 0/0 | 6020 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0003c0009t0002 | 0/0 | 6020 | 6 | 6 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0004c0012t0001 | 0/0 | 6020 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0005c0021t0002 | 0/0 | 6020 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0006c0022t0002 | 0/0 | 6007 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0007c0038t0002 | 0/0 | 6020 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0008c0031t0002 | 0/0 | 6020 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0009c0037t0002 | 0/0 | 6020 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0010c0023t0001 | 0/0 | 6020 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0011c0041t0002 | 0/0 | 6020 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0012c0039t0003 | 0/0 | 6020 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| a0013c0040t0001 | 0/0 | 6020 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | copy fasta | chr8 | 142444649 | 142550007 |
| 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 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0175 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0003g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0005g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0006g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0009g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0011g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0013g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0001t0014g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0002t0012g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0003t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0003t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0003t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0003t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0003t0001g0196 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0003t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0003t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0003t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0003t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0003t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0003t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0003t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0004t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0004t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0004t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0004t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0004t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0004t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0004t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0004t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0004t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0004t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0004t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0004t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0004t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0004t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0004t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0004t0015g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0006t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0006t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0006t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0006t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0006t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0006t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0006t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0007t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0007t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0007t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0007t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0007t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0007t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0007t0007g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0008t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0008t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0008t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0008t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0008t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0008t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0008t0010g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0010t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0010t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0010t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0011t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0011t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0011t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0013t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0013t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0014t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0014t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0015t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0015t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0016t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0016t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0017t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0017t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0018t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0018t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0024t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0025t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0026t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0027t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0028t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0029t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0030t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0032t0008g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0033t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0034t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0035t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0001c0036t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0002c0005t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0002c0005t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0002c0005t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0002c0005t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0002c0005t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0002c0005t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0002c0005t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0002c0005t0005g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0002c0019t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0002c0020t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0003c0009t0002g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0003c0009t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0003c0009t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0003c0009t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0004c0012t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0004c0012t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0005c0021t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0006c0022t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0007c0038t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0008c0031t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0009c0037t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0010c0023t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0011c0041t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0012c0039t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| a0013c0040t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0165 | EUR | GBR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0080 | EUR | GBR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00140 | hp1 | a0010 | c0023 | t0001 | g0166 | EUR | GBR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | GBR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0206 | EUR | FIN | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0181 | EUR | FIN | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0185 | EUR | FIN | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0255 | EUR | FIN | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00408 | hp2 | a0001 | c0004 | t0001 | g0161 | EAS | CHS | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00423 | hp2 | a0002 | c0005 | t0001 | g0022 | EAS | CHS | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | CHS | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | CHS | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00544 | hp2 | a0004 | c0012 | t0001 | g0108 | EAS | CHS | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00597 | hp1 | a0001 | c0016 | t0001 | g0273 | EAS | CHS | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0115 | EAS | CHS | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0172 | EAS | CHS | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00673 | hp1 | a0002 | c0005 | t0001 | g0016 | EAS | CHS | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | CHS | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00735 | hp2 | a0001 | c0006 | t0001 | g0052 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01167 | hp1 | a0001 | c0001 | t0006 | g0003 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01169 | hp1 | a0001 | c0001 | t0006 | g0003 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01169 | hp2 | a0011 | c0041 | t0002 | g0090 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01192 | hp2 | a0001 | c0034 | t0002 | g0071 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01255 | hp1 | a0001 | c0003 | t0003 | g0094 | AMR | CLM | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0301 | AMR | CLM | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | CLM | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01516 | hp1 | a0001 | c0001 | t0009 | g0203 | EUR | IBS | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0214 | EUR | IBS | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01517 | hp1 | a0001 | c0032 | t0008 | g0202 | EUR | IBS | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0230 | EUR | IBS | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01891 | hp1 | a0001 | c0007 | t0001 | g0069 | AFR | ACB | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0047 | AMR | PEL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0126 | AMR | PEL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01975 | hp2 | a0001 | c0014 | t0002 | g0082 | AMR | PEL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | PEL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02015 | hp1 | a0002 | c0005 | t0001 | g0018 | EAS | KHV | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02015 | hp2 | a0004 | c0012 | t0001 | g0114 | EAS | KHV | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0028 | EAS | KHV | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02055 | hp1 | a0001 | c0008 | t0001 | g0297 | AFR | ACB | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | KHV | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02056 | hp2 | a0005 | c0021 | t0002 | g0102 | EAS | KHV | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | KHV | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0233 | EAS | KHV | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0251 | EAS | KHV | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02074 | hp2 | a0001 | c0029 | t0002 | g0248 | EAS | KHV | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0118 | EAS | KHV | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0262 | EAS | KHV | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02083 | hp1 | a0002 | c0005 | t0001 | g0021 | EAS | KHV | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02083 | hp2 | a0001 | c0003 | t0002 | g0101 | EAS | KHV | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0179 | EAS | KHV | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | KHV | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02132 | hp1 | a0002 | c0020 | t0002 | g0053 | EAS | KHV | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | KHV | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0225 | EAS | KHV | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | KHV | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02145 | hp1 | a0003 | c0009 | t0002 | g0295 | AFR | ACB | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02145 | hp2 | a0001 | c0011 | t0003 | g0072 | AFR | ACB | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | CDX | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CDX | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02257 | hp2 | a0003 | c0009 | t0002 | g0001 | AFR | ACB | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0138 | AFR | ACB | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | ACB | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0086 | AFR | ACB | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02280 | hp2 | a0001 | c0003 | t0003 | g0131 | AFR | ACB | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0128 | AMR | PEL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02300 | hp1 | a0001 | c0011 | t0002 | g0149 | AMR | PEL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02300 | hp2 | a0001 | c0028 | t0002 | g0254 | AMR | PEL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02451 | hp1 | a0001 | c0018 | t0003 | g0009 | AFR | ACB | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02451 | hp2 | a0001 | c0006 | t0004 | g0243 | AFR | ACB | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02572 | hp1 | a0001 | c0007 | t0003 | g0276 | AFR | GWD | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0076 | AFR | GWD | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02615 | hp1 | a0001 | c0008 | t0001 | g0298 | AFR | GWD | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02615 | hp2 | a0003 | c0009 | t0002 | g0296 | AFR | GWD | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0241 | AFR | GWD | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02622 | hp2 | a0001 | c0006 | t0001 | g0289 | AFR | GWD | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02630 | hp1 | a0001 | c0001 | t0013 | g0051 | AFR | GWD | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02630 | hp2 | a0001 | c0007 | t0001 | g0068 | AFR | GWD | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | GWD | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02683 | hp1 | a0001 | c0008 | t0010 | g0173 | SAS | PJL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0125 | SAS | PJL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02717 | hp1 | a0001 | c0013 | t0001 | g0096 | AFR | GWD | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02717 | hp2 | a0001 | c0036 | t0002 | g0012 | AFR | GWD | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02735 | hp1 | a0006 | c0022 | t0002 | g0270 | SAS | PJL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0136 | SAS | PJL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0231 | AFR | GWD | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02809 | hp2 | a0001 | c0006 | t0001 | g0288 | AFR | GWD | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02818 | hp1 | a0001 | c0004 | t0015 | g0011 | AFR | GWD | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02818 | hp2 | a0001 | c0015 | t0001 | g0024 | AFR | GWD | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0070 | AFR | GWD | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02897 | hp1 | a0001 | c0006 | t0001 | g0291 | AFR | GWD | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ESN | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02965 | hp1 | a0001 | c0003 | t0002 | g0050 | AFR | ESN | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02965 | hp2 | a0001 | c0035 | t0001 | g0084 | AFR | ESN | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0073 | AFR | ESN | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02970 | hp2 | a0001 | c0010 | t0001 | g0302 | AFR | ESN | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | ESN | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02976 | hp2 | a0001 | c0007 | t0001 | g0253 | AFR | ESN | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0194 | SAS | PJL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0098 | SAS | PJL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03041 | hp1 | a0001 | c0033 | t0003 | g0027 | AFR | GWD | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03041 | hp2 | a0001 | c0004 | t0001 | g0249 | AFR | GWD | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03098 | hp1 | a0001 | c0024 | t0001 | g0085 | AFR | MSL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0242 | AFR | MSL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03139 | hp1 | a0001 | c0010 | t0004 | g0287 | AFR | ESN | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0089 | AFR | ESN | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03195 | hp1 | a0001 | c0008 | t0002 | g0232 | AFR | ESN | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03195 | hp2 | a0001 | c0014 | t0002 | g0083 | AFR | ESN | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | MSL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03209 | hp2 | a0001 | c0011 | t0003 | g0239 | AFR | MSL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03453 | hp1 | a0001 | c0004 | t0001 | g0153 | AFR | MSL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03516 | hp1 | a0001 | c0007 | t0001 | g0067 | AFR | ESN | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0135 | AFR | ESN | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03540 | hp1 | a0001 | c0007 | t0001 | g0133 | AFR | GWD | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03579 | hp1 | a0001 | c0006 | t0002 | g0303 | AFR | MSL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03579 | hp2 | a0001 | c0008 | t0003 | g0013 | AFR | MSL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03654 | hp1 | a0008 | c0031 | t0002 | g0141 | SAS | PJL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0159 | SAS | PJL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03669 | hp2 | a0001 | c0001 | t0011 | g0064 | SAS | PJL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0187 | SAS | PJL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03704 | hp2 | a0001 | c0003 | t0001 | g0097 | SAS | PJL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03710 | hp2 | a0001 | c0004 | t0001 | g0091 | SAS | PJL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | BEB | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0143 | SAS | BEB | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0217 | SAS | BEB | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | STU | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0197 | SAS | STU | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG04184 | hp1 | a0013 | c0040 | t0001 | g0266 | SAS | BEB | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0207 | SAS | BEB | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0065 | SAS | STU | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | STU | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18522 | hp1 | a0001 | c0015 | t0004 | g0282 | AFR | YRI | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18522 | hp2 | a0001 | c0004 | t0001 | g0154 | AFR | YRI | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | CHB | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | CHB | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | CHB | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | YRI | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18906 | hp2 | a0003 | c0009 | t0002 | g0001 | AFR | YRI | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0218 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18945 | hp2 | a0001 | c0001 | t0005 | g0105 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18961 | hp1 | a0002 | c0005 | t0002 | g0020 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18962 | hp1 | a0001 | c0004 | t0001 | g0210 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18963 | hp1 | a0001 | c0004 | t0001 | g0168 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18963 | hp2 | a0001 | c0001 | t0005 | g0106 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18964 | hp1 | a0001 | c0026 | t0001 | g0201 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18966 | hp1 | a0001 | c0002 | t0012 | g0039 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18966 | hp2 | a0001 | c0001 | t0005 | g0204 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18967 | hp2 | a0001 | c0002 | t0002 | g0180 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18970 | hp1 | a0002 | c0019 | t0002 | g0017 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18973 | hp2 | a0001 | c0004 | t0001 | g0103 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18974 | hp1 | a0001 | c0004 | t0001 | g0211 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18975 | hp1 | a0001 | c0025 | t0002 | g0200 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18983 | hp1 | a0002 | c0005 | t0002 | g0019 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18983 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18994 | hp1 | a0001 | c0004 | t0001 | g0038 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0116 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18997 | hp1 | a0001 | c0008 | t0002 | g0061 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18997 | hp2 | a0001 | c0002 | t0002 | g0124 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19002 | hp1 | a0001 | c0004 | t0001 | g0121 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19002 | hp2 | a0007 | c0038 | t0002 | g0056 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19009 | hp1 | a0009 | c0037 | t0002 | g0271 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19011 | hp1 | a0002 | c0005 | t0002 | g0099 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19011 | hp2 | a0002 | c0005 | t0005 | g0245 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19012 | hp1 | a0001 | c0004 | t0001 | g0209 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19030 | hp1 | a0001 | c0010 | t0004 | g0244 | AFR | LWK | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19030 | hp2 | a0001 | c0017 | t0001 | g0008 | AFR | LWK | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19043 | hp1 | a0001 | c0003 | t0003 | g0026 | AFR | LWK | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19043 | hp2 | a0001 | c0018 | t0003 | g0007 | AFR | LWK | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19054 | hp1 | a0001 | c0030 | t0001 | g0263 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19054 | hp2 | a0001 | c0008 | t0002 | g0062 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19066 | hp1 | a0001 | c0004 | t0001 | g0123 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19081 | hp2 | a0001 | c0016 | t0001 | g0272 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19240 | hp1 | a0001 | c0006 | t0001 | g0290 | AFR | YRI | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA19240 | hp2 | a0001 | c0004 | t0003 | g0250 | AFR | YRI | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA20129 | hp1 | a0001 | c0001 | t0014 | g0155 | AFR | ASW | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0055 | AFR | ASW | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA20752 | hp1 | a0001 | c0027 | t0001 | g0213 | EUR | TSI | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0182 | EUR | TSI | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | GIH | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | GIH | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | CLM | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02109 | hp1 | a0001 | c0003 | t0001 | g0152 | AFR | ACB | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02109 | hp2 | a0001 | c0003 | t0003 | g0137 | AFR | ACB | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02486 | hp2 | a0001 | c0007 | t0007 | g0240 | AFR | ACB | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02559 | hp1 | a0001 | c0004 | t0001 | g0292 | AFR | ACB | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG02559 | hp2 | a0003 | c0009 | t0002 | g0001 | AFR | ACB | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03471 | hp1 | a0001 | c0013 | t0003 | g0049 | AFR | MSL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| HG03471 | hp2 | a0012 | c0039 | t0003 | g0237 | AFR | MSL | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA20300 | hp1 | a0003 | c0009 | t0002 | g0092 | AFR | USA | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | USA | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | LWK | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| NA21309 | hp2 | a0001 | c0017 | t0001 | g0010 | AFR | LWK | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0175 | REF | REF | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0196 | REF | REF | ADGRB1_chr8_142444649_142550007 | ADGRB1 | chr8 | 142444649 | 142550007 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:142464283
|
C | T | 1 | a0013 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.85C>T | p.Arg29Trp | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/31 | 760/6020 | 85/4755 | 29/1584 | chr8 | 142464283 | ||
| chr8:142464448
|
A | G | 1 | a0012 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.250A>G | p.Met84Val | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/31 | 925/6020 | 250/4755 | 84/1584 | chr8 | 142464448 | ||
| chr8:142464556
|
T | A | 1 | a0011 | 1 | HG01169.hp2 | missense_variant | MODERATE | c.358T>A | p.Phe120Ile | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/31 | 1033/6020 | 358/4755 | 120/1584 | chr8 | 142464556 | ||
| chr8:142464674
|
G | C | 1 | a0002 | 10 | HG00423.hp2 HG00673.hp1 HG02015.hp1 others(7): Show |
missense_variant | MODERATE | c.476G>C | p.Arg159Pro | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/31 | 1151/6020 | 476/4755 | 159/1584 | chr8 | 142464674 | ||
| chr8:142464794
|
G | A | 1 | a0005 | 1 | HG02056.hp2 | missense_variant | MODERATE | c.596G>A | p.Gly199Asp | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/31 | 1271/6020 | 596/4755 | 199/1584 | chr8 | 142464794 | ||
| chr8:142475496
|
GTGGGGCG others(6): Show |
G | 1 | a0006 | 1 | HG02735.hp1 | frameshift_variant | HIGH | c.808_820delTGGGGCGA others(5): Show |
p.Trp270fs | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 3/31 | 1483/6020 | 808/4755 | 270/1584 | chr8 | 142475496 | ||
| chr8:142476597
|
C | T | 1 | a0007 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.959C>T | p.Thr320Ile | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 4/31 | 1634/6020 | 959/4755 | 320/1584 | chr8 | 142476597 | ||
| chr8:142476639
|
G | A | 1 | a0004 | 2 | HG00544.hp2 HG02015.hp2 |
missense_variant | MODERATE | c.1001G>A | p.Arg334Gln | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 4/31 | 1676/6020 | 1001/4755 | 334/1584 | chr8 | 142476639 | ||
| chr8:142477399
|
G | A | 1 | a0010 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.1237G>A | p.Asp413Asn | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 6/31 | 1912/6020 | 1237/4755 | 413/1584 | chr8 | 142477399 | ||
| chr8:142477493
|
A | G | 1 | a0009 | 1 | NA19009.hp1 | missense_variant | MODERATE | c.1331A>G | p.Asn444Ser | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 6/31 | 2006/6020 | 1331/4755 | 444/1584 | chr8 | 142477493 | ||
| chr8:142524290
|
G | T | 1 | a0008 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.3298G>T | p.Ala1100Ser | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 23/31 | 3973/6020 | 3298/4755 | 1100/1584 | chr8 | 142524290 | ||
| chr8:142543671
|
C | T | 1 | a0003 | 6 | HG02145.hp1 HG02257.hp2 HG02559.hp2 others(3): Show |
missense_variant | MODERATE | c.4520C>T | p.Ala1507Val | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 30/31 | 5195/6020 | 4520/4755 | 1507/1584 | chr8 | 142543671 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:142464270
|
G | T | 1 | a0011c0041 | 1 | HG01169.hp2 | synonymous_variant | LOW | c.72G>T | p.Leu24Leu | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/31 | 747/6020 | 72/4755 | 24/1584 | chr8 | 142464270 | ||
| chr8:142464954
|
C | G | 2 | a0001c0017a0001c0018 | 4 | HG02451.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
synonymous_variant | LOW | c.756C>G | p.Thr252Thr | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/31 | 1431/6020 | 756/4755 | 252/1584 | chr8 | 142464954 | ||
| chr8:142478200
|
T | C | 3 | a0001c0006a0001c0010a0001c0024 | 11 | HG00735.hp2 HG02451.hp2 HG02622.hp2 others(8): Show |
synonymous_variant | LOW | c.1401T>C | p.Asp467Asp | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 7/31 | 2076/6020 | 1401/4755 | 467/1584 | chr8 | 142478200 | ||
| chr8:142479348
|
G | A | 2 | a0001c0025a0001c0026 | 2 | NA18964.hp1 NA18975.hp1 |
synonymous_variant | LOW | c.1587G>A | p.Ala529Ala | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 8/31 | 2262/6020 | 1587/4755 | 529/1584 | chr8 | 142479348 | ||
| chr8:142479372
|
G | A | 1 | a0001c0027 | 1 | NA20752.hp1 | synonymous_variant | LOW | c.1611G>A | p.Thr537Thr | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 8/31 | 2286/6020 | 1611/4755 | 537/1584 | chr8 | 142479372 | ||
| chr8:142518233
|
C | T | 6 | a0001c0008a0001c0015a0001c0016others(3): Show | 14 | HG00597.hp1 HG02055.hp1 HG02132.hp1 others(11): Show |
synonymous_variant | LOW | c.2913C>T | p.Ser971Ser | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/31 | 3588/6020 | 2913/4755 | 971/1584 | chr8 | 142518233 | ||
| chr8:142521976
|
G | A | 1 | a0001c0028 | 1 | HG02300.hp2 | synonymous_variant | LOW | c.3036G>A | p.Thr1012Thr | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 21/31 | 3711/6020 | 3036/4755 | 1012/1584 | chr8 | 142521976 | ||
| chr8:142522018
|
C | T | 2 | a0001c0014a0001c0035 | 3 | HG01975.hp2 HG02965.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.3078C>T | p.Phe1026Phe | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 21/31 | 3753/6020 | 3078/4755 | 1026/1584 | chr8 | 142522018 | ||
| chr8:142522057
|
G | C | 31 | a0001c0001a0001c0002a0001c0004others(28): Show | 277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
synonymous_variant | LOW | c.3117G>C | p.Ala1039Ala | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 21/31 | 3792/6020 | 3117/4755 | 1039/1584 | chr8 | 142522057 | ||
| chr8:142524289
|
C | T | 1 | a0001c0032 | 1 | HG01517.hp1 | synonymous_variant | LOW | c.3297C>T | p.Ala1099Ala | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 23/31 | 3972/6020 | 3297/4755 | 1099/1584 | chr8 | 142524289 | ||
| chr8:142526583
|
G | A | 1 | a0001c0036 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.3354G>A | p.Val1118Val | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/31 | 4029/6020 | 3354/4755 | 1118/1584 | chr8 | 142526583 | ||
| chr8:142526601
|
G | A | 1 | a0001c0029 | 1 | HG02074.hp2 | synonymous_variant | LOW | c.3372G>A | p.Thr1124Thr | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/31 | 4047/6020 | 3372/4755 | 1124/1584 | chr8 | 142526601 | ||
| chr8:142533337
|
G | A | 2 | a0001c0007a0001c0015 | 9 | HG01891.hp1 HG02486.hp2 HG02572.hp1 others(6): Show |
synonymous_variant | LOW | c.3441G>A | p.Ala1147Ala | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/31 | 4116/6020 | 3441/4755 | 1147/1584 | chr8 | 142533337 | ||
| chr8:142542011
|
C | A | 4 | a0001c0004a0001c0011a0001c0016others(1): Show | 22 | HG00408.hp2 HG00597.hp1 HG02145.hp2 others(19): Show |
synonymous_variant | LOW | c.3777C>A | p.Pro1259Pro | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 28/31 | 4452/6020 | 3777/4755 | 1259/1584 | chr8 | 142542011 | ||
| chr8:142542056
|
C | A | 1 | a0001c0013 | 2 | HG02717.hp1 HG03471.hp1 |
synonymous_variant | LOW | c.3822C>A | p.Thr1274Thr | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 28/31 | 4497/6020 | 3822/4755 | 1274/1584 | chr8 | 142542056 | ||
| chr8:142542098
|
G | T | 8 | a0001c0002a0001c0014a0001c0026others(5): Show | 41 | HG00597.hp2 HG00609.hp2 HG00673.hp2 others(38): Show |
synonymous_variant | LOW | c.3864G>T | p.Leu1288Leu | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 28/31 | 4539/6020 | 3864/4755 | 1288/1584 | chr8 | 142542098 | ||
| chr8:142542233
|
G | C | 1 | a0001c0033 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.3999G>C | p.Leu1333Leu | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 28/31 | 4674/6020 | 3999/4755 | 1333/1584 | chr8 | 142542233 | ||
| chr8:142542521
|
G | T | 1 | a0001c0030 | 1 | NA19054.hp1 | synonymous_variant | LOW | c.4287G>T | p.Pro1429Pro | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 28/31 | 4962/6020 | 4287/4755 | 1429/1584 | chr8 | 142542521 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:142449703
|
G | A | 1 | a0001c0007t0007 | 1 | HG02486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-621G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/31 | 14496 | chr8 | 142449703 | |||||
| chr8:142449765
|
G | A | 2 | a0001c0001t0009a0001c0032t0008 | 2 | HG01516.hp1 HG01517.hp1 |
5_prime_UTR_variant | MODIFIER | c.-559G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/31 | 14434 | chr8 | 142449765 | |||||
| chr8:142449989
|
C | A | 3 | a0001c0006t0004a0001c0010t0004a0001c0015t0004 | 4 | HG02451.hp2 HG03139.hp1 NA18522.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-335C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/31 | 14210 | chr8 | 142449989 | |||||
| chr8:142449996
|
C | G | 1 | a0001c0001t0006 | 2 | HG01167.hp1 HG01169.hp1 |
5_prime_UTR_variant | MODIFIER | c.-328C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/31 | 14203 | chr8 | 142449996 | |||||
| chr8:142450085
|
G | A | 1 | a0001c0008t0010 | 1 | HG02683.hp1 | 5_prime_UTR_variant | MODIFIER | c.-239G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/31 | 14114 | chr8 | 142450085 | |||||
| chr8:142464005
|
A | G | 1 | a0001c0004t0015 | 1 | HG02818.hp1 | 5_prime_UTR_variant | MODIFIER | c.-194A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/31 | 194 | chr8 | 142464005 | |||||
| chr8:142464176
|
C | T | 1 | a0001c0001t0014 | 1 | NA20129.hp1 | 5_prime_UTR_variant | MODIFIER | c.-23C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/31 | 23 | chr8 | 142464176 | |||||
| chr8:142544448
|
C | T | 1 | a0001c0001t0013 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*31C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 31/31 | 31 | chr8 | 142544448 | |||||
| chr8:142544480
|
C | T | 1 | a0001c0002t0012 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*63C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 31/31 | 63 | chr8 | 142544480 | |||||
| chr8:142544552
|
G | A | 1 | a0001c0001t0011 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*135G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 31/31 | 135 | chr8 | 142544552 | |||||
| chr8:142544657
|
C | G | 2 | a0001c0001t0005a0002c0005t0005 | 4 | NA18945.hp2 NA18963.hp2 NA18966.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*240C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 31/31 | 240 | chr8 | 142544657 | |||||
| chr8:142544657
|
C | T | 1 | a0001c0001t0013 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*240C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 31/31 | 240 | chr8 | 142544657 | |||||
| chr8:142544672
|
G | C | 25 | a0001c0001t0002a0001c0001t0011a0001c0002t0002others(22): Show | 103 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*255G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 31/31 | 255 | chr8 | 142544672 | |||||
| chr8:142544886
|
G | A | 11 | a0001c0001t0003a0001c0001t0013a0001c0003t0003others(8): Show | 21 | HG01255.hp1 HG02109.hp2 HG02145.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*469G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 31/31 | 469 | chr8 | 142544886 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:142450279
|
CT | C | 7 | a0001c0004t0015g0011a0001c0008t0003g0013a0001c0017t0001g0008others(4): Show | 7 | HG02451.hp1 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-220+176delT | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142450279 | ||||||
| chr8:142450302
|
G | A | 1 | a0001c0001t0002g0014 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-220+198G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142450302 | ||||||
| chr8:142450519
|
GC | G | 7 | a0001c0004t0015g0011a0001c0008t0003g0013a0001c0017t0001g0008others(4): Show | 7 | HG02451.hp1 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-220+421delC | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 142450519 | |||||
| chr8:142450721
|
C | G | 2 | a0001c0006t0002g0303a0001c0010t0001g0302 | 2 | HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-220+617C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142450721 | ||||||
| chr8:142450940
|
G | T | 2 | a0001c0001t0001g0300a0001c0001t0002g0301 | 2 | HG01192.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.-220+836G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142450940 | ||||||
| chr8:142450978
|
G | T | 2 | a0001c0001t0001g0300a0001c0001t0002g0301 | 2 | HG01192.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.-220+874G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142450978 | ||||||
| chr8:142451106
|
G | A | 10 | a0001c0001t0001g0023a0001c0002t0002g0015a0001c0015t0001g0024others(7): Show | 10 | HG00423.hp2 HG00673.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.-220+1002G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142451106 | ||||||
| chr8:142451182
|
G | T | 2 | a0001c0001t0001g0299a0001c0008t0001g0298 | 2 | HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-220+1078G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142451182 | ||||||
| chr8:142451224
|
G | A | 1 | a0001c0001t0001g0025 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-220+1120G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142451224 | ||||||
| chr8:142451347
|
T | C | 1 | a0001c0003t0003g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-220+1243T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142451347 | ||||||
| chr8:142451352
|
T | C | 1 | a0001c0033t0003g0027 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-220+1248T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142451352 | ||||||
| chr8:142451384
|
T | C | 91 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0025others(88): Show | 91 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.-220+1280T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142451384 | ||||||
| chr8:142451396
|
C | T | 8 | a0001c0001t0001g0095a0001c0004t0015g0011a0001c0008t0003g0013others(5): Show | 8 | HG02451.hp1 HG02717.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-220+1292C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142451396 | ||||||
| chr8:142451450
|
GTTC | G | 24 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0029others(21): Show | 24 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(21): Show |
intron_variant | MODIFIER | c.-220+1350_-220+135 others(7): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 142451450 | |||||
| chr8:142451691
|
G | A | 81 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0025others(78): Show | 81 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.-220+1587G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142451691 | ||||||
| chr8:142451928
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-220+1824C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142451928 | ||||||
| chr8:142452067
|
T | C | 1 | a0001c0001t0002g0048 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-220+1963T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142452067 | ||||||
| chr8:142452100
|
T | C | 1 | a0001c0013t0001g0096 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-220+1996T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142452100 | ||||||
| chr8:142452102
|
C | A | 2 | a0001c0002t0002g0098a0001c0003t0001g0097 | 2 | HG03017.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-220+1998C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142452102 | ||||||
| chr8:142452120
|
G | A | 2 | a0001c0001t0001g0029a0001c0002t0002g0028 | 2 | HG02040.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.-220+2016G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142452120 | ||||||
| chr8:142452184
|
C | T | 29 | a0001c0001t0001g0066a0001c0001t0001g0075a0001c0001t0001g0077others(26): Show | 29 | HG00099.hp2 HG01071.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.-220+2080C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142452184 | ||||||
| chr8:142452237
|
T | C | 27 | a0001c0001t0001g0093a0001c0001t0001g0100a0001c0001t0001g0104others(24): Show | 27 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.-220+2133T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142452237 | ||||||
| chr8:142452378
|
A | G | 191 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0025others(188): Show | 193 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.-220+2274A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142452378 | ||||||
| chr8:142452531
|
C | T | 7 | a0001c0001t0002g0048a0001c0001t0002g0060a0001c0001t0002g0065others(4): Show | 7 | HG03669.hp2 HG03834.hp1 HG04204.hp1 others(4): Show |
intron_variant | MODIFIER | c.-220+2427C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142452531 | ||||||
| chr8:142452754
|
G | T | 24 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0029others(21): Show | 24 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(21): Show |
intron_variant | MODIFIER | c.-220+2650G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142452754 | ||||||
| chr8:142452756
|
C | T | 188 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0025others(185): Show | 190 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.-220+2652C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142452756 | ||||||
| chr8:142452930
|
C | T | 8 | a0001c0001t0001g0093a0001c0001t0002g0048a0001c0001t0002g0060others(5): Show | 8 | HG02040.hp1 HG03669.hp2 HG03834.hp1 others(5): Show |
intron_variant | MODIFIER | c.-220+2826C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142452930 | ||||||
| chr8:142453024
|
TCCCG | T | 4 | a0001c0001t0001g0294a0003c0009t0002g0001a0003c0009t0002g0295others(1): Show | 5 | HG02145.hp1 HG02257.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-220+2938_-220+294 others(8): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 142453024 | |||||
| chr8:142453038
|
CCGCCCGC others(9): Show |
C | 4 | a0001c0001t0001g0293a0001c0004t0001g0292a0001c0008t0001g0297others(1): Show | 4 | HG02055.hp1 HG02559.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-220+2938_-220+295 others(20): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 142453038 | |||||
| chr8:142453042
|
CCGCT | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0025others(180): Show | 183 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.-220+2954_-220+295 others(8): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 142453042 | |||||
| chr8:142453042
|
CCGCTCGC others(5): Show |
C | 4 | a0001c0001t0001g0294a0003c0009t0002g0001a0003c0009t0002g0295others(1): Show | 5 | HG02145.hp1 HG02257.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-220+2946_-220+295 others(16): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 142453042 | |||||
| chr8:142453046
|
T | C | 2 | a0001c0001t0001g0066a0001c0002t0001g0125 | 2 | HG01109.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.-220+2942T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142453046 | ||||||
| chr8:142453083
|
C | T | 1 | a0001c0001t0001g0059 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-220+2979C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142453083 | ||||||
| chr8:142453112
|
GC | G | 29 | a0001c0001t0001g0066a0001c0001t0001g0075a0001c0001t0001g0077others(26): Show | 29 | HG00099.hp2 HG01071.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.-220+3014delC | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 142453112 | |||||
| chr8:142453204
|
CGTGCGTG others(25): Show |
C | 1 | a0001c0001t0001g0230 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-220+3104_-220+313 others(36): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 142453204 | |||||
| chr8:142453416
|
T | C | 157 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0025others(154): Show | 159 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.-220+3312T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142453416 | ||||||
| chr8:142453464
|
G | A | 1 | a0001c0002t0001g0129 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-220+3360G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142453464 | ||||||
| chr8:142453596
|
C | T | 4 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0286others(1): Show | 4 | HG02132.hp2 HG02165.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.-220+3492C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142453596 | ||||||
| chr8:142453715
|
C | T | 4 | a0001c0017t0001g0008a0001c0017t0001g0010a0001c0018t0003g0007others(1): Show | 4 | HG02451.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-220+3611C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142453715 | ||||||
| chr8:142453737
|
G | T | 7 | a0001c0001t0002g0048a0001c0001t0002g0060a0001c0001t0002g0065others(4): Show | 7 | HG03669.hp2 HG03834.hp1 HG04204.hp1 others(4): Show |
intron_variant | MODIFIER | c.-220+3633G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142453737 | ||||||
| chr8:142453811
|
G | A | 4 | a0001c0017t0001g0008a0001c0017t0001g0010a0001c0018t0003g0007others(1): Show | 4 | HG02451.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-220+3707G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142453811 | ||||||
| chr8:142453815
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-220+3711T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142453815 | ||||||
| chr8:142453828
|
T | C | 81 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0025others(78): Show | 83 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.-220+3724T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142453828 | ||||||
| chr8:142453904
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-220+3800G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142453904 | ||||||
| chr8:142454110
|
C | T | 16 | a0001c0001t0001g0023a0001c0001t0001g0058a0001c0001t0001g0059others(13): Show | 16 | HG00423.hp2 HG00673.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.-220+4006C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142454110 | ||||||
| chr8:142454188
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-220+4084G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142454188 | ||||||
| chr8:142454349
|
C | T | 1 | a0001c0015t0004g0282 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-220+4245C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142454349 | ||||||
| chr8:142454384
|
T | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0031others(25): Show | 30 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.-220+4280T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142454384 | ||||||
| chr8:142454428
|
C | T | 1 | a0001c0001t0001g0006 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-220+4324C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142454428 | ||||||
| chr8:142454434
|
G | C | 1 | a0001c0008t0002g0232 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-220+4330G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142454434 | ||||||
| chr8:142454489
|
C | T | 1 | a0003c0009t0002g0092 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-220+4385C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142454489 | ||||||
| chr8:142455151
|
G | A | 1 | a0001c0001t0002g0032 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-220+5047G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142455151 | ||||||
| chr8:142455334
|
T | C | 5 | a0001c0001t0001g0095a0001c0003t0001g0241a0001c0003t0003g0094others(2): Show | 5 | HG01255.hp1 HG02486.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-220+5230T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142455334 | ||||||
| chr8:142455471
|
C | A | 1 | a0001c0002t0002g0033 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-220+5367C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142455471 | ||||||
| chr8:142455549
|
A | G | 47 | a0001c0001t0001g0040a0001c0001t0001g0215a0001c0001t0001g0216others(44): Show | 47 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-220+5445A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142455549 | ||||||
| chr8:142455729
|
C | T | 7 | a0001c0001t0002g0048a0001c0001t0002g0065a0001c0001t0011g0064others(4): Show | 7 | HG02717.hp1 HG03209.hp2 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.-220+5625C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142455729 | ||||||
| chr8:142455766
|
G | A | 38 | a0001c0001t0001g0040a0001c0001t0001g0215a0001c0001t0001g0216others(35): Show | 38 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.-220+5662G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142455766 | ||||||
| chr8:142455793
|
G | A | 3 | a0001c0001t0001g0132a0001c0003t0003g0131a0001c0007t0001g0133 | 3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-220+5689G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142455793 | ||||||
| chr8:142456029
|
G | C | 19 | a0001c0001t0001g0059a0001c0001t0001g0095a0001c0001t0002g0054others(16): Show | 19 | HG00423.hp2 HG00438.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.-220+5925G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142456029 | ||||||
| chr8:142456063
|
A | G | 55 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0031others(52): Show | 55 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.-220+5959A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142456063 | ||||||
| chr8:142456159
|
G | T | 1 | a0001c0007t0003g0276 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-220+6055G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142456159 | ||||||
| chr8:142456314
|
C | T | 7 | a0001c0001t0001g0059a0001c0001t0002g0054a0001c0001t0002g0134others(4): Show | 7 | HG00438.hp1 HG02071.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.-220+6210C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142456314 | ||||||
| chr8:142456429
|
A | G | 1 | a0007c0038t0002g0056 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-220+6325A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142456429 | ||||||
| chr8:142456482
|
C | T | 4 | a0001c0006t0001g0288a0001c0006t0001g0289a0001c0006t0001g0290others(1): Show | 4 | HG02622.hp2 HG02809.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-220+6378C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142456482 | ||||||
| chr8:142456518
|
C | T | 2 | a0001c0008t0003g0013a0001c0036t0002g0012 | 2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-220+6414C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142456518 | ||||||
| chr8:142456612
|
G | C | 203 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0031others(200): Show | 205 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.-220+6508G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142456612 | ||||||
| chr8:142456637
|
A | G | 55 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0031others(52): Show | 55 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.-220+6533A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142456637 | ||||||
| chr8:142456749
|
C | T | 124 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0079others(121): Show | 126 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.-220+6645C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142456749 | ||||||
| chr8:142456764
|
G | A | 20 | a0001c0001t0001g0059a0001c0001t0001g0095a0001c0001t0002g0054others(17): Show | 20 | HG00423.hp2 HG00438.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.-220+6660G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142456764 | ||||||
| chr8:142457042
|
G | A | 1 | a0001c0001t0006g0003 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-220+6938G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142457042 | ||||||
| chr8:142457114
|
G | A | 4 | a0001c0006t0001g0288a0001c0006t0001g0289a0001c0006t0001g0290others(1): Show | 4 | HG02622.hp2 HG02809.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-219-6866G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142457114 | ||||||
| chr8:142457121
|
G | A | 4 | a0001c0017t0001g0008a0001c0017t0001g0010a0001c0018t0003g0007others(1): Show | 4 | HG02451.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-219-6859G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142457121 | ||||||
| chr8:142457226
|
A | G | 55 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0031others(52): Show | 55 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.-219-6754A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142457226 | ||||||
| chr8:142457274
|
C | A | 8 | a0001c0001t0002g0048a0001c0001t0002g0065a0001c0001t0011g0064others(5): Show | 8 | HG02717.hp1 HG03209.hp2 HG03669.hp2 others(5): Show |
intron_variant | MODIFIER | c.-219-6706C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142457274 | ||||||
| chr8:142457303
|
G | C | 20 | a0001c0001t0001g0059a0001c0001t0001g0095a0001c0001t0002g0054others(17): Show | 20 | HG00423.hp2 HG00438.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.-219-6677G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142457303 | ||||||
| chr8:142457311
|
T | TGAAGGTC others(15): Show |
1 | a0011c0041t0002g0090 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-219-6668_-219-664 others(26): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 142457311 | |||||
| chr8:142457639
|
G | A | 1 | a0001c0001t0001g0277 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-219-6341G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142457639 | ||||||
| chr8:142457654
|
C | A | 45 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0031others(42): Show | 45 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.-219-6326C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142457654 | ||||||
| chr8:142457685
|
GC | G | 46 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0031others(43): Show | 46 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.-219-6294delC | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142457685 | ||||||
| chr8:142458012
|
G | A | 1 | a0001c0034t0002g0071 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-219-5968G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142458012 | ||||||
| chr8:142458369
|
G | A | 1 | a0001c0027t0001g0213 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-219-5611G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142458369 | ||||||
| chr8:142458689
|
A | C | 1 | a0012c0039t0003g0237 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-219-5291A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142458689 | ||||||
| chr8:142458976
|
C | T | 45 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0031others(42): Show | 45 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.-219-5004C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142458976 | ||||||
| chr8:142459237
|
C | T | 1 | a0001c0011t0003g0239 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-219-4743C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142459237 | ||||||
| chr8:142459466
|
C | T | 1 | a0001c0008t0002g0232 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-219-4514C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142459466 | ||||||
| chr8:142459520
|
G | A | 1 | a0001c0001t0002g0214 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-219-4460G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142459520 | ||||||
| chr8:142459586
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-219-4394G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142459586 | ||||||
| chr8:142459665
|
C | A | 2 | a0001c0001t0001g0095a0001c0011t0002g0149 | 2 | HG02300.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-219-4315C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142459665 | ||||||
| chr8:142459680
|
A | G | 55 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0031others(52): Show | 55 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.-219-4300A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142459680 | ||||||
| chr8:142459702
|
G | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG00738.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.-219-4278G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142459702 | ||||||
| chr8:142459799
|
C | T | 1 | a0001c0004t0001g0121 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-219-4181C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142459799 | ||||||
| chr8:142459881
|
G | A | 2 | a0001c0003t0001g0073a0001c0003t0001g0135 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-219-4099G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142459881 | ||||||
| chr8:142459942
|
G | A | 1 | a0001c0015t0001g0024 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-219-4038G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142459942 | ||||||
| chr8:142460240
|
G | C | 1 | a0001c0006t0004g0243 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-219-3740G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142460240 | ||||||
| chr8:142460284
|
A | G | 1 | a0001c0001t0001g0274 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-219-3696A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142460284 | ||||||
| chr8:142460654
|
C | T | 1 | a0001c0001t0001g0029 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-219-3326C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142460654 | ||||||
| chr8:142460655
|
G | A | 2 | a0001c0008t0003g0013a0001c0036t0002g0012 | 2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-219-3325G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142460655 | ||||||
| chr8:142460778
|
T | C | 3 | a0001c0006t0004g0243a0001c0010t0004g0244a0001c0010t0004g0287 | 3 | HG02451.hp2 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-219-3202T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142460778 | ||||||
| chr8:142460818
|
G | C | 4 | a0001c0001t0001g0132a0001c0003t0003g0131a0001c0007t0001g0133others(1): Show | 4 | HG02280.hp2 HG02717.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-219-3162G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142460818 | ||||||
| chr8:142460864
|
C | T | 2 | a0001c0001t0001g0095a0001c0011t0002g0149 | 2 | HG02300.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-219-3116C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142460864 | ||||||
| chr8:142460926
|
AG | A | 26 | a0001c0001t0001g0132a0001c0001t0002g0054a0001c0001t0002g0134others(23): Show | 27 | HG00423.hp2 HG00438.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.-219-3050delG | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 142460926 | |||||
| chr8:142461172
|
G | T | 1 | a0001c0006t0002g0303 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-219-2808G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142461172 | ||||||
| chr8:142461348
|
C | G | 5 | a0001c0001t0001g0293a0001c0001t0001g0294a0003c0009t0002g0001others(2): Show | 7 | HG02145.hp1 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-219-2632C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142461348 | ||||||
| chr8:142461446
|
C | T | 1 | a0001c0002t0002g0207 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-219-2534C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142461446 | ||||||
| chr8:142461631
|
C | T | 2 | a0001c0008t0003g0013a0001c0036t0002g0012 | 2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-219-2349C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142461631 | ||||||
| chr8:142461632
|
G | A | 2 | a0001c0001t0001g0075a0001c0001t0002g0074 | 2 | HG02647.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-219-2348G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142461632 | ||||||
| chr8:142461676
|
G | A | 3 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158 | 3 | HG01123.hp2 HG01975.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.-219-2304G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142461676 | ||||||
| chr8:142461691
|
G | A | 2 | a0001c0008t0003g0013a0001c0036t0002g0012 | 2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-219-2289G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142461691 | ||||||
| chr8:142461725
|
G | A | 2 | a0001c0001t0002g0054a0001c0001t0002g0134 | 2 | HG00438.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.-219-2255G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142461725 | ||||||
| chr8:142461816
|
G | C | 2 | a0001c0008t0003g0013a0001c0036t0002g0012 | 2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-219-2164G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142461816 | ||||||
| chr8:142461927
|
C | T | 2 | a0001c0011t0003g0072a0001c0034t0002g0071 | 2 | HG01192.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-219-2053C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142461927 | ||||||
| chr8:142461935
|
T | C | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | NA18747.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.-219-2045T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142461935 | ||||||
| chr8:142461941
|
G | A | 2 | a0001c0008t0003g0013a0001c0036t0002g0012 | 2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-219-2039G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142461941 | ||||||
| chr8:142461950
|
G | A | 1 | a0001c0011t0002g0149 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-219-2030G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142461950 | ||||||
| chr8:142461989
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-219-1991C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142461989 | ||||||
| chr8:142462117
|
A | T | 1 | a0011c0041t0002g0090 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-219-1863A>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142462117 | ||||||
| chr8:142462213
|
C | T | 23 | a0001c0001t0001g0132a0001c0001t0002g0134a0001c0001t0003g0004others(20): Show | 24 | HG00423.hp2 HG00438.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.-219-1767C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142462213 | ||||||
| chr8:142462227
|
G | C | 1 | a0001c0013t0003g0049 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-219-1753G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142462227 | ||||||
| chr8:142462298
|
C | T | 3 | a0001c0003t0003g0094a0001c0011t0003g0072a0001c0034t0002g0071 | 3 | HG01192.hp2 HG01255.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.-219-1682C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142462298 | ||||||
| chr8:142462328
|
T | C | 1 | a0001c0002t0002g0159 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-219-1652T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142462328 | ||||||
| chr8:142462384
|
A | G | 1 | a0001c0001t0006g0003 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-219-1596A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142462384 | ||||||
| chr8:142462570
|
G | C | 1 | a0001c0008t0002g0232 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-219-1410G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142462570 | ||||||
| chr8:142462690
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-219-1290C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142462690 | ||||||
| chr8:142462703
|
G | A | 1 | a0001c0015t0001g0024 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-219-1277G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142462703 | ||||||
| chr8:142462888
|
C | T | 1 | a0001c0002t0001g0129 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-219-1092C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142462888 | ||||||
| chr8:142462909
|
G | C | 5 | a0001c0001t0013g0051a0001c0003t0002g0050a0001c0008t0001g0297others(2): Show | 5 | HG02055.hp1 HG02630.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-219-1071G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142462909 | ||||||
| chr8:142462939
|
A | G | 2 | a0001c0001t0001g0023a0001c0001t0001g0206 | 2 | HG00280.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.-219-1041A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142462939 | ||||||
| chr8:142462947
|
C | T | 61 | a0001c0001t0001g0025a0001c0001t0001g0059a0001c0001t0001g0104others(58): Show | 61 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.-219-1033C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142462947 | ||||||
| chr8:142463040
|
G | A | 1 | a0001c0015t0001g0024 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-219-940G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142463040 | ||||||
| chr8:142463052
|
C | T | 1 | a0001c0002t0001g0047 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-219-928C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142463052 | ||||||
| chr8:142463070
|
G | T | 1 | a0011c0041t0002g0090 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-219-910G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142463070 | ||||||
| chr8:142463193
|
C | T | 6 | a0001c0001t0013g0051a0001c0003t0002g0050a0001c0008t0001g0297others(3): Show | 6 | HG02055.hp1 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-219-787C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142463193 | ||||||
| chr8:142463228
|
G | A | 1 | a0001c0001t0002g0214 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-219-752G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142463228 | ||||||
| chr8:142463248
|
C | T | 2 | a0001c0001t0001g0088a0001c0002t0001g0125 | 2 | HG01175.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.-219-732C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142463248 | ||||||
| chr8:142463290
|
T | C | 4 | a0001c0003t0002g0050a0001c0008t0001g0297a0001c0008t0003g0013others(1): Show | 4 | HG02055.hp1 HG02717.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-219-690T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142463290 | ||||||
| chr8:142463360
|
C | A | 1 | a0001c0001t0001g0100 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-219-620C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142463360 | ||||||
| chr8:142463402
|
C | T | 2 | a0001c0025t0002g0200a0001c0026t0001g0201 | 2 | NA18964.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.-219-578C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142463402 | ||||||
| chr8:142463558
|
CAG | C | 3 | a0001c0001t0013g0051a0001c0003t0002g0050a0001c0008t0001g0297 | 3 | HG02055.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-219-419_-219-418d others(4): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 142463558 | |||||
| chr8:142463570
|
G | A | 1 | a0001c0029t0002g0248 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-219-410G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142463570 | ||||||
| chr8:142463685
|
A | C | 1 | a0001c0001t0001g0059 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-219-295A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142463685 | ||||||
| chr8:142463743
|
A | G | 2 | a0001c0008t0003g0013a0001c0036t0002g0012 | 2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-219-237A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142463743 | ||||||
| chr8:142463779
|
T | C | 18 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0002g0048others(15): Show | 20 | HG01891.hp1 HG02145.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.-219-201T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 1/30 | chr8 | 142463779 | ||||||
| chr8:142465020
|
TGGGCAGA others(10): Show |
T | 84 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0034others(81): Show | 85 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.784+60_784+76delAG others(15): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 142465020 | |||||
| chr8:142465046
|
A | G | 1 | a0001c0001t0002g0197 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.784+64A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142465046 | ||||||
| chr8:142465119
|
G | A | 1 | a0001c0001t0002g0160 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.784+137G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142465119 | ||||||
| chr8:142465131
|
G | A | 1 | a0012c0039t0003g0237 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.784+149G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142465131 | ||||||
| chr8:142465227
|
A | G | 1 | a0001c0001t0003g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.784+245A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142465227 | ||||||
| chr8:142465353
|
C | T | 5 | a0001c0001t0003g0086a0001c0003t0001g0138a0001c0003t0001g0241others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.784+371C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142465353 | ||||||
| chr8:142465361
|
C | T | 1 | a0001c0004t0001g0103 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.784+379C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142465361 | ||||||
| chr8:142465366
|
C | T | 4 | a0001c0017t0001g0008a0001c0017t0001g0010a0001c0018t0003g0007others(1): Show | 4 | HG02451.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.784+384C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142465366 | ||||||
| chr8:142465498
|
G | A | 2 | a0001c0008t0003g0013a0001c0036t0002g0012 | 2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.784+516G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142465498 | ||||||
| chr8:142465652
|
C | T | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.784+670C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142465652 | ||||||
| chr8:142465706
|
G | A | 1 | a0001c0016t0001g0272 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.784+724G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142465706 | ||||||
| chr8:142466019
|
C | T | 1 | a0001c0007t0001g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.784+1037C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142466019 | ||||||
| chr8:142466270
|
G | T | 1 | a0007c0038t0002g0056 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.784+1288G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142466270 | ||||||
| chr8:142466278
|
A | G | 3 | a0001c0001t0013g0051a0001c0003t0002g0050a0001c0008t0001g0297 | 3 | HG02055.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.784+1296A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142466278 | ||||||
| chr8:142466817
|
A | T | 1 | a0011c0041t0002g0090 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.784+1835A>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142466817 | ||||||
| chr8:142467080
|
G | A | 1 | a0001c0007t0001g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.784+2098G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142467080 | ||||||
| chr8:142467137
|
C | T | 2 | a0001c0001t0001g0299a0001c0008t0001g0298 | 2 | HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.784+2155C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142467137 | ||||||
| chr8:142467139
|
T | C | 83 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(80): Show | 86 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.784+2157T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142467139 | ||||||
| chr8:142467186
|
G | A | 1 | a0013c0040t0001g0266 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.784+2204G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142467186 | ||||||
| chr8:142467384
|
G | A | 6 | a0001c0001t0001g0079a0001c0001t0001g0215a0001c0001t0002g0078others(3): Show | 6 | HG00099.hp2 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.784+2402G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142467384 | ||||||
| chr8:142467476
|
C | T | 3 | a0001c0003t0003g0094a0001c0011t0003g0072a0001c0034t0002g0071 | 3 | HG01192.hp2 HG01255.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.784+2494C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142467476 | ||||||
| chr8:142467661
|
A | G | 1 | a0001c0001t0001g0229 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.784+2679A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142467661 | ||||||
| chr8:142467764
|
G | A | 2 | a0001c0001t0001g0095a0001c0011t0002g0149 | 2 | HG02300.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.784+2782G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142467764 | ||||||
| chr8:142467885
|
C | T | 29 | a0001c0001t0001g0132a0001c0001t0001g0156a0001c0001t0001g0157others(26): Show | 30 | HG00423.hp2 HG00673.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.784+2903C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142467885 | ||||||
| chr8:142467902
|
G | C | 3 | a0001c0001t0013g0051a0001c0003t0002g0050a0001c0008t0001g0297 | 3 | HG02055.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.784+2920G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142467902 | ||||||
| chr8:142467994
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.784+3012G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142467994 | ||||||
| chr8:142468033
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.784+3051G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142468033 | ||||||
| chr8:142468207
|
T | G | 1 | a0001c0001t0001g0234 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.784+3225T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142468207 | ||||||
| chr8:142468209
|
C | CGT | 3 | a0001c0001t0001g0230a0001c0002t0002g0098a0001c0002t0002g0194 | 3 | HG01517.hp2 HG03017.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.784+3243_784+3244d others(4): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 142468209 | |||||
| chr8:142468209
|
C | T | 3 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236 | 3 | HG01109.hp2 HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.784+3227C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142468209 | ||||||
| chr8:142468209
|
CGT | C | 10 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0003t0001g0076others(7): Show | 12 | HG01891.hp1 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.784+3243_784+3244d others(4): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 142468209 | |||||
| chr8:142468223
|
T | C | 88 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0034others(85): Show | 89 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.784+3241T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142468223 | ||||||
| chr8:142468227
|
C | CGTGT | 3 | a0001c0001t0013g0051a0001c0003t0002g0050a0001c0008t0001g0297 | 3 | HG02055.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.784+3247_784+3250d others(6): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 142468227 | |||||
| chr8:142468227
|
C | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0034others(85): Show | 89 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.784+3245C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142468227 | ||||||
| chr8:142468236
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.784+3254T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142468236 | ||||||
| chr8:142468245
|
C | A | 1 | a0001c0003t0001g0097 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.784+3263C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142468245 | ||||||
| chr8:142468364
|
G | T | 60 | a0001c0001t0001g0025a0001c0001t0001g0059a0001c0001t0001g0104others(57): Show | 60 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.784+3382G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142468364 | ||||||
| chr8:142468523
|
C | T | 2 | a0001c0001t0002g0193a0001c0002t0001g0192 | 2 | NA18612.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.784+3541C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142468523 | ||||||
| chr8:142468654
|
G | A | 2 | a0001c0001t0001g0299a0001c0008t0001g0298 | 2 | HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.784+3672G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142468654 | ||||||
| chr8:142468718
|
C | T | 1 | a0001c0001t0002g0191 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.784+3736C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142468718 | ||||||
| chr8:142468755
|
G | T | 2 | a0001c0001t0001g0077a0001c0002t0002g0136 | 2 | HG01071.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.784+3773G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142468755 | ||||||
| chr8:142469162
|
T | TGA | 3 | a0001c0003t0003g0094a0001c0011t0003g0072a0001c0034t0002g0071 | 3 | HG01192.hp2 HG01255.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.784+4181_784+4182i others(4): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 142469162 | |||||
| chr8:142469162
|
T | TGTGA | 242 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(239): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.784+4183_784+4184i others(6): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 142469162 | |||||
| chr8:142469164
|
T | A | 50 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0034others(47): Show | 50 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.784+4182T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142469164 | ||||||
| chr8:142469171
|
GCA | G | 50 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0034others(47): Show | 50 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.784+4190_784+4191d others(4): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142469171 | ||||||
| chr8:142469176
|
T | C | 50 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0034others(47): Show | 50 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.784+4194T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142469176 | ||||||
| chr8:142469177
|
G | A | 50 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0034others(47): Show | 50 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.784+4195G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142469177 | ||||||
| chr8:142469183
|
A | G | 58 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0034others(55): Show | 58 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.784+4201A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142469183 | ||||||
| chr8:142469205
|
G | A | 50 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0034others(47): Show | 50 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.784+4223G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142469205 | ||||||
| chr8:142469254
|
TGTGAATG others(19): Show |
T | 1 | a0001c0001t0001g0255 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.784+4290_784+4315d others(28): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 142469254 | |||||
| chr8:142469274
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.784+4292C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142469274 | ||||||
| chr8:142469349
|
G | T | 1 | a0001c0024t0001g0085 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.784+4367G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142469349 | ||||||
| chr8:142469353
|
C | CTATGTGC others(29): Show |
2 | a0001c0004t0001g0249a0001c0004t0003g0250 | 2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.784+4381_784+4416d others(38): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 142469353 | |||||
| chr8:142469414
|
TGA | T | 4 | a0001c0006t0001g0288a0001c0006t0001g0289a0001c0006t0001g0290others(1): Show | 4 | HG02622.hp2 HG02809.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.784+4434_784+4435d others(4): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 142469414 | |||||
| chr8:142469436
|
AGT | A | 53 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0034others(50): Show | 53 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.784+4460_784+4461d others(4): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 142469436 | |||||
| chr8:142469450
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.784+4468C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142469450 | ||||||
| chr8:142469451
|
G | A | 8 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0286others(5): Show | 8 | HG02055.hp1 HG02132.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.784+4469G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142469451 | ||||||
| chr8:142469468
|
C | T | 54 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0034others(51): Show | 54 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.784+4486C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142469468 | ||||||
| chr8:142469487
|
A | G | 1 | a0001c0011t0003g0239 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.784+4505A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142469487 | ||||||
| chr8:142469510
|
T | A | 2 | a0001c0006t0002g0303a0001c0010t0001g0302 | 2 | HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.784+4528T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142469510 | ||||||
| chr8:142469510
|
TGTGTATG others(21): Show |
T | 1 | a0006c0022t0002g0270 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.784+4550_784+4577d others(30): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 142469510 | |||||
| chr8:142469530
|
T | C | 2 | a0001c0001t0001g0299a0001c0008t0001g0298 | 2 | HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.784+4548T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142469530 | ||||||
| chr8:142469535
|
G | T | 2 | a0001c0008t0003g0013a0001c0036t0002g0012 | 2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.784+4553G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142469535 | ||||||
| chr8:142469565
|
GTGTGTGC others(1): Show |
G | 4 | a0001c0001t0013g0051a0001c0003t0001g0055a0001c0003t0002g0050others(1): Show | 4 | HG02055.hp1 HG02630.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.784+4598_784+4605d others(10): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 142469565 | |||||
| chr8:142469580
|
C | A | 1 | a0001c0004t0001g0038 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.784+4598C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142469580 | ||||||
| chr8:142469582
|
T | C | 2 | a0001c0006t0002g0303a0001c0010t0001g0302 | 2 | HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.784+4600T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142469582 | ||||||
| chr8:142469584
|
T | A | 1 | a0001c0008t0002g0061 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.784+4602T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142469584 | ||||||
| chr8:142469586
|
T | C | 2 | a0001c0006t0002g0303a0001c0010t0001g0302 | 2 | HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.784+4604T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142469586 | ||||||
| chr8:142469587
|
G | A | 2 | a0001c0006t0002g0303a0001c0010t0001g0302 | 2 | HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.784+4605G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142469587 | ||||||
| chr8:142469588
|
A | T | 2 | a0001c0006t0002g0303a0001c0010t0001g0302 | 2 | HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.784+4606A>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142469588 | ||||||
| chr8:142469589
|
A | G | 2 | a0001c0006t0002g0303a0001c0010t0001g0302 | 2 | HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.784+4607A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142469589 | ||||||
| chr8:142469597
|
G | A | 2 | a0001c0006t0002g0303a0001c0010t0001g0302 | 2 | HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.784+4615G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142469597 | ||||||
| chr8:142469597
|
GTGCACGT others(13): Show |
G | 2 | a0001c0001t0001g0095a0001c0011t0002g0149 | 2 | HG02300.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.784+4633_784+4652d others(22): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 142469597 | |||||
| chr8:142469612
|
TGTGTATG others(3): Show |
T | 3 | a0001c0006t0002g0303a0001c0010t0001g0302a0001c0015t0001g0024 | 3 | HG02818.hp2 HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.784+4634_784+4643d others(12): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 142469612 | |||||
| chr8:142469622
|
C | CGTGCATG others(3): Show |
87 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0034others(84): Show | 88 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.784+4643_784+4652d others(12): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 142469622 | |||||
| chr8:142469629
|
G | GTGTGTGC others(1): Show |
3 | a0001c0001t0013g0051a0001c0003t0002g0050a0001c0008t0001g0297 | 3 | HG02055.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.784+4652_784+4653i others(10): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 142469629 | |||||
| chr8:142469652
|
A | G | 12 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0183others(9): Show | 12 | HG00323.hp1 HG00738.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.784+4670A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142469652 | ||||||
| chr8:142469679
|
ATG | A | 3 | a0001c0001t0013g0051a0001c0003t0002g0050a0001c0008t0001g0297 | 3 | HG02055.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.784+4704_784+4705d others(4): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 142469679 | |||||
| chr8:142469686
|
TGAATGTG others(3): Show |
T | 1 | a0001c0001t0002g0228 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.784+4706_784+4715d others(12): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 142469686 | |||||
| chr8:142469705
|
G | T | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.784+4723G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142469705 | ||||||
| chr8:142469760
|
A | T | 54 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0034others(51): Show | 54 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.784+4778A>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142469760 | ||||||
| chr8:142470091
|
C | T | 7 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0002g0002others(4): Show | 7 | HG00423.hp1 HG00544.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.784+5109C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142470091 | ||||||
| chr8:142470098
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.784+5116C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142470098 | ||||||
| chr8:142470170
|
G | C | 2 | a0001c0001t0001g0299a0001c0008t0001g0298 | 2 | HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.784+5188G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142470170 | ||||||
| chr8:142470344
|
G | A | 2 | a0001c0008t0003g0013a0001c0036t0002g0012 | 2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.785-5130G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142470344 | ||||||
| chr8:142470394
|
C | T | 2 | a0001c0008t0003g0013a0001c0036t0002g0012 | 2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.785-5080C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142470394 | ||||||
| chr8:142470550
|
T | A | 1 | a0001c0001t0001g0216 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.785-4924T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142470550 | ||||||
| chr8:142470820
|
C | G | 1 | a0001c0015t0001g0024 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.785-4654C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142470820 | ||||||
| chr8:142470862
|
G | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0034others(86): Show | 90 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.785-4612G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142470862 | ||||||
| chr8:142470998
|
G | A | 1 | a0001c0033t0003g0027 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.785-4476G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142470998 | ||||||
| chr8:142471356
|
T | A | 2 | a0001c0006t0002g0303a0001c0010t0001g0302 | 2 | HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.785-4118T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142471356 | ||||||
| chr8:142471371
|
G | A | 2 | a0001c0001t0001g0088a0001c0002t0001g0125 | 2 | HG01175.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.785-4103G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142471371 | ||||||
| chr8:142471409
|
G | A | 1 | a0002c0005t0001g0016 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.785-4065G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142471409 | ||||||
| chr8:142471432
|
C | T | 2 | a0001c0008t0003g0013a0001c0036t0002g0012 | 2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.785-4042C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142471432 | ||||||
| chr8:142471857
|
C | T | 3 | a0001c0001t0001g0079a0001c0001t0001g0215a0001c0003t0001g0080 | 3 | HG00099.hp2 HG01358.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.785-3617C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142471857 | ||||||
| chr8:142471883
|
C | T | 1 | a0001c0001t0002g0197 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.785-3591C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142471883 | ||||||
| chr8:142471894
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.785-3580C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142471894 | ||||||
| chr8:142471982
|
C | T | 1 | a0001c0004t0001g0123 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.785-3492C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142471982 | ||||||
| chr8:142472093
|
A | G | 1 | a0001c0001t0003g0089 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.785-3381A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142472093 | ||||||
| chr8:142472443
|
C | A | 4 | a0001c0001t0003g0004a0001c0001t0014g0155a0001c0003t0001g0055others(1): Show | 5 | HG02257.hp1 HG02486.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.785-3031C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142472443 | ||||||
| chr8:142472467
|
T | C | 59 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0034others(56): Show | 59 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.785-3007T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142472467 | ||||||
| chr8:142472507
|
T | C | 192 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(189): Show | 196 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.785-2967T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142472507 | ||||||
| chr8:142472741
|
A | T | 3 | a0001c0001t0013g0051a0001c0003t0002g0050a0001c0008t0001g0297 | 3 | HG02055.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.785-2733A>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142472741 | ||||||
| chr8:142473007
|
C | T | 38 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0215others(35): Show | 40 | HG00099.hp2 HG01168.hp1 HG01169.hp2 others(37): Show |
intron_variant | MODIFIER | c.785-2467C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142473007 | ||||||
| chr8:142473253
|
G | A | 1 | a0007c0038t0002g0056 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.785-2221G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142473253 | ||||||
| chr8:142473256
|
G | A | 2 | a0001c0003t0003g0137a0001c0007t0007g0240 | 2 | HG02109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.785-2218G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142473256 | ||||||
| chr8:142473352
|
T | C | 1 | a0001c0004t0015g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.785-2122T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142473352 | ||||||
| chr8:142473597
|
C | G | 4 | a0001c0001t0001g0075a0001c0001t0002g0074a0001c0001t0003g0231others(1): Show | 4 | HG02647.hp1 HG02647.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.785-1877C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142473597 | ||||||
| chr8:142473955
|
G | A | 95 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0034others(92): Show | 96 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.785-1519G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142473955 | ||||||
| chr8:142473992
|
C | T | 93 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0034others(90): Show | 94 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.785-1482C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142473992 | ||||||
| chr8:142474120
|
A | G | 296 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(293): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.785-1354A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142474120 | ||||||
| chr8:142474162
|
TGA | T | 3 | a0001c0003t0003g0094a0001c0011t0003g0072a0001c0034t0002g0071 | 3 | HG01192.hp2 HG01255.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.785-1310_785-1309d others(4): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 142474162 | |||||
| chr8:142474222
|
C | T | 1 | a0001c0002t0001g0047 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.785-1252C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142474222 | ||||||
| chr8:142474223
|
G | A | 3 | a0001c0001t0013g0051a0001c0003t0002g0050a0001c0008t0001g0297 | 3 | HG02055.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.785-1251G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142474223 | ||||||
| chr8:142474283
|
C | T | 4 | a0001c0003t0001g0152a0001c0004t0001g0153a0001c0004t0001g0154others(1): Show | 4 | HG02109.hp1 HG02559.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.785-1191C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142474283 | ||||||
| chr8:142474375
|
C | T | 1 | a0001c0015t0001g0024 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.785-1099C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142474375 | ||||||
| chr8:142474412
|
C | A | 2 | a0001c0001t0001g0299a0001c0008t0001g0298 | 2 | HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.785-1062C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142474412 | ||||||
| chr8:142474428
|
A | G | 1 | a0001c0003t0001g0070 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.785-1046A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142474428 | ||||||
| chr8:142474494
|
C | T | 15 | a0001c0001t0001g0104a0001c0001t0001g0109a0001c0001t0001g0110others(12): Show | 15 | HG00544.hp2 HG00597.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.785-980C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142474494 | ||||||
| chr8:142474497
|
G | A | 2 | a0001c0006t0002g0303a0001c0010t0001g0302 | 2 | HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.785-977G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142474497 | ||||||
| chr8:142474790
|
G | A | 1 | a0001c0008t0002g0062 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.785-684G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142474790 | ||||||
| chr8:142474795
|
G | T | 55 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0034others(52): Show | 55 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.785-679G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142474795 | ||||||
| chr8:142474841
|
G | A | 2 | a0001c0001t0001g0299a0001c0008t0001g0298 | 2 | HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.785-633G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142474841 | ||||||
| chr8:142474904
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.785-570G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142474904 | ||||||
| chr8:142474965
|
G | T | 1 | a0001c0011t0003g0239 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.785-509G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142474965 | ||||||
| chr8:142474994
|
T | G | 1 | a0001c0003t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.785-480T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142474994 | ||||||
| chr8:142475025
|
C | T | 7 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(4): Show | 7 | HG01123.hp2 HG01928.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.785-449C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142475025 | ||||||
| chr8:142475253
|
A | G | 6 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(3): Show | 6 | HG01109.hp2 HG02886.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.785-221A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142475253 | ||||||
| chr8:142475338
|
C | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0066 | 3 | HG01109.hp1 HG01257.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.785-136C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142475338 | ||||||
| chr8:142475429
|
G | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0034others(91): Show | 95 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.785-45G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 2/30 | chr8 | 142475429 | ||||||
| chr8:142475699
|
A | AG | 41 | a0001c0001t0001g0006a0001c0001t0001g0087a0001c0001t0001g0132others(38): Show | 44 | HG00423.hp2 HG00673.hp1 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.946+70dupG | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr8 | 142475699 | |||||
| chr8:142475711
|
C | G | 15 | a0001c0001t0001g0104a0001c0001t0001g0109a0001c0001t0001g0110others(12): Show | 15 | HG00544.hp2 HG00597.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.946+76C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 3/30 | chr8 | 142475711 | ||||||
| chr8:142475810
|
G | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0034others(95): Show | 99 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.946+175G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 3/30 | chr8 | 142475810 | ||||||
| chr8:142475896
|
C | CGGGGCTG others(13): Show |
172 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(169): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.946+265_946+284dup others(20): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr8 | 142475896 | |||||
| chr8:142475896
|
C | CGGGGCTG others(33): Show |
1 | a0001c0006t0001g0052 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.946+284_946+285ins others(40): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr8 | 142475896 | |||||
| chr8:142475896
|
C | CGGGGCTG others(13): Show |
63 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0034others(60): Show | 63 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.946+272_946+273ins others(20): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr8 | 142475896 | |||||
| chr8:142475927
|
G | C | 1 | a0001c0001t0001g0165 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.946+292G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 3/30 | chr8 | 142475927 | ||||||
| chr8:142476147
|
C | T | 5 | a0001c0001t0001g0075a0001c0001t0002g0074a0001c0001t0003g0231others(2): Show | 5 | HG02647.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.947-438C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 3/30 | chr8 | 142476147 | ||||||
| chr8:142476205
|
T | C | 1 | a0001c0002t0002g0098 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.947-380T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 3/30 | chr8 | 142476205 | ||||||
| chr8:142476506
|
A | G | 3 | a0001c0001t0001g0095a0001c0011t0002g0149a0001c0013t0003g0049 | 3 | HG02300.hp1 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.947-79A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 3/30 | chr8 | 142476506 | ||||||
| chr8:142476988
|
C | T | 3 | a0001c0001t0001g0132a0001c0003t0003g0131a0001c0007t0001g0133 | 3 | HG02280.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1058-126C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 4/30 | chr8 | 142476988 | ||||||
| chr8:142477075
|
A | C | 1 | a0001c0001t0003g0242 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1058-39A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 4/30 | chr8 | 142477075 | ||||||
| chr8:142477080
|
C | T | 3 | a0001c0001t0002g0127a0001c0002t0002g0126a0001c0002t0002g0128 | 3 | HG01928.hp2 HG01981.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.1058-34C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 4/30 | chr8 | 142477080 | ||||||
| chr8:142477306
|
G | A | 1 | a0001c0002t0002g0098 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1222+28G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 5/30 | chr8 | 142477306 | ||||||
| chr8:142477309
|
CAGCCAGG others(9): Show |
C | 1 | a0001c0015t0001g0024 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1222+32_1222+47del others(16): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 5/30 | chr8 | 142477309 | ||||||
| chr8:142477310
|
A | AGCCAGGG others(25): Show |
14 | a0001c0001t0001g0299a0001c0001t0003g0089a0001c0006t0001g0052others(11): Show | 14 | HG00735.hp2 HG01192.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1222+51_1222+52ins others(32): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr8 | 142477310 | |||||
| chr8:142477326
|
G | GGCCGAGG others(9): Show |
16 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0215others(13): Show | 16 | HG00438.hp1 HG01071.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1222+51_1222+52ins others(16): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr8 | 142477326 | |||||
| chr8:142477326
|
G | GGCCGAGG others(8): Show |
1 | a0006c0022t0002g0270 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1222+51_1222+52ins others(15): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr8 | 142477326 | |||||
| chr8:142477326
|
G | T | 1 | a0001c0015t0001g0024 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1222+48G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 5/30 | chr8 | 142477326 | ||||||
| chr8:142477562
|
G | A | 1 | a0001c0001t0002g0197 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1387+13G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 6/30 | chr8 | 142477562 | ||||||
| chr8:142477805
|
T | C | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(243): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1387+256T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 6/30 | chr8 | 142477805 | ||||||
| chr8:142477806
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1387+257G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 6/30 | chr8 | 142477806 | ||||||
| chr8:142477909
|
A | C | 1 | a0001c0001t0002g0264 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1388-278A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 6/30 | chr8 | 142477909 | ||||||
| chr8:142478023
|
C | T | 2 | a0001c0001t0001g0299a0001c0008t0001g0298 | 2 | HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1388-164C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 6/30 | chr8 | 142478023 | ||||||
| chr8:142478070
|
T | C | 210 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(207): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1388-117T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 6/30 | chr8 | 142478070 | ||||||
| chr8:142478396
|
T | C | 2 | a0001c0001t0001g0040a0001c0002t0012g0039 | 2 | HG00140.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1561+36T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 7/30 | chr8 | 142478396 | ||||||
| chr8:142478397
|
A | G | 4 | a0001c0003t0001g0070a0001c0014t0002g0082a0001c0014t0002g0083others(1): Show | 4 | HG01975.hp2 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1561+37A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 7/30 | chr8 | 142478397 | ||||||
| chr8:142478441
|
G | T | 3 | a0001c0004t0001g0209a0001c0004t0001g0210a0001c0004t0001g0211 | 3 | NA18962.hp1 NA18974.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1561+81G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 7/30 | chr8 | 142478441 | ||||||
| chr8:142478577
|
T | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0079a0001c0001t0001g0167others(1): Show | 5 | HG00140.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1561+217T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 7/30 | chr8 | 142478577 | ||||||
| chr8:142478681
|
A | AGGGTGCA others(53): Show |
1 | a0001c0004t0001g0168 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1561+346_1561+347i others(62): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr8 | 142478681 | |||||
| chr8:142478707
|
T | C | 244 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(241): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1561+347T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 7/30 | chr8 | 142478707 | ||||||
| chr8:142478792
|
A | G | 2 | a0001c0008t0003g0013a0001c0036t0002g0012 | 2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1561+432A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 7/30 | chr8 | 142478792 | ||||||
| chr8:142478938
|
G | A | 2 | a0001c0001t0002g0193a0001c0002t0001g0192 | 2 | NA18612.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1562-385G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 7/30 | chr8 | 142478938 | ||||||
| chr8:142479051
|
G | C | 2 | a0001c0001t0001g0299a0001c0008t0001g0298 | 2 | HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1562-272G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 7/30 | chr8 | 142479051 | ||||||
| chr8:142479105
|
T | G | 1 | a0001c0001t0001g0256 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1562-218T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 7/30 | chr8 | 142479105 | ||||||
| chr8:142479143
|
A | G | 209 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(206): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1562-180A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 7/30 | chr8 | 142479143 | ||||||
| chr8:142479192
|
A | G | 1 | a0001c0011t0003g0239 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1562-131A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 7/30 | chr8 | 142479192 | ||||||
| chr8:142479194
|
T | C | 209 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(206): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1562-129T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 7/30 | chr8 | 142479194 | ||||||
| chr8:142479228
|
T | C | 1 | a0001c0011t0003g0239 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1562-95T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 7/30 | chr8 | 142479228 | ||||||
| chr8:142479534
|
G | A | 209 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(206): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1726+47G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 8/30 | chr8 | 142479534 | ||||||
| chr8:142479537
|
T | C | 244 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(241): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1726+50T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 8/30 | chr8 | 142479537 | ||||||
| chr8:142479618
|
C | T | 1 | a0001c0002t0002g0207 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1727-75C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 8/30 | chr8 | 142479618 | ||||||
| chr8:142479635
|
AGCCAGCT | A | 206 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(203): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1727-54_1727-48del others(7): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 8/30 | INFO_REALIGN_3_PRIME | chr8 | 142479635 | |||||
| chr8:142479640
|
G | T | 1 | a0001c0008t0001g0297 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1727-53G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 8/30 | chr8 | 142479640 | ||||||
| chr8:142479832
|
G | A | 3 | a0001c0001t0001g0299a0001c0001t0013g0051a0001c0008t0001g0298 | 3 | HG02615.hp1 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1828+38G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 9/30 | chr8 | 142479832 | ||||||
| chr8:142479845
|
G | A | 206 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(203): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1828+51G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 9/30 | chr8 | 142479845 | ||||||
| chr8:142479894
|
C | T | 1 | a0001c0003t0002g0101 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1828+100C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 9/30 | chr8 | 142479894 | ||||||
| chr8:142479940
|
C | A | 6 | a0001c0001t0001g0299a0001c0001t0013g0051a0001c0003t0002g0050others(3): Show | 6 | HG02055.hp1 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1828+146C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 9/30 | chr8 | 142479940 | ||||||
| chr8:142480032
|
G | T | 2 | a0001c0001t0013g0051a0001c0003t0002g0050 | 2 | HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1828+238G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 9/30 | chr8 | 142480032 | ||||||
| chr8:142480195
|
C | T | 3 | a0001c0001t0001g0255a0001c0001t0001g0299a0001c0008t0001g0298 | 3 | HG00323.hp2 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1828+401C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 9/30 | chr8 | 142480195 | ||||||
| chr8:142480438
|
T | C | 236 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(233): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1828+644T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 9/30 | chr8 | 142480438 | ||||||
| chr8:142480673
|
C | T | 1 | a0001c0011t0002g0149 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1829-581C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 9/30 | chr8 | 142480673 | ||||||
| chr8:142480713
|
C | T | 3 | a0001c0007t0001g0067a0001c0007t0001g0068a0001c0007t0001g0069 | 3 | HG01891.hp1 HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1829-541C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 9/30 | chr8 | 142480713 | ||||||
| chr8:142480734
|
C | G | 207 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(204): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1829-520C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 9/30 | chr8 | 142480734 | ||||||
| chr8:142480790
|
C | T | 2 | a0001c0001t0013g0051a0001c0003t0002g0050 | 2 | HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1829-464C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 9/30 | chr8 | 142480790 | ||||||
| chr8:142480829
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0167a0001c0001t0002g0191others(1): Show | 5 | HG00140.hp1 HG00639.hp1 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.1829-425C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 9/30 | chr8 | 142480829 | ||||||
| chr8:142480841
|
C | G | 1 | a0001c0001t0006g0003 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1829-413C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 9/30 | chr8 | 142480841 | ||||||
| chr8:142480907
|
T | C | 4 | a0001c0003t0001g0152a0001c0004t0001g0153a0001c0004t0001g0154others(1): Show | 4 | HG02109.hp1 HG02559.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1829-347T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 9/30 | chr8 | 142480907 | ||||||
| chr8:142480923
|
G | A | 2 | a0001c0007t0001g0253a0001c0015t0001g0024 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1829-331G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 9/30 | chr8 | 142480923 | ||||||
| chr8:142481073
|
A | G | 6 | a0001c0001t0002g0127a0001c0002t0002g0126a0001c0002t0002g0128others(3): Show | 6 | HG01928.hp2 HG01981.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.1829-181A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 9/30 | chr8 | 142481073 | ||||||
| chr8:142481081
|
G | A | 1 | a0001c0011t0003g0239 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1829-173G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 9/30 | chr8 | 142481081 | ||||||
| chr8:142481104
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1829-150G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 9/30 | chr8 | 142481104 | ||||||
| chr8:142481124
|
G | C | 1 | a0001c0011t0003g0239 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1829-130G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 9/30 | chr8 | 142481124 | ||||||
| chr8:142481410
|
C | T | 7 | a0001c0001t0001g0299a0001c0001t0002g0074a0001c0001t0003g0004others(4): Show | 8 | HG01192.hp2 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1935+50C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 10/30 | chr8 | 142481410 | ||||||
| chr8:142481726
|
C | G | 136 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(133): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.2130+15C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | chr8 | 142481726 | ||||||
| chr8:142481800
|
G | A | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(115): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.2130+89G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | chr8 | 142481800 | ||||||
| chr8:142481929
|
C | G | 10 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(7): Show | 11 | HG01109.hp2 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2130+218C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | chr8 | 142481929 | ||||||
| chr8:142482041
|
G | GGCTGAGC others(17): Show |
125 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(122): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.2130+340_2130+363d others(26): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr8 | 142482041 | |||||
| chr8:142482041
|
G | GGCTGAGC others(1451): Show |
2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG00738.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.2130+363_2130+364i others(1460): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr8 | 142482041 | |||||
| chr8:142482091
|
C | A | 9 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(6): Show | 10 | HG01109.hp2 HG02257.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2130+380C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | chr8 | 142482091 | ||||||
| chr8:142482175
|
C | T | 127 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(124): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.2130+464C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | chr8 | 142482175 | ||||||
| chr8:142482314
|
C | G | 4 | a0001c0003t0003g0094a0001c0017t0001g0008a0001c0018t0003g0007others(1): Show | 4 | HG01255.hp1 HG02451.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.2130+603C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | chr8 | 142482314 | ||||||
| chr8:142482413
|
C | T | 1 | a0001c0026t0001g0201 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2130+702C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | chr8 | 142482413 | ||||||
| chr8:142482536
|
ACTGAGCC others(15): Show |
A | 1 | a0001c0001t0001g0087 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2130+846_2130+867d others(24): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr8 | 142482536 | |||||
| chr8:142482594
|
C | A | 1 | a0001c0001t0002g0054 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2130+883C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | chr8 | 142482594 | ||||||
| chr8:142482732
|
CCCTGGTC others(35): Show |
C | 3 | a0001c0003t0001g0070a0001c0010t0004g0244a0001c0010t0004g0287 | 3 | HG02886.hp1 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2130+1048_2130+108 others(46): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr8 | 142482732 | |||||
| chr8:142482950
|
T | G | 3 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236 | 3 | HG01109.hp2 HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2131-1027T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | chr8 | 142482950 | ||||||
| chr8:142482974
|
A | C | 1 | a0001c0002t0002g0033 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2131-1003A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | chr8 | 142482974 | ||||||
| chr8:142482979
|
A | T | 10 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(7): Show | 11 | HG01109.hp2 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2131-998A>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | chr8 | 142482979 | ||||||
| chr8:142482993
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2131-984C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | chr8 | 142482993 | ||||||
| chr8:142482994
|
A | T | 1 | a0001c0001t0001g0269 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2131-983A>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | chr8 | 142482994 | ||||||
| chr8:142483119
|
C | G | 1 | a0001c0011t0003g0239 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2131-858C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | chr8 | 142483119 | ||||||
| chr8:142483131
|
C | T | 1 | a0001c0001t0001g0278 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2131-846C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | chr8 | 142483131 | ||||||
| chr8:142483159
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2131-818C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | chr8 | 142483159 | ||||||
| chr8:142483160
|
GCTGAGCC others(15): Show |
G | 8 | a0001c0001t0002g0127a0001c0001t0013g0051a0001c0002t0002g0126others(5): Show | 8 | HG01928.hp2 HG01981.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.2131-793_2131-772d others(24): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr8 | 142483160 | |||||
| chr8:142483180
|
ACACTGAG others(39): Show |
A | 2 | a0001c0001t0003g0242a0001c0003t0001g0241 | 2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2131-759_2131-714d others(48): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr8 | 142483180 | |||||
| chr8:142483195
|
C | T | 10 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(7): Show | 11 | HG01109.hp2 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2131-782C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | chr8 | 142483195 | ||||||
| chr8:142483226
|
G | A | 249 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(246): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.2131-751G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | chr8 | 142483226 | ||||||
| chr8:142483298
|
ACTGAGCC others(87): Show |
A | 103 | a0001c0001t0001g0025a0001c0001t0001g0059a0001c0001t0001g0104others(100): Show | 105 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.2131-650_2131-557d others(96): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr8 | 142483298 | |||||
| chr8:142483327
|
ACCCTGAC others(15): Show |
A | 1 | a0001c0008t0002g0232 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2131-631_2131-610d others(24): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr8 | 142483327 | |||||
| chr8:142483341
|
C | T | 1 | a0001c0002t0002g0217 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2131-636C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | chr8 | 142483341 | ||||||
| chr8:142483344
|
ACTGAGCC others(17): Show |
A | 1 | a0001c0001t0001g0226 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2131-609_2131-586d others(26): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr8 | 142483344 | |||||
| chr8:142483474
|
A | G | 2 | a0001c0011t0003g0072a0001c0034t0002g0071 | 2 | HG01192.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2131-503A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | chr8 | 142483474 | ||||||
| chr8:142483594
|
T | G | 115 | a0001c0001t0001g0025a0001c0001t0001g0059a0001c0001t0001g0104others(112): Show | 118 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.2131-383T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | chr8 | 142483594 | ||||||
| chr8:142483694
|
ACTGGTCA others(17): Show |
A | 118 | a0001c0001t0001g0025a0001c0001t0001g0059a0001c0001t0001g0104others(115): Show | 121 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.2131-243_2131-220d others(26): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr8 | 142483694 | |||||
| chr8:142484246
|
A | G | 251 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(248): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.2199+201A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 12/30 | chr8 | 142484246 | ||||||
| chr8:142484364
|
C | T | 10 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(7): Show | 11 | HG01109.hp2 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2200-292C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 12/30 | chr8 | 142484364 | ||||||
| chr8:142484399
|
G | A | 5 | a0001c0001t0002g0127a0001c0002t0002g0126a0001c0002t0002g0128others(2): Show | 5 | HG01928.hp2 HG01981.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.2200-257G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 12/30 | chr8 | 142484399 | ||||||
| chr8:142484409
|
C | T | 6 | a0001c0001t0001g0095a0001c0001t0003g0086a0001c0001t0003g0242others(3): Show | 6 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2200-247C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 12/30 | chr8 | 142484409 | ||||||
| chr8:142484410
|
G | A | 1 | a0001c0011t0003g0072 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2200-246G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 12/30 | chr8 | 142484410 | ||||||
| chr8:142484770
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA18952.hp2 | splice_region_variant&intron_variant | LOW | c.2308+6C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142484770 | ||||||
| chr8:142484834
|
A | C | 1 | a0001c0002t0001g0129 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2308+70A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142484834 | ||||||
| chr8:142485035
|
G | A | 1 | a0001c0003t0002g0101 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2308+271G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142485035 | ||||||
| chr8:142485143
|
G | A | 98 | a0001c0001t0001g0025a0001c0001t0001g0059a0001c0001t0001g0104others(95): Show | 100 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.2308+379G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142485143 | ||||||
| chr8:142485173
|
G | A | 1 | a0001c0013t0003g0049 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2308+409G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142485173 | ||||||
| chr8:142485368
|
T | G | 108 | a0001c0001t0001g0025a0001c0001t0001g0059a0001c0001t0001g0095others(105): Show | 110 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.2308+604T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142485368 | ||||||
| chr8:142485459
|
G | A | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | HG01099.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.2308+695G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142485459 | ||||||
| chr8:142485591
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2308+827A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142485591 | ||||||
| chr8:142485685
|
G | C | 2 | a0001c0011t0003g0072a0001c0034t0002g0071 | 2 | HG01192.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2308+921G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142485685 | ||||||
| chr8:142486009
|
C | A | 117 | a0001c0001t0001g0025a0001c0001t0001g0059a0001c0001t0001g0095others(114): Show | 120 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.2308+1245C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142486009 | ||||||
| chr8:142486128
|
T | G | 1 | a0001c0002t0002g0126 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2308+1364T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142486128 | ||||||
| chr8:142486213
|
C | T | 10 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(7): Show | 11 | HG01109.hp2 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2308+1449C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142486213 | ||||||
| chr8:142486475
|
C | G | 10 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(7): Show | 11 | HG01109.hp2 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2308+1711C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142486475 | ||||||
| chr8:142486505
|
T | A | 1 | a0001c0001t0002g0301 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2308+1741T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142486505 | ||||||
| chr8:142486536
|
A | G | 11 | a0001c0001t0013g0051a0001c0003t0002g0050a0001c0003t0003g0094others(8): Show | 11 | HG01192.hp2 HG01255.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2308+1772A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142486536 | ||||||
| chr8:142486549
|
G | A | 1 | a0001c0011t0003g0239 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2308+1785G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142486549 | ||||||
| chr8:142486565
|
C | T | 114 | a0001c0001t0001g0025a0001c0001t0001g0059a0001c0001t0001g0095others(111): Show | 117 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.2309-1799C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142486565 | ||||||
| chr8:142486593
|
T | C | 125 | a0001c0001t0001g0025a0001c0001t0001g0059a0001c0001t0001g0095others(122): Show | 128 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.2309-1771T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142486593 | ||||||
| chr8:142486736
|
A | G | 41 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0040others(38): Show | 41 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.2309-1628A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142486736 | ||||||
| chr8:142486757
|
G | A | 104 | a0001c0001t0001g0025a0001c0001t0001g0059a0001c0001t0001g0095others(101): Show | 106 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.2309-1607G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142486757 | ||||||
| chr8:142486776
|
C | T | 116 | a0001c0001t0001g0025a0001c0001t0001g0059a0001c0001t0001g0095others(113): Show | 119 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.2309-1588C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142486776 | ||||||
| chr8:142486847
|
T | G | 7 | a0001c0001t0001g0216a0001c0001t0001g0219a0001c0001t0001g0220others(4): Show | 7 | HG01261.hp1 HG01943.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.2309-1517T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142486847 | ||||||
| chr8:142486886
|
G | A | 10 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(7): Show | 11 | HG01109.hp2 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2309-1478G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142486886 | ||||||
| chr8:142486934
|
C | T | 1 | a0001c0011t0003g0239 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2309-1430C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142486934 | ||||||
| chr8:142487271
|
C | T | 6 | a0001c0001t0001g0095a0001c0001t0003g0086a0001c0001t0003g0242others(3): Show | 6 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2309-1093C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142487271 | ||||||
| chr8:142487335
|
C | T | 119 | a0001c0001t0001g0025a0001c0001t0001g0059a0001c0001t0001g0104others(116): Show | 122 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.2309-1029C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142487335 | ||||||
| chr8:142487408
|
T | C | 250 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(247): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.2309-956T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142487408 | ||||||
| chr8:142487757
|
T | C | 2 | a0001c0006t0002g0303a0001c0010t0001g0302 | 2 | HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2309-607T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142487757 | ||||||
| chr8:142487788
|
G | A | 10 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(7): Show | 11 | HG01109.hp2 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2309-576G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142487788 | ||||||
| chr8:142487855
|
A | G | 147 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(144): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.2309-509A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142487855 | ||||||
| chr8:142487979
|
G | A | 4 | a0001c0001t0001g0171a0001c0001t0001g0208a0001c0004t0001g0103others(1): Show | 4 | NA18952.hp1 NA18973.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.2309-385G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142487979 | ||||||
| chr8:142488023
|
G | A | 1 | a0001c0001t0002g0163 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2309-341G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142488023 | ||||||
| chr8:142488128
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2309-236A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142488128 | ||||||
| chr8:142488282
|
C | T | 3 | a0001c0001t0002g0074a0001c0001t0003g0004a0001c0001t0014g0155 | 4 | HG02257.hp1 HG02486.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2309-82C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142488282 | ||||||
| chr8:142488292
|
C | T | 7 | a0001c0001t0001g0299a0001c0001t0002g0074a0001c0001t0003g0004others(4): Show | 8 | HG02257.hp1 HG02486.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2309-72C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 13/30 | chr8 | 142488292 | ||||||
| chr8:142488568
|
G | A | 9 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(6): Show | 10 | HG01109.hp2 HG02257.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2452+61G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 14/30 | chr8 | 142488568 | ||||||
| chr8:142488576
|
C | T | 1 | a0001c0003t0003g0137 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2452+69C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 14/30 | chr8 | 142488576 | ||||||
| chr8:142488579
|
T | C | 113 | a0001c0001t0001g0025a0001c0001t0001g0059a0001c0001t0001g0095others(110): Show | 116 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(113): Show |
intron_variant | MODIFIER | c.2452+72T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 14/30 | chr8 | 142488579 | ||||||
| chr8:142488597
|
G | A | 2 | a0001c0006t0002g0303a0001c0010t0001g0302 | 2 | HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2452+90G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 14/30 | chr8 | 142488597 | ||||||
| chr8:142488616
|
C | T | 2 | a0001c0006t0002g0303a0001c0010t0001g0302 | 2 | HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2452+109C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 14/30 | chr8 | 142488616 | ||||||
| chr8:142488793
|
G | A | 250 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(247): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.2453-242G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 14/30 | chr8 | 142488793 | ||||||
| chr8:142488920
|
G | A | 127 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(124): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.2453-115G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 14/30 | chr8 | 142488920 | ||||||
| chr8:142489008
|
C | T | 1 | a0001c0011t0003g0239 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2453-27C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 14/30 | chr8 | 142489008 | ||||||
| chr8:142489138
|
G | A | 1 | a0001c0001t0002g0264 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2528+28G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 15/30 | chr8 | 142489138 | ||||||
| chr8:142489243
|
G | A | 4 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(1): Show | 4 | HG01109.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2529-93G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 15/30 | chr8 | 142489243 | ||||||
| chr8:142489465
|
G | C | 2 | a0001c0008t0003g0013a0001c0036t0002g0012 | 2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2631+27G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 16/30 | chr8 | 142489465 | ||||||
| chr8:142489550
|
TTCGAGAG others(28): Show |
T | 1 | a0001c0003t0003g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2631+113_2631+147d others(37): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 16/30 | chr8 | 142489550 | ||||||
| chr8:142489560
|
A | G | 250 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(247): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.2631+122A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 16/30 | chr8 | 142489560 | ||||||
| chr8:142489637
|
A | G | 2 | a0001c0002t0002g0180a0002c0019t0002g0017 | 2 | NA18967.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.2631+199A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 16/30 | chr8 | 142489637 | ||||||
| chr8:142489732
|
G | A | 2 | a0001c0006t0002g0303a0001c0010t0001g0302 | 2 | HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2631+294G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 16/30 | chr8 | 142489732 | ||||||
| chr8:142489827
|
A | G | 147 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(144): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.2631+389A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 16/30 | chr8 | 142489827 | ||||||
| chr8:142489870
|
C | T | 9 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(6): Show | 10 | HG01109.hp2 HG02257.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2631+432C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 16/30 | chr8 | 142489870 | ||||||
| chr8:142489883
|
C | T | 1 | a0001c0001t0002g0189 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2631+445C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 16/30 | chr8 | 142489883 | ||||||
| chr8:142490019
|
G | A | 1 | a0001c0015t0001g0024 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2631+581G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 16/30 | chr8 | 142490019 | ||||||
| chr8:142490120
|
G | A | 1 | a0001c0013t0003g0049 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2632-652G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 16/30 | chr8 | 142490120 | ||||||
| chr8:142490358
|
C | T | 7 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(4): Show | 8 | HG01109.hp2 HG02257.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.2632-414C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 16/30 | chr8 | 142490358 | ||||||
| chr8:142490376
|
G | A | 6 | a0001c0001t0001g0139a0001c0001t0001g0215a0001c0001t0001g0223others(3): Show | 6 | HG00733.hp1 HG01243.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.2632-396G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 16/30 | chr8 | 142490376 | ||||||
| chr8:142490384
|
A | C | 1 | a0001c0011t0003g0239 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2632-388A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 16/30 | chr8 | 142490384 | ||||||
| chr8:142490483
|
G | A | 86 | a0001c0001t0001g0025a0001c0001t0001g0059a0001c0001t0001g0104others(83): Show | 88 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.2632-289G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 16/30 | chr8 | 142490483 | ||||||
| chr8:142490643
|
G | A | 5 | a0001c0001t0013g0051a0001c0003t0002g0050a0001c0008t0001g0297others(2): Show | 5 | HG02055.hp1 HG02300.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2632-129G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 16/30 | chr8 | 142490643 | ||||||
| chr8:142490662
|
G | A | 2 | a0001c0011t0003g0072a0001c0034t0002g0071 | 2 | HG01192.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2632-110G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 16/30 | chr8 | 142490662 | ||||||
| chr8:142490863
|
G | A | 3 | a0001c0003t0001g0070a0001c0010t0004g0244a0001c0010t0004g0287 | 3 | HG02886.hp1 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2675+48G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142490863 | ||||||
| chr8:142490882
|
G | C | 1 | a0001c0001t0001g0246 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2675+67G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142490882 | ||||||
| chr8:142491081
|
C | T | 1 | a0004c0012t0001g0114 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2675+266C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142491081 | ||||||
| chr8:142491100
|
C | T | 3 | a0001c0001t0002g0074a0001c0001t0003g0004a0001c0001t0014g0155 | 4 | HG02257.hp1 HG02486.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2675+285C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142491100 | ||||||
| chr8:142491349
|
G | A | 1 | a0001c0017t0001g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2675+534G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142491349 | ||||||
| chr8:142491365
|
C | G | 1 | a0001c0002t0002g0118 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2675+550C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142491365 | ||||||
| chr8:142491367
|
A | T | 1 | a0001c0011t0003g0239 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2675+552A>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142491367 | ||||||
| chr8:142491471
|
C | T | 1 | a0001c0011t0003g0239 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2675+656C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142491471 | ||||||
| chr8:142491483
|
C | A | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2675+668C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142491483 | ||||||
| chr8:142491495
|
G | A | 15 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(12): Show | 15 | HG01109.hp2 HG01255.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2675+680G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142491495 | ||||||
| chr8:142491589
|
A | G | 134 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(131): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.2675+774A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142491589 | ||||||
| chr8:142491654
|
C | A | 3 | a0001c0001t0002g0074a0001c0001t0003g0004a0001c0001t0014g0155 | 4 | HG02257.hp1 HG02486.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2675+839C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142491654 | ||||||
| chr8:142491753
|
C | T | 2 | a0001c0001t0001g0257a0001c0011t0002g0149 | 2 | HG02273.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.2675+938C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142491753 | ||||||
| chr8:142491754
|
G | A | 2 | a0001c0011t0003g0072a0001c0034t0002g0071 | 2 | HG01192.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2675+939G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142491754 | ||||||
| chr8:142491758
|
C | T | 128 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(125): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.2675+943C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142491758 | ||||||
| chr8:142491776
|
A | G | 1 | a0001c0003t0001g0055 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2675+961A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142491776 | ||||||
| chr8:142491793
|
G | A | 137 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(134): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.2675+978G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142491793 | ||||||
| chr8:142492021
|
T | G | 1 | a0001c0008t0002g0232 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2675+1206T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142492021 | ||||||
| chr8:142492103
|
T | G | 15 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(12): Show | 15 | HG01109.hp2 HG01255.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2675+1288T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142492103 | ||||||
| chr8:142492197
|
T | C | 239 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(236): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.2675+1382T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142492197 | ||||||
| chr8:142492198
|
T | C | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2675+1383T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142492198 | ||||||
| chr8:142492231
|
G | A | 1 | a0001c0002t0002g0028 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2675+1416G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142492231 | ||||||
| chr8:142492307
|
A | G | 1 | a0001c0006t0004g0243 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2675+1492A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142492307 | ||||||
| chr8:142492395
|
C | T | 6 | a0001c0003t0003g0094a0001c0011t0002g0149a0001c0017t0001g0008others(3): Show | 6 | HG01255.hp1 HG02300.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2675+1580C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142492395 | ||||||
| chr8:142492429
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2675+1614G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142492429 | ||||||
| chr8:142492500
|
G | C | 2 | a0001c0011t0003g0239a0001c0015t0001g0024 | 2 | HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2675+1685G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142492500 | ||||||
| chr8:142492550
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2675+1735G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142492550 | ||||||
| chr8:142492553
|
G | A | 1 | a0001c0015t0001g0024 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2675+1738G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142492553 | ||||||
| chr8:142492566
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2675+1751C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142492566 | ||||||
| chr8:142492738
|
G | A | 6 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(3): Show | 6 | HG01109.hp2 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2675+1923G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142492738 | ||||||
| chr8:142492797
|
A | C | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2675+1982A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142492797 | ||||||
| chr8:142492798
|
C | A | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2675+1983C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142492798 | ||||||
| chr8:142492818
|
A | AG | 5 | a0001c0001t0001g0066a0001c0001t0001g0169a0001c0001t0001g0198others(2): Show | 5 | HG00741.hp1 HG01099.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.2675+2008dupG | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142492818 | |||||
| chr8:142492885
|
C | T | 2 | a0001c0003t0002g0101a0002c0020t0002g0053 | 2 | HG02083.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.2675+2070C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142492885 | ||||||
| chr8:142492929
|
G | A | 1 | a0001c0001t0006g0003 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2675+2114G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142492929 | ||||||
| chr8:142492941
|
A | C | 4 | a0001c0001t0001g0087a0001c0007t0001g0067a0001c0007t0001g0068others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2675+2126A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142492941 | ||||||
| chr8:142492942
|
G | C | 4 | a0001c0001t0001g0087a0001c0007t0001g0067a0001c0007t0001g0068others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2675+2127G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142492942 | ||||||
| chr8:142493046
|
G | A | 1 | a0001c0004t0001g0209 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2675+2231G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142493046 | ||||||
| chr8:142493048
|
G | A | 8 | a0001c0001t0001g0095a0001c0001t0003g0086a0001c0001t0003g0242others(5): Show | 8 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2675+2233G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142493048 | ||||||
| chr8:142493064
|
G | A | 1 | a0001c0013t0003g0049 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2675+2249G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142493064 | ||||||
| chr8:142493164
|
G | GAATACAG others(27): Show |
1 | a0001c0003t0003g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2675+2349_2675+235 others(38): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142493164 | ||||||
| chr8:142493222
|
C | T | 2 | a0001c0006t0002g0303a0001c0010t0001g0302 | 2 | HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2675+2407C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142493222 | ||||||
| chr8:142493260
|
G | A | 2 | a0001c0008t0002g0232a0001c0018t0003g0007 | 2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2675+2445G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142493260 | ||||||
| chr8:142493282
|
T | G | 41 | a0001c0001t0001g0258a0001c0001t0001g0293a0001c0001t0001g0294others(38): Show | 43 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(40): Show |
intron_variant | MODIFIER | c.2675+2467T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142493282 | ||||||
| chr8:142493326
|
T | C | 1 | a0001c0003t0003g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2675+2511T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142493326 | ||||||
| chr8:142493333
|
G | T | 1 | a0001c0001t0002g0301 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2675+2518G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142493333 | ||||||
| chr8:142493405
|
G | C | 4 | a0001c0001t0001g0258a0001c0001t0002g0078a0001c0002t0001g0047others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.2675+2590G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142493405 | ||||||
| chr8:142493714
|
C | T | 2 | a0001c0006t0002g0303a0001c0010t0001g0302 | 2 | HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2675+2899C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142493714 | ||||||
| chr8:142493730
|
T | A | 28 | a0001c0001t0001g0087a0001c0001t0001g0234a0001c0001t0001g0235others(25): Show | 29 | HG01109.hp2 HG01192.hp2 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.2675+2915T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142493730 | ||||||
| chr8:142493737
|
C | G | 2 | a0001c0001t0009g0203a0001c0032t0008g0202 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2675+2922C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142493737 | ||||||
| chr8:142493788
|
A | G | 28 | a0001c0001t0001g0087a0001c0001t0001g0234a0001c0001t0001g0235others(25): Show | 29 | HG01109.hp2 HG01192.hp2 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.2675+2973A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142493788 | ||||||
| chr8:142493799
|
T | C | 2 | a0001c0001t0001g0293a0003c0009t0002g0001 | 4 | HG02257.hp2 HG02559.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2675+2984T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142493799 | ||||||
| chr8:142493805
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2675+2990C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142493805 | ||||||
| chr8:142493945
|
C | T | 1 | a0001c0001t0002g0264 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2675+3130C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142493945 | ||||||
| chr8:142493946
|
G | T | 2 | a0001c0011t0003g0072a0001c0034t0002g0071 | 2 | HG01192.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2675+3131G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142493946 | ||||||
| chr8:142494003
|
G | A | 1 | a0001c0007t0003g0276 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2675+3188G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142494003 | ||||||
| chr8:142494015
|
C | T | 2 | a0001c0001t0009g0203a0001c0032t0008g0202 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2675+3200C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142494015 | ||||||
| chr8:142494248
|
A | C | 1 | a0001c0003t0003g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2675+3433A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142494248 | ||||||
| chr8:142494259
|
GAGCCCTG others(41): Show |
G | 8 | a0001c0001t0001g0258a0001c0001t0002g0078a0001c0002t0001g0047others(5): Show | 8 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.2675+3462_2675+350 others(52): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142494259 | |||||
| chr8:142494376
|
A | G | 1 | a0001c0001t0003g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2675+3561A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142494376 | ||||||
| chr8:142494466
|
TCACATGC others(16): Show |
T | 1 | a0001c0002t0002g0098 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2675+3652_2675+367 others(27): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142494466 | ||||||
| chr8:142494476
|
G | A | 2 | a0001c0006t0002g0303a0001c0010t0001g0302 | 2 | HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2675+3661G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142494476 | ||||||
| chr8:142494588
|
G | A | 5 | a0001c0001t0001g0087a0001c0007t0001g0067a0001c0007t0001g0068others(2): Show | 5 | HG01891.hp1 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2675+3773G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142494588 | ||||||
| chr8:142494701
|
T | C | 18 | a0001c0001t0001g0087a0001c0001t0002g0074a0001c0001t0014g0155others(15): Show | 18 | HG01192.hp2 HG01255.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.2675+3886T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142494701 | ||||||
| chr8:142494708
|
G | A | 5 | a0001c0001t0001g0087a0001c0007t0001g0067a0001c0007t0001g0068others(2): Show | 5 | HG01891.hp1 HG02630.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2675+3893G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142494708 | ||||||
| chr8:142494722
|
A | G | 3 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0003g0131 | 3 | HG02280.hp2 HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2675+3907A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142494722 | ||||||
| chr8:142494734
|
C | T | 4 | a0001c0003t0001g0152a0001c0004t0001g0153a0001c0004t0001g0154others(1): Show | 4 | HG02109.hp1 HG02559.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2675+3919C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142494734 | ||||||
| chr8:142494762
|
C | A | 8 | a0001c0001t0001g0139a0001c0001t0001g0198a0001c0001t0001g0199others(5): Show | 8 | HG00733.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.2675+3947C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142494762 | ||||||
| chr8:142494763
|
G | A | 12 | a0001c0001t0002g0074a0001c0001t0014g0155a0001c0006t0002g0303others(9): Show | 12 | HG01192.hp2 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.2675+3948G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142494763 | ||||||
| chr8:142494767
|
G | C | 1 | a0001c0010t0001g0302 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2675+3952G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142494767 | ||||||
| chr8:142494879
|
G | GC | 5 | a0001c0001t0001g0087a0001c0007t0001g0067a0001c0007t0001g0068others(2): Show | 5 | HG01891.hp1 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2675+4065dupC | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142494879 | |||||
| chr8:142494887
|
T | G | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2675+4072T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142494887 | ||||||
| chr8:142494937
|
C | T | 1 | a0001c0002t0001g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2675+4122C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142494937 | ||||||
| chr8:142495242
|
G | C | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2675+4427G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142495242 | ||||||
| chr8:142495296
|
G | A | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2675+4481G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142495296 | ||||||
| chr8:142495299
|
A | G | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2675+4484A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142495299 | ||||||
| chr8:142495489
|
T | A | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2675+4674T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142495489 | ||||||
| chr8:142495709
|
T | C | 1 | a0001c0002t0002g0172 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2675+4894T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142495709 | ||||||
| chr8:142495731
|
G | A | 13 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(10): Show | 13 | HG01109.hp2 HG01192.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.2675+4916G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142495731 | ||||||
| chr8:142495776
|
C | T | 7 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(4): Show | 7 | HG01109.hp2 HG02615.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2675+4961C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142495776 | ||||||
| chr8:142495801
|
T | C | 1 | a0001c0008t0002g0232 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2675+4986T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142495801 | ||||||
| chr8:142496010
|
A | T | 6 | a0001c0001t0002g0032a0001c0001t0002g0035a0001c0001t0002g0045others(3): Show | 6 | HG00438.hp2 HG02300.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.2675+5195A>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142496010 | ||||||
| chr8:142496156
|
G | C | 1 | a0001c0007t0001g0133 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2675+5341G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142496156 | ||||||
| chr8:142496528
|
G | T | 5 | a0001c0001t0002g0074a0001c0001t0014g0155a0001c0006t0002g0303others(2): Show | 5 | HG01192.hp2 HG02145.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2675+5713G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142496528 | ||||||
| chr8:142496605
|
T | G | 5 | a0001c0001t0001g0087a0001c0007t0001g0067a0001c0007t0001g0068others(2): Show | 5 | HG01891.hp1 HG02630.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2675+5790T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142496605 | ||||||
| chr8:142496745
|
G | T | 2 | a0001c0001t0001g0299a0001c0008t0001g0298 | 2 | HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2675+5930G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142496745 | ||||||
| chr8:142496797
|
G | T | 1 | a0001c0004t0001g0091 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2675+5982G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142496797 | ||||||
| chr8:142496896
|
C | T | 1 | a0001c0002t0002g0207 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2675+6081C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142496896 | ||||||
| chr8:142496995
|
G | C | 1 | a0001c0013t0003g0049 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2675+6180G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142496995 | ||||||
| chr8:142496999
|
G | A | 1 | a0001c0001t0002g0185 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2675+6184G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142496999 | ||||||
| chr8:142497307
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2675+6492G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142497307 | ||||||
| chr8:142497383
|
G | T | 2 | a0001c0004t0001g0121a0001c0004t0001g0161 | 2 | HG00408.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.2675+6568G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142497383 | ||||||
| chr8:142497384
|
G | T | 3 | a0001c0001t0001g0005a0001c0001t0002g0035a0001c0001t0002g0130 | 4 | HG01257.hp1 HG01993.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.2675+6569G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142497384 | ||||||
| chr8:142497422
|
T | C | 1 | a0004c0012t0001g0108 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2675+6607T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142497422 | ||||||
| chr8:142497519
|
C | T | 6 | a0001c0003t0001g0152a0001c0003t0002g0101a0001c0004t0001g0153others(3): Show | 6 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.2675+6704C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142497519 | ||||||
| chr8:142497520
|
G | A | 5 | a0001c0001t0002g0014a0001c0002t0002g0041a0001c0002t0002g0063others(2): Show | 5 | NA18940.hp1 NA18997.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.2675+6705G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142497520 | ||||||
| chr8:142497893
|
C | T | 6 | a0001c0001t0001g0087a0001c0007t0001g0067a0001c0007t0001g0068others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2675+7078C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142497893 | ||||||
| chr8:142497925
|
C | G | 16 | a0001c0001t0001g0087a0001c0001t0001g0234a0001c0001t0001g0235others(13): Show | 16 | HG01109.hp2 HG01891.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.2675+7110C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142497925 | ||||||
| chr8:142497992
|
A | G | 6 | a0001c0003t0003g0094a0001c0011t0002g0149a0001c0017t0001g0008others(3): Show | 6 | HG01255.hp1 HG02300.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2675+7177A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142497992 | ||||||
| chr8:142498039
|
T | C | 5 | a0001c0001t0001g0077a0001c0001t0002g0127a0001c0002t0002g0126others(2): Show | 5 | HG01071.hp1 HG01928.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.2675+7224T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142498039 | ||||||
| chr8:142498058
|
C | T | 5 | a0001c0001t0001g0087a0001c0007t0001g0067a0001c0007t0001g0068others(2): Show | 5 | HG01891.hp1 HG02630.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2675+7243C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142498058 | ||||||
| chr8:142498107
|
G | A | 1 | a0001c0015t0001g0024 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2675+7292G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142498107 | ||||||
| chr8:142498167
|
G | A | 2 | a0001c0011t0003g0072a0001c0034t0002g0071 | 2 | HG01192.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2675+7352G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142498167 | ||||||
| chr8:142498209
|
T | C | 3 | a0001c0001t0013g0051a0001c0003t0002g0050a0001c0008t0001g0297 | 3 | HG02055.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2675+7394T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142498209 | ||||||
| chr8:142498232
|
A | G | 3 | a0001c0001t0002g0074a0001c0001t0014g0155a0001c0006t0002g0303 | 3 | HG02647.hp2 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2675+7417A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142498232 | ||||||
| chr8:142498576
|
TCA | T | 9 | a0001c0001t0001g0087a0001c0001t0013g0051a0001c0003t0002g0050others(6): Show | 9 | HG01891.hp1 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2675+7762_2675+776 others(6): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142498576 | ||||||
| chr8:142498639
|
C | A | 3 | a0001c0001t0002g0074a0001c0001t0014g0155a0001c0006t0002g0303 | 3 | HG02647.hp2 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2675+7824C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142498639 | ||||||
| chr8:142498662
|
C | T | 7 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(4): Show | 7 | HG01109.hp2 HG02615.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2675+7847C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142498662 | ||||||
| chr8:142498716
|
C | G | 1 | a0001c0001t0001g0229 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2675+7901C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142498716 | ||||||
| chr8:142498891
|
C | T | 1 | a0001c0003t0003g0137 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2675+8076C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142498891 | ||||||
| chr8:142498920
|
A | G | 9 | a0001c0001t0001g0087a0001c0001t0013g0051a0001c0003t0002g0050others(6): Show | 9 | HG01891.hp1 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2675+8105A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142498920 | ||||||
| chr8:142498928
|
G | A | 177 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(174): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.2675+8113G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142498928 | ||||||
| chr8:142498929
|
C | T | 5 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(2): Show | 5 | HG01109.hp2 HG02886.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2675+8114C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142498929 | ||||||
| chr8:142498933
|
T | C | 9 | a0001c0001t0001g0087a0001c0001t0013g0051a0001c0003t0002g0050others(6): Show | 9 | HG01891.hp1 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2675+8118T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142498933 | ||||||
| chr8:142499139
|
C | T | 2 | a0001c0011t0003g0072a0001c0034t0002g0071 | 2 | HG01192.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2675+8324C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142499139 | ||||||
| chr8:142499191
|
T | A | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2675+8376T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142499191 | ||||||
| chr8:142499207
|
T | C | 14 | a0001c0001t0001g0087a0001c0001t0002g0074a0001c0001t0013g0051others(11): Show | 14 | HG01192.hp2 HG01891.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2675+8392T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142499207 | ||||||
| chr8:142499314
|
T | C | 3 | a0001c0001t0002g0074a0001c0001t0014g0155a0001c0006t0002g0303 | 3 | HG02647.hp2 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2675+8499T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142499314 | ||||||
| chr8:142499427
|
C | T | 4 | a0001c0001t0001g0119a0001c0002t0002g0115a0001c0002t0002g0116others(1): Show | 4 | HG00597.hp2 NA18952.hp2 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.2675+8612C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142499427 | ||||||
| chr8:142499437
|
C | T | 1 | a0001c0006t0004g0243 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2675+8622C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142499437 | ||||||
| chr8:142499438
|
G | A | 5 | a0001c0001t0001g0087a0001c0007t0001g0067a0001c0007t0001g0068others(2): Show | 5 | HG01891.hp1 HG02630.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2675+8623G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142499438 | ||||||
| chr8:142499452
|
C | T | 3 | a0001c0001t0002g0074a0001c0001t0014g0155a0001c0006t0002g0303 | 3 | HG02647.hp2 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2675+8637C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142499452 | ||||||
| chr8:142499460
|
C | CGCGTGCT others(5): Show |
7 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(4): Show | 7 | HG01109.hp2 HG02615.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2675+8646_2675+865 others(16): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142499460 | |||||
| chr8:142499500
|
C | T | 1 | a0001c0018t0003g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2675+8685C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142499500 | ||||||
| chr8:142499525
|
C | T | 174 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(171): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.2675+8710C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142499525 | ||||||
| chr8:142499566
|
C | T | 3 | a0001c0014t0002g0082a0001c0014t0002g0083a0001c0035t0001g0084 | 3 | HG01975.hp2 HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2675+8751C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142499566 | ||||||
| chr8:142499593
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2675+8778C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142499593 | ||||||
| chr8:142499594
|
GCGGTGGG others(8): Show |
G | 2 | a0001c0008t0003g0013a0001c0036t0002g0012 | 2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2675+8781_2675+879 others(19): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142499594 | |||||
| chr8:142499644
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2675+8829G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142499644 | ||||||
| chr8:142499710
|
G | A | 2 | a0001c0006t0001g0288a0001c0006t0001g0289 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2675+8895G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142499710 | ||||||
| chr8:142499720
|
AGCAGACA others(67): Show |
A | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2675+8906_2675+897 others(78): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142499720 | ||||||
| chr8:142499787
|
G | A | 4 | a0001c0004t0015g0011a0001c0008t0002g0232a0001c0008t0003g0013others(1): Show | 4 | HG02717.hp2 HG02818.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2675+8972G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142499787 | ||||||
| chr8:142499799
|
G | A | 3 | a0001c0001t0013g0051a0001c0003t0002g0050a0001c0008t0001g0297 | 3 | HG02055.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2675+8984G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142499799 | ||||||
| chr8:142499824
|
C | T | 7 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(4): Show | 7 | HG01109.hp2 HG02615.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2675+9009C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142499824 | ||||||
| chr8:142499921
|
G | GT | 302 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.2675+9108dupT | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142499921 | |||||
| chr8:142499924
|
G | T | 1 | a0001c0001t0001g0183 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2675+9109G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142499924 | ||||||
| chr8:142499927
|
C | G | 4 | a0001c0001t0001g0034a0001c0001t0001g0183a0001c0001t0002g0043others(1): Show | 4 | HG03490.hp2 NA18983.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.2675+9112C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142499927 | ||||||
| chr8:142499957
|
C | G | 4 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(1): Show | 4 | HG01109.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2675+9142C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142499957 | ||||||
| chr8:142499960
|
T | C | 303 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2675+9145T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142499960 | ||||||
| chr8:142499978
|
G | GC | 303 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2675+9166dupC | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142499978 | |||||
| chr8:142499982
|
T | TGGCAGCC others(16): Show |
1 | a0001c0002t0001g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2675+9169_2675+919 others(27): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142499982 | |||||
| chr8:142500007
|
T | G | 303 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2675+9192T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500007 | ||||||
| chr8:142500101
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2675+9286C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500101 | ||||||
| chr8:142500145
|
C | T | 2 | a0001c0011t0003g0072a0001c0034t0002g0071 | 2 | HG01192.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2675+9330C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500145 | ||||||
| chr8:142500149
|
G | A | 5 | a0001c0001t0001g0087a0001c0007t0001g0067a0001c0007t0001g0068others(2): Show | 5 | HG01891.hp1 HG02630.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2675+9334G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500149 | ||||||
| chr8:142500188
|
G | GC | 5 | a0001c0001t0001g0183a0001c0002t0002g0115a0001c0003t0003g0094others(2): Show | 5 | HG00597.hp2 HG01255.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.2675+9378dupC | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500188 | |||||
| chr8:142500214
|
T | TTCCCCCC others(16): Show |
1 | a0001c0024t0001g0085 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2675+9405_2675+942 others(27): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500214 | |||||
| chr8:142500215
|
T | TCCCCCCG others(408): Show |
1 | a0001c0002t0002g0262 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2675+9442_2675+944 others(419): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500215 | |||||
| chr8:142500220
|
C | CCGCGCCG others(16): Show |
25 | a0001c0001t0001g0220a0001c0001t0001g0234a0001c0001t0001g0235others(22): Show | 25 | HG00438.hp2 HG00733.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2675+9489_2675+951 others(27): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500220 | |||||
| chr8:142500220
|
C | CCGCGCCG others(39): Show |
3 | a0001c0001t0001g0087a0001c0001t0001g0280a0001c0001t0002g0081 | 3 | HG02976.hp1 HG03540.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.2675+9466_2675+951 others(50): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500220 | |||||
| chr8:142500220
|
C | CCGCGCCG others(62): Show |
7 | a0001c0003t0001g0152a0001c0004t0001g0153a0001c0004t0001g0154others(4): Show | 7 | HG01891.hp1 HG02109.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.2675+9443_2675+951 others(73): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500220 | |||||
| chr8:142500220
|
C | CCGCGCCG others(246): Show |
1 | a0001c0007t0001g0133 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2675+9511_2675+951 others(257): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500220 | |||||
| chr8:142500220
|
CCGCGCCG others(16): Show |
C | 53 | a0001c0001t0001g0031a0001c0001t0001g0059a0001c0001t0001g0104others(50): Show | 53 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.2675+9489_2675+951 others(27): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500220 | |||||
| chr8:142500220
|
CCGCGCCG others(39): Show |
C | 71 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(68): Show | 74 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.2675+9466_2675+951 others(50): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500220 | |||||
| chr8:142500220
|
CCGCGCCG others(62): Show |
C | 3 | a0001c0001t0001g0025a0001c0001t0001g0034a0001c0030t0001g0263 | 3 | NA19054.hp1 NA19065.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2675+9443_2675+951 others(73): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500220 | |||||
| chr8:142500221
|
CGCGCCGC others(84): Show |
C | 1 | a0005c0021t0002g0102 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2675+9407_2675+949 others(95): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500221 | ||||||
| chr8:142500222
|
G | GCGCCGCT others(62): Show |
2 | a0001c0001t0002g0193a0001c0002t0001g0192 | 2 | NA18612.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.2675+9465_2675+946 others(73): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500222 | |||||
| chr8:142500227
|
G | A | 1 | a0001c0001t0002g0048 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2675+9412G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500227 | ||||||
| chr8:142500227
|
GCTCCTCC others(169): Show |
G | 1 | a0001c0001t0014g0155 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2675+9415_2675+959 others(4): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500227 | |||||
| chr8:142500228
|
C | CTCCTCCA others(16): Show |
11 | a0001c0001t0001g0216a0001c0001t0001g0229a0001c0001t0001g0257others(8): Show | 11 | HG00673.hp2 HG01167.hp2 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.2675+9435_2675+943 others(27): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500228 | |||||
| chr8:142500243
|
A | C | 1 | a0001c0001t0001g0252 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2675+9428A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500243 | ||||||
| chr8:142500245
|
G | GCGCCGCT others(199): Show |
9 | a0001c0003t0003g0026a0001c0006t0001g0288a0001c0006t0001g0289others(6): Show | 9 | HG02572.hp1 HG02622.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2675+9465_2675+946 others(210): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500245 | |||||
| chr8:142500247
|
G | C | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2675+9432G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500247 | ||||||
| chr8:142500251
|
C | G | 3 | a0001c0001t0001g0040a0001c0001t0001g0219a0001c0001t0001g0221 | 3 | HG00140.hp2 HG01261.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.2675+9436C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500251 | ||||||
| chr8:142500260
|
C | T | 4 | a0001c0003t0003g0094a0001c0017t0001g0008a0001c0018t0003g0007others(1): Show | 4 | HG01255.hp1 HG02451.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.2675+9445C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500260 | ||||||
| chr8:142500261
|
TCCCCACG others(62): Show |
T | 1 | a0001c0001t0002g0264 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2675+9451_2675+951 others(73): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500261 | |||||
| chr8:142500266
|
A | ACGCGCCG others(16): Show |
3 | a0001c0001t0001g0247a0001c0004t0001g0249a0001c0004t0003g0250 | 3 | HG03041.hp2 NA18962.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2675+9465_2675+946 others(27): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500266 | |||||
| chr8:142500266
|
A | ACGCGCCG others(61): Show |
12 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0003g0004others(9): Show | 15 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.2675+9465_2675+946 others(72): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500266 | |||||
| chr8:142500266
|
A | C | 5 | a0001c0001t0001g0252a0001c0003t0003g0094a0001c0017t0001g0008others(2): Show | 5 | HG01255.hp1 HG02451.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.2675+9451A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500266 | ||||||
| chr8:142500266
|
ACGCGCCG others(62): Show |
A | 12 | a0001c0001t0001g0075a0001c0001t0001g0164a0001c0001t0002g0014others(9): Show | 12 | HG00099.hp2 HG02647.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.2675+9466_2675+953 others(73): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500266 | |||||
| chr8:142500268
|
G | GCGCCGCT others(131): Show |
1 | a0001c0002t0002g0116 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2675+9465_2675+946 others(142): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500268 | |||||
| chr8:142500268
|
G | GCGCCGCT others(176): Show |
1 | a0001c0001t0003g0089 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2675+9465_2675+946 others(187): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500268 | |||||
| chr8:142500274
|
C | CTCCTCCC others(210): Show |
1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2675+9465_2675+946 others(221): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500274 | |||||
| chr8:142500274
|
C | CTCCTCCC others(522): Show |
2 | a0002c0005t0002g0099a0002c0005t0005g0245 | 2 | NA19011.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.2675+9465_2675+946 others(533): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500274 | |||||
| chr8:142500279
|
CCACCTCC others(38): Show |
C | 2 | a0001c0001t0001g0151a0001c0026t0001g0201 | 2 | HG00738.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.2675+9466_2675+951 others(49): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500279 | |||||
| chr8:142500281
|
A | C | 22 | a0001c0001t0001g0148a0001c0001t0001g0178a0001c0001t0001g0246others(19): Show | 22 | HG00423.hp2 HG00735.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.2675+9466A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500281 | ||||||
| chr8:142500281
|
ACCTCCCC others(39): Show |
A | 1 | a0001c0002t0001g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2675+9469_2675+951 others(50): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500281 | |||||
| chr8:142500283
|
C | CGCCCCCC others(62): Show |
1 | a0002c0005t0001g0022 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2675+9468_2675+946 others(73): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500283 | ||||||
| chr8:142500284
|
T | G | 22 | a0001c0001t0001g0148a0001c0001t0001g0178a0001c0001t0001g0246others(19): Show | 22 | HG00423.hp2 HG00735.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.2675+9469T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500284 | ||||||
| chr8:142500286
|
CCCACGCG others(14): Show |
C | 5 | a0001c0001t0001g0148a0001c0001t0002g0197a0001c0002t0002g0098others(2): Show | 5 | HG01192.hp2 HG03017.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.2675+9474_2675+949 others(25): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500286 | |||||
| chr8:142500289
|
A | ACGCGCCG others(62): Show |
2 | a0001c0001t0013g0051a0001c0003t0002g0050 | 2 | HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2675+9488_2675+948 others(73): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500289 | |||||
| chr8:142500289
|
A | C | 18 | a0001c0001t0001g0029a0001c0001t0001g0178a0001c0001t0001g0246others(15): Show | 18 | HG00423.hp2 HG00735.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.2675+9474A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500289 | ||||||
| chr8:142500289
|
ACGCGCCG others(39): Show |
A | 4 | a0001c0001t0001g0077a0001c0001t0001g0219a0001c0001t0002g0074others(1): Show | 4 | HG01071.hp1 HG01261.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2675+9489_2675+953 others(50): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500289 | |||||
| chr8:142500291
|
G | A | 2 | a0001c0001t0001g0178a0001c0017t0001g0010 | 2 | HG01261.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2675+9476G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500291 | ||||||
| chr8:142500302
|
CCACCTCC others(61): Show |
C | 1 | a0001c0001t0001g0178 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2675+9489_2675+955 others(72): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500302 | |||||
| chr8:142500304
|
A | C | 61 | a0001c0001t0001g0031a0001c0001t0001g0059a0001c0001t0001g0104others(58): Show | 61 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.2675+9489A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500304 | ||||||
| chr8:142500306
|
C | CGCCCCCC others(39): Show |
1 | a0001c0004t0001g0038 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2675+9491_2675+949 others(50): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500306 | ||||||
| chr8:142500307
|
T | G | 61 | a0001c0001t0001g0031a0001c0001t0001g0059a0001c0001t0001g0104others(58): Show | 61 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.2675+9492T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500307 | ||||||
| chr8:142500312
|
A | ACGCGCCG others(62): Show |
2 | a0001c0001t0003g0242a0001c0003t0001g0241 | 2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2675+9511_2675+951 others(73): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500312 | |||||
| chr8:142500312
|
A | ACGCGCCG others(62): Show |
4 | a0001c0001t0001g0095a0001c0001t0003g0086a0001c0006t0004g0243others(1): Show | 4 | HG02280.hp1 HG02451.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2675+9511_2675+951 others(73): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500312 | |||||
| chr8:142500312
|
A | ACGCGCCG others(292): Show |
1 | a0001c0003t0001g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2675+9511_2675+951 others(303): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500312 | |||||
| chr8:142500312
|
A | ACGCGCCG others(39): Show |
5 | a0001c0001t0001g0139a0001c0001t0001g0215a0001c0001t0001g0223others(2): Show | 5 | HG00733.hp1 HG01243.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.2675+9511_2675+951 others(50): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500312 | |||||
| chr8:142500312
|
A | ACGCGCCG others(16): Show |
4 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0002g0060others(1): Show | 4 | HG00741.hp1 HG01070.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2675+9527_2675+954 others(27): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500312 | |||||
| chr8:142500312
|
A | C | 64 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0059others(61): Show | 64 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.2675+9497A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500312 | ||||||
| chr8:142500312
|
ACG | A | 5 | a0001c0001t0001g0148a0001c0001t0002g0197a0001c0002t0002g0098others(2): Show | 5 | HG01192.hp2 HG03017.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.2675+9501_2675+950 others(6): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500312 | |||||
| chr8:142500314
|
G | A | 2 | a0001c0001t0001g0284a0001c0017t0001g0010 | 2 | HG02165.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2675+9499G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500314 | ||||||
| chr8:142500314
|
G | GCGCCGCT others(39): Show |
1 | a0001c0001t0001g0221 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2675+9511_2675+951 others(50): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500314 | |||||
| chr8:142500314
|
GCGCCGCT others(87): Show |
G | 5 | a0001c0001t0001g0258a0001c0001t0002g0078a0001c0002t0001g0047others(2): Show | 5 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.2675+9501_2675+959 others(98): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500314 | |||||
| chr8:142500327
|
C | A | 33 | a0001c0001t0001g0087a0001c0001t0001g0095a0001c0001t0001g0293others(30): Show | 36 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(33): Show |
intron_variant | MODIFIER | c.2675+9512C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500327 | ||||||
| chr8:142500329
|
C | A | 1 | a0001c0026t0001g0201 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2675+9514C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500329 | ||||||
| chr8:142500329
|
C | G | 1 | a0001c0001t0001g0151 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2675+9514C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500329 | ||||||
| chr8:142500330
|
G | C | 2 | a0001c0001t0001g0151a0001c0026t0001g0201 | 2 | HG00738.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.2675+9515G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500330 | ||||||
| chr8:142500330
|
G | T | 33 | a0001c0001t0001g0087a0001c0001t0001g0095a0001c0001t0001g0293others(30): Show | 36 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(33): Show |
intron_variant | MODIFIER | c.2675+9515G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500330 | ||||||
| chr8:142500335
|
C | A | 27 | a0001c0001t0001g0087a0001c0001t0001g0293a0001c0001t0001g0294others(24): Show | 30 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.2675+9520C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500335 | ||||||
| chr8:142500337
|
G | A | 83 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0058others(80): Show | 86 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.2675+9522G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500337 | ||||||
| chr8:142500342
|
G | T | 1 | a0001c0001t0001g0284 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2675+9527G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500342 | ||||||
| chr8:142500343
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2675+9528C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500343 | ||||||
| chr8:142500343
|
CTCCTCCC others(16): Show |
C | 3 | a0001c0001t0001g0029a0001c0001t0001g0132a0001c0003t0003g0131 | 3 | HG02280.hp2 HG03453.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.2675+9537_2675+955 others(27): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500343 | |||||
| chr8:142500352
|
C | T | 7 | a0001c0001t0001g0079a0001c0001t0001g0278a0001c0001t0001g0284others(4): Show | 7 | HG00423.hp2 HG02055.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.2675+9537C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500352 | ||||||
| chr8:142500353
|
G | A | 1 | a0001c0001t0002g0054 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2675+9538G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500353 | ||||||
| chr8:142500353
|
G | C | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2675+9538G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500353 | ||||||
| chr8:142500353
|
G | GC | 8 | a0001c0001t0001g0142a0001c0001t0001g0146a0001c0001t0001g0151others(5): Show | 8 | HG00738.hp1 HG00738.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.2675+9544dupC | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500353 | |||||
| chr8:142500353
|
G | GCCCCCCG others(109): Show |
1 | a0001c0008t0001g0297 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2675+9549_2675+955 others(120): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500353 | |||||
| chr8:142500354
|
CCCCCCGC others(15): Show |
C | 1 | a0001c0003t0002g0101 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2675+9545_2675+956 others(26): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500354 | |||||
| chr8:142500360
|
G | A | 92 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0058others(89): Show | 95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.2675+9545G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500360 | ||||||
| chr8:142500362
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2675+9547G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500362 | ||||||
| chr8:142500365
|
T | G | 192 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0025others(189): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.2675+9550T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500365 | ||||||
| chr8:142500366
|
T | C | 192 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0025others(189): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.2675+9551T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500366 | ||||||
| chr8:142500366
|
T | TTCCTCCC others(454): Show |
1 | a0001c0001t0005g0105 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2675+9559_2675+956 others(465): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500366 | |||||
| chr8:142500366
|
TTCCTCCC others(16): Show |
T | 5 | a0001c0003t0003g0094a0001c0017t0001g0008a0001c0018t0003g0007others(2): Show | 5 | HG01255.hp1 HG02132.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.2675+9560_2675+958 others(27): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500366 | |||||
| chr8:142500373
|
C | A | 4 | a0001c0003t0001g0152a0001c0004t0001g0153a0001c0004t0001g0154others(1): Show | 4 | HG02109.hp1 HG02559.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2675+9558C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500373 | ||||||
| chr8:142500374
|
CTG | C | 4 | a0001c0003t0001g0152a0001c0004t0001g0153a0001c0004t0001g0154others(1): Show | 4 | HG02109.hp1 HG02559.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2675+9560_2675+956 others(6): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500374 | ||||||
| chr8:142500375
|
T | C | 20 | a0001c0001t0001g0079a0001c0001t0001g0087a0001c0001t0001g0120others(17): Show | 22 | HG00280.hp2 HG01074.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.2675+9560T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500375 | ||||||
| chr8:142500375
|
T | G | 1 | a0001c0001t0001g0178 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2675+9560T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500375 | ||||||
| chr8:142500375
|
T | TGCCCCCC others(85): Show |
9 | a0001c0001t0003g0004a0001c0003t0001g0055a0001c0003t0001g0073others(6): Show | 10 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2675+9567_2675+956 others(96): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500375 | |||||
| chr8:142500376
|
G | C | 1 | a0001c0001t0001g0178 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2675+9561G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500376 | ||||||
| chr8:142500378
|
C | T | 4 | a0001c0003t0001g0152a0001c0004t0001g0153a0001c0004t0001g0154others(1): Show | 4 | HG02109.hp1 HG02559.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2675+9563C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500378 | ||||||
| chr8:142500381
|
C | G | 5 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(2): Show | 5 | HG01109.hp2 HG02886.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2675+9566C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500381 | ||||||
| chr8:142500382
|
C | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0278 | 2 | HG02055.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2675+9567C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500382 | ||||||
| chr8:142500382
|
CGCGCCGC others(16): Show |
C | 1 | a0001c0015t0004g0282 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2675+9568_2675+959 others(27): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500382 | ||||||
| chr8:142500383
|
G | A | 215 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0025others(212): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.2675+9568G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500383 | ||||||
| chr8:142500383
|
G | GCGCCGCT others(39): Show |
1 | a0001c0001t0001g0246 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2675+9589_2675+959 others(50): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500383 | |||||
| chr8:142500385
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0278 | 2 | HG02055.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2675+9570G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500385 | ||||||
| chr8:142500388
|
G | T | 8 | a0001c0001t0001g0087a0001c0001t0001g0293a0001c0001t0001g0294others(5): Show | 10 | HG01891.hp1 HG02257.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.2675+9573G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500388 | ||||||
| chr8:142500389
|
C | T | 8 | a0001c0001t0001g0087a0001c0001t0001g0293a0001c0001t0001g0294others(5): Show | 10 | HG01891.hp1 HG02257.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.2675+9574C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500389 | ||||||
| chr8:142500396
|
C | A | 3 | a0001c0014t0002g0082a0001c0014t0002g0083a0001c0035t0001g0084 | 3 | HG01975.hp2 HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2675+9581C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500396 | ||||||
| chr8:142500398
|
C | CGCCCCCC others(16): Show |
9 | a0001c0001t0003g0004a0001c0003t0001g0055a0001c0003t0001g0073others(6): Show | 10 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2675+9589_2675+959 others(27): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142500398 | |||||
| chr8:142500398
|
C | T | 7 | a0001c0001t0001g0087a0001c0001t0001g0293a0001c0001t0001g0294others(4): Show | 9 | HG01891.hp1 HG02257.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2675+9583C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500398 | ||||||
| chr8:142500399
|
G | A | 3 | a0001c0014t0002g0082a0001c0014t0002g0083a0001c0035t0001g0084 | 3 | HG01975.hp2 HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2675+9584G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500399 | ||||||
| chr8:142500405
|
T | C | 16 | a0001c0001t0001g0087a0001c0001t0001g0293a0001c0001t0001g0294others(13): Show | 19 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.2675+9590T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500405 | ||||||
| chr8:142500408
|
A | G | 17 | a0001c0001t0001g0087a0001c0001t0001g0293a0001c0001t0001g0294others(14): Show | 20 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.2675+9593A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500408 | ||||||
| chr8:142500419
|
A | C | 4 | a0001c0001t0001g0087a0001c0007t0001g0067a0001c0007t0001g0068others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2675+9604A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500419 | ||||||
| chr8:142500422
|
A | C | 1 | a0001c0007t0007g0240 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2675+9607A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500422 | ||||||
| chr8:142500422
|
A | G | 4 | a0001c0001t0001g0087a0001c0007t0001g0067a0001c0007t0001g0068others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2675+9607A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500422 | ||||||
| chr8:142500428
|
C | T | 4 | a0001c0001t0001g0087a0001c0007t0001g0067a0001c0007t0001g0068others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2675+9613C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500428 | ||||||
| chr8:142500429
|
C | A | 4 | a0001c0001t0001g0087a0001c0007t0001g0067a0001c0007t0001g0068others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2675+9614C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500429 | ||||||
| chr8:142500430
|
A | C | 4 | a0001c0001t0001g0087a0001c0007t0001g0067a0001c0007t0001g0068others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2675+9615A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500430 | ||||||
| chr8:142500431
|
T | A | 4 | a0001c0001t0001g0087a0001c0007t0001g0067a0001c0007t0001g0068others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2675+9616T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500431 | ||||||
| chr8:142500432
|
G | C | 4 | a0001c0001t0001g0087a0001c0007t0001g0067a0001c0007t0001g0068others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2675+9617G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500432 | ||||||
| chr8:142500434
|
C | G | 4 | a0001c0001t0001g0087a0001c0007t0001g0067a0001c0007t0001g0068others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2675+9619C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500434 | ||||||
| chr8:142500904
|
T | C | 2 | a0001c0001t0001g0258a0001c0002t0001g0047 | 2 | HG01361.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.2676-10028T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142500904 | ||||||
| chr8:142501235
|
G | A | 3 | a0001c0001t0001g0075a0001c0013t0001g0096a0001c0015t0004g0282 | 3 | HG02647.hp1 HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2676-9697G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501235 | ||||||
| chr8:142501238
|
A | G | 3 | a0001c0001t0001g0075a0001c0013t0001g0096a0001c0015t0004g0282 | 3 | HG02647.hp1 HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2676-9694A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501238 | ||||||
| chr8:142501391
|
TGATGGAG others(56): Show |
T | 11 | a0001c0001t0001g0087a0001c0001t0001g0277a0001c0001t0002g0074others(8): Show | 11 | HG00673.hp2 HG01891.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.2676-9450_2676-938 others(67): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142501391 | |||||
| chr8:142501454
|
C | T | 1 | a0008c0031t0002g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2676-9478C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501454 | ||||||
| chr8:142501482
|
A | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9450A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501482 | ||||||
| chr8:142501483
|
T | TGAGGGTG others(40): Show |
9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9448_2676-944 others(51): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142501483 | |||||
| chr8:142501502
|
T | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9430T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501502 | ||||||
| chr8:142501503
|
T | C | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9429T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501503 | ||||||
| chr8:142501503
|
T | TTGTGTGG others(163): Show |
1 | a0001c0002t0002g0172 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2676-9388_2676-938 others(174): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142501503 | |||||
| chr8:142501503
|
T | TTGTGTGG others(100): Show |
10 | a0001c0001t0001g0095a0001c0001t0001g0156a0001c0001t0003g0086others(7): Show | 10 | HG02258.hp1 HG02273.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2676-9387_2676-928 others(111): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142501503 | |||||
| chr8:142501517
|
C | T | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9415C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501517 | ||||||
| chr8:142501527
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9405G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501527 | ||||||
| chr8:142501544
|
G | GAT | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9388_2676-938 others(6): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501544 | ||||||
| chr8:142501546
|
T | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9386T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501546 | ||||||
| chr8:142501549
|
T | TG | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9382dupG | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142501549 | |||||
| chr8:142501551
|
T | G | 1 | a0008c0031t0002g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2676-9381T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501551 | ||||||
| chr8:142501552
|
G | GATAGTGA others(22): Show |
9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9380_2676-937 others(33): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501552 | ||||||
| chr8:142501561
|
G | A | 1 | a0008c0031t0002g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2676-9371G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501561 | ||||||
| chr8:142501568
|
G | T | 1 | a0008c0031t0002g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2676-9364G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501568 | ||||||
| chr8:142501570
|
G | T | 1 | a0008c0031t0002g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2676-9362G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501570 | ||||||
| chr8:142501573
|
G | C | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9359G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501573 | ||||||
| chr8:142501575
|
C | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9357C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501575 | ||||||
| chr8:142501575
|
C | T | 1 | a0008c0031t0002g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2676-9357C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501575 | ||||||
| chr8:142501579
|
G | T | 1 | a0008c0031t0002g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2676-9353G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501579 | ||||||
| chr8:142501580
|
A | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9352A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501580 | ||||||
| chr8:142501580
|
A | T | 1 | a0008c0031t0002g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2676-9352A>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501580 | ||||||
| chr8:142501581
|
T | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9351T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501581 | ||||||
| chr8:142501583
|
G | A | 1 | a0008c0031t0002g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2676-9349G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501583 | ||||||
| chr8:142501584
|
C | T | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9348C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501584 | ||||||
| chr8:142501589
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9343G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501589 | ||||||
| chr8:142501596
|
G | T | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9336G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501596 | ||||||
| chr8:142501602
|
A | G | 1 | a0008c0031t0002g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2676-9330A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501602 | ||||||
| chr8:142501605
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9327G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501605 | ||||||
| chr8:142501609
|
A | G | 10 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(7): Show | 10 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.2676-9323A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501609 | ||||||
| chr8:142501610
|
C | T | 10 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(7): Show | 10 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.2676-9322C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501610 | ||||||
| chr8:142501611
|
T | G | 1 | a0008c0031t0002g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2676-9321T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501611 | ||||||
| chr8:142501612
|
G | A | 1 | a0008c0031t0002g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2676-9320G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501612 | ||||||
| chr8:142501613
|
T | C | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9319T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501613 | ||||||
| chr8:142501617
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9315G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501617 | ||||||
| chr8:142501619
|
T | G | 1 | a0008c0031t0002g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2676-9313T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501619 | ||||||
| chr8:142501620
|
T | G | 1 | a0008c0031t0002g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2676-9312T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501620 | ||||||
| chr8:142501623
|
A | G | 1 | a0008c0031t0002g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2676-9309A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501623 | ||||||
| chr8:142501624
|
C | T | 10 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(7): Show | 10 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.2676-9308C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501624 | ||||||
| chr8:142501626
|
A | G | 1 | a0008c0031t0002g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2676-9306A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501626 | ||||||
| chr8:142501627
|
T | C | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9305T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501627 | ||||||
| chr8:142501629
|
G | A | 1 | a0008c0031t0002g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2676-9303G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501629 | ||||||
| chr8:142501630
|
A | T | 1 | a0008c0031t0002g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2676-9302A>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501630 | ||||||
| chr8:142501632
|
G | A | 1 | a0001c0003t0001g0055 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2676-9300G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501632 | ||||||
| chr8:142501632
|
G | GTGAGGTG others(13): Show |
9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9298_2676-929 others(24): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142501632 | |||||
| chr8:142501636
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9296G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501636 | ||||||
| chr8:142501638
|
T | C | 1 | a0008c0031t0002g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2676-9294T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501638 | ||||||
| chr8:142501643
|
G | A | 1 | a0008c0031t0002g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2676-9289G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501643 | ||||||
| chr8:142501647
|
T | C | 1 | a0008c0031t0002g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2676-9285T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501647 | ||||||
| chr8:142501647
|
T | TGATGGTG others(37): Show |
11 | a0001c0001t0001g0104a0001c0001t0001g0109a0001c0001t0001g0110others(8): Show | 11 | HG00639.hp2 HG01074.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.2676-9281_2676-928 others(48): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142501647 | |||||
| chr8:142501650
|
TGATGGGG others(62): Show |
T | 1 | a0001c0008t0002g0062 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2676-9280_2676-921 others(73): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142501650 | |||||
| chr8:142501652
|
A | G | 168 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(165): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.2676-9280A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501652 | ||||||
| chr8:142501655
|
G | A | 156 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(153): Show | 159 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.2676-9277G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501655 | ||||||
| chr8:142501656
|
G | T | 156 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(153): Show | 159 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.2676-9276G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501656 | ||||||
| chr8:142501659
|
GGTGGTAG others(59): Show |
G | 156 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(153): Show | 159 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.2676-9267_2676-920 others(70): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142501659 | |||||
| chr8:142501668
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9264G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501668 | ||||||
| chr8:142501670
|
T | A | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | HG00741.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.2676-9262T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501670 | ||||||
| chr8:142501672
|
T | A | 12 | a0001c0001t0001g0104a0001c0001t0001g0109a0001c0001t0001g0110others(9): Show | 12 | HG00639.hp2 HG01074.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.2676-9260T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501672 | ||||||
| chr8:142501672
|
T | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9260T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501672 | ||||||
| chr8:142501673
|
T | C | 12 | a0001c0001t0001g0104a0001c0001t0001g0109a0001c0001t0001g0110others(9): Show | 12 | HG00639.hp2 HG01074.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.2676-9259T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501673 | ||||||
| chr8:142501676
|
T | C | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9256T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501676 | ||||||
| chr8:142501687
|
C | T | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9245C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501687 | ||||||
| chr8:142501692
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9240G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501692 | ||||||
| chr8:142501693
|
A | C | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9239A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501693 | ||||||
| chr8:142501694
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9238G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501694 | ||||||
| chr8:142501696
|
TGG | T | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9233_2676-923 others(6): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142501696 | |||||
| chr8:142501701
|
T | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9231T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501701 | ||||||
| chr8:142501712
|
A | ATGGTGAT others(201): Show |
2 | a0001c0001t0001g0156a0001c0002t0002g0172 | 2 | HG00609.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.2676-9214_2676-921 others(212): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142501712 | |||||
| chr8:142501712
|
A | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9220A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501712 | ||||||
| chr8:142501718
|
AGGG | A | 12 | a0001c0001t0001g0104a0001c0001t0001g0109a0001c0001t0001g0110others(9): Show | 12 | HG00639.hp2 HG01074.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.2676-9213_2676-921 others(7): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501718 | ||||||
| chr8:142501719
|
G | T | 11 | a0001c0001t0001g0132a0001c0001t0001g0156a0001c0001t0002g0081others(8): Show | 11 | HG00609.hp2 HG02083.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.2676-9213G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501719 | ||||||
| chr8:142501720
|
G | A | 3 | a0001c0001t0013g0051a0001c0003t0002g0050a0001c0008t0001g0297 | 3 | HG02055.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2676-9212G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501720 | ||||||
| chr8:142501724
|
A | T | 12 | a0001c0001t0001g0104a0001c0001t0001g0109a0001c0001t0001g0110others(9): Show | 12 | HG00639.hp2 HG01074.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.2676-9208A>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501724 | ||||||
| chr8:142501725
|
T | G | 12 | a0001c0001t0001g0104a0001c0001t0001g0109a0001c0001t0001g0110others(9): Show | 12 | HG00639.hp2 HG01074.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.2676-9207T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501725 | ||||||
| chr8:142501725
|
T | TA | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9207_2676-920 others(5): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501725 | ||||||
| chr8:142501725
|
T | TGTG | 26 | a0001c0001t0001g0087a0001c0001t0001g0156a0001c0001t0001g0234others(23): Show | 26 | HG01109.hp2 HG01192.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.2676-9197_2676-919 others(7): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142501725 | |||||
| chr8:142501728
|
GGTGGTGG others(163): Show |
G | 2 | a0001c0001t0001g0079a0001c0003t0001g0080 | 2 | HG00099.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2676-9174_2676-900 others(4): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142501728 | |||||
| chr8:142501732
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9200G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501732 | ||||||
| chr8:142501733
|
T | TGGTGGTG others(11): Show |
1 | a0001c0002t0002g0172 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2676-9195_2676-919 others(22): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142501733 | |||||
| chr8:142501738
|
A | G | 1 | a0001c0008t0002g0062 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2676-9194A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501738 | ||||||
| chr8:142501748
|
C | T | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9184C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501748 | ||||||
| chr8:142501750
|
G | C | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9182G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501750 | ||||||
| chr8:142501753
|
A | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9179A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501753 | ||||||
| chr8:142501757
|
C | T | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9175C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501757 | ||||||
| chr8:142501758
|
A | G | 180 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(177): Show | 183 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.2676-9174A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501758 | ||||||
| chr8:142501762
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9170G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501762 | ||||||
| chr8:142501771
|
T | C | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9161T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501771 | ||||||
| chr8:142501775
|
AGGG | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9156_2676-915 others(7): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501775 | ||||||
| chr8:142501777
|
G | T | 171 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(168): Show | 174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.2676-9155G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501777 | ||||||
| chr8:142501782
|
G | A | 180 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(177): Show | 183 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.2676-9150G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501782 | ||||||
| chr8:142501783
|
C | T | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9149C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501783 | ||||||
| chr8:142501796
|
A | ATTATGAC others(5): Show |
9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9135_2676-913 others(16): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142501796 | |||||
| chr8:142501797
|
T | C | 171 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(168): Show | 174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.2676-9135T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501797 | ||||||
| chr8:142501803
|
A | T | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9129A>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501803 | ||||||
| chr8:142501805
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9127G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501805 | ||||||
| chr8:142501808
|
G | GTGGGGTA others(5): Show |
9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9124_2676-912 others(16): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501808 | ||||||
| chr8:142501813
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9119G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501813 | ||||||
| chr8:142501813
|
G | C | 1 | a0001c0001t0001g0212 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2676-9119G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501813 | ||||||
| chr8:142501822
|
A | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9110A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501822 | ||||||
| chr8:142501831
|
T | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9101T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501831 | ||||||
| chr8:142501839
|
T | G | 180 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(177): Show | 183 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.2676-9093T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501839 | ||||||
| chr8:142501841
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9091G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501841 | ||||||
| chr8:142501845
|
T | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9087T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501845 | ||||||
| chr8:142501849
|
T | C | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9083T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501849 | ||||||
| chr8:142501860
|
C | T | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9072C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501860 | ||||||
| chr8:142501863
|
TGGAGGTG others(1): Show |
T | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9066_2676-905 others(12): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142501863 | |||||
| chr8:142501873
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9059G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501873 | ||||||
| chr8:142501874
|
T | C | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9058T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501874 | ||||||
| chr8:142501875
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9057G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501875 | ||||||
| chr8:142501891
|
A | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9041A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501891 | ||||||
| chr8:142501892
|
G | T | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9040G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501892 | ||||||
| chr8:142501896
|
GAT | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9035_2676-903 others(6): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501896 | ||||||
| chr8:142501898
|
T | TGTG | 238 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(235): Show | 244 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.2676-9027_2676-902 others(7): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142501898 | |||||
| chr8:142501908
|
A | G | 22 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0003g0004others(19): Show | 25 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.2676-9024A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501908 | ||||||
| chr8:142501915
|
TGGC | T | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9014_2676-901 others(7): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142501915 | |||||
| chr8:142501919
|
G | A | 1 | a0001c0006t0001g0052 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2676-9013G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501919 | ||||||
| chr8:142501923
|
A | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9009A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501923 | ||||||
| chr8:142501927
|
C | T | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9005C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501927 | ||||||
| chr8:142501932
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-9000G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501932 | ||||||
| chr8:142501933
|
C | T | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8999C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501933 | ||||||
| chr8:142501946
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8986G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501946 | ||||||
| chr8:142501950
|
TGGC | T | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8981_2676-897 others(7): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501950 | ||||||
| chr8:142501957
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8975G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501957 | ||||||
| chr8:142501971
|
GGAGGT | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8960_2676-895 others(9): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501971 | ||||||
| chr8:142501978
|
G | C | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8954G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501978 | ||||||
| chr8:142501978
|
GGGT | G | 176 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(173): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.2676-8943_2676-894 others(7): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142501978 | |||||
| chr8:142501979
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8953G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501979 | ||||||
| chr8:142501986
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8946G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501986 | ||||||
| chr8:142501989
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2676-8943G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142501989 | ||||||
| chr8:142501998
|
GGAT | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8932_2676-893 others(7): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142501998 | |||||
| chr8:142502006
|
A | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8926A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502006 | ||||||
| chr8:142502009
|
G | T | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8923G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502009 | ||||||
| chr8:142502016
|
T | C | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8916T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502016 | ||||||
| chr8:142502034
|
A | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8898A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502034 | ||||||
| chr8:142502036
|
T | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8896T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502036 | ||||||
| chr8:142502039
|
T | TGGGGTAG others(1): Show |
9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8891_2676-889 others(12): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502039 | |||||
| chr8:142502043
|
G | T | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8889G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502043 | ||||||
| chr8:142502049
|
G | T | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8883G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502049 | ||||||
| chr8:142502050
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8882G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502050 | ||||||
| chr8:142502053
|
GT | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8878delT | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502053 | ||||||
| chr8:142502055
|
C | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8877C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502055 | ||||||
| chr8:142502057
|
G | T | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8875G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502057 | ||||||
| chr8:142502063
|
G | T | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8869G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502063 | ||||||
| chr8:142502064
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8868G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502064 | ||||||
| chr8:142502078
|
T | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8854T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502078 | ||||||
| chr8:142502095
|
C | T | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8837C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502095 | ||||||
| chr8:142502099
|
A | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8833A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502099 | ||||||
| chr8:142502106
|
T | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8826T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502106 | ||||||
| chr8:142502109
|
C | T | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8823C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502109 | ||||||
| chr8:142502116
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8816G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502116 | ||||||
| chr8:142502117
|
A | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8815A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502117 | ||||||
| chr8:142502123
|
TG | T | 10 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(7): Show | 10 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.2676-8804delG | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502123 | |||||
| chr8:142502138
|
A | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8794A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502138 | ||||||
| chr8:142502174
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8758G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502174 | ||||||
| chr8:142502178
|
C | T | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8754C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502178 | ||||||
| chr8:142502196
|
A | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8736A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502196 | ||||||
| chr8:142502201
|
A | T | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8731A>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502201 | ||||||
| chr8:142502207
|
T | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8725T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502207 | ||||||
| chr8:142502212
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8720G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502212 | ||||||
| chr8:142502218
|
A | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8714A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502218 | ||||||
| chr8:142502221
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8711G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502221 | ||||||
| chr8:142502224
|
A | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8708A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502224 | ||||||
| chr8:142502226
|
A | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8706A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502226 | ||||||
| chr8:142502234
|
T | TGGTGGGG others(308): Show |
9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8694_2676-869 others(319): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502234 | |||||
| chr8:142502239
|
A | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8693A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502239 | ||||||
| chr8:142502246
|
T | C | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8686T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502246 | ||||||
| chr8:142502251
|
C | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8681C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502251 | ||||||
| chr8:142502272
|
C | T | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8660C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502272 | ||||||
| chr8:142502281
|
T | C | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8651T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502281 | ||||||
| chr8:142502296
|
T | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8636T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502296 | ||||||
| chr8:142502313
|
T | TGGGGTAG others(69): Show |
9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8618_2676-861 others(80): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502313 | |||||
| chr8:142502318
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8614G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502318 | ||||||
| chr8:142502323
|
G | GTGGTAA | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8608_2676-860 others(10): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502323 | |||||
| chr8:142502330
|
T | TTATGG | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8602_2676-860 others(9): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502330 | ||||||
| chr8:142502335
|
A | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8597A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502335 | ||||||
| chr8:142502344
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8588G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502344 | ||||||
| chr8:142502352
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8580G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502352 | ||||||
| chr8:142502353
|
A | T | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8579A>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502353 | ||||||
| chr8:142502371
|
C | T | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8561C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502371 | ||||||
| chr8:142502372
|
G | A | 11 | a0001c0001t0001g0087a0001c0001t0002g0074a0001c0001t0013g0051others(8): Show | 11 | HG01891.hp1 HG02055.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.2676-8560G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502372 | ||||||
| chr8:142502387
|
AC | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8544delC | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502387 | ||||||
| chr8:142502391
|
T | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8541T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502391 | ||||||
| chr8:142502392
|
G | T | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8540G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502392 | ||||||
| chr8:142502394
|
T | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8538T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502394 | ||||||
| chr8:142502399
|
A | G | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8533A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502399 | ||||||
| chr8:142502400
|
T | TGGTGTGG others(886): Show |
1 | a0001c0008t0002g0062 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2676-8528_2676-852 others(897): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502400 | |||||
| chr8:142502414
|
G | A | 9 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(6): Show | 9 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.2676-8518G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502414 | ||||||
| chr8:142502414
|
G | GTGATGGT others(895): Show |
1 | a0001c0001t0001g0206 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2676-8516_2676-851 others(906): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502414 | |||||
| chr8:142502420
|
A | G | 10 | a0001c0001t0001g0132a0001c0001t0001g0206a0001c0001t0002g0081others(7): Show | 10 | HG00280.hp1 HG02083.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.2676-8512A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502420 | ||||||
| chr8:142502426
|
G | A | 10 | a0001c0001t0001g0132a0001c0001t0001g0206a0001c0001t0002g0081others(7): Show | 10 | HG00280.hp1 HG02083.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.2676-8506G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502426 | ||||||
| chr8:142502426
|
G | GTGGTGGT others(895): Show |
1 | a0001c0004t0015g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2676-8498_2676-849 others(906): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502426 | |||||
| chr8:142502426
|
G | GTGGTGGT others(816): Show |
1 | a0005c0021t0002g0102 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2676-8496_2676-849 others(827): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502426 | |||||
| chr8:142502426
|
G | GTGGTGGT others(895): Show |
1 | a0001c0006t0004g0243 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2676-8496_2676-849 others(906): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502426 | |||||
| chr8:142502426
|
G | GTGGTGGT others(898): Show |
1 | a0001c0001t0001g0088 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2676-8496_2676-849 others(909): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502426 | |||||
| chr8:142502426
|
G | GTGGTGGT others(899): Show |
1 | a0001c0002t0002g0117 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2676-8496_2676-849 others(910): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502426 | |||||
| chr8:142502426
|
G | GTGGTGGT others(898): Show |
1 | a0002c0005t0001g0018 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2676-8496_2676-849 others(909): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502426 | |||||
| chr8:142502426
|
G | GTGGTGGT others(899): Show |
1 | a0001c0001t0001g0146 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2676-8496_2676-849 others(910): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502426 | |||||
| chr8:142502426
|
G | GTGGTGGT others(895): Show |
1 | a0001c0001t0001g0079 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2676-8496_2676-849 others(906): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502426 | |||||
| chr8:142502426
|
G | GTGGTGGT others(898): Show |
174 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(171): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.2676-8496_2676-849 others(909): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502426 | |||||
| chr8:142502426
|
G | GTGGTGGT others(895): Show |
1 | a0001c0001t0001g0183 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2676-8496_2676-849 others(906): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502426 | |||||
| chr8:142502426
|
G | GTGGTGGT others(898): Show |
9 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(6): Show | 9 | HG01109.hp2 HG02451.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.2676-8496_2676-849 others(909): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502426 | |||||
| chr8:142502426
|
G | GTGGTGGT others(898): Show |
1 | a0001c0011t0002g0149 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2676-8496_2676-849 others(909): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502426 | |||||
| chr8:142502426
|
G | GTGGTGGT others(901): Show |
1 | a0001c0004t0001g0161 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2676-8496_2676-849 others(912): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502426 | |||||
| chr8:142502426
|
G | GTGGTGGT others(902): Show |
1 | a0001c0003t0003g0094 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2676-8496_2676-849 others(913): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502426 | |||||
| chr8:142502426
|
G | GTGGTGGT others(903): Show |
1 | a0001c0025t0002g0200 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2676-8496_2676-849 others(914): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502426 | |||||
| chr8:142502426
|
G | GTGGTGGT others(901): Show |
2 | a0001c0001t0001g0293a0003c0009t0002g0001 | 4 | HG02257.hp2 HG02559.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2676-8496_2676-849 others(912): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502426 | |||||
| chr8:142502426
|
G | GTGGTGGT others(898): Show |
2 | a0001c0011t0003g0072a0001c0034t0002g0071 | 2 | HG01192.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2676-8496_2676-849 others(909): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502426 | |||||
| chr8:142502426
|
G | GTGGTGGT others(902): Show |
1 | a0001c0001t0011g0064 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2676-8496_2676-849 others(913): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502426 | |||||
| chr8:142502426
|
G | GTGGTGGT others(901): Show |
48 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0040others(45): Show | 48 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.2676-8496_2676-849 others(912): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502426 | |||||
| chr8:142502426
|
G | GTGGTGGT others(904): Show |
2 | a0001c0001t0002g0035a0001c0001t0002g0130 | 2 | NA18940.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.2676-8496_2676-849 others(915): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502426 | |||||
| chr8:142502426
|
G | GTGGTGGT others(898): Show |
1 | a0001c0010t0001g0302 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2676-8496_2676-849 others(909): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502426 | |||||
| chr8:142502426
|
G | GTGGTGGT others(904): Show |
4 | a0001c0001t0001g0087a0001c0007t0001g0067a0001c0007t0001g0068others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2676-8496_2676-849 others(915): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502426 | |||||
| chr8:142502426
|
G | GTGGTGGT others(901): Show |
3 | a0001c0001t0013g0051a0001c0003t0002g0050a0001c0008t0001g0297 | 3 | HG02055.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2676-8496_2676-849 others(912): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502426 | |||||
| chr8:142502426
|
G | GTGGTGGT others(904): Show |
3 | a0001c0001t0002g0074a0001c0001t0014g0155a0001c0006t0002g0303 | 3 | HG02647.hp2 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2676-8496_2676-849 others(915): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502426 | |||||
| chr8:142502426
|
G | GTGGTGGT others(904): Show |
2 | a0001c0001t0002g0078a0011c0041t0002g0090 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2676-8496_2676-849 others(915): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502426 | |||||
| chr8:142502426
|
G | GTGGTGGT others(907): Show |
1 | a0001c0007t0003g0276 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2676-8496_2676-849 others(918): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502426 | |||||
| chr8:142502426
|
G | GTGGTGGT others(907): Show |
24 | a0001c0001t0001g0258a0001c0001t0001g0294a0001c0001t0003g0004others(21): Show | 25 | HG00735.hp2 HG01361.hp2 HG01928.hp1 others(22): Show |
intron_variant | MODIFIER | c.2676-8496_2676-849 others(918): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502426 | |||||
| chr8:142502426
|
G | GTGGTGGT others(901): Show |
1 | a0001c0006t0001g0291 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.2676-8496_2676-849 others(912): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502426 | |||||
| chr8:142502433
|
T | TGGTGATG others(625): Show |
1 | a0001c0001t0005g0204 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2676-8496_2676-849 others(636): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502433 | |||||
| chr8:142502437
|
A | G | 1 | a0001c0001t0005g0204 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2676-8495A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502437 | ||||||
| chr8:142502460
|
GCA | G | 303 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2676-8471_2676-847 others(6): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502460 | ||||||
| chr8:142502465
|
C | A | 303 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2676-8467C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502465 | ||||||
| chr8:142502468
|
C | G | 303 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2676-8464C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502468 | ||||||
| chr8:142502469
|
A | ATT | 300 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(297): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.2676-8463_2676-846 others(6): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502469 | ||||||
| chr8:142502470
|
C | G | 300 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(297): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.2676-8462C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502470 | ||||||
| chr8:142502470
|
C | T | 2 | a0001c0003t0003g0094a0009c0037t0002g0271 | 2 | HG01255.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.2676-8462C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502470 | ||||||
| chr8:142502476
|
T | G | 1 | a0001c0003t0003g0094 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2676-8456T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502476 | ||||||
| chr8:142502490
|
G | A | 29 | a0001c0001t0001g0258a0001c0001t0001g0293a0001c0001t0001g0294others(26): Show | 32 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.2676-8442G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502490 | ||||||
| chr8:142502490
|
G | T | 1 | a0001c0006t0001g0291 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.2676-8442G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502490 | ||||||
| chr8:142502492
|
G | GGTGATGG others(79): Show |
1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2676-8434_2676-843 others(90): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502492 | |||||
| chr8:142502499
|
A | G | 1 | a0001c0001t0005g0204 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2676-8433A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502499 | ||||||
| chr8:142502506
|
G | A | 1 | a0001c0001t0005g0204 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2676-8426G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502506 | ||||||
| chr8:142502508
|
C | T | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2676-8424C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502508 | ||||||
| chr8:142502510
|
T | G | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2676-8422T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502510 | ||||||
| chr8:142502510
|
T | TTAGTAAT others(115): Show |
1 | a0001c0001t0005g0204 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2676-8418_2676-841 others(126): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502510 | |||||
| chr8:142502513
|
G | A | 1 | a0006c0022t0002g0270 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2676-8419G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502513 | ||||||
| chr8:142502513
|
G | GTGATGGT others(60): Show |
3 | a0001c0001t0013g0051a0001c0003t0002g0050a0001c0013t0003g0049 | 3 | HG02630.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2676-8354_2676-835 others(71): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502513 | |||||
| chr8:142502515
|
G | A | 2 | a0001c0001t0005g0204a0009c0037t0002g0271 | 2 | NA18966.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.2676-8417G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502515 | ||||||
| chr8:142502534
|
G | T | 1 | a0001c0001t0005g0204 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2676-8398G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502534 | ||||||
| chr8:142502539
|
G | A | 1 | a0001c0001t0005g0204 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2676-8393G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502539 | ||||||
| chr8:142502543
|
C | T | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2676-8389C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502543 | ||||||
| chr8:142502544
|
A | T | 1 | a0001c0001t0005g0204 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2676-8388A>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502544 | ||||||
| chr8:142502546
|
AGGT | A | 32 | a0001c0001t0001g0023a0001c0001t0001g0258a0001c0001t0001g0293others(29): Show | 35 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.2676-8369_2676-836 others(7): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502546 | |||||
| chr8:142502549
|
T | TGGTGGTG others(57): Show |
1 | a0001c0010t0001g0302 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2676-8354_2676-835 others(68): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502549 | |||||
| chr8:142502553
|
G | GGGGTGAT others(871): Show |
1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2676-8378_2676-837 others(882): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502553 | |||||
| chr8:142502560
|
G | T | 2 | a0001c0001t0002g0074a0001c0001t0014g0155 | 2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2676-8372G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502560 | ||||||
| chr8:142502574
|
G | C | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2676-8358G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502574 | ||||||
| chr8:142502578
|
T | G | 1 | a0001c0006t0001g0291 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.2676-8354T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502578 | ||||||
| chr8:142502579
|
T | A | 302 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.2676-8353T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502579 | ||||||
| chr8:142502580
|
C | CTGATGGT others(55): Show |
4 | a0001c0001t0001g0087a0001c0007t0001g0067a0001c0007t0001g0068others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2676-8352_2676-835 others(66): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502580 | ||||||
| chr8:142502580
|
C | CTGATGGT others(58): Show |
1 | a0001c0008t0001g0297 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2676-8352_2676-835 others(69): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502580 | ||||||
| chr8:142502580
|
C | CTGATGGT others(58): Show |
10 | a0001c0001t0001g0132a0001c0001t0002g0081a0001c0003t0001g0152others(7): Show | 10 | HG02083.hp2 HG02109.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.2676-8352_2676-835 others(69): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502580 | ||||||
| chr8:142502580
|
C | T | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2676-8352C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502580 | ||||||
| chr8:142502581
|
A | G | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2676-8351A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502581 | ||||||
| chr8:142502581
|
A | T | 286 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(283): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.2676-8351A>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502581 | ||||||
| chr8:142502582
|
G | A | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2676-8350G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502582 | ||||||
| chr8:142502582
|
G | C | 16 | a0001c0001t0001g0087a0001c0001t0001g0132a0001c0001t0002g0081others(13): Show | 16 | HG01891.hp1 HG02055.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.2676-8350G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502582 | ||||||
| chr8:142502583
|
T | A | 286 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(283): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.2676-8349T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502583 | ||||||
| chr8:142502584
|
C | G | 17 | a0001c0001t0001g0087a0001c0001t0001g0132a0001c0001t0002g0081others(14): Show | 17 | HG01891.hp1 HG02055.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.2676-8348C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502584 | ||||||
| chr8:142502584
|
C | T | 286 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(283): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.2676-8348C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502584 | ||||||
| chr8:142502585
|
A | G | 287 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(284): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.2676-8347A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502585 | ||||||
| chr8:142502586
|
T | A | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2676-8346T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502586 | ||||||
| chr8:142502586
|
T | G | 286 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(283): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.2676-8346T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502586 | ||||||
| chr8:142502586
|
T | TGG | 16 | a0001c0001t0001g0087a0001c0001t0001g0132a0001c0001t0002g0081others(13): Show | 16 | HG01891.hp1 HG02055.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.2676-8346_2676-834 others(6): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502586 | ||||||
| chr8:142502587
|
C | T | 302 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.2676-8345C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502587 | ||||||
| chr8:142502588
|
A | T | 303 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2676-8344A>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502588 | ||||||
| chr8:142502589
|
C | G | 302 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.2676-8343C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502589 | ||||||
| chr8:142502597
|
T | A | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2676-8335T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502597 | ||||||
| chr8:142502623
|
A | C | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2676-8309A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502623 | ||||||
| chr8:142502624
|
A | C | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2676-8308A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502624 | ||||||
| chr8:142502633
|
C | T | 247 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(244): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2676-8299C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502633 | ||||||
| chr8:142502638
|
A | C | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2676-8294A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502638 | ||||||
| chr8:142502662
|
A | ATGCTGGG others(2): Show |
253 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(250): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.2676-8268_2676-826 others(13): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142502662 | |||||
| chr8:142502673
|
A | G | 253 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(250): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.2676-8259A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502673 | ||||||
| chr8:142502674
|
A | C | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2676-8258A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502674 | ||||||
| chr8:142502714
|
A | C | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2676-8218A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502714 | ||||||
| chr8:142502762
|
T | A | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2676-8170T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502762 | ||||||
| chr8:142502767
|
A | C | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2676-8165A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502767 | ||||||
| chr8:142502798
|
A | C | 1 | a0009c0037t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2676-8134A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502798 | ||||||
| chr8:142502811
|
A | G | 11 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(8): Show | 11 | HG01109.hp2 HG01255.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.2676-8121A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502811 | ||||||
| chr8:142502906
|
G | C | 3 | a0001c0001t0002g0074a0001c0001t0014g0155a0001c0006t0002g0303 | 3 | HG02647.hp2 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2676-8026G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142502906 | ||||||
| chr8:142503066
|
G | T | 1 | a0001c0001t0001g0195 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2676-7866G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142503066 | ||||||
| chr8:142503165
|
AC | A | 10 | a0001c0001t0001g0258a0001c0001t0002g0078a0001c0002t0001g0047others(7): Show | 10 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.2676-7761delC | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142503165 | |||||
| chr8:142503271
|
G | A | 44 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0034others(41): Show | 44 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.2676-7661G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142503271 | ||||||
| chr8:142503331
|
T | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0167a0010c0023t0001g0166 | 4 | HG00140.hp1 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.2676-7601T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142503331 | ||||||
| chr8:142503381
|
G | A | 1 | a0001c0007t0001g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2676-7551G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142503381 | ||||||
| chr8:142503505
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2676-7427G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142503505 | ||||||
| chr8:142503631
|
G | T | 1 | a0001c0011t0003g0239 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2676-7301G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142503631 | ||||||
| chr8:142504006
|
G | A | 3 | a0001c0002t0002g0115a0001c0002t0002g0116a0001c0002t0002g0117 | 3 | HG00597.hp2 NA18961.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.2676-6926G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142504006 | ||||||
| chr8:142504037
|
G | A | 210 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(207): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.2676-6895G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142504037 | ||||||
| chr8:142504115
|
A | G | 1 | a0001c0013t0003g0049 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2676-6817A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142504115 | ||||||
| chr8:142504132
|
C | G | 1 | a0005c0021t0002g0102 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2676-6800C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142504132 | ||||||
| chr8:142504289
|
G | C | 28 | a0001c0001t0001g0258a0001c0001t0001g0293a0001c0001t0001g0294others(25): Show | 31 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.2676-6643G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142504289 | ||||||
| chr8:142504312
|
C | T | 1 | a0001c0003t0003g0137 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2676-6620C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142504312 | ||||||
| chr8:142504729
|
C | G | 31 | a0001c0001t0001g0258a0001c0001t0001g0293a0001c0001t0001g0294others(28): Show | 34 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.2676-6203C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142504729 | ||||||
| chr8:142504734
|
G | T | 52 | a0001c0001t0001g0087a0001c0001t0001g0234a0001c0001t0001g0235others(49): Show | 55 | HG00735.hp2 HG01109.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.2676-6198G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142504734 | ||||||
| chr8:142504746
|
G | A | 1 | a0001c0003t0003g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2676-6186G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142504746 | ||||||
| chr8:142505058
|
G | C | 1 | a0001c0001t0005g0106 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2676-5874G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142505058 | ||||||
| chr8:142505102
|
A | G | 2 | a0001c0001t0001g0002a0001c0001t0002g0002 | 2 | HG00423.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.2676-5830A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142505102 | ||||||
| chr8:142505127
|
A | G | 1 | a0001c0001t0001g0255 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2676-5805A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142505127 | ||||||
| chr8:142505218
|
C | A | 1 | a0001c0007t0001g0133 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2676-5714C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142505218 | ||||||
| chr8:142505256
|
C | T | 1 | a0001c0036t0002g0012 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2676-5676C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142505256 | ||||||
| chr8:142505289
|
G | C | 3 | a0001c0001t0013g0051a0001c0003t0002g0050a0001c0008t0001g0297 | 3 | HG02055.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2676-5643G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142505289 | ||||||
| chr8:142505299
|
G | T | 2 | a0001c0002t0002g0172a0001c0016t0001g0272 | 2 | HG00609.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.2676-5633G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142505299 | ||||||
| chr8:142505359
|
G | A | 2 | a0001c0011t0002g0149a0001c0013t0003g0049 | 2 | HG02300.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2676-5573G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142505359 | ||||||
| chr8:142505390
|
C | T | 1 | a0004c0012t0001g0108 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2676-5542C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142505390 | ||||||
| chr8:142505489
|
C | T | 6 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(3): Show | 6 | HG01109.hp2 HG02886.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2676-5443C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142505489 | ||||||
| chr8:142505562
|
G | C | 2 | a0001c0001t0001g0256a0008c0031t0002g0141 | 2 | HG00741.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.2676-5370G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142505562 | ||||||
| chr8:142505613
|
G | A | 9 | a0001c0001t0001g0258a0001c0001t0002g0078a0001c0002t0001g0047others(6): Show | 9 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.2676-5319G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142505613 | ||||||
| chr8:142505625
|
G | A | 2 | a0001c0011t0003g0072a0001c0034t0002g0071 | 2 | HG01192.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2676-5307G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142505625 | ||||||
| chr8:142505641
|
G | A | 12 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0183others(9): Show | 12 | HG00323.hp1 HG00738.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.2676-5291G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142505641 | ||||||
| chr8:142505729
|
C | T | 1 | a0001c0008t0002g0232 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2676-5203C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142505729 | ||||||
| chr8:142505760
|
T | C | 261 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(258): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.2676-5172T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142505760 | ||||||
| chr8:142505789
|
A | T | 2 | a0001c0002t0002g0225a0001c0002t0002g0233 | 2 | HG02071.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.2676-5143A>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142505789 | ||||||
| chr8:142505922
|
G | A | 1 | a0001c0011t0002g0149 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2676-5010G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142505922 | ||||||
| chr8:142506152
|
G | A | 3 | a0001c0014t0002g0082a0001c0014t0002g0083a0001c0035t0001g0084 | 3 | HG01975.hp2 HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2676-4780G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142506152 | ||||||
| chr8:142506169
|
G | T | 1 | a0001c0006t0004g0243 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2676-4763G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142506169 | ||||||
| chr8:142506235
|
C | G | 1 | a0001c0001t0002g0130 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2676-4697C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142506235 | ||||||
| chr8:142506347
|
C | T | 1 | a0001c0011t0002g0149 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2676-4585C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142506347 | ||||||
| chr8:142506459
|
G | A | 1 | a0001c0011t0002g0149 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2676-4473G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142506459 | ||||||
| chr8:142506572
|
G | A | 30 | a0001c0001t0001g0258a0001c0001t0001g0293a0001c0001t0001g0294others(27): Show | 33 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.2676-4360G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142506572 | ||||||
| chr8:142506961
|
T | G | 2 | a0001c0011t0003g0072a0001c0034t0002g0071 | 2 | HG01192.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2676-3971T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142506961 | ||||||
| chr8:142507085
|
C | T | 1 | a0001c0002t0012g0039 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2676-3847C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142507085 | ||||||
| chr8:142507537
|
G | A | 3 | a0001c0001t0013g0051a0001c0003t0002g0050a0001c0008t0001g0297 | 3 | HG02055.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2676-3395G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142507537 | ||||||
| chr8:142507566
|
C | T | 18 | a0001c0001t0001g0006a0001c0001t0001g0150a0001c0001t0001g0151others(15): Show | 20 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.2676-3366C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142507566 | ||||||
| chr8:142507606
|
C | G | 6 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(3): Show | 6 | HG01109.hp2 HG02886.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2676-3326C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142507606 | ||||||
| chr8:142507636
|
G | A | 1 | a0007c0038t0002g0056 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2676-3296G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142507636 | ||||||
| chr8:142507663
|
G | T | 1 | a0001c0003t0001g0097 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2676-3269G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142507663 | ||||||
| chr8:142507747
|
G | A | 1 | a0001c0001t0001g0260 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2676-3185G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142507747 | ||||||
| chr8:142507847
|
C | T | 30 | a0001c0001t0001g0258a0001c0001t0001g0293a0001c0001t0001g0294others(27): Show | 33 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.2676-3085C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142507847 | ||||||
| chr8:142507849
|
G | T | 9 | a0001c0001t0001g0258a0001c0001t0002g0078a0001c0002t0001g0047others(6): Show | 9 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.2676-3083G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142507849 | ||||||
| chr8:142508005
|
C | T | 9 | a0001c0001t0001g0258a0001c0001t0002g0078a0001c0002t0001g0047others(6): Show | 9 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.2676-2927C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142508005 | ||||||
| chr8:142508022
|
A | G | 9 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0003g0004others(6): Show | 12 | HG02145.hp1 HG02257.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2676-2910A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142508022 | ||||||
| chr8:142508053
|
T | A | 3 | a0001c0003t0001g0070a0001c0010t0004g0244a0001c0010t0004g0287 | 3 | HG02886.hp1 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2676-2879T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142508053 | ||||||
| chr8:142508206
|
C | T | 1 | a0001c0001t0001g0034 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2676-2726C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142508206 | ||||||
| chr8:142508289
|
G | A | 5 | a0001c0001t0001g0087a0001c0007t0001g0067a0001c0007t0001g0068others(2): Show | 5 | HG01891.hp1 HG02630.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2676-2643G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142508289 | ||||||
| chr8:142508358
|
G | A | 1 | a0001c0003t0001g0055 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2676-2574G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142508358 | ||||||
| chr8:142508427
|
C | T | 3 | a0001c0001t0002g0074a0001c0001t0014g0155a0001c0006t0002g0303 | 3 | HG02647.hp2 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2676-2505C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142508427 | ||||||
| chr8:142508636
|
C | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0034a0001c0002t0002g0262others(1): Show | 4 | HG02080.hp2 NA19054.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.2676-2296C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142508636 | ||||||
| chr8:142508773
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2676-2159C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142508773 | ||||||
| chr8:142508938
|
G | A | 1 | a0007c0038t0002g0056 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2676-1994G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142508938 | ||||||
| chr8:142508987
|
G | C | 3 | a0001c0007t0001g0067a0001c0007t0001g0068a0001c0007t0001g0069 | 3 | HG01891.hp1 HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2676-1945G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142508987 | ||||||
| chr8:142509077
|
C | G | 260 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(257): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.2676-1855C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142509077 | ||||||
| chr8:142509083
|
T | TC | 6 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(3): Show | 6 | HG01109.hp2 HG02886.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2676-1844dupC | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr8 | 142509083 | |||||
| chr8:142509109
|
A | T | 197 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(194): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.2676-1823A>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142509109 | ||||||
| chr8:142509223
|
C | T | 1 | a0001c0007t0001g0069 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2676-1709C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142509223 | ||||||
| chr8:142509285
|
T | C | 44 | a0001c0001t0001g0087a0001c0001t0001g0234a0001c0001t0001g0235others(41): Show | 47 | HG00735.hp2 HG01109.hp2 HG01169.hp2 others(44): Show |
intron_variant | MODIFIER | c.2676-1647T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142509285 | ||||||
| chr8:142509369
|
C | T | 1 | a0001c0001t0002g0185 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2676-1563C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142509369 | ||||||
| chr8:142509444
|
G | A | 3 | a0001c0001t0002g0074a0001c0001t0014g0155a0001c0006t0002g0303 | 3 | HG02647.hp2 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2676-1488G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142509444 | ||||||
| chr8:142509566
|
G | A | 2 | a0001c0004t0001g0103a0001c0004t0001g0123 | 2 | NA18973.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.2676-1366G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142509566 | ||||||
| chr8:142509858
|
C | T | 39 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0040others(36): Show | 39 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.2676-1074C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142509858 | ||||||
| chr8:142509968
|
G | A | 2 | a0001c0001t0001g0079a0001c0003t0001g0080 | 2 | HG00099.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2676-964G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142509968 | ||||||
| chr8:142509991
|
G | A | 9 | a0001c0001t0001g0095a0001c0001t0003g0086a0001c0001t0003g0242others(6): Show | 9 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2676-941G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142509991 | ||||||
| chr8:142510129
|
G | A | 3 | a0001c0001t0013g0051a0001c0003t0002g0050a0001c0008t0001g0297 | 3 | HG02055.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2676-803G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142510129 | ||||||
| chr8:142510299
|
C | T | 5 | a0001c0001t0001g0087a0001c0007t0001g0067a0001c0007t0001g0068others(2): Show | 5 | HG01891.hp1 HG02630.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2676-633C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142510299 | ||||||
| chr8:142510431
|
C | T | 1 | a0001c0010t0001g0302 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2676-501C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142510431 | ||||||
| chr8:142510441
|
C | G | 45 | a0001c0001t0001g0087a0001c0001t0001g0095a0001c0001t0001g0258others(42): Show | 46 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(43): Show |
intron_variant | MODIFIER | c.2676-491C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142510441 | ||||||
| chr8:142510512
|
G | T | 2 | a0001c0004t0001g0249a0001c0004t0003g0250 | 2 | HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2676-420G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142510512 | ||||||
| chr8:142510518
|
C | T | 2 | a0001c0001t0002g0134a0005c0021t0002g0102 | 2 | HG00438.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.2676-414C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142510518 | ||||||
| chr8:142510538
|
C | G | 1 | a0001c0004t0001g0091 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2676-394C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142510538 | ||||||
| chr8:142510565
|
C | T | 6 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(3): Show | 6 | HG01109.hp2 HG02886.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2676-367C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142510565 | ||||||
| chr8:142510852
|
C | G | 1 | a0001c0001t0001g0269 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2676-80C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 17/30 | chr8 | 142510852 | ||||||
| chr8:142511107
|
C | T | 1 | a0001c0001t0002g0197 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2817+34C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142511107 | ||||||
| chr8:142511172
|
T | C | 1 | a0001c0003t0001g0076 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2817+99T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142511172 | ||||||
| chr8:142511312
|
C | G | 2 | a0001c0001t0001g0142a0001c0001t0001g0144 | 2 | HG03490.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.2817+239C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142511312 | ||||||
| chr8:142511426
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2817+353G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142511426 | ||||||
| chr8:142511458
|
T | C | 1 | a0001c0006t0002g0303 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2817+385T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142511458 | ||||||
| chr8:142511612
|
C | G | 1 | a0005c0021t0002g0102 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2817+539C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142511612 | ||||||
| chr8:142511753
|
G | A | 3 | a0001c0001t0002g0074a0001c0001t0014g0155a0001c0006t0002g0303 | 3 | HG02647.hp2 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2817+680G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142511753 | ||||||
| chr8:142511811
|
G | C | 25 | a0001c0001t0001g0087a0001c0001t0001g0132a0001c0001t0002g0074others(22): Show | 25 | HG01192.hp2 HG01255.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.2817+738G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142511811 | ||||||
| chr8:142511823
|
A | C | 7 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(4): Show | 7 | HG01109.hp2 HG02886.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.2817+750A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142511823 | ||||||
| chr8:142511901
|
G | A | 1 | a0001c0008t0001g0297 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2817+828G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142511901 | ||||||
| chr8:142511932
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2817+859G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142511932 | ||||||
| chr8:142512072
|
T | C | 7 | a0001c0001t0001g0087a0001c0003t0003g0026a0001c0007t0001g0067others(4): Show | 7 | HG01891.hp1 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2817+999T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142512072 | ||||||
| chr8:142512138
|
C | A | 4 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(1): Show | 4 | HG01109.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2817+1065C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142512138 | ||||||
| chr8:142512314
|
A | C | 1 | a0001c0007t0001g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2817+1241A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142512314 | ||||||
| chr8:142512332
|
G | A | 1 | a0003c0009t0002g0296 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2817+1259G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142512332 | ||||||
| chr8:142512361
|
T | C | 13 | a0001c0001t0001g0087a0001c0001t0002g0078a0001c0003t0001g0055others(10): Show | 13 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.2817+1288T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142512361 | ||||||
| chr8:142512415
|
C | T | 1 | a0001c0002t0002g0179 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2817+1342C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142512415 | ||||||
| chr8:142512450
|
A | G | 7 | a0001c0001t0002g0074a0001c0001t0014g0155a0001c0011t0003g0072others(4): Show | 7 | HG01975.hp2 HG02145.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2817+1377A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142512450 | ||||||
| chr8:142512563
|
G | T | 1 | a0001c0008t0001g0297 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2817+1490G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142512563 | ||||||
| chr8:142512584
|
G | A | 164 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0025others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.2817+1511G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142512584 | ||||||
| chr8:142512743
|
G | A | 2 | a0002c0005t0001g0016a0002c0005t0001g0022 | 2 | HG00423.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.2817+1670G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142512743 | ||||||
| chr8:142512806
|
C | T | 2 | a0001c0001t0001g0267a0001c0025t0002g0200 | 2 | NA18975.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.2817+1733C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142512806 | ||||||
| chr8:142512917
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2817+1844A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142512917 | ||||||
| chr8:142513030
|
T | C | 35 | a0001c0001t0001g0087a0001c0001t0001g0234a0001c0001t0001g0235others(32): Show | 37 | HG00735.hp2 HG01109.hp2 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.2817+1957T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142513030 | ||||||
| chr8:142513080
|
G | A | 1 | a0002c0005t0002g0019 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2817+2007G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142513080 | ||||||
| chr8:142513144
|
T | C | 2 | a0001c0001t0013g0051a0001c0013t0003g0049 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2817+2071T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142513144 | ||||||
| chr8:142513248
|
G | A | 1 | a0001c0001t0002g0143 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2817+2175G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142513248 | ||||||
| chr8:142513265
|
G | A | 1 | a0001c0001t0003g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2817+2192G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142513265 | ||||||
| chr8:142513416
|
C | A | 1 | a0001c0008t0001g0298 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2817+2343C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142513416 | ||||||
| chr8:142513429
|
T | C | 14 | a0001c0001t0013g0051a0001c0003t0001g0070a0001c0003t0001g0138others(11): Show | 14 | HG02055.hp1 HG02258.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2817+2356T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142513429 | ||||||
| chr8:142513433
|
C | T | 16 | a0001c0001t0001g0087a0001c0001t0001g0258a0001c0001t0001g0293others(13): Show | 18 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.2817+2360C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142513433 | ||||||
| chr8:142513675
|
C | G | 1 | a0004c0012t0001g0114 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2817+2602C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142513675 | ||||||
| chr8:142513742
|
G | A | 15 | a0001c0001t0001g0095a0001c0001t0001g0132a0001c0001t0001g0294others(12): Show | 16 | HG02071.hp2 HG02135.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.2817+2669G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142513742 | ||||||
| chr8:142513896
|
C | G | 1 | a0001c0004t0015g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2817+2823C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142513896 | ||||||
| chr8:142513922
|
C | T | 4 | a0001c0001t0002g0074a0001c0001t0014g0155a0001c0011t0003g0072others(1): Show | 4 | HG01192.hp2 HG02145.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2817+2849C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142513922 | ||||||
| chr8:142514125
|
G | A | 1 | a0001c0004t0015g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2817+3052G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142514125 | ||||||
| chr8:142514170
|
C | T | 1 | a0001c0007t0007g0240 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2817+3097C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142514170 | ||||||
| chr8:142514284
|
T | C | 1 | a0001c0006t0004g0243 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2817+3211T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142514284 | ||||||
| chr8:142514351
|
C | T | 190 | a0001c0001t0001g0006a0001c0001t0001g0025a0001c0001t0001g0034others(187): Show | 195 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.2817+3278C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142514351 | ||||||
| chr8:142514375
|
C | T | 5 | a0001c0001t0003g0242a0001c0003t0001g0138a0001c0003t0001g0241others(2): Show | 5 | HG02258.hp1 HG02622.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2817+3302C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142514375 | ||||||
| chr8:142514424
|
G | A | 1 | a0001c0004t0015g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2817+3351G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142514424 | ||||||
| chr8:142514527
|
T | C | 16 | a0001c0001t0001g0087a0001c0001t0001g0258a0001c0001t0001g0293others(13): Show | 18 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.2817+3454T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142514527 | ||||||
| chr8:142514557
|
G | A | 1 | a0001c0001t0002g0222 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2817+3484G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142514557 | ||||||
| chr8:142514609
|
C | T | 18 | a0001c0001t0001g0087a0001c0001t0001g0258a0001c0001t0001g0293others(15): Show | 20 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.2818-3529C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142514609 | ||||||
| chr8:142514632
|
T | C | 289 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.2818-3506T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142514632 | ||||||
| chr8:142515136
|
C | T | 72 | a0001c0001t0001g0058a0001c0001t0001g0066a0001c0001t0001g0087others(69): Show | 74 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.2818-3002C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142515136 | ||||||
| chr8:142515146
|
T | A | 23 | a0001c0001t0001g0087a0001c0001t0001g0132a0001c0001t0001g0293others(20): Show | 25 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.2818-2992T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142515146 | ||||||
| chr8:142515153
|
T | C | 23 | a0001c0001t0001g0087a0001c0001t0001g0132a0001c0001t0001g0293others(20): Show | 25 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.2818-2985T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142515153 | ||||||
| chr8:142515166
|
G | A | 5 | a0001c0001t0001g0277a0001c0001t0001g0280a0001c0002t0001g0251others(2): Show | 5 | HG02074.hp1 NA18967.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2818-2972G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142515166 | ||||||
| chr8:142515310
|
C | T | 1 | a0001c0001t0003g0242 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2818-2828C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142515310 | ||||||
| chr8:142515325
|
C | G | 4 | a0001c0001t0013g0051a0001c0003t0001g0241a0001c0006t0004g0243others(1): Show | 4 | HG02451.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2818-2813C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142515325 | ||||||
| chr8:142515420
|
C | T | 1 | a0001c0034t0002g0071 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2818-2718C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142515420 | ||||||
| chr8:142515468
|
C | T | 6 | a0001c0001t0001g0095a0001c0003t0001g0152a0001c0004t0001g0153others(3): Show | 6 | HG02109.hp1 HG02559.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2818-2670C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142515468 | ||||||
| chr8:142515509
|
A | T | 3 | a0001c0002t0002g0063a0001c0008t0002g0061a0001c0008t0002g0062 | 3 | NA18940.hp1 NA18997.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.2818-2629A>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142515509 | ||||||
| chr8:142515586
|
C | T | 1 | a0001c0011t0003g0239 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2818-2552C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142515586 | ||||||
| chr8:142515675
|
G | A | 1 | a0002c0005t0001g0016 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2818-2463G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142515675 | ||||||
| chr8:142515782
|
C | T | 9 | a0001c0001t0001g0087a0001c0001t0001g0293a0001c0007t0001g0067others(6): Show | 11 | HG01891.hp1 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2818-2356C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142515782 | ||||||
| chr8:142515829
|
G | A | 2 | a0001c0001t0013g0051a0001c0013t0003g0049 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2818-2309G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142515829 | ||||||
| chr8:142516019
|
A | G | 6 | a0001c0003t0001g0070a0001c0010t0004g0244a0001c0010t0004g0287others(3): Show | 6 | HG02886.hp1 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2818-2119A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142516019 | ||||||
| chr8:142516032
|
G | A | 2 | a0001c0003t0001g0073a0001c0003t0001g0135 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2818-2106G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142516032 | ||||||
| chr8:142516034
|
G | A | 4 | a0001c0004t0001g0168a0001c0004t0001g0209a0001c0004t0001g0210others(1): Show | 4 | NA18962.hp1 NA18963.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.2818-2104G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142516034 | ||||||
| chr8:142516150
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2818-1988C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142516150 | ||||||
| chr8:142516160
|
G | A | 34 | a0001c0003t0001g0055a0001c0003t0001g0070a0001c0003t0001g0073others(31): Show | 34 | HG00099.hp2 HG00597.hp1 HG01975.hp2 others(31): Show |
intron_variant | MODIFIER | c.2818-1978G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142516160 | ||||||
| chr8:142516169
|
A | AGCCCCAG others(513): Show |
1 | a0001c0001t0001g0176 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2818-1929_2818-192 others(524): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr8 | 142516169 | |||||
| chr8:142516169
|
A | AGCCCCAG others(166): Show |
1 | a0001c0001t0002g0205 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2818-1946_2818-177 others(177): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr8 | 142516169 | |||||
| chr8:142516181
|
G | A | 2 | a0001c0001t0003g0231a0001c0034t0002g0071 | 2 | HG01192.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2818-1957G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142516181 | ||||||
| chr8:142516210
|
G | A | 74 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(71): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.2818-1928G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142516210 | ||||||
| chr8:142516238
|
C | T | 4 | a0001c0003t0001g0070a0001c0010t0004g0244a0001c0010t0004g0287others(1): Show | 4 | HG02886.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2818-1900C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142516238 | ||||||
| chr8:142516239
|
G | A | 1 | a0001c0001t0001g0277 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2818-1899G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142516239 | ||||||
| chr8:142516290
|
T | C | 148 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(145): Show | 151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.2818-1848T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142516290 | ||||||
| chr8:142516290
|
TGGGCCCC others(18): Show |
T | 15 | a0001c0001t0001g0104a0001c0001t0001g0109a0001c0001t0001g0111others(12): Show | 15 | HG00639.hp2 HG01074.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.2818-1809_2818-178 others(29): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr8 | 142516290 | |||||
| chr8:142516292
|
G | T | 1 | a0001c0004t0001g0091 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2818-1846G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142516292 | ||||||
| chr8:142516383
|
G | A | 148 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(145): Show | 151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.2818-1755G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142516383 | ||||||
| chr8:142516447
|
C | T | 2 | a0001c0003t0001g0241a0001c0003t0003g0137 | 2 | HG02109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.2818-1691C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142516447 | ||||||
| chr8:142516447
|
CGTGTGTC others(18): Show |
C | 1 | a0001c0011t0002g0149 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2818-1684_2818-166 others(29): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr8 | 142516447 | |||||
| chr8:142516448
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2818-1690G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142516448 | ||||||
| chr8:142516490
|
T | C | 14 | a0001c0008t0001g0297a0001c0008t0001g0298a0001c0008t0002g0061others(11): Show | 14 | HG00597.hp1 HG02055.hp1 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.2818-1648T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142516490 | ||||||
| chr8:142516510
|
G | A | 6 | a0001c0003t0001g0070a0001c0010t0004g0244a0001c0010t0004g0287others(3): Show | 6 | HG02886.hp1 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2818-1628G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142516510 | ||||||
| chr8:142516520
|
G | A | 5 | a0001c0001t0001g0095a0001c0001t0002g0074a0001c0004t0001g0153others(2): Show | 5 | HG02451.hp2 HG02647.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2818-1618G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142516520 | ||||||
| chr8:142516558
|
A | G | 1 | a0001c0008t0002g0062 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2818-1580A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142516558 | ||||||
| chr8:142516609
|
T | G | 18 | a0001c0001t0001g0025a0001c0001t0001g0034a0001c0001t0001g0093others(15): Show | 18 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.2818-1529T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142516609 | ||||||
| chr8:142516623
|
TGCATGTG others(70): Show |
T | 13 | a0001c0008t0001g0297a0001c0008t0001g0298a0001c0008t0002g0061others(10): Show | 13 | HG00597.hp1 HG02055.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.2818-1513_2818-143 others(81): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr8 | 142516623 | |||||
| chr8:142516642
|
G | GGT | 4 | a0001c0001t0001g0075a0001c0001t0002g0264a0001c0017t0001g0008others(1): Show | 4 | HG02056.hp1 HG02647.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.2818-1476_2818-147 others(6): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr8 | 142516642 | |||||
| chr8:142516642
|
G | GGTGT | 111 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0034others(108): Show | 114 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.2818-1478_2818-147 others(8): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr8 | 142516642 | |||||
| chr8:142516642
|
GGT | G | 14 | a0001c0001t0002g0045a0001c0001t0002g0046a0001c0001t0002g0127others(11): Show | 14 | HG00438.hp2 HG01928.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.2818-1476_2818-147 others(6): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr8 | 142516642 | |||||
| chr8:142516666
|
TCCCAGGT others(18): Show |
T | 1 | a0001c0002t0002g0098 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2818-1462_2818-143 others(29): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr8 | 142516666 | |||||
| chr8:142516676
|
A | G | 266 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(263): Show | 272 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.2818-1462A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142516676 | ||||||
| chr8:142516705
|
A | C | 1 | a0001c0002t0002g0098 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2818-1433A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142516705 | ||||||
| chr8:142516716
|
C | T | 13 | a0001c0008t0001g0297a0001c0008t0001g0298a0001c0008t0002g0061others(10): Show | 13 | HG00597.hp1 HG02055.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.2818-1422C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142516716 | ||||||
| chr8:142516784
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2818-1354C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142516784 | ||||||
| chr8:142517080
|
A | C | 4 | a0001c0003t0003g0026a0001c0003t0003g0094a0001c0018t0003g0007others(1): Show | 4 | HG01255.hp1 HG02451.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.2818-1058A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142517080 | ||||||
| chr8:142517215
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2818-923C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142517215 | ||||||
| chr8:142517327
|
G | T | 267 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(264): Show | 273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.2818-811G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142517327 | ||||||
| chr8:142517342
|
A | G | 285 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(282): Show | 291 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.2818-796A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142517342 | ||||||
| chr8:142517508
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2818-630C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142517508 | ||||||
| chr8:142517701
|
G | A | 1 | a0003c0009t0002g0092 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2818-437G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142517701 | ||||||
| chr8:142517704
|
C | T | 14 | a0001c0008t0001g0297a0001c0008t0001g0298a0001c0008t0002g0061others(11): Show | 14 | HG00597.hp1 HG02055.hp1 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.2818-434C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142517704 | ||||||
| chr8:142517800
|
C | T | 1 | a0002c0005t0001g0016 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2818-338C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142517800 | ||||||
| chr8:142518062
|
G | A | 13 | a0001c0008t0001g0297a0001c0008t0001g0298a0001c0008t0002g0061others(10): Show | 13 | HG00597.hp1 HG02055.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.2818-76G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142518062 | ||||||
| chr8:142518126
|
C | T | 10 | a0001c0008t0001g0297a0001c0008t0001g0298a0001c0008t0002g0061others(7): Show | 10 | HG00597.hp1 HG02055.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.2818-12C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 18/30 | chr8 | 142518126 | ||||||
| chr8:142518270
|
A | G | 284 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(281): Show | 290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.2921+29A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142518270 | ||||||
| chr8:142518273
|
T | G | 303 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2921+32T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142518273 | ||||||
| chr8:142518290
|
A | C | 303 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2921+49A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142518290 | ||||||
| chr8:142518304
|
T | C | 303 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2921+63T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142518304 | ||||||
| chr8:142518343
|
A | C | 303 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2921+102A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142518343 | ||||||
| chr8:142518355
|
G | C | 303 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2921+114G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142518355 | ||||||
| chr8:142518373
|
A | C | 303 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2921+132A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142518373 | ||||||
| chr8:142518385
|
A | C | 303 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2921+144A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142518385 | ||||||
| chr8:142518392
|
A | C | 303 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2921+151A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142518392 | ||||||
| chr8:142518413
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2921+172C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142518413 | ||||||
| chr8:142518421
|
G | GT | 291 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(288): Show | 297 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.2921+181dupT | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr8 | 142518421 | |||||
| chr8:142518430
|
C | G | 1 | a0001c0001t0001g0176 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2921+189C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142518430 | ||||||
| chr8:142518448
|
A | C | 303 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2921+207A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142518448 | ||||||
| chr8:142518454
|
A | C | 303 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2921+213A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142518454 | ||||||
| chr8:142518496
|
T | G | 1 | a0002c0005t0002g0099 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2921+255T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142518496 | ||||||
| chr8:142518510
|
T | C | 303 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2921+269T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142518510 | ||||||
| chr8:142518548
|
A | C | 303 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2921+307A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142518548 | ||||||
| chr8:142518574
|
G | A | 1 | a0001c0004t0015g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2921+333G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142518574 | ||||||
| chr8:142518691
|
T | C | 4 | a0001c0001t0001g0171a0001c0002t0002g0225a0001c0004t0001g0103others(1): Show | 4 | HG02135.hp1 NA18952.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.2921+450T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142518691 | ||||||
| chr8:142518768
|
G | A | 1 | a0001c0002t0001g0251 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2921+527G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142518768 | ||||||
| chr8:142518960
|
T | G | 170 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(167): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.2921+719T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142518960 | ||||||
| chr8:142519147
|
C | T | 5 | a0001c0001t0001g0293a0001c0013t0001g0096a0003c0009t0002g0001others(2): Show | 7 | HG02145.hp1 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2921+906C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142519147 | ||||||
| chr8:142519170
|
A | G | 1 | a0001c0001t0002g0222 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2921+929A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142519170 | ||||||
| chr8:142519509
|
G | A | 13 | a0001c0008t0001g0297a0001c0008t0001g0298a0001c0008t0002g0061others(10): Show | 13 | HG00597.hp1 HG02055.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.2921+1268G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142519509 | ||||||
| chr8:142519705
|
TTGG | T | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(135): Show | 141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.2922-1112_2922-111 others(7): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr8 | 142519705 | |||||
| chr8:142519752
|
G | C | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(135): Show | 141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.2922-1071G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142519752 | ||||||
| chr8:142519783
|
ATGG | A | 18 | a0001c0001t0001g0025a0001c0001t0001g0034a0001c0001t0001g0093others(15): Show | 18 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.2922-1035_2922-103 others(7): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr8 | 142519783 | |||||
| chr8:142519840
|
G | A | 7 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(4): Show | 7 | HG01109.hp2 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2922-983G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142519840 | ||||||
| chr8:142519884
|
G | A | 11 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0146others(8): Show | 11 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.2922-939G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142519884 | ||||||
| chr8:142519980
|
G | A | 1 | a0001c0001t0002g0127 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2922-843G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142519980 | ||||||
| chr8:142520034
|
ATGG | A | 6 | a0001c0001t0001g0107a0001c0003t0003g0026a0001c0003t0003g0094others(3): Show | 6 | HG01255.hp1 HG02451.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2922-784_2922-782d others(5): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr8 | 142520034 | |||||
| chr8:142520096
|
T | G | 276 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(273): Show | 282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.2922-727T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142520096 | ||||||
| chr8:142520148
|
TGTGATG | T | 14 | a0001c0008t0001g0297a0001c0008t0001g0298a0001c0008t0002g0061others(11): Show | 14 | HG00597.hp1 HG02055.hp1 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.2922-671_2922-666d others(8): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr8 | 142520148 | |||||
| chr8:142520192
|
T | G | 1 | a0001c0001t0003g0004 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2922-631T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142520192 | ||||||
| chr8:142520253
|
GTGA | G | 8 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(5): Show | 8 | HG01109.hp2 HG02622.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.2922-564_2922-562d others(5): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr8 | 142520253 | |||||
| chr8:142520372
|
G | GCGTGGTG others(87): Show |
1 | a0001c0001t0001g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2922-451_2922-450i others(96): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142520372 | ||||||
| chr8:142520374
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2922-449G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142520374 | ||||||
| chr8:142520375
|
G | A | 1 | a0001c0013t0001g0096 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2922-448G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142520375 | ||||||
| chr8:142520381
|
G | C | 1 | a0001c0001t0001g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2922-442G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142520381 | ||||||
| chr8:142520383
|
GATGGTAG others(96): Show |
G | 1 | a0001c0013t0001g0096 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2922-434_2922-332d others(2): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr8 | 142520383 | |||||
| chr8:142520389
|
A | G | 18 | a0001c0001t0001g0025a0001c0001t0001g0034a0001c0001t0001g0093others(15): Show | 18 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.2922-434A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142520389 | ||||||
| chr8:142520393
|
A | ATGG | 17 | a0001c0001t0001g0025a0001c0001t0001g0034a0001c0001t0001g0093others(14): Show | 17 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.2922-429_2922-428i others(5): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr8 | 142520393 | |||||
| chr8:142520395
|
T | G | 1 | a0001c0001t0001g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2922-428T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142520395 | ||||||
| chr8:142520397
|
T | C | 1 | a0001c0001t0001g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2922-426T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142520397 | ||||||
| chr8:142520398
|
G | GTTGGTGA others(191): Show |
17 | a0001c0001t0001g0025a0001c0001t0001g0034a0001c0001t0001g0093others(14): Show | 17 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.2922-425_2922-424i others(200): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142520398 | ||||||
| chr8:142520398
|
G | T | 1 | a0001c0001t0001g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2922-425G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142520398 | ||||||
| chr8:142520399
|
A | ATGGTGGT others(218): Show |
272 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(269): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.2922-422_2922-421i others(227): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr8 | 142520399 | |||||
| chr8:142520399
|
A | ATGGTGGT others(206): Show |
1 | a0001c0001t0001g0087 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2922-422_2922-421i others(215): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr8 | 142520399 | |||||
| chr8:142520399
|
A | ATGGTGGT others(209): Show |
3 | a0001c0007t0001g0067a0001c0007t0001g0068a0001c0007t0001g0069 | 3 | HG01891.hp1 HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2922-422_2922-421i others(218): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr8 | 142520399 | |||||
| chr8:142520399
|
A | G | 18 | a0001c0001t0001g0025a0001c0001t0001g0034a0001c0001t0001g0093others(15): Show | 18 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.2922-424A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142520399 | ||||||
| chr8:142520402
|
T | G | 8 | a0001c0001t0001g0293a0001c0001t0013g0051a0001c0007t0003g0276others(5): Show | 10 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2922-421T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142520402 | ||||||
| chr8:142520407
|
A | G | 8 | a0001c0001t0001g0293a0001c0001t0013g0051a0001c0007t0003g0276others(5): Show | 10 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2922-416A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142520407 | ||||||
| chr8:142520408
|
A | ATGGTTGT others(2): Show |
8 | a0001c0001t0001g0293a0001c0001t0013g0051a0001c0007t0003g0276others(5): Show | 10 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2922-411_2922-410i others(11): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr8 | 142520408 | |||||
| chr8:142520416
|
A | G | 8 | a0001c0001t0001g0293a0001c0001t0013g0051a0001c0007t0003g0276others(5): Show | 10 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2922-407A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142520416 | ||||||
| chr8:142520423
|
A | C | 8 | a0001c0001t0001g0293a0001c0001t0013g0051a0001c0007t0003g0276others(5): Show | 10 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2922-400A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142520423 | ||||||
| chr8:142520427
|
T | G | 1 | a0001c0003t0003g0137 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2922-396T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142520427 | ||||||
| chr8:142520431
|
A | G | 8 | a0001c0001t0001g0293a0001c0001t0013g0051a0001c0007t0003g0276others(5): Show | 10 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2922-392A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142520431 | ||||||
| chr8:142520436
|
G | A | 8 | a0001c0001t0001g0293a0001c0001t0013g0051a0001c0007t0003g0276others(5): Show | 10 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2922-387G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142520436 | ||||||
| chr8:142520442
|
G | GATGGTGA others(55): Show |
8 | a0001c0001t0001g0293a0001c0001t0013g0051a0001c0007t0003g0276others(5): Show | 10 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2922-381_2922-380i others(64): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142520442 | ||||||
| chr8:142520467
|
GTGGTGAT others(19): Show |
G | 244 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(241): Show | 248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.2922-347_2922-322d others(28): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr8 | 142520467 | |||||
| chr8:142520475
|
GGTT | G | 8 | a0001c0001t0001g0293a0001c0001t0013g0051a0001c0007t0003g0276others(5): Show | 10 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2922-345_2922-343d others(5): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr8 | 142520475 | |||||
| chr8:142520480
|
T | A | 8 | a0001c0001t0001g0293a0001c0001t0013g0051a0001c0007t0003g0276others(5): Show | 10 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2922-343T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142520480 | ||||||
| chr8:142520486
|
A | G | 8 | a0001c0001t0001g0293a0001c0001t0013g0051a0001c0007t0003g0276others(5): Show | 10 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2922-337A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142520486 | ||||||
| chr8:142520487
|
A | G | 1 | a0001c0013t0001g0096 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2922-336A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142520487 | ||||||
| chr8:142520493
|
A | ATGGTGGT others(112): Show |
1 | a0001c0007t0007g0240 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2922-325_2922-324i others(121): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr8 | 142520493 | |||||
| chr8:142520493
|
A | ATGGTGGT others(115): Show |
7 | a0001c0001t0001g0293a0001c0001t0013g0051a0001c0007t0003g0276others(4): Show | 9 | HG02145.hp1 HG02257.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2922-325_2922-324i others(124): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr8 | 142520493 | |||||
| chr8:142520493
|
A | G | 1 | a0001c0013t0001g0096 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2922-330A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | chr8 | 142520493 | ||||||
| chr8:142520512
|
AGTG | A | 4 | a0001c0003t0003g0026a0001c0003t0003g0094a0001c0018t0003g0007others(1): Show | 4 | HG01255.hp1 HG02451.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.2922-301_2922-299d others(5): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr8 | 142520512 | |||||
| chr8:142520979
|
A | G | 1 | a0001c0013t0001g0096 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3024+54A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 20/30 | chr8 | 142520979 | ||||||
| chr8:142521031
|
C | T | 1 | a0001c0013t0003g0049 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3024+106C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 20/30 | chr8 | 142521031 | ||||||
| chr8:142521253
|
G | A | 1 | a0001c0003t0003g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3024+328G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 20/30 | chr8 | 142521253 | ||||||
| chr8:142521318
|
G | C | 241 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(238): Show | 247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.3024+393G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 20/30 | chr8 | 142521318 | ||||||
| chr8:142521321
|
C | T | 1 | a0001c0002t0002g0172 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3024+396C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 20/30 | chr8 | 142521321 | ||||||
| chr8:142521376
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3024+451C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 20/30 | chr8 | 142521376 | ||||||
| chr8:142521433
|
T | C | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.3024+508T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 20/30 | chr8 | 142521433 | ||||||
| chr8:142521470
|
G | C | 1 | a0001c0011t0002g0149 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3025-495G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 20/30 | chr8 | 142521470 | ||||||
| chr8:142521474
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3025-491C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 20/30 | chr8 | 142521474 | ||||||
| chr8:142521484
|
C | G | 235 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(232): Show | 241 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.3025-481C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 20/30 | chr8 | 142521484 | ||||||
| chr8:142521532
|
C | T | 1 | a0001c0001t0003g0086 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3025-433C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 20/30 | chr8 | 142521532 | ||||||
| chr8:142521599
|
G | T | 7 | a0001c0003t0001g0070a0001c0003t0002g0101a0001c0010t0004g0244others(4): Show | 7 | HG02083.hp2 HG02886.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.3025-366G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 20/30 | chr8 | 142521599 | ||||||
| chr8:142521664
|
C | T | 1 | a0001c0011t0003g0239 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3025-301C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 20/30 | chr8 | 142521664 | ||||||
| chr8:142521908
|
A | G | 303 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.3025-57A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 20/30 | chr8 | 142521908 | ||||||
| chr8:142521939
|
C | T | 3 | a0001c0006t0001g0288a0001c0006t0001g0289a0001c0006t0001g0291 | 3 | HG02622.hp2 HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3025-26C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 20/30 | chr8 | 142521939 | ||||||
| chr8:142521957
|
C | T | 152 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(149): Show | 157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
splice_region_variant&intron_variant | LOW | c.3025-8C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 20/30 | chr8 | 142521957 | ||||||
| chr8:142522307
|
T | C | 242 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(239): Show | 248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.3175+192T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 21/30 | chr8 | 142522307 | ||||||
| chr8:142522314
|
T | G | 90 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0034others(87): Show | 91 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.3175+199T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 21/30 | chr8 | 142522314 | ||||||
| chr8:142522423
|
C | T | 1 | a0008c0031t0002g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3176-218C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 21/30 | chr8 | 142522423 | ||||||
| chr8:142522459
|
G | A | 2 | a0001c0001t0003g0086a0001c0001t0003g0231 | 2 | HG02280.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.3176-182G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 21/30 | chr8 | 142522459 | ||||||
| chr8:142522553
|
C | T | 1 | a0001c0001t0001g0059 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3176-88C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 21/30 | chr8 | 142522553 | ||||||
| chr8:142522770
|
G | A | 2 | a0001c0001t0002g0078a0011c0041t0002g0090 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.3245+60G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 22/30 | chr8 | 142522770 | ||||||
| chr8:142523270
|
G | A | 1 | a0001c0004t0001g0168 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3245+560G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 22/30 | chr8 | 142523270 | ||||||
| chr8:142523324
|
T | TGGAG | 89 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0034others(86): Show | 90 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.3245+615_3245+616i others(6): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 22/30 | INFO_REALIGN_3_PRIME | chr8 | 142523324 | |||||
| chr8:142523326
|
A | G | 303 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.3245+616A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 22/30 | chr8 | 142523326 | ||||||
| chr8:142523366
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3245+656G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 22/30 | chr8 | 142523366 | ||||||
| chr8:142523404
|
A | AG | 303 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.3245+697dupG | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 22/30 | INFO_REALIGN_3_PRIME | chr8 | 142523404 | |||||
| chr8:142523410
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3245+700G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 22/30 | chr8 | 142523410 | ||||||
| chr8:142523526
|
GCTGAGAG others(3): Show |
G | 1 | a0001c0001t0002g0043 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.3246-711_3246-702d others(12): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 22/30 | chr8 | 142523526 | ||||||
| chr8:142523544
|
A | C | 1 | a0001c0001t0002g0043 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.3246-694A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 22/30 | chr8 | 142523544 | ||||||
| chr8:142523692
|
G | A | 2 | a0001c0002t0012g0039a0005c0021t0002g0102 | 2 | HG02056.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.3246-546G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 22/30 | chr8 | 142523692 | ||||||
| chr8:142523778
|
A | AG | 28 | a0001c0001t0001g0079a0001c0001t0001g0088a0001c0001t0001g0147others(25): Show | 28 | HG00408.hp2 HG00438.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.3246-454dupG | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 22/30 | INFO_REALIGN_3_PRIME | chr8 | 142523778 | |||||
| chr8:142523840
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3246-398G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 22/30 | chr8 | 142523840 | ||||||
| chr8:142523958
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3246-280T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 22/30 | chr8 | 142523958 | ||||||
| chr8:142524109
|
G | A | 89 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0034others(86): Show | 90 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.3246-129G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 22/30 | chr8 | 142524109 | ||||||
| chr8:142524174
|
C | T | 1 | a0001c0008t0002g0232 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3246-64C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 22/30 | chr8 | 142524174 | ||||||
| chr8:142524175
|
G | A | 2 | a0001c0001t0001g0075a0001c0017t0001g0008 | 2 | HG02647.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3246-63G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 22/30 | chr8 | 142524175 | ||||||
| chr8:142524176
|
G | T | 1 | a0001c0003t0001g0152 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3246-62G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 22/30 | chr8 | 142524176 | ||||||
| chr8:142524207
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3246-31G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 22/30 | chr8 | 142524207 | ||||||
| chr8:142524626
|
T | C | 12 | a0001c0003t0001g0070a0001c0003t0002g0101a0001c0003t0003g0026others(9): Show | 12 | HG01255.hp1 HG02083.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.3312+322T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 23/30 | chr8 | 142524626 | ||||||
| chr8:142524630
|
C | T | 1 | a0001c0001t0002g0143 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3312+326C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 23/30 | chr8 | 142524630 | ||||||
| chr8:142524743
|
G | A | 141 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0034others(138): Show | 144 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.3312+439G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 23/30 | chr8 | 142524743 | ||||||
| chr8:142525443
|
C | A | 102 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0034others(99): Show | 105 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.3313-1099C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 23/30 | chr8 | 142525443 | ||||||
| chr8:142525583
|
C | G | 1 | a0001c0008t0002g0232 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3313-959C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 23/30 | chr8 | 142525583 | ||||||
| chr8:142525642
|
G | A | 4 | a0001c0004t0001g0153a0001c0004t0001g0154a0001c0004t0001g0292others(1): Show | 4 | HG02559.hp1 HG02818.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.3313-900G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 23/30 | chr8 | 142525642 | ||||||
| chr8:142525774
|
T | C | 103 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0034others(100): Show | 106 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.3313-768T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 23/30 | chr8 | 142525774 | ||||||
| chr8:142525901
|
C | T | 102 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0034others(99): Show | 105 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.3313-641C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 23/30 | chr8 | 142525901 | ||||||
| chr8:142525978
|
G | T | 1 | a0001c0001t0002g0081 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3313-564G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 23/30 | chr8 | 142525978 | ||||||
| chr8:142526065
|
A | G | 1 | a0001c0008t0002g0232 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3313-477A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 23/30 | chr8 | 142526065 | ||||||
| chr8:142526068
|
C | T | 131 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.3313-474C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 23/30 | chr8 | 142526068 | ||||||
| chr8:142526118
|
G | A | 102 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0034others(99): Show | 105 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.3313-424G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 23/30 | chr8 | 142526118 | ||||||
| chr8:142526511
|
C | A | 1 | a0001c0001t0001g0299 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3313-31C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 23/30 | chr8 | 142526511 | ||||||
| chr8:142526694
|
G | C | 1 | a0001c0002t0002g0063 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3398+67G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142526694 | ||||||
| chr8:142526785
|
C | A | 4 | a0001c0001t0001g0293a0003c0009t0002g0001a0003c0009t0002g0295others(1): Show | 6 | HG02145.hp1 HG02257.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.3398+158C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142526785 | ||||||
| chr8:142526935
|
C | A | 1 | a0001c0001t0002g0130 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3398+308C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142526935 | ||||||
| chr8:142527001
|
CA | C | 8 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(5): Show | 10 | HG01109.hp2 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.3398+375delA | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142527001 | ||||||
| chr8:142527004
|
G | C | 1 | a0001c0002t0002g0063 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3398+377G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142527004 | ||||||
| chr8:142527074
|
C | G | 143 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.3398+447C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142527074 | ||||||
| chr8:142527084
|
G | A | 3 | a0001c0001t0001g0095a0001c0001t0002g0074a0001c0006t0004g0243 | 3 | HG02451.hp2 HG02647.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3398+457G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142527084 | ||||||
| chr8:142527174
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3398+547C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142527174 | ||||||
| chr8:142527278
|
G | T | 94 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0034others(91): Show | 95 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.3398+651G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142527278 | ||||||
| chr8:142527617
|
A | G | 1 | a0001c0001t0001g0255 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3398+990A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142527617 | ||||||
| chr8:142527640
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3398+1013A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142527640 | ||||||
| chr8:142527823
|
G | A | 92 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0034others(89): Show | 93 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.3398+1196G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142527823 | ||||||
| chr8:142527841
|
A | G | 1 | a0001c0028t0002g0254 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3398+1214A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142527841 | ||||||
| chr8:142527945
|
G | A | 1 | a0013c0040t0001g0266 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3398+1318G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142527945 | ||||||
| chr8:142528125
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3398+1498A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142528125 | ||||||
| chr8:142528219
|
A | G | 14 | a0001c0001t0001g0087a0001c0001t0001g0299a0001c0001t0003g0242others(11): Show | 14 | HG01891.hp1 HG02451.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.3398+1592A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142528219 | ||||||
| chr8:142528263
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3398+1636C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142528263 | ||||||
| chr8:142528304
|
G | A | 125 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0034others(122): Show | 128 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.3398+1677G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142528304 | ||||||
| chr8:142528385
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3398+1758C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142528385 | ||||||
| chr8:142528426
|
T | A | 1 | a0001c0014t0002g0082 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3398+1799T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142528426 | ||||||
| chr8:142528426
|
T | C | 19 | a0001c0001t0001g0075a0001c0001t0001g0234a0001c0001t0001g0235others(16): Show | 19 | HG01109.hp2 HG01891.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.3398+1799T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142528426 | ||||||
| chr8:142528431
|
G | A | 1 | a0001c0013t0001g0096 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3398+1804G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142528431 | ||||||
| chr8:142528433
|
G | A | 1 | a0001c0001t0003g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3398+1806G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142528433 | ||||||
| chr8:142528453
|
G | T | 1 | a0012c0039t0003g0237 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3398+1826G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142528453 | ||||||
| chr8:142528552
|
T | C | 169 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0023others(166): Show | 170 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.3398+1925T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142528552 | ||||||
| chr8:142528682
|
C | T | 3 | a0001c0001t0001g0132a0001c0001t0014g0155a0001c0003t0001g0138 | 3 | HG02258.hp1 HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3398+2055C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142528682 | ||||||
| chr8:142528774
|
A | G | 2 | a0001c0001t0001g0075a0001c0017t0001g0008 | 2 | HG02647.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3398+2147A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142528774 | ||||||
| chr8:142528820
|
C | T | 1 | a0001c0001t0002g0228 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3398+2193C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142528820 | ||||||
| chr8:142528907
|
G | A | 2 | a0001c0001t0001g0075a0001c0017t0001g0008 | 2 | HG02647.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3398+2280G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142528907 | ||||||
| chr8:142528921
|
G | A | 1 | a0001c0002t0002g0028 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3398+2294G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142528921 | ||||||
| chr8:142528935
|
G | A | 1 | a0001c0029t0002g0248 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3398+2308G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142528935 | ||||||
| chr8:142528963
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.3398+2336G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142528963 | ||||||
| chr8:142529034
|
G | T | 56 | a0001c0001t0001g0025a0001c0001t0001g0034a0001c0001t0001g0058others(53): Show | 56 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.3398+2407G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142529034 | ||||||
| chr8:142529055
|
G | A | 1 | a0001c0003t0003g0137 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3398+2428G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142529055 | ||||||
| chr8:142529094
|
G | A | 5 | a0001c0001t0002g0134a0001c0001t0002g0222a0001c0001t0002g0279others(2): Show | 5 | HG00438.hp1 HG00673.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.3398+2467G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142529094 | ||||||
| chr8:142529175
|
CAT | C | 60 | a0001c0001t0001g0025a0001c0001t0001g0034a0001c0001t0001g0040others(57): Show | 60 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.3398+2549_3398+255 others(6): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142529175 | ||||||
| chr8:142529306
|
G | A | 37 | a0001c0001t0001g0031a0001c0001t0001g0151a0001c0001t0001g0174others(34): Show | 37 | HG00544.hp1 HG00597.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.3398+2679G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142529306 | ||||||
| chr8:142529349
|
T | C | 1 | a0001c0013t0001g0096 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3398+2722T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142529349 | ||||||
| chr8:142529355
|
T | C | 1 | a0001c0003t0003g0137 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3398+2728T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142529355 | ||||||
| chr8:142529392
|
T | C | 21 | a0001c0001t0001g0088a0001c0001t0001g0206a0001c0001t0001g0234others(18): Show | 22 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.3398+2765T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142529392 | ||||||
| chr8:142529534
|
A | C | 1 | a0001c0001t0001g0268 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3398+2907A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142529534 | ||||||
| chr8:142529554
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3398+2927A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142529554 | ||||||
| chr8:142529567
|
C | A | 1 | a0001c0001t0001g0269 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3398+2940C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142529567 | ||||||
| chr8:142529590
|
G | A | 1 | a0001c0003t0003g0137 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3398+2963G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142529590 | ||||||
| chr8:142529628
|
G | A | 1 | a0001c0001t0002g0162 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3398+3001G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142529628 | ||||||
| chr8:142529671
|
TGTGTACC others(15): Show |
T | 27 | a0001c0001t0001g0088a0001c0001t0001g0095a0001c0001t0001g0206others(24): Show | 28 | HG00140.hp1 HG00280.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.3398+3066_3398+308 others(26): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | INFO_REALIGN_3_PRIME | chr8 | 142529671 | |||||
| chr8:142529796
|
CTGTGAGT others(35): Show |
C | 1 | a0001c0002t0002g0217 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3398+3190_3398+323 others(46): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | INFO_REALIGN_3_PRIME | chr8 | 142529796 | |||||
| chr8:142529880
|
A | G | 1 | a0001c0002t0002g0217 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3398+3253A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142529880 | ||||||
| chr8:142529888
|
G | A | 11 | a0001c0001t0001g0031a0001c0001t0002g0264a0001c0001t0002g0283others(8): Show | 11 | HG00544.hp1 HG00597.hp2 HG00673.hp2 others(8): Show |
intron_variant | MODIFIER | c.3398+3261G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142529888 | ||||||
| chr8:142530013
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3399-3282C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142530013 | ||||||
| chr8:142530014
|
G | A | 3 | a0001c0001t0001g0212a0001c0002t0002g0262a0001c0002t0012g0039 | 3 | HG02080.hp2 NA18966.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3399-3281G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142530014 | ||||||
| chr8:142530095
|
T | C | 116 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0093others(113): Show | 118 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.3399-3200T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142530095 | ||||||
| chr8:142530106
|
C | T | 54 | a0001c0001t0001g0031a0001c0001t0001g0293a0001c0001t0002g0037others(51): Show | 56 | HG00544.hp1 HG00597.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.3399-3189C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142530106 | ||||||
| chr8:142530109
|
TAGTG | T | 4 | a0001c0001t0001g0132a0001c0001t0001g0294a0001c0001t0014g0155others(1): Show | 4 | HG02258.hp1 HG02897.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-3185_3399-318 others(8): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142530109 | ||||||
| chr8:142530164
|
C | T | 1 | a0001c0003t0001g0076 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3399-3131C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142530164 | ||||||
| chr8:142530231
|
C | CGT | 4 | a0001c0001t0001g0132a0001c0001t0001g0294a0001c0001t0014g0155others(1): Show | 4 | HG02258.hp1 HG02897.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-3051_3399-305 others(6): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | INFO_REALIGN_3_PRIME | chr8 | 142530231 | |||||
| chr8:142530232
|
G | C | 1 | a0001c0001t0001g0227 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3399-3063G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142530232 | ||||||
| chr8:142530312
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3399-2983C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142530312 | ||||||
| chr8:142530456
|
G | T | 1 | a0001c0001t0001g0005 | 2 | HG01257.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.3399-2839G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142530456 | ||||||
| chr8:142530462
|
G | A | 63 | a0001c0001t0001g0031a0001c0001t0001g0132a0001c0001t0001g0293others(60): Show | 65 | HG00544.hp1 HG00597.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.3399-2833G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142530462 | ||||||
| chr8:142530508
|
C | G | 1 | a0001c0001t0002g0275 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.3399-2787C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142530508 | ||||||
| chr8:142530532
|
A | T | 65 | a0001c0001t0001g0031a0001c0001t0001g0132a0001c0001t0001g0293others(62): Show | 67 | HG00544.hp1 HG00597.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.3399-2763A>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142530532 | ||||||
| chr8:142530758
|
G | A | 4 | a0001c0004t0001g0168a0001c0004t0001g0209a0001c0004t0001g0210others(1): Show | 4 | NA18962.hp1 NA18963.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.3399-2537G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142530758 | ||||||
| chr8:142530766
|
G | A | 54 | a0001c0001t0001g0031a0001c0001t0001g0293a0001c0001t0002g0037others(51): Show | 56 | HG00544.hp1 HG00597.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.3399-2529G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142530766 | ||||||
| chr8:142530788
|
C | A | 252 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0031others(249): Show | 255 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.3399-2507C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142530788 | ||||||
| chr8:142530809
|
C | G | 53 | a0001c0001t0001g0031a0001c0001t0001g0293a0001c0001t0002g0037others(50): Show | 55 | HG00544.hp1 HG00597.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.3399-2486C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142530809 | ||||||
| chr8:142530839
|
G | A | 1 | a0001c0001t0013g0051 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3399-2456G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142530839 | ||||||
| chr8:142530940
|
G | A | 2 | a0004c0012t0001g0108a0004c0012t0001g0114 | 2 | HG00544.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.3399-2355G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142530940 | ||||||
| chr8:142530974
|
A | T | 1 | a0001c0007t0001g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3399-2321A>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142530974 | ||||||
| chr8:142531093
|
A | G | 1 | a0001c0001t0001g0267 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3399-2202A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142531093 | ||||||
| chr8:142531331
|
G | A | 2 | a0001c0001t0001g0142a0001c0001t0001g0144 | 2 | HG03490.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.3399-1964G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142531331 | ||||||
| chr8:142531350
|
C | T | 1 | a0001c0001t0002g0127 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3399-1945C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142531350 | ||||||
| chr8:142531450
|
T | A | 1 | a0001c0001t0003g0086 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3399-1845T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142531450 | ||||||
| chr8:142531620
|
G | C | 107 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0293others(104): Show | 109 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.3399-1675G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142531620 | ||||||
| chr8:142531677
|
T | C | 253 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0031others(250): Show | 256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.3399-1618T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142531677 | ||||||
| chr8:142531764
|
G | A | 1 | a0001c0011t0003g0072 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3399-1531G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142531764 | ||||||
| chr8:142531972
|
G | C | 1 | a0001c0002t0002g0063 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3399-1323G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142531972 | ||||||
| chr8:142531973
|
G | T | 1 | a0001c0002t0002g0063 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3399-1322G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142531973 | ||||||
| chr8:142531977
|
G | C | 1 | a0001c0002t0002g0063 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3399-1318G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142531977 | ||||||
| chr8:142531978
|
A | T | 1 | a0001c0002t0002g0063 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3399-1317A>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142531978 | ||||||
| chr8:142531979
|
G | A | 1 | a0001c0002t0002g0063 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3399-1316G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142531979 | ||||||
| chr8:142531981
|
A | T | 1 | a0001c0002t0002g0063 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3399-1314A>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142531981 | ||||||
| chr8:142531987
|
G | A | 1 | a0001c0002t0002g0063 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3399-1308G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142531987 | ||||||
| chr8:142531989
|
G | A | 1 | a0001c0002t0002g0063 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3399-1306G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142531989 | ||||||
| chr8:142531990
|
T | C | 1 | a0001c0002t0002g0063 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3399-1305T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142531990 | ||||||
| chr8:142531991
|
G | A | 1 | a0002c0020t0002g0053 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3399-1304G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142531991 | ||||||
| chr8:142531991
|
G | C | 1 | a0001c0002t0002g0063 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3399-1304G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142531991 | ||||||
| chr8:142532000
|
G | C | 1 | a0001c0002t0002g0063 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3399-1295G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142532000 | ||||||
| chr8:142532004
|
C | G | 1 | a0001c0002t0002g0063 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3399-1291C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142532004 | ||||||
| chr8:142532007
|
T | A | 1 | a0001c0002t0002g0063 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3399-1288T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142532007 | ||||||
| chr8:142532008
|
T | G | 1 | a0001c0002t0002g0063 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3399-1287T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142532008 | ||||||
| chr8:142532009
|
G | C | 1 | a0001c0002t0002g0063 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3399-1286G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142532009 | ||||||
| chr8:142532009
|
G | T | 1 | a0001c0001t0002g0193 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3399-1286G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142532009 | ||||||
| chr8:142532010
|
T | C | 1 | a0001c0002t0002g0063 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3399-1285T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142532010 | ||||||
| chr8:142532013
|
T | A | 1 | a0001c0002t0002g0063 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3399-1282T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142532013 | ||||||
| chr8:142532014
|
G | A | 1 | a0001c0002t0002g0063 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3399-1281G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142532014 | ||||||
| chr8:142532016
|
C | G | 1 | a0001c0002t0002g0063 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3399-1279C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142532016 | ||||||
| chr8:142532017
|
A | G | 1 | a0001c0002t0002g0063 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3399-1278A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142532017 | ||||||
| chr8:142532018
|
G | T | 1 | a0001c0002t0002g0063 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3399-1277G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142532018 | ||||||
| chr8:142532038
|
T | C | 1 | a0001c0002t0002g0063 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3399-1257T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142532038 | ||||||
| chr8:142532045
|
T | A | 1 | a0001c0002t0002g0063 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3399-1250T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142532045 | ||||||
| chr8:142532051
|
C | G | 1 | a0001c0002t0002g0063 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3399-1244C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142532051 | ||||||
| chr8:142532058
|
G | C | 1 | a0001c0002t0002g0063 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3399-1237G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142532058 | ||||||
| chr8:142532217
|
T | C | 129 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0100others(126): Show | 131 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.3399-1078T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142532217 | ||||||
| chr8:142532246
|
G | A | 4 | a0001c0001t0001g0132a0001c0001t0001g0294a0001c0001t0014g0155others(1): Show | 4 | HG02258.hp1 HG02897.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-1049G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142532246 | ||||||
| chr8:142532257
|
G | A | 1 | a0001c0008t0003g0013 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3399-1038G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142532257 | ||||||
| chr8:142532328
|
G | A | 1 | a0001c0013t0001g0096 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3399-967G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142532328 | ||||||
| chr8:142532367
|
G | C | 1 | a0001c0001t0001g0139 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3399-928G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142532367 | ||||||
| chr8:142532431
|
A | G | 20 | a0001c0001t0001g0119a0001c0001t0003g0089a0001c0004t0001g0038others(17): Show | 20 | HG00408.hp2 HG00597.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.3399-864A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142532431 | ||||||
| chr8:142532520
|
G | A | 3 | a0001c0007t0001g0067a0001c0007t0001g0068a0001c0007t0001g0069 | 3 | HG01891.hp1 HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3399-775G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142532520 | ||||||
| chr8:142532610
|
T | C | 56 | a0001c0001t0001g0002a0001c0001t0002g0002a0001c0001t0002g0014others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.3399-685T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142532610 | ||||||
| chr8:142532615
|
T | C | 10 | a0001c0001t0001g0119a0001c0004t0001g0038a0001c0004t0001g0103others(7): Show | 10 | HG00408.hp2 NA18952.hp2 NA18962.hp1 others(7): Show |
intron_variant | MODIFIER | c.3399-680T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142532615 | ||||||
| chr8:142532673
|
C | T | 1 | a0001c0003t0003g0137 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3399-622C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142532673 | ||||||
| chr8:142532701
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3399-594C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142532701 | ||||||
| chr8:142532807
|
T | C | 1 | a0001c0001t0013g0051 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3399-488T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142532807 | ||||||
| chr8:142533117
|
T | C | 142 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0034others(139): Show | 142 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.3399-178T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142533117 | ||||||
| chr8:142533157
|
T | C | 1 | a0001c0001t0002g0143 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3399-138T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142533157 | ||||||
| chr8:142533239
|
A | G | 93 | a0001c0001t0001g0002a0001c0001t0001g0088a0001c0001t0001g0095others(90): Show | 94 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.3399-56A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142533239 | ||||||
| chr8:142533261
|
C | T | 3 | a0001c0003t0001g0073a0001c0003t0001g0135a0001c0003t0001g0187 | 3 | HG02970.hp1 HG03516.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.3399-34C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142533261 | ||||||
| chr8:142533262
|
G | A | 155 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0034others(152): Show | 155 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.3399-33G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142533262 | ||||||
| chr8:142533280
|
A | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0034others(157): Show | 160 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.3399-15A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 24/30 | chr8 | 142533280 | ||||||
| chr8:142533517
|
G | A | 1 | a0001c0003t0003g0137 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3570+51G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142533517 | ||||||
| chr8:142533519
|
C | T | 4 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(1): Show | 4 | HG01109.hp2 HG02886.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.3570+53C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142533519 | ||||||
| chr8:142533549
|
G | C | 4 | a0001c0004t0001g0249a0001c0004t0003g0250a0001c0011t0002g0149others(1): Show | 4 | HG02300.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3570+83G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142533549 | ||||||
| chr8:142533565
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3570+99G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142533565 | ||||||
| chr8:142533669
|
A | G | 1 | a0001c0004t0003g0250 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3570+203A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142533669 | ||||||
| chr8:142533739
|
A | G | 4 | a0001c0001t0001g0132a0001c0001t0001g0294a0001c0001t0014g0155others(1): Show | 4 | HG02258.hp1 HG02897.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3570+273A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142533739 | ||||||
| chr8:142533742
|
G | A | 47 | a0001c0001t0001g0002a0001c0001t0002g0002a0001c0001t0002g0014others(44): Show | 47 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.3570+276G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142533742 | ||||||
| chr8:142533743
|
G | A | 1 | a0001c0008t0002g0232 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3570+277G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142533743 | ||||||
| chr8:142533908
|
G | A | 1 | a0001c0001t0013g0051 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3570+442G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142533908 | ||||||
| chr8:142533956
|
G | A | 1 | a0001c0003t0001g0097 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3570+490G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142533956 | ||||||
| chr8:142534141
|
A | G | 253 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0031others(250): Show | 256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.3570+675A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142534141 | ||||||
| chr8:142534163
|
A | G | 155 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0034others(152): Show | 155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.3570+697A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142534163 | ||||||
| chr8:142534241
|
C | A | 4 | a0001c0004t0001g0249a0001c0004t0003g0250a0001c0011t0002g0149others(1): Show | 4 | HG02300.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3570+775C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142534241 | ||||||
| chr8:142534345
|
T | C | 4 | a0001c0001t0001g0132a0001c0001t0001g0294a0001c0001t0014g0155others(1): Show | 4 | HG02258.hp1 HG02897.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3570+879T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142534345 | ||||||
| chr8:142534358
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3570+892G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142534358 | ||||||
| chr8:142534540
|
T | C | 67 | a0001c0001t0001g0002a0001c0001t0001g0100a0001c0001t0001g0119others(64): Show | 67 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.3570+1074T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142534540 | ||||||
| chr8:142534732
|
G | A | 1 | a0001c0001t0002g0045 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.3570+1266G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142534732 | ||||||
| chr8:142535398
|
C | T | 3 | a0001c0003t0001g0070a0001c0010t0004g0244a0001c0010t0004g0287 | 3 | HG02886.hp1 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3571-1589C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142535398 | ||||||
| chr8:142535466
|
G | T | 4 | a0001c0004t0001g0249a0001c0004t0003g0250a0001c0011t0002g0149others(1): Show | 4 | HG02300.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3571-1521G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142535466 | ||||||
| chr8:142535786
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3571-1201G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142535786 | ||||||
| chr8:142535868
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3571-1119G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142535868 | ||||||
| chr8:142535989
|
C | T | 1 | a0001c0001t0001g0267 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3571-998C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142535989 | ||||||
| chr8:142536076
|
G | A | 1 | a0001c0013t0003g0049 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3571-911G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142536076 | ||||||
| chr8:142536235
|
T | TG | 158 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0034others(155): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.3571-752_3571-751i others(3): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142536235 | ||||||
| chr8:142536238
|
T | A | 158 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0034others(155): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.3571-749T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142536238 | ||||||
| chr8:142536239
|
A | C | 158 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0034others(155): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.3571-748A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142536239 | ||||||
| chr8:142536244
|
G | A | 1 | a0001c0001t0002g0185 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3571-743G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142536244 | ||||||
| chr8:142536616
|
C | T | 4 | a0001c0001t0001g0169a0001c0001t0001g0216a0001c0001t0001g0220others(1): Show | 4 | HG01099.hp2 HG01952.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.3571-371C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142536616 | ||||||
| chr8:142536699
|
A | T | 1 | a0001c0002t0002g0124 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.3571-288A>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142536699 | ||||||
| chr8:142536765
|
G | A | 1 | a0001c0001t0002g0189 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3571-222G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142536765 | ||||||
| chr8:142536905
|
C | T | 4 | a0001c0001t0001g0132a0001c0001t0001g0294a0001c0001t0014g0155others(1): Show | 4 | HG02258.hp1 HG02897.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3571-82C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 25/30 | chr8 | 142536905 | ||||||
| chr8:142537218
|
C | A | 1 | a0001c0033t0003g0027 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3666+136C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142537218 | ||||||
| chr8:142537221
|
T | A | 1 | a0001c0033t0003g0027 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3666+139T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142537221 | ||||||
| chr8:142537239
|
G | A | 14 | a0001c0001t0001g0132a0001c0001t0001g0186a0001c0001t0001g0293others(11): Show | 16 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.3666+157G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142537239 | ||||||
| chr8:142537308
|
C | T | 3 | a0001c0007t0001g0067a0001c0007t0001g0068a0001c0007t0001g0069 | 3 | HG01891.hp1 HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3666+226C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142537308 | ||||||
| chr8:142537318
|
C | A | 1 | a0001c0001t0001g0284 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3666+236C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142537318 | ||||||
| chr8:142537356
|
G | C | 11 | a0001c0003t0001g0070a0001c0003t0003g0131a0001c0007t0001g0067others(8): Show | 11 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.3666+274G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142537356 | ||||||
| chr8:142537420
|
C | T | 3 | a0001c0001t0001g0088a0001c0001t0001g0206a0010c0023t0001g0166 | 3 | HG00140.hp1 HG00280.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.3666+338C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142537420 | ||||||
| chr8:142537439
|
C | G | 1 | a0003c0009t0002g0296 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3666+357C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142537439 | ||||||
| chr8:142537523
|
A | G | 3 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236 | 3 | HG01109.hp2 HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3666+441A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142537523 | ||||||
| chr8:142537548
|
C | T | 8 | a0001c0002t0002g0015a0001c0002t0002g0028a0001c0002t0002g0115others(5): Show | 8 | HG00597.hp2 HG02040.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.3666+466C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142537548 | ||||||
| chr8:142537561
|
C | A | 13 | a0001c0001t0001g0132a0001c0001t0001g0293a0001c0001t0001g0294others(10): Show | 15 | HG02109.hp2 HG02145.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.3666+479C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142537561 | ||||||
| chr8:142537740
|
C | T | 1 | a0001c0011t0002g0149 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3666+658C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142537740 | ||||||
| chr8:142537753
|
T | C | 253 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0031others(250): Show | 256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.3666+671T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142537753 | ||||||
| chr8:142537786
|
G | A | 2 | a0001c0008t0002g0061a0001c0008t0002g0062 | 2 | NA18997.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.3666+704G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142537786 | ||||||
| chr8:142537798
|
A | C | 1 | a0001c0003t0003g0137 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3666+716A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142537798 | ||||||
| chr8:142537798
|
A | G | 1 | a0001c0002t0002g0194 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3666+716A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142537798 | ||||||
| chr8:142537923
|
C | G | 1 | a0001c0001t0001g0029 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.3666+841C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142537923 | ||||||
| chr8:142538061
|
T | C | 70 | a0001c0001t0001g0031a0001c0001t0001g0095a0001c0001t0001g0234others(67): Show | 71 | HG00544.hp1 HG00597.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.3666+979T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142538061 | ||||||
| chr8:142538114
|
G | C | 103 | a0001c0001t0001g0025a0001c0001t0001g0034a0001c0001t0001g0040others(100): Show | 105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.3666+1032G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142538114 | ||||||
| chr8:142538125
|
C | T | 86 | a0001c0001t0001g0025a0001c0001t0001g0034a0001c0001t0001g0040others(83): Show | 86 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.3666+1043C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142538125 | ||||||
| chr8:142538204
|
C | T | 1 | a0001c0013t0001g0096 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3666+1122C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142538204 | ||||||
| chr8:142538232
|
G | A | 1 | a0001c0015t0001g0024 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3667-1142G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142538232 | ||||||
| chr8:142538234
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3667-1140G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142538234 | ||||||
| chr8:142538254
|
C | T | 13 | a0001c0001t0001g0132a0001c0001t0001g0293a0001c0001t0001g0294others(10): Show | 15 | HG02109.hp2 HG02145.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.3667-1120C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142538254 | ||||||
| chr8:142538292
|
C | T | 1 | a0001c0003t0003g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3667-1082C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142538292 | ||||||
| chr8:142538342
|
C | A | 1 | a0001c0002t0002g0217 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3667-1032C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142538342 | ||||||
| chr8:142538365
|
C | T | 1 | a0001c0013t0001g0096 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3667-1009C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142538365 | ||||||
| chr8:142538375
|
G | A | 1 | a0003c0009t0002g0296 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3667-999G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142538375 | ||||||
| chr8:142538380
|
G | A | 1 | a0001c0001t0013g0051 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3667-994G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142538380 | ||||||
| chr8:142538391
|
C | A | 49 | a0001c0001t0001g0031a0001c0001t0002g0081a0001c0001t0002g0197others(46): Show | 49 | HG00544.hp1 HG00597.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.3667-983C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142538391 | ||||||
| chr8:142538417
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.3667-957C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142538417 | ||||||
| chr8:142538516
|
C | T | 1 | a0001c0001t0003g0086 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3667-858C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142538516 | ||||||
| chr8:142538518
|
C | T | 1 | a0001c0001t0002g0264 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3667-856C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142538518 | ||||||
| chr8:142538536
|
G | A | 1 | a0001c0001t0003g0004 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.3667-838G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142538536 | ||||||
| chr8:142538687
|
C | T | 44 | a0001c0001t0001g0002a0001c0001t0002g0002a0001c0001t0002g0014others(41): Show | 44 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.3667-687C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142538687 | ||||||
| chr8:142538750
|
C | T | 1 | a0001c0002t0002g0207 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3667-624C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142538750 | ||||||
| chr8:142538784
|
C | T | 4 | a0001c0001t0001g0132a0001c0001t0001g0294a0001c0001t0014g0155others(1): Show | 4 | HG02258.hp1 HG02897.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3667-590C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142538784 | ||||||
| chr8:142538785
|
C | T | 170 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0034others(167): Show | 173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.3667-589C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142538785 | ||||||
| chr8:142539032
|
C | T | 79 | a0001c0001t0001g0031a0001c0001t0001g0095a0001c0001t0001g0132others(76): Show | 82 | HG00544.hp1 HG00597.hp2 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.3667-342C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142539032 | ||||||
| chr8:142539039
|
G | A | 41 | a0001c0001t0001g0031a0001c0001t0002g0197a0001c0001t0002g0205others(38): Show | 41 | HG00544.hp1 HG00597.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.3667-335G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142539039 | ||||||
| chr8:142539051
|
C | T | 1 | a0001c0002t0002g0207 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3667-323C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142539051 | ||||||
| chr8:142539055
|
G | A | 1 | a0001c0014t0002g0082 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3667-319G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142539055 | ||||||
| chr8:142539075
|
C | G | 64 | a0001c0001t0001g0025a0001c0001t0001g0034a0001c0001t0001g0040others(61): Show | 64 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.3667-299C>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142539075 | ||||||
| chr8:142539075
|
C | T | 5 | a0001c0003t0003g0026a0001c0003t0003g0094a0001c0008t0003g0013others(2): Show | 5 | HG01255.hp1 HG02451.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.3667-299C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142539075 | ||||||
| chr8:142539081
|
C | A | 11 | a0001c0003t0001g0070a0001c0003t0003g0131a0001c0007t0001g0067others(8): Show | 11 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.3667-293C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142539081 | ||||||
| chr8:142539109
|
C | T | 1 | a0001c0013t0001g0096 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3667-265C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142539109 | ||||||
| chr8:142539152
|
G | A | 48 | a0001c0001t0001g0002a0001c0001t0002g0002a0001c0001t0002g0014others(45): Show | 48 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.3667-222G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142539152 | ||||||
| chr8:142539209
|
A | G | 214 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0034others(211): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.3667-165A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142539209 | ||||||
| chr8:142539298
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3667-76C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142539298 | ||||||
| chr8:142539314
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3667-60G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 26/30 | chr8 | 142539314 | ||||||
| chr8:142539461
|
T | C | 253 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0031others(250): Show | 256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.3706+48T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142539461 | ||||||
| chr8:142539597
|
C | T | 1 | a0001c0003t0003g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3706+184C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142539597 | ||||||
| chr8:142539601
|
C | T | 1 | a0001c0001t0013g0051 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3706+188C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142539601 | ||||||
| chr8:142539612
|
CCT | C | 3 | a0001c0003t0001g0070a0001c0010t0004g0244a0001c0010t0004g0287 | 3 | HG02886.hp1 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3706+200_3706+201d others(4): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142539612 | ||||||
| chr8:142539789
|
C | A | 253 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0031others(250): Show | 256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.3706+376C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142539789 | ||||||
| chr8:142539827
|
T | C | 1 | a0001c0003t0001g0187 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3706+414T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142539827 | ||||||
| chr8:142539947
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3706+534C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142539947 | ||||||
| chr8:142539991
|
G | A | 2 | a0001c0001t0001g0075a0001c0017t0001g0008 | 2 | HG02647.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3706+578G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142539991 | ||||||
| chr8:142540000
|
A | G | 104 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0119others(101): Show | 107 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.3706+587A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142540000 | ||||||
| chr8:142540036
|
A | C | 1 | a0001c0010t0004g0287 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3706+623A>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142540036 | ||||||
| chr8:142540082
|
T | C | 1 | a0001c0001t0002g0193 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3706+669T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142540082 | ||||||
| chr8:142540215
|
G | A | 1 | a0001c0003t0003g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3706+802G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142540215 | ||||||
| chr8:142540288
|
G | C | 1 | a0001c0013t0001g0096 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3706+875G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142540288 | ||||||
| chr8:142540337
|
G | A | 1 | a0001c0011t0002g0149 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3706+924G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142540337 | ||||||
| chr8:142540430
|
C | T | 1 | a0001c0007t0001g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3706+1017C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142540430 | ||||||
| chr8:142540514
|
G | T | 2 | a0001c0001t0002g0014a0001c0001t0002g0043 | 2 | NA19057.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.3706+1101G>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142540514 | ||||||
| chr8:142540531
|
G | A | 50 | a0001c0001t0001g0031a0001c0001t0002g0081a0001c0001t0002g0197others(47): Show | 50 | HG00544.hp1 HG00597.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.3706+1118G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142540531 | ||||||
| chr8:142540542
|
C | CG | 6 | a0001c0001t0001g0079a0001c0001t0001g0174a0001c0001t0002g0275others(3): Show | 6 | HG01175.hp1 HG01255.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.3706+1133dupG | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | INFO_REALIGN_3_PRIME | chr8 | 142540542 | |||||
| chr8:142540607
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3706+1194C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142540607 | ||||||
| chr8:142540649
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3706+1236G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142540649 | ||||||
| chr8:142540752
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3707-1189G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142540752 | ||||||
| chr8:142540887
|
G | A | 1 | a0010c0023t0001g0166 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3707-1054G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142540887 | ||||||
| chr8:142540894
|
T | C | 89 | a0001c0001t0001g0025a0001c0001t0001g0034a0001c0001t0001g0040others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.3707-1047T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142540894 | ||||||
| chr8:142540904
|
A | G | 1 | a0001c0001t0013g0051 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3707-1037A>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142540904 | ||||||
| chr8:142541050
|
G | C | 1 | a0001c0013t0001g0096 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3707-891G>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142541050 | ||||||
| chr8:142541056
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3707-885C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142541056 | ||||||
| chr8:142541057
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3707-884G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142541057 | ||||||
| chr8:142541097
|
C | T | 49 | a0001c0001t0002g0081a0001c0001t0002g0197a0001c0001t0002g0301others(46): Show | 49 | HG00597.hp2 HG00609.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.3707-844C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142541097 | ||||||
| chr8:142541136
|
C | T | 1 | a0001c0001t0003g0004 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.3707-805C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142541136 | ||||||
| chr8:142541226
|
C | T | 10 | a0001c0001t0001g0293a0001c0001t0001g0299a0001c0001t0003g0231others(7): Show | 12 | HG02109.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.3707-715C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142541226 | ||||||
| chr8:142541311
|
G | A | 1 | a0001c0013t0001g0096 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3707-630G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142541311 | ||||||
| chr8:142541431
|
C | T | 2 | a0001c0001t0002g0060a0001c0001t0002g0065 | 2 | HG03834.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.3707-510C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142541431 | ||||||
| chr8:142541447
|
G | A | 1 | a0001c0008t0002g0232 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3707-494G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142541447 | ||||||
| chr8:142541497
|
G | A | 2 | a0001c0008t0002g0061a0001c0008t0002g0062 | 2 | NA18997.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.3707-444G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142541497 | ||||||
| chr8:142541547
|
G | A | 1 | a0001c0011t0003g0072 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3707-394G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142541547 | ||||||
| chr8:142541681
|
C | T | 6 | a0001c0007t0001g0067a0001c0007t0001g0068a0001c0007t0001g0069others(3): Show | 6 | HG01891.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.3707-260C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142541681 | ||||||
| chr8:142541691
|
C | T | 2 | a0001c0003t0001g0073a0001c0003t0001g0135 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3707-250C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142541691 | ||||||
| chr8:142541840
|
C | T | 3 | a0001c0014t0002g0082a0001c0014t0002g0083a0001c0034t0002g0071 | 3 | HG01192.hp2 HG01975.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3707-101C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142541840 | ||||||
| chr8:142541889
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3707-52G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142541889 | ||||||
| chr8:142541928
|
G | A | 1 | a0001c0001t0002g0134 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3707-13G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 27/30 | chr8 | 142541928 | ||||||
| chr8:142542667
|
G | A | 3 | a0001c0001t0001g0293a0003c0009t0002g0001a0003c0009t0002g0295 | 5 | HG02145.hp1 HG02257.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.4413+20G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 28/30 | chr8 | 142542667 | ||||||
| chr8:142542788
|
C | A | 1 | a0001c0001t0003g0089 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4413+141C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 28/30 | chr8 | 142542788 | ||||||
| chr8:142542856
|
C | T | 1 | a0001c0001t0013g0051 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4413+209C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 28/30 | chr8 | 142542856 | ||||||
| chr8:142542949
|
C | T | 1 | a0001c0001t0002g0045 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.4413+302C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 28/30 | chr8 | 142542949 | ||||||
| chr8:142543112
|
C | T | 2 | a0001c0002t0002g0126a0001c0002t0002g0128 | 2 | HG01928.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.4414-291C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 28/30 | chr8 | 142543112 | ||||||
| chr8:142543320
|
T | C | 1 | a0001c0001t0001g0278 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4414-83T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 28/30 | chr8 | 142543320 | ||||||
| chr8:142543328
|
T | A | 1 | a0001c0024t0001g0085 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4414-75T>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 28/30 | chr8 | 142543328 | ||||||
| chr8:142543460
|
C | A | 1 | a0002c0005t0001g0021 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.4449+22C>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 29/30 | chr8 | 142543460 | ||||||
| chr8:142543566
|
T | C | 7 | a0001c0001t0002g0074a0001c0001t0002g0081a0001c0006t0002g0303others(4): Show | 7 | HG01192.hp2 HG01975.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.4450-35T>C | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 29/30 | chr8 | 142543566 | ||||||
| chr8:142543578
|
C | T | 1 | a0001c0024t0001g0085 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4450-23C>T | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 29/30 | chr8 | 142543578 | ||||||
| chr8:142543873
|
G | A | 1 | a0001c0002t0002g0118 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.4557+165G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 30/30 | chr8 | 142543873 | ||||||
| chr8:142543918
|
G | A | 1 | a0001c0003t0003g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4557+210G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 30/30 | chr8 | 142543918 | ||||||
| chr8:142544057
|
G | A | 1 | a0001c0001t0013g0051 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4558-163G>A | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 30/30 | chr8 | 142544057 | ||||||
| chr8:142544085
|
T | TCCTGTCC | 9 | a0001c0001t0001g0075a0001c0001t0001g0095a0001c0001t0001g0235others(6): Show | 9 | HG02572.hp2 HG02647.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.4558-118_4558-112d others(9): Show |
ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr8 | 142544085 | |||||
| chr8:142544113
|
T | G | 1 | a0001c0001t0002g0301 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.4558-107T>G | ADGRB1 | ENSG00000181790.13 | transcript | ENST00000517894.6 | protein_coding | 30/30 | chr8 | 142544113 |