| geneid | 221395 |
|---|---|
| ensemblid | ENSG00000069122.19 |
| hgncid | 19030 |
| symbol | ADGRF5 |
| name | adhesion G protein-coupled receptor F5 |
| refseq_nuc | NM_001098518.2 |
| refseq_prot | NP_001091988.1 |
| ensembl_nuc | ENST00000283296.12 |
| ensembl_prot | ENSP00000283296.7 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 46852522 |
| end | 46921938 |
| strand | - |
| ver | v1.2 |
| region | chr6:46852522-46921938 |
| region5000 | chr6:46847522-46926938 |
| regionname0 | ADGRF5_chr6_46852522_46921938 |
| regionname5000 | ADGRF5_chr6_46847522_46926938 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1346 | 167 | 13 | 41 | 82 | 9 | 22 | 62 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0002 | 0/0 | 1346 | 134 | 27 | 15 | 74 | 4 | 14 | 55 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0003 | 1/0 | 1346 | 52 | 39 | 8 | 1 | 1 | 2 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0004 | 0/0 | 1346 | 11 | 10 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0005 | 0/1 | 1346 | 2 | 0 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0006 | 0/0 | 1346 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0007 | 0/0 | 1346 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0008 | 0/0 | 1346 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0009 | 0/0 | 1346 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0010 | 0/0 | 1346 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0011 | 0/0 | 1346 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0012 | 0/0 | 1346 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0013 | 0/0 | 1346 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0014 | 0/0 | 1346 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0015 | 0/0 | 1346 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0016 | 0/0 | 1346 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0017 | 0/0 | 1346 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0018 | 0/0 | 1346 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0019 | 0/0 | 1346 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0020 | 0/0 | 1346 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 4041 | 133 | 11 | 39 | 63 | 7 | 13 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0002 | 0/0 | 4041 | 114 | 19 | 13 | 64 | 4 | 14 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0003 | 0/0 | 4041 | 44 | 36 | 5 | 1 | 0 | 2 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0004 | 0/0 | 4041 | 28 | 1 | 2 | 14 | 2 | 9 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0005 | 0/0 | 4041 | 10 | 2 | 1 | 7 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0006 | 0/0 | 4041 | 7 | 6 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0007 | 1/0 | 4041 | 6 | 1 | 3 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0008 | 0/0 | 4041 | 5 | 5 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0009 | 0/0 | 4041 | 3 | 2 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0010 | 0/0 | 4041 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0011 | 0/0 | 4041 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0012 | 0/0 | 4041 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0013 | 0/0 | 4041 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0014 | 0/0 | 4041 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0015 | 0/1 | 4041 | 2 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0016 | 0/0 | 4041 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0017 | 0/0 | 4041 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0018 | 0/0 | 4041 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0019 | 0/0 | 4041 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0020 | 0/0 | 4041 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0021 | 0/0 | 4041 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0022 | 0/0 | 4041 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0023 | 0/0 | 4041 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0024 | 0/0 | 4041 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0025 | 0/0 | 4041 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0026 | 0/0 | 4041 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0027 | 0/0 | 4041 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0028 | 0/0 | 4041 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0029 | 0/0 | 4041 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0030 | 0/0 | 4041 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0031 | 0/0 | 4041 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0032 | 0/0 | 4041 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0033 | 0/0 | 4041 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0034 | 0/0 | 4041 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| c0035 | 0/0 | 4041 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 1721 | 146 | 13 | 32 | 71 | 7 | 22 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0002 | 0/0 | 1721 | 85 | 14 | 11 | 47 | 2 | 11 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0003 | 0/0 | 1721 | 45 | 10 | 5 | 24 | 2 | 4 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0004 | 0/0 | 1720 | 32 | 24 | 5 | 1 | 0 | 2 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0005 | 0/0 | 1721 | 24 | 0 | 11 | 9 | 2 | 2 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0006 | 0/0 | 1721 | 9 | 8 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0007 | 1/0 | 1721 | 5 | 1 | 2 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0008 | 0/0 | 1720 | 4 | 4 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0009 | 0/0 | 1721 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0010 | 0/0 | 1720 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0011 | 0/0 | 1721 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0012 | 0/0 | 1721 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0013 | 0/0 | 1720 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0014 | 0/0 | 1771 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0015 | 0/0 | 1721 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0016 | 0/0 | 1721 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0017 | 0/0 | 1720 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0018 | 0/0 | 1721 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0019 | 0/0 | 1687 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0020 | 0/0 | 1721 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0021 | 0/0 | 1721 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0022 | 0/0 | 1721 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0023 | 0/0 | 1721 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0024 | 0/0 | 1721 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0025 | 0/0 | 1721 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0026 | 0/0 | 1721 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0027 | 0/0 | 1721 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0028 | 0/0 | 1721 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0029 | 0/0 | 1720 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0030 | 0/0 | 1721 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0031 | 0/0 | 1721 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0032 | 0/0 | 1721 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| t0033 | 0/0 | 1721 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0145 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0216 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0363 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0369 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0370 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0373 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0374 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0376 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| 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 | 0/0 | 4041 | 133 | 11 | 39 | 63 | 7 | 13 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0001c0004 | 0/0 | 4041 | 28 | 1 | 2 | 14 | 2 | 9 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0001c0012 | 0/0 | 4041 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0001c0013 | 0/0 | 4041 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0001c0019 | 0/0 | 4041 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0001c0028 | 0/0 | 4041 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0002c0002 | 0/0 | 4041 | 114 | 19 | 13 | 64 | 4 | 14 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0002c0005 | 0/0 | 4041 | 10 | 2 | 1 | 7 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0002c0006 | 0/0 | 4041 | 7 | 6 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0002c0014 | 0/0 | 4041 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0002c0017 | 0/0 | 4041 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0003c0003 | 0/0 | 4041 | 44 | 36 | 5 | 1 | 0 | 2 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0003c0007 | 1/0 | 4041 | 6 | 1 | 3 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0003c0025 | 0/0 | 4041 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0003c0034 | 0/0 | 4041 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0004c0008 | 0/0 | 4041 | 5 | 5 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0004c0009 | 0/0 | 4041 | 3 | 2 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0004c0011 | 0/0 | 4041 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0004c0029 | 0/0 | 4041 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0005c0015 | 0/1 | 4041 | 2 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0006c0010 | 0/0 | 4041 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0007c0016 | 0/0 | 4041 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0008c0035 | 0/0 | 4041 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0009c0023 | 0/0 | 4041 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0010c0032 | 0/0 | 4041 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0011c0018 | 0/0 | 4041 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0012c0027 | 0/0 | 4041 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0013c0030 | 0/0 | 4041 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0014c0020 | 0/0 | 4041 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0015c0026 | 0/0 | 4041 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0016c0021 | 0/0 | 4041 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0017c0031 | 0/0 | 4041 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0018c0024 | 0/0 | 4041 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0019c0033 | 0/0 | 4041 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0020c0022 | 0/0 | 4041 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5761 | 110 | 10 | 30 | 52 | 7 | 11 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0001c0001t0002 | 0/0 | 5761 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0001c0001t0005 | 0/0 | 5761 | 18 | 0 | 9 | 8 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0001c0001t0015 | 0/0 | 5761 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0001c0001t0023 | 0/0 | 5761 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0001c0001t0032 | 0/0 | 5761 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0001c0001t0033 | 0/0 | 5761 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0001c0004t0001 | 0/0 | 5761 | 21 | 0 | 1 | 12 | 0 | 8 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0001c0004t0005 | 0/0 | 5761 | 5 | 0 | 1 | 1 | 2 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0001c0004t0018 | 0/0 | 5761 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0001c0004t0030 | 0/0 | 5761 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0001c0012t0001 | 0/0 | 5761 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0001c0013t0001 | 0/0 | 5761 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0001c0019t0001 | 0/0 | 5761 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0001c0028t0006 | 0/0 | 5761 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0002c0002t0002 | 0/0 | 5761 | 67 | 11 | 8 | 37 | 2 | 9 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0002c0002t0003 | 0/0 | 5761 | 38 | 4 | 5 | 23 | 2 | 4 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0002c0002t0012 | 0/0 | 5761 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0002c0002t0016 | 0/0 | 5761 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0002c0002t0020 | 0/0 | 5761 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0002c0002t0021 | 0/0 | 5761 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0002c0002t0022 | 0/0 | 5761 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0002c0002t0025 | 0/0 | 5761 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0002c0002t0026 | 0/0 | 5761 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0002c0002t0031 | 0/0 | 5761 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0002c0005t0002 | 0/0 | 5761 | 8 | 1 | 1 | 6 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0002c0005t0003 | 0/0 | 5761 | 2 | 1 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0002c0006t0002 | 0/0 | 5761 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0002c0006t0003 | 0/0 | 5761 | 5 | 5 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0002c0014t0002 | 0/0 | 5761 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0002c0017t0002 | 0/0 | 5761 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0003c0003t0004 | 0/0 | 5760 | 28 | 21 | 4 | 1 | 0 | 2 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0003c0003t0006 | 0/0 | 5761 | 6 | 5 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0003c0003t0008 | 0/0 | 5760 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0003c0003t0011 | 0/0 | 5761 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0003c0003t0013 | 0/0 | 5760 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0003c0003t0014 | 0/0 | 5811 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0003c0003t0017 | 0/0 | 5760 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0003c0003t0019 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0003c0007t0004 | 0/0 | 5760 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0003c0007t0007 | 1/0 | 5761 | 5 | 1 | 2 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0003c0025t0004 | 0/0 | 5760 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0003c0034t0008 | 0/0 | 5760 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0004c0008t0006 | 0/0 | 5761 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0004c0008t0009 | 0/0 | 5761 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0004c0008t0027 | 0/0 | 5761 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0004c0009t0010 | 0/0 | 5760 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0004c0009t0029 | 0/0 | 5760 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0004c0011t0006 | 0/0 | 5761 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0004c0011t0024 | 0/0 | 5761 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0004c0029t0028 | 0/0 | 5761 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0005c0015t0001 | 0/1 | 5761 | 2 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0006c0010t0001 | 0/0 | 5761 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0007c0016t0001 | 0/0 | 5761 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0008c0035t0002 | 0/0 | 5761 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0009c0023t0002 | 0/0 | 5761 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0010c0032t0004 | 0/0 | 5760 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0011c0018t0001 | 0/0 | 5761 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0012c0027t0002 | 0/0 | 5761 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0013c0030t0005 | 0/0 | 5761 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0014c0020t0001 | 0/0 | 5761 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0015c0026t0001 | 0/0 | 5761 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0016c0021t0001 | 0/0 | 5761 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0017c0031t0004 | 0/0 | 5760 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0018c0024t0002 | 0/0 | 5761 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0019c0033t0014 | 0/0 | 5811 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| a0020c0022t0001 | 0/0 | 5761 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | copy fasta | chr6 | 46847522 | 46926938 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0373 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0374 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0376 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0001g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0002g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0005g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0005g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0005g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0005g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0005g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0005g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0005g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0005g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0005g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0005g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0015g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0023g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0032g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0001t0033g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0004t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0004t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0004t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0004t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0004t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0004t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0004t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0004t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0004t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0004t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0004t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0004t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0004t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0004t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0004t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0004t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0004t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0004t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0004t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0004t0005g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0004t0005g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0004t0005g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0004t0005g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0004t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0004t0018g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0004t0030g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0012t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0012t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0013t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0013t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0019t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0001c0028t0006g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0363 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0002g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0012g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0012g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0016g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0020g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0021g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0022g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0025g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0026g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0002t0031g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0005t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0005t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0005t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0005t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0005t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0005t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0005t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0005t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0005t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0005t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0006t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0006t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0006t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0006t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0006t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0006t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0006t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0014t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0014t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0002c0017t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0004g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0004g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0004g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0004g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0004g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0004g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0004g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0004g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0006g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0006g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0006g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0006g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0006g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0008g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0008g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0008g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0011g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0011g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0013g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0013g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0014g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0017g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0003t0019g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0007t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0007t0007g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0007t0007g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0007t0007g0145 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0007t0007g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0007t0007g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0025t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0003c0034t0008g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0004c0008t0006g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0004c0008t0009g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0004c0008t0009g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0004c0008t0009g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0004c0008t0027g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0004c0009t0010g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0004c0009t0010g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0004c0009t0029g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0004c0011t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0004c0011t0024g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0004c0029t0028g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0005c0015t0001g0216 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0005c0015t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0006c0010t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0006c0010t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0007c0016t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0008c0035t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0009c0023t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0010c0032t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0011c0018t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0012c0027t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0013c0030t0005g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0014c0020t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0015c0026t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0016c0021t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0017c0031t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0018c0024t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0019c0033t0014g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| a0020c0022t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0373 | EUR | GBR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0312 | EUR | GBR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0247 | EUR | FIN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00280 | hp2 | a0003 | c0007 | t0007 | g0122 | EUR | FIN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0363 | EUR | FIN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0370 | EUR | FIN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0222 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00423 | hp1 | a0002 | c0002 | t0002 | g0341 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0258 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00438 | hp1 | a0002 | c0002 | t0003 | g0018 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0263 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00544 | hp1 | a0014 | c0020 | t0001 | g0339 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0252 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00558 | hp2 | a0001 | c0001 | t0005 | g0073 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0272 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00621 | hp1 | a0001 | c0001 | t0005 | g0080 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00639 | hp1 | a0001 | c0001 | t0005 | g0041 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0332 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00642 | hp1 | a0002 | c0006 | t0002 | g0197 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00673 | hp2 | a0002 | c0005 | t0002 | g0136 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00733 | hp1 | a0002 | c0002 | t0003 | g0040 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0340 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0368 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00738 | hp2 | a0020 | c0022 | t0001 | g0301 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00741 | hp1 | a0002 | c0002 | t0003 | g0048 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG00741 | hp2 | a0003 | c0003 | t0004 | g0192 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0248 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01071 | hp2 | a0003 | c0007 | t0007 | g0234 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01074 | hp1 | a0003 | c0003 | t0004 | g0356 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0364 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0365 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0093 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01099 | hp2 | a0002 | c0002 | t0003 | g0049 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0126 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01106 | hp2 | a0004 | c0009 | t0010 | g0013 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0219 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0082 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01167 | hp2 | a0002 | c0002 | t0002 | g0123 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01168 | hp1 | a0002 | c0002 | t0003 | g0092 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0251 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0336 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01192 | hp1 | a0001 | c0004 | t0005 | g0036 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01243 | hp2 | a0003 | c0003 | t0006 | g0350 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01255 | hp1 | a0003 | c0007 | t0004 | g0185 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0371 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01261 | hp1 | a0003 | c0003 | t0004 | g0238 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01346 | hp1 | a0003 | c0003 | t0004 | g0204 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01346 | hp2 | a0003 | c0007 | t0007 | g0144 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0372 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0085 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0314 | EUR | IBS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0369 | EUR | IBS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0374 | EUR | IBS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01516 | hp2 | a0002 | c0002 | t0003 | g0084 | EUR | IBS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01884 | hp1 | a0002 | c0002 | t0002 | g0244 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01884 | hp2 | a0003 | c0003 | t0006 | g0344 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01891 | hp1 | a0003 | c0003 | t0004 | g0171 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01891 | hp2 | a0002 | c0005 | t0003 | g0025 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01943 | hp1 | a0002 | c0002 | t0002 | g0172 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01943 | hp2 | a0002 | c0002 | t0003 | g0038 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01952 | hp2 | a0001 | c0001 | t0005 | g0046 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01975 | hp1 | a0001 | c0004 | t0001 | g0142 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01975 | hp2 | a0001 | c0001 | t0005 | g0045 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01978 | hp1 | a0013 | c0030 | t0005 | g0068 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0042 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01993 | hp2 | a0001 | c0001 | t0005 | g0069 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02004 | hp1 | a0002 | c0005 | t0002 | g0143 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02004 | hp2 | a0008 | c0035 | t0002 | g0183 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02015 | hp1 | a0002 | c0014 | t0002 | g0099 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02055 | hp1 | a0002 | c0006 | t0003 | g0027 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02055 | hp2 | a0003 | c0007 | t0007 | g0159 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0245 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02056 | hp2 | a0002 | c0002 | t0003 | g0087 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0230 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02080 | hp1 | a0001 | c0001 | t0005 | g0081 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02083 | hp1 | a0002 | c0005 | t0002 | g0328 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02083 | hp2 | a0002 | c0002 | t0003 | g0074 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02129 | hp1 | a0002 | c0005 | t0002 | g0151 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0231 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02135 | hp2 | a0002 | c0002 | t0003 | g0078 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02145 | hp1 | a0001 | c0001 | t0015 | g0007 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02145 | hp2 | a0003 | c0003 | t0004 | g0343 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CDX | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CDX | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02257 | hp1 | a0004 | c0009 | t0010 | g0012 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02257 | hp2 | a0002 | c0002 | t0003 | g0091 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02258 | hp1 | a0006 | c0010 | t0001 | g0170 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02258 | hp2 | a0002 | c0005 | t0002 | g0348 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0174 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02273 | hp2 | a0001 | c0001 | t0005 | g0059 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02280 | hp1 | a0003 | c0003 | t0008 | g0008 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02280 | hp2 | a0004 | c0008 | t0009 | g0355 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0240 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0377 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02523 | hp1 | a0001 | c0004 | t0001 | g0119 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02572 | hp1 | a0003 | c0003 | t0004 | g0121 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02572 | hp2 | a0003 | c0034 | t0008 | g0004 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02602 | hp1 | a0005 | c0015 | t0001 | g0233 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0375 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02615 | hp1 | a0002 | c0002 | t0002 | g0362 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02615 | hp2 | a0003 | c0003 | t0004 | g0094 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02622 | hp1 | a0002 | c0006 | t0003 | g0030 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02622 | hp2 | a0003 | c0003 | t0008 | g0006 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02630 | hp1 | a0001 | c0004 | t0018 | g0015 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02630 | hp2 | a0002 | c0006 | t0002 | g0196 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02647 | hp1 | a0003 | c0003 | t0004 | g0162 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02647 | hp2 | a0002 | c0006 | t0003 | g0031 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02683 | hp2 | a0009 | c0023 | t0002 | g0286 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02698 | hp1 | a0001 | c0004 | t0001 | g0203 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02698 | hp2 | a0002 | c0002 | t0003 | g0086 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02717 | hp1 | a0003 | c0003 | t0006 | g0345 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02717 | hp2 | a0003 | c0003 | t0011 | g0011 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02723 | hp1 | a0003 | c0003 | t0011 | g0010 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02723 | hp2 | a0003 | c0003 | t0013 | g0032 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02809 | hp1 | a0019 | c0033 | t0014 | g0342 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02809 | hp2 | a0003 | c0003 | t0004 | g0194 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02818 | hp1 | a0010 | c0032 | t0004 | g0200 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02818 | hp2 | a0006 | c0010 | t0001 | g0193 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02886 | hp1 | a0002 | c0002 | t0003 | g0034 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02886 | hp2 | a0004 | c0009 | t0029 | g0095 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02895 | hp1 | a0018 | c0024 | t0002 | g0187 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02896 | hp1 | a0004 | c0008 | t0027 | g0357 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02896 | hp2 | a0003 | c0003 | t0004 | g0353 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02897 | hp1 | a0003 | c0003 | t0004 | g0352 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02922 | hp1 | a0002 | c0002 | t0002 | g0242 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02922 | hp2 | a0003 | c0003 | t0004 | g0125 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02965 | hp1 | a0003 | c0003 | t0004 | g0163 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02965 | hp2 | a0003 | c0003 | t0014 | g0337 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02970 | hp1 | a0003 | c0003 | t0004 | g0191 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02970 | hp2 | a0002 | c0006 | t0003 | g0029 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02976 | hp1 | a0003 | c0003 | t0006 | g0346 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02976 | hp2 | a0015 | c0026 | t0001 | g0338 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0106 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03017 | hp2 | a0002 | c0002 | t0003 | g0051 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03041 | hp1 | a0002 | c0002 | t0002 | g0169 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03098 | hp1 | a0003 | c0003 | t0004 | g0190 | AFR | MSL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03130 | hp1 | a0004 | c0008 | t0009 | g0354 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03130 | hp2 | a0002 | c0002 | t0012 | g0089 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03139 | hp1 | a0004 | c0008 | t0006 | g0358 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03139 | hp2 | a0004 | c0008 | t0009 | g0096 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03195 | hp1 | a0002 | c0006 | t0003 | g0026 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0102 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | MSL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0359 | AFR | MSL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03225 | hp1 | a0004 | c0029 | t0028 | g0124 | AFR | MSL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03225 | hp2 | a0003 | c0003 | t0006 | g0241 | AFR | MSL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03239 | hp1 | a0016 | c0021 | t0001 | g0156 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03453 | hp1 | a0003 | c0003 | t0004 | g0165 | AFR | MSL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03453 | hp2 | a0003 | c0025 | t0004 | g0239 | AFR | MSL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03486 | hp1 | a0003 | c0003 | t0004 | g0188 | AFR | MSL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03486 | hp2 | a0003 | c0003 | t0004 | g0120 | AFR | MSL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0307 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03491 | hp2 | a0007 | c0016 | t0001 | g0201 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0306 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03516 | hp1 | a0003 | c0003 | t0004 | g0186 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03516 | hp2 | a0003 | c0003 | t0004 | g0195 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03540 | hp1 | a0003 | c0003 | t0017 | g0014 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03540 | hp2 | a0002 | c0002 | t0020 | g0028 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | MSL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03579 | hp2 | a0003 | c0003 | t0004 | g0347 | AFR | MSL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03654 | hp2 | a0001 | c0004 | t0001 | g0155 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03688 | hp1 | a0001 | c0004 | t0005 | g0017 | SAS | STU | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03688 | hp2 | a0001 | c0004 | t0001 | g0166 | SAS | STU | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03704 | hp1 | a0002 | c0002 | t0003 | g0056 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03710 | hp1 | a0001 | c0004 | t0001 | g0167 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0318 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | BEB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | BEB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0315 | SAS | BEB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03834 | hp2 | a0003 | c0003 | t0004 | g0226 | SAS | BEB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03927 | hp2 | a0002 | c0002 | t0026 | g0098 | SAS | BEB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0107 | SAS | BEB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03942 | hp2 | a0001 | c0001 | t0005 | g0047 | SAS | BEB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0367 | SAS | STU | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG04115 | hp2 | a0001 | c0004 | t0001 | g0158 | SAS | STU | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG04184 | hp1 | a0002 | c0002 | t0003 | g0075 | SAS | BEB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0168 | SAS | STU | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG04199 | hp2 | a0001 | c0004 | t0001 | g0157 | SAS | STU | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG04204 | hp1 | a0003 | c0003 | t0004 | g0237 | SAS | STU | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0321 | SAS | STU | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0101 | SAS | STU | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG04228 | hp2 | a0001 | c0004 | t0001 | g0154 | SAS | STU | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18522 | hp1 | a0002 | c0002 | t0012 | g0033 | AFR | YRI | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18522 | hp2 | a0002 | c0002 | t0016 | g0009 | AFR | YRI | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18747 | hp1 | a0002 | c0002 | t0003 | g0076 | EAS | CHB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18747 | hp2 | a0002 | c0017 | t0002 | g0139 | EAS | CHB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18939 | hp1 | a0001 | c0013 | t0001 | g0250 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18941 | hp2 | a0001 | c0004 | t0001 | g0146 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18943 | hp2 | a0002 | c0002 | t0025 | g0179 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18944 | hp1 | a0012 | c0027 | t0002 | g0132 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18945 | hp2 | a0002 | c0002 | t0003 | g0019 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18946 | hp1 | a0002 | c0002 | t0003 | g0058 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18946 | hp2 | a0003 | c0003 | t0004 | g0227 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0177 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18948 | hp1 | a0001 | c0012 | t0001 | g0275 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18948 | hp2 | a0002 | c0005 | t0003 | g0043 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18949 | hp2 | a0002 | c0002 | t0022 | g0071 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18950 | hp1 | a0002 | c0002 | t0003 | g0062 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18951 | hp1 | a0002 | c0002 | t0003 | g0020 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18951 | hp2 | a0001 | c0004 | t0001 | g0140 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18952 | hp1 | a0001 | c0004 | t0001 | g0128 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18952 | hp2 | a0001 | c0004 | t0001 | g0127 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18953 | hp1 | a0002 | c0002 | t0021 | g0022 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18954 | hp1 | a0001 | c0013 | t0001 | g0277 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18956 | hp2 | a0002 | c0002 | t0003 | g0057 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18959 | hp1 | a0001 | c0001 | t0032 | g0289 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18959 | hp2 | a0002 | c0005 | t0002 | g0135 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0182 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18960 | hp2 | a0001 | c0004 | t0001 | g0292 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18965 | hp1 | a0001 | c0001 | t0023 | g0088 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0150 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18966 | hp2 | a0002 | c0002 | t0002 | g0327 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0298 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18968 | hp2 | a0001 | c0001 | t0005 | g0052 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18969 | hp2 | a0002 | c0002 | t0003 | g0055 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18971 | hp1 | a0002 | c0002 | t0003 | g0023 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0282 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18972 | hp2 | a0001 | c0001 | t0005 | g0060 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18973 | hp2 | a0001 | c0001 | t0005 | g0053 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18975 | hp2 | a0002 | c0002 | t0003 | g0072 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18979 | hp1 | a0002 | c0002 | t0003 | g0077 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18979 | hp2 | a0001 | c0012 | t0001 | g0295 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0253 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18981 | hp2 | a0001 | c0004 | t0001 | g0147 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0311 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0254 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18984 | hp2 | a0002 | c0005 | t0002 | g0130 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18989 | hp1 | a0001 | c0004 | t0001 | g0138 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18989 | hp2 | a0002 | c0002 | t0003 | g0021 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18990 | hp1 | a0002 | c0002 | t0003 | g0064 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18993 | hp1 | a0002 | c0014 | t0002 | g0209 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18993 | hp2 | a0001 | c0001 | t0033 | g0379 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18994 | hp2 | a0002 | c0002 | t0002 | g0223 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18997 | hp1 | a0002 | c0002 | t0003 | g0079 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA18997 | hp2 | a0002 | c0002 | t0002 | g0181 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19001 | hp1 | a0002 | c0002 | t0003 | g0067 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0133 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0291 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0257 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19006 | hp2 | a0001 | c0001 | t0005 | g0070 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19007 | hp1 | a0001 | c0019 | t0001 | g0270 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19010 | hp1 | a0002 | c0002 | t0003 | g0063 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19010 | hp2 | a0001 | c0001 | t0005 | g0083 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19012 | hp2 | a0002 | c0002 | t0002 | g0273 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19030 | hp1 | a0002 | c0002 | t0002 | g0361 | AFR | LWK | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19030 | hp2 | a0004 | c0011 | t0006 | g0103 | AFR | LWK | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19043 | hp1 | a0003 | c0003 | t0019 | g0016 | AFR | LWK | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0378 | AFR | LWK | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19056 | hp1 | a0001 | c0004 | t0001 | g0118 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19056 | hp2 | a0002 | c0002 | t0003 | g0061 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19057 | hp1 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19058 | hp1 | a0002 | c0002 | t0003 | g0065 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19060 | hp1 | a0001 | c0004 | t0001 | g0129 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0173 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19062 | hp1 | a0001 | c0004 | t0001 | g0131 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0224 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0207 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19065 | hp2 | a0002 | c0002 | t0003 | g0054 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0249 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19070 | hp1 | a0001 | c0004 | t0030 | g0137 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0246 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19078 | hp2 | a0011 | c0018 | t0001 | g0152 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19079 | hp1 | a0002 | c0002 | t0002 | g0175 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19079 | hp2 | a0001 | c0004 | t0001 | g0141 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19080 | hp2 | a0002 | c0002 | t0002 | g0178 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19083 | hp2 | a0002 | c0002 | t0002 | g0176 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19085 | hp2 | a0002 | c0002 | t0031 | g0278 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0218 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19086 | hp2 | a0001 | c0004 | t0005 | g0044 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19091 | hp1 | a0002 | c0002 | t0003 | g0024 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19091 | hp2 | a0002 | c0005 | t0002 | g0148 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | YRI | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA19240 | hp2 | a0002 | c0002 | t0002 | g0360 | AFR | YRI | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA20129 | hp1 | a0002 | c0002 | t0003 | g0066 | AFR | ASW | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA20129 | hp2 | a0003 | c0003 | t0004 | g0189 | AFR | ASW | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA20752 | hp1 | a0001 | c0004 | t0005 | g0035 | EUR | TSI | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA20752 | hp2 | a0002 | c0002 | t0003 | g0050 | EUR | TSI | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA20805 | hp1 | a0001 | c0004 | t0005 | g0037 | EUR | TSI | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0376 | EUR | TSI | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA20905 | hp1 | a0001 | c0004 | t0001 | g0153 | SAS | GIH | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0351 | SAS | GIH | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0366 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0114 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02109 | hp2 | a0003 | c0003 | t0013 | g0090 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02486 | hp1 | a0004 | c0011 | t0024 | g0262 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02486 | hp2 | a0003 | c0003 | t0004 | g0199 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02559 | hp1 | a0003 | c0003 | t0008 | g0005 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG02559 | hp2 | a0017 | c0031 | t0004 | g0198 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03471 | hp1 | a0003 | c0003 | t0006 | g0349 | AFR | MSL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| HG03471 | hp2 | a0002 | c0002 | t0002 | g0243 | AFR | MSL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA20300 | hp1 | a0003 | c0003 | t0004 | g0164 | AFR | USA | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA20300 | hp2 | a0002 | c0002 | t0003 | g0039 | AFR | USA | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA21309 | hp1 | a0001 | c0028 | t0006 | g0235 | AFR | LWK | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0113 | AFR | LWK | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| homoSapiens_chm13v2 | hp1 | a0005 | c0015 | t0001 | g0216 | REF | REF | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| homoSapiens_grch38 | hp1 | a0003 | c0007 | t0007 | g0145 | REF | REF | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:46856740
|
C | T | 1 | a0014 | 1 | HG00544.hp1 | missense_variant | MODERATE | c.3854G>A | p.Arg1285Lys | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 19/21 | 4104/5761 | 3854/4041 | 1285/1346 | chr6 | 46856740 | ||
| chr6:46859336
|
A | G | 10 | a0001a0005a0006others(7): Show | 178 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(175): Show |
missense_variant | MODERATE | c.2567T>C | p.Met856Thr | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 2817/5761 | 2567/4041 | 856/1346 | chr6 | 46859336 | ||
| chr6:46859358
|
T | C | 1 | a0012 | 1 | NA18944.hp1 | missense_variant | MODERATE | c.2545A>G | p.Thr849Ala | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 2795/5761 | 2545/4041 | 849/1346 | chr6 | 46859358 | ||
| chr6:46859466
|
C | T | 1 | a0013 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.2437G>A | p.Val813Ile | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 2687/5761 | 2437/4041 | 813/1346 | chr6 | 46859466 | ||
| chr6:46859502
|
C | T | 5 | a0002a0008a0009others(2): Show | 138 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(135): Show |
missense_variant | MODERATE | c.2401G>A | p.Val801Ile | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 2651/5761 | 2401/4041 | 801/1346 | chr6 | 46859502 | ||
| chr6:46863070
|
C | T | 1 | a0011 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.2017G>A | p.Val673Ile | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/21 | 2267/5761 | 2017/4041 | 673/1346 | chr6 | 46863070 | ||
| chr6:46866948
|
G | A | 15 | a0001a0002a0004others(12): Show | 326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
missense_variant | MODERATE | c.1811C>T | p.Thr604Met | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/21 | 2061/5761 | 1811/4041 | 604/1346 | chr6 | 46866948 | ||
| chr6:46867077
|
A | G | 1 | a0016 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.1682T>C | p.Ile561Thr | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/21 | 1932/5761 | 1682/4041 | 561/1346 | chr6 | 46867077 | ||
| chr6:46871962
|
G | A | 2 | a0010a0017 | 2 | HG02559.hp2 HG02818.hp1 |
missense_variant | MODERATE | c.1292C>T | p.Ala431Val | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/21 | 1542/5761 | 1292/4041 | 431/1346 | chr6 | 46871962 | ||
| chr6:46871995
|
A | C | 1 | a0018 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.1259T>G | p.Ile420Arg | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/21 | 1509/5761 | 1259/4041 | 420/1346 | chr6 | 46871995 | ||
| chr6:46872008
|
G | C | 1 | a0010 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.1246C>G | p.Pro416Ala | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/21 | 1496/5761 | 1246/4041 | 416/1346 | chr6 | 46872008 | ||
| chr6:46878306
|
T | A | 1 | a0005 | 2 | HG02602.hp1 homoSapiens_chm13v2.hp1 |
missense_variant | MODERATE | c.1136A>T | p.Lys379Met | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/21 | 1386/5761 | 1136/4041 | 379/1346 | chr6 | 46878306 | ||
| chr6:46879836
|
T | C | 1 | a0019 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.1018A>G | p.Ile340Val | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/21 | 1268/5761 | 1018/4041 | 340/1346 | chr6 | 46879836 | ||
| chr6:46881517
|
A | G | 1 | a0009 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.752T>C | p.Val251Ala | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/21 | 1002/5761 | 752/4041 | 251/1346 | chr6 | 46881517 | ||
| chr6:46882092
|
C | T | 1 | a0006 | 2 | HG02258.hp1 HG02818.hp2 |
missense_variant | MODERATE | c.628G>A | p.Gly210Arg | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 7/21 | 878/5761 | 628/4041 | 210/1346 | chr6 | 46882092 | ||
| chr6:46883597
|
C | T | 1 | a0020 | 1 | HG00738.hp2 | missense_variant | MODERATE | c.574G>A | p.Ala192Thr | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/21 | 824/5761 | 574/4041 | 192/1346 | chr6 | 46883597 | ||
| chr6:46888404
|
G | A | 1 | a0008 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.259C>T | p.Leu87Phe | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/21 | 509/5761 | 259/4041 | 87/1346 | chr6 | 46888404 | ||
| chr6:46900034
|
C | T | 1 | a0007 | 1 | HG03491.hp2 | missense_variant | MODERATE | c.152G>A | p.Arg51Gln | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/21 | 402/5761 | 152/4041 | 51/1346 | chr6 | 46900034 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:46858240
|
A | G | 1 | a0001c0019 | 1 | NA19007.hp1 | synonymous_variant | LOW | c.3663T>C | p.Ile1221Ile | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 3913/5761 | 3663/4041 | 1221/1346 | chr6 | 46858240 | ||
| chr6:46858285
|
T | C | 2 | a0004c0011a0004c0029 | 3 | HG02486.hp1 HG03225.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.3618A>G | p.Pro1206Pro | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 3868/5761 | 3618/4041 | 1206/1346 | chr6 | 46858285 | ||
| chr6:46858399
|
G | A | 1 | a0002c0017 | 1 | NA18747.hp2 | synonymous_variant | LOW | c.3504C>T | p.Asp1168Asp | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 3754/5761 | 3504/4041 | 1168/1346 | chr6 | 46858399 | ||
| chr6:46858690
|
G | A | 1 | a0004c0029 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.3213C>T | p.Val1071Val | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 3463/5761 | 3213/4041 | 1071/1346 | chr6 | 46858690 | ||
| chr6:46858771
|
G | A | 28 | a0001c0001a0001c0004a0001c0012others(25): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
synonymous_variant | LOW | c.3132C>T | p.Asn1044Asn | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 3382/5761 | 3132/4041 | 1044/1346 | chr6 | 46858771 | ||
| chr6:46858978
|
T | A | 28 | a0001c0001a0001c0004a0001c0012others(25): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
synonymous_variant | LOW | c.2925A>T | p.Val975Val | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 3175/5761 | 2925/4041 | 975/1346 | chr6 | 46858978 | ||
| chr6:46859056
|
G | A | 1 | a0001c0028 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.2847C>T | p.Gly949Gly | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 3097/5761 | 2847/4041 | 949/1346 | chr6 | 46859056 | ||
| chr6:46859107
|
T | C | 28 | a0001c0001a0001c0004a0001c0012others(25): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
synonymous_variant | LOW | c.2796A>G | p.Thr932Thr | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 3046/5761 | 2796/4041 | 932/1346 | chr6 | 46859107 | ||
| chr6:46859173
|
G | A | 28 | a0001c0001a0001c0004a0001c0012others(25): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
synonymous_variant | LOW | c.2730C>T | p.Ala910Ala | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 2980/5761 | 2730/4041 | 910/1346 | chr6 | 46859173 | ||
| chr6:46859218
|
C | T | 1 | a0003c0025 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.2685G>A | p.Ser895Ser | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 2935/5761 | 2685/4041 | 895/1346 | chr6 | 46859218 | ||
| chr6:46859242
|
A | G | 11 | a0002c0002a0002c0005a0002c0006others(8): Show | 146 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(143): Show |
synonymous_variant | LOW | c.2661T>C | p.Tyr887Tyr | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 2911/5761 | 2661/4041 | 887/1346 | chr6 | 46859242 | ||
| chr6:46859389
|
C | T | 28 | a0001c0001a0001c0004a0001c0012others(25): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
synonymous_variant | LOW | c.2514G>A | p.Ser838Ser | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 2764/5761 | 2514/4041 | 838/1346 | chr6 | 46859389 | ||
| chr6:46862900
|
G | C | 1 | a0001c0013 | 2 | NA18939.hp1 NA18954.hp1 |
synonymous_variant | LOW | c.2187C>G | p.Leu729Leu | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/21 | 2437/5761 | 2187/4041 | 729/1346 | chr6 | 46862900 | ||
| chr6:46863050
|
C | T | 1 | a0001c0012 | 2 | NA18948.hp1 NA18979.hp2 |
synonymous_variant | LOW | c.2037G>A | p.Pro679Pro | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/21 | 2287/5761 | 2037/4041 | 679/1346 | chr6 | 46863050 | ||
| chr6:46865076
|
G | A | 14 | a0001c0001a0001c0004a0001c0012others(11): Show | 177 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(174): Show |
synonymous_variant | LOW | c.1956C>T | p.Val652Val | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/21 | 2206/5761 | 1956/4041 | 652/1346 | chr6 | 46865076 | ||
| chr6:46866998
|
G | A | 1 | a0002c0014 | 2 | HG02015.hp1 NA18993.hp1 |
synonymous_variant | LOW | c.1761C>T | p.His587His | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/21 | 2011/5761 | 1761/4041 | 587/1346 | chr6 | 46866998 | ||
| chr6:46879885
|
G | A | 1 | a0016c0021 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.969C>T | p.Thr323Thr | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/21 | 1219/5761 | 969/4041 | 323/1346 | chr6 | 46879885 | ||
| chr6:46883559
|
C | T | 1 | a0002c0006 | 7 | HG00642.hp1 HG02055.hp1 HG02622.hp1 others(4): Show |
splice_region_variant&synonymous_variant | LOW | c.612G>A | p.Ala204Ala | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/21 | 862/5761 | 612/4041 | 204/1346 | chr6 | 46883559 | ||
| chr6:46883598
|
G | A | 1 | a0003c0034 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.573C>T | p.Ser191Ser | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/21 | 823/5761 | 573/4041 | 191/1346 | chr6 | 46883598 | ||
| chr6:46888363
|
G | A | 26 | a0001c0001a0001c0012a0001c0013others(23): Show | 330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
synonymous_variant | LOW | c.300C>T | p.Thr100Thr | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/21 | 550/5761 | 300/4041 | 100/1346 | chr6 | 46888363 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:46852636
|
CA | C | 13 | a0003c0003t0004a0003c0003t0008a0003c0003t0013others(10): Show | 44 | HG00741.hp2 HG01074.hp1 HG01106.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1355delT | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 1355 | chr6 | 46852636 | |||||
| chr6:46852653
|
G | A | 1 | a0002c0002t0022 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1339C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 1339 | chr6 | 46852653 | |||||
| chr6:46852660
|
A | G | 1 | a0002c0002t0021 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1332T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 1332 | chr6 | 46852660 | |||||
| chr6:46852675
|
A | AATCCTTG others(44): Show |
2 | a0003c0003t0014a0019c0033t0014 | 2 | HG02809.hp1 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1316_*1317insCCCA others(47): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 1316 | chr6 | 46852675 | |||||
| chr6:46852710
|
G | C | 3 | a0003c0003t0014a0003c0003t0017a0019c0033t0014 | 3 | HG02809.hp1 HG02965.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1282C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 1282 | chr6 | 46852710 | |||||
| chr6:46852745
|
G | C | 1 | a0004c0029t0028 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1247C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 1247 | chr6 | 46852745 | |||||
| chr6:46852749
|
A | C | 1 | a0004c0029t0028 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1243T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 1243 | chr6 | 46852749 | |||||
| chr6:46852772
|
C | T | 2 | a0004c0008t0009a0004c0008t0027 | 4 | HG02280.hp2 HG02896.hp1 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1220G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 1220 | chr6 | 46852772 | |||||
| chr6:46852887
|
G | T | 13 | a0003c0003t0004a0003c0003t0008a0003c0003t0013others(10): Show | 45 | HG00741.hp2 HG01074.hp1 HG01255.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1105C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 1105 | chr6 | 46852887 | |||||
| chr6:46852932
|
A | G | 1 | a0004c0008t0027 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1060T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 1060 | chr6 | 46852932 | |||||
| chr6:46853162
|
G | A | 30 | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(27): Show | 191 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*830C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 830 | chr6 | 46853162 | |||||
| chr6:46853169
|
T | C | 1 | a0002c0002t0026 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*823A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 823 | chr6 | 46853169 | |||||
| chr6:46853348
|
C | G | 22 | a0001c0001t0002a0001c0001t0023a0002c0002t0002others(19): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*644G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 644 | chr6 | 46853348 | |||||
| chr6:46853419
|
A | C | 1 | a0002c0002t0025 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*573T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 573 | chr6 | 46853419 | |||||
| chr6:46853515
|
T | C | 1 | a0001c0004t0030 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*477A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 477 | chr6 | 46853515 | |||||
| chr6:46853580
|
T | C | 22 | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(19): Show | 176 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*412A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 412 | chr6 | 46853580 | |||||
| chr6:46853696
|
G | A | 1 | a0002c0002t0031 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*296C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 296 | chr6 | 46853696 | |||||
| chr6:46853798
|
G | A | 1 | a0001c0001t0032 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*194C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 194 | chr6 | 46853798 | |||||
| chr6:46853900
|
C | T | 1 | a0002c0002t0012 | 2 | HG03130.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*92G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 92 | chr6 | 46853900 | |||||
| chr6:46853970
|
C | T | 2 | a0002c0002t0020a0004c0011t0024 | 2 | HG02486.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*22G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 22 | chr6 | 46853970 | |||||
| chr6:46921812
|
G | A | 1 | a0001c0001t0033 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-124C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/21 | 15050 | chr6 | 46921812 | |||||
| chr6:46921838
|
GAGAACCA others(27): Show |
G | 1 | a0003c0003t0019 | 1 | NA19043.hp1 | 5_prime_UTR_variant | MODIFIER | c.-184_-151delGCCTGA others(28): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/21 | 15077 | chr6 | 46921838 | |||||
| chr6:46921840
|
G | T | 12 | a0001c0001t0005a0001c0001t0023a0001c0004t0005others(9): Show | 77 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(74): Show |
5_prime_UTR_variant | MODIFIER | c.-152C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/21 | 15078 | chr6 | 46921840 | |||||
| chr6:46921884
|
C | T | 5 | a0001c0004t0018a0002c0002t0016a0003c0003t0011others(2): Show | 7 | HG01106.hp2 HG02257.hp1 HG02630.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-196G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/21 | 15122 | chr6 | 46921884 | |||||
| chr6:46921897
|
C | G | 3 | a0001c0001t0015a0003c0003t0008a0003c0034t0008 | 5 | HG02145.hp1 HG02280.hp1 HG02559.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-209G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/21 | 15135 | chr6 | 46921897 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:46854283
|
C | G | 9 | a0003c0003t0006g0241a0003c0003t0006g0344a0003c0003t0006g0345others(6): Show | 9 | HG01243.hp2 HG01884.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3962-212G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46854283 | ||||||
| chr6:46854455
|
C | G | 345 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(342): Show | 348 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.3962-384G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46854455 | ||||||
| chr6:46854612
|
A | G | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.3962-541T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46854612 | ||||||
| chr6:46854637
|
G | A | 5 | a0004c0008t0006g0358a0004c0008t0009g0096a0004c0008t0009g0354others(2): Show | 5 | HG02280.hp2 HG02896.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.3962-566C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46854637 | ||||||
| chr6:46854669
|
A | G | 323 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(320): Show | 326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.3962-598T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46854669 | ||||||
| chr6:46854709
|
C | T | 1 | a0002c0002t0003g0087 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3962-638G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46854709 | ||||||
| chr6:46854779
|
C | A | 1 | a0001c0004t0001g0138 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3962-708G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46854779 | ||||||
| chr6:46854791
|
T | C | 3 | a0004c0009t0010g0012a0004c0009t0010g0013a0004c0009t0029g0095 | 3 | HG01106.hp2 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3962-720A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46854791 | ||||||
| chr6:46854804
|
C | T | 1 | a0001c0004t0005g0017 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3962-733G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46854804 | ||||||
| chr6:46854852
|
A | C | 138 | a0002c0002t0002g0101a0002c0002t0002g0102a0002c0002t0002g0106others(135): Show | 138 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.3962-781T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46854852 | ||||||
| chr6:46854900
|
G | GA | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.3962-830dupT | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46854900 | ||||||
| chr6:46854917
|
G | A | 1 | a0004c0029t0028g0124 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3962-846C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46854917 | ||||||
| chr6:46855014
|
G | C | 1 | a0002c0002t0002g0133 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.3962-943C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46855014 | ||||||
| chr6:46855032
|
A | C | 1 | a0004c0029t0028g0124 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3961+942T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46855032 | ||||||
| chr6:46855132
|
A | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0359a0001c0001t0015g0007others(6): Show | 10 | HG02145.hp1 HG02572.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.3961+842T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46855132 | ||||||
| chr6:46855191
|
T | G | 1 | a0001c0001t0001g0228 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3961+783A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46855191 | ||||||
| chr6:46855232
|
A | G | 1 | a0002c0002t0002g0263 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3961+742T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46855232 | ||||||
| chr6:46855297
|
T | C | 1 | a0001c0004t0001g0153 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3961+677A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46855297 | ||||||
| chr6:46855632
|
C | T | 319 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0097others(316): Show | 321 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.3961+342G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46855632 | ||||||
| chr6:46855763
|
T | A | 2 | a0001c0001t0001g0274a0001c0001t0001g0296 | 2 | HG02080.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.3961+211A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46855763 | ||||||
| chr6:46855775
|
G | T | 9 | a0003c0003t0006g0241a0003c0003t0006g0344a0003c0003t0006g0345others(6): Show | 9 | HG01243.hp2 HG01884.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3961+199C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46855775 | ||||||
| chr6:46855795
|
C | T | 1 | a0001c0001t0001g0266 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.3961+179G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46855795 | ||||||
| chr6:46855952
|
G | A | 1 | a0013c0030t0005g0068 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.3961+22C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46855952 | ||||||
| chr6:46855958
|
G | A | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.3961+16C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46855958 | ||||||
| chr6:46856068
|
A | AG | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.3877-11dupC | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 19/20 | chr6 | 46856068 | ||||||
| chr6:46856089
|
A | G | 6 | a0002c0002t0002g0257a0002c0002t0002g0258a0002c0002t0002g0298others(3): Show | 6 | HG00423.hp2 HG03491.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.3877-31T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 19/20 | chr6 | 46856089 | ||||||
| chr6:46856162
|
G | A | 2 | a0002c0014t0002g0099a0002c0014t0002g0209 | 2 | HG02015.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.3877-104C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 19/20 | chr6 | 46856162 | ||||||
| chr6:46856428
|
T | A | 143 | a0002c0002t0002g0101a0002c0002t0002g0102a0002c0002t0002g0106others(140): Show | 143 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.3876+290A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 19/20 | chr6 | 46856428 | ||||||
| chr6:46856542
|
A | G | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(175): Show | 181 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.3876+176T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 19/20 | chr6 | 46856542 | ||||||
| chr6:46856711
|
A | G | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
splice_region_variant&intron_variant | LOW | c.3876+7T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 19/20 | chr6 | 46856711 | ||||||
| chr6:46856823
|
C | T | 5 | a0004c0008t0006g0358a0004c0008t0009g0096a0004c0008t0009g0354others(2): Show | 5 | HG02280.hp2 HG02896.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.3816+44G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 18/20 | chr6 | 46856823 | ||||||
| chr6:46856838
|
T | C | 1 | a0002c0005t0002g0151 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3816+29A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 18/20 | chr6 | 46856838 | ||||||
| chr6:46856860
|
C | T | 1 | a0002c0002t0003g0061 | 1 | NA19056.hp2 | splice_region_variant&intron_variant | LOW | c.3816+7G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 18/20 | chr6 | 46856860 | ||||||
| chr6:46856913
|
G | GA | 9 | a0003c0003t0006g0241a0003c0003t0006g0344a0003c0003t0006g0345others(6): Show | 9 | HG01243.hp2 HG01884.hp2 HG02717.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.3775-6dupT | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46856913 | ||||||
| chr6:46857061
|
C | G | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.3775-153G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857061 | ||||||
| chr6:46857331
|
G | T | 1 | a0001c0001t0005g0082 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3775-423C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857331 | ||||||
| chr6:46857349
|
C | G | 1 | a0001c0028t0006g0235 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3775-441G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857349 | ||||||
| chr6:46857431
|
A | G | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.3775-523T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857431 | ||||||
| chr6:46857458
|
C | T | 1 | a0002c0002t0003g0087 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3775-550G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857458 | ||||||
| chr6:46857509
|
C | T | 2 | a0003c0003t0004g0191a0003c0003t0004g0192 | 2 | HG00741.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3775-601G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857509 | ||||||
| chr6:46857582
|
G | A | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.3774+547C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857582 | ||||||
| chr6:46857707
|
A | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(171): Show | 177 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.3774+422T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857707 | ||||||
| chr6:46857735
|
AAGGTCTC others(4): Show |
A | 1 | a0003c0003t0004g0171 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3774+383_3774+393d others(13): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857735 | ||||||
| chr6:46857748
|
G | C | 1 | a0001c0001t0001g0314 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3774+381C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857748 | ||||||
| chr6:46857760
|
T | C | 1 | a0002c0002t0002g0101 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3774+369A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857760 | ||||||
| chr6:46857787
|
C | CT | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.3774+341dupA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857787 | ||||||
| chr6:46857791
|
C | G | 1 | a0001c0001t0005g0085 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3774+338G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857791 | ||||||
| chr6:46857858
|
G | A | 146 | a0002c0002t0002g0101a0002c0002t0002g0102a0002c0002t0002g0106others(143): Show | 146 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.3774+271C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857858 | ||||||
| chr6:46857873
|
A | C | 4 | a0003c0003t0004g0226a0003c0003t0004g0227a0003c0025t0004g0239others(1): Show | 4 | HG02572.hp2 HG03453.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.3774+256T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857873 | ||||||
| chr6:46857895
|
G | C | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.3774+234C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857895 | ||||||
| chr6:46858084
|
T | C | 1 | a0002c0006t0003g0030 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3774+45A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46858084 | ||||||
| chr6:46859608
|
T | C | 1 | a0003c0003t0004g0125 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2380-85A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859608 | ||||||
| chr6:46859728
|
T | C | 1 | a0001c0001t0002g0375 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2380-205A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859728 | ||||||
| chr6:46859773
|
C | T | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.2380-250G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859773 | ||||||
| chr6:46859817
|
C | CTATTT | 5 | a0002c0002t0002g0360a0002c0002t0002g0361a0002c0002t0002g0362others(2): Show | 5 | HG02615.hp1 HG03540.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.2380-299_2380-295d others(7): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859817 | ||||||
| chr6:46859817
|
C | CTATTTTA others(3): Show |
210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.2380-304_2380-295d others(12): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859817 | ||||||
| chr6:46859817
|
C | CTATTTTA others(8): Show |
33 | a0001c0001t0001g0116a0001c0001t0001g0228a0001c0001t0001g0229others(30): Show | 33 | HG00544.hp1 HG00741.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.2380-309_2380-295d others(17): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859817 | ||||||
| chr6:46859817
|
C | CTATTTTA others(11): Show |
1 | a0002c0002t0031g0278 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2380-312_2380-295d others(20): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859817 | ||||||
| chr6:46859817
|
C | CTATTTTA others(13): Show |
65 | a0002c0002t0002g0114a0002c0002t0002g0123a0002c0002t0002g0133others(62): Show | 65 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.2380-314_2380-295d others(22): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859817 | ||||||
| chr6:46859817
|
C | CTATTTTA others(18): Show |
6 | a0002c0002t0002g0252a0002c0002t0002g0341a0002c0002t0003g0024others(3): Show | 6 | HG00423.hp1 HG00558.hp1 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.2380-319_2380-295d others(27): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859817 | ||||||
| chr6:46859817
|
CTATTT | C | 9 | a0003c0003t0006g0241a0003c0003t0006g0344a0003c0003t0006g0345others(6): Show | 9 | HG01243.hp2 HG01884.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2380-299_2380-295d others(7): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859817 | ||||||
| chr6:46859821
|
T | TTTATTTT others(8): Show |
1 | a0002c0002t0003g0075 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2380-299_2380-298i others(17): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859821 | ||||||
| chr6:46859825
|
T | TTTTATTT others(3): Show |
3 | a0004c0009t0010g0012a0004c0009t0010g0013a0004c0009t0029g0095 | 3 | HG01106.hp2 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2380-303_2380-302i others(12): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859825 | ||||||
| chr6:46859876
|
G | A | 146 | a0002c0002t0002g0101a0002c0002t0002g0102a0002c0002t0002g0106others(143): Show | 146 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.2380-353C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859876 | ||||||
| chr6:46859919
|
A | G | 1 | a0003c0003t0008g0005 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2380-396T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859919 | ||||||
| chr6:46859937
|
G | T | 2 | a0002c0002t0003g0077a0002c0002t0003g0078 | 2 | HG02135.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.2380-414C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859937 | ||||||
| chr6:46859953
|
A | G | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.2380-430T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859953 | ||||||
| chr6:46859981
|
C | T | 4 | a0003c0003t0004g0120a0003c0003t0004g0121a0003c0003t0004g0194others(1): Show | 4 | HG02572.hp1 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2380-458G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859981 | ||||||
| chr6:46860232
|
C | G | 1 | a0002c0017t0002g0139 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2379+483G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46860232 | ||||||
| chr6:46860371
|
C | T | 1 | a0001c0001t0005g0042 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2379+344G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46860371 | ||||||
| chr6:46860422
|
G | A | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.2379+293C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46860422 | ||||||
| chr6:46860437
|
C | T | 1 | a0003c0003t0006g0241 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2379+278G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46860437 | ||||||
| chr6:46860599
|
A | G | 1 | a0010c0032t0004g0200 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2379+116T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46860599 | ||||||
| chr6:46860643
|
G | A | 1 | a0001c0001t0001g0256 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2379+72C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46860643 | ||||||
| chr6:46860933
|
A | G | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.2200-39T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46860933 | ||||||
| chr6:46861058
|
C | T | 1 | a0001c0001t0001g0300 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2200-164G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861058 | ||||||
| chr6:46861099
|
A | G | 28 | a0002c0002t0002g0117a0002c0002t0002g0172a0002c0002t0002g0173others(25): Show | 28 | HG00438.hp1 HG00741.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.2200-205T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861099 | ||||||
| chr6:46861137
|
T | C | 325 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(322): Show | 328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.2200-243A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861137 | ||||||
| chr6:46861190
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0359a0001c0001t0015g0007others(2): Show | 6 | HG02145.hp1 HG02630.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2200-296C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861190 | ||||||
| chr6:46861305
|
G | A | 1 | a0001c0028t0006g0235 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2200-411C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861305 | ||||||
| chr6:46861456
|
T | C | 345 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(342): Show | 348 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.2200-562A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861456 | ||||||
| chr6:46861484
|
C | T | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.2200-590G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861484 | ||||||
| chr6:46861509
|
AC | A | 5 | a0002c0002t0002g0219a0002c0002t0003g0039a0002c0002t0003g0040others(2): Show | 5 | HG00733.hp1 HG01109.hp1 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.2200-616delG | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861509 | ||||||
| chr6:46861558
|
C | T | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.2200-664G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861558 | ||||||
| chr6:46861618
|
C | T | 3 | a0004c0009t0010g0012a0004c0009t0010g0013a0004c0009t0029g0095 | 3 | HG01106.hp2 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2200-724G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861618 | ||||||
| chr6:46861627
|
T | C | 1 | a0003c0003t0011g0011 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2200-733A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861627 | ||||||
| chr6:46861642
|
C | T | 4 | a0003c0003t0004g0120a0003c0003t0004g0121a0003c0003t0004g0194others(1): Show | 4 | HG02572.hp1 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2200-748G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861642 | ||||||
| chr6:46861711
|
A | G | 71 | a0002c0002t0002g0114a0002c0002t0002g0123a0002c0002t0002g0133others(68): Show | 71 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.2200-817T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861711 | ||||||
| chr6:46861791
|
T | A | 2 | a0001c0004t0001g0118a0001c0004t0001g0127 | 2 | NA18952.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.2200-897A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861791 | ||||||
| chr6:46861817
|
G | A | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0097others(114): Show | 119 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.2200-923C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861817 | ||||||
| chr6:46861891
|
T | C | 2 | a0002c0002t0002g0123a0002c0002t0003g0092 | 2 | HG01167.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.2199+997A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861891 | ||||||
| chr6:46862012
|
A | T | 2 | a0003c0003t0014g0337a0019c0033t0014g0342 | 2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2199+876T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862012 | ||||||
| chr6:46862079
|
T | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(175): Show | 181 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.2199+809A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862079 | ||||||
| chr6:46862115
|
G | A | 4 | a0003c0003t0004g0120a0003c0003t0004g0121a0003c0003t0004g0194others(1): Show | 4 | HG02572.hp1 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2199+773C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862115 | ||||||
| chr6:46862199
|
G | C | 1 | a0001c0001t0001g0366 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2199+689C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862199 | ||||||
| chr6:46862253
|
T | A | 1 | a0002c0002t0026g0098 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2199+635A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862253 | ||||||
| chr6:46862323
|
A | G | 1 | a0001c0028t0006g0235 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2199+565T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862323 | ||||||
| chr6:46862358
|
T | A | 2 | a0001c0001t0001g0261a0001c0001t0001g0288 | 2 | HG01243.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.2199+530A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862358 | ||||||
| chr6:46862361
|
C | T | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.2199+527G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862361 | ||||||
| chr6:46862363
|
G | A | 6 | a0001c0001t0001g0202a0001c0001t0001g0368a0001c0001t0001g0369others(3): Show | 6 | HG00738.hp1 HG01515.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2199+525C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862363 | ||||||
| chr6:46862396
|
G | A | 1 | a0001c0001t0001g0310 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2199+492C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862396 | ||||||
| chr6:46862506
|
T | C | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.2199+382A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862506 | ||||||
| chr6:46862561
|
T | C | 1 | a0001c0001t0001g0290 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2199+327A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862561 | ||||||
| chr6:46862622
|
G | A | 1 | a0004c0011t0024g0262 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2199+266C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862622 | ||||||
| chr6:46862637
|
G | T | 1 | a0001c0001t0001g0221 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2199+251C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862637 | ||||||
| chr6:46862703
|
C | CT | 11 | a0001c0004t0005g0017a0002c0002t0003g0039a0003c0003t0004g0164others(8): Show | 11 | HG00741.hp2 HG01071.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.2199+184dupA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | ||||||
| chr6:46862703
|
C | CTTTTT | 31 | a0001c0001t0001g0112a0001c0001t0001g0116a0001c0001t0001g0202others(28): Show | 31 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.2199+180_2199+184d others(7): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | ||||||
| chr6:46862703
|
C | CTTTTTT | 17 | a0001c0001t0001g0149a0001c0001t0001g0225a0001c0001t0001g0236others(14): Show | 17 | HG01106.hp2 HG01934.hp2 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.2199+179_2199+184d others(8): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | ||||||
| chr6:46862703
|
C | CTTTTTTT others(2): Show |
16 | a0002c0002t0002g0113a0002c0002t0002g0172a0002c0002t0002g0181others(13): Show | 16 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.2199+176_2199+184d others(11): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | ||||||
| chr6:46862703
|
C | CTTTTTTT others(3): Show |
33 | a0002c0002t0002g0101a0002c0002t0002g0106a0002c0002t0002g0117others(30): Show | 33 | HG00280.hp1 HG00438.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.2199+175_2199+184d others(12): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | ||||||
| chr6:46862703
|
C | CTTTTTTT others(4): Show |
20 | a0002c0002t0002g0102a0002c0002t0002g0123a0002c0002t0002g0176others(17): Show | 20 | HG00642.hp1 HG01070.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.2199+174_2199+184d others(13): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | ||||||
| chr6:46862703
|
C | CTTTTTTT others(5): Show |
14 | a0002c0002t0002g0107a0002c0002t0002g0114a0002c0002t0002g0134others(11): Show | 14 | HG01168.hp1 HG02055.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.2199+173_2199+184d others(14): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | ||||||
| chr6:46862703
|
C | CTTTTTTT others(6): Show |
23 | a0002c0002t0002g0133a0002c0002t0002g0168a0002c0002t0002g0222others(20): Show | 23 | HG00408.hp2 HG00423.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.2199+172_2199+184d others(15): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | ||||||
| chr6:46862703
|
C | CTTTTTTT others(7): Show |
18 | a0002c0002t0002g0150a0002c0002t0002g0243a0002c0002t0003g0050others(15): Show | 18 | HG00673.hp2 HG01516.hp2 HG02129.hp1 others(15): Show |
intron_variant | MODIFIER | c.2199+171_2199+184d others(16): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | ||||||
| chr6:46862703
|
C | CTTTTTTT others(8): Show |
8 | a0002c0002t0002g0219a0002c0002t0002g0224a0002c0002t0002g0249others(5): Show | 8 | HG00438.hp2 HG00597.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.2199+170_2199+184d others(17): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | ||||||
| chr6:46862703
|
C | CTTTTTTT others(9): Show |
4 | a0002c0002t0002g0251a0002c0002t0002g0341a0002c0002t0003g0040others(1): Show | 4 | HG00423.hp1 HG00733.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.2199+169_2199+184d others(18): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | ||||||
| chr6:46862703
|
C | CTTTTTTT others(11): Show |
1 | a0002c0002t0002g0254 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2199+167_2199+184d others(20): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | ||||||
| chr6:46862703
|
C | CTTTTTTT others(12): Show |
1 | a0002c0002t0002g0253 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2199+166_2199+184d others(21): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | ||||||
| chr6:46862703
|
CT | C | 47 | a0001c0001t0001g0108a0001c0001t0001g0206a0001c0001t0001g0210others(44): Show | 47 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.2199+184delA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | ||||||
| chr6:46862703
|
CTT | C | 84 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0100others(81): Show | 85 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.2199+183_2199+184d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | ||||||
| chr6:46862703
|
CTTT | C | 9 | a0001c0001t0001g0003a0001c0001t0001g0115a0001c0001t0001g0208others(6): Show | 10 | HG01515.hp1 HG02630.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.2199+182_2199+184d others(5): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | ||||||
| chr6:46862711
|
T | A | 2 | a0001c0013t0001g0250a0001c0013t0001g0277 | 2 | NA18939.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.2199+177A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862711 | ||||||
| chr6:46862754
|
T | C | 1 | a0002c0006t0002g0197 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2199+134A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862754 | ||||||
| chr6:46863166
|
C | T | 1 | a0001c0001t0001g0351 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1991-70G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46863166 | ||||||
| chr6:46863230
|
A | T | 1 | a0003c0003t0004g0171 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1991-134T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46863230 | ||||||
| chr6:46863231
|
C | T | 1 | a0001c0001t0001g0330 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1991-135G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46863231 | ||||||
| chr6:46863323
|
C | T | 323 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(320): Show | 326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1991-227G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46863323 | ||||||
| chr6:46863452
|
G | T | 1 | a0001c0004t0001g0203 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1991-356C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46863452 | ||||||
| chr6:46863490
|
G | A | 1 | a0001c0001t0001g0308 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1991-394C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46863490 | ||||||
| chr6:46863527
|
C | T | 1 | a0003c0003t0004g0171 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1991-431G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46863527 | ||||||
| chr6:46863540
|
T | C | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.1991-444A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46863540 | ||||||
| chr6:46863633
|
T | C | 1 | a0003c0003t0004g0125 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1991-537A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46863633 | ||||||
| chr6:46863655
|
T | C | 1 | a0004c0009t0029g0095 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1991-559A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46863655 | ||||||
| chr6:46863710
|
C | T | 2 | a0001c0001t0001g0368a0001c0001t0001g0369 | 2 | HG00738.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1991-614G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46863710 | ||||||
| chr6:46863759
|
T | C | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.1991-663A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46863759 | ||||||
| chr6:46863776
|
A | G | 3 | a0004c0009t0010g0012a0004c0009t0010g0013a0004c0009t0029g0095 | 3 | HG01106.hp2 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1991-680T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46863776 | ||||||
| chr6:46863783
|
A | G | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.1991-687T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46863783 | ||||||
| chr6:46864035
|
T | G | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.1991-939A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864035 | ||||||
| chr6:46864082
|
A | T | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.1990+960T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864082 | ||||||
| chr6:46864092
|
G | A | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.1990+950C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864092 | ||||||
| chr6:46864107
|
T | C | 3 | a0004c0009t0010g0012a0004c0009t0010g0013a0004c0009t0029g0095 | 3 | HG01106.hp2 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1990+935A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864107 | ||||||
| chr6:46864135
|
C | T | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.1990+907G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864135 | ||||||
| chr6:46864218
|
C | T | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.1990+824G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864218 | ||||||
| chr6:46864320
|
G | A | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.1990+722C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864320 | ||||||
| chr6:46864361
|
T | C | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.1990+681A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864361 | ||||||
| chr6:46864509
|
C | G | 1 | a0004c0011t0024g0262 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1990+533G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864509 | ||||||
| chr6:46864526
|
A | AT | 9 | a0001c0001t0001g0319a0001c0001t0005g0070a0001c0001t0005g0081others(6): Show | 9 | HG00741.hp2 HG01109.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1990+515dupA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864526 | ||||||
| chr6:46864526
|
A | ATT | 13 | a0003c0003t0004g0186a0003c0003t0004g0188a0003c0003t0004g0189others(10): Show | 13 | HG01106.hp2 HG01255.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1990+514_1990+515d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864526 | ||||||
| chr6:46864526
|
AT | A | 26 | a0001c0001t0001g0225a0001c0001t0001g0260a0001c0001t0001g0294others(23): Show | 26 | HG01074.hp1 HG01891.hp1 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.1990+515delA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864526 | ||||||
| chr6:46864526
|
ATT | A | 11 | a0002c0002t0002g0150a0002c0002t0002g0230a0002c0002t0002g0245others(8): Show | 11 | HG02056.hp1 HG02071.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1990+514_1990+515d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864526 | ||||||
| chr6:46864526
|
ATTT | A | 132 | a0002c0002t0002g0102a0002c0002t0002g0106a0002c0002t0002g0113others(129): Show | 132 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1990+513_1990+515d others(5): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864526 | ||||||
| chr6:46864628
|
G | A | 3 | a0004c0011t0006g0103a0004c0011t0024g0262a0004c0029t0028g0124 | 3 | HG02486.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1990+414C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864628 | ||||||
| chr6:46864753
|
T | C | 3 | a0003c0003t0004g0199a0010c0032t0004g0200a0017c0031t0004g0198 | 3 | HG02486.hp2 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1990+289A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864753 | ||||||
| chr6:46864799
|
T | C | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.1990+243A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864799 | ||||||
| chr6:46864816
|
A | G | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.1990+226T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864816 | ||||||
| chr6:46864820
|
G | A | 1 | a0020c0022t0001g0301 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1990+222C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864820 | ||||||
| chr6:46864825
|
A | G | 2 | a0003c0003t0014g0337a0019c0033t0014g0342 | 2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1990+217T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864825 | ||||||
| chr6:46864905
|
A | C | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.1990+137T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864905 | ||||||
| chr6:46865004
|
T | C | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.1990+38A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46865004 | ||||||
| chr6:46865231
|
A | G | 11 | a0001c0001t0001g0002a0001c0001t0001g0160a0001c0001t0001g0161others(8): Show | 12 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.1835-34T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46865231 | ||||||
| chr6:46865652
|
C | G | 1 | a0001c0001t0001g0264 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1835-455G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46865652 | ||||||
| chr6:46865925
|
C | T | 1 | a0004c0029t0028g0124 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1835-728G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46865925 | ||||||
| chr6:46865935
|
G | A | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.1835-738C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46865935 | ||||||
| chr6:46865958
|
A | G | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.1835-761T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46865958 | ||||||
| chr6:46865974
|
A | G | 1 | a0001c0004t0001g0167 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1835-777T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46865974 | ||||||
| chr6:46866005
|
AT | A | 362 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(359): Show | 365 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.1835-809delA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866005 | ||||||
| chr6:46866046
|
G | A | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.1835-849C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866046 | ||||||
| chr6:46866107
|
C | A | 143 | a0002c0002t0002g0101a0002c0002t0002g0102a0002c0002t0002g0106others(140): Show | 143 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1834+818G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866107 | ||||||
| chr6:46866165
|
A | T | 1 | a0003c0003t0004g0194 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1834+760T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866165 | ||||||
| chr6:46866311
|
A | G | 1 | a0001c0028t0006g0235 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1834+614T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866311 | ||||||
| chr6:46866316
|
CTT | C | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.1834+607_1834+608d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866316 | ||||||
| chr6:46866346
|
T | G | 1 | a0002c0002t0003g0091 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1834+579A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866346 | ||||||
| chr6:46866393
|
G | A | 146 | a0002c0002t0002g0101a0002c0002t0002g0102a0002c0002t0002g0106others(143): Show | 146 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.1834+532C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866393 | ||||||
| chr6:46866444
|
G | A | 2 | a0004c0011t0024g0262a0004c0029t0028g0124 | 2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1834+481C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866444 | ||||||
| chr6:46866564
|
AT | A | 4 | a0003c0003t0006g0241a0003c0003t0006g0344a0003c0003t0006g0345others(1): Show | 4 | HG01884.hp2 HG02717.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1834+360delA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866564 | ||||||
| chr6:46866659
|
A | C | 323 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(320): Show | 326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1834+266T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866659 | ||||||
| chr6:46866662
|
A | G | 1 | a0001c0001t0001g0370 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1834+263T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866662 | ||||||
| chr6:46866699
|
T | C | 8 | a0003c0003t0004g0171a0003c0003t0004g0226a0003c0003t0004g0227others(5): Show | 8 | HG01891.hp1 HG02572.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1834+226A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866699 | ||||||
| chr6:46866704
|
A | T | 146 | a0002c0002t0002g0101a0002c0002t0002g0102a0002c0002t0002g0106others(143): Show | 146 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.1834+221T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866704 | ||||||
| chr6:46866730
|
C | T | 3 | a0004c0009t0010g0012a0004c0009t0010g0013a0004c0009t0029g0095 | 3 | HG01106.hp2 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1834+195G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866730 | ||||||
| chr6:46866736
|
T | G | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.1834+189A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866736 | ||||||
| chr6:46867169
|
TG | T | 323 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(320): Show | 326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1622-33delC | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 12/20 | chr6 | 46867169 | ||||||
| chr6:46867467
|
A | G | 9 | a0003c0003t0006g0241a0003c0003t0006g0344a0003c0003t0006g0345others(6): Show | 9 | HG01243.hp2 HG01884.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1622-330T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 12/20 | chr6 | 46867467 | ||||||
| chr6:46867491
|
G | C | 4 | a0003c0003t0004g0199a0010c0032t0004g0200a0015c0026t0001g0338others(1): Show | 4 | HG02486.hp2 HG02559.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1622-354C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 12/20 | chr6 | 46867491 | ||||||
| chr6:46867565
|
C | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0232a0001c0001t0001g0266others(9): Show | 13 | HG00609.hp1 NA18939.hp1 NA18943.hp1 others(10): Show |
intron_variant | MODIFIER | c.1622-428G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 12/20 | chr6 | 46867565 | ||||||
| chr6:46867638
|
G | C | 1 | a0001c0028t0006g0235 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1622-501C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 12/20 | chr6 | 46867638 | ||||||
| chr6:46867760
|
C | T | 4 | a0001c0004t0001g0142a0001c0004t0001g0153a0001c0004t0005g0044others(1): Show | 4 | HG00544.hp1 HG01975.hp1 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.1622-623G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 12/20 | chr6 | 46867760 | ||||||
| chr6:46867794
|
TGC | T | 323 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(320): Show | 326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1622-659_1622-658d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 12/20 | chr6 | 46867794 | ||||||
| chr6:46867941
|
T | A | 323 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(320): Show | 326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1622-804A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 12/20 | chr6 | 46867941 | ||||||
| chr6:46868017
|
T | C | 14 | a0003c0003t0004g0186a0003c0003t0004g0188a0003c0003t0004g0189others(11): Show | 14 | HG00741.hp2 HG01255.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1621+866A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 12/20 | chr6 | 46868017 | ||||||
| chr6:46868035
|
C | A | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.1621+848G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 12/20 | chr6 | 46868035 | ||||||
| chr6:46868669
|
G | C | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.1621+214C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 12/20 | chr6 | 46868669 | ||||||
| chr6:46868785
|
T | C | 1 | a0003c0003t0004g0199 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1621+98A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 12/20 | chr6 | 46868785 | ||||||
| chr6:46868815
|
A | G | 1 | a0002c0002t0002g0102 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1621+68T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 12/20 | chr6 | 46868815 | ||||||
| chr6:46869109
|
C | G | 2 | a0002c0002t0002g0222a0002c0002t0002g0223 | 2 | HG00408.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1412-17G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46869109 | ||||||
| chr6:46869140
|
A | G | 1 | a0004c0029t0028g0124 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1412-48T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46869140 | ||||||
| chr6:46869258
|
T | C | 346 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(343): Show | 349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.1412-166A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46869258 | ||||||
| chr6:46869270
|
G | A | 4 | a0003c0003t0004g0120a0003c0003t0004g0121a0003c0003t0004g0194others(1): Show | 4 | HG02572.hp1 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1412-178C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46869270 | ||||||
| chr6:46869468
|
C | T | 136 | a0002c0002t0002g0101a0002c0002t0002g0102a0002c0002t0002g0106others(133): Show | 136 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1412-376G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46869468 | ||||||
| chr6:46869653
|
C | T | 144 | a0002c0002t0002g0101a0002c0002t0002g0102a0002c0002t0002g0106others(141): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.1412-561G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46869653 | ||||||
| chr6:46869770
|
C | T | 3 | a0004c0009t0010g0012a0004c0009t0010g0013a0004c0009t0029g0095 | 3 | HG01106.hp2 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1412-678G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46869770 | ||||||
| chr6:46869812
|
G | A | 2 | a0002c0002t0003g0020a0002c0002t0003g0021 | 2 | NA18951.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1412-720C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46869812 | ||||||
| chr6:46869832
|
A | G | 1 | a0003c0003t0004g0199 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1412-740T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46869832 | ||||||
| chr6:46869967
|
A | G | 6 | a0001c0001t0001g0112a0001c0004t0001g0154a0001c0004t0001g0155others(3): Show | 6 | HG03239.hp1 HG03492.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.1412-875T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46869967 | ||||||
| chr6:46870263
|
A | C | 323 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(320): Show | 326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1412-1171T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46870263 | ||||||
| chr6:46870279
|
A | G | 1 | a0002c0002t0003g0050 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1412-1187T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46870279 | ||||||
| chr6:46870304
|
C | T | 2 | a0004c0009t0010g0012a0004c0009t0010g0013 | 2 | HG01106.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1412-1212G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46870304 | ||||||
| chr6:46870305
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1412-1213G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46870305 | ||||||
| chr6:46870330
|
A | T | 1 | a0001c0019t0001g0270 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1412-1238T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46870330 | ||||||
| chr6:46870379
|
G | A | 1 | a0001c0012t0001g0295 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1412-1287C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46870379 | ||||||
| chr6:46870390
|
C | G | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.1412-1298G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46870390 | ||||||
| chr6:46870737
|
GCTTAACA others(4): Show |
G | 1 | a0001c0001t0001g0325 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1411+1095_1411+110 others(15): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46870737 | ||||||
| chr6:46870837
|
G | A | 2 | a0003c0003t0014g0337a0019c0033t0014g0342 | 2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1411+1006C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46870837 | ||||||
| chr6:46870922
|
T | TTG | 356 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(353): Show | 359 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.1411+919_1411+920d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46870922 | ||||||
| chr6:46870957
|
T | C | 1 | a0002c0002t0002g0245 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1411+886A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46870957 | ||||||
| chr6:46870961
|
T | C | 1 | a0003c0025t0004g0239 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1411+882A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46870961 | ||||||
| chr6:46870981
|
A | G | 3 | a0001c0001t0001g0116a0001c0001t0001g0271a0001c0004t0001g0146 | 3 | HG03831.hp1 NA18941.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1411+862T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46870981 | ||||||
| chr6:46871026
|
C | T | 1 | a0002c0017t0002g0139 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1411+817G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46871026 | ||||||
| chr6:46871072
|
A | G | 2 | a0001c0001t0001g0323a0001c0001t0001g0324 | 2 | HG01167.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.1411+771T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46871072 | ||||||
| chr6:46871183
|
A | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0359a0001c0001t0001g0364others(151): Show | 155 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.1411+660T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46871183 | ||||||
| chr6:46871211
|
T | C | 14 | a0003c0003t0004g0186a0003c0003t0004g0188a0003c0003t0004g0189others(11): Show | 14 | HG00741.hp2 HG01255.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1411+632A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46871211 | ||||||
| chr6:46871325
|
A | G | 1 | a0003c0003t0017g0014 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1411+518T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46871325 | ||||||
| chr6:46871453
|
A | G | 3 | a0001c0004t0001g0118a0001c0004t0001g0119a0001c0004t0001g0127 | 3 | HG02523.hp1 NA18952.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1411+390T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46871453 | ||||||
| chr6:46871524
|
A | G | 10 | a0002c0002t0002g0244a0002c0002t0016g0009a0003c0003t0006g0350others(7): Show | 10 | HG01243.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1411+319T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46871524 | ||||||
| chr6:46871571
|
C | A | 5 | a0003c0003t0004g0199a0003c0003t0004g0226a0003c0003t0011g0010others(2): Show | 5 | HG02486.hp2 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1411+272G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46871571 | ||||||
| chr6:46871620
|
T | G | 309 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(306): Show | 312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1411+223A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46871620 | ||||||
| chr6:46871698
|
T | C | 22 | a0001c0001t0001g0003a0001c0001t0001g0202a0001c0001t0001g0236others(19): Show | 23 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.1411+145A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46871698 | ||||||
| chr6:46871725
|
A | T | 2 | a0002c0002t0016g0009a0004c0008t0009g0096 | 2 | HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1411+118T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46871725 | ||||||
| chr6:46871738
|
G | A | 3 | a0001c0001t0001g0313a0001c0001t0005g0093a0020c0022t0001g0301 | 3 | HG00738.hp2 HG01099.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1411+105C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46871738 | ||||||
| chr6:46871807
|
C | G | 1 | a0003c0003t0004g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1411+36G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46871807 | ||||||
| chr6:46872021
|
G | A | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | NA18956.hp1 NA18984.hp1 |
splice_region_variant&intron_variant | LOW | c.1241-8C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46872021 | ||||||
| chr6:46872085
|
A | AT | 7 | a0002c0002t0002g0240a0002c0002t0002g0360a0002c0002t0002g0361others(4): Show | 7 | HG02451.hp1 HG02615.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.1241-73dupA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46872085 | ||||||
| chr6:46872337
|
T | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0097a0001c0001t0001g0100others(114): Show | 118 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.1241-324A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46872337 | ||||||
| chr6:46872369
|
G | C | 1 | a0001c0001t0001g0215 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1241-356C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46872369 | ||||||
| chr6:46872646
|
G | A | 1 | a0002c0002t0003g0066 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1241-633C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46872646 | ||||||
| chr6:46872681
|
A | G | 1 | a0002c0002t0003g0055 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1241-668T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46872681 | ||||||
| chr6:46872709
|
A | C | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(317): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.1241-696T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46872709 | ||||||
| chr6:46872799
|
C | T | 1 | a0003c0003t0019g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1241-786G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46872799 | ||||||
| chr6:46872875
|
C | T | 1 | a0002c0017t0002g0139 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1241-862G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46872875 | ||||||
| chr6:46872876
|
G | A | 1 | a0003c0003t0013g0032 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1241-863C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46872876 | ||||||
| chr6:46872967
|
G | C | 6 | a0001c0001t0001g0359a0001c0001t0015g0007a0002c0002t0002g0169others(3): Show | 6 | HG02145.hp1 HG02572.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1241-954C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46872967 | ||||||
| chr6:46873024
|
C | T | 16 | a0001c0001t0001g0206a0001c0001t0001g0210a0001c0001t0001g0211others(13): Show | 16 | HG00423.hp1 HG01243.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.1241-1011G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46873024 | ||||||
| chr6:46873101
|
T | G | 17 | a0001c0001t0001g0001a0001c0001t0001g0256a0001c0001t0001g0266others(14): Show | 18 | HG02071.hp2 NA18939.hp1 NA18941.hp1 others(15): Show |
intron_variant | MODIFIER | c.1241-1088A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46873101 | ||||||
| chr6:46873102
|
A | C | 1 | a0001c0001t0001g0221 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1241-1089T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46873102 | ||||||
| chr6:46873119
|
C | A | 1 | a0002c0002t0003g0034 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1241-1106G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46873119 | ||||||
| chr6:46873138
|
C | T | 1 | a0003c0003t0004g0189 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1241-1125G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46873138 | ||||||
| chr6:46873146
|
G | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0097a0001c0001t0001g0100others(111): Show | 115 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.1241-1133C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46873146 | ||||||
| chr6:46873296
|
G | A | 1 | a0004c0011t0006g0103 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1241-1283C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46873296 | ||||||
| chr6:46873569
|
T | C | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(317): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.1241-1556A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46873569 | ||||||
| chr6:46873630
|
C | G | 64 | a0001c0001t0005g0047a0001c0001t0005g0073a0001c0001t0005g0080others(61): Show | 64 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.1241-1617G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46873630 | ||||||
| chr6:46873813
|
T | A | 4 | a0002c0002t0002g0360a0002c0002t0002g0361a0002c0002t0002g0362others(1): Show | 4 | HG02615.hp1 HG03540.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1241-1800A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46873813 | ||||||
| chr6:46873853
|
A | G | 3 | a0001c0001t0001g0359a0001c0001t0015g0007a0015c0026t0001g0338 | 3 | HG02145.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1241-1840T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46873853 | ||||||
| chr6:46873864
|
C | T | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0097others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.1241-1851G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46873864 | ||||||
| chr6:46873980
|
C | A | 1 | a0003c0003t0004g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1241-1967G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46873980 | ||||||
| chr6:46874001
|
T | C | 7 | a0002c0006t0002g0196a0002c0006t0002g0197a0002c0006t0003g0026others(4): Show | 7 | HG00642.hp1 HG02055.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1241-1988A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46874001 | ||||||
| chr6:46874069
|
C | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0097others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.1241-2056G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46874069 | ||||||
| chr6:46874132
|
T | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0108a0001c0001t0001g0109 | 3 | NA18950.hp2 NA18973.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1241-2119A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46874132 | ||||||
| chr6:46874170
|
C | T | 1 | a0003c0003t0004g0227 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1241-2157G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46874170 | ||||||
| chr6:46874400
|
C | T | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0097others(225): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1241-2387G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46874400 | ||||||
| chr6:46874472
|
G | T | 10 | a0003c0003t0004g0186a0003c0003t0004g0188a0003c0003t0004g0189others(7): Show | 10 | HG00741.hp2 HG01255.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241-2459C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46874472 | ||||||
| chr6:46874664
|
C | A | 6 | a0001c0004t0018g0015a0002c0005t0002g0348a0002c0005t0003g0025others(3): Show | 6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1241-2651G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46874664 | ||||||
| chr6:46874714
|
T | G | 2 | a0001c0001t0001g0368a0001c0001t0001g0369 | 2 | HG00738.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1241-2701A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46874714 | ||||||
| chr6:46874732
|
G | A | 1 | a0002c0014t0002g0209 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1241-2719C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46874732 | ||||||
| chr6:46874746
|
T | G | 1 | a0001c0001t0023g0088 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1241-2733A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46874746 | ||||||
| chr6:46874899
|
G | A | 3 | a0002c0002t0002g0240a0003c0003t0017g0014a0003c0025t0004g0239 | 3 | HG02451.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1241-2886C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46874899 | ||||||
| chr6:46874952
|
G | T | 16 | a0001c0001t0001g0206a0001c0001t0001g0210a0001c0001t0001g0211others(13): Show | 16 | HG00423.hp1 HG01243.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.1241-2939C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46874952 | ||||||
| chr6:46875008
|
G | A | 1 | a0003c0003t0004g0194 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1241-2995C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46875008 | ||||||
| chr6:46875144
|
C | T | 1 | a0006c0010t0001g0193 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1240+3058G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46875144 | ||||||
| chr6:46875154
|
T | A | 17 | a0001c0001t0001g0206a0001c0001t0001g0210a0001c0001t0001g0211others(14): Show | 17 | HG00423.hp1 HG01243.hp1 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.1240+3048A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46875154 | ||||||
| chr6:46875197
|
G | T | 1 | a0001c0001t0005g0081 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1240+3005C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46875197 | ||||||
| chr6:46875442
|
C | T | 1 | a0001c0004t0018g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1240+2760G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46875442 | ||||||
| chr6:46875981
|
C | T | 6 | a0001c0001t0001g0260a0001c0001t0001g0332a0001c0001t0001g0333others(3): Show | 6 | HG00639.hp2 HG01175.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1240+2221G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46875981 | ||||||
| chr6:46876015
|
G | A | 321 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(318): Show | 324 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.1240+2187C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876015 | ||||||
| chr6:46876056
|
T | A | 1 | a0001c0004t0001g0153 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1240+2146A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876056 | ||||||
| chr6:46876139
|
A | G | 1 | a0002c0002t0002g0249 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1240+2063T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876139 | ||||||
| chr6:46876227
|
G | T | 6 | a0001c0004t0018g0015a0002c0005t0002g0348a0002c0005t0003g0025others(3): Show | 6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240+1975C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876227 | ||||||
| chr6:46876359
|
G | T | 3 | a0002c0002t0002g0247a0002c0002t0002g0248a0003c0003t0004g0226 | 3 | HG00280.hp1 HG01070.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1240+1843C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876359 | ||||||
| chr6:46876585
|
G | C | 1 | a0002c0002t0002g0106 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1240+1617C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876585 | ||||||
| chr6:46876605
|
T | C | 2 | a0001c0001t0001g0111a0001c0001t0001g0351 | 2 | HG02683.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1240+1597A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876605 | ||||||
| chr6:46876613
|
T | C | 1 | a0003c0003t0004g0186 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1240+1589A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876613 | ||||||
| chr6:46876689
|
G | T | 1 | a0003c0007t0007g0159 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1240+1513C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876689 | ||||||
| chr6:46876720
|
C | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0351 | 2 | HG02683.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1240+1482G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876720 | ||||||
| chr6:46876729
|
A | G | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(317): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.1240+1473T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876729 | ||||||
| chr6:46876777
|
G | A | 1 | a0002c0002t0003g0087 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1240+1425C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876777 | ||||||
| chr6:46876832
|
C | T | 1 | a0003c0003t0013g0090 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1240+1370G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876832 | ||||||
| chr6:46876841
|
A | T | 45 | a0001c0001t0005g0047a0001c0001t0005g0073a0001c0001t0005g0080others(42): Show | 45 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.1240+1361T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876841 | ||||||
| chr6:46876899
|
CT | C | 230 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0097others(227): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.1240+1302delA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876899 | ||||||
| chr6:46876939
|
A | G | 3 | a0001c0001t0001g0359a0001c0001t0015g0007a0015c0026t0001g0338 | 3 | HG02145.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1240+1263T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876939 | ||||||
| chr6:46877046
|
T | C | 2 | a0003c0003t0011g0010a0003c0003t0011g0011 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1240+1156A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877046 | ||||||
| chr6:46877056
|
A | C | 1 | a0002c0002t0003g0050 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1240+1146T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877056 | ||||||
| chr6:46877094
|
A | G | 111 | a0001c0001t0001g0002a0001c0001t0001g0202a0001c0001t0001g0206others(108): Show | 112 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.1240+1108T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877094 | ||||||
| chr6:46877100
|
C | A | 1 | a0002c0002t0003g0061 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1240+1102G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877100 | ||||||
| chr6:46877225
|
C | CTCTT | 4 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0293others(1): Show | 4 | HG00544.hp2 HG01175.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+973_1240+976d others(6): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877225 | ||||||
| chr6:46877225
|
C | CTCTTTCT others(1): Show |
5 | a0001c0001t0001g0100a0001c0001t0001g0374a0002c0002t0002g0101others(2): Show | 5 | HG01516.hp1 HG03195.hp2 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240+969_1240+976d others(10): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877225 | ||||||
| chr6:46877225
|
C | CTCTTTCT others(5): Show |
2 | a0002c0002t0026g0098a0007c0016t0001g0201 | 2 | HG03491.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1240+965_1240+976d others(14): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877225 | ||||||
| chr6:46877225
|
CTCTT | C | 13 | a0001c0001t0001g0110a0001c0001t0001g0305a0001c0001t0005g0053others(10): Show | 13 | HG00597.hp1 HG00621.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1240+973_1240+976d others(6): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877225 | ||||||
| chr6:46877225
|
CTCTTTCT others(1): Show |
C | 11 | a0001c0001t0001g0160a0001c0001t0001g0255a0001c0001t0001g0323others(8): Show | 11 | HG00099.hp1 HG00408.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.1240+969_1240+976d others(10): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877225 | ||||||
| chr6:46877225
|
CTCTTTCT others(5): Show |
C | 7 | a0001c0001t0001g0279a0001c0001t0001g0280a0002c0002t0002g0253others(4): Show | 7 | HG01106.hp2 HG02257.hp1 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240+965_1240+976d others(14): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877225 | ||||||
| chr6:46877225
|
CTCTTTCT others(9): Show |
C | 2 | a0001c0004t0005g0044a0014c0020t0001g0339 | 2 | HG00544.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1240+961_1240+976d others(18): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877225 | ||||||
| chr6:46877236
|
T | C | 1 | a0001c0001t0001g0329 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1240+966A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877236 | ||||||
| chr6:46877275
|
CTTTCTTT others(7): Show |
C | 5 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0217others(2): Show | 5 | HG01358.hp2 HG01952.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240+913_1240+926d others(16): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877275 | ||||||
| chr6:46877277
|
TTCTTTCT others(9): Show |
T | 4 | a0001c0001t0001g0265a0001c0001t0001g0303a0002c0002t0002g0251others(1): Show | 4 | HG01175.hp1 HG01346.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+909_1240+924d others(18): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877277 | ||||||
| chr6:46877279
|
CTTTCTT | C | 3 | a0003c0003t0004g0226a0003c0003t0004g0347a0003c0003t0017g0014 | 3 | HG03540.hp1 HG03579.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1240+917_1240+922d others(8): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877279 | ||||||
| chr6:46877281
|
T | C | 1 | a0003c0025t0004g0239 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1240+921A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877281 | ||||||
| chr6:46877281
|
TTCTTTCT others(3): Show |
T | 1 | a0003c0003t0004g0195 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1240+911_1240+920d others(12): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877281 | ||||||
| chr6:46877281
|
TTCTTTCT others(5): Show |
T | 15 | a0001c0001t0001g0105a0001c0001t0001g0112a0001c0001t0001g0228others(12): Show | 15 | HG00639.hp2 HG01361.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1240+909_1240+920d others(14): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877281 | ||||||
| chr6:46877283
|
CTT | C | 3 | a0001c0001t0001g0378a0002c0002t0003g0021a0002c0002t0025g0179 | 3 | NA18943.hp2 NA18989.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1240+917_1240+918d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877283 | ||||||
| chr6:46877283
|
CTTTCTT | C | 5 | a0001c0001t0001g0370a0001c0001t0005g0045a0002c0002t0020g0028others(2): Show | 5 | HG00323.hp2 HG01975.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240+913_1240+918d others(8): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877283 | ||||||
| chr6:46877285
|
T | C | 16 | a0001c0001t0001g0220a0001c0001t0001g0283a0001c0001t0001g0340others(13): Show | 16 | HG00408.hp2 HG00597.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.1240+917A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877285 | ||||||
| chr6:46877285
|
TTCTTTC | T | 5 | a0001c0001t0001g0003a0001c0004t0001g0129a0001c0028t0006g0235others(2): Show | 6 | HG01261.hp1 HG02145.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1240+911_1240+916d others(8): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877285 | ||||||
| chr6:46877285
|
TTCTTTCT others(1): Show |
T | 18 | a0001c0001t0001g0208a0001c0001t0001g0267a0001c0001t0001g0290others(15): Show | 18 | HG00099.hp2 HG01168.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1240+909_1240+916d others(10): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877285 | ||||||
| chr6:46877287
|
CTT | C | 13 | a0001c0001t0001g0202a0001c0001t0001g0261a0001c0001t0002g0375others(10): Show | 13 | HG00423.hp1 HG01243.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1240+913_1240+914d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877287 | ||||||
| chr6:46877289
|
T | C | 48 | a0001c0001t0001g0220a0001c0001t0001g0232a0001c0001t0001g0236others(45): Show | 48 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.1240+913A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877289 | ||||||
| chr6:46877289
|
T | TTCTTTCT others(7): Show |
1 | a0006c0010t0001g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1240+912_1240+913i others(16): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877289 | ||||||
| chr6:46877289
|
TTC | T | 8 | a0001c0001t0001g0115a0003c0003t0004g0199a0004c0008t0009g0354others(5): Show | 8 | HG02280.hp2 HG02486.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1240+911_1240+912d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877289 | ||||||
| chr6:46877289
|
TTCTCTCT others(3): Show |
T | 1 | a0003c0003t0004g0162 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1240+903_1240+912d others(12): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877289 | ||||||
| chr6:46877291
|
C | CTT | 6 | a0001c0004t0001g0146a0003c0003t0004g0237a0003c0003t0006g0350others(3): Show | 6 | HG01243.hp2 HG02622.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240+910_1240+911i others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877291 | ||||||
| chr6:46877293
|
C | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0097others(98): Show | 103 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.1240+909G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877293 | ||||||
| chr6:46877295
|
C | CCTTCCTT others(7): Show |
1 | a0003c0025t0004g0239 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1240+906_1240+907i others(16): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877295 | ||||||
| chr6:46877295
|
C | T | 3 | a0001c0001t0001g0283a0001c0001t0001g0340a0003c0003t0006g0350 | 3 | HG00733.hp2 HG01243.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.1240+907G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877295 | ||||||
| chr6:46877297
|
C | T | 29 | a0001c0001t0001g0212a0001c0001t0001g0310a0001c0001t0001g0325others(26): Show | 29 | HG01071.hp2 HG01168.hp1 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.1240+905G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877297 | ||||||
| chr6:46877298
|
T | C | 3 | a0001c0001t0001g0340a0002c0006t0003g0029a0003c0025t0004g0239 | 3 | HG00733.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1240+904A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877298 | ||||||
| chr6:46877299
|
C | CCT | 4 | a0001c0001t0001g0283a0002c0002t0002g0177a0002c0002t0002g0222others(1): Show | 4 | HG00408.hp2 HG02015.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1240+902_1240+903i others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877299 | ||||||
| chr6:46877299
|
C | CCTTCCT | 6 | a0001c0001t0001g0220a0002c0002t0002g0169a0002c0002t0002g0315others(3): Show | 6 | HG00597.hp2 HG02572.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1240+902_1240+903i others(8): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877299 | ||||||
| chr6:46877299
|
C | CCTTCCTT others(7): Show |
1 | a0001c0001t0015g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1240+902_1240+903i others(16): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877299 | ||||||
| chr6:46877299
|
C | T | 9 | a0001c0001t0001g0287a0001c0001t0001g0330a0001c0001t0001g0340others(6): Show | 9 | HG00642.hp2 HG00673.hp1 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.1240+903G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877299 | ||||||
| chr6:46877301
|
C | T | 4 | a0001c0001t0001g0359a0001c0004t0001g0155a0002c0002t0002g0367others(1): Show | 4 | HG02698.hp2 HG03209.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+901G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877301 | ||||||
| chr6:46877302
|
T | C | 25 | a0001c0001t0001g0220a0001c0001t0001g0283a0001c0001t0001g0287others(22): Show | 25 | HG00408.hp2 HG00597.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.1240+900A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877302 | ||||||
| chr6:46877303
|
C | CCT | 7 | a0001c0001t0001g0232a0001c0001t0001g0236a0001c0001t0001g0377others(4): Show | 7 | HG00609.hp1 HG00741.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.1240+898_1240+899i others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877303 | ||||||
| chr6:46877303
|
C | CCTTCCT | 4 | a0002c0002t0002g0172a0002c0002t0002g0176a0002c0002t0002g0246others(1): Show | 4 | HG01943.hp1 HG02809.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+898_1240+899i others(8): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877303 | ||||||
| chr6:46877303
|
C | CCTTCCTT others(3): Show |
6 | a0001c0001t0001g0364a0002c0002t0002g0107a0002c0002t0002g0113others(3): Show | 6 | HG01074.hp2 HG02055.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1240+898_1240+899i others(12): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877303 | ||||||
| chr6:46877303
|
C | CCTTCCTT others(15): Show |
1 | a0001c0001t0001g0359 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1240+898_1240+899i others(24): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877303 | ||||||
| chr6:46877303
|
C | CTTTCCTT others(19): Show |
1 | a0002c0002t0002g0240 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1240+898_1240+899i others(28): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877303 | ||||||
| chr6:46877303
|
C | T | 91 | a0001c0001t0001g0104a0001c0001t0001g0110a0001c0001t0001g0116others(88): Show | 91 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1240+899G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877303 | ||||||
| chr6:46877305
|
C | T | 1 | a0001c0004t0001g0155 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1240+897G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877305 | ||||||
| chr6:46877305
|
CTT | C | 7 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0004t0001g0131others(4): Show | 7 | HG00741.hp2 HG01884.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.1240+895_1240+896d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877305 | ||||||
| chr6:46877306
|
T | C | 137 | a0001c0001t0001g0104a0001c0001t0001g0110a0001c0001t0001g0116others(134): Show | 137 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1240+896A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877306 | ||||||
| chr6:46877306
|
T | TCC | 3 | a0001c0001t0001g0366a0002c0002t0002g0181a0003c0003t0004g0191 | 3 | HG01123.hp1 HG02970.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.1240+895_1240+896i others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877306 | ||||||
| chr6:46877306
|
T | TCCTTCC | 7 | a0002c0002t0002g0173a0002c0002t0002g0218a0002c0002t0002g0219others(4): Show | 7 | HG01070.hp2 HG01099.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240+895_1240+896i others(8): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877306 | ||||||
| chr6:46877306
|
T | TCCTTCCT others(3): Show |
14 | a0001c0001t0001g0225a0001c0001t0001g0368a0001c0001t0001g0374others(11): Show | 14 | HG00438.hp1 HG00738.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.1240+895_1240+896i others(12): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877306 | ||||||
| chr6:46877306
|
T | TCCTTCCT others(7): Show |
7 | a0002c0002t0002g0102a0002c0002t0002g0184a0002c0002t0002g0224others(4): Show | 7 | HG00323.hp1 HG00642.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240+895_1240+896i others(16): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877306 | ||||||
| chr6:46877306
|
T | TCTCTCCT others(3): Show |
2 | a0001c0001t0001g0369a0002c0002t0003g0020 | 2 | HG01515.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.1240+895_1240+896i others(12): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877306 | ||||||
| chr6:46877306
|
T | TCTCTCCT others(7): Show |
2 | a0001c0001t0001g0002a0002c0002t0003g0019 | 3 | HG01070.hp1 HG01071.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.1240+895_1240+896i others(16): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877306 | ||||||
| chr6:46877306
|
T | TCTCTTTC others(5): Show |
2 | a0001c0001t0001g0325a0002c0002t0002g0327 | 2 | NA18966.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1240+895_1240+896i others(14): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877306 | ||||||
| chr6:46877306
|
TTTCCTTC others(9): Show |
T | 2 | a0002c0002t0002g0367a0002c0002t0003g0086 | 2 | HG02698.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1240+880_1240+895d others(18): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877306 | ||||||
| chr6:46877307
|
T | C | 44 | a0001c0001t0001g0206a0001c0001t0001g0212a0001c0001t0001g0213others(41): Show | 44 | HG01071.hp2 HG01168.hp1 HG01192.hp1 others(41): Show |
intron_variant | MODIFIER | c.1240+895A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877307 | ||||||
| chr6:46877309
|
CCT | C | 6 | a0001c0001t0001g0206a0001c0001t0001g0212a0001c0001t0001g0213others(3): Show | 6 | HG01496.hp1 HG02602.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240+891_1240+892d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877309 | ||||||
| chr6:46877310
|
C | T | 39 | a0001c0001t0001g0310a0001c0001t0005g0060a0001c0001t0005g0069others(36): Show | 39 | HG01071.hp2 HG01168.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.1240+892G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877310 | ||||||
| chr6:46877311
|
T | C | 8 | a0001c0001t0005g0060a0001c0001t0023g0088a0001c0004t0001g0127others(5): Show | 8 | HG01071.hp2 HG01243.hp2 HG03654.hp2 others(5): Show |
intron_variant | MODIFIER | c.1240+891A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877311 | ||||||
| chr6:46877314
|
C | T | 10 | a0001c0001t0001g0212a0001c0001t0005g0060a0001c0001t0023g0088others(7): Show | 10 | HG01071.hp2 HG02647.hp1 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.1240+888G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877314 | ||||||
| chr6:46877315
|
T | C | 3 | a0001c0001t0001g0212a0001c0004t0001g0155a0002c0014t0002g0209 | 3 | HG03654.hp2 NA18990.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1240+887A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877315 | ||||||
| chr6:46877318
|
C | T | 1 | a0001c0004t0001g0155 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1240+884G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877318 | ||||||
| chr6:46877319
|
T | C | 1 | a0001c0004t0001g0155 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1240+883A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877319 | ||||||
| chr6:46877322
|
C | T | 2 | a0001c0004t0001g0155a0003c0003t0004g0162 | 2 | HG02647.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1240+880G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877322 | ||||||
| chr6:46877322
|
CTTCT | C | 7 | a0001c0001t0001g0149a0001c0001t0005g0052a0001c0001t0005g0070others(4): Show | 7 | HG01106.hp2 HG01192.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.1240+876_1240+879d others(6): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877322 | ||||||
| chr6:46877322
|
CTTCTTTC others(1): Show |
C | 13 | a0001c0001t0005g0053a0001c0001t0005g0083a0001c0001t0023g0088others(10): Show | 13 | HG01891.hp1 HG02055.hp2 HG02698.hp1 others(10): Show |
intron_variant | MODIFIER | c.1240+872_1240+879d others(10): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877322 | ||||||
| chr6:46877322
|
CTTCTTTC others(5): Show |
C | 11 | a0001c0001t0005g0085a0001c0004t0001g0142a0001c0004t0001g0157others(8): Show | 11 | HG00280.hp2 HG00544.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.1240+868_1240+879d others(14): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877322 | ||||||
| chr6:46877322
|
CTTCTTTC others(9): Show |
C | 19 | a0001c0001t0005g0041a0001c0001t0005g0042a0001c0001t0005g0059others(16): Show | 19 | HG00639.hp1 HG00673.hp2 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.1240+864_1240+879d others(18): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877322 | ||||||
| chr6:46877322
|
CTTCTTTC others(13): Show |
C | 18 | a0001c0004t0001g0166a0002c0002t0002g0230a0002c0002t0002g0231others(15): Show | 18 | HG01168.hp1 HG01346.hp1 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1240+860_1240+879d others(22): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877322 | ||||||
| chr6:46877322
|
CTTCTTTC others(17): Show |
C | 30 | a0001c0001t0001g0003a0001c0001t0005g0047a0001c0001t0005g0073others(27): Show | 31 | HG00558.hp2 HG00621.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.1240+856_1240+879d others(26): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877322 | ||||||
| chr6:46877322
|
CTTCTTTC others(21): Show |
C | 31 | a0001c0001t0001g0115a0001c0028t0006g0235a0002c0002t0002g0123others(28): Show | 31 | HG00733.hp1 HG01167.hp2 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.1240+852_1240+879d others(30): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877322 | ||||||
| chr6:46877322
|
CTTCTTTC others(25): Show |
C | 2 | a0002c0002t0002g0243a0003c0003t0004g0094 | 2 | HG02615.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1240+848_1240+879d others(34): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877322 | ||||||
| chr6:46877323
|
T | C | 3 | a0002c0002t0002g0367a0002c0002t0003g0086a0003c0003t0004g0162 | 3 | HG02647.hp1 HG02698.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1240+879A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877323 | ||||||
| chr6:46877326
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0097others(205): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1240+876A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877326 | ||||||
| chr6:46877327
|
T | C | 3 | a0002c0002t0002g0367a0002c0002t0003g0086a0003c0003t0004g0162 | 3 | HG02647.hp1 HG02698.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1240+875A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877327 | ||||||
| chr6:46877330
|
T | C | 180 | a0001c0001t0001g0001a0001c0001t0001g0097a0001c0001t0001g0100others(177): Show | 181 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.1240+872A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877330 | ||||||
| chr6:46877334
|
T | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0097a0001c0001t0001g0100others(137): Show | 141 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.1240+868A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877334 | ||||||
| chr6:46877338
|
T | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0097a0001c0001t0001g0100others(88): Show | 92 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1240+864A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877338 | ||||||
| chr6:46877342
|
T | C | 19 | a0001c0001t0001g0111a0001c0001t0001g0161a0001c0001t0001g0212others(16): Show | 19 | HG00099.hp2 HG01081.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.1240+860A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877342 | ||||||
| chr6:46877346
|
T | C | 22 | a0001c0001t0001g0111a0001c0001t0001g0285a0002c0002t0002g0230others(19): Show | 22 | HG01168.hp1 HG01192.hp2 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.1240+856A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877346 | ||||||
| chr6:46877350
|
T | C | 44 | a0001c0001t0001g0003a0001c0001t0005g0047a0001c0001t0005g0073others(41): Show | 45 | HG00558.hp2 HG00621.hp1 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.1240+852A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877350 | ||||||
| chr6:46877351
|
T | C | 1 | a0003c0034t0008g0004 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1240+851A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877351 | ||||||
| chr6:46877354
|
T | C | 18 | a0001c0001t0001g0115a0001c0028t0006g0235a0002c0002t0003g0072others(15): Show | 18 | HG01261.hp1 HG01884.hp2 HG02083.hp2 others(15): Show |
intron_variant | MODIFIER | c.1240+848A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877354 | ||||||
| chr6:46877357
|
CTTTCTTT others(14): Show |
C | 8 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0217others(5): Show | 8 | HG00423.hp1 HG01243.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.1240+824_1240+844d others(23): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877357 | ||||||
| chr6:46877358
|
T | C | 2 | a0003c0003t0004g0094a0004c0011t0006g0103 | 2 | HG02615.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1240+844A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877358 | ||||||
| chr6:46877361
|
CTTTCTTT others(10): Show |
C | 3 | a0001c0001t0001g0214a0001c0001t0001g0215a0005c0015t0001g0216 | 3 | HG02129.hp2 HG02155.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1240+824_1240+840d others(19): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877361 | ||||||
| chr6:46877362
|
T | C | 1 | a0001c0004t0001g0155 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1240+840A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877362 | ||||||
| chr6:46877365
|
CTTTCTTT others(6): Show |
C | 7 | a0001c0001t0001g0206a0001c0001t0001g0213a0001c0001t0001g0288others(4): Show | 7 | HG01496.hp1 HG02109.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240+824_1240+836d others(15): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877365 | ||||||
| chr6:46877369
|
CTTTCTTT others(2): Show |
C | 3 | a0001c0001t0001g0212a0001c0001t0001g0294a0002c0014t0002g0209 | 3 | NA18990.hp2 NA18993.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1240+824_1240+832d others(11): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877369 | ||||||
| chr6:46877373
|
CTTTCT | C | 31 | a0001c0001t0001g0104a0001c0001t0001g0116a0001c0001t0001g0229others(28): Show | 31 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.1240+824_1240+828d others(7): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877373 | ||||||
| chr6:46877377
|
CT | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0097others(138): Show | 143 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.1240+824delA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877377 | ||||||
| chr6:46877378
|
T | TTTC | 27 | a0001c0001t0001g0161a0001c0001t0001g0266a0001c0001t0001g0284others(24): Show | 27 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.1240+821_1240+823d others(5): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877378 | ||||||
| chr6:46877378
|
T | TTTCTTTC | 5 | a0001c0001t0001g0111a0001c0001t0001g0285a0001c0001t0001g0319others(2): Show | 5 | HG01192.hp2 HG01258.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+817_1240+823d others(9): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877378 | ||||||
| chr6:46877384
|
T | C | 1 | a0001c0001t0005g0060 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1240+818A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877384 | ||||||
| chr6:46877385
|
C | T | 1 | a0001c0001t0005g0060 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1240+817G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877385 | ||||||
| chr6:46877487
|
G | C | 1 | a0003c0003t0004g0121 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1240+715C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877487 | ||||||
| chr6:46877536
|
A | G | 1 | a0003c0003t0013g0090 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1240+666T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877536 | ||||||
| chr6:46877545
|
C | T | 2 | a0002c0002t0002g0133a0002c0002t0002g0134 | 2 | NA19002.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1240+657G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877545 | ||||||
| chr6:46877710
|
G | C | 1 | a0001c0001t0001g0274 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1240+492C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877710 | ||||||
| chr6:46877736
|
T | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0097a0001c0001t0001g0100others(111): Show | 115 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.1240+466A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877736 | ||||||
| chr6:46877753
|
T | C | 1 | a0001c0001t0001g0310 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1240+449A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877753 | ||||||
| chr6:46877759
|
G | C | 1 | a0003c0003t0004g0356 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1240+443C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877759 | ||||||
| chr6:46877860
|
G | T | 2 | a0002c0002t0002g0247a0002c0002t0002g0248 | 2 | HG00280.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.1240+342C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877860 | ||||||
| chr6:46878042
|
G | A | 6 | a0001c0004t0018g0015a0002c0005t0002g0348a0002c0005t0003g0025others(3): Show | 6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240+160C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46878042 | ||||||
| chr6:46878052
|
A | T | 1 | a0003c0034t0008g0004 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1240+150T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46878052 | ||||||
| chr6:46878489
|
A | T | 3 | a0003c0003t0004g0199a0010c0032t0004g0200a0017c0031t0004g0198 | 3 | HG02486.hp2 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1037-84T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46878489 | ||||||
| chr6:46878540
|
G | A | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(317): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.1037-135C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46878540 | ||||||
| chr6:46878554
|
C | G | 2 | a0001c0001t0001g0359a0001c0001t0015g0007 | 2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1037-149G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46878554 | ||||||
| chr6:46878657
|
A | G | 6 | a0001c0004t0018g0015a0002c0005t0002g0348a0002c0005t0003g0025others(3): Show | 6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1037-252T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46878657 | ||||||
| chr6:46878811
|
A | G | 2 | a0001c0001t0001g0359a0001c0001t0015g0007 | 2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1037-406T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46878811 | ||||||
| chr6:46878967
|
G | A | 1 | a0002c0005t0003g0025 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1037-562C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46878967 | ||||||
| chr6:46879034
|
C | T | 3 | a0003c0003t0004g0199a0010c0032t0004g0200a0017c0031t0004g0198 | 3 | HG02486.hp2 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1037-629G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46879034 | ||||||
| chr6:46879088
|
A | G | 230 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0097others(227): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.1037-683T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46879088 | ||||||
| chr6:46879306
|
G | GA | 7 | a0003c0003t0004g0199a0003c0003t0008g0005a0003c0003t0008g0006others(4): Show | 7 | HG02280.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1036+511_1036+512i others(3): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46879306 | ||||||
| chr6:46879307
|
T | C | 7 | a0003c0003t0004g0199a0003c0003t0008g0005a0003c0003t0008g0006others(4): Show | 7 | HG02280.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1036+511A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46879307 | ||||||
| chr6:46879308
|
G | A | 3 | a0003c0003t0004g0199a0010c0032t0004g0200a0017c0031t0004g0198 | 3 | HG02486.hp2 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1036+510C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46879308 | ||||||
| chr6:46879311
|
C | A | 1 | a0001c0001t0001g0340 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1036+507G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46879311 | ||||||
| chr6:46879329
|
C | T | 89 | a0001c0001t0001g0003a0001c0001t0001g0100a0001c0001t0001g0108others(86): Show | 90 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.1036+489G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46879329 | ||||||
| chr6:46879348
|
G | A | 1 | a0001c0001t0001g0330 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1036+470C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46879348 | ||||||
| chr6:46879418
|
G | A | 6 | a0001c0001t0001g0260a0001c0001t0001g0332a0001c0001t0001g0333others(3): Show | 6 | HG00639.hp2 HG01175.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+400C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46879418 | ||||||
| chr6:46879547
|
G | C | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0097others(283): Show | 288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.1036+271C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46879547 | ||||||
| chr6:46879564
|
C | G | 1 | a0002c0002t0003g0024 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1036+254G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46879564 | ||||||
| chr6:46879747
|
A | G | 2 | a0002c0002t0002g0244a0018c0024t0002g0187 | 2 | HG01884.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1036+71T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46879747 | ||||||
| chr6:46879764
|
T | G | 87 | a0001c0001t0001g0002a0001c0001t0001g0202a0001c0001t0001g0206others(84): Show | 88 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1036+54A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46879764 | ||||||
| chr6:46880289
|
C | T | 1 | a0002c0002t0003g0072 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.815-250G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46880289 | ||||||
| chr6:46880358
|
T | TA | 301 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0097others(298): Show | 303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.815-320dupT | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46880358 | ||||||
| chr6:46880522
|
C | T | 7 | a0001c0001t0001g0206a0001c0001t0001g0210a0001c0001t0001g0211others(4): Show | 7 | HG01358.hp2 HG01952.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.815-483G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46880522 | ||||||
| chr6:46880561
|
T | TAAGAGTG others(3): Show |
1 | a0001c0001t0001g0326 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.815-532_815-523dup others(10): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46880561 | ||||||
| chr6:46880625
|
T | G | 2 | a0001c0001t0001g0359a0001c0001t0015g0007 | 2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.815-586A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46880625 | ||||||
| chr6:46880708
|
T | C | 4 | a0002c0002t0002g0360a0002c0002t0002g0361a0002c0002t0002g0362others(1): Show | 4 | HG02615.hp1 HG03540.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.815-669A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46880708 | ||||||
| chr6:46880740
|
A | T | 1 | a0002c0002t0002g0173 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.815-701T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46880740 | ||||||
| chr6:46880787
|
T | A | 1 | a0001c0001t0001g0115 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.814+668A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46880787 | ||||||
| chr6:46880894
|
C | T | 1 | a0003c0003t0013g0032 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.814+561G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46880894 | ||||||
| chr6:46880924
|
C | G | 1 | a0002c0002t0016g0009 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.814+531G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46880924 | ||||||
| chr6:46880940
|
A | T | 2 | a0003c0003t0004g0094a0003c0034t0008g0004 | 2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.814+515T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46880940 | ||||||
| chr6:46881014
|
C | T | 8 | a0002c0002t0002g0244a0002c0002t0002g0247a0002c0002t0002g0248others(5): Show | 8 | HG00280.hp1 HG01070.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.814+441G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46881014 | ||||||
| chr6:46881104
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.814+351T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46881104 | ||||||
| chr6:46881320
|
G | T | 19 | a0001c0001t0001g0202a0001c0001t0001g0236a0001c0001t0001g0359others(16): Show | 19 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.814+135C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46881320 | ||||||
| chr6:46881336
|
A | C | 1 | a0003c0034t0008g0004 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.814+119T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46881336 | ||||||
| chr6:46881338
|
C | A | 7 | a0003c0003t0006g0241a0003c0003t0006g0344a0003c0003t0006g0345others(4): Show | 7 | HG01884.hp2 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.814+117G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46881338 | ||||||
| chr6:46881630
|
T | C | 3 | a0002c0002t0016g0009a0003c0003t0006g0350a0004c0008t0009g0096 | 3 | HG01243.hp2 HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.672-33A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 7/20 | chr6 | 46881630 | ||||||
| chr6:46881883
|
T | C | 12 | a0001c0001t0001g0003a0001c0001t0001g0115a0001c0028t0006g0235others(9): Show | 13 | HG01261.hp1 HG02145.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.671+166A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 7/20 | chr6 | 46881883 | ||||||
| chr6:46882432
|
T | G | 327 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(324): Show | 330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.613-325A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46882432 | ||||||
| chr6:46882456
|
G | A | 1 | a0003c0003t0013g0032 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.613-349C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46882456 | ||||||
| chr6:46882533
|
C | T | 1 | a0005c0015t0001g0233 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.613-426G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46882533 | ||||||
| chr6:46882536
|
T | C | 1 | a0003c0003t0019g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.613-429A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46882536 | ||||||
| chr6:46882543
|
C | T | 2 | a0002c0002t0002g0243a0002c0002t0003g0091 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.613-436G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46882543 | ||||||
| chr6:46882686
|
C | T | 3 | a0002c0005t0002g0135a0002c0005t0002g0328a0002c0005t0003g0043 | 3 | HG02083.hp1 NA18948.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.613-579G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46882686 | ||||||
| chr6:46882969
|
T | C | 1 | a0003c0003t0004g0204 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.612+590A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46882969 | ||||||
| chr6:46883047
|
A | T | 2 | a0006c0010t0001g0170a0006c0010t0001g0193 | 2 | HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.612+512T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46883047 | ||||||
| chr6:46883166
|
G | A | 333 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(330): Show | 336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.612+393C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46883166 | ||||||
| chr6:46883179
|
C | T | 1 | a0001c0001t0001g0329 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.612+380G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46883179 | ||||||
| chr6:46883185
|
C | T | 1 | a0001c0001t0005g0042 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.612+374G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46883185 | ||||||
| chr6:46883219
|
A | G | 6 | a0002c0002t0002g0169a0003c0003t0004g0120a0003c0003t0004g0121others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.612+340T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46883219 | ||||||
| chr6:46883229
|
T | C | 1 | a0002c0002t0003g0018 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.612+330A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46883229 | ||||||
| chr6:46883293
|
C | T | 1 | a0002c0002t0022g0071 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.612+266G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46883293 | ||||||
| chr6:46883434
|
T | C | 7 | a0003c0003t0006g0241a0003c0003t0006g0344a0003c0003t0006g0345others(4): Show | 7 | HG01884.hp2 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.612+125A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46883434 | ||||||
| chr6:46883526
|
G | A | 1 | a0002c0002t0002g0247 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.612+33C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46883526 | ||||||
| chr6:46883774
|
C | G | 7 | a0003c0003t0006g0241a0003c0003t0006g0344a0003c0003t0006g0345others(4): Show | 7 | HG01884.hp2 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.506-109G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 5/20 | chr6 | 46883774 | ||||||
| chr6:46883776
|
C | T | 1 | a0001c0001t0005g0085 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.506-111G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 5/20 | chr6 | 46883776 | ||||||
| chr6:46883788
|
C | A | 12 | a0001c0001t0001g0003a0001c0001t0001g0115a0001c0028t0006g0235others(9): Show | 13 | HG01261.hp1 HG02145.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.506-123G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 5/20 | chr6 | 46883788 | ||||||
| chr6:46883799
|
C | T | 1 | a0004c0011t0006g0103 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.506-134G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 5/20 | chr6 | 46883799 | ||||||
| chr6:46883856
|
C | T | 5 | a0002c0002t0002g0244a0002c0002t0016g0009a0003c0003t0006g0350others(2): Show | 5 | HG01243.hp2 HG01884.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.506-191G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 5/20 | chr6 | 46883856 | ||||||
| chr6:46883934
|
G | T | 1 | a0002c0002t0002g0102 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.505+161C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 5/20 | chr6 | 46883934 | ||||||
| chr6:46883993
|
C | A | 5 | a0001c0001t0001g0211a0001c0001t0001g0217a0001c0001t0001g0221others(2): Show | 5 | HG01358.hp2 HG01952.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.505+102G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 5/20 | chr6 | 46883993 | ||||||
| chr6:46884415
|
T | A | 1 | a0002c0006t0003g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.329-144A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46884415 | ||||||
| chr6:46884436
|
T | G | 1 | a0003c0007t0004g0185 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.329-165A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46884436 | ||||||
| chr6:46884456
|
C | T | 327 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(324): Show | 330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.329-185G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46884456 | ||||||
| chr6:46884685
|
G | A | 1 | a0001c0001t0001g0369 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.329-414C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46884685 | ||||||
| chr6:46884801
|
G | C | 8 | a0001c0001t0001g0100a0001c0001t0001g0108a0001c0001t0001g0109others(5): Show | 8 | HG02071.hp1 HG02135.hp1 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.329-530C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46884801 | ||||||
| chr6:46884810
|
C | T | 2 | a0003c0003t0004g0195a0003c0003t0004g0343 | 2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.329-539G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46884810 | ||||||
| chr6:46885194
|
CA | C | 14 | a0001c0001t0001g0100a0001c0001t0001g0108a0001c0001t0001g0109others(11): Show | 14 | HG00621.hp1 HG01346.hp1 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.329-924delT | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46885194 | ||||||
| chr6:46885194
|
CAA | C | 80 | a0001c0001t0001g0149a0001c0001t0001g0285a0001c0001t0001g0287others(77): Show | 80 | HG00558.hp2 HG00639.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.329-925_329-924del others(2): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46885194 | ||||||
| chr6:46885194
|
CAAA | C | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(233): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.329-926_329-924del others(3): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46885194 | ||||||
| chr6:46885240
|
G | T | 1 | a0002c0002t0012g0089 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.329-969C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46885240 | ||||||
| chr6:46885328
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.329-1057G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46885328 | ||||||
| chr6:46885373
|
C | A | 3 | a0002c0002t0002g0240a0003c0003t0017g0014a0003c0025t0004g0239 | 3 | HG02451.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.329-1102G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46885373 | ||||||
| chr6:46885495
|
G | C | 1 | a0002c0002t0003g0018 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.329-1224C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46885495 | ||||||
| chr6:46885511
|
G | A | 16 | a0001c0001t0001g0100a0001c0001t0001g0108a0001c0001t0001g0109others(13): Show | 16 | HG01074.hp1 HG01106.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.329-1240C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46885511 | ||||||
| chr6:46885513
|
T | C | 6 | a0001c0004t0018g0015a0002c0005t0002g0348a0002c0005t0003g0025others(3): Show | 6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.329-1242A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46885513 | ||||||
| chr6:46885535
|
G | T | 1 | a0005c0015t0001g0233 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.329-1264C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46885535 | ||||||
| chr6:46885683
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.329-1412T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46885683 | ||||||
| chr6:46885760
|
T | C | 1 | a0014c0020t0001g0339 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.329-1489A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46885760 | ||||||
| chr6:46885849
|
A | G | 1 | a0001c0001t0001g0276 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.329-1578T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46885849 | ||||||
| chr6:46885925
|
C | A | 333 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(330): Show | 336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.329-1654G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46885925 | ||||||
| chr6:46886128
|
A | T | 5 | a0001c0001t0001g0267a0001c0001t0001g0293a0001c0001t0001g0299others(2): Show | 5 | HG00544.hp2 HG00609.hp2 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.329-1857T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46886128 | ||||||
| chr6:46886144
|
T | C | 4 | a0002c0002t0002g0367a0002c0002t0003g0050a0002c0002t0003g0084others(1): Show | 4 | HG01516.hp2 HG02698.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.329-1873A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46886144 | ||||||
| chr6:46886307
|
T | A | 3 | a0001c0004t0018g0015a0004c0009t0010g0012a0004c0009t0010g0013 | 3 | HG01106.hp2 HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.328+2028A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46886307 | ||||||
| chr6:46886426
|
T | C | 13 | a0001c0001t0001g0202a0001c0001t0001g0236a0001c0001t0001g0366others(10): Show | 13 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.328+1909A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46886426 | ||||||
| chr6:46886624
|
T | A | 9 | a0003c0003t0004g0186a0003c0003t0004g0188a0003c0003t0004g0189others(6): Show | 9 | HG00741.hp2 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.328+1711A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46886624 | ||||||
| chr6:46886666
|
G | A | 71 | a0001c0001t0001g0002a0001c0001t0001g0206a0001c0001t0001g0210others(68): Show | 72 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.328+1669C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46886666 | ||||||
| chr6:46886670
|
G | A | 8 | a0002c0002t0020g0028a0002c0006t0002g0196a0002c0006t0002g0197others(5): Show | 8 | HG00642.hp1 HG02055.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.328+1665C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46886670 | ||||||
| chr6:46886893
|
A | T | 333 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(330): Show | 336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.328+1442T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46886893 | ||||||
| chr6:46887003
|
C | T | 327 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(324): Show | 330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.328+1332G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46887003 | ||||||
| chr6:46887024
|
G | C | 1 | a0002c0002t0002g0219 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.328+1311C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46887024 | ||||||
| chr6:46887224
|
A | G | 3 | a0002c0002t0002g0240a0003c0003t0017g0014a0003c0025t0004g0239 | 3 | HG02451.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.328+1111T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46887224 | ||||||
| chr6:46887358
|
G | A | 1 | a0003c0003t0004g0227 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.328+977C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46887358 | ||||||
| chr6:46887393
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0097a0001c0001t0001g0104others(106): Show | 110 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.328+942T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46887393 | ||||||
| chr6:46887545
|
T | G | 6 | a0001c0004t0018g0015a0002c0005t0002g0348a0002c0005t0003g0025others(3): Show | 6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.328+790A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46887545 | ||||||
| chr6:46887605
|
C | T | 1 | a0002c0002t0003g0091 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.328+730G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46887605 | ||||||
| chr6:46887798
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.328+537T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46887798 | ||||||
| chr6:46887903
|
T | G | 7 | a0003c0003t0004g0199a0003c0003t0008g0005a0003c0003t0008g0006others(4): Show | 7 | HG02280.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.328+432A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46887903 | ||||||
| chr6:46887997
|
C | CAGGGAAG others(24): Show |
71 | a0001c0001t0001g0100a0001c0001t0001g0108a0001c0001t0001g0109others(68): Show | 71 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.328+307_328+337dup others(31): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46887997 | ||||||
| chr6:46888095
|
C | T | 1 | a0004c0011t0006g0103 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.328+240G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46888095 | ||||||
| chr6:46888119
|
C | T | 1 | a0003c0034t0008g0004 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.328+216G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46888119 | ||||||
| chr6:46888219
|
C | T | 1 | a0003c0003t0013g0090 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.328+116G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46888219 | ||||||
| chr6:46888526
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0097a0001c0001t0001g0104others(106): Show | 110 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.158-21C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46888526 | ||||||
| chr6:46888547
|
G | A | 1 | a0001c0001t0001g0296 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.158-42C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46888547 | ||||||
| chr6:46888728
|
G | A | 1 | a0002c0002t0003g0034 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.158-223C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46888728 | ||||||
| chr6:46888755
|
G | T | 1 | a0001c0004t0005g0044 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.158-250C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46888755 | ||||||
| chr6:46888844
|
T | G | 333 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(330): Show | 336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.158-339A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46888844 | ||||||
| chr6:46888847
|
G | A | 2 | a0002c0002t0003g0077a0002c0002t0003g0078 | 2 | HG02135.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.158-342C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46888847 | ||||||
| chr6:46888942
|
C | G | 6 | a0001c0004t0018g0015a0002c0005t0002g0348a0002c0005t0003g0025others(3): Show | 6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.158-437G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46888942 | ||||||
| chr6:46889186
|
C | CAT | 10 | a0001c0004t0018g0015a0002c0002t0002g0240a0002c0002t0012g0033others(7): Show | 10 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.158-683_158-682dup others(2): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889186 | ||||||
| chr6:46889186
|
CAT | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0097others(202): Show | 207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.158-683_158-682del others(2): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889186 | ||||||
| chr6:46889186
|
CATAT | C | 45 | a0001c0001t0001g0003a0001c0001t0001g0115a0001c0028t0006g0235others(42): Show | 46 | HG00280.hp1 HG00741.hp2 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.158-685_158-682del others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889186 | ||||||
| chr6:46889209
|
T | C | 6 | a0001c0004t0018g0015a0002c0005t0002g0348a0002c0005t0003g0025others(3): Show | 6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.158-704A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889209 | ||||||
| chr6:46889213
|
T | G | 3 | a0002c0002t0003g0087a0003c0003t0011g0010a0003c0003t0011g0011 | 3 | HG02056.hp2 HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.158-708A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889213 | ||||||
| chr6:46889279
|
TATATAGT others(29): Show |
T | 1 | a0003c0003t0013g0090 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.158-810_158-775del others(36): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889279 | ||||||
| chr6:46889299
|
GTATA | G | 4 | a0002c0002t0002g0367a0002c0002t0003g0050a0002c0002t0003g0084others(1): Show | 4 | HG01516.hp2 HG02698.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-798_158-795del others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889299 | ||||||
| chr6:46889368
|
A | C | 1 | a0001c0001t0001g0310 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.158-863T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889368 | ||||||
| chr6:46889450
|
T | C | 13 | a0001c0001t0001g0149a0001c0001t0005g0041a0001c0001t0005g0042others(10): Show | 13 | HG00639.hp1 HG01496.hp2 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.158-945A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889450 | ||||||
| chr6:46889499
|
T | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0097a0001c0001t0001g0104others(101): Show | 105 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.158-994A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889499 | ||||||
| chr6:46889501
|
G | T | 7 | a0002c0002t0002g0247a0002c0002t0002g0248a0003c0003t0004g0226others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.158-996C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889501 | ||||||
| chr6:46889552
|
A | ATG | 39 | a0001c0001t0001g0100a0001c0001t0001g0108a0001c0001t0001g0109others(36): Show | 39 | HG00438.hp1 HG00741.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.158-1049_158-1048d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889552 | ||||||
| chr6:46889552
|
A | G | 1 | a0003c0003t0019g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.158-1047T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889552 | ||||||
| chr6:46889552
|
ATG | A | 4 | a0001c0001t0001g0265a0001c0001t0001g0309a0001c0001t0001g0351others(1): Show | 4 | NA18945.hp1 NA18952.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-1049_158-1048d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889552 | ||||||
| chr6:46889566
|
GTGTA | G | 106 | a0001c0001t0001g0001a0001c0001t0001g0097a0001c0001t0001g0104others(103): Show | 107 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.158-1065_158-1062d others(6): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889566 | ||||||
| chr6:46889568
|
G | A | 2 | a0001c0004t0001g0146a0003c0034t0008g0004 | 2 | HG02572.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.158-1063C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889568 | ||||||
| chr6:46889568
|
G | GTA | 4 | a0001c0004t0001g0142a0002c0002t0002g0240a0002c0005t0002g0143others(1): Show | 4 | HG01975.hp1 HG02004.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-1065_158-1064d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889568 | ||||||
| chr6:46889568
|
G | GTGTA | 71 | a0001c0001t0001g0149a0001c0001t0001g0202a0001c0001t0001g0236others(68): Show | 71 | HG00323.hp2 HG00558.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.158-1064_158-1063i others(6): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889568 | ||||||
| chr6:46889568
|
G | GTGTATA | 10 | a0001c0001t0001g0372a0001c0001t0001g0373a0001c0001t0005g0060others(7): Show | 10 | HG00099.hp1 HG00280.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-1064_158-1063i others(8): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889568 | ||||||
| chr6:46889568
|
G | GTGTATAT others(1): Show |
4 | a0002c0002t0002g0169a0003c0003t0004g0120a0003c0003t0004g0121others(1): Show | 4 | HG02572.hp1 HG02723.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-1064_158-1063i others(10): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889568 | ||||||
| chr6:46889568
|
GTATA | G | 7 | a0001c0004t0018g0015a0002c0005t0002g0348a0002c0005t0003g0025others(4): Show | 7 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.158-1067_158-1064d others(6): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889568 | ||||||
| chr6:46889570
|
A | G | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0115others(92): Show | 97 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.158-1065T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889570 | ||||||
| chr6:46889572
|
A | G | 4 | a0001c0001t0001g0003a0003c0003t0004g0195a0003c0003t0004g0343others(1): Show | 5 | HG02109.hp2 HG02145.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.158-1067T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889572 | ||||||
| chr6:46889621
|
G | A | 1 | a0002c0014t0002g0099 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.158-1116C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889621 | ||||||
| chr6:46889677
|
T | C | 17 | a0001c0001t0001g0206a0001c0001t0001g0210a0001c0001t0001g0211others(14): Show | 17 | HG00423.hp1 HG01243.hp1 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.158-1172A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889677 | ||||||
| chr6:46889767
|
AT | A | 6 | a0001c0004t0018g0015a0002c0005t0002g0348a0002c0005t0003g0025others(3): Show | 6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.158-1263delA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889767 | ||||||
| chr6:46889780
|
G | GTA | 3 | a0001c0001t0001g0370a0002c0005t0002g0130a0003c0003t0019g0016 | 3 | HG00323.hp2 NA18984.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.158-1277_158-1276d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889780 | ||||||
| chr6:46889780
|
GTA | G | 196 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0104others(193): Show | 197 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.158-1277_158-1276d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889780 | ||||||
| chr6:46889782
|
A | G | 2 | a0002c0002t0002g0219a0003c0003t0017g0014 | 2 | HG01109.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.158-1277T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889782 | ||||||
| chr6:46889784
|
A | G | 1 | a0001c0001t0001g0225 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.158-1279T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889784 | ||||||
| chr6:46889799
|
T | C | 4 | a0003c0003t0008g0005a0003c0003t0008g0006a0003c0003t0008g0008others(1): Show | 4 | HG02280.hp1 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-1294A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889799 | ||||||
| chr6:46889940
|
T | C | 6 | a0001c0004t0018g0015a0002c0005t0002g0348a0002c0005t0003g0025others(3): Show | 6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.158-1435A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889940 | ||||||
| chr6:46889992
|
T | C | 2 | a0003c0003t0004g0191a0003c0003t0004g0192 | 2 | HG00741.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.158-1487A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889992 | ||||||
| chr6:46890054
|
A | G | 1 | a0002c0005t0002g0148 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.158-1549T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46890054 | ||||||
| chr6:46890090
|
T | C | 1 | a0003c0003t0019g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.158-1585A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46890090 | ||||||
| chr6:46890132
|
G | A | 31 | a0001c0001t0001g0220a0001c0001t0001g0225a0001c0001t0001g0232others(28): Show | 31 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.158-1627C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46890132 | ||||||
| chr6:46890205
|
G | C | 74 | a0001c0001t0001g0100a0001c0001t0001g0108a0001c0001t0001g0109others(71): Show | 74 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.158-1700C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46890205 | ||||||
| chr6:46890262
|
T | G | 1 | a0002c0002t0002g0242 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.158-1757A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46890262 | ||||||
| chr6:46890332
|
A | T | 1 | a0002c0002t0002g0150 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.158-1827T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46890332 | ||||||
| chr6:46890344
|
T | C | 333 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(330): Show | 336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.158-1839A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46890344 | ||||||
| chr6:46890489
|
G | A | 5 | a0001c0001t0001g0296a0001c0001t0001g0305a0001c0001t0001g0331others(2): Show | 5 | HG00621.hp2 NA18947.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-1984C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46890489 | ||||||
| chr6:46890537
|
G | GT | 378 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(375): Show | 381 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.158-2033_158-2032i others(3): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46890537 | ||||||
| chr6:46890843
|
A | G | 1 | a0004c0029t0028g0124 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.158-2338T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46890843 | ||||||
| chr6:46890856
|
T | C | 1 | a0002c0002t0002g0263 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.158-2351A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46890856 | ||||||
| chr6:46890962
|
T | C | 1 | a0001c0001t0001g0325 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.158-2457A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46890962 | ||||||
| chr6:46890972
|
G | A | 1 | a0003c0003t0004g0171 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.158-2467C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46890972 | ||||||
| chr6:46891250
|
C | A | 6 | a0002c0002t0002g0169a0003c0003t0004g0120a0003c0003t0004g0121others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.158-2745G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46891250 | ||||||
| chr6:46891256
|
C | T | 71 | a0001c0001t0001g0100a0001c0001t0001g0108a0001c0001t0001g0109others(68): Show | 71 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.158-2751G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46891256 | ||||||
| chr6:46891306
|
T | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0097a0001c0001t0001g0104others(106): Show | 110 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.158-2801A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46891306 | ||||||
| chr6:46891401
|
C | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0097a0001c0001t0001g0104others(106): Show | 110 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.158-2896G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46891401 | ||||||
| chr6:46891409
|
C | A | 10 | a0001c0001t0001g0271a0002c0002t0002g0249a0002c0002t0002g0251others(7): Show | 10 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(7): Show |
intron_variant | MODIFIER | c.158-2904G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46891409 | ||||||
| chr6:46891611
|
C | T | 332 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(329): Show | 335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.158-3106G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46891611 | ||||||
| chr6:46891655
|
C | T | 1 | a0002c0002t0002g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.158-3150G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46891655 | ||||||
| chr6:46891721
|
G | A | 71 | a0001c0001t0001g0100a0001c0001t0001g0108a0001c0001t0001g0109others(68): Show | 71 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.158-3216C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46891721 | ||||||
| chr6:46891804
|
G | A | 1 | a0002c0002t0003g0038 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.158-3299C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46891804 | ||||||
| chr6:46892054
|
C | T | 1 | a0003c0034t0008g0004 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.158-3549G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892054 | ||||||
| chr6:46892147
|
TACACAAA others(5): Show |
T | 1 | a0001c0001t0001g0329 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.158-3654_158-3643d others(14): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892147 | ||||||
| chr6:46892155
|
TACAC | T | 4 | a0001c0004t0005g0037a0003c0007t0004g0185a0003c0007t0007g0122others(1): Show | 4 | HG00280.hp2 HG01255.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-3654_158-3651d others(6): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892155 | ||||||
| chr6:46892155
|
TACACAC | T | 22 | a0001c0001t0001g0161a0001c0001t0001g0236a0001c0004t0001g0131others(19): Show | 22 | HG00642.hp1 HG00673.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.158-3656_158-3651d others(8): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892155 | ||||||
| chr6:46892155
|
TACACACA others(1): Show |
T | 37 | a0001c0001t0001g0274a0001c0001t0001g0366a0001c0004t0001g0118others(34): Show | 37 | HG00544.hp1 HG01071.hp2 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.158-3658_158-3651d others(10): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892155 | ||||||
| chr6:46892155
|
TACACACA others(3): Show |
T | 67 | a0001c0001t0001g0202a0001c0001t0001g0276a0001c0001t0001g0290others(64): Show | 67 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.158-3660_158-3651d others(12): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892155 | ||||||
| chr6:46892155
|
TACACACA others(5): Show |
T | 129 | a0001c0001t0001g0001a0001c0001t0001g0097a0001c0001t0001g0104others(126): Show | 130 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.158-3662_158-3651d others(14): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892155 | ||||||
| chr6:46892155
|
TACACACA others(7): Show |
T | 81 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0115others(78): Show | 83 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.158-3664_158-3651d others(16): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892155 | ||||||
| chr6:46892155
|
TACACACA others(9): Show |
T | 21 | a0001c0001t0001g0221a0001c0001t0001g0256a0001c0001t0001g0264others(18): Show | 21 | HG00280.hp1 HG01070.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.158-3666_158-3651d others(18): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892155 | ||||||
| chr6:46892155
|
TACACACA others(11): Show |
T | 9 | a0002c0002t0002g0113a0002c0002t0002g0126a0002c0002t0002g0207others(6): Show | 9 | HG01106.hp1 HG01175.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.158-3668_158-3651d others(20): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892155 | ||||||
| chr6:46892155
|
TACACACA others(13): Show |
T | 5 | a0001c0001t0001g0100a0001c0001t0001g0108a0001c0001t0001g0109others(2): Show | 5 | NA18950.hp2 NA18973.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-3670_158-3651d others(22): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892155 | ||||||
| chr6:46892167
|
C | T | 1 | a0001c0001t0001g0329 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.158-3662G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892167 | ||||||
| chr6:46892177
|
C | T | 1 | a0003c0003t0013g0090 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.158-3672G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892177 | ||||||
| chr6:46892235
|
C | T | 74 | a0001c0001t0001g0100a0001c0001t0001g0108a0001c0001t0001g0109others(71): Show | 74 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.158-3730G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892235 | ||||||
| chr6:46892417
|
G | A | 3 | a0002c0002t0002g0240a0003c0003t0017g0014a0003c0025t0004g0239 | 3 | HG02451.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.158-3912C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892417 | ||||||
| chr6:46892438
|
A | G | 1 | a0004c0008t0027g0357 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.158-3933T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892438 | ||||||
| chr6:46892480
|
G | A | 2 | a0003c0003t0011g0010a0003c0003t0011g0011 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.158-3975C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892480 | ||||||
| chr6:46892504
|
C | T | 3 | a0002c0002t0002g0247a0002c0002t0002g0248a0003c0003t0004g0226 | 3 | HG00280.hp1 HG01070.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.158-3999G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892504 | ||||||
| chr6:46892575
|
C | T | 6 | a0001c0004t0018g0015a0002c0005t0002g0348a0002c0005t0003g0025others(3): Show | 6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.158-4070G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892575 | ||||||
| chr6:46892671
|
A | T | 71 | a0001c0001t0001g0100a0001c0001t0001g0108a0001c0001t0001g0109others(68): Show | 71 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.158-4166T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892671 | ||||||
| chr6:46892706
|
C | A | 2 | a0002c0002t0002g0114a0002c0002t0002g0242 | 2 | HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.158-4201G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892706 | ||||||
| chr6:46892783
|
A | G | 92 | a0001c0001t0001g0002a0001c0001t0001g0202a0001c0001t0001g0206others(89): Show | 93 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.158-4278T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892783 | ||||||
| chr6:46892790
|
T | C | 3 | a0002c0002t0002g0240a0003c0003t0017g0014a0003c0025t0004g0239 | 3 | HG02451.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.158-4285A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892790 | ||||||
| chr6:46892901
|
C | T | 1 | a0003c0003t0004g0199 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.158-4396G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892901 | ||||||
| chr6:46893053
|
C | T | 1 | a0001c0001t0001g0330 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.158-4548G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893053 | ||||||
| chr6:46893055
|
G | A | 1 | a0001c0001t0001g0336 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.158-4550C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893055 | ||||||
| chr6:46893058
|
A | AT | 37 | a0001c0001t0001g0115a0001c0001t0001g0210a0001c0001t0001g0211others(34): Show | 37 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.158-4554dupA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893058 | ||||||
| chr6:46893058
|
A | ATT | 6 | a0001c0004t0001g0158a0002c0006t0003g0027a0003c0003t0004g0191others(3): Show | 6 | HG00741.hp2 HG02055.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.158-4555_158-4554d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893058 | ||||||
| chr6:46893058
|
A | ATTT | 9 | a0001c0001t0001g0097a0001c0001t0001g0104a0001c0001t0001g0105others(6): Show | 9 | HG02155.hp2 HG03579.hp2 NA18945.hp1 others(6): Show |
intron_variant | MODIFIER | c.158-4556_158-4554d others(5): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893058 | ||||||
| chr6:46893058
|
A | ATTTT | 67 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0111others(64): Show | 68 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.158-4557_158-4554d others(6): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893058 | ||||||
| chr6:46893058
|
A | ATTTTT | 29 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0205others(26): Show | 29 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.158-4558_158-4554d others(7): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893058 | ||||||
| chr6:46893058
|
AT | A | 63 | a0001c0001t0001g0002a0001c0001t0001g0108a0001c0001t0001g0149others(60): Show | 64 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.158-4554delA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893058 | ||||||
| chr6:46893058
|
ATT | A | 62 | a0001c0001t0001g0100a0001c0001t0001g0109a0001c0001t0001g0225others(59): Show | 62 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.158-4555_158-4554d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893058 | ||||||
| chr6:46893058
|
ATTT | A | 12 | a0001c0004t0018g0015a0002c0002t0002g0123a0002c0002t0003g0092others(9): Show | 12 | HG01106.hp2 HG01167.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.158-4556_158-4554d others(5): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893058 | ||||||
| chr6:46893058
|
ATTTTTTT others(4): Show |
A | 1 | a0014c0020t0001g0339 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.158-4564_158-4554d others(13): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893058 | ||||||
| chr6:46893058
|
ATTTTTTT others(6): Show |
A | 5 | a0003c0003t0004g0162a0003c0003t0004g0163a0003c0003t0004g0164others(2): Show | 5 | HG02647.hp1 HG02965.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-4566_158-4554d others(15): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893058 | ||||||
| chr6:46893105
|
C | T | 3 | a0001c0004t0001g0146a0001c0004t0030g0137a0002c0005t0002g0136 | 3 | HG00673.hp2 NA18941.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.158-4600G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893105 | ||||||
| chr6:46893165
|
C | T | 1 | a0001c0001t0001g0370 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.158-4660G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893165 | ||||||
| chr6:46893191
|
T | G | 333 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(330): Show | 336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.158-4686A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893191 | ||||||
| chr6:46893276
|
C | T | 6 | a0001c0001t0001g0260a0001c0001t0001g0332a0001c0001t0001g0333others(3): Show | 6 | HG00639.hp2 HG01175.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.158-4771G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893276 | ||||||
| chr6:46893324
|
T | A | 6 | a0002c0002t0002g0169a0003c0003t0004g0120a0003c0003t0004g0121others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.158-4819A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893324 | ||||||
| chr6:46893409
|
T | G | 1 | a0002c0002t0002g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.158-4904A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893409 | ||||||
| chr6:46893433
|
G | A | 1 | a0002c0002t0002g0249 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.158-4928C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893433 | ||||||
| chr6:46893450
|
T | C | 1 | a0001c0001t0001g0236 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.158-4945A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893450 | ||||||
| chr6:46893615
|
C | G | 1 | a0003c0003t0013g0090 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.158-5110G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893615 | ||||||
| chr6:46893617
|
G | A | 1 | a0002c0002t0002g0114 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.158-5112C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893617 | ||||||
| chr6:46893727
|
A | G | 1 | a0003c0003t0013g0090 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.158-5222T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893727 | ||||||
| chr6:46893999
|
G | A | 1 | a0004c0011t0006g0103 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.158-5494C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893999 | ||||||
| chr6:46894053
|
C | G | 6 | a0001c0004t0018g0015a0002c0005t0002g0348a0002c0005t0003g0025others(3): Show | 6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.158-5548G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46894053 | ||||||
| chr6:46894107
|
C | T | 4 | a0003c0003t0004g0162a0003c0003t0004g0163a0003c0003t0004g0164others(1): Show | 4 | HG02647.hp1 HG02965.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-5602G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46894107 | ||||||
| chr6:46894167
|
T | A | 3 | a0003c0003t0004g0199a0010c0032t0004g0200a0017c0031t0004g0198 | 3 | HG02486.hp2 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.158-5662A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46894167 | ||||||
| chr6:46894303
|
C | T | 2 | a0002c0002t0003g0077a0002c0002t0003g0078 | 2 | HG02135.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.157+5726G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46894303 | ||||||
| chr6:46894950
|
G | A | 3 | a0002c0002t0002g0240a0003c0003t0017g0014a0003c0025t0004g0239 | 3 | HG02451.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.157+5079C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46894950 | ||||||
| chr6:46894953
|
C | T | 4 | a0002c0002t0002g0169a0003c0003t0004g0120a0003c0003t0004g0121others(1): Show | 4 | HG02572.hp1 HG02723.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+5076G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46894953 | ||||||
| chr6:46894963
|
G | A | 4 | a0002c0002t0002g0133a0002c0002t0002g0134a0002c0002t0002g0327others(1): Show | 4 | NA18944.hp1 NA18966.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.157+5066C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46894963 | ||||||
| chr6:46894979
|
C | T | 1 | a0003c0003t0019g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.157+5050G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46894979 | ||||||
| chr6:46894984
|
C | A | 1 | a0003c0003t0019g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.157+5045G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46894984 | ||||||
| chr6:46895131
|
C | T | 6 | a0001c0004t0018g0015a0002c0005t0002g0348a0002c0005t0003g0025others(3): Show | 6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.157+4898G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46895131 | ||||||
| chr6:46895191
|
G | A | 2 | a0003c0007t0004g0185a0014c0020t0001g0339 | 2 | HG00544.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.157+4838C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46895191 | ||||||
| chr6:46895223
|
G | T | 16 | a0002c0002t0002g0244a0002c0002t0016g0009a0003c0003t0004g0186others(13): Show | 16 | HG00741.hp2 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.157+4806C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46895223 | ||||||
| chr6:46895346
|
G | A | 3 | a0002c0002t0002g0240a0003c0003t0017g0014a0003c0025t0004g0239 | 3 | HG02451.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.157+4683C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46895346 | ||||||
| chr6:46895394
|
G | A | 1 | a0007c0016t0001g0201 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.157+4635C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46895394 | ||||||
| chr6:46895410
|
T | A | 7 | a0003c0003t0006g0241a0003c0003t0006g0344a0003c0003t0006g0345others(4): Show | 7 | HG01884.hp2 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.157+4619A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46895410 | ||||||
| chr6:46895418
|
G | C | 6 | a0001c0004t0018g0015a0002c0005t0002g0348a0002c0005t0003g0025others(3): Show | 6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.157+4611C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46895418 | ||||||
| chr6:46895519
|
C | T | 4 | a0001c0004t0001g0128a0001c0004t0001g0129a0001c0004t0001g0131others(1): Show | 4 | NA18952.hp1 NA18984.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+4510G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46895519 | ||||||
| chr6:46895523
|
C | A | 22 | a0002c0002t0002g0169a0002c0002t0002g0244a0002c0002t0016g0009others(19): Show | 22 | HG00741.hp2 HG01243.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.157+4506G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46895523 | ||||||
| chr6:46895542
|
G | A | 1 | a0003c0003t0019g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.157+4487C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46895542 | ||||||
| chr6:46895688
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.157+4341C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46895688 | ||||||
| chr6:46895697
|
T | C | 1 | a0002c0002t0002g0311 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.157+4332A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46895697 | ||||||
| chr6:46895782
|
G | A | 9 | a0003c0003t0004g0186a0003c0003t0004g0188a0003c0003t0004g0189others(6): Show | 9 | HG00741.hp2 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.157+4247C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46895782 | ||||||
| chr6:46895815
|
T | C | 1 | a0003c0034t0008g0004 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.157+4214A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46895815 | ||||||
| chr6:46895880
|
G | C | 1 | a0001c0001t0001g0312 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.157+4149C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46895880 | ||||||
| chr6:46896099
|
G | A | 1 | a0001c0001t0005g0073 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.157+3930C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46896099 | ||||||
| chr6:46896132
|
C | A | 3 | a0002c0002t0002g0360a0002c0002t0002g0361a0002c0002t0002g0362 | 3 | HG02615.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.157+3897G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46896132 | ||||||
| chr6:46896136
|
G | T | 2 | a0001c0001t0001g0220a0002c0002t0003g0018 | 2 | HG00438.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.157+3893C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46896136 | ||||||
| chr6:46896211
|
C | T | 1 | a0003c0003t0004g0192 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.157+3818G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46896211 | ||||||
| chr6:46896231
|
T | C | 1 | a0003c0003t0019g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.157+3798A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46896231 | ||||||
| chr6:46896299
|
C | T | 15 | a0002c0002t0002g0172a0002c0002t0002g0173a0002c0002t0002g0174others(12): Show | 15 | HG00741.hp1 HG01099.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.157+3730G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46896299 | ||||||
| chr6:46896517
|
C | T | 1 | a0003c0003t0013g0090 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.157+3512G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46896517 | ||||||
| chr6:46896539
|
T | C | 1 | a0003c0003t0004g0194 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.157+3490A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46896539 | ||||||
| chr6:46896549
|
T | C | 1 | a0017c0031t0004g0198 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.157+3480A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46896549 | ||||||
| chr6:46896660
|
A | ATG | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0115others(148): Show | 153 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.157+3367_157+3368d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46896660 | ||||||
| chr6:46896714
|
CAT | C | 4 | a0002c0002t0002g0114a0002c0002t0002g0242a0003c0003t0019g0016others(1): Show | 4 | HG02109.hp1 HG02922.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.157+3313_157+3314d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46896714 | ||||||
| chr6:46896977
|
T | C | 3 | a0002c0002t0002g0240a0003c0003t0017g0014a0003c0025t0004g0239 | 3 | HG02451.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.157+3052A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46896977 | ||||||
| chr6:46897011
|
G | A | 1 | a0001c0001t0001g0336 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.157+3018C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897011 | ||||||
| chr6:46897079
|
T | TAC | 5 | a0002c0002t0002g0240a0003c0003t0017g0014a0003c0003t0019g0016others(2): Show | 5 | HG02451.hp1 HG03139.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.157+2948_157+2949d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897079 | ||||||
| chr6:46897137
|
C | CAT | 24 | a0001c0001t0001g0003a0001c0001t0001g0206a0001c0001t0001g0210others(21): Show | 25 | HG00423.hp1 HG00741.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.157+2890_157+2891d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897137 | ||||||
| chr6:46897137
|
C | CATAT | 6 | a0001c0004t0018g0015a0002c0005t0002g0348a0002c0005t0003g0025others(3): Show | 6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.157+2888_157+2891d others(6): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897137 | ||||||
| chr6:46897137
|
CAT | C | 3 | a0001c0004t0001g0127a0001c0019t0001g0270a0002c0005t0002g0151 | 3 | HG02129.hp1 NA18952.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.157+2890_157+2891d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897137 | ||||||
| chr6:46897145
|
T | C | 3 | a0001c0001t0001g0266a0001c0004t0001g0292a0004c0011t0006g0103 | 3 | NA18960.hp2 NA19007.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.157+2884A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897145 | ||||||
| chr6:46897145
|
T | TAC | 81 | a0001c0001t0001g0001a0001c0001t0001g0100a0001c0001t0001g0108others(78): Show | 82 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.157+2882_157+2883d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897145 | ||||||
| chr6:46897145
|
T | TACACACA others(1): Show |
4 | a0003c0003t0008g0005a0003c0003t0008g0006a0003c0003t0008g0008others(1): Show | 4 | HG02280.hp1 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.157+2876_157+2883d others(10): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897145 | ||||||
| chr6:46897145
|
T | TATAC | 62 | a0001c0001t0001g0002a0001c0001t0001g0220a0001c0001t0001g0221others(59): Show | 63 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.157+2883_157+2884i others(6): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897145 | ||||||
| chr6:46897145
|
T | TATACAC | 17 | a0001c0001t0001g0115a0002c0002t0002g0247a0003c0003t0004g0186others(14): Show | 17 | HG00280.hp1 HG01261.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.157+2883_157+2884i others(8): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897145 | ||||||
| chr6:46897145
|
T | TATACACA others(1): Show |
12 | a0002c0002t0002g0248a0003c0003t0004g0199a0003c0003t0006g0241others(9): Show | 12 | HG01070.hp2 HG01884.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.157+2883_157+2884i others(10): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897145 | ||||||
| chr6:46897145
|
T | TATACACA others(3): Show |
2 | a0003c0003t0006g0346a0003c0003t0011g0011 | 2 | HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.157+2883_157+2884i others(12): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897145 | ||||||
| chr6:46897145
|
TAC | T | 5 | a0001c0001t0001g0264a0002c0002t0002g0360a0002c0002t0002g0361others(2): Show | 5 | HG01071.hp2 HG01261.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+2882_157+2883d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897145 | ||||||
| chr6:46897145
|
TACACACA others(5): Show |
T | 3 | a0002c0002t0002g0240a0003c0003t0017g0014a0003c0025t0004g0239 | 3 | HG02451.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.157+2872_157+2883d others(14): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897145 | ||||||
| chr6:46897147
|
C | T | 5 | a0001c0001t0001g0359a0001c0001t0015g0007a0003c0003t0004g0226others(2): Show | 5 | HG02145.hp1 HG02572.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.157+2882G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897147 | ||||||
| chr6:46897149
|
C | T | 4 | a0002c0002t0002g0360a0002c0002t0002g0361a0002c0002t0002g0362others(1): Show | 4 | HG02615.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+2880G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897149 | ||||||
| chr6:46897159
|
C | T | 3 | a0002c0002t0002g0240a0003c0003t0017g0014a0003c0025t0004g0239 | 3 | HG02451.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.157+2870G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897159 | ||||||
| chr6:46897161
|
C | T | 3 | a0002c0002t0002g0240a0003c0003t0017g0014a0003c0025t0004g0239 | 3 | HG02451.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.157+2868G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897161 | ||||||
| chr6:46897179
|
T | C | 1 | a0002c0002t0003g0074 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.157+2850A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897179 | ||||||
| chr6:46897198
|
T | A | 3 | a0002c0005t0002g0348a0002c0005t0003g0025a0004c0009t0029g0095 | 3 | HG01891.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.157+2831A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897198 | ||||||
| chr6:46897257
|
A | G | 4 | a0003c0003t0008g0005a0003c0003t0008g0006a0003c0003t0008g0008others(1): Show | 4 | HG02280.hp1 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.157+2772T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897257 | ||||||
| chr6:46897523
|
T | C | 333 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(330): Show | 336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.157+2506A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897523 | ||||||
| chr6:46897570
|
G | A | 2 | a0002c0002t0002g0253a0002c0002t0002g0254 | 2 | NA18981.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.157+2459C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897570 | ||||||
| chr6:46897596
|
A | G | 1 | a0015c0026t0001g0338 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.157+2433T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897596 | ||||||
| chr6:46897606
|
G | A | 2 | a0002c0002t0002g0240a0003c0025t0004g0239 | 2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.157+2423C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897606 | ||||||
| chr6:46897638
|
G | A | 1 | a0001c0001t0001g0314 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.157+2391C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897638 | ||||||
| chr6:46897659
|
C | A | 6 | a0001c0004t0018g0015a0002c0005t0002g0348a0002c0005t0003g0025others(3): Show | 6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.157+2370G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897659 | ||||||
| chr6:46897660
|
C | A | 6 | a0001c0004t0018g0015a0002c0005t0002g0348a0002c0005t0003g0025others(3): Show | 6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.157+2369G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897660 | ||||||
| chr6:46897716
|
G | T | 3 | a0002c0002t0002g0240a0003c0003t0017g0014a0003c0025t0004g0239 | 3 | HG02451.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.157+2313C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897716 | ||||||
| chr6:46897823
|
C | T | 1 | a0001c0028t0006g0235 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.157+2206G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897823 | ||||||
| chr6:46898021
|
T | A | 335 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(332): Show | 338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.157+2008A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46898021 | ||||||
| chr6:46898106
|
T | G | 5 | a0002c0002t0002g0244a0002c0002t0016g0009a0003c0003t0006g0350others(2): Show | 5 | HG01243.hp2 HG01884.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+1923A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46898106 | ||||||
| chr6:46898224
|
C | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0097a0001c0001t0001g0104others(106): Show | 110 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.157+1805G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46898224 | ||||||
| chr6:46898718
|
T | G | 1 | a0003c0003t0017g0014 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.157+1311A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46898718 | ||||||
| chr6:46898723
|
T | G | 1 | a0001c0004t0001g0203 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.157+1306A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46898723 | ||||||
| chr6:46898898
|
G | A | 1 | a0003c0003t0004g0226 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.157+1131C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46898898 | ||||||
| chr6:46898914
|
C | T | 1 | a0002c0002t0002g0291 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.157+1115G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46898914 | ||||||
| chr6:46898935
|
C | T | 2 | a0002c0005t0002g0348a0002c0005t0003g0025 | 2 | HG01891.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.157+1094G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46898935 | ||||||
| chr6:46898936
|
G | A | 3 | a0002c0002t0002g0240a0003c0003t0017g0014a0003c0025t0004g0239 | 3 | HG02451.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.157+1093C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46898936 | ||||||
| chr6:46899062
|
G | T | 1 | a0002c0005t0002g0135 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.157+967C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899062 | ||||||
| chr6:46899088
|
A | G | 7 | a0003c0003t0004g0199a0003c0003t0008g0005a0003c0003t0008g0006others(4): Show | 7 | HG02280.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.157+941T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899088 | ||||||
| chr6:46899145
|
C | T | 1 | a0003c0003t0013g0090 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.157+884G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899145 | ||||||
| chr6:46899179
|
G | A | 3 | a0002c0002t0016g0009a0003c0003t0006g0350a0004c0008t0009g0096 | 3 | HG01243.hp2 HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.157+850C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899179 | ||||||
| chr6:46899240
|
CAGA | C | 3 | a0001c0001t0001g0097a0001c0001t0001g0104a0001c0001t0001g0105 | 3 | HG02155.hp2 NA18994.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.157+786_157+788del others(3): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899240 | ||||||
| chr6:46899309
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.157+720G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899309 | ||||||
| chr6:46899344
|
G | A | 20 | a0001c0001t0001g0003a0001c0028t0006g0235a0003c0003t0004g0195others(17): Show | 21 | HG01074.hp1 HG01261.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.157+685C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899344 | ||||||
| chr6:46899404
|
C | T | 1 | a0002c0002t0002g0249 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.157+625G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899404 | ||||||
| chr6:46899480
|
C | T | 3 | a0001c0001t0001g0370a0001c0001t0001g0372a0001c0001t0001g0373 | 3 | HG00099.hp1 HG00323.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.157+549G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899480 | ||||||
| chr6:46899532
|
G | A | 8 | a0003c0003t0004g0186a0003c0003t0004g0188a0003c0003t0004g0189others(5): Show | 8 | HG00741.hp2 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.157+497C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899532 | ||||||
| chr6:46899656
|
GT | G | 6 | a0001c0004t0018g0015a0002c0002t0003g0024a0003c0003t0017g0014others(3): Show | 6 | HG01106.hp2 HG01255.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.157+372delA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899656 | ||||||
| chr6:46899665
|
T | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0160others(96): Show | 100 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.157+364A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899665 | ||||||
| chr6:46899666
|
TTG | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0160others(96): Show | 100 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.157+361_157+362del others(2): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899666 | ||||||
| chr6:46899746
|
G | A | 1 | a0002c0002t0021g0022 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.157+283C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899746 | ||||||
| chr6:46899863
|
G | T | 1 | a0001c0001t0001g0359 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.157+166C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899863 | ||||||
| chr6:46899975
|
A | T | 1 | a0001c0001t0001g0290 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.157+54T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899975 | ||||||
| chr6:46899977
|
A | G | 1 | a0001c0013t0001g0250 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.157+52T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899977 | ||||||
| chr6:46899980
|
C | T | 331 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(328): Show | 334 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.157+49G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899980 | ||||||
| chr6:46900109
|
T | G | 6 | a0001c0004t0018g0015a0003c0003t0011g0010a0003c0003t0011g0011others(3): Show | 6 | HG01106.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-26A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46900109 | ||||||
| chr6:46900161
|
TA | T | 231 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0097others(228): Show | 233 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.103-79delT | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46900161 | ||||||
| chr6:46900309
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0160others(96): Show | 100 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.103-226C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46900309 | ||||||
| chr6:46900376
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.103-293G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46900376 | ||||||
| chr6:46900462
|
G | A | 2 | a0001c0001t0001g0318a0001c0001t0001g0319 | 2 | HG01258.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.103-379C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46900462 | ||||||
| chr6:46900521
|
A | AG | 98 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0161others(95): Show | 99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.103-439dupC | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46900521 | ||||||
| chr6:46901004
|
C | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0161others(95): Show | 99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.103-921G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46901004 | ||||||
| chr6:46901026
|
T | C | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0359others(19): Show | 24 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.103-943A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46901026 | ||||||
| chr6:46901073
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0161others(95): Show | 99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.103-990C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46901073 | ||||||
| chr6:46901180
|
C | T | 1 | a0001c0001t0005g0042 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.103-1097G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46901180 | ||||||
| chr6:46901330
|
C | T | 1 | a0001c0001t0032g0289 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.103-1247G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46901330 | ||||||
| chr6:46901414
|
C | T | 5 | a0003c0003t0004g0356a0004c0008t0006g0358a0004c0008t0009g0354others(2): Show | 5 | HG01074.hp1 HG02280.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-1331G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46901414 | ||||||
| chr6:46901429
|
C | G | 8 | a0001c0001t0001g0261a0001c0001t0001g0284a0001c0001t0001g0285others(5): Show | 8 | HG00642.hp2 HG01192.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.103-1346G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46901429 | ||||||
| chr6:46901727
|
G | A | 5 | a0003c0003t0004g0356a0004c0008t0006g0358a0004c0008t0009g0354others(2): Show | 5 | HG01074.hp1 HG02280.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-1644C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46901727 | ||||||
| chr6:46901890
|
C | T | 4 | a0001c0001t0015g0007a0003c0003t0008g0005a0003c0003t0008g0006others(1): Show | 4 | HG02145.hp1 HG02280.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-1807G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46901890 | ||||||
| chr6:46901907
|
T | C | 2 | a0002c0002t0003g0091a0003c0003t0006g0350 | 2 | HG01243.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.103-1824A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46901907 | ||||||
| chr6:46901930
|
G | A | 2 | a0001c0001t0015g0007a0003c0003t0008g0006 | 2 | HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.103-1847C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46901930 | ||||||
| chr6:46902081
|
C | T | 1 | a0001c0001t0005g0041 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.103-1998G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46902081 | ||||||
| chr6:46902121
|
G | A | 6 | a0001c0004t0018g0015a0003c0003t0011g0010a0003c0003t0011g0011others(3): Show | 6 | HG01106.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-2038C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46902121 | ||||||
| chr6:46902158
|
T | G | 330 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(327): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.103-2075A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46902158 | ||||||
| chr6:46902297
|
A | G | 1 | a0002c0002t0002g0168 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.103-2214T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46902297 | ||||||
| chr6:46902421
|
G | A | 6 | a0001c0004t0018g0015a0003c0003t0011g0010a0003c0003t0011g0011others(3): Show | 6 | HG01106.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-2338C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46902421 | ||||||
| chr6:46902591
|
C | T | 1 | a0003c0034t0008g0004 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.103-2508G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46902591 | ||||||
| chr6:46902746
|
A | T | 1 | a0003c0003t0004g0347 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.103-2663T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46902746 | ||||||
| chr6:46902842
|
G | A | 1 | a0002c0006t0002g0197 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.103-2759C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46902842 | ||||||
| chr6:46902861
|
T | C | 61 | a0001c0001t0005g0041a0001c0001t0005g0042a0001c0001t0005g0045others(58): Show | 61 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.103-2778A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46902861 | ||||||
| chr6:46902864
|
C | G | 5 | a0003c0003t0004g0356a0004c0008t0006g0358a0004c0008t0009g0354others(2): Show | 5 | HG01074.hp1 HG02280.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-2781G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46902864 | ||||||
| chr6:46902904
|
C | G | 336 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(333): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.103-2821G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46902904 | ||||||
| chr6:46903036
|
T | A | 3 | a0002c0002t0003g0091a0003c0003t0006g0350a0003c0003t0013g0090 | 3 | HG01243.hp2 HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.103-2953A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903036 | ||||||
| chr6:46903087
|
C | T | 2 | a0002c0002t0002g0102a0004c0011t0006g0103 | 2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.103-3004G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903087 | ||||||
| chr6:46903147
|
G | A | 1 | a0002c0002t0002g0126 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.103-3064C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903147 | ||||||
| chr6:46903214
|
G | C | 1 | a0001c0001t0001g0261 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.103-3131C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903214 | ||||||
| chr6:46903245
|
C | T | 1 | a0017c0031t0004g0198 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.103-3162G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903245 | ||||||
| chr6:46903367
|
G | A | 2 | a0001c0001t0001g0320a0001c0001t0005g0082 | 2 | HG01109.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.103-3284C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903367 | ||||||
| chr6:46903394
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0161others(95): Show | 99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.102+3267C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903394 | ||||||
| chr6:46903448
|
C | T | 161 | a0001c0001t0001g0202a0001c0001t0001g0206a0001c0001t0001g0208others(158): Show | 161 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.102+3213G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903448 | ||||||
| chr6:46903497
|
G | A | 1 | a0002c0002t0003g0075 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.102+3164C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903497 | ||||||
| chr6:46903527
|
T | A | 4 | a0001c0001t0001g0260a0001c0001t0001g0333a0001c0001t0001g0334others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+3134A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903527 | ||||||
| chr6:46903541
|
G | C | 6 | a0001c0004t0018g0015a0003c0003t0011g0010a0003c0003t0011g0011others(3): Show | 6 | HG01106.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+3120C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903541 | ||||||
| chr6:46903589
|
G | A | 1 | a0002c0002t0002g0321 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.102+3072C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903589 | ||||||
| chr6:46903608
|
T | C | 8 | a0002c0002t0002g0244a0003c0003t0004g0186a0003c0003t0004g0188others(5): Show | 8 | HG01884.hp1 HG02895.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.102+3053A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903608 | ||||||
| chr6:46903626
|
GCCCTGCC others(8): Show |
G | 1 | a0001c0001t0001g0322 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.102+3020_102+3034d others(17): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903626 | ||||||
| chr6:46903669
|
T | C | 2 | a0001c0004t0001g0127a0002c0005t0002g0151 | 2 | HG02129.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.102+2992A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903669 | ||||||
| chr6:46903714
|
C | A | 3 | a0002c0002t0003g0091a0003c0003t0006g0350a0003c0003t0013g0090 | 3 | HG01243.hp2 HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.102+2947G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903714 | ||||||
| chr6:46903906
|
C | T | 6 | a0001c0004t0018g0015a0003c0003t0011g0010a0003c0003t0011g0011others(3): Show | 6 | HG01106.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+2755G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903906 | ||||||
| chr6:46903972
|
T | C | 1 | a0011c0018t0001g0152 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.102+2689A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903972 | ||||||
| chr6:46904017
|
C | G | 23 | a0002c0002t0002g0169a0002c0002t0002g0244a0002c0006t0002g0196others(20): Show | 23 | HG00642.hp1 HG00741.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.102+2644G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46904017 | ||||||
| chr6:46904178
|
T | C | 330 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(327): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.102+2483A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46904178 | ||||||
| chr6:46904205
|
T | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0161others(95): Show | 99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.102+2456A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46904205 | ||||||
| chr6:46904248
|
T | C | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0359others(19): Show | 24 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.102+2413A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46904248 | ||||||
| chr6:46904257
|
A | T | 1 | a0002c0014t0002g0209 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.102+2404T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46904257 | ||||||
| chr6:46904305
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.102+2356C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46904305 | ||||||
| chr6:46904377
|
G | T | 1 | a0007c0016t0001g0201 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.102+2284C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46904377 | ||||||
| chr6:46904624
|
G | T | 18 | a0001c0001t0001g0097a0001c0001t0001g0100a0001c0001t0001g0104others(15): Show | 18 | HG02015.hp1 HG02155.hp2 HG02683.hp1 others(15): Show |
intron_variant | MODIFIER | c.102+2037C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46904624 | ||||||
| chr6:46904691
|
T | A | 1 | a0001c0001t0001g0376 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.102+1970A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46904691 | ||||||
| chr6:46904728
|
C | G | 1 | a0002c0002t0003g0034 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.102+1933G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46904728 | ||||||
| chr6:46904884
|
A | G | 1 | a0001c0001t0001g0276 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.102+1777T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46904884 | ||||||
| chr6:46904902
|
G | T | 6 | a0001c0004t0018g0015a0003c0003t0011g0010a0003c0003t0011g0011others(3): Show | 6 | HG01106.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+1759C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46904902 | ||||||
| chr6:46904916
|
A | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0161others(95): Show | 99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.102+1745T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46904916 | ||||||
| chr6:46905088
|
T | C | 1 | a0001c0001t0001g0266 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.102+1573A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46905088 | ||||||
| chr6:46905223
|
A | C | 16 | a0001c0001t0001g0097a0001c0001t0001g0100a0001c0001t0001g0104others(13): Show | 16 | HG02015.hp1 HG02155.hp2 HG02683.hp1 others(13): Show |
intron_variant | MODIFIER | c.102+1438T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46905223 | ||||||
| chr6:46905257
|
A | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0161others(95): Show | 99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.102+1404T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46905257 | ||||||
| chr6:46905409
|
G | A | 1 | a0001c0004t0001g0153 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.102+1252C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46905409 | ||||||
| chr6:46905647
|
T | C | 1 | a0003c0034t0008g0004 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.102+1014A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46905647 | ||||||
| chr6:46905658
|
G | A | 1 | a0007c0016t0001g0201 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.102+1003C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46905658 | ||||||
| chr6:46905733
|
C | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0161others(95): Show | 99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.102+928G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46905733 | ||||||
| chr6:46905743
|
CAAT | C | 23 | a0002c0002t0002g0169a0002c0002t0002g0244a0002c0006t0002g0196others(20): Show | 23 | HG00642.hp1 HG00741.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.102+915_102+917del others(3): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46905743 | ||||||
| chr6:46905791
|
G | A | 4 | a0003c0003t0004g0171a0003c0003t0004g0194a0003c0003t0004g0195others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+870C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46905791 | ||||||
| chr6:46905812
|
G | T | 23 | a0002c0002t0002g0169a0002c0002t0002g0244a0002c0006t0002g0196others(20): Show | 23 | HG00642.hp1 HG00741.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.102+849C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46905812 | ||||||
| chr6:46905880
|
G | A | 4 | a0002c0002t0002g0169a0003c0003t0004g0120a0003c0003t0004g0121others(1): Show | 4 | HG02145.hp2 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+781C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46905880 | ||||||
| chr6:46905931
|
T | C | 37 | a0001c0001t0001g0097a0001c0001t0001g0100a0001c0001t0001g0104others(34): Show | 37 | HG01106.hp1 HG01891.hp2 HG02015.hp1 others(34): Show |
intron_variant | MODIFIER | c.102+730A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46905931 | ||||||
| chr6:46906000
|
A | G | 4 | a0002c0002t0003g0091a0003c0003t0006g0350a0003c0003t0013g0090others(1): Show | 4 | HG01243.hp2 HG02109.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+661T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46906000 | ||||||
| chr6:46906371
|
G | C | 1 | a0001c0001t0001g0336 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.102+290C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46906371 | ||||||
| chr6:46906544
|
A | G | 2 | a0002c0005t0003g0025a0002c0006t0003g0026 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.102+117T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46906544 | ||||||
| chr6:46906588
|
T | G | 5 | a0001c0001t0001g0368a0001c0001t0001g0369a0001c0001t0001g0374others(2): Show | 5 | HG00738.hp1 HG01515.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.102+73A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46906588 | ||||||
| chr6:46907030
|
G | T | 2 | a0002c0002t0002g0102a0004c0011t0006g0103 | 2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-24-244C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46907030 | ||||||
| chr6:46907399
|
T | C | 1 | a0001c0001t0001g0322 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-24-613A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46907399 | ||||||
| chr6:46907413
|
C | A | 7 | a0001c0001t0015g0007a0003c0003t0004g0199a0003c0003t0008g0005others(4): Show | 7 | HG02145.hp1 HG02280.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-24-627G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46907413 | ||||||
| chr6:46907434
|
G | T | 161 | a0001c0001t0001g0202a0001c0001t0001g0206a0001c0001t0001g0208others(158): Show | 161 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-24-648C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46907434 | ||||||
| chr6:46907480
|
C | A | 2 | a0002c0002t0002g0230a0002c0002t0002g0231 | 2 | HG02071.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.-24-694G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46907480 | ||||||
| chr6:46907521
|
T | A | 1 | a0003c0003t0004g0227 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-24-735A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46907521 | ||||||
| chr6:46907582
|
T | C | 6 | a0001c0004t0018g0015a0003c0003t0011g0010a0003c0003t0011g0011others(3): Show | 6 | HG01106.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-24-796A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46907582 | ||||||
| chr6:46907614
|
A | T | 1 | a0002c0002t0003g0040 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-24-828T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46907614 | ||||||
| chr6:46907824
|
T | C | 3 | a0002c0002t0002g0114a0002c0002t0002g0242a0002c0002t0012g0033 | 3 | HG02109.hp1 HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-24-1038A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46907824 | ||||||
| chr6:46908010
|
G | A | 2 | a0001c0001t0001g0323a0001c0001t0001g0324 | 2 | HG01167.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.-24-1224C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46908010 | ||||||
| chr6:46908048
|
G | A | 1 | a0001c0001t0001g0325 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-24-1262C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46908048 | ||||||
| chr6:46908183
|
G | T | 100 | a0001c0001t0001g0202a0001c0001t0001g0206a0001c0001t0001g0208others(97): Show | 100 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.-24-1397C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46908183 | ||||||
| chr6:46908348
|
G | A | 1 | a0001c0012t0001g0275 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-24-1562C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46908348 | ||||||
| chr6:46908354
|
T | C | 1 | a0002c0002t0012g0089 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-24-1568A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46908354 | ||||||
| chr6:46908362
|
G | C | 2 | a0001c0001t0001g0326a0002c0002t0002g0327 | 2 | NA18966.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-24-1576C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46908362 | ||||||
| chr6:46908469
|
T | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0161others(95): Show | 99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.-24-1683A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46908469 | ||||||
| chr6:46908506
|
C | T | 100 | a0001c0001t0001g0202a0001c0001t0001g0206a0001c0001t0001g0208others(97): Show | 100 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.-24-1720G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46908506 | ||||||
| chr6:46908637
|
G | C | 3 | a0001c0001t0001g0202a0003c0003t0004g0237a0003c0003t0004g0238 | 3 | HG01261.hp1 HG03831.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-24-1851C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46908637 | ||||||
| chr6:46908708
|
A | T | 1 | a0001c0001t0001g0208 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-24-1922T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46908708 | ||||||
| chr6:46909032
|
T | G | 10 | a0002c0002t0002g0244a0003c0003t0004g0186a0003c0003t0004g0188others(7): Show | 10 | HG00741.hp2 HG01884.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.-24-2246A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46909032 | ||||||
| chr6:46909138
|
A | G | 1 | a0002c0002t0003g0039 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-24-2352T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46909138 | ||||||
| chr6:46909274
|
T | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0359others(19): Show | 24 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.-24-2488A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46909274 | ||||||
| chr6:46909514
|
C | G | 4 | a0001c0004t0001g0128a0001c0004t0001g0129a0001c0004t0001g0131others(1): Show | 4 | NA18952.hp1 NA18984.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.-24-2728G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46909514 | ||||||
| chr6:46909609
|
C | A | 11 | a0002c0002t0016g0009a0002c0002t0020g0028a0002c0005t0003g0025others(8): Show | 11 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-24-2823G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46909609 | ||||||
| chr6:46909687
|
G | A | 1 | a0003c0003t0004g0171 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-24-2901C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46909687 | ||||||
| chr6:46909835
|
G | GT | 6 | a0001c0004t0018g0015a0003c0003t0011g0010a0003c0003t0011g0011others(3): Show | 6 | HG01106.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-24-3050dupA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46909835 | ||||||
| chr6:46910007
|
C | CAATAA | 64 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0366others(61): Show | 64 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.-24-3226_-24-3222d others(7): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910007 | ||||||
| chr6:46910007
|
C | CAATAAAA others(3): Show |
8 | a0001c0001t0005g0080a0001c0001t0005g0081a0002c0002t0003g0076others(5): Show | 8 | HG00621.hp1 HG01243.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.-24-3231_-24-3222d others(12): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910007 | ||||||
| chr6:46910007
|
CAATAAAA others(3): Show |
C | 104 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0161others(101): Show | 105 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.-24-3231_-24-3222d others(12): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910007 | ||||||
| chr6:46910056
|
G | T | 2 | a0001c0001t0001g0255a0001c0001t0001g0283 | 2 | HG00408.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.-24-3270C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910056 | ||||||
| chr6:46910115
|
G | A | 39 | a0001c0001t0001g0097a0001c0001t0001g0100a0001c0001t0001g0104others(36): Show | 39 | HG01106.hp1 HG01891.hp2 HG02015.hp1 others(36): Show |
intron_variant | MODIFIER | c.-24-3329C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910115 | ||||||
| chr6:46910169
|
G | A | 2 | a0001c0001t0001g0274a0002c0005t0002g0328 | 2 | HG02080.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.-24-3383C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910169 | ||||||
| chr6:46910212
|
C | G | 1 | a0001c0004t0001g0127 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-24-3426G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910212 | ||||||
| chr6:46910278
|
G | T | 1 | a0001c0001t0001g0359 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-24-3492C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910278 | ||||||
| chr6:46910474
|
G | A | 5 | a0003c0003t0004g0356a0004c0008t0006g0358a0004c0008t0009g0354others(2): Show | 5 | HG01074.hp1 HG02280.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-24-3688C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910474 | ||||||
| chr6:46910552
|
A | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0161others(95): Show | 99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.-24-3766T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910552 | ||||||
| chr6:46910592
|
C | T | 2 | a0003c0003t0004g0120a0003c0003t0004g0343 | 2 | HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-24-3806G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910592 | ||||||
| chr6:46910608
|
C | T | 1 | a0001c0001t0001g0370 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-24-3822G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910608 | ||||||
| chr6:46910610
|
G | A | 1 | a0001c0001t0001g0329 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-24-3824C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910610 | ||||||
| chr6:46910656
|
G | A | 1 | a0001c0001t0001g0330 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-24-3870C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910656 | ||||||
| chr6:46910693
|
TCAAC | T | 11 | a0002c0002t0016g0009a0002c0002t0020g0028a0002c0005t0003g0025others(8): Show | 11 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-24-3911_-24-3908d others(6): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910693 | ||||||
| chr6:46910709
|
A | C | 65 | a0001c0001t0005g0041a0001c0001t0005g0042a0001c0001t0005g0045others(62): Show | 65 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.-24-3923T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910709 | ||||||
| chr6:46910713
|
A | C | 7 | a0001c0004t0005g0035a0001c0004t0005g0036a0001c0004t0005g0037others(4): Show | 7 | HG01192.hp1 HG02615.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-24-3927T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910713 | ||||||
| chr6:46910766
|
G | A | 1 | a0001c0001t0005g0093 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-24-3980C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910766 | ||||||
| chr6:46910870
|
G | T | 7 | a0001c0001t0015g0007a0003c0003t0004g0199a0003c0003t0008g0005others(4): Show | 7 | HG02145.hp1 HG02280.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-24-4084C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910870 | ||||||
| chr6:46910933
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-24-4147A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910933 | ||||||
| chr6:46911027
|
C | A | 1 | a0001c0001t0005g0083 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-24-4241G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46911027 | ||||||
| chr6:46911155
|
C | A | 1 | a0005c0015t0001g0233 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-24-4369G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46911155 | ||||||
| chr6:46911263
|
T | C | 331 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(328): Show | 334 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.-24-4477A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46911263 | ||||||
| chr6:46911449
|
A | T | 1 | a0007c0016t0001g0201 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-24-4663T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46911449 | ||||||
| chr6:46911555
|
C | T | 1 | a0007c0016t0001g0201 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-24-4769G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46911555 | ||||||
| chr6:46911699
|
C | T | 23 | a0002c0002t0002g0169a0002c0002t0002g0244a0002c0006t0002g0196others(20): Show | 23 | HG00642.hp1 HG00741.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.-24-4913G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46911699 | ||||||
| chr6:46911910
|
A | G | 1 | a0001c0004t0001g0166 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-24-5124T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46911910 | ||||||
| chr6:46911929
|
C | T | 2 | a0004c0008t0009g0354a0004c0008t0009g0355 | 2 | HG02280.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-24-5143G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46911929 | ||||||
| chr6:46912221
|
A | G | 4 | a0003c0003t0006g0241a0003c0003t0006g0344a0003c0003t0006g0345others(1): Show | 4 | HG01884.hp2 HG02717.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-24-5435T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46912221 | ||||||
| chr6:46912400
|
G | T | 54 | a0001c0001t0001g0206a0001c0001t0001g0208a0001c0001t0001g0210others(51): Show | 54 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.-24-5614C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46912400 | ||||||
| chr6:46912556
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-24-5770A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46912556 | ||||||
| chr6:46912559
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0161others(95): Show | 99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.-24-5773C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46912559 | ||||||
| chr6:46912672
|
G | T | 1 | a0002c0002t0016g0009 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-24-5886C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46912672 | ||||||
| chr6:46912814
|
C | A | 1 | a0001c0001t0001g0340 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-24-6028G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46912814 | ||||||
| chr6:46912959
|
T | C | 1 | a0007c0016t0001g0201 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-24-6173A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46912959 | ||||||
| chr6:46913144
|
G | C | 3 | a0003c0003t0014g0337a0015c0026t0001g0338a0019c0033t0014g0342 | 3 | HG02809.hp1 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-24-6358C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46913144 | ||||||
| chr6:46913187
|
C | T | 1 | a0004c0029t0028g0124 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-6401G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46913187 | ||||||
| chr6:46913205
|
A | G | 1 | a0001c0004t0001g0166 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-24-6419T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46913205 | ||||||
| chr6:46913223
|
C | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0161others(95): Show | 99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.-24-6437G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46913223 | ||||||
| chr6:46913262
|
C | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0266a0001c0001t0001g0268others(9): Show | 13 | NA18939.hp1 NA18943.hp1 NA18954.hp1 others(10): Show |
intron_variant | MODIFIER | c.-24-6476G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46913262 | ||||||
| chr6:46913271
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0161others(95): Show | 99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.-24-6485C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46913271 | ||||||
| chr6:46913392
|
G | A | 62 | a0001c0001t0005g0041a0001c0001t0005g0042a0001c0001t0005g0045others(59): Show | 62 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.-24-6606C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46913392 | ||||||
| chr6:46913409
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0364a0002c0002t0002g0365 | 4 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24-6623C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46913409 | ||||||
| chr6:46913499
|
CA | C | 267 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0097others(264): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.-24-6714delT | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46913499 | ||||||
| chr6:46913528
|
G | C | 1 | a0007c0016t0001g0201 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-24-6742C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46913528 | ||||||
| chr6:46913650
|
A | C | 2 | a0002c0002t0002g0240a0003c0025t0004g0239 | 2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24-6864T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46913650 | ||||||
| chr6:46913787
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-24-7001C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46913787 | ||||||
| chr6:46913856
|
A | T | 325 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(322): Show | 328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.-24-7070T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46913856 | ||||||
| chr6:46914103
|
A | C | 1 | a0001c0012t0001g0275 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-24-7317T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46914103 | ||||||
| chr6:46914283
|
G | A | 1 | a0015c0026t0001g0338 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-25+7430C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46914283 | ||||||
| chr6:46914323
|
G | A | 2 | a0002c0002t0003g0091a0003c0003t0006g0350 | 2 | HG01243.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-25+7390C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46914323 | ||||||
| chr6:46914428
|
C | T | 70 | a0001c0001t0001g0202a0001c0001t0001g0206a0001c0001t0001g0208others(67): Show | 70 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.-25+7285G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46914428 | ||||||
| chr6:46914429
|
A | T | 1 | a0003c0003t0004g0194 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-25+7284T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46914429 | ||||||
| chr6:46914432
|
T | C | 1 | a0003c0003t0008g0008 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-25+7281A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46914432 | ||||||
| chr6:46914656
|
G | T | 8 | a0002c0002t0002g0244a0003c0003t0004g0186a0003c0003t0004g0188others(5): Show | 8 | HG01884.hp1 HG02895.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-25+7057C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46914656 | ||||||
| chr6:46914857
|
G | T | 1 | a0002c0002t0002g0123 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-25+6856C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46914857 | ||||||
| chr6:46914869
|
T | G | 100 | a0001c0001t0001g0202a0001c0001t0001g0206a0001c0001t0001g0208others(97): Show | 100 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.-25+6844A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46914869 | ||||||
| chr6:46914878
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-25+6835G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46914878 | ||||||
| chr6:46914879
|
G | A | 6 | a0001c0004t0018g0015a0003c0003t0011g0010a0003c0003t0011g0011others(3): Show | 6 | HG01106.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+6834C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46914879 | ||||||
| chr6:46914908
|
T | G | 1 | a0001c0001t0001g0205 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-25+6805A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46914908 | ||||||
| chr6:46915134
|
A | C | 1 | a0007c0016t0001g0201 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-25+6579T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915134 | ||||||
| chr6:46915135
|
C | T | 1 | a0001c0001t0001g0332 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-25+6578G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915135 | ||||||
| chr6:46915151
|
C | T | 3 | a0002c0002t0003g0091a0003c0003t0006g0350a0003c0003t0013g0090 | 3 | HG01243.hp2 HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-25+6562G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915151 | ||||||
| chr6:46915167
|
A | G | 100 | a0001c0001t0001g0202a0001c0001t0001g0206a0001c0001t0001g0208others(97): Show | 100 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.-25+6546T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915167 | ||||||
| chr6:46915288
|
T | TTAA | 12 | a0001c0001t0005g0085a0001c0004t0001g0118a0001c0004t0001g0119others(9): Show | 12 | HG01496.hp2 HG01516.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.-25+6422_-25+6424d others(5): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915288 | ||||||
| chr6:46915288
|
T | TTAATAAT others(2): Show |
20 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0359others(17): Show | 22 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.-25+6416_-25+6424d others(11): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915288 | ||||||
| chr6:46915288
|
T | TTAATAAT others(5): Show |
3 | a0001c0001t0001g0377a0001c0001t0001g0378a0003c0003t0004g0186 | 3 | HG02451.hp2 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-25+6413_-25+6424d others(14): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915288 | ||||||
| chr6:46915288
|
T | TTAATAAT others(11): Show |
8 | a0002c0002t0002g0244a0003c0003t0004g0188a0003c0003t0004g0189others(5): Show | 8 | HG01884.hp1 HG02895.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-25+6407_-25+6424d others(20): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915288 | ||||||
| chr6:46915288
|
T | TTAATAAT others(14): Show |
1 | a0003c0003t0004g0192 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-25+6404_-25+6424d others(23): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915288 | ||||||
| chr6:46915320
|
C | G | 10 | a0002c0002t0002g0244a0003c0003t0004g0186a0003c0003t0004g0188others(7): Show | 10 | HG00741.hp2 HG01884.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.-25+6393G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915320 | ||||||
| chr6:46915448
|
G | C | 1 | a0002c0002t0003g0023 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-25+6265C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915448 | ||||||
| chr6:46915529
|
C | T | 1 | a0006c0010t0001g0193 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-25+6184G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915529 | ||||||
| chr6:46915552
|
G | A | 1 | a0001c0001t0001g0331 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-25+6161C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915552 | ||||||
| chr6:46915736
|
C | G | 1 | a0003c0007t0007g0234 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-25+5977G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915736 | ||||||
| chr6:46915757
|
C | T | 9 | a0001c0001t0001g0271a0001c0019t0001g0270a0002c0002t0002g0251others(6): Show | 9 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+5956G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915757 | ||||||
| chr6:46915823
|
A | C | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | NA18943.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-25+5890T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915823 | ||||||
| chr6:46915980
|
G | A | 8 | a0001c0004t0018g0015a0002c0002t0003g0091a0003c0003t0011g0010others(5): Show | 8 | HG01106.hp2 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-25+5733C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915980 | ||||||
| chr6:46916003
|
A | C | 1 | a0001c0004t0001g0203 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-25+5710T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46916003 | ||||||
| chr6:46916042
|
C | T | 54 | a0001c0001t0001g0206a0001c0001t0001g0208a0001c0001t0001g0210others(51): Show | 54 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.-25+5671G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46916042 | ||||||
| chr6:46916097
|
A | G | 54 | a0001c0001t0001g0206a0001c0001t0001g0208a0001c0001t0001g0210others(51): Show | 54 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.-25+5616T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46916097 | ||||||
| chr6:46916259
|
G | A | 1 | a0010c0032t0004g0200 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-25+5454C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46916259 | ||||||
| chr6:46916473
|
G | A | 1 | a0002c0002t0003g0086 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-25+5240C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46916473 | ||||||
| chr6:46916551
|
T | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0161others(95): Show | 99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.-25+5162A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46916551 | ||||||
| chr6:46916556
|
C | A | 1 | a0001c0004t0018g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-25+5157G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46916556 | ||||||
| chr6:46916782
|
A | T | 6 | a0001c0004t0018g0015a0003c0003t0011g0010a0003c0003t0011g0011others(3): Show | 6 | HG01106.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+4931T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46916782 | ||||||
| chr6:46916944
|
G | A | 328 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(325): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.-25+4769C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46916944 | ||||||
| chr6:46916945
|
C | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0161others(86): Show | 90 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.-25+4768G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46916945 | ||||||
| chr6:46917458
|
C | T | 1 | a0003c0007t0007g0122 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-25+4255G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46917458 | ||||||
| chr6:46917562
|
T | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0161others(118): Show | 122 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.-25+4151A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46917562 | ||||||
| chr6:46917597
|
G | A | 1 | a0007c0016t0001g0201 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-25+4116C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46917597 | ||||||
| chr6:46917622
|
G | A | 1 | a0003c0007t0007g0159 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-25+4091C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46917622 | ||||||
| chr6:46918075
|
T | G | 1 | a0002c0002t0003g0087 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-25+3638A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918075 | ||||||
| chr6:46918106
|
G | A | 1 | a0001c0001t0023g0088 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-25+3607C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918106 | ||||||
| chr6:46918107
|
G | A | 62 | a0001c0001t0001g0202a0001c0001t0001g0206a0001c0001t0001g0208others(59): Show | 62 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.-25+3606C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918107 | ||||||
| chr6:46918206
|
T | C | 1 | a0001c0001t0001g0261 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-25+3507A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918206 | ||||||
| chr6:46918220
|
A | T | 2 | a0001c0001t0001g0368a0001c0001t0001g0369 | 2 | HG00738.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.-25+3493T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918220 | ||||||
| chr6:46918278
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-25+3435T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918278 | ||||||
| chr6:46918420
|
T | G | 328 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(325): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.-25+3293A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918420 | ||||||
| chr6:46918427
|
C | T | 1 | a0001c0001t0001g0266 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-25+3286G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918427 | ||||||
| chr6:46918435
|
C | T | 13 | a0002c0002t0002g0169a0002c0006t0002g0196a0002c0006t0002g0197others(10): Show | 13 | HG00642.hp1 HG01255.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.-25+3278G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918435 | ||||||
| chr6:46918568
|
G | A | 2 | a0001c0004t0001g0166a0001c0004t0001g0167 | 2 | HG03688.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-25+3145C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918568 | ||||||
| chr6:46918677
|
T | C | 1 | a0014c0020t0001g0339 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-25+3036A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918677 | ||||||
| chr6:46918768
|
G | A | 1 | a0001c0001t0001g0340 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-25+2945C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918768 | ||||||
| chr6:46918780
|
C | T | 1 | a0002c0002t0002g0172 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-25+2933G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918780 | ||||||
| chr6:46918825
|
C | T | 2 | a0002c0002t0002g0240a0003c0025t0004g0239 | 2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-25+2888G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918825 | ||||||
| chr6:46918941
|
A | G | 1 | a0002c0002t0003g0024 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-25+2772T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918941 | ||||||
| chr6:46918953
|
A | G | 10 | a0002c0002t0002g0244a0003c0003t0004g0186a0003c0003t0004g0188others(7): Show | 10 | HG00741.hp2 HG01884.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.-25+2760T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918953 | ||||||
| chr6:46919000
|
T | C | 6 | a0001c0004t0018g0015a0003c0003t0011g0010a0003c0003t0011g0011others(3): Show | 6 | HG01106.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+2713A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46919000 | ||||||
| chr6:46919037
|
G | GTT | 95 | a0001c0001t0001g0001a0001c0001t0001g0255a0001c0001t0001g0256others(92): Show | 96 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.-25+2674_-25+2675d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46919037 | ||||||
| chr6:46919067
|
G | T | 1 | a0007c0016t0001g0201 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-25+2646C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46919067 | ||||||
| chr6:46919132
|
A | G | 1 | a0003c0007t0004g0185 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-25+2581T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46919132 | ||||||
| chr6:46919215
|
T | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0097others(136): Show | 141 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.-25+2498A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46919215 | ||||||
| chr6:46919449
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-25+2264T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46919449 | ||||||
| chr6:46919529
|
T | C | 1 | a0001c0001t0001g0003 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-25+2184A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46919529 | ||||||
| chr6:46919645
|
G | T | 2 | a0001c0004t0001g0118a0001c0004t0001g0119 | 2 | HG02523.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.-25+2068C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46919645 | ||||||
| chr6:46919656
|
T | C | 1 | a0002c0002t0002g0169 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-25+2057A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46919656 | ||||||
| chr6:46919674
|
C | A | 6 | a0001c0004t0018g0015a0003c0003t0011g0010a0003c0003t0011g0011others(3): Show | 6 | HG01106.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+2039G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46919674 | ||||||
| chr6:46919816
|
T | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0255a0001c0001t0001g0256others(94): Show | 98 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.-25+1897A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46919816 | ||||||
| chr6:46919902
|
T | G | 1 | a0007c0016t0001g0201 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-25+1811A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46919902 | ||||||
| chr6:46919965
|
A | G | 1 | a0001c0001t0001g0116 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-25+1748T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46919965 | ||||||
| chr6:46919966
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-25+1747C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46919966 | ||||||
| chr6:46920177
|
C | A | 1 | a0002c0002t0012g0089 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-25+1536G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46920177 | ||||||
| chr6:46920357
|
A | G | 1 | a0003c0003t0004g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-25+1356T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46920357 | ||||||
| chr6:46920407
|
A | T | 6 | a0001c0001t0015g0007a0003c0003t0004g0094a0003c0003t0008g0005others(3): Show | 6 | HG02145.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+1306T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46920407 | ||||||
| chr6:46920415
|
A | G | 5 | a0001c0001t0015g0007a0003c0003t0008g0005a0003c0003t0008g0006others(2): Show | 5 | HG02145.hp1 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25+1298T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46920415 | ||||||
| chr6:46920500
|
C | T | 1 | a0003c0003t0004g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-25+1213G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46920500 | ||||||
| chr6:46920523
|
AT | A | 13 | a0002c0002t0002g0172a0002c0002t0002g0173a0002c0002t0002g0174others(10): Show | 13 | HG01943.hp1 HG02004.hp2 HG02273.hp1 others(10): Show |
intron_variant | MODIFIER | c.-25+1189delA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46920523 | ||||||
| chr6:46920525
|
T | TG | 6 | a0002c0002t0002g0245a0002c0002t0002g0246a0002c0002t0002g0247others(3): Show | 6 | HG00280.hp1 HG01070.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+1187_-25+1188i others(3): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46920525 | ||||||
| chr6:46920526
|
T | G | 124 | a0001c0001t0001g0202a0001c0001t0001g0205a0001c0001t0001g0206others(121): Show | 124 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.-25+1187A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46920526 | ||||||
| chr6:46920526
|
T | TG | 58 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0264others(55): Show | 60 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.-25+1186dupC | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46920526 | ||||||
| chr6:46920526
|
T | TGG | 100 | a0001c0001t0001g0001a0001c0001t0001g0104a0001c0001t0001g0105others(97): Show | 101 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.-25+1185_-25+1186d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46920526 | ||||||
| chr6:46920533
|
G | GT | 75 | a0001c0001t0005g0041a0001c0001t0005g0042a0001c0001t0005g0045others(72): Show | 75 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.-25+1179_-25+1180i others(3): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46920533 | ||||||
| chr6:46920591
|
G | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0359others(19): Show | 24 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.-25+1122C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46920591 | ||||||
| chr6:46920770
|
G | A | 2 | a0001c0001t0005g0093a0002c0002t0003g0092 | 2 | HG01099.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.-25+943C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46920770 | ||||||
| chr6:46920841
|
C | T | 6 | a0001c0001t0015g0007a0003c0003t0004g0094a0003c0003t0008g0005others(3): Show | 6 | HG02145.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+872G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46920841 | ||||||
| chr6:46920974
|
C | T | 1 | a0006c0010t0001g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-25+739G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46920974 | ||||||
| chr6:46921033
|
A | T | 52 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0097others(49): Show | 54 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.-25+680T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921033 | ||||||
| chr6:46921062
|
G | T | 1 | a0001c0013t0001g0250 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-25+651C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921062 | ||||||
| chr6:46921141
|
T | C | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(317): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.-25+572A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921141 | ||||||
| chr6:46921173
|
G | T | 97 | a0001c0001t0001g0001a0001c0001t0001g0255a0001c0001t0001g0256others(94): Show | 98 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.-25+540C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921173 | ||||||
| chr6:46921262
|
GCTCC | G | 6 | a0001c0001t0015g0007a0003c0003t0004g0094a0003c0003t0008g0005others(3): Show | 6 | HG02145.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+447_-25+450del others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921262 | ||||||
| chr6:46921277
|
T | C | 1 | a0001c0001t0001g0351 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-25+436A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921277 | ||||||
| chr6:46921418
|
A | G | 1 | a0002c0002t0002g0249 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-25+295T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921418 | ||||||
| chr6:46921426
|
G | GA | 183 | a0001c0001t0001g0001a0001c0001t0001g0116a0001c0001t0001g0255others(180): Show | 184 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.-25+286dupT | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921426 | ||||||
| chr6:46921482
|
A | T | 77 | a0001c0001t0005g0041a0001c0001t0005g0042a0001c0001t0005g0045others(74): Show | 77 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.-25+231T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921482 | ||||||
| chr6:46921485
|
C | T | 5 | a0001c0001t0015g0007a0003c0003t0008g0005a0003c0003t0008g0006others(2): Show | 5 | HG02145.hp1 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25+228G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921485 | ||||||
| chr6:46921486
|
G | A | 7 | a0003c0003t0004g0352a0003c0003t0004g0353a0003c0003t0004g0356others(4): Show | 7 | HG01074.hp1 HG02280.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-25+227C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921486 | ||||||
| chr6:46921547
|
G | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0359others(19): Show | 24 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.-25+166C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921547 | ||||||
| chr6:46921577
|
A | G | 23 | a0001c0001t0001g0097a0001c0001t0001g0100a0001c0001t0001g0104others(20): Show | 23 | HG02015.hp1 HG02109.hp1 HG02155.hp2 others(20): Show |
intron_variant | MODIFIER | c.-25+136T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921577 | ||||||
| chr6:46921584
|
C | A | 11 | a0001c0001t0001g0368a0001c0001t0001g0369a0001c0001t0001g0370others(8): Show | 11 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.-25+129G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921584 | ||||||
| chr6:46921680
|
A | C | 6 | a0001c0001t0015g0007a0003c0003t0004g0094a0003c0003t0008g0005others(3): Show | 6 | HG02145.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+33T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921680 | ||||||
| chr6:46921691
|
C | T | 6 | a0001c0001t0015g0007a0003c0003t0004g0094a0003c0003t0008g0005others(3): Show | 6 | HG02145.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+22G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921691 |