Item | Value |
---|---|
geneid | 222487 |
ensemblid | ENSG00000182885.17 |
hgncid | 13728 |
symbol | ADGRG3 |
name | adhesion G protein-coupled receptor G3 |
refseq_nuc | NM_170776.5 |
refseq_prot | NP_740746.4 |
ensembl_nuc | ENST00000333493.9 |
ensembl_prot | ENSP00000332900.4 |
mane_status | MANE Select |
chr | chr16 |
start | 57668306 |
end | 57689378 |
strand | + |
ver | v1.2 |
region | chr16:57668306-57689378 |
region5000 | chr16:57663306-57694378 |
regionname0 | ADGRG3_chr16_57668306_57689378 |
regionname5000 | ADGRG3_chr16_57663306_57694378 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 549 | 381 | 84 | 70 | 167 | 12 | 46 | 131 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | MATPR others(544): Show |
chr16 | 57663306 | 57694378 |
a0002 | 0/0 | 549 | 51 | 5 | 6 | 32 | 6 | 2 | 22 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | MATPS others(544): Show |
chr16 | 57663306 | 57694378 |
a0003 | 0/0 | 549 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | MATPR others(544): Show |
chr16 | 57663306 | 57694378 |
a0004 | 0/0 | 549 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | MATPR others(544): Show |
chr16 | 57663306 | 57694378 |
a0005 | 0/0 | 549 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | MATPR others(544): Show |
chr16 | 57663306 | 57694378 |
a0006 | 0/0 | 549 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | MATPR others(544): Show |
chr16 | 57663306 | 57694378 |
a0007 | 0/0 | 549 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | MATPR others(544): Show |
chr16 | 57663306 | 57694378 |
a0008 | 0/0 | 549 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | MATPR others(544): Show |
chr16 | 57663306 | 57694378 |
a0009 | 0/0 | 549 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | MATPR others(544): Show |
chr16 | 57663306 | 57694378 |
a0010 | 0/0 | 549 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | MATPR others(544): Show |
chr16 | 57663306 | 57694378 |
a0011 | 0/0 | 549 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | MATPR others(544): Show |
chr16 | 57663306 | 57694378 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1647 | 258 | 40 | 45 | 138 | 6 | 27 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | ATGGC others(1642): Show |
chr16 | 57663306 | 57694378 | ||
a0001c0002 | 0/0 | 1647 | 94 | 19 | 23 | 29 | 5 | 18 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | ATGGC others(1642): Show |
chr16 | 57663306 | 57694378 | ||
a0001c0005 | 0/0 | 1647 | 13 | 13 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | ATGGC others(1642): Show |
chr16 | 57663306 | 57694378 | ||
a0001c0007 | 0/0 | 1647 | 7 | 7 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | ATGGC others(1642): Show |
chr16 | 57663306 | 57694378 | ||
a0001c0008 | 0/0 | 1647 | 3 | 0 | 2 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | ATGGC others(1642): Show |
chr16 | 57663306 | 57694378 | ||
a0001c0009 | 0/0 | 1647 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | ATGGC others(1642): Show |
chr16 | 57663306 | 57694378 | ||
a0001c0015 | 0/0 | 1647 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | ATGGC others(1642): Show |
chr16 | 57663306 | 57694378 | ||
a0001c0017 | 0/0 | 1647 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | ATGGC others(1642): Show |
chr16 | 57663306 | 57694378 | ||
a0001c0019 | 0/0 | 1647 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | ATGGC others(1642): Show |
chr16 | 57663306 | 57694378 | ||
a0001c0021 | 0/0 | 1647 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | ATGGC others(1642): Show |
chr16 | 57663306 | 57694378 | ||
a0002c0003 | 0/0 | 1647 | 26 | 0 | 0 | 24 | 1 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | ATGGC others(1642): Show |
chr16 | 57663306 | 57694378 | ||
a0002c0004 | 0/0 | 1647 | 22 | 4 | 4 | 8 | 5 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | ATGGC others(1642): Show |
chr16 | 57663306 | 57694378 | ||
a0002c0022 | 0/0 | 1647 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | ATGGC others(1642): Show |
chr16 | 57663306 | 57694378 | ||
a0002c0023 | 0/0 | 1647 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | ATGGC others(1642): Show |
chr16 | 57663306 | 57694378 | ||
a0002c0024 | 0/0 | 1647 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | ATGGC others(1642): Show |
chr16 | 57663306 | 57694378 | ||
a0003c0006 | 0/0 | 1647 | 7 | 6 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | ATGGC others(1642): Show |
chr16 | 57663306 | 57694378 | ||
a0004c0010 | 0/0 | 1647 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | ATGGC others(1642): Show |
chr16 | 57663306 | 57694378 | ||
a0005c0016 | 0/0 | 1647 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | ATGGC others(1642): Show |
chr16 | 57663306 | 57694378 | ||
a0006c0011 | 0/0 | 1647 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | ATGGC others(1642): Show |
chr16 | 57663306 | 57694378 | ||
a0007c0018 | 0/0 | 1647 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | ATGGC others(1642): Show |
chr16 | 57663306 | 57694378 | ||
a0008c0013 | 0/0 | 1647 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | ATGGC others(1642): Show |
chr16 | 57663306 | 57694378 | ||
a0009c0012 | 0/0 | 1647 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | ATGGC others(1642): Show |
chr16 | 57663306 | 57694378 | ||
a0010c0020 | 0/0 | 1647 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | ATGGC others(1642): Show |
chr16 | 57663306 | 57694378 | ||
a0011c0014 | 0/0 | 1647 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | ATGGC others(1642): Show |
chr16 | 57663306 | 57694378 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2609 | 136 | 20 | 25 | 68 | 3 | 18 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0001c0001t0002 | 0/0 | 2609 | 70 | 7 | 16 | 40 | 0 | 7 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0001c0001t0005 | 0/0 | 2609 | 31 | 0 | 0 | 30 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0001c0001t0006 | 0/0 | 2609 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0001c0001t0007 | 0/0 | 2609 | 7 | 7 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0001c0001t0009 | 0/0 | 2609 | 5 | 0 | 3 | 0 | 2 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0001c0001t0010 | 0/0 | 2609 | 4 | 3 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0001c0001t0014 | 0/0 | 2609 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0001c0001t0016 | 0/0 | 2609 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0001c0001t0017 | 0/0 | 2609 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0001c0001t0019 | 0/0 | 2609 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0001c0002t0001 | 0/0 | 2609 | 42 | 4 | 14 | 16 | 0 | 8 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0001c0002t0003 | 0/0 | 2609 | 8 | 3 | 0 | 4 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0001c0002t0004 | 0/0 | 2609 | 31 | 1 | 8 | 8 | 5 | 9 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0001c0002t0008 | 0/0 | 2609 | 5 | 5 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0001c0002t0012 | 0/0 | 2609 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0001c0002t0013 | 0/0 | 2609 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0001c0002t0015 | 0/0 | 2609 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0001c0002t0020 | 0/0 | 2609 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0001c0002t0021 | 0/0 | 2609 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0001c0005t0001 | 0/0 | 2609 | 13 | 13 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0001c0007t0001 | 0/0 | 2609 | 6 | 6 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0001c0007t0008 | 0/0 | 2609 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0001c0008t0002 | 0/0 | 2609 | 3 | 0 | 2 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0001c0009t0003 | 0/0 | 2609 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0001c0015t0009 | 0/0 | 2609 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0001c0017t0011 | 0/0 | 2609 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0001c0019t0008 | 0/0 | 2609 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0001c0021t0001 | 0/0 | 2609 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0002c0003t0001 | 0/0 | 2609 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0002c0003t0003 | 0/0 | 2609 | 24 | 0 | 0 | 23 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0002c0003t0004 | 0/0 | 2609 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0002c0004t0001 | 0/0 | 2609 | 17 | 1 | 4 | 7 | 5 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0002c0004t0005 | 0/0 | 2609 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0002c0004t0006 | 0/0 | 2609 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0002c0004t0011 | 0/0 | 2609 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0002c0004t0018 | 0/0 | 2609 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0002c0022t0011 | 0/0 | 2609 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0002c0023t0001 | 0/0 | 2609 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0002c0024t0004 | 0/0 | 2609 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0003c0006t0006 | 0/0 | 2609 | 7 | 6 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0004c0010t0001 | 0/0 | 2609 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0005c0016t0002 | 0/0 | 2609 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0006c0011t0008 | 0/0 | 2609 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0007c0018t0007 | 0/0 | 2609 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0008c0013t0001 | 0/0 | 2609 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0009c0012t0005 | 0/0 | 2609 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0010c0020t0001 | 0/0 | 2609 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
a0011c0014t0001 | 0/0 | 2609 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | AGACA others(2604): Show |
chr16 | 57663306 | 57694378 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0020 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0111 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0263 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0001 | 0/0 | 14 | 0 | 3 | 9 | 0 | 2 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0007 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0014 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0015 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0005g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0005g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0005g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0005g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0005g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0005g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0005g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0005g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0005g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0005g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0005g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0005g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0007g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0007g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0007g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0007g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0009g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0009g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0009g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0009g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0010g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0010g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0010g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0010g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0014g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0016g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0017g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0001t0019g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0001g0002 | 0/0 | 12 | 1 | 4 | 5 | 0 | 2 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0004g0005 | 0/0 | 7 | 0 | 2 | 0 | 3 | 2 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0004g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0004g0023 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0004g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0004g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0004g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0004g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0004g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0004g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0004g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0004g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0004g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0004g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0004g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0004g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0008g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0008g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0008g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0012g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0012g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0012g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0013g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0013g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0015g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0020g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0002t0021g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0005t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0005t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0005t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0005t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0005t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0005t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0005t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0005t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0005t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0005t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0005t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0007t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0007t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0007t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0007t0008g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0008t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0008t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0008t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0009t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0009t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0015t0009g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0017t0011g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0019t0008g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0001c0021t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0003t0003g0009 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0003t0003g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0003t0003g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0003t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0003t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0003t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0003t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0003t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0003t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0003t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0003t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0003t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0003t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0003t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0004t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0004t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0004t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0004t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0004t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0004t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0004t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0004t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0004t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0004t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0004t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0004t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0004t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0004t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0004t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0004t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0004t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0004t0006g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0004t0011g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0004t0018g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0022t0011g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0023t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0002c0024t0004g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0003c0006t0006g0008 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0003c0006t0006g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0004c0010t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0004c0010t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0005c0016t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0006c0011t0008g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0007c0018t0007g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0008c0013t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0009c0012t0005g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0010c0020t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
a0011c0014t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0003 | t0001 | g0211 | EUR | GBR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00099 | hp2 | a0001 | c0001 | t0019 | g0038 | EUR | GBR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00140 | hp1 | a0002 | c0004 | t0001 | g0209 | EUR | GBR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0115 | EUR | GBR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00280 | hp1 | a0001 | c0002 | t0004 | g0005 | EUR | FIN | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | FIN | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | FIN | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00323 | hp2 | a0001 | c0002 | t0004 | g0005 | EUR | FIN | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00408 | hp2 | a0002 | c0003 | t0003 | g0011 | EAS | CHS | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00423 | hp1 | a0002 | c0003 | t0003 | g0011 | EAS | CHS | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | CHS | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00438 | hp1 | a0001 | c0002 | t0004 | g0026 | EAS | CHS | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0307 | EAS | CHS | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00558 | hp2 | a0001 | c0002 | t0004 | g0010 | EAS | CHS | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00597 | hp1 | a0001 | c0001 | t0005 | g0097 | EAS | CHS | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00609 | hp1 | a0001 | c0001 | t0005 | g0260 | EAS | CHS | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00621 | hp1 | a0001 | c0001 | t0005 | g0303 | EAS | CHS | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00639 | hp1 | a0001 | c0002 | t0004 | g0005 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00639 | hp2 | a0005 | c0016 | t0002 | g0071 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0317 | EAS | CHS | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | CHS | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00735 | hp1 | a0002 | c0023 | t0001 | g0226 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0318 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG00741 | hp2 | a0004 | c0010 | t0001 | g0296 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01070 | hp1 | a0001 | c0002 | t0004 | g0256 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01070 | hp2 | a0002 | c0004 | t0001 | g0044 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01071 | hp2 | a0002 | c0004 | t0001 | g0044 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01074 | hp1 | a0001 | c0002 | t0004 | g0005 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0076 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01106 | hp1 | a0001 | c0002 | t0004 | g0269 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01109 | hp2 | a0003 | c0006 | t0006 | g0008 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01167 | hp1 | a0001 | c0001 | t0010 | g0129 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01168 | hp1 | a0002 | c0004 | t0001 | g0213 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01168 | hp2 | a0001 | c0002 | t0004 | g0046 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01169 | hp1 | a0001 | c0002 | t0004 | g0046 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01192 | hp1 | a0001 | c0008 | t0002 | g0186 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01192 | hp2 | a0001 | c0001 | t0009 | g0268 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0112 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0319 | AMR | PUR | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01255 | hp1 | a0001 | c0002 | t0004 | g0262 | AMR | CLM | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | CLM | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01256 | hp2 | a0001 | c0008 | t0002 | g0187 | AMR | CLM | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0293 | AMR | CLM | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01257 | hp2 | a0001 | c0001 | t0009 | g0110 | AMR | CLM | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01346 | hp2 | a0002 | c0004 | t0001 | g0216 | AMR | CLM | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01496 | hp1 | a0002 | c0024 | t0004 | g0215 | AMR | CLM | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01515 | hp1 | a0002 | c0004 | t0001 | g0218 | EUR | IBS | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01515 | hp2 | a0002 | c0004 | t0001 | g0207 | EUR | IBS | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01516 | hp1 | a0001 | c0002 | t0004 | g0265 | EUR | IBS | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01516 | hp2 | a0001 | c0001 | t0009 | g0006 | EUR | IBS | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01517 | hp1 | a0002 | c0004 | t0001 | g0208 | EUR | IBS | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01517 | hp2 | a0001 | c0001 | t0009 | g0006 | EUR | IBS | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01884 | hp1 | a0001 | c0005 | t0001 | g0095 | AFR | ACB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01884 | hp2 | a0002 | c0004 | t0001 | g0214 | AFR | ACB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01891 | hp1 | a0001 | c0007 | t0008 | g0254 | AFR | ACB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01891 | hp2 | a0007 | c0018 | t0007 | g0045 | AFR | ACB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0107 | AMR | PEL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0310 | AMR | PEL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0025 | AMR | PEL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0025 | AMR | PEL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PEL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0034 | AMR | PEL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0168 | AMR | PEL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PEL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0104 | AMR | PEL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02004 | hp2 | a0001 | c0002 | t0020 | g0057 | AMR | PEL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02015 | hp1 | a0002 | c0004 | t0001 | g0043 | EAS | KHV | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | KHV | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02027 | hp2 | a0001 | c0002 | t0003 | g0150 | EAS | KHV | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02040 | hp2 | a0002 | c0003 | t0003 | g0011 | EAS | KHV | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02055 | hp1 | a0001 | c0002 | t0008 | g0251 | AFR | ACB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02071 | hp1 | a0001 | c0001 | t0005 | g0239 | EAS | KHV | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02071 | hp2 | a0002 | c0004 | t0001 | g0225 | EAS | KHV | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | KHV | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02074 | hp2 | a0002 | c0003 | t0003 | g0219 | EAS | KHV | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02080 | hp1 | a0008 | c0013 | t0001 | g0174 | EAS | KHV | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02083 | hp2 | a0001 | c0001 | t0005 | g0237 | EAS | KHV | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | KHV | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02132 | hp1 | a0001 | c0002 | t0003 | g0311 | EAS | KHV | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02132 | hp2 | a0002 | c0003 | t0003 | g0011 | EAS | KHV | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02135 | hp1 | a0002 | c0004 | t0001 | g0224 | EAS | KHV | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02135 | hp2 | a0001 | c0002 | t0003 | g0234 | EAS | KHV | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02145 | hp1 | a0002 | c0022 | t0011 | g0288 | AFR | ACB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02145 | hp2 | a0001 | c0002 | t0003 | g0259 | AFR | ACB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02148 | hp2 | a0001 | c0001 | t0009 | g0041 | AMR | PEL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CDX | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | CDX | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CDX | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02165 | hp2 | a0009 | c0012 | t0005 | g0004 | EAS | CDX | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02257 | hp1 | a0001 | c0002 | t0008 | g0013 | AFR | ACB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | ACB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02258 | hp1 | a0003 | c0006 | t0006 | g0008 | AFR | ACB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02258 | hp2 | a0001 | c0007 | t0001 | g0021 | AFR | ACB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | PEL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0092 | AMR | PEL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02280 | hp1 | a0001 | c0001 | t0007 | g0012 | AFR | ACB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02280 | hp2 | a0001 | c0002 | t0012 | g0054 | AFR | ACB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02300 | hp2 | a0001 | c0002 | t0004 | g0264 | AMR | PEL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02451 | hp1 | a0001 | c0005 | t0001 | g0282 | AFR | ACB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02451 | hp2 | a0004 | c0010 | t0001 | g0295 | AFR | ACB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02523 | hp2 | a0002 | c0003 | t0003 | g0009 | EAS | KHV | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02572 | hp1 | a0001 | c0007 | t0001 | g0042 | AFR | GWD | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0109 | AFR | GWD | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02615 | hp2 | a0001 | c0005 | t0001 | g0284 | AFR | GWD | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02622 | hp1 | a0001 | c0002 | t0012 | g0253 | AFR | GWD | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02622 | hp2 | a0001 | c0001 | t0006 | g0185 | AFR | GWD | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02630 | hp1 | a0001 | c0001 | t0007 | g0045 | AFR | GWD | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | GWD | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02647 | hp1 | a0001 | c0007 | t0001 | g0021 | AFR | GWD | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02647 | hp2 | a0003 | c0006 | t0006 | g0008 | AFR | GWD | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0247 | SAS | PJL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02683 | hp2 | a0001 | c0002 | t0004 | g0106 | SAS | PJL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02698 | hp1 | a0001 | c0008 | t0002 | g0188 | SAS | PJL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | GWD | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02723 | hp1 | a0001 | c0009 | t0003 | g0149 | AFR | GWD | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02723 | hp2 | a0001 | c0005 | t0001 | g0198 | AFR | GWD | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02735 | hp2 | a0002 | c0004 | t0018 | g0212 | SAS | PJL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02738 | hp2 | a0001 | c0002 | t0004 | g0314 | SAS | PJL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0274 | AFR | GWD | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02818 | hp1 | a0001 | c0001 | t0014 | g0249 | AFR | GWD | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02886 | hp1 | a0003 | c0006 | t0006 | g0008 | AFR | GWD | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02886 | hp2 | a0002 | c0004 | t0006 | g0228 | AFR | GWD | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02895 | hp1 | a0001 | c0005 | t0001 | g0277 | AFR | GWD | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02895 | hp2 | a0001 | c0007 | t0001 | g0021 | AFR | GWD | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02897 | hp1 | a0001 | c0007 | t0001 | g0042 | AFR | GWD | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02897 | hp2 | a0001 | c0005 | t0001 | g0024 | AFR | GWD | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02922 | hp1 | a0001 | c0002 | t0012 | g0052 | AFR | ESN | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02922 | hp2 | a0002 | c0004 | t0011 | g0287 | AFR | ESN | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02965 | hp2 | a0010 | c0020 | t0001 | g0285 | AFR | ESN | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02970 | hp1 | a0001 | c0009 | t0003 | g0162 | AFR | ESN | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02970 | hp2 | a0001 | c0001 | t0010 | g0320 | AFR | ESN | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | ESN | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02976 | hp2 | a0001 | c0001 | t0007 | g0012 | AFR | ESN | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0081 | SAS | PJL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03041 | hp2 | a0001 | c0002 | t0003 | g0290 | AFR | GWD | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03098 | hp1 | a0001 | c0005 | t0001 | g0278 | AFR | MSL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03098 | hp2 | a0001 | c0002 | t0013 | g0148 | AFR | MSL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03130 | hp1 | a0003 | c0006 | t0006 | g0008 | AFR | ESN | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03130 | hp2 | a0001 | c0002 | t0003 | g0257 | AFR | ESN | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03139 | hp1 | a0001 | c0001 | t0007 | g0050 | AFR | ESN | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ESN | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03195 | hp1 | a0001 | c0007 | t0001 | g0193 | AFR | ESN | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ESN | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0171 | AFR | MSL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03225 | hp1 | a0001 | c0005 | t0001 | g0280 | AFR | MSL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03225 | hp2 | a0001 | c0002 | t0021 | g0013 | AFR | MSL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03453 | hp1 | a0001 | c0002 | t0008 | g0013 | AFR | MSL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03453 | hp2 | a0003 | c0006 | t0006 | g0276 | AFR | MSL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03486 | hp1 | a0001 | c0001 | t0007 | g0012 | AFR | MSL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | MSL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03490 | hp1 | a0001 | c0002 | t0004 | g0023 | SAS | PJL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03490 | hp2 | a0001 | c0002 | t0004 | g0266 | SAS | PJL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03491 | hp1 | a0001 | c0002 | t0003 | g0144 | SAS | PJL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03492 | hp2 | a0001 | c0002 | t0004 | g0023 | SAS | PJL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03516 | hp1 | a0001 | c0001 | t0016 | g0166 | AFR | ESN | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03516 | hp2 | a0003 | c0006 | t0006 | g0008 | AFR | ESN | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03540 | hp1 | a0001 | c0005 | t0001 | g0283 | AFR | GWD | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0250 | AFR | GWD | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03579 | hp1 | a0001 | c0002 | t0008 | g0013 | AFR | MSL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03579 | hp2 | a0001 | c0002 | t0004 | g0258 | AFR | MSL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03654 | hp1 | a0001 | c0002 | t0004 | g0023 | SAS | PJL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0139 | SAS | PJL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03688 | hp1 | a0001 | c0001 | t0005 | g0056 | SAS | STU | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | STU | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0065 | SAS | PJL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03710 | hp1 | a0001 | c0002 | t0004 | g0005 | SAS | PJL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0301 | SAS | BEB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | BEB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0140 | SAS | BEB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG04115 | hp1 | a0001 | c0001 | t0017 | g0085 | SAS | STU | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0299 | SAS | STU | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | BEB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0167 | SAS | BEB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG04199 | hp1 | a0002 | c0003 | t0003 | g0009 | SAS | STU | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG04199 | hp2 | a0001 | c0002 | t0004 | g0005 | SAS | STU | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0103 | SAS | STU | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG04204 | hp2 | a0001 | c0002 | t0004 | g0176 | SAS | STU | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | STU | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | STU | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18522 | hp1 | a0001 | c0005 | t0001 | g0024 | AFR | YRI | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18522 | hp2 | a0001 | c0001 | t0007 | g0051 | AFR | YRI | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0309 | EAS | CHB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18747 | hp1 | a0002 | c0003 | t0003 | g0203 | EAS | CHB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | CHB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | YRI | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | YRI | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18939 | hp1 | a0001 | c0001 | t0005 | g0077 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18943 | hp1 | a0001 | c0001 | t0005 | g0178 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18948 | hp1 | a0001 | c0001 | t0005 | g0074 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18950 | hp2 | a0001 | c0002 | t0004 | g0010 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18951 | hp1 | a0001 | c0001 | t0005 | g0246 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18953 | hp2 | a0002 | c0003 | t0003 | g0009 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18954 | hp1 | a0002 | c0003 | t0003 | g0022 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18954 | hp2 | a0002 | c0003 | t0003 | g0009 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18960 | hp1 | a0001 | c0001 | t0005 | g0267 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18960 | hp2 | a0002 | c0004 | t0001 | g0205 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18961 | hp1 | a0002 | c0003 | t0003 | g0221 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18962 | hp1 | a0002 | c0003 | t0003 | g0011 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18963 | hp1 | a0001 | c0001 | t0005 | g0121 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18966 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18967 | hp2 | a0002 | c0003 | t0003 | g0223 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18971 | hp1 | a0002 | c0003 | t0003 | g0022 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18971 | hp2 | a0001 | c0002 | t0004 | g0064 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18972 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18973 | hp1 | a0001 | c0001 | t0005 | g0030 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18975 | hp2 | a0002 | c0003 | t0003 | g0201 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18977 | hp1 | a0002 | c0003 | t0003 | g0009 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18978 | hp2 | a0001 | c0002 | t0001 | g0308 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18979 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18981 | hp2 | a0001 | c0001 | t0005 | g0073 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18982 | hp2 | a0002 | c0003 | t0003 | g0222 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18983 | hp1 | a0002 | c0003 | t0003 | g0009 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18985 | hp1 | a0002 | c0003 | t0003 | g0202 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18987 | hp2 | a0001 | c0002 | t0004 | g0026 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18990 | hp1 | a0002 | c0004 | t0005 | g0200 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18991 | hp1 | a0001 | c0002 | t0004 | g0010 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18991 | hp2 | a0001 | c0001 | t0005 | g0230 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18992 | hp2 | a0001 | c0002 | t0015 | g0010 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18993 | hp2 | a0001 | c0001 | t0005 | g0236 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18994 | hp1 | a0002 | c0004 | t0001 | g0220 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18995 | hp2 | a0001 | c0001 | t0005 | g0036 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18997 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18997 | hp2 | a0001 | c0002 | t0003 | g0117 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18998 | hp1 | a0002 | c0003 | t0004 | g0062 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18999 | hp1 | a0001 | c0002 | t0004 | g0063 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19000 | hp1 | a0001 | c0001 | t0005 | g0175 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19001 | hp2 | a0002 | c0004 | t0001 | g0043 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19002 | hp2 | a0011 | c0014 | t0001 | g0179 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19003 | hp1 | a0001 | c0001 | t0005 | g0138 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19005 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19006 | hp2 | a0001 | c0001 | t0005 | g0069 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19010 | hp2 | a0002 | c0003 | t0003 | g0227 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19011 | hp2 | a0002 | c0003 | t0003 | g0022 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0289 | AFR | LWK | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19030 | hp2 | a0001 | c0001 | t0010 | g0040 | AFR | LWK | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | LWK | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19043 | hp2 | a0001 | c0005 | t0001 | g0279 | AFR | LWK | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19055 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19056 | hp1 | a0001 | c0002 | t0004 | g0010 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19060 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19065 | hp2 | a0002 | c0004 | t0001 | g0206 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19067 | hp1 | a0001 | c0001 | t0005 | g0315 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19074 | hp2 | a0001 | c0001 | t0005 | g0036 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19077 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19080 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19081 | hp2 | a0002 | c0003 | t0003 | g0204 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19084 | hp1 | a0001 | c0001 | t0005 | g0030 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19088 | hp1 | a0001 | c0001 | t0005 | g0126 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19088 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19090 | hp1 | a0002 | c0003 | t0003 | g0199 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19240 | hp1 | a0001 | c0021 | t0001 | g0194 | AFR | YRI | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA19240 | hp2 | a0001 | c0002 | t0013 | g0191 | AFR | YRI | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ASW | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | ASW | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA20752 | hp1 | a0001 | c0002 | t0004 | g0146 | EUR | TSI | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA20752 | hp2 | a0001 | c0002 | t0004 | g0005 | EUR | TSI | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA20805 | hp1 | a0002 | c0004 | t0001 | g0217 | EUR | TSI | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA20805 | hp2 | a0001 | c0015 | t0009 | g0114 | EUR | TSI | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0147 | SAS | GIH | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | GIH | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | CLM | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG01123 | hp2 | a0006 | c0011 | t0008 | g0255 | AMR | CLM | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02486 | hp1 | a0001 | c0005 | t0001 | g0294 | AFR | ACB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ACB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02559 | hp1 | a0001 | c0005 | t0001 | g0024 | AFR | ACB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03471 | hp1 | a0001 | c0002 | t0008 | g0053 | AFR | MSL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG03471 | hp2 | a0001 | c0001 | t0010 | g0033 | AFR | MSL | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG06807 | hp1 | a0001 | c0001 | t0007 | g0012 | AFR | USA | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
HG06807 | hp2 | a0001 | c0019 | t0008 | g0252 | AFR | USA | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | USA | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA20300 | hp2 | a0002 | c0004 | t0006 | g0210 | AFR | USA | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA21309 | hp1 | a0001 | c0017 | t0011 | g0312 | AFR | LWK | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | LWK | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0111 | REF | REF | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0263 | REF | REF | ADGRG3_chr16_57663306_57694378 | ADGRG3 | chr16 | 57663306 | 57694378 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:57668362 | G | T | 1 | a0002 | 51 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(48): Show |
missense_variant | MODERATE | c.15G>T | p.Arg5Ser | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/12 | 57/2609 | 15/1650 | 5/549 | chr16 | 57668362 | |||
chr16:57673384 | T | A | 1 | a0006 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.122T>A | p.Ile41Asn | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/12 | 164/2609 | 122/1650 | 41/549 | chr16 | 57673384 | |||
chr16:57676216 | G | A | 1 | a0009 | 1 | HG02165.hp2 | missense_variant | MODERATE | c.223G>A | p.Glu75Lys | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 3/12 | 265/2609 | 223/1650 | 75/549 | chr16 | 57676216 | |||
chr16:57676244 | C | T | 2 | a0003 a0010 |
8 | HG01109.hp2 HG02258.hp1 HG02647.hp2 others(5): Show |
missense_variant | MODERATE | c.251C>T | p.Thr84Met | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 3/12 | 293/2609 | 251/1650 | 84/549 | chr16 | 57676244 | |||
chr16:57679258 | A | C | 1 | a0007 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.574A>C | p.Thr192Pro | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 5/12 | 616/2609 | 574/1650 | 192/549 | chr16 | 57679258 | |||
chr16:57679274 | C | T | 1 | a0004 | 2 | HG00741.hp2 HG02451.hp2 |
missense_variant | MODERATE | c.590C>T | p.Pro197Leu | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 5/12 | 632/2609 | 590/1650 | 197/549 | chr16 | 57679274 | |||
chr16:57684158 | G | A | 1 | a0008 | 1 | HG02080.hp1 | missense_variant | MODERATE | c.1108G>A | p.Val370Ile | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 9/12 | 1150/2609 | 1108/1650 | 370/549 | chr16 | 57684158 | |||
chr16:57684413 | G | A | 1 | a0003 | 7 | HG01109.hp2 HG02258.hp1 HG02647.hp2 others(4): Show |
missense_variant | MODERATE | c.1186G>A | p.Gly396Ser | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 10/12 | 1228/2609 | 1186/1650 | 396/549 | chr16 | 57684413 | |||
chr16:57685674 | G | A | 1 | a0011 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.1288G>A | p.Ala430Thr | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/12 | 1330/2609 | 1288/1650 | 430/549 | chr16 | 57685674 | |||
chr16:57685780 | C | T | 1 | a0005 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.1394C>T | p.Ala465Val | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/12 | 1436/2609 | 1394/1650 | 465/549 | chr16 | 57685780 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:57668392 | G | T | 2 | a0002c0023 a0002c0024 |
2 | HG00735.hp1 HG01496.hp1 |
synonymous_variant | LOW | c.45G>T | p.Leu15Leu | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/12 | 87/2609 | 45/1650 | 15/549 | chr16 | 57668392 | |||
chr16:57673337 | C | T | 3 | a0001c0007 a0001c0008 a0001c0021 |
11 | HG01192.hp1 HG01256.hp2 HG01891.hp1 others(8): Show |
synonymous_variant | LOW | c.75C>T | p.Thr25Thr | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/12 | 117/2609 | 75/1650 | 25/549 | chr16 | 57673337 | |||
chr16:57676317 | T | C | 2 | a0003c0006 a0010c0020 |
8 | HG01109.hp2 HG02258.hp1 HG02647.hp2 others(5): Show |
synonymous_variant | LOW | c.324T>C | p.Tyr108Tyr | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 3/12 | 366/2609 | 324/1650 | 108/549 | chr16 | 57676317 | |||
chr16:57679197 | A | G | 1 | a0001c0019 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.513A>G | p.Gly171Gly | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 5/12 | 555/2609 | 513/1650 | 171/549 | chr16 | 57679197 | |||
chr16:57683977 | C | T | 3 | a0001c0005 a0001c0007 a0001c0021 |
21 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(18): Show |
synonymous_variant | LOW | c.927C>T | p.His309His | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 9/12 | 969/2609 | 927/1650 | 309/549 | chr16 | 57683977 | |||
chr16:57684148 | C | T | 2 | a0001c0017 a0002c0022 |
2 | HG02145.hp1 NA21309.hp1 |
synonymous_variant | LOW | c.1098C>T | p.Leu366Leu | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 9/12 | 1140/2609 | 1098/1650 | 366/549 | chr16 | 57684148 | |||
chr16:57685835 | G | A | 3 | a0001c0005 a0001c0007 a0001c0009 |
22 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(19): Show |
synonymous_variant | LOW | c.1449G>A | p.Ser483Ser | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/12 | 1491/2609 | 1449/1650 | 483/549 | chr16 | 57685835 | |||
chr16:57685859 | G | T | 1 | a0001c0015 | 1 | NA20805.hp2 | synonymous_variant | LOW | c.1473G>T | p.Gly491Gly | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/12 | 1515/2609 | 1473/1650 | 491/549 | chr16 | 57685859 | |||
chr16:57688416 | C | T | 9 | a0001c0002 a0001c0005 a0001c0007 others(6): Show |
147 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(144): Show |
synonymous_variant | LOW | c.1605C>T | p.Ser535Ser | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 12/12 | 1647/2609 | 1605/1650 | 535/549 | chr16 | 57688416 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:57668320 | C | T | 8 | a0001c0001t0007 a0001c0002t0008 a0001c0002t0012 others(5): Show |
20 | HG01123.hp2 HG01891.hp1 HG01891.hp2 others(17): Show |
5_prime_UTR_variant | MODIFIER | c.-28C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/12 | 28 | chr16 | 57668320 | ||||||
chr16:57668328 | G | T | 1 | a0001c0002t0020 | 1 | HG02004.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-20G>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/12 | chr16 | 57668328 | |||||||
chr16:57668341 | G | C | 1 | a0001c0001t0014 | 1 | HG02818.hp1 | 5_prime_UTR_variant | MODIFIER | c.-7G>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/12 | 7 | chr16 | 57668341 | ||||||
chr16:57688664 | T | A | 7 | a0001c0002t0003 a0001c0002t0004 a0001c0002t0015 others(4): Show |
68 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*203T>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 12/12 | 203 | chr16 | 57688664 | ||||||
chr16:57688722 | A | G | 3 | a0001c0001t0006 a0002c0004t0006 a0003c0006t0006 |
10 | HG01109.hp2 HG02258.hp1 HG02622.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*261A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 12/12 | 261 | chr16 | 57688722 | ||||||
chr16:57688921 | C | T | 22 | a0001c0001t0001 a0001c0001t0014 a0001c0002t0001 others(19): Show |
151 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*460C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 12/12 | 460 | chr16 | 57688921 | ||||||
chr16:57688923 | G | T | 1 | a0001c0002t0015 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*462G>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 12/12 | 462 | chr16 | 57688923 | ||||||
chr16:57688954 | C | T | 4 | a0001c0002t0004 a0001c0002t0015 a0002c0003t0004 others(1): Show |
34 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*493C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 12/12 | 493 | chr16 | 57688954 | ||||||
chr16:57689106 | C | A | 1 | a0001c0001t0016 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*645C>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 12/12 | 645 | chr16 | 57689106 | ||||||
chr16:57689136 | G | C | 3 | a0001c0001t0006 a0002c0004t0006 a0003c0006t0006 |
10 | HG01109.hp2 HG02258.hp1 HG02622.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*675G>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 12/12 | 675 | chr16 | 57689136 | ||||||
chr16:57689165 | G | A | 9 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(6): Show |
96 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*704G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 12/12 | 704 | chr16 | 57689165 | ||||||
chr16:57689188 | T | C | 1 | a0001c0001t0010 | 4 | HG01167.hp1 HG02970.hp2 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*727T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 12/12 | 727 | chr16 | 57689188 | ||||||
chr16:57689208 | G | C | 1 | a0001c0001t0017 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*747G>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 12/12 | 747 | chr16 | 57689208 | ||||||
chr16:57689244 | C | A | 1 | a0001c0002t0013 | 2 | HG03098.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*783C>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 12/12 | 783 | chr16 | 57689244 | ||||||
chr16:57689250 | C | G | 1 | a0001c0001t0019 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*789C>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 12/12 | 789 | chr16 | 57689250 | ||||||
chr16:57689267 | G | A | 15 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(12): Show |
132 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*806G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 12/12 | 806 | chr16 | 57689267 | ||||||
chr16:57689285 | A | G | 16 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(13): Show |
133 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*824A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 12/12 | 824 | chr16 | 57689285 | ||||||
chr16:57689290 | G | A | 2 | a0001c0001t0009 a0001c0015t0009 |
6 | HG01192.hp2 HG01257.hp2 HG01516.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*829G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 12/12 | 829 | chr16 | 57689290 | ||||||
chr16:57689316 | C | T | 1 | a0001c0002t0021 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*855C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 12/12 | 855 | chr16 | 57689316 | ||||||
chr16:57689327 | A | G | 16 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(13): Show |
133 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*866A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 12/12 | 866 | chr16 | 57689327 | ||||||
chr16:57689337 | T | C | 16 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(13): Show |
133 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*876T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 12/12 | 876 | chr16 | 57689337 | ||||||
chr16:57689341 | G | C | 3 | a0001c0017t0011 a0002c0004t0011 a0002c0022t0011 |
3 | HG02145.hp1 HG02922.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*880G>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 12/12 | 880 | chr16 | 57689341 | ||||||
chr16:57689367 | T | C | 1 | a0001c0002t0012 | 3 | HG02280.hp2 HG02622.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*906T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 12/12 | 906 | chr16 | 57689367 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:57668447 | G | T | 26 | a0001c0001t0001g0048 a0001c0001t0001g0297 a0001c0001t0001g0298 others(23): Show |
28 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.58+42G>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57668447 | |||||||
chr16:57668490 | A | G | 9 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0002g0047 others(6): Show |
10 | HG00642.hp1 HG00741.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.58+85A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57668490 | |||||||
chr16:57668542 | C | T | 13 | a0001c0001t0001g0281 a0001c0001t0001g0286 a0001c0005t0001g0024 others(10): Show |
15 | HG02109.hp1 HG02145.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.58+137C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57668542 | |||||||
chr16:57668561 | T | C | 295 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(292): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.58+156T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57668561 | |||||||
chr16:57668793 | A | G | 299 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(296): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.58+388A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57668793 | |||||||
chr16:57668927 | A | G | 68 | a0001c0001t0001g0229 a0001c0001t0001g0231 a0001c0001t0001g0233 others(65): Show |
87 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.58+522A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57668927 | |||||||
chr16:57668981 | G | A | 30 | a0001c0001t0001g0048 a0001c0001t0001g0272 a0001c0001t0001g0297 others(27): Show |
33 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.58+576G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57668981 | |||||||
chr16:57669003 | C | T | 2 | a0001c0007t0008g0254 a0006c0011t0008g0255 |
2 | HG01123.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.58+598C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57669003 | |||||||
chr16:57669089 | G | C | 37 | a0001c0001t0001g0275 a0002c0003t0001g0211 a0002c0003t0003g0009 others(34): Show |
50 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.58+684G>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57669089 | |||||||
chr16:57669181 | A | G | 309 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(306): Show |
419 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(416): Show |
intron_variant | MODIFIER | c.58+776A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57669181 | |||||||
chr16:57669192 | T | G | 264 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(261): Show |
361 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(358): Show |
intron_variant | MODIFIER | c.58+787T>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57669192 | |||||||
chr16:57669274 | G | C | 1 | a0001c0001t0002g0289 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.58+869G>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57669274 | |||||||
chr16:57669440 | G | A | 30 | a0001c0001t0001g0048 a0001c0001t0001g0272 a0001c0001t0001g0297 others(27): Show |
33 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.58+1035G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57669440 | |||||||
chr16:57669442 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.58+1037T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57669442 | |||||||
chr16:57669462 | T | C | 1 | a0001c0002t0004g0256 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.58+1057T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57669462 | |||||||
chr16:57669472 | G | C | 1 | a0001c0001t0001g0060 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.58+1067G>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57669472 | |||||||
chr16:57669529 | G | A | 7 | a0001c0001t0001g0061 a0001c0002t0004g0010 a0001c0002t0004g0026 others(4): Show |
11 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(8): Show |
intron_variant | MODIFIER | c.58+1124G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57669529 | |||||||
chr16:57669530 | C | G | 71 | a0001c0001t0001g0048 a0001c0001t0001g0055 a0001c0001t0001g0195 others(68): Show |
80 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.58+1125C>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57669530 | |||||||
chr16:57669569 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.58+1164G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57669569 | |||||||
chr16:57669622 | A | C | 1 | a0001c0002t0012g0054 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.58+1217A>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57669622 | |||||||
chr16:57669694 | G | GCATTCAT others(5): Show |
1 | a0002c0004t0006g0228 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.58+1304_58+1315dup others(12): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 57669694 | ||||||
chr16:57669694 | GCATT | G | 29 | a0001c0001t0001g0048 a0001c0001t0001g0272 a0001c0001t0001g0297 others(26): Show |
32 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.58+1312_58+1315del others(4): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 57669694 | ||||||
chr16:57669928 | G | T | 1 | a0001c0001t0014g0249 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.58+1523G>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57669928 | |||||||
chr16:57669984 | G | A | 167 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(164): Show |
242 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.58+1579G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57669984 | |||||||
chr16:57670022 | G | T | 2 | a0002c0004t0011g0287 a0002c0022t0011g0288 |
2 | HG02145.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.58+1617G>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57670022 | |||||||
chr16:57670048 | G | A | 29 | a0001c0001t0001g0048 a0001c0001t0001g0272 a0001c0001t0001g0297 others(26): Show |
32 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.58+1643G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57670048 | |||||||
chr16:57670062 | G | A | 3 | a0001c0001t0002g0192 a0001c0001t0002g0273 a0001c0001t0002g0274 |
3 | HG02630.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.58+1657G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57670062 | |||||||
chr16:57670204 | T | C | 1 | a0001c0002t0003g0290 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.58+1799T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57670204 | |||||||
chr16:57670327 | T | C | 5 | a0001c0001t0001g0027 a0001c0001t0001g0066 a0001c0001t0001g0067 others(2): Show |
6 | NA18944.hp1 NA18998.hp2 NA19006.hp2 others(3): Show |
intron_variant | MODIFIER | c.58+1922T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57670327 | |||||||
chr16:57670355 | T | G | 1 | a0002c0003t0003g0022 | 3 | NA18954.hp1 NA18971.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.58+1950T>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57670355 | |||||||
chr16:57670371 | G | A | 3 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0005c0016t0002g0071 |
3 | HG00639.hp2 HG00738.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.58+1966G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57670371 | |||||||
chr16:57670465 | C | A | 11 | a0001c0002t0001g0250 a0001c0002t0008g0251 a0001c0007t0001g0021 others(8): Show |
14 | HG01123.hp2 HG01192.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.58+2060C>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57670465 | |||||||
chr16:57670560 | T | C | 90 | a0001c0001t0001g0048 a0001c0001t0001g0189 a0001c0001t0001g0229 others(87): Show |
112 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.58+2155T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57670560 | |||||||
chr16:57670723 | C | G | 1 | a0001c0019t0008g0252 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.58+2318C>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57670723 | |||||||
chr16:57670841 | AAC | A | 33 | a0001c0001t0001g0048 a0001c0001t0001g0272 a0001c0001t0001g0300 others(30): Show |
39 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.58+2438_58+2439del others(2): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 57670841 | ||||||
chr16:57670957 | C | A | 3 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0002t0003g0290 |
3 | HG02486.hp2 HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.59-2364C>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57670957 | |||||||
chr16:57671057 | G | A | 3 | a0001c0002t0008g0013 a0001c0002t0008g0053 a0001c0002t0021g0013 |
5 | HG02257.hp1 HG03225.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-2264G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57671057 | |||||||
chr16:57671172 | A | G | 25 | a0001c0001t0001g0055 a0001c0001t0001g0190 a0001c0001t0001g0195 others(22): Show |
32 | HG01099.hp2 HG01109.hp2 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.59-2149A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57671172 | |||||||
chr16:57671332 | G | GT | 74 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0059 others(71): Show |
84 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.59-1964dupT | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 57671332 | ||||||
chr16:57671332 | GT | G | 64 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(61): Show |
85 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.59-1964delT | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 57671332 | ||||||
chr16:57671332 | GTT | G | 18 | a0001c0001t0001g0190 a0001c0001t0002g0192 a0001c0001t0002g0274 others(15): Show |
27 | HG01109.hp2 HG01192.hp1 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.59-1965_59-1964del others(2): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 57671332 | ||||||
chr16:57671359 | G | A | 3 | a0001c0002t0008g0013 a0001c0002t0008g0053 a0001c0002t0021g0013 |
5 | HG02257.hp1 HG03225.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-1962G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57671359 | |||||||
chr16:57671374 | T | C | 1 | a0001c0002t0013g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.59-1947T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57671374 | |||||||
chr16:57671414 | C | G | 1 | a0001c0001t0010g0320 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.59-1907C>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57671414 | |||||||
chr16:57671427 | G | A | 3 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0002t0003g0290 |
3 | HG02486.hp2 HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.59-1894G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57671427 | |||||||
chr16:57671434 | G | A | 1 | a0001c0007t0001g0193 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.59-1887G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57671434 | |||||||
chr16:57671629 | T | C | 1 | a0001c0009t0003g0149 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.59-1692T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57671629 | |||||||
chr16:57671865 | A | G | 1 | a0001c0002t0001g0250 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.59-1456A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57671865 | |||||||
chr16:57671919 | A | G | 124 | a0001c0001t0001g0048 a0001c0001t0001g0078 a0001c0001t0001g0079 others(121): Show |
158 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.59-1402A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57671919 | |||||||
chr16:57671933 | C | T | 2 | a0001c0001t0002g0047 a0001c0001t0002g0293 |
3 | HG00642.hp1 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.59-1388C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57671933 | |||||||
chr16:57671967 | T | C | 6 | a0001c0001t0001g0190 a0001c0001t0002g0192 a0001c0001t0002g0274 others(3): Show |
11 | HG01109.hp2 HG02258.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-1354T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57671967 | |||||||
chr16:57672211 | A | T | 3 | a0001c0005t0001g0294 a0004c0010t0001g0295 a0004c0010t0001g0296 |
3 | HG00741.hp2 HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.59-1110A>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57672211 | |||||||
chr16:57672224 | A | G | 8 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0002g0047 others(5): Show |
9 | HG00642.hp1 HG00741.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.59-1097A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57672224 | |||||||
chr16:57672237 | G | A | 5 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0002g0047 others(2): Show |
6 | HG00642.hp1 HG01257.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-1084G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57672237 | |||||||
chr16:57672414 | T | C | 1 | a0001c0002t0004g0023 | 3 | HG03490.hp1 HG03492.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.59-907T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57672414 | |||||||
chr16:57672567 | C | T | 1 | a0001c0001t0002g0147 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.59-754C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57672567 | |||||||
chr16:57672614 | C | T | 3 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0002t0004g0146 |
3 | HG01361.hp2 HG02602.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.59-707C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57672614 | |||||||
chr16:57672667 | G | A | 2 | a0001c0008t0002g0186 a0001c0008t0002g0187 |
2 | HG01192.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.59-654G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57672667 | |||||||
chr16:57672671 | C | T | 32 | a0001c0001t0001g0048 a0001c0001t0001g0272 a0001c0001t0001g0300 others(29): Show |
38 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.59-650C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57672671 | |||||||
chr16:57672694 | G | A | 1 | a0001c0002t0012g0054 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.59-627G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57672694 | |||||||
chr16:57673150 | A | G | 1 | a0001c0001t0002g0145 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.59-171A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 1/11 | chr16 | 57673150 | |||||||
chr16:57673521 | C | T | 3 | a0001c0005t0001g0294 a0004c0010t0001g0295 a0004c0010t0001g0296 |
3 | HG00741.hp2 HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.206+53C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57673521 | |||||||
chr16:57673523 | A | G | 33 | a0001c0001t0001g0048 a0001c0001t0001g0272 a0001c0001t0001g0300 others(30): Show |
39 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.206+55A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57673523 | |||||||
chr16:57673544 | C | G | 2 | a0001c0001t0001g0291 a0001c0001t0001g0292 |
2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.206+76C>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57673544 | |||||||
chr16:57673673 | G | T | 1 | a0001c0001t0002g0289 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.206+205G>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57673673 | |||||||
chr16:57673877 | T | C | 35 | a0001c0001t0001g0048 a0001c0001t0001g0272 a0001c0001t0001g0300 others(32): Show |
43 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.206+409T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57673877 | |||||||
chr16:57673881 | G | C | 2 | a0001c0001t0010g0320 a0001c0002t0013g0191 |
2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.206+413G>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57673881 | |||||||
chr16:57673912 | G | A | 1 | a0001c0002t0003g0150 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.206+444G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57673912 | |||||||
chr16:57673920 | G | A | 71 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0189 others(68): Show |
89 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.206+452G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57673920 | |||||||
chr16:57673949 | C | T | 17 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(14): Show |
19 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.206+481C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57673949 | |||||||
chr16:57673952 | G | A | 2 | a0001c0002t0001g0250 a0001c0002t0008g0251 |
2 | HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.206+484G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57673952 | |||||||
chr16:57674113 | G | A | 2 | a0001c0001t0010g0320 a0001c0002t0013g0191 |
2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.206+645G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57674113 | |||||||
chr16:57674122 | T | A | 96 | a0001c0001t0001g0028 a0001c0001t0001g0048 a0001c0001t0001g0083 others(93): Show |
118 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.206+654T>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57674122 | |||||||
chr16:57674144 | C | G | 98 | a0001c0001t0001g0028 a0001c0001t0001g0048 a0001c0001t0001g0083 others(95): Show |
122 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.206+676C>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57674144 | |||||||
chr16:57674163 | G | A | 1 | a0001c0001t0001g0300 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.206+695G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57674163 | |||||||
chr16:57674239 | C | T | 123 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0019 others(120): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.206+771C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57674239 | |||||||
chr16:57674277 | G | A | 2 | a0001c0002t0003g0257 a0001c0002t0003g0259 |
2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.206+809G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57674277 | |||||||
chr16:57674281 | T | C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0118 a0001c0001t0001g0119 |
4 | HG02109.hp2 HG02809.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.206+813T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57674281 | |||||||
chr16:57674288 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.206+820C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57674288 | |||||||
chr16:57674314 | G | C | 1 | a0001c0002t0012g0253 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.206+846G>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57674314 | |||||||
chr16:57674328 | T | C | 20 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(17): Show |
24 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.206+860T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57674328 | |||||||
chr16:57674385 | T | C | 143 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(140): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.206+917T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57674385 | |||||||
chr16:57674504 | C | T | 123 | a0001c0001t0001g0028 a0001c0001t0001g0038 a0001c0001t0001g0041 others(120): Show |
148 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.206+1036C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57674504 | |||||||
chr16:57674571 | T | C | 136 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(133): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.206+1103T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57674571 | |||||||
chr16:57674655 | T | C | 1 | a0001c0019t0008g0252 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.206+1187T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57674655 | |||||||
chr16:57674675 | A | G | 5 | a0001c0001t0007g0045 a0001c0002t0001g0250 a0001c0005t0001g0284 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.206+1207A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57674675 | |||||||
chr16:57674725 | A | T | 6 | a0001c0017t0011g0312 a0002c0004t0011g0287 a0002c0022t0011g0288 others(3): Show |
11 | HG01109.hp2 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.206+1257A>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57674725 | |||||||
chr16:57674730 | T | G | 143 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(140): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.206+1262T>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57674730 | |||||||
chr16:57674829 | C | CA | 91 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0019 others(88): Show |
132 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.207-1353dupA | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 57674829 | ||||||
chr16:57674829 | C | CAA | 12 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0086 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.207-1354_207-1353d others(4): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 57674829 | ||||||
chr16:57674829 | C | CAAA | 6 | a0001c0001t0001g0195 a0001c0001t0006g0185 a0002c0004t0006g0210 others(3): Show |
11 | HG01109.hp2 HG02258.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.207-1355_207-1353d others(5): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 57674829 | ||||||
chr16:57674829 | CA | C | 11 | a0001c0001t0001g0142 a0001c0001t0001g0180 a0001c0001t0002g0047 others(8): Show |
12 | HG00642.hp1 HG01168.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.207-1353delA | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 57674829 | ||||||
chr16:57674889 | G | A | 3 | a0003c0006t0006g0008 a0003c0006t0006g0276 a0010c0020t0001g0285 |
8 | HG01109.hp2 HG02258.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.207-1311G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57674889 | |||||||
chr16:57674932 | G | T | 1 | a0001c0002t0001g0109 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.207-1268G>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57674932 | |||||||
chr16:57674977 | CAG | C | 3 | a0001c0017t0011g0312 a0002c0004t0011g0287 a0002c0022t0011g0288 |
3 | HG02145.hp1 HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.207-1220_207-1219d others(4): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 57674977 | ||||||
chr16:57674995 | C | CA | 37 | a0001c0001t0001g0080 a0001c0001t0001g0105 a0001c0001t0001g0189 others(34): Show |
47 | HG00741.hp2 HG01123.hp2 HG01346.hp1 others(44): Show |
intron_variant | MODIFIER | c.207-1187dupA | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 57674995 | ||||||
chr16:57674995 | C | CAAA | 24 | a0001c0001t0001g0048 a0001c0001t0001g0197 a0001c0001t0002g0033 others(21): Show |
29 | HG00642.hp2 HG01109.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.207-1189_207-1187d others(5): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 57674995 | ||||||
chr16:57674995 | C | CAAAA | 31 | a0001c0001t0001g0242 a0001c0001t0002g0001 a0001c0001t0002g0007 others(28): Show |
61 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.207-1190_207-1187d others(6): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 57674995 | ||||||
chr16:57674995 | C | CAAAAA | 12 | a0001c0001t0002g0032 a0001c0001t0002g0075 a0001c0001t0002g0098 others(9): Show |
13 | HG00621.hp1 HG00639.hp2 HG02738.hp2 others(10): Show |
intron_variant | MODIFIER | c.207-1191_207-1187d others(7): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 57674995 | ||||||
chr16:57675012 | A | AAAAAAGC | 18 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0100 others(15): Show |
18 | HG01123.hp1 HG01192.hp2 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.207-1187_207-1186i others(9): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 57675012 | ||||||
chr16:57675012 | A | AAAAAGC | 122 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(119): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.207-1187_207-1186i others(8): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 57675012 | ||||||
chr16:57675012 | A | AAAAGC | 5 | a0001c0001t0001g0272 a0001c0001t0002g0289 a0001c0001t0002g0310 others(2): Show |
6 | HG00597.hp2 HG01934.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.207-1187_207-1186i others(7): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 57675012 | ||||||
chr16:57675015 | C | A | 6 | a0001c0002t0012g0052 a0001c0002t0012g0054 a0001c0002t0012g0253 others(3): Show |
11 | HG01109.hp2 HG02258.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.207-1185C>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57675015 | |||||||
chr16:57675223 | C | T | 27 | a0001c0001t0002g0047 a0001c0001t0002g0293 a0001c0001t0005g0004 others(24): Show |
36 | HG00597.hp1 HG00609.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.207-977C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57675223 | |||||||
chr16:57675321 | A | C | 3 | a0001c0002t0012g0052 a0001c0002t0012g0054 a0001c0002t0012g0253 |
3 | HG02280.hp2 HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.207-879A>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57675321 | |||||||
chr16:57675364 | C | T | 1 | a0002c0004t0001g0218 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.207-836C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57675364 | |||||||
chr16:57675404 | C | T | 6 | a0001c0002t0012g0052 a0001c0002t0012g0054 a0001c0002t0012g0253 others(3): Show |
11 | HG01109.hp2 HG02258.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.207-796C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57675404 | |||||||
chr16:57675405 | G | A | 6 | a0001c0002t0012g0052 a0001c0002t0012g0054 a0001c0002t0012g0253 others(3): Show |
11 | HG01109.hp2 HG02258.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.207-795G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57675405 | |||||||
chr16:57675504 | A | G | 6 | a0001c0002t0012g0052 a0001c0002t0012g0054 a0001c0002t0012g0253 others(3): Show |
11 | HG01109.hp2 HG02258.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.207-696A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57675504 | |||||||
chr16:57675527 | A | C | 6 | a0001c0002t0012g0052 a0001c0002t0012g0054 a0001c0002t0012g0253 others(3): Show |
11 | HG01109.hp2 HG02258.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.207-673A>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57675527 | |||||||
chr16:57675563 | G | A | 4 | a0001c0001t0002g0047 a0001c0001t0002g0293 a0001c0001t0007g0045 others(1): Show |
5 | HG00642.hp1 HG01257.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.207-637G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57675563 | |||||||
chr16:57675595 | C | A | 1 | a0001c0002t0001g0250 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.207-605C>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57675595 | |||||||
chr16:57675663 | A | G | 12 | a0001c0001t0010g0320 a0001c0002t0012g0052 a0001c0002t0012g0054 others(9): Show |
15 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.207-537A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57675663 | |||||||
chr16:57675669 | T | C | 3 | a0001c0002t0012g0052 a0001c0002t0012g0054 a0001c0002t0012g0253 |
3 | HG02280.hp2 HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.207-531T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57675669 | |||||||
chr16:57675714 | CA | C | 6 | a0001c0002t0012g0052 a0001c0002t0012g0054 a0001c0002t0012g0253 others(3): Show |
11 | HG01109.hp2 HG02258.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.207-482delA | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 57675714 | ||||||
chr16:57675838 | CGGGTTTC others(7): Show |
C | 1 | a0001c0001t0001g0125 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.207-360_207-347del others(14): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 57675838 | ||||||
chr16:57675980 | T | G | 10 | a0001c0005t0001g0024 a0001c0005t0001g0198 a0001c0005t0001g0277 others(7): Show |
12 | HG02451.hp1 HG02486.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.207-220T>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57675980 | |||||||
chr16:57676003 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.207-197A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57676003 | |||||||
chr16:57676132 | A | G | 3 | a0001c0001t0006g0185 a0002c0004t0006g0210 a0002c0004t0006g0228 |
3 | HG02622.hp2 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.207-68A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57676132 | |||||||
chr16:57676133 | G | A | 6 | a0001c0002t0012g0052 a0001c0002t0012g0054 a0001c0002t0012g0253 others(3): Show |
11 | HG01109.hp2 HG02258.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.207-67G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57676133 | |||||||
chr16:57676157 | G | A | 3 | a0003c0006t0006g0008 a0003c0006t0006g0276 a0010c0020t0001g0285 |
8 | HG01109.hp2 HG02258.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.207-43G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57676157 | |||||||
chr16:57676164 | G | A | 4 | a0001c0001t0002g0047 a0001c0001t0002g0293 a0001c0001t0007g0045 others(1): Show |
5 | HG00642.hp1 HG01257.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.207-36G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57676164 | |||||||
chr16:57676165 | G | A | 64 | a0001c0001t0001g0048 a0001c0001t0001g0190 a0001c0001t0001g0291 others(61): Show |
94 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.207-35G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57676165 | |||||||
chr16:57676180 | C | A | 1 | a0001c0001t0005g0056 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.207-20C>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57676180 | |||||||
chr16:57676181 | C | G | 154 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(151): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.207-19C>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 2/11 | chr16 | 57676181 | |||||||
chr16:57676412 | G | C | 3 | a0003c0006t0006g0008 a0003c0006t0006g0276 a0010c0020t0001g0285 |
8 | HG01109.hp2 HG02258.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.345+74G>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 3/11 | chr16 | 57676412 | |||||||
chr16:57676566 | C | A | 1 | a0001c0001t0002g0241 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.345+228C>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 3/11 | chr16 | 57676566 | |||||||
chr16:57676623 | A | C | 6 | a0001c0001t0002g0192 a0001c0001t0002g0274 a0001c0001t0014g0249 others(3): Show |
6 | HG00741.hp2 HG01123.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.345+285A>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 3/11 | chr16 | 57676623 | |||||||
chr16:57676627 | G | T | 66 | a0001c0001t0001g0048 a0001c0001t0002g0001 a0001c0001t0002g0007 others(63): Show |
99 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.345+289G>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 3/11 | chr16 | 57676627 | |||||||
chr16:57676667 | T | C | 155 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(152): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.345+329T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 3/11 | chr16 | 57676667 | |||||||
chr16:57676697 | G | A | 5 | a0001c0007t0001g0021 a0001c0007t0001g0042 a0001c0007t0001g0193 others(2): Show |
8 | HG01891.hp1 HG02258.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+359G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 3/11 | chr16 | 57676697 | |||||||
chr16:57676742 | G | A | 12 | a0001c0001t0005g0004 a0001c0001t0005g0036 a0001c0001t0005g0069 others(9): Show |
19 | HG00597.hp1 HG02071.hp1 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.345+404G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 3/11 | chr16 | 57676742 | |||||||
chr16:57676748 | T | A | 1 | a0001c0001t0001g0270 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.345+410T>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 3/11 | chr16 | 57676748 | |||||||
chr16:57676987 | G | A | 3 | a0003c0006t0006g0008 a0003c0006t0006g0276 a0010c0020t0001g0285 |
8 | HG01109.hp2 HG02258.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.345+649G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 3/11 | chr16 | 57676987 | |||||||
chr16:57677137 | C | T | 3 | a0003c0006t0006g0008 a0003c0006t0006g0276 a0010c0020t0001g0285 |
8 | HG01109.hp2 HG02258.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.345+799C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 3/11 | chr16 | 57677137 | |||||||
chr16:57677164 | A | G | 1 | a0001c0001t0001g0270 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.345+826A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 3/11 | chr16 | 57677164 | |||||||
chr16:57677165 | A | G | 1 | a0001c0001t0001g0270 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.345+827A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 3/11 | chr16 | 57677165 | |||||||
chr16:57677167 | T | C | 4 | a0002c0004t0005g0200 a0003c0006t0006g0008 a0003c0006t0006g0276 others(1): Show |
9 | HG01109.hp2 HG02258.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.345+829T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 3/11 | chr16 | 57677167 | |||||||
chr16:57677168 | T | G | 1 | a0001c0001t0001g0270 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.345+830T>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 3/11 | chr16 | 57677168 | |||||||
chr16:57677219 | T | G | 1 | a0001c0001t0001g0270 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.345+881T>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 3/11 | chr16 | 57677219 | |||||||
chr16:57677274 | T | C | 1 | a0002c0003t0004g0062 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.346-896T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 3/11 | chr16 | 57677274 | |||||||
chr16:57677358 | G | A | 1 | a0001c0005t0001g0284 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.346-812G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 3/11 | chr16 | 57677358 | |||||||
chr16:57677456 | C | T | 31 | a0001c0001t0001g0080 a0001c0001t0001g0195 a0001c0001t0001g0196 others(28): Show |
40 | HG00597.hp1 HG00609.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.346-714C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 3/11 | chr16 | 57677456 | |||||||
chr16:57677514 | G | A | 6 | a0001c0001t0002g0192 a0001c0001t0002g0274 a0001c0001t0014g0249 others(3): Show |
6 | HG00741.hp2 HG01123.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.346-656G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 3/11 | chr16 | 57677514 | |||||||
chr16:57677651 | G | A | 176 | a0001c0001t0001g0048 a0001c0001t0001g0059 a0001c0001t0001g0080 others(173): Show |
262 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(259): Show |
intron_variant | MODIFIER | c.346-519G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 3/11 | chr16 | 57677651 | |||||||
chr16:57677757 | C | T | 3 | a0001c0001t0006g0185 a0002c0004t0006g0210 a0002c0004t0006g0228 |
3 | HG02622.hp2 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.346-413C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 3/11 | chr16 | 57677757 | |||||||
chr16:57677794 | C | T | 3 | a0001c0001t0006g0185 a0002c0004t0006g0210 a0002c0004t0006g0228 |
3 | HG02622.hp2 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.346-376C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 3/11 | chr16 | 57677794 | |||||||
chr16:57677865 | C | T | 21 | a0001c0002t0003g0117 a0001c0002t0003g0144 a0001c0002t0003g0150 others(18): Show |
38 | HG00408.hp2 HG00423.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.346-305C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 3/11 | chr16 | 57677865 | |||||||
chr16:57677870 | C | G | 2 | a0001c0001t0005g0121 a0001c0001t0005g0138 |
2 | NA18963.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.346-300C>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 3/11 | chr16 | 57677870 | |||||||
chr16:57677922 | C | A | 1 | a0001c0002t0003g0290 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.346-248C>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 3/11 | chr16 | 57677922 | |||||||
chr16:57677943 | T | C | 3 | a0001c0001t0010g0320 a0001c0002t0013g0148 a0001c0002t0013g0191 |
3 | HG02970.hp2 HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.346-227T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 3/11 | chr16 | 57677943 | |||||||
chr16:57678121 | C | T | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG02055.hp2 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.346-49C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 3/11 | chr16 | 57678121 | |||||||
chr16:57678378 | T | C | 4 | a0001c0001t0002g0047 a0001c0001t0002g0293 a0001c0001t0007g0045 others(1): Show |
5 | HG00642.hp1 HG01257.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.492+62T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 4/11 | chr16 | 57678378 | |||||||
chr16:57678394 | C | A | 1 | a0001c0001t0002g0289 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.492+78C>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 4/11 | chr16 | 57678394 | |||||||
chr16:57678450 | T | G | 2 | a0001c0002t0001g0250 a0001c0002t0008g0251 |
2 | HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.492+134T>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 4/11 | chr16 | 57678450 | |||||||
chr16:57678517 | C | T | 1 | a0001c0008t0002g0188 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.492+201C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 4/11 | chr16 | 57678517 | |||||||
chr16:57678521 | C | G | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG02055.hp2 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.492+205C>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 4/11 | chr16 | 57678521 | |||||||
chr16:57678565 | A | G | 1 | a0001c0002t0003g0117 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.492+249A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 4/11 | chr16 | 57678565 | |||||||
chr16:57678596 | T | G | 1 | a0001c0001t0001g0197 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.492+280T>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 4/11 | chr16 | 57678596 | |||||||
chr16:57678761 | C | T | 1 | a0011c0014t0001g0179 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.493-416C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 4/11 | chr16 | 57678761 | |||||||
chr16:57678810 | A | G | 23 | a0001c0001t0005g0004 a0001c0001t0005g0030 a0001c0001t0005g0036 others(20): Show |
31 | HG00597.hp1 HG00609.hp1 HG02071.hp1 others(28): Show |
intron_variant | MODIFIER | c.493-367A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 4/11 | chr16 | 57678810 | |||||||
chr16:57678834 | C | T | 7 | a0001c0002t0003g0311 a0002c0003t0003g0199 a0002c0003t0003g0203 others(4): Show |
7 | HG02132.hp1 NA18747.hp1 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.493-343C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 4/11 | chr16 | 57678834 | |||||||
chr16:57678844 | C | G | 18 | a0001c0002t0003g0117 a0001c0002t0003g0144 a0001c0002t0003g0150 others(15): Show |
30 | HG00408.hp2 HG00423.hp1 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.493-333C>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 4/11 | chr16 | 57678844 | |||||||
chr16:57678951 | G | C | 23 | a0001c0001t0005g0004 a0001c0001t0005g0030 a0001c0001t0005g0036 others(20): Show |
31 | HG00597.hp1 HG00609.hp1 HG02071.hp1 others(28): Show |
intron_variant | MODIFIER | c.493-226G>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 4/11 | chr16 | 57678951 | |||||||
chr16:57679118 | G | C | 23 | a0001c0001t0005g0004 a0001c0001t0005g0030 a0001c0001t0005g0036 others(20): Show |
31 | HG00597.hp1 HG00609.hp1 HG02071.hp1 others(28): Show |
intron_variant | MODIFIER | c.493-59G>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 4/11 | chr16 | 57679118 | |||||||
chr16:57679125 | G | A | 23 | a0001c0001t0005g0004 a0001c0001t0005g0030 a0001c0001t0005g0036 others(20): Show |
31 | HG00597.hp1 HG00609.hp1 HG02071.hp1 others(28): Show |
intron_variant | MODIFIER | c.493-52G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 4/11 | chr16 | 57679125 | |||||||
chr16:57679141 | T | G | 1 | a0001c0001t0005g0237 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.493-36T>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 4/11 | chr16 | 57679141 | |||||||
chr16:57679338 | C | T | 179 | a0001c0001t0001g0048 a0001c0001t0001g0059 a0001c0001t0001g0080 others(176): Show |
265 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(262): Show |
intron_variant | MODIFIER | c.627+27C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 5/11 | chr16 | 57679338 | |||||||
chr16:57679411 | C | T | 3 | a0001c0002t0012g0052 a0001c0002t0012g0054 a0001c0002t0012g0253 |
3 | HG02280.hp2 HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.627+100C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 5/11 | chr16 | 57679411 | |||||||
chr16:57679427 | C | T | 2 | a0001c0002t0001g0250 a0001c0002t0008g0251 |
2 | HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.627+116C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 5/11 | chr16 | 57679427 | |||||||
chr16:57679564 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.628-252C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 5/11 | chr16 | 57679564 | |||||||
chr16:57679565 | G | C | 23 | a0001c0001t0005g0004 a0001c0001t0005g0030 a0001c0001t0005g0036 others(20): Show |
31 | HG00597.hp1 HG00609.hp1 HG02071.hp1 others(28): Show |
intron_variant | MODIFIER | c.628-251G>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 5/11 | chr16 | 57679565 | |||||||
chr16:57679596 | T | C | 23 | a0001c0001t0005g0004 a0001c0001t0005g0030 a0001c0001t0005g0036 others(20): Show |
31 | HG00597.hp1 HG00609.hp1 HG02071.hp1 others(28): Show |
intron_variant | MODIFIER | c.628-220T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 5/11 | chr16 | 57679596 | |||||||
chr16:57679622 | A | G | 105 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0014 others(102): Show |
157 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.628-194A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 5/11 | chr16 | 57679622 | |||||||
chr16:57679624 | G | A | 39 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0124 others(36): Show |
64 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.628-192G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 5/11 | chr16 | 57679624 | |||||||
chr16:57679673 | G | A | 1 | a0001c0002t0001g0171 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.628-143G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 5/11 | chr16 | 57679673 | |||||||
chr16:57679683 | T | C | 5 | a0001c0001t0002g0192 a0001c0001t0002g0274 a0004c0010t0001g0295 others(2): Show |
5 | HG00741.hp2 HG01123.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.628-133T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 5/11 | chr16 | 57679683 | |||||||
chr16:57679735 | G | T | 25 | a0001c0001t0005g0004 a0001c0001t0005g0030 a0001c0001t0005g0036 others(22): Show |
33 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.628-81G>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 5/11 | chr16 | 57679735 | |||||||
chr16:57679744 | G | A | 4 | a0001c0001t0002g0192 a0001c0001t0002g0274 a0004c0010t0001g0295 others(1): Show |
4 | HG00741.hp2 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-72G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 5/11 | chr16 | 57679744 | |||||||
chr16:57679767 | C | A | 72 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0014 others(69): Show |
113 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.628-49C>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 5/11 | chr16 | 57679767 | |||||||
chr16:57679773 | A | C | 97 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0014 others(94): Show |
146 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.628-43A>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 5/11 | chr16 | 57679773 | |||||||
chr16:57679900 | G | A | 3 | a0001c0001t0010g0129 a0001c0001t0010g0320 a0001c0002t0013g0148 |
3 | HG01167.hp1 HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.667+45G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 6/11 | chr16 | 57679900 | |||||||
chr16:57680015 | T | C | 1 | a0001c0001t0009g0268 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.667+160T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 6/11 | chr16 | 57680015 | |||||||
chr16:57680015 | T | TC | 27 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0060 others(24): Show |
30 | HG00738.hp1 HG00738.hp2 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.667+168dupC | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr16 | 57680015 | ||||||
chr16:57680019 | C | CT | 113 | a0001c0001t0001g0059 a0001c0001t0001g0080 a0001c0001t0001g0108 others(110): Show |
169 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.667+164_667+165ins others(1): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 6/11 | chr16 | 57680019 | |||||||
chr16:57680019 | C | CTCCCCT | 7 | a0001c0002t0003g0311 a0002c0003t0003g0199 a0002c0003t0003g0203 others(4): Show |
7 | HG02132.hp1 NA18747.hp1 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.667+164_667+165ins others(6): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 6/11 | chr16 | 57680019 | |||||||
chr16:57680019 | C | CTCCTCTC others(132): Show |
2 | a0001c0001t0002g0192 a0001c0001t0002g0274 |
2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.667+164_667+165ins others(139): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 6/11 | chr16 | 57680019 | |||||||
chr16:57680022 | C | CCT | 13 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0002g0015 others(10): Show |
17 | HG00642.hp2 HG01192.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.667+169_667+170dup others(2): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr16 | 57680022 | ||||||
chr16:57680022 | C | CT | 54 | a0001c0001t0001g0100 a0001c0001t0001g0197 a0001c0001t0002g0001 others(51): Show |
81 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.667+167_667+168ins others(1): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 6/11 | chr16 | 57680022 | |||||||
chr16:57680022 | C | T | 122 | a0001c0001t0001g0059 a0001c0001t0001g0080 a0001c0001t0001g0108 others(119): Show |
178 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.667+167C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 6/11 | chr16 | 57680022 | |||||||
chr16:57680032 | T | C | 1 | a0001c0001t0002g0101 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.667+177T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 6/11 | chr16 | 57680032 | |||||||
chr16:57680053 | T | C | 3 | a0003c0006t0006g0008 a0003c0006t0006g0276 a0010c0020t0001g0285 |
8 | HG01109.hp2 HG02258.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.667+198T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 6/11 | chr16 | 57680053 | |||||||
chr16:57680072 | C | T | 25 | a0001c0001t0005g0004 a0001c0001t0005g0030 a0001c0001t0005g0036 others(22): Show |
33 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.668-193C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 6/11 | chr16 | 57680072 | |||||||
chr16:57680086 | C | T | 3 | a0001c0001t0010g0129 a0001c0001t0010g0320 a0001c0002t0013g0148 |
3 | HG01167.hp1 HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.668-179C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 6/11 | chr16 | 57680086 | |||||||
chr16:57680091 | C | T | 1 | a0004c0010t0001g0296 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.668-174C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 6/11 | chr16 | 57680091 | |||||||
chr16:57680095 | C | CTCACCTC others(163): Show |
1 | a0004c0010t0001g0296 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.668-170_668-169ins others(170): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 6/11 | chr16 | 57680095 | |||||||
chr16:57680097 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.668-168C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 6/11 | chr16 | 57680097 | |||||||
chr16:57680098 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.668-167T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 6/11 | chr16 | 57680098 | |||||||
chr16:57680103 | T | C | 1 | a0004c0010t0001g0296 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.668-162T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 6/11 | chr16 | 57680103 | |||||||
chr16:57680105 | T | TCCTCCCC others(101): Show |
1 | a0004c0010t0001g0295 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.668-137_668-30dupC others(107): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr16 | 57680105 | ||||||
chr16:57680105 | T | TCCTCCCC others(101): Show |
3 | a0001c0017t0011g0312 a0002c0004t0011g0287 a0002c0022t0011g0288 |
3 | HG02145.hp1 HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.668-127_668-126ins others(108): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr16 | 57680105 | ||||||
chr16:57680105 | TCCTCCCC others(47): Show |
T | 5 | a0001c0001t0006g0185 a0001c0002t0001g0250 a0001c0002t0008g0251 others(2): Show |
5 | HG02055.hp1 HG02622.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.668-126_668-73delA others(53): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr16 | 57680105 | ||||||
chr16:57680139 | A | ACCTCCTC others(101): Show |
1 | a0001c0001t0001g0108 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.668-30_668-29insCC others(106): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr16 | 57680139 | ||||||
chr16:57680139 | A | C | 3 | a0001c0017t0011g0312 a0002c0004t0011g0287 a0002c0022t0011g0288 |
3 | HG02145.hp1 HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.668-126A>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 6/11 | chr16 | 57680139 | |||||||
chr16:57680158 | A | ACCCTCCC others(47): Show |
4 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0297 others(1): Show |
4 | HG02486.hp2 HG02976.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.668-83_668-30dupCC others(52): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr16 | 57680158 | ||||||
chr16:57680182 | C | CCCCTCTG others(101): Show |
1 | a0001c0001t0001g0190 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.668-30_668-29insCC others(106): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr16 | 57680182 | ||||||
chr16:57680182 | C | CCCCTCTG others(47): Show |
8 | a0001c0001t0002g0047 a0001c0001t0002g0293 a0001c0001t0007g0045 others(5): Show |
11 | HG00642.hp1 HG01257.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.668-68_668-15dupCC others(52): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr16 | 57680182 | ||||||
chr16:57680182 | C | T | 1 | a0006c0011t0008g0255 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.668-83C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 6/11 | chr16 | 57680182 | |||||||
chr16:57680236 | T | C | 20 | a0001c0001t0017g0085 a0001c0002t0003g0117 a0001c0002t0003g0144 others(17): Show |
32 | HG00408.hp2 HG00423.hp1 HG02015.hp1 others(29): Show |
intron_variant | MODIFIER | c.668-29T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 6/11 | chr16 | 57680236 | |||||||
chr16:57680261 | C | G | 1 | a0001c0019t0008g0252 | 1 | HG06807.hp2 | splice_region_variant&intron_variant | LOW | c.668-4C>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 6/11 | chr16 | 57680261 | |||||||
chr16:57680399 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.768+34C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 7/11 | chr16 | 57680399 | |||||||
chr16:57680410 | C | T | 2 | a0001c0001t0001g0116 a0001c0001t0001g0180 |
2 | HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.768+45C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 7/11 | chr16 | 57680410 | |||||||
chr16:57680499 | C | A | 3 | a0001c0017t0011g0312 a0002c0004t0011g0287 a0002c0022t0011g0288 |
3 | HG02145.hp1 HG02922.hp2 NA21309.hp1 |
splice_region_variant&intron_variant | LOW | c.769-6C>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 7/11 | chr16 | 57680499 | |||||||
chr16:57680720 | C | T | 3 | a0001c0001t0006g0185 a0002c0004t0006g0210 a0002c0004t0006g0228 |
3 | HG02622.hp2 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.881+103C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57680720 | |||||||
chr16:57680730 | G | A | 2 | a0002c0003t0003g0201 a0002c0003t0003g0221 |
2 | NA18961.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.881+113G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57680730 | |||||||
chr16:57680819 | C | T | 77 | a0001c0001t0001g0018 a0001c0001t0001g0035 a0001c0001t0001g0060 others(74): Show |
93 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.881+202C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57680819 | |||||||
chr16:57680820 | T | G | 1 | a0001c0001t0001g0128 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.881+203T>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57680820 | |||||||
chr16:57680843 | G | A | 40 | a0001c0001t0001g0018 a0001c0001t0001g0035 a0001c0001t0001g0060 others(37): Show |
46 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.881+226G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57680843 | |||||||
chr16:57680854 | T | C | 2 | a0001c0005t0001g0278 a0001c0005t0001g0279 |
2 | HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.881+237T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57680854 | |||||||
chr16:57680877 | G | C | 1 | a0001c0002t0001g0109 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.881+260G>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57680877 | |||||||
chr16:57681005 | A | T | 50 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0014 others(47): Show |
79 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.881+388A>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57681005 | |||||||
chr16:57681144 | T | TTTTGAGA others(12): Show |
1 | a0001c0001t0001g0170 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.881+528_881+546dup others(19): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 57681144 | ||||||
chr16:57681187 | G | A | 3 | a0001c0002t0004g0264 a0001c0002t0004g0265 a0001c0002t0004g0269 |
3 | HG01106.hp1 HG01516.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.881+570G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57681187 | |||||||
chr16:57681267 | C | T | 1 | a0001c0019t0008g0252 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.881+650C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57681267 | |||||||
chr16:57681298 | C | T | 20 | a0001c0001t0001g0080 a0001c0001t0010g0129 a0001c0001t0010g0320 others(17): Show |
34 | HG00733.hp1 HG01099.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.881+681C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57681298 | |||||||
chr16:57681336 | CTGTGTGT others(9): Show |
C | 1 | a0001c0001t0001g0316 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.881+731_881+746del others(16): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 57681336 | ||||||
chr16:57681348 | C | CTG | 24 | a0001c0001t0001g0037 a0001c0001t0001g0080 a0001c0001t0001g0091 others(21): Show |
37 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.881+758_881+759dup others(2): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 57681348 | ||||||
chr16:57681348 | C | CTGTG | 4 | a0001c0002t0001g0171 a0001c0002t0008g0013 a0001c0002t0008g0053 others(1): Show |
6 | HG02257.hp1 HG03209.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.881+756_881+759dup others(4): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 57681348 | ||||||
chr16:57681348 | CTG | C | 28 | a0001c0001t0001g0041 a0001c0001t0001g0059 a0001c0001t0001g0094 others(25): Show |
41 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.881+758_881+759del others(2): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 57681348 | ||||||
chr16:57681348 | CTGTG | C | 6 | a0001c0001t0001g0120 a0001c0001t0002g0047 a0001c0001t0002g0293 others(3): Show |
6 | HG01257.hp1 HG01258.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.881+756_881+759del others(4): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 57681348 | ||||||
chr16:57681366 | G | T | 7 | a0001c0002t0004g0046 a0001c0002t0004g0256 a0001c0002t0004g0264 others(4): Show |
8 | HG01070.hp1 HG01106.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.881+749G>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57681366 | |||||||
chr16:57681367 | TGTGTGTG others(7): Show |
T | 1 | a0001c0005t0001g0280 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.881+754_881+767del others(14): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 57681367 | ||||||
chr16:57681371 | TGTGTGCG others(1): Show |
T | 2 | a0003c0006t0006g0008 a0003c0006t0006g0276 |
5 | HG01109.hp2 HG02258.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.881+756_881+763del others(8): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 57681371 | ||||||
chr16:57681371 | TGTGTGCG others(3): Show |
T | 52 | a0001c0001t0001g0018 a0001c0001t0001g0035 a0001c0001t0001g0060 others(49): Show |
61 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.881+758_881+767del others(10): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 57681371 | ||||||
chr16:57681373 | TGTGCGCG others(1): Show |
T | 18 | a0001c0001t0005g0030 a0001c0001t0005g0069 a0001c0001t0005g0073 others(15): Show |
20 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.881+762_881+769del others(8): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 57681373 | ||||||
chr16:57681375 | TGC | T | 9 | a0001c0001t0002g0134 a0001c0001t0002g0192 a0001c0001t0002g0274 others(6): Show |
12 | HG01243.hp2 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.881+764_881+765del others(2): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 57681375 | ||||||
chr16:57681375 | TGCGC | T | 47 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0014 others(44): Show |
76 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.881+762_881+765del others(4): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 57681375 | ||||||
chr16:57681377 | C | T | 32 | a0001c0001t0001g0108 a0001c0001t0001g0190 a0001c0001t0001g0291 others(29): Show |
40 | HG00423.hp1 HG02027.hp2 HG02040.hp2 others(37): Show |
intron_variant | MODIFIER | c.881+760C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57681377 | |||||||
chr16:57681377 | CGCGCGT | C | 4 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(1): Show |
4 | HG02055.hp2 HG02615.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+764_881+769del others(6): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 57681377 | ||||||
chr16:57681379 | C | T | 36 | a0001c0001t0001g0108 a0001c0001t0001g0190 a0001c0001t0001g0291 others(33): Show |
47 | HG00423.hp1 HG01243.hp2 HG02027.hp2 others(44): Show |
intron_variant | MODIFIER | c.881+762C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57681379 | |||||||
chr16:57681381 | C | T | 10 | a0001c0001t0001g0108 a0001c0001t0001g0190 a0001c0001t0001g0229 others(7): Show |
10 | HG02015.hp2 HG02486.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.881+764C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57681381 | |||||||
chr16:57681381 | CGT | C | 3 | a0002c0004t0006g0228 a0002c0004t0011g0287 a0002c0022t0011g0288 |
3 | HG02145.hp1 HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.881+766_881+767del others(2): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 57681381 | ||||||
chr16:57681383 | T | C | 77 | a0001c0001t0001g0018 a0001c0001t0001g0035 a0001c0001t0001g0060 others(74): Show |
94 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.881+766T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57681383 | |||||||
chr16:57681383 | T | TGTGC | 4 | a0001c0001t0001g0108 a0001c0001t0001g0190 a0001c0001t0001g0292 others(1): Show |
4 | HG02486.hp2 HG02717.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+767_881+768ins others(4): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 57681383 | ||||||
chr16:57681389 | C | T | 2 | a0001c0002t0001g0250 a0001c0002t0008g0251 |
2 | HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.881+772C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57681389 | |||||||
chr16:57681447 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0182 |
2 | HG00735.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.881+830G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57681447 | |||||||
chr16:57681452 | A | T | 1 | a0001c0002t0012g0253 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.881+835A>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57681452 | |||||||
chr16:57681469 | C | A | 2 | a0001c0002t0001g0250 a0001c0002t0008g0251 |
2 | HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.881+852C>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57681469 | |||||||
chr16:57681516 | T | C | 1 | a0001c0001t0001g0048 | 2 | HG01261.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.881+899T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57681516 | |||||||
chr16:57681641 | G | A | 14 | a0001c0001t0005g0030 a0001c0001t0005g0056 a0001c0001t0005g0069 others(11): Show |
15 | HG00609.hp1 HG00621.hp1 HG03688.hp1 others(12): Show |
intron_variant | MODIFIER | c.881+1024G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57681641 | |||||||
chr16:57681668 | G | A | 16 | a0001c0005t0001g0024 a0001c0005t0001g0095 a0001c0005t0001g0198 others(13): Show |
21 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.881+1051G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57681668 | |||||||
chr16:57681726 | C | CA | 12 | a0001c0001t0001g0061 a0001c0001t0001g0086 a0001c0001t0001g0170 others(9): Show |
12 | HG00621.hp2 HG00741.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.881+1129dupA | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 57681726 | ||||||
chr16:57681726 | CA | C | 7 | a0001c0001t0001g0141 a0001c0001t0001g0177 a0001c0001t0001g0182 others(4): Show |
8 | HG00735.hp2 HG01167.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.881+1129delA | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 57681726 | ||||||
chr16:57681745 | A | AAG | 8 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0039 others(5): Show |
9 | HG01243.hp2 HG01952.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.881+1144_881+1145d others(4): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 57681745 | ||||||
chr16:57681745 | A | AG | 47 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0014 others(44): Show |
69 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.881+1128_881+1129i others(3): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57681745 | |||||||
chr16:57681745 | A | G | 4 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0273 others(1): Show |
5 | HG02630.hp2 HG03491.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.881+1128A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57681745 | |||||||
chr16:57681745 | AAG | A | 19 | a0001c0001t0001g0108 a0001c0002t0001g0301 a0001c0002t0012g0052 others(16): Show |
24 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.881+1144_881+1145d others(4): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 57681745 | ||||||
chr16:57681746 | AG | A | 60 | a0001c0001t0001g0018 a0001c0001t0001g0035 a0001c0001t0001g0060 others(57): Show |
66 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.881+1130delG | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57681746 | |||||||
chr16:57681747 | G | A | 13 | a0001c0001t0001g0196 a0001c0001t0001g0291 a0001c0001t0001g0292 others(10): Show |
18 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.881+1130G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57681747 | |||||||
chr16:57681840 | G | A | 1 | a0001c0021t0001g0194 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.881+1223G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57681840 | |||||||
chr16:57681843 | T | A | 78 | a0001c0001t0001g0018 a0001c0001t0001g0035 a0001c0001t0001g0060 others(75): Show |
94 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.881+1226T>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57681843 | |||||||
chr16:57681970 | C | G | 21 | a0001c0001t0017g0085 a0001c0002t0003g0117 a0001c0002t0003g0144 others(18): Show |
33 | HG00408.hp2 HG00423.hp1 HG02015.hp1 others(30): Show |
intron_variant | MODIFIER | c.881+1353C>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57681970 | |||||||
chr16:57682108 | C | T | 51 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0014 others(48): Show |
80 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.881+1491C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682108 | |||||||
chr16:57682149 | G | A | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1532G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682149 | |||||||
chr16:57682150 | T | A | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1533T>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682150 | |||||||
chr16:57682151 | G | T | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1534G>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682151 | |||||||
chr16:57682153 | G | T | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1536G>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682153 | |||||||
chr16:57682154 | A | C | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1537A>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682154 | |||||||
chr16:57682155 | G | C | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1538G>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682155 | |||||||
chr16:57682157 | G | C | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1540G>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682157 | |||||||
chr16:57682159 | G | A | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1542G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682159 | |||||||
chr16:57682162 | C | A | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1545C>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682162 | |||||||
chr16:57682164 | G | C | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1547G>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682164 | |||||||
chr16:57682167 | C | A | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1550C>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682167 | |||||||
chr16:57682168 | A | T | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1551A>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682168 | |||||||
chr16:57682169 | G | T | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1552G>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682169 | |||||||
chr16:57682171 | C | A | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1554C>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682171 | |||||||
chr16:57682172 | A | T | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1555A>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682172 | |||||||
chr16:57682173 | G | C | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1556G>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682173 | |||||||
chr16:57682176 | A | G | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1559A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682176 | |||||||
chr16:57682177 | C | G | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1560C>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682177 | |||||||
chr16:57682180 | C | A | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1563C>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682180 | |||||||
chr16:57682184 | G | A | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1567G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682184 | |||||||
chr16:57682187 | C | A | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1570C>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682187 | |||||||
chr16:57682189 | C | T | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1572C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682189 | |||||||
chr16:57682192 | C | T | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1575C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682192 | |||||||
chr16:57682193 | A | G | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1576A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682193 | |||||||
chr16:57682194 | G | A | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1577G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682194 | |||||||
chr16:57682198 | G | A | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1581G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682198 | |||||||
chr16:57682199 | G | A | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1582G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682199 | |||||||
chr16:57682200 | G | A | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1583G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682200 | |||||||
chr16:57682201 | C | G | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1584C>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682201 | |||||||
chr16:57682202 | C | A | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1585C>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682202 | |||||||
chr16:57682205 | G | A | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1588G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682205 | |||||||
chr16:57682208 | C | T | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1591C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682208 | |||||||
chr16:57682217 | G | A | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1600G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682217 | |||||||
chr16:57682218 | G | A | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1601G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682218 | |||||||
chr16:57682219 | G | A | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1602G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682219 | |||||||
chr16:57682221 | C | A | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1604C>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682221 | |||||||
chr16:57682222 | C | A | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1605C>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682222 | |||||||
chr16:57682223 | C | T | 1 | a0001c0001t0007g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+1606C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682223 | |||||||
chr16:57682287 | T | C | 14 | a0001c0001t0005g0030 a0001c0001t0005g0056 a0001c0001t0005g0069 others(11): Show |
15 | HG00609.hp1 HG00621.hp1 HG03688.hp1 others(12): Show |
intron_variant | MODIFIER | c.882-1645T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682287 | |||||||
chr16:57682342 | C | T | 18 | a0001c0002t0001g0250 a0001c0002t0008g0251 a0001c0005t0001g0024 others(15): Show |
23 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.882-1590C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682342 | |||||||
chr16:57682360 | T | A | 1 | a0001c0001t0001g0170 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.882-1572T>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682360 | |||||||
chr16:57682362 | C | T | 1 | a0001c0002t0003g0290 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.882-1570C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682362 | |||||||
chr16:57682488 | T | C | 24 | a0001c0001t0017g0085 a0001c0002t0003g0117 a0001c0002t0003g0144 others(21): Show |
36 | HG00408.hp2 HG00423.hp1 HG02015.hp1 others(33): Show |
intron_variant | MODIFIER | c.882-1444T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682488 | |||||||
chr16:57682515 | A | G | 48 | a0001c0001t0006g0185 a0001c0001t0014g0249 a0001c0001t0017g0085 others(45): Show |
70 | HG00408.hp2 HG00423.hp1 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.882-1417A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682515 | |||||||
chr16:57682668 | G | A | 2 | a0001c0002t0001g0250 a0001c0002t0008g0251 |
2 | HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.882-1264G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682668 | |||||||
chr16:57682681 | C | T | 1 | a0001c0002t0003g0290 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.882-1251C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682681 | |||||||
chr16:57682699 | G | A | 1 | a0002c0003t0001g0211 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.882-1233G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682699 | |||||||
chr16:57682740 | A | G | 1 | a0001c0002t0003g0290 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.882-1192A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682740 | |||||||
chr16:57682819 | T | TA | 29 | a0001c0001t0001g0108 a0001c0001t0001g0190 a0001c0001t0001g0195 others(26): Show |
31 | HG00099.hp1 HG00544.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.882-1111dupA | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 57682819 | ||||||
chr16:57682912 | C | A | 145 | a0001c0001t0001g0108 a0001c0001t0001g0190 a0001c0001t0001g0195 others(142): Show |
199 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.882-1020C>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682912 | |||||||
chr16:57682920 | A | T | 145 | a0001c0001t0001g0108 a0001c0001t0001g0190 a0001c0001t0001g0195 others(142): Show |
199 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.882-1012A>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682920 | |||||||
chr16:57682933 | C | A | 8 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0066 others(5): Show |
10 | HG00408.hp1 HG02015.hp2 NA18612.hp2 others(7): Show |
intron_variant | MODIFIER | c.882-999C>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682933 | |||||||
chr16:57682953 | A | G | 149 | a0001c0001t0001g0108 a0001c0001t0001g0190 a0001c0001t0001g0195 others(146): Show |
203 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.882-979A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682953 | |||||||
chr16:57682960 | G | A | 50 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0014 others(47): Show |
79 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.882-972G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682960 | |||||||
chr16:57682962 | G | A | 1 | a0001c0001t0002g0134 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.882-970G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57682962 | |||||||
chr16:57683004 | T | TCCAGTTC others(29): Show |
1 | a0001c0001t0001g0128 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.882-910_882-909ins others(36): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 57683004 | ||||||
chr16:57683077 | G | A | 1 | a0002c0004t0001g0206 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.882-855G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57683077 | |||||||
chr16:57683151 | AGAGCTGA others(20): Show |
A | 1 | a0001c0001t0002g0098 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.882-780_882-754del others(27): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57683151 | |||||||
chr16:57683301 | C | T | 20 | a0001c0002t0003g0117 a0001c0002t0003g0144 a0001c0002t0003g0150 others(17): Show |
32 | HG00408.hp2 HG00423.hp1 HG02015.hp1 others(29): Show |
intron_variant | MODIFIER | c.882-631C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57683301 | |||||||
chr16:57683344 | A | T | 8 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0066 others(5): Show |
10 | HG00408.hp1 HG02015.hp2 NA18612.hp2 others(7): Show |
intron_variant | MODIFIER | c.882-588A>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57683344 | |||||||
chr16:57683428 | T | C | 1 | a0001c0019t0008g0252 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.882-504T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57683428 | |||||||
chr16:57683483 | G | A | 4 | a0001c0007t0001g0021 a0001c0007t0001g0042 a0001c0007t0001g0193 others(1): Show |
7 | HG02258.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.882-449G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57683483 | |||||||
chr16:57683491 | G | A | 1 | a0002c0003t0003g0011 | 5 | HG00408.hp2 HG00423.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.882-441G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57683491 | |||||||
chr16:57683656 | C | A | 1 | a0001c0005t0001g0198 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.882-276C>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57683656 | |||||||
chr16:57683696 | A | C | 1 | a0001c0005t0001g0280 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.882-236A>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57683696 | |||||||
chr16:57683887 | C | T | 1 | a0001c0002t0004g0265 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.882-45C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 8/11 | chr16 | 57683887 | |||||||
chr16:57684492 | C | T | 10 | a0001c0005t0001g0024 a0001c0005t0001g0198 a0001c0005t0001g0277 others(7): Show |
12 | HG02451.hp1 HG02486.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1256+9C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 10/11 | chr16 | 57684492 | |||||||
chr16:57684611 | C | G | 1 | a0001c0002t0004g0063 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1256+128C>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 10/11 | chr16 | 57684611 | |||||||
chr16:57684700 | A | G | 1 | a0001c0002t0004g0176 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1256+217A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 10/11 | chr16 | 57684700 | |||||||
chr16:57684719 | C | T | 14 | a0001c0001t0005g0030 a0001c0001t0005g0056 a0001c0001t0005g0069 others(11): Show |
15 | HG00609.hp1 HG00621.hp1 HG03688.hp1 others(12): Show |
intron_variant | MODIFIER | c.1256+236C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 10/11 | chr16 | 57684719 | |||||||
chr16:57684799 | C | T | 3 | a0001c0017t0011g0312 a0002c0004t0011g0287 a0002c0022t0011g0288 |
3 | HG02145.hp1 HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1256+316C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 10/11 | chr16 | 57684799 | |||||||
chr16:57684800 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1256+317G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 10/11 | chr16 | 57684800 | |||||||
chr16:57684809 | C | A | 1 | a0001c0002t0003g0290 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1256+326C>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 10/11 | chr16 | 57684809 | |||||||
chr16:57684871 | C | G | 26 | a0001c0001t0001g0059 a0001c0001t0001g0124 a0001c0002t0004g0005 others(23): Show |
39 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.1256+388C>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 10/11 | chr16 | 57684871 | |||||||
chr16:57684892 | C | T | 1 | a0001c0001t0002g0289 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1256+409C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 10/11 | chr16 | 57684892 | |||||||
chr16:57684910 | A | C | 319 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(316): Show |
437 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(434): Show |
intron_variant | MODIFIER | c.1256+427A>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 10/11 | chr16 | 57684910 | |||||||
chr16:57685011 | T | C | 5 | a0001c0001t0006g0185 a0002c0004t0006g0210 a0002c0004t0006g0228 others(2): Show |
10 | HG01109.hp2 HG02258.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1256+528T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 10/11 | chr16 | 57685011 | |||||||
chr16:57685114 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1257-529G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 10/11 | chr16 | 57685114 | |||||||
chr16:57685313 | C | T | 3 | a0001c0017t0011g0312 a0002c0004t0011g0287 a0002c0022t0011g0288 |
3 | HG02145.hp1 HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1257-330C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 10/11 | chr16 | 57685313 | |||||||
chr16:57685400 | A | G | 1 | a0001c0002t0008g0251 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1257-243A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 10/11 | chr16 | 57685400 | |||||||
chr16:57685406 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1257-237G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 10/11 | chr16 | 57685406 | |||||||
chr16:57685522 | G | T | 1 | a0001c0007t0008g0254 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1257-121G>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 10/11 | chr16 | 57685522 | |||||||
chr16:57686060 | A | C | 25 | a0001c0001t0005g0004 a0001c0001t0005g0030 a0001c0001t0005g0036 others(22): Show |
33 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1540+134A>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57686060 | |||||||
chr16:57686110 | CGTTTGTG others(6): Show |
C | 1 | a0001c0001t0001g0118 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1540+186_1540+198d others(15): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr16 | 57686110 | ||||||
chr16:57686111 | G | A | 1 | a0002c0004t0001g0044 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1540+185G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57686111 | |||||||
chr16:57686141 | C | G | 89 | a0001c0001t0005g0004 a0001c0001t0005g0030 a0001c0001t0005g0036 others(86): Show |
120 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1540+215C>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57686141 | |||||||
chr16:57686329 | C | T | 90 | a0001c0001t0001g0059 a0001c0002t0001g0025 a0001c0002t0001g0049 others(87): Show |
126 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.1540+403C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57686329 | |||||||
chr16:57686377 | A | G | 1 | a0001c0001t0002g0089 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1540+451A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57686377 | |||||||
chr16:57686392 | G | T | 1 | a0001c0002t0013g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1540+466G>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57686392 | |||||||
chr16:57686401 | C | T | 1 | a0001c0017t0011g0312 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1540+475C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57686401 | |||||||
chr16:57686407 | T | TGAGGATC others(6): Show |
15 | a0001c0005t0001g0024 a0001c0005t0001g0095 a0001c0005t0001g0198 others(12): Show |
20 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.1540+482_1540+494d others(15): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr16 | 57686407 | ||||||
chr16:57686425 | A | T | 15 | a0001c0005t0001g0024 a0001c0005t0001g0095 a0001c0005t0001g0198 others(12): Show |
20 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.1540+499A>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57686425 | |||||||
chr16:57686473 | T | C | 2 | a0001c0002t0003g0257 a0001c0002t0003g0259 |
2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1540+547T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57686473 | |||||||
chr16:57686493 | C | G | 114 | a0001c0001t0001g0059 a0001c0001t0005g0004 a0001c0001t0005g0030 others(111): Show |
158 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.1540+567C>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57686493 | |||||||
chr16:57686504 | C | G | 1 | a0001c0002t0004g0266 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1540+578C>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57686504 | |||||||
chr16:57686576 | G | A | 103 | a0001c0001t0005g0030 a0001c0001t0005g0056 a0001c0001t0005g0069 others(100): Show |
140 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1540+650G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57686576 | |||||||
chr16:57686616 | A | G | 2 | a0001c0002t0001g0250 a0001c0002t0008g0251 |
2 | HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1540+690A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57686616 | |||||||
chr16:57686622 | T | C | 1 | a0001c0001t0002g0161 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1540+696T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57686622 | |||||||
chr16:57686651 | T | C | 179 | a0001c0001t0001g0059 a0001c0001t0001g0108 a0001c0001t0001g0190 others(176): Show |
252 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.1540+725T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57686651 | |||||||
chr16:57686698 | G | A | 104 | a0001c0001t0001g0059 a0001c0001t0005g0030 a0001c0001t0005g0056 others(101): Show |
141 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.1540+772G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57686698 | |||||||
chr16:57686758 | C | T | 1 | a0001c0002t0003g0290 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1540+832C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57686758 | |||||||
chr16:57686867 | C | T | 90 | a0001c0001t0001g0059 a0001c0002t0001g0025 a0001c0002t0001g0049 others(87): Show |
126 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.1540+941C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57686867 | |||||||
chr16:57686885 | A | G | 116 | a0001c0001t0001g0059 a0001c0001t0005g0004 a0001c0001t0005g0030 others(113): Show |
160 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1540+959A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57686885 | |||||||
chr16:57686905 | G | GAGC | 26 | a0001c0001t0005g0004 a0001c0001t0005g0030 a0001c0001t0005g0036 others(23): Show |
34 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.1540+982_1540+984d others(5): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr16 | 57686905 | ||||||
chr16:57686959 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1540+1033G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57686959 | |||||||
chr16:57686977 | G | A | 15 | a0001c0005t0001g0024 a0001c0005t0001g0095 a0001c0005t0001g0198 others(12): Show |
20 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.1540+1051G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57686977 | |||||||
chr16:57687047 | C | T | 1 | a0001c0002t0004g0064 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1540+1121C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57687047 | |||||||
chr16:57687053 | C | T | 88 | a0001c0001t0001g0059 a0001c0002t0001g0025 a0001c0002t0001g0049 others(85): Show |
119 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1540+1127C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57687053 | |||||||
chr16:57687078 | C | T | 2 | a0004c0010t0001g0295 a0004c0010t0001g0296 |
2 | HG00741.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1540+1152C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57687078 | |||||||
chr16:57687111 | G | C | 2 | a0001c0001t0001g0130 a0001c0001t0001g0182 |
2 | HG00735.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1540+1185G>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57687111 | |||||||
chr16:57687145 | G | A | 2 | a0001c0001t0001g0108 a0001c0021t0001g0194 |
2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1541-1207G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57687145 | |||||||
chr16:57687215 | G | T | 179 | a0001c0001t0001g0059 a0001c0001t0001g0108 a0001c0001t0001g0190 others(176): Show |
252 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.1541-1137G>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57687215 | |||||||
chr16:57687234 | G | A | 233 | a0001c0001t0001g0018 a0001c0001t0001g0035 a0001c0001t0001g0059 others(230): Show |
325 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.1541-1118G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57687234 | |||||||
chr16:57687250 | CT | C | 93 | a0001c0001t0001g0059 a0001c0001t0001g0128 a0001c0001t0001g0141 others(90): Show |
124 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.1541-1088delT | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr16 | 57687250 | ||||||
chr16:57687250 | CTT | C | 25 | a0001c0001t0005g0004 a0001c0001t0005g0030 a0001c0001t0005g0036 others(22): Show |
33 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1541-1089_1541-108 others(6): Show |
ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr16 | 57687250 | ||||||
chr16:57687330 | G | A | 4 | a0001c0001t0002g0273 a0001c0001t0007g0012 a0001c0001t0007g0050 others(1): Show |
7 | HG02280.hp1 HG02630.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1541-1022G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57687330 | |||||||
chr16:57687360 | T | C | 121 | a0001c0001t0001g0059 a0001c0001t0001g0108 a0001c0001t0001g0190 others(118): Show |
160 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1541-992T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57687360 | |||||||
chr16:57687518 | C | G | 2 | a0001c0001t0002g0192 a0001c0001t0002g0274 |
2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1541-834C>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57687518 | |||||||
chr16:57687521 | G | A | 1 | a0001c0002t0001g0107 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1541-831G>A | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57687521 | |||||||
chr16:57687714 | T | C | 3 | a0001c0017t0011g0312 a0002c0004t0011g0287 a0002c0022t0011g0288 |
3 | HG02145.hp1 HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1541-638T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57687714 | |||||||
chr16:57687738 | T | C | 1 | a0001c0001t0005g0237 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1541-614T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57687738 | |||||||
chr16:57687760 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1541-592A>G | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57687760 | |||||||
chr16:57687933 | G | C | 1 | a0001c0001t0002g0102 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1541-419G>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57687933 | |||||||
chr16:57688040 | T | C | 44 | a0001c0002t0003g0117 a0001c0002t0003g0144 a0001c0002t0003g0150 others(41): Show |
68 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.1541-312T>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57688040 | |||||||
chr16:57688052 | A | C | 1 | a0001c0001t0001g0271 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1541-300A>C | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57688052 | |||||||
chr16:57688126 | G | T | 112 | a0001c0001t0005g0004 a0001c0001t0005g0030 a0001c0001t0005g0036 others(109): Show |
151 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.1541-226G>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57688126 | |||||||
chr16:57688271 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1541-81C>T | ADGRG3 | ENSG00000182885.17 | transcript | ENST00000333493.9 | protein_coding | 11/11 | chr16 | 57688271 |