Item | Value |
---|---|
geneid | 84873 |
ensemblid | ENSG00000144820.8 |
hgncid | 19241 |
symbol | ADGRG7 |
name | adhesion G protein-coupled receptor G7 |
refseq_nuc | NM_032787.3 |
refseq_prot | NP_116176.2 |
ensembl_nuc | ENST00000273352.8 |
ensembl_prot | ENSP00000273352.3 |
mane_status | MANE Select |
chr | chr3 |
start | 100609601 |
end | 100695479 |
strand | + |
ver | v1.2 |
region | chr3:100609601-100695479 |
region5000 | chr3:100604601-100700479 |
regionname0 | ADGRG7_chr3_100609601_100695479 |
regionname5000 | ADGRG7_chr3_100604601_100700479 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 797 | 212 | 58 | 34 | 91 | 12 | 15 | 66 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | MASCR others(792): Show |
chr3 | 100604601 | 100700479 |
a0002 | 0/0 | 797 | 74 | 9 | 11 | 50 | 2 | 2 | 42 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | MASCR others(792): Show |
chr3 | 100604601 | 100700479 |
a0003 | 0/0 | 797 | 35 | 8 | 14 | 4 | 2 | 7 | 2 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | MASCR others(792): Show |
chr3 | 100604601 | 100700479 |
a0004 | 0/0 | 797 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | MASCR others(792): Show |
chr3 | 100604601 | 100700479 |
a0005 | 0/0 | 797 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | MASCR others(792): Show |
chr3 | 100604601 | 100700479 |
a0006 | 0/0 | 797 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | MASCR others(792): Show |
chr3 | 100604601 | 100700479 |
a0007 | 0/0 | 797 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | MASCR others(792): Show |
chr3 | 100604601 | 100700479 |
a0008 | 0/0 | 797 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | MASCR others(792): Show |
chr3 | 100604601 | 100700479 |
a0009 | 0/0 | 797 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | MASCR others(792): Show |
chr3 | 100604601 | 100700479 |
a0010 | 0/0 | 797 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | MASCR others(792): Show |
chr3 | 100604601 | 100700479 |
a0011 | 0/0 | 797 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | MASCR others(792): Show |
chr3 | 100604601 | 100700479 |
a0012 | 0/0 | 797 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | MASCR others(792): Show |
chr3 | 100604601 | 100700479 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2391 | 204 | 51 | 34 | 91 | 11 | 15 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ATGGC others(2386): Show |
chr3 | 100604601 | 100700479 | ||
a0001c0005 | 0/0 | 2391 | 4 | 3 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ATGGC others(2386): Show |
chr3 | 100604601 | 100700479 | ||
a0001c0008 | 0/0 | 2391 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ATGGC others(2386): Show |
chr3 | 100604601 | 100700479 | ||
a0001c0010 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ATGGC others(2386): Show |
chr3 | 100604601 | 100700479 | ||
a0001c0011 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ATGGC others(2386): Show |
chr3 | 100604601 | 100700479 | ||
a0002c0002 | 0/0 | 2391 | 74 | 9 | 11 | 50 | 2 | 2 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ATGGC others(2386): Show |
chr3 | 100604601 | 100700479 | ||
a0003c0003 | 0/0 | 2391 | 35 | 8 | 14 | 4 | 2 | 7 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ATGGC others(2386): Show |
chr3 | 100604601 | 100700479 | ||
a0004c0004 | 0/0 | 2391 | 4 | 4 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ATGGC others(2386): Show |
chr3 | 100604601 | 100700479 | ||
a0004c0009 | 0/0 | 2391 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ATGGC others(2386): Show |
chr3 | 100604601 | 100700479 | ||
a0005c0006 | 0/0 | 2391 | 4 | 3 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ATGGC others(2386): Show |
chr3 | 100604601 | 100700479 | ||
a0006c0007 | 0/0 | 2391 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ATGGC others(2386): Show |
chr3 | 100604601 | 100700479 | ||
a0007c0016 | 0/0 | 2391 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ATGGC others(2386): Show |
chr3 | 100604601 | 100700479 | ||
a0008c0017 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ATGGC others(2386): Show |
chr3 | 100604601 | 100700479 | ||
a0009c0012 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ATGGC others(2386): Show |
chr3 | 100604601 | 100700479 | ||
a0010c0015 | 0/0 | 2391 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ATGGC others(2386): Show |
chr3 | 100604601 | 100700479 | ||
a0011c0013 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ATGGC others(2386): Show |
chr3 | 100604601 | 100700479 | ||
a0012c0014 | 0/0 | 2391 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ATGGC others(2386): Show |
chr3 | 100604601 | 100700479 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3128 | 193 | 41 | 34 | 91 | 10 | 15 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ACTTT others(3123): Show |
chr3 | 100604601 | 100700479 |
a0001c0001t0002 | 0/0 | 3128 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ACTTT others(3123): Show |
chr3 | 100604601 | 100700479 |
a0001c0001t0003 | 0/0 | 3128 | 6 | 6 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ACTTT others(3123): Show |
chr3 | 100604601 | 100700479 |
a0001c0001t0005 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ACTTT others(3123): Show |
chr3 | 100604601 | 100700479 |
a0001c0001t0006 | 0/0 | 3128 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ACTTT others(3123): Show |
chr3 | 100604601 | 100700479 |
a0001c0001t0007 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ACTTT others(3123): Show |
chr3 | 100604601 | 100700479 |
a0001c0005t0001 | 0/0 | 3128 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ACTTT others(3123): Show |
chr3 | 100604601 | 100700479 |
a0001c0005t0008 | 0/0 | 3128 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ACTTT others(3123): Show |
chr3 | 100604601 | 100700479 |
a0001c0008t0001 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ACTTT others(3123): Show |
chr3 | 100604601 | 100700479 |
a0001c0008t0009 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ACTTT others(3123): Show |
chr3 | 100604601 | 100700479 |
a0001c0010t0001 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ACTTT others(3123): Show |
chr3 | 100604601 | 100700479 |
a0001c0011t0001 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ACTTT others(3123): Show |
chr3 | 100604601 | 100700479 |
a0002c0002t0001 | 0/0 | 3128 | 74 | 9 | 11 | 50 | 2 | 2 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ACTTT others(3123): Show |
chr3 | 100604601 | 100700479 |
a0003c0003t0001 | 0/0 | 3128 | 34 | 7 | 14 | 4 | 2 | 7 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ACTTT others(3123): Show |
chr3 | 100604601 | 100700479 |
a0003c0003t0003 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ACTTT others(3123): Show |
chr3 | 100604601 | 100700479 |
a0004c0004t0002 | 0/0 | 3128 | 4 | 4 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ACTTT others(3123): Show |
chr3 | 100604601 | 100700479 |
a0004c0009t0002 | 0/0 | 3128 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ACTTT others(3123): Show |
chr3 | 100604601 | 100700479 |
a0005c0006t0001 | 0/0 | 3128 | 4 | 3 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ACTTT others(3123): Show |
chr3 | 100604601 | 100700479 |
a0006c0007t0004 | 0/0 | 3128 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ACTTT others(3123): Show |
chr3 | 100604601 | 100700479 |
a0007c0016t0001 | 0/0 | 3128 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ACTTT others(3123): Show |
chr3 | 100604601 | 100700479 |
a0008c0017t0001 | 0/0 | 3128 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ACTTT others(3123): Show |
chr3 | 100604601 | 100700479 |
a0009c0012t0001 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ACTTT others(3123): Show |
chr3 | 100604601 | 100700479 |
a0010c0015t0001 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ACTTT others(3123): Show |
chr3 | 100604601 | 100700479 |
a0011c0013t0001 | 0/0 | 3128 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ACTTT others(3123): Show |
chr3 | 100604601 | 100700479 |
a0012c0014t0001 | 0/0 | 3128 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | ACTTT others(3123): Show |
chr3 | 100604601 | 100700479 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0006g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0001t0007g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0005t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0005t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0005t0008g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0008t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0008t0009g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0010t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0001c0011t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0002c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0003c0003t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0004c0004t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0004c0004t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0004c0004t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0004c0004t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0004c0009t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0004c0009t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0005c0006t0001g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0005c0006t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0005c0006t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0006c0007t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0006c0007t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0006c0007t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0007c0016t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0008c0017t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0009c0012t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0010c0015t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0011c0013t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
a0012c0014t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | GBR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0101 | EUR | GBR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0219 | EUR | GBR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG00140 | hp2 | a0001 | c0001 | t0006 | g0204 | EUR | GBR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG00280 | hp1 | a0001 | c0005 | t0008 | g0106 | EUR | FIN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0073 | EUR | FIN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0269 | EAS | CHS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | CHS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG00597 | hp1 | a0003 | c0003 | t0001 | g0136 | EAS | CHS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | CHS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0281 | EAS | CHS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG00735 | hp2 | a0004 | c0009 | t0002 | g0049 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG00741 | hp2 | a0003 | c0003 | t0001 | g0244 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01071 | hp2 | a0003 | c0003 | t0001 | g0131 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01074 | hp1 | a0003 | c0003 | t0001 | g0132 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01081 | hp2 | a0003 | c0003 | t0001 | g0140 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0262 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01109 | hp2 | a0003 | c0003 | t0001 | g0147 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01167 | hp1 | a0003 | c0003 | t0001 | g0142 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0293 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01168 | hp1 | a0003 | c0003 | t0001 | g0146 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01243 | hp2 | a0003 | c0003 | t0001 | g0141 | AMR | PUR | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0015 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01256 | hp2 | a0003 | c0003 | t0001 | g0020 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01257 | hp1 | a0003 | c0003 | t0001 | g0009 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01258 | hp2 | a0003 | c0003 | t0001 | g0019 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0258 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0301 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01433 | hp2 | a0003 | c0003 | t0001 | g0021 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0015 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01496 | hp2 | a0003 | c0003 | t0001 | g0143 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01515 | hp1 | a0003 | c0003 | t0001 | g0148 | EUR | IBS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0277 | EUR | IBS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0080 | EUR | IBS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | IBS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0079 | EUR | IBS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0276 | EUR | IBS | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01891 | hp1 | a0002 | c0002 | t0001 | g0308 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01928 | hp2 | a0002 | c0002 | t0001 | g0272 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0279 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01943 | hp2 | a0003 | c0003 | t0001 | g0133 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01975 | hp2 | a0005 | c0006 | t0001 | g0006 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0294 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0260 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02055 | hp2 | a0003 | c0003 | t0001 | g0026 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02145 | hp2 | a0003 | c0003 | t0001 | g0245 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02165 | hp1 | a0003 | c0003 | t0001 | g0099 | EAS | CDX | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0304 | EAS | CDX | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02257 | hp1 | a0001 | c0008 | t0009 | g0036 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0168 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0261 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02280 | hp2 | a0003 | c0003 | t0001 | g0029 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02300 | hp1 | a0007 | c0016 | t0001 | g0144 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02300 | hp2 | a0002 | c0002 | t0001 | g0287 | AMR | PEL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02451 | hp1 | a0001 | c0011 | t0001 | g0060 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0300 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02523 | hp2 | a0008 | c0017 | t0001 | g0138 | EAS | KHV | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02602 | hp2 | a0003 | c0003 | t0001 | g0252 | SAS | PJL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02615 | hp1 | a0004 | c0009 | t0002 | g0069 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0312 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02630 | hp1 | a0006 | c0007 | t0004 | g0044 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02630 | hp2 | a0003 | c0003 | t0001 | g0009 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02647 | hp1 | a0002 | c0002 | t0001 | g0071 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02683 | hp1 | a0003 | c0003 | t0001 | g0134 | SAS | PJL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02698 | hp2 | a0003 | c0003 | t0001 | g0253 | SAS | PJL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02723 | hp2 | a0010 | c0015 | t0001 | g0024 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02735 | hp1 | a0003 | c0003 | t0001 | g0139 | SAS | PJL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02886 | hp1 | a0001 | c0001 | t0007 | g0299 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02895 | hp2 | a0001 | c0005 | t0001 | g0007 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0108 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02897 | hp1 | a0001 | c0005 | t0001 | g0007 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02922 | hp1 | a0003 | c0003 | t0001 | g0243 | AFR | ESN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0169 | AFR | ESN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0306 | AFR | ESN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02970 | hp1 | a0005 | c0006 | t0001 | g0030 | AFR | ESN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | ESN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03041 | hp2 | a0004 | c0004 | t0002 | g0022 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03098 | hp2 | a0005 | c0006 | t0001 | g0006 | AFR | MSL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | ESN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03195 | hp2 | a0003 | c0003 | t0001 | g0130 | AFR | ESN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0307 | AFR | MSL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03225 | hp2 | a0001 | c0008 | t0001 | g0041 | AFR | MSL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03239 | hp2 | a0003 | c0003 | t0001 | g0129 | SAS | PJL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03453 | hp1 | a0001 | c0005 | t0001 | g0070 | AFR | MSL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03453 | hp2 | a0004 | c0004 | t0002 | g0038 | AFR | MSL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03486 | hp2 | a0003 | c0003 | t0003 | g0025 | AFR | MSL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03516 | hp2 | a0006 | c0007 | t0004 | g0042 | AFR | ESN | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0311 | AFR | GWD | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0126 | AFR | MSL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03579 | hp2 | a0001 | c0001 | t0005 | g0072 | AFR | MSL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03654 | hp2 | a0003 | c0003 | t0001 | g0251 | SAS | PJL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | BEB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03834 | hp2 | a0003 | c0003 | t0001 | g0135 | SAS | BEB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | BEB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0263 | SAS | BEB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0264 | SAS | STU | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | STU | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | STU | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | STU | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | YRI | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18522 | hp2 | a0005 | c0006 | t0001 | g0031 | AFR | YRI | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0275 | EAS | CHB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CHB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | YRI | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | YRI | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0286 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0290 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0297 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0284 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18970 | hp1 | a0011 | c0013 | t0001 | g0190 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0283 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18974 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0313 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0298 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18986 | hp2 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18987 | hp2 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18990 | hp2 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0303 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18995 | hp1 | a0012 | c0014 | t0001 | g0278 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0305 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19003 | hp2 | a0002 | c0002 | t0001 | g0296 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19006 | hp1 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | LWK | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | LWK | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19043 | hp1 | a0003 | c0003 | t0001 | g0028 | AFR | LWK | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | LWK | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19055 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19055 | hp2 | a0003 | c0003 | t0001 | g0137 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19062 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0282 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0280 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19077 | hp2 | a0003 | c0003 | t0001 | g0149 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0289 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0302 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0288 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19240 | hp1 | a0001 | c0010 | t0001 | g0039 | AFR | YRI | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0310 | AFR | YRI | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ASW | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ASW | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0213 | EUR | TSI | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | TSI | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0212 | EUR | TSI | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA20805 | hp2 | a0003 | c0003 | t0001 | g0145 | EUR | TSI | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | GIH | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | GIH | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02109 | hp1 | a0006 | c0007 | t0004 | g0043 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02486 | hp2 | a0004 | c0004 | t0002 | g0040 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0167 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG02559 | hp2 | a0009 | c0012 | t0001 | g0067 | AFR | ACB | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0309 | AFR | MSL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
HG03471 | hp2 | a0004 | c0004 | t0002 | g0037 | AFR | MSL | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18955 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | USA | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | USA | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0155 | REF | REF | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0051 | REF | REF | ADGRG7_chr3_100604601_100700479 | ADGRG7 | chr3 | 100604601 | 100700479 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:100635680 | A | G | 3 | a0003 a0007 a0008 |
37 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(34): Show |
missense_variant | MODERATE | c.451A>G | p.Lys151Glu | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/16 | 707/3128 | 451/2394 | 151/797 | chr3 | 100635680 | |||
chr3:100635812 | A | G | 1 | a0010 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.583A>G | p.Asn195Asp | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/16 | 839/3128 | 583/2394 | 195/797 | chr3 | 100635812 | |||
chr3:100643628 | C | T | 1 | a0012 | 1 | NA18995.hp1 | missense_variant | MODERATE | c.941C>T | p.Thr314Met | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/16 | 1197/3128 | 941/2394 | 314/797 | chr3 | 100643628 | |||
chr3:100646070 | G | A | 1 | a0007 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.1072G>A | p.Asp358Asn | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 9/16 | 1328/3128 | 1072/2394 | 358/797 | chr3 | 100646070 | |||
chr3:100649702 | A | G | 2 | a0002 a0012 |
75 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(72): Show |
missense_variant | MODERATE | c.1274A>G | p.Lys425Arg | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/16 | 1530/3128 | 1274/2394 | 425/797 | chr3 | 100649702 | |||
chr3:100654863 | G | A | 1 | a0009 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.1408G>A | p.Val470Ile | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 12/16 | 1664/3128 | 1408/2394 | 470/797 | chr3 | 100654863 | |||
chr3:100655922 | A | G | 1 | a0008 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.1750A>G | p.Ile584Val | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/16 | 2006/3128 | 1750/2394 | 584/797 | chr3 | 100655922 | |||
chr3:100659797 | A | T | 1 | a0006 | 3 | HG02109.hp1 HG02630.hp1 HG03516.hp2 |
missense_variant | MODERATE | c.1933A>T | p.Thr645Ser | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/16 | 2189/3128 | 1933/2394 | 645/797 | chr3 | 100659797 | |||
chr3:100659833 | A | C | 1 | a0011 | 1 | NA18970.hp1 | missense_variant | MODERATE | c.1969A>C | p.Asn657His | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/16 | 2225/3128 | 1969/2394 | 657/797 | chr3 | 100659833 | |||
chr3:100694874 | G | A | 2 | a0004 a0006 |
9 | HG00735.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
missense_variant | MODERATE | c.2267G>A | p.Arg756His | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 16/16 | 2523/3128 | 2267/2394 | 756/797 | chr3 | 100694874 | |||
chr3:100694910 | C | A | 1 | a0005 | 4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
missense_variant | MODERATE | c.2303C>A | p.Thr768Asn | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 16/16 | 2559/3128 | 2303/2394 | 768/797 | chr3 | 100694910 | |||
chr3:100694916 | A | G | 1 | a0005 | 4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
missense_variant | MODERATE | c.2309A>G | p.His770Arg | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 16/16 | 2565/3128 | 2309/2394 | 770/797 | chr3 | 100694916 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:100609889 | G | C | 4 | a0001c0008 a0001c0010 a0004c0004 others(1): Show |
10 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(7): Show |
synonymous_variant | LOW | c.33G>C | p.Val11Val | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/16 | 289/3128 | 33/2394 | 11/797 | chr3 | 100609889 | |||
chr3:100643317 | G | A | 1 | a0001c0010 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.750G>A | p.Val250Val | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 7/16 | 1006/3128 | 750/2394 | 250/797 | chr3 | 100643317 | |||
chr3:100646628 | G | A | 1 | a0001c0011 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.1170G>A | p.Ala390Ala | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/16 | 1426/3128 | 1170/2394 | 390/797 | chr3 | 100646628 | |||
chr3:100655966 | G | A | 1 | a0001c0005 | 4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
synonymous_variant | LOW | c.1794G>A | p.Gln598Gln | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/16 | 2050/3128 | 1794/2394 | 598/797 | chr3 | 100655966 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:100609682 | A | G | 1 | a0001c0008t0009 | 1 | HG02257.hp1 | 5_prime_UTR_variant | MODIFIER | c.-175A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/16 | 175 | chr3 | 100609682 | ||||||
chr3:100609716 | C | T | 1 | a0001c0005t0008 | 1 | HG00280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-141C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/16 | 141 | chr3 | 100609716 | ||||||
chr3:100609779 | C | T | 1 | a0001c0005t0008 | 1 | HG00280.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-78C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/16 | chr3 | 100609779 | |||||||
chr3:100609783 | T | C | 1 | a0001c0001t0005 | 1 | HG03579.hp2 | 5_prime_UTR_variant | MODIFIER | c.-74T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/16 | 74 | chr3 | 100609783 | ||||||
chr3:100609797 | C | G | 1 | a0001c0001t0007 | 1 | HG02886.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-60C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/16 | chr3 | 100609797 | |||||||
chr3:100695137 | G | C | 4 | a0001c0001t0002 a0004c0004t0002 a0004c0009t0002 others(1): Show |
11 | HG00735.hp2 HG02109.hp1 HG02486.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*136G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 16/16 | 136 | chr3 | 100695137 | ||||||
chr3:100695199 | C | G | 1 | a0001c0001t0006 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*198C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 16/16 | 198 | chr3 | 100695199 | ||||||
chr3:100695263 | C | A | 2 | a0001c0001t0003 a0003c0003t0003 |
7 | HG02258.hp1 HG02559.hp1 HG02896.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*262C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 16/16 | 262 | chr3 | 100695263 | ||||||
chr3:100695274 | A | G | 1 | a0006c0007t0004 | 3 | HG02109.hp1 HG02630.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*273A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 16/16 | 273 | chr3 | 100695274 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:100610207 | T | G | 3 | a0003c0003t0001g0019 a0003c0003t0001g0020 a0003c0003t0001g0021 |
3 | HG01256.hp2 HG01258.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.115+236T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100610207 | |||||||
chr3:100610356 | A | G | 264 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(261): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.115+385A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100610356 | |||||||
chr3:100610408 | A | G | 1 | a0001c0001t0001g0315 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.115+437A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100610408 | |||||||
chr3:100610482 | C | A | 3 | a0001c0005t0001g0007 a0001c0005t0001g0070 a0004c0009t0002g0069 |
4 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+511C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100610482 | |||||||
chr3:100610501 | C | A | 1 | a0002c0002t0001g0071 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.115+530C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100610501 | |||||||
chr3:100610593 | G | C | 3 | a0001c0005t0001g0007 a0001c0005t0001g0070 a0004c0009t0002g0069 |
4 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+622G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100610593 | |||||||
chr3:100610635 | A | G | 1 | a0001c0001t0001g0314 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.115+664A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100610635 | |||||||
chr3:100610646 | C | T | 2 | a0002c0002t0001g0018 a0002c0002t0001g0313 |
3 | NA18961.hp1 NA18966.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.115+675C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100610646 | |||||||
chr3:100610915 | G | C | 289 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(286): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.115+944G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100610915 | |||||||
chr3:100610985 | C | T | 3 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0009c0012t0001g0067 |
3 | HG02559.hp2 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.115+1014C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100610985 | |||||||
chr3:100611043 | G | A | 1 | a0004c0004t0002g0022 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.115+1072G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611043 | |||||||
chr3:100611171 | T | C | 1 | a0001c0001t0005g0072 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.115+1200T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611171 | |||||||
chr3:100611243 | T | TTTTCCTT others(1): Show |
25 | a0001c0001t0001g0010 a0001c0001t0001g0162 a0001c0001t0001g0163 others(22): Show |
26 | HG00438.hp1 HG00544.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.115+1273_115+1280d others(10): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100611243 | ||||||
chr3:100611244 | T | TTTCC | 7 | a0001c0001t0001g0005 a0001c0001t0001g0046 a0001c0001t0001g0047 others(4): Show |
8 | HG00735.hp2 HG01106.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.115+1328_115+1331d others(6): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100611244 | ||||||
chr3:100611244 | T | TTTCCTTC others(1): Show |
3 | a0001c0001t0001g0023 a0001c0001t0001g0045 a0001c0001t0001g0066 |
3 | HG01952.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.115+1324_115+1331d others(10): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100611244 | ||||||
chr3:100611244 | T | TTTCCTTC others(5): Show |
6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG00423.hp1 HG01168.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.115+1280_115+1281i others(14): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100611244 | ||||||
chr3:100611244 | TTTCC | T | 10 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0063 others(7): Show |
13 | HG01884.hp1 HG01975.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.115+1328_115+1331d others(6): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100611244 | ||||||
chr3:100611244 | TTTCCTTC others(5): Show |
T | 1 | a0001c0001t0001g0032 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.115+1320_115+1331d others(14): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100611244 | ||||||
chr3:100611244 | TTTCCTTC others(9): Show |
T | 8 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0003g0033 others(5): Show |
8 | HG02145.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.115+1316_115+1331d others(18): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100611244 | ||||||
chr3:100611244 | TTTCCTTC others(13): Show |
T | 4 | a0001c0008t0001g0041 a0006c0007t0004g0042 a0006c0007t0004g0043 others(1): Show |
4 | HG02109.hp1 HG02630.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.115+1312_115+1331d others(22): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100611244 | ||||||
chr3:100611248 | C | CTTCT | 81 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0073 others(78): Show |
85 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.115+1280_115+1281i others(6): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100611248 | ||||||
chr3:100611252 | C | T | 148 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0153 others(145): Show |
164 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.115+1281C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611252 | |||||||
chr3:100611253 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.115+1282T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611253 | |||||||
chr3:100611257 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.115+1286T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611257 | |||||||
chr3:100611283 | C | CCTTCCTT others(5): Show |
1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115+1323_115+1324i others(14): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100611283 | ||||||
chr3:100611283 | C | T | 12 | a0002c0002t0001g0071 a0002c0002t0001g0302 a0002c0002t0001g0303 others(9): Show |
12 | HG01891.hp1 HG02165.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.115+1312C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611283 | |||||||
chr3:100611287 | C | T | 46 | a0001c0001t0001g0273 a0001c0001t0001g0295 a0001c0001t0007g0299 others(43): Show |
59 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.115+1316C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611287 | |||||||
chr3:100611291 | C | T | 15 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(12): Show |
15 | HG01099.hp1 HG01346.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.115+1320C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611291 | |||||||
chr3:100611291 | CCTTCCTT others(5): Show |
C | 12 | a0002c0002t0001g0071 a0002c0002t0001g0302 a0002c0002t0001g0303 others(9): Show |
12 | HG01891.hp1 HG02165.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.115+1325_115+1336d others(14): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100611291 | ||||||
chr3:100611295 | C | CCTTCCTT others(3): Show |
1 | a0001c0001t0001g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.115+1331_115+1332i others(12): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100611295 | ||||||
chr3:100611295 | C | T | 60 | a0001c0001t0001g0073 a0001c0001t0001g0107 a0001c0001t0001g0109 others(57): Show |
62 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.115+1324C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611295 | |||||||
chr3:100611295 | CCTTCCTT others(1): Show |
C | 46 | a0001c0001t0001g0273 a0001c0001t0001g0295 a0001c0001t0007g0299 others(43): Show |
59 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.115+1329_115+1336d others(10): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100611295 | ||||||
chr3:100611296 | C | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115+1325C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611296 | |||||||
chr3:100611299 | CCTTT | C | 18 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(15): Show |
18 | HG01099.hp1 HG01346.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.115+1332_115+1335d others(6): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100611299 | ||||||
chr3:100611303 | T | C | 64 | a0001c0001t0001g0073 a0001c0001t0001g0107 a0001c0001t0001g0109 others(61): Show |
66 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.115+1332T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611303 | |||||||
chr3:100611303 | T | TCTTCCTT others(1): Show |
124 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(121): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.115+1336_115+1337i others(10): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100611303 | ||||||
chr3:100611345 | G | A | 164 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(161): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.115+1374G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611345 | |||||||
chr3:100611358 | T | C | 1 | a0001c0001t0005g0072 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.115+1387T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611358 | |||||||
chr3:100611734 | G | A | 6 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0003c0003t0001g0026 others(3): Show |
6 | HG01952.hp1 HG02055.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.115+1763G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611734 | |||||||
chr3:100611914 | T | C | 1 | a0002c0002t0001g0265 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.115+1943T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611914 | |||||||
chr3:100611936 | T | A | 250 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(247): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.115+1965T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100611936 | |||||||
chr3:100612052 | T | C | 7 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(4): Show |
7 | HG00438.hp1 HG02080.hp2 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.115+2081T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100612052 | |||||||
chr3:100612110 | G | T | 58 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0032 others(55): Show |
60 | HG00280.hp1 HG00597.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.115+2139G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100612110 | |||||||
chr3:100612164 | A | T | 1 | a0002c0002t0001g0301 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.115+2193A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100612164 | |||||||
chr3:100612201 | G | T | 1 | a0001c0001t0001g0242 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.115+2230G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100612201 | |||||||
chr3:100612317 | T | C | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115+2346T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100612317 | |||||||
chr3:100612467 | T | C | 3 | a0001c0005t0001g0007 a0001c0005t0001g0070 a0004c0009t0002g0069 |
4 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+2496T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100612467 | |||||||
chr3:100612680 | C | T | 3 | a0001c0005t0001g0007 a0001c0005t0001g0070 a0004c0009t0002g0069 |
4 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+2709C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100612680 | |||||||
chr3:100612913 | A | T | 287 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(284): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.115+2942A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100612913 | |||||||
chr3:100612922 | A | G | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115+2951A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100612922 | |||||||
chr3:100612992 | C | T | 11 | a0001c0005t0008g0106 a0001c0008t0001g0041 a0001c0008t0009g0036 others(8): Show |
11 | HG00280.hp1 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.115+3021C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100612992 | |||||||
chr3:100613060 | G | A | 1 | a0002c0002t0001g0071 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.115+3089G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100613060 | |||||||
chr3:100613060 | G | T | 61 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0032 others(58): Show |
64 | HG00280.hp1 HG00597.hp1 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.115+3089G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100613060 | |||||||
chr3:100613142 | G | A | 3 | a0001c0005t0001g0007 a0001c0005t0001g0070 a0004c0009t0002g0069 |
4 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+3171G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100613142 | |||||||
chr3:100613169 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0153 |
2 | HG00280.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.115+3198C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100613169 | |||||||
chr3:100613538 | TA | T | 169 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(166): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.115+3580delA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100613538 | ||||||
chr3:100613539 | A | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115+3568A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100613539 | |||||||
chr3:100613588 | T | A | 3 | a0001c0005t0001g0007 a0001c0005t0001g0070 a0004c0009t0002g0069 |
4 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+3617T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100613588 | |||||||
chr3:100613697 | G | A | 5 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0003c0003t0001g0026 others(2): Show |
5 | HG01952.hp1 HG02055.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+3726G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100613697 | |||||||
chr3:100613747 | AT | A | 3 | a0001c0005t0001g0007 a0001c0005t0001g0070 a0004c0009t0002g0069 |
4 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+3781delT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100613747 | ||||||
chr3:100613794 | C | T | 7 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.115+3823C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100613794 | |||||||
chr3:100614554 | G | A | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115+4583G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100614554 | |||||||
chr3:100614589 | C | T | 1 | a0003c0003t0001g0149 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.115+4618C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100614589 | |||||||
chr3:100614630 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.115+4659A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100614630 | |||||||
chr3:100614692 | C | T | 160 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(157): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.115+4721C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100614692 | |||||||
chr3:100614852 | T | A | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.115+4881T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100614852 | |||||||
chr3:100614870 | G | A | 1 | a0002c0002t0001g0302 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.115+4899G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100614870 | |||||||
chr3:100614969 | T | C | 10 | a0002c0002t0001g0004 a0002c0002t0001g0013 a0002c0002t0001g0266 others(7): Show |
13 | HG00423.hp2 HG01928.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.115+4998T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100614969 | |||||||
chr3:100615011 | C | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115+5040C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615011 | |||||||
chr3:100615038 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.115+5067C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615038 | |||||||
chr3:100615104 | C | G | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.115+5133C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615104 | |||||||
chr3:100615137 | G | A | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.115+5166G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615137 | |||||||
chr3:100615205 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.115+5234G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615205 | |||||||
chr3:100615252 | A | G | 1 | a0002c0002t0001g0300 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.115+5281A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615252 | |||||||
chr3:100615252 | A | T | 1 | a0001c0001t0001g0241 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.115+5281A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615252 | |||||||
chr3:100615313 | C | A | 1 | a0001c0001t0001g0077 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.115+5342C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615313 | |||||||
chr3:100615369 | G | T | 2 | a0001c0001t0001g0066 a0009c0012t0001g0067 |
2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.115+5398G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615369 | |||||||
chr3:100615378 | G | T | 1 | a0002c0002t0001g0264 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.115+5407G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615378 | |||||||
chr3:100615412 | T | C | 58 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0032 others(55): Show |
60 | HG00280.hp1 HG00597.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.115+5441T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615412 | |||||||
chr3:100615635 | G | A | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115+5664G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615635 | |||||||
chr3:100615681 | A | G | 161 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(158): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.115+5710A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615681 | |||||||
chr3:100615688 | T | C | 1 | a0001c0001t0005g0072 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.115+5717T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615688 | |||||||
chr3:100615690 | G | A | 57 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0032 others(54): Show |
59 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(56): Show |
intron_variant | MODIFIER | c.115+5719G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615690 | |||||||
chr3:100615724 | A | T | 161 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(158): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.115+5753A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615724 | |||||||
chr3:100615736 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.115+5765T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615736 | |||||||
chr3:100615799 | C | G | 61 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0032 others(58): Show |
64 | HG00280.hp1 HG00597.hp1 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.115+5828C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615799 | |||||||
chr3:100615872 | G | T | 1 | a0001c0001t0001g0240 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.115+5901G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615872 | |||||||
chr3:100615967 | G | A | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.115+5996G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100615967 | |||||||
chr3:100616019 | C | T | 1 | a0002c0002t0001g0071 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.115+6048C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100616019 | |||||||
chr3:100616244 | A | G | 31 | a0003c0003t0001g0009 a0003c0003t0001g0019 a0003c0003t0001g0020 others(28): Show |
32 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.115+6273A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100616244 | |||||||
chr3:100616332 | C | A | 292 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(289): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.115+6361C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100616332 | |||||||
chr3:100616335 | C | T | 289 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(286): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.115+6364C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100616335 | |||||||
chr3:100616406 | A | T | 13 | a0003c0003t0001g0019 a0003c0003t0001g0020 a0003c0003t0001g0021 others(10): Show |
13 | HG01109.hp2 HG01167.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.115+6435A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100616406 | |||||||
chr3:100616675 | A | G | 58 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0032 others(55): Show |
60 | HG00280.hp1 HG00597.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.115+6704A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100616675 | |||||||
chr3:100616721 | T | C | 1 | a0003c0003t0001g0141 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.115+6750T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100616721 | |||||||
chr3:100616753 | G | A | 10 | a0001c0008t0001g0041 a0001c0008t0009g0036 a0001c0010t0001g0039 others(7): Show |
10 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.115+6782G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100616753 | |||||||
chr3:100616762 | A | C | 12 | a0001c0001t0001g0002 a0001c0001t0001g0045 a0001c0001t0001g0056 others(9): Show |
14 | HG00735.hp2 HG01884.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.115+6791A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100616762 | |||||||
chr3:100616786 | A | T | 1 | a0001c0001t0005g0072 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.115+6815A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100616786 | |||||||
chr3:100617012 | A | G | 1 | a0011c0013t0001g0190 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.115+7041A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100617012 | |||||||
chr3:100617083 | T | C | 4 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(1): Show |
4 | HG02145.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+7112T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100617083 | |||||||
chr3:100617121 | A | C | 1 | a0001c0001t0001g0185 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.115+7150A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100617121 | |||||||
chr3:100617371 | C | T | 3 | a0001c0001t0001g0105 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | HG00099.hp1 HG01192.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.115+7400C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100617371 | |||||||
chr3:100617462 | A | G | 54 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0032 others(51): Show |
56 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(53): Show |
intron_variant | MODIFIER | c.115+7491A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100617462 | |||||||
chr3:100617517 | G | A | 4 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(1): Show |
4 | HG02145.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+7546G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100617517 | |||||||
chr3:100617616 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.115+7645G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100617616 | |||||||
chr3:100617651 | T | G | 160 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(157): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.115+7680T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100617651 | |||||||
chr3:100617696 | G | A | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115+7725G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100617696 | |||||||
chr3:100617747 | G | C | 1 | a0001c0008t0009g0036 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.115+7776G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100617747 | |||||||
chr3:100617894 | C | A | 4 | a0001c0005t0001g0007 a0001c0005t0001g0070 a0001c0005t0008g0106 others(1): Show |
5 | HG00280.hp1 HG02615.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.115+7923C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100617894 | |||||||
chr3:100617900 | C | T | 3 | a0001c0005t0001g0007 a0001c0005t0001g0070 a0004c0009t0002g0069 |
4 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+7929C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100617900 | |||||||
chr3:100617920 | GA | G | 3 | a0001c0005t0001g0007 a0001c0005t0001g0070 a0004c0009t0002g0069 |
4 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+7951delA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100617920 | ||||||
chr3:100617977 | C | T | 1 | a0002c0002t0001g0272 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.115+8006C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100617977 | |||||||
chr3:100617978 | A | G | 65 | a0001c0001t0001g0273 a0001c0001t0001g0295 a0001c0001t0007g0299 others(62): Show |
78 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.115+8007A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100617978 | |||||||
chr3:100618042 | C | T | 37 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0003c0003t0001g0009 others(34): Show |
38 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.115+8071C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618042 | |||||||
chr3:100618045 | T | C | 287 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(284): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.115+8074T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618045 | |||||||
chr3:100618047 | G | A | 65 | a0001c0001t0001g0273 a0001c0001t0001g0295 a0001c0001t0007g0299 others(62): Show |
78 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.115+8076G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618047 | |||||||
chr3:100618076 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.115+8105T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618076 | |||||||
chr3:100618145 | A | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0233 a0001c0001t0001g0234 others(3): Show |
7 | HG02129.hp1 NA18960.hp2 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+8174A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618145 | |||||||
chr3:100618155 | A | G | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.115+8184A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618155 | |||||||
chr3:100618260 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.115+8289C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618260 | |||||||
chr3:100618273 | C | A | 54 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0032 others(51): Show |
56 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(53): Show |
intron_variant | MODIFIER | c.115+8302C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618273 | |||||||
chr3:100618274 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.115+8303G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618274 | |||||||
chr3:100618339 | T | TA | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.115+8369dupA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100618339 | ||||||
chr3:100618398 | G | T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0180 a0001c0001t0001g0181 others(5): Show |
9 | NA18946.hp2 NA18960.hp1 NA18966.hp2 others(6): Show |
intron_variant | MODIFIER | c.115+8427G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618398 | |||||||
chr3:100618414 | T | C | 287 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(284): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.115+8443T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618414 | |||||||
chr3:100618433 | T | A | 2 | a0001c0001t0001g0242 a0001c0005t0008g0106 |
2 | HG00280.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.115+8462T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618433 | |||||||
chr3:100618434 | C | T | 2 | a0001c0001t0001g0242 a0001c0005t0008g0106 |
2 | HG00280.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.115+8463C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618434 | |||||||
chr3:100618449 | C | T | 1 | a0003c0003t0001g0149 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.115+8478C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618449 | |||||||
chr3:100618534 | A | C | 292 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(289): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.115+8563A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618534 | |||||||
chr3:100618535 | G | A | 3 | a0002c0002t0001g0302 a0002c0002t0001g0304 a0002c0002t0001g0305 |
3 | HG02165.hp2 NA18999.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.115+8564G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618535 | |||||||
chr3:100618570 | T | G | 7 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.115+8599T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618570 | |||||||
chr3:100618612 | T | G | 1 | a0001c0001t0001g0273 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.115+8641T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618612 | |||||||
chr3:100618655 | C | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(1): Show |
4 | HG02145.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+8684C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618655 | |||||||
chr3:100618669 | C | G | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115+8698C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618669 | |||||||
chr3:100618694 | A | G | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.115+8723A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618694 | |||||||
chr3:100618765 | G | C | 51 | a0001c0001t0001g0295 a0002c0002t0001g0001 a0002c0002t0001g0004 others(48): Show |
64 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.115+8794G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618765 | |||||||
chr3:100618787 | G | GA | 58 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0032 others(55): Show |
60 | HG00280.hp1 HG00597.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.115+8817dupA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100618787 | ||||||
chr3:100618909 | G | A | 3 | a0005c0006t0001g0006 a0005c0006t0001g0030 a0005c0006t0001g0031 |
4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.115+8938G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100618909 | |||||||
chr3:100619084 | G | C | 1 | a0001c0001t0001g0008 | 2 | NA18969.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.115+9113G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100619084 | |||||||
chr3:100619299 | G | A | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115+9328G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100619299 | |||||||
chr3:100619315 | A | C | 1 | a0002c0002t0001g0071 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.115+9344A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100619315 | |||||||
chr3:100619378 | C | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115+9407C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100619378 | |||||||
chr3:100619396 | A | T | 1 | a0010c0015t0001g0024 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.115+9425A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100619396 | |||||||
chr3:100619470 | T | G | 12 | a0001c0001t0001g0002 a0001c0001t0001g0045 a0001c0001t0001g0056 others(9): Show |
14 | HG00735.hp2 HG01884.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.115+9499T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100619470 | |||||||
chr3:100619540 | C | T | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.115+9569C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100619540 | |||||||
chr3:100619592 | C | A | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115+9621C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100619592 | |||||||
chr3:100619622 | G | T | 37 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0003c0003t0001g0009 others(34): Show |
38 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.115+9651G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100619622 | |||||||
chr3:100619656 | G | A | 2 | a0001c0001t0001g0164 a0001c0001t0001g0240 |
2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.115+9685G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100619656 | |||||||
chr3:100619765 | G | A | 12 | a0003c0003t0001g0019 a0003c0003t0001g0020 a0003c0003t0001g0021 others(9): Show |
12 | HG01109.hp2 HG01167.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.115+9794G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100619765 | |||||||
chr3:100619780 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.115+9809C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100619780 | |||||||
chr3:100619828 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.116-9770G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100619828 | |||||||
chr3:100620022 | A | T | 47 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0008t0001g0041 others(44): Show |
48 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.116-9576A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620022 | |||||||
chr3:100620024 | T | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0153 |
2 | HG00280.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.116-9574T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620024 | |||||||
chr3:100620048 | G | A | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.116-9550G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620048 | |||||||
chr3:100620136 | G | A | 7 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.116-9462G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620136 | |||||||
chr3:100620358 | G | A | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.116-9240G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620358 | |||||||
chr3:100620392 | A | G | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.116-9206A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620392 | |||||||
chr3:100620445 | T | C | 60 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0032 others(57): Show |
63 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.116-9153T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620445 | |||||||
chr3:100620537 | T | C | 3 | a0001c0005t0001g0007 a0001c0005t0001g0070 a0004c0009t0002g0069 |
4 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-9061T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620537 | |||||||
chr3:100620617 | G | C | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.116-8981G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620617 | |||||||
chr3:100620744 | C | T | 32 | a0003c0003t0001g0009 a0003c0003t0001g0019 a0003c0003t0001g0020 others(29): Show |
33 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.116-8854C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620744 | |||||||
chr3:100620832 | TG | T | 47 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0008t0001g0041 others(44): Show |
48 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.116-8765delG | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620832 | |||||||
chr3:100620864 | G | A | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.116-8734G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620864 | |||||||
chr3:100620912 | G | T | 7 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.116-8686G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620912 | |||||||
chr3:100620917 | C | T | 2 | a0002c0002t0001g0297 a0002c0002t0001g0298 |
2 | NA18950.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.116-8681C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620917 | |||||||
chr3:100620923 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.116-8675A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620923 | |||||||
chr3:100620992 | G | C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.116-8606G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100620992 | |||||||
chr3:100621097 | G | T | 1 | a0001c0001t0001g0237 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.116-8501G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100621097 | |||||||
chr3:100621184 | G | A | 54 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0032 others(51): Show |
56 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(53): Show |
intron_variant | MODIFIER | c.116-8414G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100621184 | |||||||
chr3:100621279 | A | C | 1 | a0001c0001t0001g0229 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.116-8319A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100621279 | |||||||
chr3:100621301 | A | G | 60 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0032 others(57): Show |
63 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.116-8297A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100621301 | |||||||
chr3:100621304 | A | T | 9 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0107 others(6): Show |
9 | HG02027.hp2 NA18747.hp2 NA18964.hp1 others(6): Show |
intron_variant | MODIFIER | c.116-8294A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100621304 | |||||||
chr3:100621571 | G | A | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.116-8027G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100621571 | |||||||
chr3:100621612 | T | C | 3 | a0002c0002t0001g0018 a0002c0002t0001g0274 a0002c0002t0001g0313 |
4 | NA18961.hp1 NA18966.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.116-7986T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100621612 | |||||||
chr3:100621813 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.116-7785C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100621813 | |||||||
chr3:100621869 | T | G | 1 | a0002c0002t0001g0275 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.116-7729T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100621869 | |||||||
chr3:100621887 | C | A | 1 | a0001c0001t0001g0081 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.116-7711C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100621887 | |||||||
chr3:100621952 | C | T | 47 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0008t0001g0041 others(44): Show |
48 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.116-7646C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100621952 | |||||||
chr3:100621976 | C | G | 2 | a0001c0001t0001g0236 a0001c0001t0001g0237 |
2 | HG02129.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.116-7622C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100621976 | |||||||
chr3:100621983 | C | T | 10 | a0001c0008t0001g0041 a0001c0008t0009g0036 a0001c0010t0001g0039 others(7): Show |
10 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.116-7615C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100621983 | |||||||
chr3:100622008 | A | C | 1 | a0003c0003t0001g0140 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.116-7590A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100622008 | |||||||
chr3:100622053 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.116-7545C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100622053 | |||||||
chr3:100622264 | A | AT | 30 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0052 others(27): Show |
32 | HG00735.hp2 HG01099.hp1 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.116-7313dupT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100622264 | ||||||
chr3:100622264 | A | ATT | 50 | a0001c0001t0001g0045 a0001c0001t0001g0063 a0001c0001t0001g0295 others(47): Show |
63 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.116-7314_116-7313d others(4): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100622264 | ||||||
chr3:100622264 | ATTTT | A | 9 | a0001c0001t0001g0023 a0001c0001t0001g0150 a0001c0001t0001g0151 others(6): Show |
10 | HG01884.hp2 HG01891.hp2 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.116-7316_116-7313d others(6): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100622264 | ||||||
chr3:100622264 | ATTTTT | A | 38 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0034 others(35): Show |
40 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.116-7317_116-7313d others(7): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100622264 | ||||||
chr3:100622264 | ATTTTTT | A | 16 | a0001c0001t0001g0100 a0001c0001t0001g0164 a0001c0001t0001g0225 others(13): Show |
16 | HG01255.hp1 HG01496.hp2 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.116-7318_116-7313d others(8): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100622264 | ||||||
chr3:100622264 | ATTTTTTT | A | 155 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(152): Show |
161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.116-7319_116-7313d others(9): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100622264 | ||||||
chr3:100622291 | T | C | 7 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.116-7307T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100622291 | |||||||
chr3:100622353 | C | T | 3 | a0001c0005t0001g0007 a0001c0005t0001g0070 a0004c0009t0002g0069 |
4 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-7245C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100622353 | |||||||
chr3:100622355 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.116-7243T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100622355 | |||||||
chr3:100622460 | A | G | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.116-7138A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100622460 | |||||||
chr3:100622539 | A | G | 1 | a0001c0001t0003g0126 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.116-7059A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100622539 | |||||||
chr3:100622637 | C | A | 7 | a0001c0001t0001g0003 a0001c0001t0001g0165 a0001c0001t0001g0166 others(4): Show |
9 | HG00544.hp1 HG02080.hp1 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.116-6961C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100622637 | |||||||
chr3:100622720 | G | A | 2 | a0001c0001t0001g0164 a0001c0001t0001g0240 |
2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.116-6878G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100622720 | |||||||
chr3:100622721 | C | T | 1 | a0001c0005t0001g0070 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.116-6877C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100622721 | |||||||
chr3:100622768 | T | A | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.116-6830T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100622768 | |||||||
chr3:100622808 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.116-6790C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100622808 | |||||||
chr3:100622899 | G | A | 2 | a0001c0001t0001g0082 a0001c0005t0008g0106 |
2 | HG00280.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.116-6699G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100622899 | |||||||
chr3:100622928 | G | GT | 34 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(31): Show |
38 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.116-6658dupT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100622928 | ||||||
chr3:100622960 | G | A | 7 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.116-6638G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100622960 | |||||||
chr3:100622994 | C | A | 10 | a0001c0008t0001g0041 a0001c0008t0009g0036 a0001c0010t0001g0039 others(7): Show |
10 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.116-6604C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100622994 | |||||||
chr3:100623126 | A | G | 3 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0009c0012t0001g0067 |
3 | HG02559.hp2 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.116-6472A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100623126 | |||||||
chr3:100623136 | A | G | 61 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0032 others(58): Show |
64 | HG00280.hp1 HG00597.hp1 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.116-6462A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100623136 | |||||||
chr3:100623153 | T | G | 1 | a0002c0002t0001g0307 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.116-6445T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100623153 | |||||||
chr3:100623535 | A | T | 13 | a0001c0001t0001g0160 a0001c0008t0001g0041 a0001c0008t0009g0036 others(10): Show |
13 | HG01928.hp2 HG01993.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.116-6063A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100623535 | |||||||
chr3:100623543 | T | A | 1 | a0002c0002t0001g0302 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.116-6055T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100623543 | |||||||
chr3:100623568 | T | C | 4 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(1): Show |
4 | HG02145.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-6030T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100623568 | |||||||
chr3:100623612 | C | A | 3 | a0001c0001t0001g0045 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG02109.hp2 HG02258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.116-5986C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100623612 | |||||||
chr3:100623649 | C | G | 288 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(285): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.116-5949C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100623649 | |||||||
chr3:100623693 | C | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.116-5905C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100623693 | |||||||
chr3:100623723 | C | A | 1 | a0001c0001t0001g0226 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.116-5875C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100623723 | |||||||
chr3:100623751 | T | G | 4 | a0002c0002t0001g0306 a0002c0002t0001g0310 a0002c0002t0001g0311 others(1): Show |
4 | HG02615.hp2 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.116-5847T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100623751 | |||||||
chr3:100623864 | T | C | 2 | a0001c0001t0001g0105 a0001c0001t0001g0238 |
2 | HG00099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.116-5734T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100623864 | |||||||
chr3:100623945 | T | G | 3 | a0001c0001t0001g0105 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | HG00099.hp1 HG01192.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.116-5653T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100623945 | |||||||
chr3:100624255 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.116-5343T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100624255 | |||||||
chr3:100624447 | A | G | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.116-5151A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100624447 | |||||||
chr3:100624453 | A | C | 44 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0032 others(41): Show |
46 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.116-5145A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100624453 | |||||||
chr3:100624554 | T | C | 48 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0032 others(45): Show |
50 | HG00280.hp1 HG00597.hp1 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.116-5044T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100624554 | |||||||
chr3:100624640 | G | A | 1 | a0003c0003t0001g0029 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.116-4958G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100624640 | |||||||
chr3:100624910 | C | G | 1 | a0002c0002t0001g0296 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.116-4688C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100624910 | |||||||
chr3:100625211 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.116-4387T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100625211 | |||||||
chr3:100625237 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.116-4361G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100625237 | |||||||
chr3:100625255 | T | A | 3 | a0001c0001t0001g0083 a0001c0001t0001g0195 a0001c0001t0001g0241 |
3 | HG01123.hp2 HG01516.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.116-4343T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100625255 | |||||||
chr3:100625359 | T | C | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.116-4239T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100625359 | |||||||
chr3:100625394 | A | G | 160 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(157): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.116-4204A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100625394 | |||||||
chr3:100625400 | A | T | 286 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(283): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.116-4198A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100625400 | |||||||
chr3:100625487 | A | G | 44 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0032 others(41): Show |
46 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.116-4111A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100625487 | |||||||
chr3:100625502 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.116-4096A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100625502 | |||||||
chr3:100625617 | GAA | G | 37 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0003c0003t0001g0009 others(34): Show |
38 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.116-3979_116-3978d others(4): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100625617 | ||||||
chr3:100625879 | C | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.116-3719C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100625879 | |||||||
chr3:100625880 | A | G | 311 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(308): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.116-3718A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100625880 | |||||||
chr3:100625892 | G | A | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.116-3706G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100625892 | |||||||
chr3:100626161 | G | A | 7 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.116-3437G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100626161 | |||||||
chr3:100626181 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.116-3417A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100626181 | |||||||
chr3:100626193 | G | A | 3 | a0001c0001t0001g0081 a0001c0001t0001g0102 a0001c0001t0001g0196 |
3 | NA18953.hp2 NA18974.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.116-3405G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100626193 | |||||||
chr3:100626317 | C | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.116-3281C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100626317 | |||||||
chr3:100626357 | G | A | 44 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0032 others(41): Show |
46 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.116-3241G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100626357 | |||||||
chr3:100626455 | C | A | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.116-3143C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100626455 | |||||||
chr3:100626779 | C | T | 7 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.116-2819C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100626779 | |||||||
chr3:100627074 | G | A | 3 | a0001c0001t0001g0105 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | HG00099.hp1 HG01192.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.116-2524G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100627074 | |||||||
chr3:100627150 | C | A | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.116-2448C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100627150 | |||||||
chr3:100627291 | T | C | 3 | a0001c0001t0001g0081 a0001c0001t0001g0102 a0001c0001t0001g0196 |
3 | NA18953.hp2 NA18974.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.116-2307T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100627291 | |||||||
chr3:100627403 | G | A | 9 | a0003c0003t0001g0009 a0003c0003t0001g0129 a0003c0003t0001g0130 others(6): Show |
10 | HG01071.hp2 HG01074.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.116-2195G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100627403 | |||||||
chr3:100627544 | G | C | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.116-2054G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100627544 | |||||||
chr3:100627568 | G | C | 60 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0032 others(57): Show |
63 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.116-2030G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100627568 | |||||||
chr3:100627755 | A | G | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.116-1843A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100627755 | |||||||
chr3:100627813 | C | G | 2 | a0002c0002t0001g0263 a0002c0002t0001g0264 |
2 | HG03927.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.116-1785C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100627813 | |||||||
chr3:100627891 | C | G | 1 | a0001c0001t0001g0075 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.116-1707C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100627891 | |||||||
chr3:100627892 | C | T | 1 | a0003c0003t0001g0244 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.116-1706C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100627892 | |||||||
chr3:100628110 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.116-1488A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100628110 | |||||||
chr3:100628112 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.116-1486C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100628112 | |||||||
chr3:100628159 | C | T | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.116-1439C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100628159 | |||||||
chr3:100628269 | T | A | 40 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(37): Show |
42 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.116-1329T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100628269 | |||||||
chr3:100628292 | C | G | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.116-1306C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100628292 | |||||||
chr3:100628374 | G | GT | 56 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0046 others(53): Show |
57 | HG00597.hp1 HG00735.hp1 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.116-1214dupT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100628374 | ||||||
chr3:100628374 | G | GTT | 10 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
12 | HG01975.hp2 HG02145.hp1 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.116-1215_116-1214d others(4): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100628374 | ||||||
chr3:100628416 | T | C | 1 | a0002c0002t0001g0267 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.116-1182T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100628416 | |||||||
chr3:100628437 | C | A | 7 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.116-1161C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100628437 | |||||||
chr3:100628445 | G | A | 224 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(221): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.116-1153G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100628445 | |||||||
chr3:100628564 | C | G | 7 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.116-1034C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100628564 | |||||||
chr3:100628599 | G | A | 64 | a0001c0001t0001g0295 a0001c0001t0007g0299 a0002c0002t0001g0001 others(61): Show |
77 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.116-999G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100628599 | |||||||
chr3:100628619 | G | C | 1 | a0002c0002t0001g0306 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.116-979G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100628619 | |||||||
chr3:100628793 | C | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.116-805C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100628793 | |||||||
chr3:100628812 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.116-786C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100628812 | |||||||
chr3:100628874 | C | T | 3 | a0001c0001t0001g0081 a0001c0001t0001g0102 a0001c0001t0001g0196 |
3 | NA18953.hp2 NA18974.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.116-724C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100628874 | |||||||
chr3:100629092 | T | C | 1 | a0001c0001t0001g0085 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.116-506T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100629092 | |||||||
chr3:100629100 | G | C | 61 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0032 others(58): Show |
64 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.116-498G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100629100 | |||||||
chr3:100629118 | C | T | 1 | a0005c0006t0001g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.116-480C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100629118 | |||||||
chr3:100629251 | T | C | 2 | a0001c0005t0001g0070 a0004c0009t0002g0069 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.116-347T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100629251 | |||||||
chr3:100629267 | C | A | 1 | a0002c0002t0001g0279 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.116-331C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100629267 | |||||||
chr3:100629267 | C | CTCTA | 55 | a0001c0001t0001g0005 a0001c0001t0001g0045 a0001c0001t0001g0047 others(52): Show |
57 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.116-290_116-287dup others(4): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100629267 | ||||||
chr3:100629267 | C | CTCTATCT others(1): Show |
14 | a0001c0001t0001g0083 a0001c0001t0001g0121 a0001c0001t0001g0125 others(11): Show |
15 | HG00609.hp1 HG00735.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.116-294_116-287dup others(8): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100629267 | ||||||
chr3:100629267 | CTCTA | C | 42 | a0001c0001t0001g0010 a0001c0001t0001g0048 a0001c0001t0001g0059 others(39): Show |
43 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.116-290_116-287del others(4): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100629267 | ||||||
chr3:100629267 | CTCTATCT others(1): Show |
C | 36 | a0001c0001t0001g0027 a0001c0001t0001g0162 a0001c0001t0003g0167 others(33): Show |
37 | HG00438.hp1 HG00597.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.116-294_116-287del others(8): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100629267 | ||||||
chr3:100629267 | CTCTATCT others(5): Show |
C | 1 | a0001c0001t0001g0197 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.116-298_116-287del others(12): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 100629267 | ||||||
chr3:100629277 | C | G | 1 | a0001c0001t0001g0295 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.116-321C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100629277 | |||||||
chr3:100629322 | A | G | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.116-276A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100629322 | |||||||
chr3:100629514 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.116-84G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100629514 | |||||||
chr3:100629547 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.116-51A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 1/15 | chr3 | 100629547 | |||||||
chr3:100629957 | C | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.229+246C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 2/15 | chr3 | 100629957 | |||||||
chr3:100629958 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.229+247G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 2/15 | chr3 | 100629958 | |||||||
chr3:100629999 | C | T | 10 | a0001c0008t0001g0041 a0001c0008t0009g0036 a0001c0010t0001g0039 others(7): Show |
10 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.229+288C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 2/15 | chr3 | 100629999 | |||||||
chr3:100630044 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0064 |
4 | HG01884.hp1 HG02486.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.229+333C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 2/15 | chr3 | 100630044 | |||||||
chr3:100630186 | CAATT | C | 9 | a0001c0005t0008g0106 a0001c0008t0001g0041 a0004c0004t0002g0022 others(6): Show |
9 | HG00280.hp1 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.229+476_229+479del others(4): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 2/15 | chr3 | 100630186 | |||||||
chr3:100630274 | G | A | 1 | a0002c0002t0001g0071 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.230-431G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 2/15 | chr3 | 100630274 | |||||||
chr3:100630340 | T | G | 1 | a0003c0003t0001g0145 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.230-365T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 2/15 | chr3 | 100630340 | |||||||
chr3:100630343 | C | T | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.230-362C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 2/15 | chr3 | 100630343 | |||||||
chr3:100630345 | T | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0118 |
2 | HG00609.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.230-360T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 2/15 | chr3 | 100630345 | |||||||
chr3:100630530 | C | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.230-175C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 2/15 | chr3 | 100630530 | |||||||
chr3:100630647 | T | A | 1 | a0001c0001t0001g0008 | 2 | NA18969.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.230-58T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 2/15 | chr3 | 100630647 | |||||||
chr3:100630851 | C | T | 1 | a0002c0002t0001g0013 | 2 | NA18988.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.334+42C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100630851 | |||||||
chr3:100630997 | A | C | 1 | a0001c0001t0005g0072 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.334+188A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100630997 | |||||||
chr3:100630999 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.334+190C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100630999 | |||||||
chr3:100631123 | TA | T | 61 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0032 others(58): Show |
64 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.334+323delA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr3 | 100631123 | ||||||
chr3:100631124 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.334+315A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100631124 | |||||||
chr3:100631400 | A | G | 33 | a0003c0003t0001g0009 a0003c0003t0001g0019 a0003c0003t0001g0020 others(30): Show |
34 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.334+591A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100631400 | |||||||
chr3:100631403 | C | A | 10 | a0001c0008t0001g0041 a0001c0008t0009g0036 a0001c0010t0001g0039 others(7): Show |
10 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.334+594C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100631403 | |||||||
chr3:100631422 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.334+613G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100631422 | |||||||
chr3:100631550 | T | C | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.334+741T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100631550 | |||||||
chr3:100631584 | T | C | 1 | a0002c0002t0001g0259 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.334+775T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100631584 | |||||||
chr3:100631663 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.334+854G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100631663 | |||||||
chr3:100631700 | A | G | 1 | a0002c0002t0001g0309 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.334+891A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100631700 | |||||||
chr3:100631844 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.334+1035C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100631844 | |||||||
chr3:100631901 | C | T | 61 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0032 others(58): Show |
64 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.334+1092C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100631901 | |||||||
chr3:100632031 | A | G | 1 | a0001c0001t0001g0178 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.334+1222A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100632031 | |||||||
chr3:100632551 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.335-714C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100632551 | |||||||
chr3:100632662 | C | T | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.335-603C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100632662 | |||||||
chr3:100632668 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.335-597A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100632668 | |||||||
chr3:100632852 | T | C | 287 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(284): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.335-413T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100632852 | |||||||
chr3:100632968 | A | C | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.335-297A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100632968 | |||||||
chr3:100633052 | C | T | 45 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0032 others(42): Show |
47 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.335-213C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100633052 | |||||||
chr3:100633199 | C | T | 32 | a0003c0003t0001g0009 a0003c0003t0001g0019 a0003c0003t0001g0020 others(29): Show |
33 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.335-66C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 3/15 | chr3 | 100633199 | |||||||
chr3:100633588 | C | T | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.447+211C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100633588 | |||||||
chr3:100633593 | C | T | 4 | a0002c0002t0001g0280 a0002c0002t0001g0281 a0002c0002t0001g0282 others(1): Show |
4 | HG00621.hp1 NA19063.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.447+216C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100633593 | |||||||
chr3:100633652 | G | T | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | HG00597.hp2 NA18946.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.447+275G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100633652 | |||||||
chr3:100633676 | C | T | 45 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0032 others(42): Show |
47 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.447+299C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100633676 | |||||||
chr3:100633764 | C | T | 7 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.447+387C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100633764 | |||||||
chr3:100633802 | G | A | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.447+425G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100633802 | |||||||
chr3:100633850 | T | C | 1 | a0003c0003t0001g0145 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.447+473T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100633850 | |||||||
chr3:100633885 | C | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0171 |
2 | HG02083.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.447+508C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100633885 | |||||||
chr3:100633899 | T | C | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.447+522T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100633899 | |||||||
chr3:100633942 | G | C | 2 | a0002c0002t0001g0263 a0002c0002t0001g0264 |
2 | HG03927.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.447+565G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100633942 | |||||||
chr3:100634051 | C | T | 7 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.447+674C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100634051 | |||||||
chr3:100634086 | G | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.447+709G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100634086 | |||||||
chr3:100634506 | A | G | 1 | a0003c0003t0001g0029 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.447+1129A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100634506 | |||||||
chr3:100634619 | A | G | 285 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(282): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.448-1058A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100634619 | |||||||
chr3:100634885 | G | C | 3 | a0003c0003t0001g0026 a0003c0003t0001g0028 a0003c0003t0003g0025 |
3 | HG02055.hp2 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.448-792G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100634885 | |||||||
chr3:100634965 | T | C | 66 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(63): Show |
79 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.448-712T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100634965 | |||||||
chr3:100635000 | G | GAC | 225 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(222): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.448-649_448-648dup others(2): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr3 | 100635000 | ||||||
chr3:100635000 | G | GACAC | 20 | a0001c0001t0001g0073 a0001c0001t0001g0081 a0001c0001t0001g0102 others(17): Show |
20 | HG00280.hp2 HG00621.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.448-651_448-648dup others(4): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr3 | 100635000 | ||||||
chr3:100635000 | G | GACACAC | 14 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
15 | HG01106.hp1 HG01516.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.448-653_448-648dup others(6): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr3 | 100635000 | ||||||
chr3:100635000 | G | GACACACA others(1): Show |
3 | a0003c0003t0001g0026 a0003c0003t0001g0028 a0003c0003t0003g0025 |
3 | HG02055.hp2 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.448-655_448-648dup others(8): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr3 | 100635000 | ||||||
chr3:100635030 | T | C | 2 | a0001c0001t0001g0254 a0001c0005t0008g0106 |
2 | HG00280.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.448-647T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100635030 | |||||||
chr3:100635034 | C | CACACACA others(3): Show |
1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.448-637_448-636ins others(10): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr3 | 100635034 | ||||||
chr3:100635047 | G | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
4 | HG03209.hp1 HG03239.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.448-630G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100635047 | |||||||
chr3:100635089 | A | T | 1 | a0003c0003t0001g0148 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.448-588A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100635089 | |||||||
chr3:100635188 | CA | C | 3 | a0003c0003t0001g0026 a0003c0003t0001g0028 a0003c0003t0003g0025 |
3 | HG02055.hp2 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.448-483delA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr3 | 100635188 | ||||||
chr3:100635231 | A | ACC | 242 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(239): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.448-446_448-445ins others(2): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100635231 | |||||||
chr3:100635247 | T | C | 1 | a0003c0003t0001g0148 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.448-430T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100635247 | |||||||
chr3:100635326 | A | G | 226 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(223): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.448-351A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | chr3 | 100635326 | |||||||
chr3:100635652 | G | GT | 7 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.448-17dupT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr3 | 100635652 | ||||||
chr3:100635839 | G | A | 248 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(245): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.597+13G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/15 | chr3 | 100635839 | |||||||
chr3:100635853 | AT | A | 7 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.597+37delT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 100635853 | ||||||
chr3:100635854 | T | A | 272 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(269): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.597+28T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/15 | chr3 | 100635854 | |||||||
chr3:100635855 | T | A | 3 | a0001c0001t0001g0111 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01884.hp2 HG01891.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.597+29T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/15 | chr3 | 100635855 | |||||||
chr3:100636013 | G | T | 3 | a0003c0003t0001g0026 a0003c0003t0001g0028 a0003c0003t0003g0025 |
3 | HG02055.hp2 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.597+187G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/15 | chr3 | 100636013 | |||||||
chr3:100636250 | G | T | 160 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(157): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.597+424G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/15 | chr3 | 100636250 | |||||||
chr3:100636260 | G | A | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.597+434G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/15 | chr3 | 100636260 | |||||||
chr3:100636494 | A | G | 2 | a0001c0001t0001g0098 a0001c0001t0001g0124 |
2 | HG01346.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.597+668A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/15 | chr3 | 100636494 | |||||||
chr3:100636575 | T | C | 242 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(239): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.598-727T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/15 | chr3 | 100636575 | |||||||
chr3:100636645 | G | GA | 237 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(234): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.598-647dupA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 100636645 | ||||||
chr3:100636750 | G | T | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.598-552G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/15 | chr3 | 100636750 | |||||||
chr3:100636871 | A | G | 1 | a0002c0002t0001g0301 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.598-431A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/15 | chr3 | 100636871 | |||||||
chr3:100637014 | C | T | 249 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(246): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.598-288C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/15 | chr3 | 100637014 | |||||||
chr3:100637180 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.598-122C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/15 | chr3 | 100637180 | |||||||
chr3:100637183 | C | G | 249 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(246): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.598-119C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 5/15 | chr3 | 100637183 | |||||||
chr3:100637437 | C | G | 1 | a0001c0001t0001g0120 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.698+35C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100637437 | |||||||
chr3:100637541 | G | A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.698+139G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100637541 | |||||||
chr3:100637738 | A | C | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.698+336A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100637738 | |||||||
chr3:100637808 | C | G | 1 | a0001c0001t0001g0078 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.698+406C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100637808 | |||||||
chr3:100637871 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0171 |
2 | HG02083.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.698+469G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100637871 | |||||||
chr3:100637908 | C | G | 4 | a0001c0008t0001g0041 a0006c0007t0004g0042 a0006c0007t0004g0043 others(1): Show |
4 | HG02109.hp1 HG02630.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.698+506C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100637908 | |||||||
chr3:100637947 | A | C | 1 | a0001c0001t0001g0077 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.698+545A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100637947 | |||||||
chr3:100637968 | A | T | 1 | a0001c0001t0001g0160 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.698+566A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100637968 | |||||||
chr3:100637974 | C | A | 1 | a0001c0008t0009g0036 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.698+572C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100637974 | |||||||
chr3:100638125 | T | G | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.698+723T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100638125 | |||||||
chr3:100638263 | T | A | 3 | a0002c0002t0001g0302 a0002c0002t0001g0304 a0002c0002t0001g0305 |
3 | HG02165.hp2 NA18999.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.698+861T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100638263 | |||||||
chr3:100638425 | A | G | 2 | a0001c0005t0001g0007 a0001c0005t0001g0070 |
3 | HG02895.hp2 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.698+1023A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100638425 | |||||||
chr3:100638538 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.698+1136G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100638538 | |||||||
chr3:100638542 | C | T | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.698+1140C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100638542 | |||||||
chr3:100638560 | A | C | 1 | a0001c0001t0001g0222 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.698+1158A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100638560 | |||||||
chr3:100638577 | G | A | 2 | a0002c0002t0001g0297 a0002c0002t0001g0298 |
2 | NA18950.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.698+1175G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100638577 | |||||||
chr3:100638731 | A | G | 7 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.698+1329A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100638731 | |||||||
chr3:100638827 | C | A | 68 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(65): Show |
71 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.698+1425C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100638827 | |||||||
chr3:100638862 | C | T | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.698+1460C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100638862 | |||||||
chr3:100639010 | CTG | C | 5 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0053 others(2): Show |
5 | HG02809.hp1 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.698+1654_698+1655d others(4): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 100639010 | ||||||
chr3:100639010 | CTGTG | C | 17 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0023 others(14): Show |
20 | HG01884.hp1 HG01952.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.698+1652_698+1655d others(6): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 100639010 | ||||||
chr3:100639010 | CTGTGTG | C | 9 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0034 others(6): Show |
10 | HG01975.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.698+1650_698+1655d others(8): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 100639010 | ||||||
chr3:100639010 | CTGTGTGT others(1): Show |
C | 13 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0066 others(10): Show |
14 | HG01081.hp2 HG01106.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.698+1648_698+1655d others(10): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 100639010 | ||||||
chr3:100639010 | CTGTGTGT others(3): Show |
C | 29 | a0003c0003t0001g0019 a0003c0003t0001g0021 a0003c0003t0001g0029 others(26): Show |
29 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.698+1646_698+1655d others(12): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 100639010 | ||||||
chr3:100639010 | CTGTGTGT others(5): Show |
C | 3 | a0002c0002t0001g0276 a0002c0002t0001g0277 a0002c0002t0001g0304 |
3 | HG01515.hp2 HG01517.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.698+1644_698+1655d others(14): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 100639010 | ||||||
chr3:100639010 | CTGTGTGT others(7): Show |
C | 53 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0013 others(50): Show |
66 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.698+1642_698+1655d others(16): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 100639010 | ||||||
chr3:100639010 | CTGTGTGT others(9): Show |
C | 15 | a0001c0001t0001g0077 a0001c0001t0001g0087 a0001c0001t0001g0088 others(12): Show |
16 | HG00597.hp2 HG01256.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.698+1640_698+1655d others(18): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 100639010 | ||||||
chr3:100639010 | CTGTGTGT others(11): Show |
C | 151 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(148): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.698+1638_698+1655d others(20): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 100639010 | ||||||
chr3:100639010 | CTGTGTGT others(15): Show |
C | 4 | a0001c0001t0001g0083 a0001c0001t0001g0195 a0001c0001t0001g0241 others(1): Show |
4 | HG01123.hp1 HG01123.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.698+1634_698+1655d others(24): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 100639010 | ||||||
chr3:100639030 | GTGTGTGT others(21): Show |
G | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.698+1632_698+1659d others(30): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 100639030 | ||||||
chr3:100639032 | GTGTGTGT others(19): Show |
G | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.698+1634_698+1659d others(28): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 100639032 | ||||||
chr3:100639196 | T | C | 285 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(282): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.698+1794T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100639196 | |||||||
chr3:100639197 | G | A | 53 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0013 others(50): Show |
66 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.698+1795G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100639197 | |||||||
chr3:100639300 | T | A | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.698+1898T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100639300 | |||||||
chr3:100639534 | G | T | 63 | a0001c0001t0001g0162 a0002c0002t0001g0001 a0002c0002t0001g0004 others(60): Show |
76 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.698+2132G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100639534 | |||||||
chr3:100639696 | C | A | 62 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0013 others(59): Show |
75 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.698+2294C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100639696 | |||||||
chr3:100639696 | C | T | 2 | a0001c0001t0001g0066 a0009c0012t0001g0067 |
2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.698+2294C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100639696 | |||||||
chr3:100639801 | G | C | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.698+2399G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100639801 | |||||||
chr3:100639938 | G | T | 3 | a0001c0001t0001g0113 a0001c0001t0001g0215 a0001c0001t0001g0216 |
3 | HG02135.hp1 NA18747.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.698+2536G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100639938 | |||||||
chr3:100639947 | C | A | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.698+2545C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100639947 | |||||||
chr3:100639951 | T | A | 12 | a0001c0008t0001g0041 a0001c0008t0009g0036 a0001c0010t0001g0039 others(9): Show |
12 | HG00735.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.698+2549T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100639951 | |||||||
chr3:100640018 | C | T | 2 | a0001c0001t0001g0066 a0009c0012t0001g0067 |
2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.698+2616C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100640018 | |||||||
chr3:100640061 | C | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.698+2659C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100640061 | |||||||
chr3:100640178 | G | A | 1 | a0003c0003t0001g0139 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.698+2776G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100640178 | |||||||
chr3:100640285 | C | A | 1 | a0001c0001t0001g0054 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.698+2883C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100640285 | |||||||
chr3:100640489 | T | C | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.699-2777T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100640489 | |||||||
chr3:100640544 | C | T | 17 | a0001c0001t0001g0010 a0001c0001t0001g0087 a0001c0001t0001g0088 others(14): Show |
18 | HG00544.hp2 HG00558.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.699-2722C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100640544 | |||||||
chr3:100640618 | T | C | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.699-2648T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100640618 | |||||||
chr3:100640665 | G | A | 2 | a0001c0005t0001g0007 a0001c0005t0001g0070 |
3 | HG02895.hp2 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.699-2601G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100640665 | |||||||
chr3:100640760 | G | T | 1 | a0001c0001t0001g0097 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.699-2506G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100640760 | |||||||
chr3:100640788 | T | C | 68 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(65): Show |
71 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.699-2478T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100640788 | |||||||
chr3:100640832 | T | G | 62 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0013 others(59): Show |
75 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.699-2434T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100640832 | |||||||
chr3:100640864 | A | G | 2 | a0001c0005t0001g0007 a0001c0005t0001g0070 |
3 | HG02895.hp2 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.699-2402A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100640864 | |||||||
chr3:100641051 | G | A | 5 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0217 others(2): Show |
5 | HG01358.hp1 HG01943.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.699-2215G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100641051 | |||||||
chr3:100641154 | G | A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.699-2112G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100641154 | |||||||
chr3:100641234 | G | A | 1 | a0002c0002t0001g0310 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.699-2032G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100641234 | |||||||
chr3:100641287 | G | A | 2 | a0001c0005t0001g0007 a0001c0005t0001g0070 |
3 | HG02895.hp2 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.699-1979G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100641287 | |||||||
chr3:100641302 | G | A | 2 | a0001c0001t0001g0210 a0001c0001t0001g0220 |
2 | HG02071.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.699-1964G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100641302 | |||||||
chr3:100641425 | A | T | 62 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0013 others(59): Show |
75 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.699-1841A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100641425 | |||||||
chr3:100641427 | G | A | 2 | a0001c0001t0001g0066 a0009c0012t0001g0067 |
2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.699-1839G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100641427 | |||||||
chr3:100641504 | C | T | 162 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(159): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.699-1762C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100641504 | |||||||
chr3:100641543 | A | C | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.699-1723A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100641543 | |||||||
chr3:100641613 | G | A | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.699-1653G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100641613 | |||||||
chr3:100641648 | A | G | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.699-1618A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100641648 | |||||||
chr3:100641894 | C | A | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.699-1372C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100641894 | |||||||
chr3:100641906 | C | T | 1 | a0003c0003t0001g0140 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.699-1360C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100641906 | |||||||
chr3:100641949 | G | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.699-1317G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100641949 | |||||||
chr3:100641973 | C | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0175 |
2 | HG02015.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.699-1293C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100641973 | |||||||
chr3:100642205 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.699-1061T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100642205 | |||||||
chr3:100642532 | C | G | 1 | a0003c0003t0001g0251 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.699-734C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100642532 | |||||||
chr3:100642818 | C | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(1): Show |
4 | HG02145.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.699-448C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100642818 | |||||||
chr3:100642847 | C | T | 2 | a0001c0001t0001g0254 a0001c0001t0001g0256 |
2 | NA18999.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.699-419C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100642847 | |||||||
chr3:100642901 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.699-365A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100642901 | |||||||
chr3:100642962 | T | C | 33 | a0003c0003t0001g0009 a0003c0003t0001g0019 a0003c0003t0001g0020 others(30): Show |
34 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.699-304T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100642962 | |||||||
chr3:100643098 | C | A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.699-168C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100643098 | |||||||
chr3:100643148 | T | C | 2 | a0001c0001t0001g0157 a0001c0001t0001g0173 |
2 | HG00423.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.699-118T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 6/15 | chr3 | 100643148 | |||||||
chr3:100643670 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.946+37C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100643670 | |||||||
chr3:100643782 | T | C | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | NA18965.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.946+149T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100643782 | |||||||
chr3:100643923 | G | C | 12 | a0001c0008t0001g0041 a0001c0008t0009g0036 a0001c0010t0001g0039 others(9): Show |
12 | HG00735.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.946+290G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100643923 | |||||||
chr3:100644061 | C | T | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.946+428C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100644061 | |||||||
chr3:100644109 | A | G | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.946+476A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100644109 | |||||||
chr3:100644155 | C | T | 249 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(246): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.946+522C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100644155 | |||||||
chr3:100644187 | T | TA | 238 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(235): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.946+564dupA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr3 | 100644187 | ||||||
chr3:100644213 | G | C | 249 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(246): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.946+580G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100644213 | |||||||
chr3:100644214 | A | G | 2 | a0001c0005t0001g0007 a0001c0005t0001g0070 |
3 | HG02895.hp2 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.946+581A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100644214 | |||||||
chr3:100644223 | C | G | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.946+590C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100644223 | |||||||
chr3:100644256 | G | A | 62 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0013 others(59): Show |
75 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.946+623G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100644256 | |||||||
chr3:100644282 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.946+649A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100644282 | |||||||
chr3:100644332 | G | A | 12 | a0001c0008t0001g0041 a0001c0008t0009g0036 a0001c0010t0001g0039 others(9): Show |
12 | HG00735.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.946+699G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100644332 | |||||||
chr3:100644379 | T | C | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.946+746T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100644379 | |||||||
chr3:100644532 | G | A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.946+899G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100644532 | |||||||
chr3:100644597 | G | A | 37 | a0001c0001t0001g0081 a0001c0001t0001g0102 a0001c0001t0001g0196 others(34): Show |
38 | HG00597.hp1 HG00735.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.946+964G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100644597 | |||||||
chr3:100644697 | A | C | 2 | a0001c0005t0001g0007 a0001c0005t0001g0070 |
3 | HG02895.hp2 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.946+1064A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100644697 | |||||||
chr3:100644728 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.946+1095G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100644728 | |||||||
chr3:100645007 | C | T | 2 | a0001c0005t0001g0007 a0001c0005t0001g0070 |
3 | HG02895.hp2 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.947-938C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100645007 | |||||||
chr3:100645014 | G | A | 1 | a0001c0001t0005g0072 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.947-931G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100645014 | |||||||
chr3:100645258 | A | G | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.947-687A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100645258 | |||||||
chr3:100645408 | G | C | 1 | a0001c0001t0001g0083 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.947-537G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100645408 | |||||||
chr3:100645431 | C | CAGA | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.947-511_947-509dup others(3): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr3 | 100645431 | ||||||
chr3:100645474 | G | A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.947-471G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100645474 | |||||||
chr3:100645633 | A | G | 1 | a0001c0001t0001g0213 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.947-312A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100645633 | |||||||
chr3:100645636 | C | T | 1 | a0001c0001t0003g0167 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.947-309C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100645636 | |||||||
chr3:100645667 | C | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0247 |
2 | HG03654.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.947-278C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100645667 | |||||||
chr3:100645749 | G | A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.947-196G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 8/15 | chr3 | 100645749 | |||||||
chr3:100646220 | G | C | 1 | a0003c0003t0001g0133 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1110+112G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 9/15 | chr3 | 100646220 | |||||||
chr3:100646220 | G | T | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1110+112G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 9/15 | chr3 | 100646220 | |||||||
chr3:100646229 | T | A | 4 | a0004c0004t0002g0022 a0004c0004t0002g0037 a0004c0009t0002g0049 others(1): Show |
4 | HG00735.hp2 HG02615.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1110+121T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 9/15 | chr3 | 100646229 | |||||||
chr3:100646280 | G | A | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01884.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1110+172G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 9/15 | chr3 | 100646280 | |||||||
chr3:100646354 | C | T | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG00280.hp1 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111-215C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 9/15 | chr3 | 100646354 | |||||||
chr3:100646488 | G | C | 1 | a0001c0001t0001g0221 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1111-81G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 9/15 | chr3 | 100646488 | |||||||
chr3:100646807 | T | C | 2 | a0002c0002t0001g0071 a0002c0002t0001g0309 |
2 | HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1266+83T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100646807 | |||||||
chr3:100646881 | C | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1266+157C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100646881 | |||||||
chr3:100646912 | A | C | 285 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(282): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.1266+188A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100646912 | |||||||
chr3:100646955 | C | T | 98 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0013 others(95): Show |
112 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.1266+231C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100646955 | |||||||
chr3:100647017 | T | C | 282 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(279): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.1266+293T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100647017 | |||||||
chr3:100647018 | G | A | 176 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(173): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1266+294G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100647018 | |||||||
chr3:100647020 | A | G | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1266+296A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100647020 | |||||||
chr3:100647031 | C | T | 281 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(278): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1266+307C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100647031 | |||||||
chr3:100647060 | G | A | 2 | a0003c0003t0001g0135 a0003c0003t0001g0244 |
2 | HG00741.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1266+336G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100647060 | |||||||
chr3:100647122 | A | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1266+398A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100647122 | |||||||
chr3:100647168 | C | G | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1266+444C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100647168 | |||||||
chr3:100647184 | A | T | 1 | a0001c0005t0001g0070 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1266+460A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100647184 | |||||||
chr3:100647370 | T | C | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1266+646T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100647370 | |||||||
chr3:100647380 | C | T | 282 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(279): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.1266+656C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100647380 | |||||||
chr3:100647699 | C | T | 1 | a0001c0008t0009g0036 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1266+975C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100647699 | |||||||
chr3:100647707 | C | CA | 280 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(277): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1266+991dupA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr3 | 100647707 | ||||||
chr3:100647759 | A | C | 1 | a0001c0001t0001g0050 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1266+1035A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100647759 | |||||||
chr3:100647829 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1266+1105G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100647829 | |||||||
chr3:100647988 | G | T | 2 | a0001c0005t0001g0007 a0001c0005t0001g0070 |
3 | HG02895.hp2 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1266+1264G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100647988 | |||||||
chr3:100648019 | C | T | 281 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(278): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1266+1295C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648019 | |||||||
chr3:100648028 | T | C | 282 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(279): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.1266+1304T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648028 | |||||||
chr3:100648055 | C | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1266+1331C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648055 | |||||||
chr3:100648260 | T | C | 282 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(279): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.1267-1435T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648260 | |||||||
chr3:100648266 | A | G | 7 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1267-1429A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648266 | |||||||
chr3:100648315 | G | GTAA | 282 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(279): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.1267-1380_1267-137 others(7): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648315 | |||||||
chr3:100648317 | T | G | 282 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(279): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.1267-1378T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648317 | |||||||
chr3:100648340 | GA | G | 282 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(279): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.1267-1350delA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr3 | 100648340 | ||||||
chr3:100648343 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1267-1352A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648343 | |||||||
chr3:100648381 | C | T | 282 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(279): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.1267-1314C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648381 | |||||||
chr3:100648383 | A | G | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1267-1312A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648383 | |||||||
chr3:100648411 | C | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1267-1284C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648411 | |||||||
chr3:100648413 | T | C | 281 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(278): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1267-1282T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648413 | |||||||
chr3:100648427 | T | A | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1267-1268T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648427 | |||||||
chr3:100648495 | G | A | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1267-1200G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648495 | |||||||
chr3:100648519 | G | A | 282 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(279): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.1267-1176G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648519 | |||||||
chr3:100648522 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1267-1173C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648522 | |||||||
chr3:100648647 | C | T | 162 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(159): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.1267-1048C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648647 | |||||||
chr3:100648672 | C | G | 5 | a0001c0001t0001g0066 a0001c0001t0001g0150 a0001c0001t0001g0151 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1267-1023C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648672 | |||||||
chr3:100648721 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1267-974C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648721 | |||||||
chr3:100648766 | A | T | 281 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(278): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1267-929A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648766 | |||||||
chr3:100648795 | TA | T | 36 | a0003c0003t0001g0009 a0003c0003t0001g0019 a0003c0003t0001g0020 others(33): Show |
37 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1267-893delA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr3 | 100648795 | ||||||
chr3:100648801 | A | T | 36 | a0003c0003t0001g0009 a0003c0003t0001g0019 a0003c0003t0001g0020 others(33): Show |
37 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1267-894A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648801 | |||||||
chr3:100648833 | T | C | 4 | a0001c0001t0001g0104 a0001c0001t0001g0107 a0001c0001t0001g0179 others(1): Show |
4 | HG02027.hp2 NA18747.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.1267-862T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648833 | |||||||
chr3:100648929 | C | T | 3 | a0003c0003t0001g0026 a0003c0003t0001g0028 a0003c0003t0003g0025 |
3 | HG02055.hp2 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1267-766C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648929 | |||||||
chr3:100648945 | G | C | 1 | a0001c0001t0001g0195 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1267-750G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100648945 | |||||||
chr3:100649288 | G | A | 3 | a0003c0003t0001g0026 a0003c0003t0001g0028 a0003c0003t0003g0025 |
3 | HG02055.hp2 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1267-407G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100649288 | |||||||
chr3:100649300 | T | C | 3 | a0003c0003t0001g0026 a0003c0003t0001g0028 a0003c0003t0003g0025 |
3 | HG02055.hp2 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1267-395T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100649300 | |||||||
chr3:100649403 | C | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1267-292C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100649403 | |||||||
chr3:100649431 | C | G | 1 | a0001c0001t0001g0153 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1267-264C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100649431 | |||||||
chr3:100649581 | A | G | 176 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(173): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1267-114A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100649581 | |||||||
chr3:100649631 | G | A | 43 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0079 others(40): Show |
45 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1267-64G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 10/15 | chr3 | 100649631 | |||||||
chr3:100649848 | A | G | 281 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(278): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1379+41A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100649848 | |||||||
chr3:100650096 | T | C | 281 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(278): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1379+289T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100650096 | |||||||
chr3:100650115 | G | T | 281 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(278): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1379+308G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100650115 | |||||||
chr3:100650302 | C | G | 238 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(235): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1379+495C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100650302 | |||||||
chr3:100650340 | T | A | 3 | a0005c0006t0001g0006 a0005c0006t0001g0030 a0005c0006t0001g0031 |
4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1379+533T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100650340 | |||||||
chr3:100650388 | G | A | 12 | a0001c0008t0001g0041 a0001c0008t0009g0036 a0001c0010t0001g0039 others(9): Show |
12 | HG00735.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1379+581G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100650388 | |||||||
chr3:100650424 | C | T | 12 | a0001c0008t0001g0041 a0001c0008t0009g0036 a0001c0010t0001g0039 others(9): Show |
12 | HG00735.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1379+617C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100650424 | |||||||
chr3:100650496 | C | G | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1379+689C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100650496 | |||||||
chr3:100650625 | A | G | 1 | a0003c0003t0001g0147 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1379+818A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100650625 | |||||||
chr3:100650641 | G | A | 36 | a0003c0003t0001g0009 a0003c0003t0001g0019 a0003c0003t0001g0020 others(33): Show |
37 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1379+834G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100650641 | |||||||
chr3:100650649 | A | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1379+842A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100650649 | |||||||
chr3:100650666 | G | T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0065 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1379+859G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100650666 | |||||||
chr3:100650824 | T | A | 1 | a0001c0001t0001g0160 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1379+1017T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100650824 | |||||||
chr3:100650851 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1379+1044G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100650851 | |||||||
chr3:100651094 | C | G | 226 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(223): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1379+1287C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100651094 | |||||||
chr3:100651179 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1379+1372A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100651179 | |||||||
chr3:100651296 | G | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1379+1489G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100651296 | |||||||
chr3:100651310 | T | G | 1 | a0001c0001t0001g0184 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1379+1503T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100651310 | |||||||
chr3:100651347 | A | G | 7 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1379+1540A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100651347 | |||||||
chr3:100651350 | A | G | 1 | a0003c0003t0003g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1379+1543A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100651350 | |||||||
chr3:100651441 | A | G | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1379+1634A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100651441 | |||||||
chr3:100651450 | C | A | 1 | a0001c0001t0001g0203 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1379+1643C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100651450 | |||||||
chr3:100651476 | T | C | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1379+1669T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100651476 | |||||||
chr3:100651524 | A | G | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1379+1717A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100651524 | |||||||
chr3:100651571 | T | C | 2 | a0001c0005t0001g0007 a0001c0005t0001g0070 |
3 | HG02895.hp2 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1379+1764T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100651571 | |||||||
chr3:100651684 | AT | A | 6 | a0001c0001t0001g0048 a0001c0011t0001g0060 a0003c0003t0001g0244 others(3): Show |
7 | HG00741.hp2 HG01975.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1379+1888delT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr3 | 100651684 | ||||||
chr3:100651695 | T | A | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1379+1888T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100651695 | |||||||
chr3:100651696 | A | T | 1 | a0001c0001t0001g0056 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1379+1889A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100651696 | |||||||
chr3:100651924 | T | A | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1379+2117T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100651924 | |||||||
chr3:100651929 | C | T | 161 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(158): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.1379+2122C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100651929 | |||||||
chr3:100652116 | C | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1379+2309C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652116 | |||||||
chr3:100652205 | G | A | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1379+2398G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652205 | |||||||
chr3:100652207 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1379+2400A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652207 | |||||||
chr3:100652232 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1379+2425G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652232 | |||||||
chr3:100652242 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1379+2435T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652242 | |||||||
chr3:100652245 | A | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1379+2438A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652245 | |||||||
chr3:100652302 | C | T | 2 | a0001c0005t0001g0007 a0001c0005t0001g0070 |
3 | HG02895.hp2 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1379+2495C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652302 | |||||||
chr3:100652340 | C | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1380-2495C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652340 | |||||||
chr3:100652352 | A | G | 223 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(220): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1380-2483A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652352 | |||||||
chr3:100652372 | A | G | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1380-2463A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652372 | |||||||
chr3:100652518 | C | G | 1 | a0001c0001t0001g0117 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1380-2317C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652518 | |||||||
chr3:100652518 | C | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1380-2317C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652518 | |||||||
chr3:100652576 | G | T | 2 | a0001c0001t0001g0066 a0009c0012t0001g0067 |
2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1380-2259G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652576 | |||||||
chr3:100652616 | T | C | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1380-2219T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652616 | |||||||
chr3:100652633 | C | T | 1 | a0002c0002t0001g0298 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1380-2202C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652633 | |||||||
chr3:100652634 | AT | A | 12 | a0001c0008t0001g0041 a0001c0008t0009g0036 a0001c0010t0001g0039 others(9): Show |
12 | HG00735.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1380-2197delT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr3 | 100652634 | ||||||
chr3:100652647 | A | G | 238 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(235): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1380-2188A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652647 | |||||||
chr3:100652843 | C | T | 1 | a0001c0001t0005g0072 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1380-1992C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652843 | |||||||
chr3:100652896 | G | C | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1380-1939G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652896 | |||||||
chr3:100652986 | C | G | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1380-1849C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652986 | |||||||
chr3:100652998 | C | G | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1380-1837C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100652998 | |||||||
chr3:100653027 | C | T | 43 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0079 others(40): Show |
45 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1380-1808C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100653027 | |||||||
chr3:100653182 | T | C | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1380-1653T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100653182 | |||||||
chr3:100653295 | G | C | 7 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
8 | HG01975.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1380-1540G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100653295 | |||||||
chr3:100653380 | G | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1380-1455G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100653380 | |||||||
chr3:100653390 | C | G | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1380-1445C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100653390 | |||||||
chr3:100653404 | T | C | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1380-1431T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100653404 | |||||||
chr3:100653577 | A | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1380-1258A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100653577 | |||||||
chr3:100653809 | C | T | 160 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(157): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.1380-1026C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100653809 | |||||||
chr3:100654042 | G | T | 1 | a0002c0002t0001g0303 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1380-793G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100654042 | |||||||
chr3:100654093 | G | A | 1 | a0003c0003t0001g0243 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1380-742G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100654093 | |||||||
chr3:100654142 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1380-693C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100654142 | |||||||
chr3:100654161 | G | A | 21 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(18): Show |
23 | HG00735.hp2 HG01975.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1380-674G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100654161 | |||||||
chr3:100654243 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1380-592G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100654243 | |||||||
chr3:100654294 | T | G | 2 | a0001c0001t0001g0089 a0001c0001t0001g0158 |
2 | NA18994.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1380-541T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100654294 | |||||||
chr3:100654396 | A | G | 4 | a0002c0002t0001g0306 a0002c0002t0001g0310 a0002c0002t0001g0311 others(1): Show |
4 | HG02615.hp2 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1380-439A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100654396 | |||||||
chr3:100654456 | C | T | 161 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(158): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.1380-379C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100654456 | |||||||
chr3:100654499 | T | C | 283 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(280): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1380-336T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100654499 | |||||||
chr3:100654562 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1380-273G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100654562 | |||||||
chr3:100654681 | C | T | 1 | a0002c0002t0001g0289 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1380-154C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100654681 | |||||||
chr3:100654708 | A | C | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1380-127A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100654708 | |||||||
chr3:100654775 | T | G | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1380-60T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 11/15 | chr3 | 100654775 | |||||||
chr3:100655229 | T | C | 63 | a0001c0001t0005g0072 a0002c0002t0001g0001 a0002c0002t0001g0004 others(60): Show |
76 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.1726+48T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 12/15 | chr3 | 100655229 | |||||||
chr3:100655277 | C | T | 62 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0013 others(59): Show |
75 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.1726+96C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 12/15 | chr3 | 100655277 | |||||||
chr3:100655320 | C | T | 1 | a0008c0017t0001g0138 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1726+139C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 12/15 | chr3 | 100655320 | |||||||
chr3:100655362 | C | T | 3 | a0001c0005t0001g0007 a0001c0005t0001g0070 a0001c0005t0008g0106 |
4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1726+181C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 12/15 | chr3 | 100655362 | |||||||
chr3:100655415 | A | G | 3 | a0001c0005t0001g0007 a0001c0005t0001g0070 a0001c0005t0008g0106 |
4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1726+234A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 12/15 | chr3 | 100655415 | |||||||
chr3:100655527 | C | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1726+346C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 12/15 | chr3 | 100655527 | |||||||
chr3:100655896 | T | C | 122 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(119): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
splice_region_variant&intron_variant | LOW | c.1727-3T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 12/15 | chr3 | 100655896 | |||||||
chr3:100656232 | C | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1823+237C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100656232 | |||||||
chr3:100656245 | T | G | 1 | a0001c0008t0001g0041 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1823+250T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100656245 | |||||||
chr3:100656401 | A | C | 3 | a0001c0005t0001g0007 a0001c0005t0001g0070 a0001c0005t0008g0106 |
4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1823+406A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100656401 | |||||||
chr3:100656623 | C | A | 1 | a0001c0001t0001g0217 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1823+628C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100656623 | |||||||
chr3:100656711 | G | T | 244 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(241): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1823+716G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100656711 | |||||||
chr3:100656728 | G | A | 244 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(241): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1823+733G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100656728 | |||||||
chr3:100656794 | T | TCA | 293 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(290): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1823+800_1823+801i others(4): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr3 | 100656794 | ||||||
chr3:100656853 | G | T | 3 | a0001c0005t0001g0007 a0001c0005t0001g0070 a0001c0005t0008g0106 |
4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1823+858G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100656853 | |||||||
chr3:100656925 | C | G | 3 | a0001c0005t0001g0007 a0001c0005t0001g0070 a0001c0005t0008g0106 |
4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1823+930C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100656925 | |||||||
chr3:100657185 | G | A | 3 | a0001c0005t0001g0007 a0001c0005t0001g0070 a0001c0005t0008g0106 |
4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1823+1190G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100657185 | |||||||
chr3:100657238 | C | G | 2 | a0002c0002t0001g0297 a0002c0002t0001g0298 |
2 | NA18950.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1823+1243C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100657238 | |||||||
chr3:100657578 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0171 |
2 | HG02083.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1823+1583G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100657578 | |||||||
chr3:100657596 | T | C | 142 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(139): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.1823+1601T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100657596 | |||||||
chr3:100657599 | T | C | 3 | a0001c0005t0001g0007 a0001c0005t0001g0070 a0001c0005t0008g0106 |
4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1823+1604T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100657599 | |||||||
chr3:100657606 | A | G | 9 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(6): Show |
10 | HG01975.hp2 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1823+1611A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100657606 | |||||||
chr3:100657626 | T | C | 9 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(6): Show |
10 | HG01975.hp2 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1823+1631T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100657626 | |||||||
chr3:100657702 | C | T | 44 | a0001c0001t0001g0010 a0001c0001t0001g0046 a0001c0001t0001g0047 others(41): Show |
45 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.1823+1707C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100657702 | |||||||
chr3:100657951 | G | A | 3 | a0001c0005t0001g0007 a0001c0005t0001g0070 a0001c0005t0008g0106 |
4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1824-1737G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100657951 | |||||||
chr3:100657999 | A | G | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1824-1689A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100657999 | |||||||
chr3:100658077 | C | T | 49 | a0001c0001t0001g0010 a0001c0001t0001g0046 a0001c0001t0001g0047 others(46): Show |
50 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.1824-1611C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100658077 | |||||||
chr3:100658191 | T | C | 1 | a0003c0003t0001g0133 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1824-1497T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100658191 | |||||||
chr3:100658279 | A | G | 49 | a0001c0001t0001g0010 a0001c0001t0001g0046 a0001c0001t0001g0047 others(46): Show |
50 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.1824-1409A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100658279 | |||||||
chr3:100658291 | G | T | 1 | a0002c0002t0001g0260 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1824-1397G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100658291 | |||||||
chr3:100658300 | T | G | 1 | a0001c0001t0001g0173 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1824-1388T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100658300 | |||||||
chr3:100658440 | G | A | 42 | a0001c0001t0001g0010 a0001c0001t0001g0066 a0001c0001t0001g0074 others(39): Show |
43 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1824-1248G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100658440 | |||||||
chr3:100658517 | G | C | 231 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(228): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1824-1171G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100658517 | |||||||
chr3:100658729 | G | A | 230 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(227): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.1824-959G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100658729 | |||||||
chr3:100658872 | T | A | 3 | a0001c0005t0001g0007 a0001c0005t0001g0070 a0001c0005t0008g0106 |
4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1824-816T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100658872 | |||||||
chr3:100658903 | T | G | 1 | a0001c0001t0001g0054 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1824-785T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100658903 | |||||||
chr3:100658906 | C | T | 1 | a0003c0003t0001g0132 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1824-782C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100658906 | |||||||
chr3:100658957 | C | A | 1 | a0002c0002t0001g0307 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1824-731C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100658957 | |||||||
chr3:100658979 | G | T | 1 | a0002c0002t0001g0304 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1824-709G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100658979 | |||||||
chr3:100659099 | A | G | 121 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(118): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.1824-589A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100659099 | |||||||
chr3:100659135 | A | T | 3 | a0001c0005t0001g0007 a0001c0005t0001g0070 a0001c0005t0008g0106 |
4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1824-553A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100659135 | |||||||
chr3:100659157 | G | C | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1824-531G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100659157 | |||||||
chr3:100659418 | C | T | 9 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(6): Show |
10 | HG01975.hp2 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1824-270C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100659418 | |||||||
chr3:100659439 | C | CA | 112 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(109): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.1824-224dupA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr3 | 100659439 | ||||||
chr3:100659439 | C | CAA | 23 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0078 others(20): Show |
23 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.1824-225_1824-224d others(4): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr3 | 100659439 | ||||||
chr3:100659439 | CA | C | 14 | a0001c0001t0001g0023 a0001c0001t0001g0032 a0001c0001t0001g0034 others(11): Show |
15 | HG01952.hp1 HG01975.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1824-224delA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr3 | 100659439 | ||||||
chr3:100659439 | CAAAAAAA others(2): Show |
C | 32 | a0003c0003t0001g0009 a0003c0003t0001g0019 a0003c0003t0001g0020 others(29): Show |
33 | HG00741.hp2 HG01071.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.1824-232_1824-224d others(11): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr3 | 100659439 | ||||||
chr3:100659448 | A | G | 9 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(6): Show |
10 | HG01975.hp2 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1824-240A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100659448 | |||||||
chr3:100659465 | G | A | 3 | a0001c0005t0001g0007 a0001c0005t0001g0070 a0001c0005t0008g0106 |
4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1824-223G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100659465 | |||||||
chr3:100659638 | T | C | 2 | a0001c0005t0001g0007 a0001c0005t0001g0070 |
3 | HG02895.hp2 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1824-50T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 13/15 | chr3 | 100659638 | |||||||
chr3:100659892 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1979+49C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100659892 | |||||||
chr3:100659898 | G | A | 3 | a0001c0005t0001g0007 a0001c0005t0001g0070 a0001c0005t0008g0106 |
4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1979+55G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100659898 | |||||||
chr3:100659906 | A | G | 12 | a0001c0008t0001g0041 a0001c0008t0009g0036 a0001c0010t0001g0039 others(9): Show |
12 | HG00735.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1979+63A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100659906 | |||||||
chr3:100660002 | G | T | 2 | a0001c0005t0001g0007 a0001c0005t0001g0070 |
3 | HG02895.hp2 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1979+159G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100660002 | |||||||
chr3:100660028 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1979+185C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100660028 | |||||||
chr3:100660086 | A | G | 1 | a0003c0003t0001g0099 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1979+243A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100660086 | |||||||
chr3:100660109 | C | T | 3 | a0001c0005t0001g0007 a0001c0005t0001g0070 a0001c0005t0008g0106 |
4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1979+266C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100660109 | |||||||
chr3:100660129 | G | T | 3 | a0003c0003t0001g0026 a0003c0003t0001g0028 a0003c0003t0003g0025 |
3 | HG02055.hp2 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1979+286G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100660129 | |||||||
chr3:100660167 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1979+324A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100660167 | |||||||
chr3:100660309 | T | C | 54 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(51): Show |
56 | HG00597.hp1 HG00735.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.1979+466T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100660309 | |||||||
chr3:100660678 | C | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1979+835C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100660678 | |||||||
chr3:100660821 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1979+978A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100660821 | |||||||
chr3:100660952 | C | CA | 9 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0005g0072 others(6): Show |
10 | HG00280.hp1 HG01884.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1979+1124dupA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 100660952 | ||||||
chr3:100660952 | C | CAA | 9 | a0001c0008t0009g0036 a0001c0010t0001g0039 a0004c0004t0002g0022 others(6): Show |
9 | HG00735.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1979+1123_1979+112 others(6): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 100660952 | ||||||
chr3:100660952 | C | CAAA | 11 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(8): Show |
12 | HG01975.hp2 HG02145.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1979+1122_1979+112 others(7): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 100660952 | ||||||
chr3:100660952 | CA | C | 49 | a0001c0001t0001g0010 a0001c0001t0001g0046 a0001c0001t0001g0047 others(46): Show |
50 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.1979+1124delA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 100660952 | ||||||
chr3:100661010 | C | G | 1 | a0002c0002t0001g0302 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1979+1167C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100661010 | |||||||
chr3:100661012 | A | G | 112 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(109): Show |
116 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1979+1169A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100661012 | |||||||
chr3:100661029 | G | A | 20 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(17): Show |
21 | HG00735.hp2 HG01975.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1979+1186G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100661029 | |||||||
chr3:100661065 | C | T | 4 | a0002c0002t0001g0001 a0002c0002t0001g0275 a0002c0002t0001g0284 others(1): Show |
9 | NA18612.hp1 NA18953.hp1 NA18955.hp1 others(6): Show |
intron_variant | MODIFIER | c.1979+1222C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100661065 | |||||||
chr3:100661098 | G | T | 9 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(6): Show |
10 | HG01975.hp2 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1979+1255G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100661098 | |||||||
chr3:100661197 | C | T | 3 | a0001c0005t0001g0007 a0001c0005t0001g0070 a0001c0005t0008g0106 |
4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1979+1354C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100661197 | |||||||
chr3:100661295 | T | C | 3 | a0001c0005t0001g0007 a0001c0005t0001g0070 a0001c0005t0008g0106 |
4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1979+1452T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100661295 | |||||||
chr3:100661373 | A | G | 1 | a0002c0002t0001g0288 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1979+1530A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100661373 | |||||||
chr3:100661897 | T | C | 3 | a0001c0005t0001g0007 a0001c0005t0001g0070 a0001c0005t0008g0106 |
4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1979+2054T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100661897 | |||||||
chr3:100661961 | C | T | 8 | a0001c0001t0001g0111 a0001c0001t0001g0114 a0001c0001t0001g0115 others(5): Show |
8 | HG00597.hp2 NA18941.hp1 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.1979+2118C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100661961 | |||||||
chr3:100661967 | A | G | 288 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(285): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1979+2124A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100661967 | |||||||
chr3:100662157 | A | G | 9 | a0004c0004t0002g0022 a0004c0004t0002g0037 a0004c0004t0002g0038 others(6): Show |
9 | HG00735.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1979+2314A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100662157 | |||||||
chr3:100662282 | A | C | 3 | a0001c0005t0001g0007 a0001c0005t0001g0070 a0001c0005t0008g0106 |
4 | HG00280.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1979+2439A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100662282 | |||||||
chr3:100662287 | G | A | 1 | a0003c0003t0001g0251 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1979+2444G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100662287 | |||||||
chr3:100662359 | G | T | 1 | a0002c0002t0001g0294 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1979+2516G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100662359 | |||||||
chr3:100662471 | G | C | 231 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(228): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1979+2628G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100662471 | |||||||
chr3:100662583 | C | T | 2 | a0001c0008t0009g0036 a0001c0010t0001g0039 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1979+2740C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100662583 | |||||||
chr3:100662599 | A | T | 7 | a0001c0001t0001g0100 a0001c0001t0001g0109 a0001c0001t0001g0198 others(4): Show |
7 | HG01192.hp2 HG01255.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.1979+2756A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100662599 | |||||||
chr3:100662629 | C | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1979+2786C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100662629 | |||||||
chr3:100662870 | G | GA | 144 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0079 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.1979+3033dupA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 100662870 | ||||||
chr3:100663027 | C | T | 3 | a0005c0006t0001g0006 a0005c0006t0001g0030 a0005c0006t0001g0031 |
4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1979+3184C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100663027 | |||||||
chr3:100663063 | T | C | 2 | a0001c0008t0009g0036 a0001c0010t0001g0039 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1979+3220T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100663063 | |||||||
chr3:100663102 | T | C | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1979+3259T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100663102 | |||||||
chr3:100663113 | A | C | 231 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(228): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1979+3270A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100663113 | |||||||
chr3:100663133 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1979+3290G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100663133 | |||||||
chr3:100663297 | T | A | 245 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(242): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1979+3454T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100663297 | |||||||
chr3:100663448 | T | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG01106.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1979+3605T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100663448 | |||||||
chr3:100663487 | C | T | 2 | a0001c0008t0009g0036 a0001c0010t0001g0039 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1979+3644C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100663487 | |||||||
chr3:100663607 | A | G | 1 | a0001c0005t0001g0070 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1979+3764A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100663607 | |||||||
chr3:100663664 | C | G | 144 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0079 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.1979+3821C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100663664 | |||||||
chr3:100663699 | G | C | 211 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(208): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1979+3856G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100663699 | |||||||
chr3:100663793 | T | A | 1 | a0001c0001t0001g0027 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1979+3950T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100663793 | |||||||
chr3:100664018 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1979+4175A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100664018 | |||||||
chr3:100664080 | A | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1979+4237A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100664080 | |||||||
chr3:100664091 | T | A | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1979+4248T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100664091 | |||||||
chr3:100664324 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1979+4481C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100664324 | |||||||
chr3:100664441 | A | G | 1 | a0002c0002t0001g0308 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1980-4508A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100664441 | |||||||
chr3:100664458 | C | G | 36 | a0001c0001t0001g0119 a0003c0003t0001g0009 a0003c0003t0001g0019 others(33): Show |
37 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1980-4491C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100664458 | |||||||
chr3:100664507 | A | G | 3 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0005t0008g0106 |
3 | HG00280.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1980-4442A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100664507 | |||||||
chr3:100664545 | C | T | 9 | a0004c0004t0002g0022 a0004c0004t0002g0037 a0004c0004t0002g0038 others(6): Show |
9 | HG00735.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1980-4404C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100664545 | |||||||
chr3:100664895 | A | C | 245 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(242): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1980-4054A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100664895 | |||||||
chr3:100664920 | G | T | 1 | a0001c0001t0001g0189 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1980-4029G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100664920 | |||||||
chr3:100664972 | A | C | 1 | a0001c0008t0001g0041 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1980-3977A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100664972 | |||||||
chr3:100665014 | C | T | 245 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(242): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1980-3935C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100665014 | |||||||
chr3:100665102 | G | A | 1 | a0001c0005t0001g0070 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1980-3847G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100665102 | |||||||
chr3:100665300 | T | C | 3 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0005t0008g0106 |
3 | HG00280.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1980-3649T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100665300 | |||||||
chr3:100665488 | C | T | 7 | a0001c0001t0003g0033 a0001c0001t0003g0108 a0001c0001t0003g0126 others(4): Show |
7 | HG02258.hp1 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1980-3461C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100665488 | |||||||
chr3:100665602 | T | C | 14 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0078 others(11): Show |
16 | HG00099.hp1 HG00438.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.1980-3347T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100665602 | |||||||
chr3:100665617 | T | C | 245 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(242): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1980-3332T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100665617 | |||||||
chr3:100666013 | T | C | 1 | a0001c0001t0001g0159 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1980-2936T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666013 | |||||||
chr3:100666017 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1980-2932C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666017 | |||||||
chr3:100666054 | C | CT | 9 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(6): Show |
9 | HG00621.hp2 HG01515.hp2 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.1980-2880dupT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 100666054 | ||||||
chr3:100666124 | C | T | 48 | a0001c0001t0001g0250 a0002c0002t0001g0001 a0002c0002t0001g0004 others(45): Show |
61 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1980-2825C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666124 | |||||||
chr3:100666157 | C | G | 5 | a0001c0001t0001g0081 a0001c0001t0001g0102 a0001c0001t0001g0196 others(2): Show |
5 | NA18953.hp2 NA18974.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.1980-2792C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666157 | |||||||
chr3:100666182 | G | T | 1 | a0001c0005t0001g0070 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1980-2767G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666182 | |||||||
chr3:100666250 | G | C | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1980-2699G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666250 | |||||||
chr3:100666254 | C | T | 13 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0045 others(10): Show |
13 | HG01891.hp1 HG02258.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1980-2695C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666254 | |||||||
chr3:100666367 | T | C | 1 | a0001c0008t0001g0041 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1980-2582T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666367 | |||||||
chr3:100666447 | T | C | 1 | a0003c0003t0001g0143 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1980-2502T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666447 | |||||||
chr3:100666455 | G | A | 208 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(205): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1980-2494G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666455 | |||||||
chr3:100666579 | G | C | 1 | a0001c0005t0001g0070 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1980-2370G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666579 | |||||||
chr3:100666807 | T | C | 1 | a0005c0006t0001g0006 | 2 | HG01975.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1980-2142T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666807 | |||||||
chr3:100666901 | G | C | 1 | a0002c0002t0001g0261 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1980-2048G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666901 | |||||||
chr3:100666933 | C | T | 144 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0079 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.1980-2016C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666933 | |||||||
chr3:100666967 | G | C | 1 | a0004c0009t0002g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1980-1982G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666967 | |||||||
chr3:100666996 | G | A | 61 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(58): Show |
64 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.1980-1953G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100666996 | |||||||
chr3:100667021 | G | A | 3 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0005t0008g0106 |
3 | HG00280.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1980-1928G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100667021 | |||||||
chr3:100667035 | C | T | 9 | a0004c0004t0002g0022 a0004c0004t0002g0037 a0004c0004t0002g0038 others(6): Show |
9 | HG00735.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1980-1914C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100667035 | |||||||
chr3:100667055 | T | C | 1 | a0001c0005t0001g0070 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1980-1894T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100667055 | |||||||
chr3:100667138 | G | A | 7 | a0001c0001t0003g0033 a0001c0001t0003g0108 a0001c0001t0003g0126 others(4): Show |
7 | HG02258.hp1 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1980-1811G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100667138 | |||||||
chr3:100667188 | T | A | 209 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(206): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1980-1761T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100667188 | |||||||
chr3:100667227 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1980-1722A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100667227 | |||||||
chr3:100667286 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1980-1663C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100667286 | |||||||
chr3:100667591 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1980-1358G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100667591 | |||||||
chr3:100667855 | C | T | 1 | a0003c0003t0001g0245 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1980-1094C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100667855 | |||||||
chr3:100667864 | C | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1980-1085C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100667864 | |||||||
chr3:100667884 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1980-1065G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100667884 | |||||||
chr3:100667952 | G | C | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1980-997G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100667952 | |||||||
chr3:100667965 | G | T | 5 | a0001c0001t0003g0108 a0001c0001t0003g0126 a0001c0001t0003g0167 others(2): Show |
5 | HG02258.hp1 HG02559.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1980-984G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100667965 | |||||||
chr3:100668073 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1980-876G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100668073 | |||||||
chr3:100668645 | C | G | 16 | a0001c0001t0003g0033 a0001c0001t0003g0108 a0001c0001t0003g0126 others(13): Show |
16 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1980-304C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100668645 | |||||||
chr3:100668672 | A | G | 1 | a0001c0001t0001g0011 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1980-277A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100668672 | |||||||
chr3:100668785 | A | G | 7 | a0001c0001t0003g0033 a0001c0001t0003g0108 a0001c0001t0003g0126 others(4): Show |
7 | HG02258.hp1 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1980-164A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100668785 | |||||||
chr3:100668865 | A | G | 230 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(227): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1980-84A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 14/15 | chr3 | 100668865 | |||||||
chr3:100669193 | T | A | 1 | a0001c0001t0001g0226 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2136+88T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100669193 | |||||||
chr3:100669296 | A | C | 231 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(228): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.2136+191A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100669296 | |||||||
chr3:100669305 | G | T | 244 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(241): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.2136+200G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100669305 | |||||||
chr3:100669406 | A | G | 9 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0056 others(6): Show |
12 | HG01884.hp1 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2136+301A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100669406 | |||||||
chr3:100669418 | T | C | 1 | a0001c0001t0003g0033 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2136+313T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100669418 | |||||||
chr3:100669488 | C | G | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2136+383C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100669488 | |||||||
chr3:100669514 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2136+409A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100669514 | |||||||
chr3:100669527 | C | A | 1 | a0001c0001t0001g0213 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2136+422C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100669527 | |||||||
chr3:100669533 | C | CA | 18 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(15): Show |
18 | HG00438.hp1 HG02027.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.2136+457dupA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100669533 | ||||||
chr3:100669533 | CA | C | 32 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0023 others(29): Show |
36 | HG01884.hp1 HG01891.hp1 HG01952.hp1 others(33): Show |
intron_variant | MODIFIER | c.2136+457delA | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100669533 | ||||||
chr3:100669533 | CAAA | C | 18 | a0001c0001t0001g0047 a0001c0001t0001g0105 a0001c0001t0001g0188 others(15): Show |
18 | HG00099.hp1 HG00735.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.2136+455_2136+457d others(5): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100669533 | ||||||
chr3:100669533 | CAAAA | C | 62 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(59): Show |
66 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.2136+454_2136+457d others(6): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100669533 | ||||||
chr3:100669533 | CAAAAA | C | 11 | a0001c0001t0001g0101 a0001c0001t0001g0166 a0001c0001t0001g0226 others(8): Show |
11 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(8): Show |
intron_variant | MODIFIER | c.2136+453_2136+457d others(7): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100669533 | ||||||
chr3:100669533 | CAAAAAA | C | 121 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0079 others(118): Show |
134 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.2136+452_2136+457d others(8): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100669533 | ||||||
chr3:100669533 | CAAAAAAA | C | 14 | a0001c0001t0001g0102 a0001c0001t0001g0120 a0001c0001t0001g0171 others(11): Show |
17 | HG00609.hp1 HG01255.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.2136+451_2136+457d others(9): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100669533 | ||||||
chr3:100669597 | G | A | 1 | a0003c0003t0001g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2136+492G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100669597 | |||||||
chr3:100669633 | A | G | 1 | a0003c0003t0001g0019 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2136+528A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100669633 | |||||||
chr3:100669678 | T | C | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2136+573T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100669678 | |||||||
chr3:100669687 | T | A | 1 | a0003c0003t0001g0026 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2136+582T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100669687 | |||||||
chr3:100669788 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2136+683C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100669788 | |||||||
chr3:100669990 | A | G | 2 | a0001c0001t0001g0174 a0001c0001t0001g0176 |
2 | HG00741.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.2136+885A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100669990 | |||||||
chr3:100670066 | A | C | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2136+961A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670066 | |||||||
chr3:100670113 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2136+1008T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670113 | |||||||
chr3:100670125 | A | G | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2136+1020A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670125 | |||||||
chr3:100670145 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2136+1040G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670145 | |||||||
chr3:100670188 | T | A | 144 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0079 others(141): Show |
160 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.2136+1083T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670188 | |||||||
chr3:100670200 | C | CT | 6 | a0001c0001t0001g0096 a0001c0001t0001g0157 a0001c0001t0001g0173 others(3): Show |
6 | HG00423.hp1 HG02015.hp1 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.2136+1096dupT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100670200 | ||||||
chr3:100670412 | T | C | 1 | a0001c0001t0003g0033 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2136+1307T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670412 | |||||||
chr3:100670481 | G | A | 1 | a0003c0003t0003g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2136+1376G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670481 | |||||||
chr3:100670490 | T | C | 1 | a0001c0001t0001g0181 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2136+1385T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670490 | |||||||
chr3:100670495 | A | G | 211 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(208): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.2136+1390A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670495 | |||||||
chr3:100670513 | T | C | 16 | a0001c0001t0003g0033 a0001c0001t0003g0108 a0001c0001t0003g0126 others(13): Show |
16 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+1408T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670513 | |||||||
chr3:100670567 | T | C | 68 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(65): Show |
72 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.2136+1462T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670567 | |||||||
chr3:100670572 | A | G | 3 | a0001c0001t0003g0167 a0001c0001t0003g0168 a0001c0001t0003g0169 |
3 | HG02258.hp1 HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2136+1467A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670572 | |||||||
chr3:100670601 | G | A | 1 | a0003c0003t0001g0029 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2136+1496G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670601 | |||||||
chr3:100670636 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2136+1531C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670636 | |||||||
chr3:100670751 | C | G | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2136+1646C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670751 | |||||||
chr3:100670845 | A | G | 2 | a0001c0008t0009g0036 a0001c0010t0001g0039 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2136+1740A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670845 | |||||||
chr3:100670869 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2136+1764T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100670869 | |||||||
chr3:100671120 | C | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2136+2015C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100671120 | |||||||
chr3:100671121 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2136+2016G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100671121 | |||||||
chr3:100671338 | C | T | 1 | a0003c0003t0001g0026 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2136+2233C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100671338 | |||||||
chr3:100671366 | G | A | 1 | a0001c0001t0003g0033 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2136+2261G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100671366 | |||||||
chr3:100671393 | A | G | 244 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(241): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.2136+2288A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100671393 | |||||||
chr3:100671428 | G | C | 18 | a0001c0001t0003g0033 a0001c0001t0003g0108 a0001c0001t0003g0126 others(15): Show |
18 | HG00735.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.2136+2323G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100671428 | |||||||
chr3:100671448 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2136+2343A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100671448 | |||||||
chr3:100671503 | G | T | 1 | a0003c0003t0003g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2136+2398G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100671503 | |||||||
chr3:100671606 | T | C | 14 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
14 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2136+2501T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100671606 | |||||||
chr3:100671694 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2136+2589A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100671694 | |||||||
chr3:100671931 | C | G | 18 | a0001c0001t0003g0033 a0001c0001t0003g0108 a0001c0001t0003g0126 others(15): Show |
18 | HG00735.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.2136+2826C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100671931 | |||||||
chr3:100672036 | T | C | 230 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(227): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.2136+2931T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100672036 | |||||||
chr3:100672037 | G | A | 17 | a0001c0001t0001g0199 a0001c0001t0003g0033 a0001c0001t0003g0108 others(14): Show |
17 | HG00735.hp2 HG01934.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.2136+2932G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100672037 | |||||||
chr3:100672422 | A | G | 214 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(211): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.2136+3317A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100672422 | |||||||
chr3:100672461 | G | A | 3 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0005t0008g0106 |
3 | HG00280.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2136+3356G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100672461 | |||||||
chr3:100672494 | G | A | 16 | a0001c0001t0003g0033 a0001c0001t0003g0108 a0001c0001t0003g0126 others(13): Show |
16 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+3389G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100672494 | |||||||
chr3:100672499 | C | G | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2136+3394C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100672499 | |||||||
chr3:100672611 | A | G | 4 | a0002c0002t0001g0306 a0002c0002t0001g0310 a0002c0002t0001g0311 others(1): Show |
4 | HG02615.hp2 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2136+3506A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100672611 | |||||||
chr3:100672621 | C | A | 1 | a0001c0001t0001g0200 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2136+3516C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100672621 | |||||||
chr3:100672627 | C | G | 16 | a0001c0001t0003g0033 a0001c0001t0003g0108 a0001c0001t0003g0126 others(13): Show |
16 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+3522C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100672627 | |||||||
chr3:100672753 | A | G | 45 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0079 others(42): Show |
47 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.2136+3648A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100672753 | |||||||
chr3:100672798 | A | G | 1 | a0002c0002t0001g0288 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2136+3693A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100672798 | |||||||
chr3:100673020 | T | G | 3 | a0005c0006t0001g0006 a0005c0006t0001g0030 a0005c0006t0001g0031 |
4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2136+3915T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100673020 | |||||||
chr3:100673022 | G | T | 119 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(116): Show |
134 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.2136+3917G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100673022 | |||||||
chr3:100673034 | G | C | 2 | a0001c0008t0009g0036 a0001c0010t0001g0039 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2136+3929G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100673034 | |||||||
chr3:100673054 | T | A | 2 | a0001c0008t0009g0036 a0001c0010t0001g0039 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2136+3949T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100673054 | |||||||
chr3:100673151 | T | G | 244 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(241): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.2136+4046T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100673151 | |||||||
chr3:100673271 | G | A | 16 | a0001c0001t0003g0033 a0001c0001t0003g0108 a0001c0001t0003g0126 others(13): Show |
16 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+4166G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100673271 | |||||||
chr3:100673276 | C | G | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2136+4171C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100673276 | |||||||
chr3:100673347 | T | C | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2136+4242T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100673347 | |||||||
chr3:100673467 | C | CT | 5 | a0001c0001t0001g0012 a0001c0001t0001g0182 a0005c0006t0001g0006 others(2): Show |
7 | HG00738.hp1 HG01071.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.2136+4376dupT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100673467 | ||||||
chr3:100673467 | CT | C | 169 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(166): Show |
186 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.2136+4376delT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100673467 | ||||||
chr3:100673502 | T | C | 229 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(226): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.2136+4397T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100673502 | |||||||
chr3:100673519 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2136+4414T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100673519 | |||||||
chr3:100673524 | T | C | 226 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(223): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.2136+4419T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100673524 | |||||||
chr3:100673544 | C | T | 208 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(205): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.2136+4439C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100673544 | |||||||
chr3:100673720 | G | A | 14 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
14 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2136+4615G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100673720 | |||||||
chr3:100673818 | T | C | 1 | a0001c0008t0009g0036 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2136+4713T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100673818 | |||||||
chr3:100673977 | T | A | 3 | a0005c0006t0001g0006 a0005c0006t0001g0030 a0005c0006t0001g0031 |
4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2136+4872T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100673977 | |||||||
chr3:100674068 | G | T | 16 | a0001c0001t0003g0033 a0001c0001t0003g0108 a0001c0001t0003g0126 others(13): Show |
16 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+4963G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100674068 | |||||||
chr3:100674207 | T | C | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2136+5102T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100674207 | |||||||
chr3:100674467 | A | G | 1 | a0001c0001t0001g0255 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2136+5362A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100674467 | |||||||
chr3:100674479 | T | C | 1 | a0003c0003t0003g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2136+5374T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100674479 | |||||||
chr3:100674487 | G | A | 7 | a0001c0001t0003g0033 a0001c0001t0003g0108 a0001c0001t0003g0126 others(4): Show |
7 | HG02258.hp1 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2136+5382G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100674487 | |||||||
chr3:100674533 | T | A | 1 | a0002c0002t0001g0071 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2136+5428T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100674533 | |||||||
chr3:100674576 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2136+5471T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100674576 | |||||||
chr3:100674579 | C | CT | 6 | a0001c0001t0001g0075 a0001c0001t0001g0104 a0001c0001t0001g0238 others(3): Show |
7 | HG01192.hp1 HG01975.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.2136+5490dupT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100674579 | ||||||
chr3:100674579 | CT | C | 157 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(154): Show |
173 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.2136+5490delT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100674579 | ||||||
chr3:100674735 | C | G | 229 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(226): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.2136+5630C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100674735 | |||||||
chr3:100674800 | A | G | 1 | a0002c0002t0001g0308 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2136+5695A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100674800 | |||||||
chr3:100674913 | T | C | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2136+5808T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100674913 | |||||||
chr3:100675126 | G | A | 229 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(226): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.2136+6021G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100675126 | |||||||
chr3:100675129 | A | G | 2 | a0001c0001t0001g0254 a0001c0001t0001g0256 |
2 | NA18999.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.2136+6024A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100675129 | |||||||
chr3:100675163 | T | G | 229 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(226): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.2136+6058T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100675163 | |||||||
chr3:100675325 | A | T | 16 | a0001c0001t0003g0033 a0001c0001t0003g0108 a0001c0001t0003g0126 others(13): Show |
16 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+6220A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100675325 | |||||||
chr3:100675534 | G | T | 1 | a0001c0001t0001g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2136+6429G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100675534 | |||||||
chr3:100675656 | T | G | 1 | a0001c0001t0001g0249 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2136+6551T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100675656 | |||||||
chr3:100675788 | G | C | 7 | a0001c0001t0003g0033 a0001c0001t0003g0108 a0001c0001t0003g0126 others(4): Show |
7 | HG02258.hp1 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2136+6683G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100675788 | |||||||
chr3:100676052 | A | T | 1 | a0003c0003t0003g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2136+6947A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100676052 | |||||||
chr3:100676361 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2136+7256C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100676361 | |||||||
chr3:100676362 | G | A | 16 | a0001c0001t0003g0033 a0001c0001t0003g0108 a0001c0001t0003g0126 others(13): Show |
16 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+7257G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100676362 | |||||||
chr3:100676443 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2136+7338T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100676443 | |||||||
chr3:100676447 | G | A | 2 | a0001c0001t0001g0082 a0001c0005t0008g0106 |
2 | HG00280.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.2136+7342G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100676447 | |||||||
chr3:100676605 | T | C | 1 | a0001c0001t0003g0033 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2136+7500T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100676605 | |||||||
chr3:100676666 | C | A | 11 | a0002c0002t0001g0015 a0002c0002t0001g0016 a0002c0002t0001g0017 others(8): Show |
14 | HG00609.hp1 HG01255.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.2136+7561C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100676666 | |||||||
chr3:100676791 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2136+7686C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100676791 | |||||||
chr3:100676812 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2136+7707G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100676812 | |||||||
chr3:100676885 | T | C | 9 | a0004c0004t0002g0022 a0004c0004t0002g0037 a0004c0004t0002g0038 others(6): Show |
9 | HG00735.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2136+7780T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100676885 | |||||||
chr3:100676976 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2136+7871G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100676976 | |||||||
chr3:100677006 | G | A | 14 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
14 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2136+7901G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100677006 | |||||||
chr3:100677115 | A | G | 9 | a0004c0004t0002g0022 a0004c0004t0002g0037 a0004c0004t0002g0038 others(6): Show |
9 | HG00735.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2136+8010A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100677115 | |||||||
chr3:100677167 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2136+8062C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100677167 | |||||||
chr3:100677295 | C | T | 18 | a0001c0001t0003g0033 a0001c0001t0003g0108 a0001c0001t0003g0126 others(15): Show |
18 | HG00735.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.2136+8190C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100677295 | |||||||
chr3:100677383 | T | C | 2 | a0002c0002t0001g0016 a0002c0002t0001g0017 |
4 | HG00609.hp1 NA19005.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.2136+8278T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100677383 | |||||||
chr3:100677539 | A | G | 2 | a0002c0002t0001g0261 a0002c0002t0001g0262 |
2 | HG01099.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2136+8434A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100677539 | |||||||
chr3:100677610 | G | T | 1 | a0001c0001t0001g0046 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2136+8505G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100677610 | |||||||
chr3:100677752 | T | C | 2 | a0001c0008t0009g0036 a0001c0010t0001g0039 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2136+8647T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100677752 | |||||||
chr3:100677761 | A | G | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2136+8656A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100677761 | |||||||
chr3:100677763 | A | C | 2 | a0003c0003t0001g0137 a0008c0017t0001g0138 |
2 | HG02523.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.2136+8658A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100677763 | |||||||
chr3:100677780 | A | G | 230 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(227): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.2136+8675A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100677780 | |||||||
chr3:100677883 | A | G | 68 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(65): Show |
72 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.2136+8778A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100677883 | |||||||
chr3:100677951 | C | T | 3 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0005t0008g0106 |
3 | HG00280.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2136+8846C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100677951 | |||||||
chr3:100678071 | G | T | 62 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(59): Show |
65 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.2136+8966G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100678071 | |||||||
chr3:100678113 | AT | A | 7 | a0001c0001t0003g0033 a0001c0001t0003g0108 a0001c0001t0003g0126 others(4): Show |
7 | HG02258.hp1 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2136+9010delT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100678113 | ||||||
chr3:100678306 | A | G | 14 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
14 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2136+9201A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100678306 | |||||||
chr3:100678358 | C | T | 16 | a0001c0001t0003g0033 a0001c0001t0003g0108 a0001c0001t0003g0126 others(13): Show |
16 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+9253C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100678358 | |||||||
chr3:100678410 | G | T | 3 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0005t0008g0106 |
3 | HG00280.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2136+9305G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100678410 | |||||||
chr3:100678748 | T | C | 18 | a0001c0001t0003g0033 a0001c0001t0003g0108 a0001c0001t0003g0126 others(15): Show |
18 | HG00735.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.2136+9643T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100678748 | |||||||
chr3:100678938 | G | C | 1 | a0001c0001t0001g0157 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2136+9833G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100678938 | |||||||
chr3:100678978 | C | G | 1 | a0001c0001t0001g0048 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2136+9873C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100678978 | |||||||
chr3:100679070 | C | G | 239 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(236): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.2136+9965C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100679070 | |||||||
chr3:100679243 | C | T | 16 | a0001c0001t0003g0033 a0001c0001t0003g0108 a0001c0001t0003g0126 others(13): Show |
16 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+10138C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100679243 | |||||||
chr3:100679383 | C | A | 2 | a0001c0001t0001g0066 a0009c0012t0001g0067 |
2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2136+10278C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100679383 | |||||||
chr3:100679397 | G | C | 1 | a0008c0017t0001g0138 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2136+10292G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100679397 | |||||||
chr3:100679460 | T | C | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2136+10355T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100679460 | |||||||
chr3:100679561 | C | T | 16 | a0001c0001t0003g0033 a0001c0001t0003g0108 a0001c0001t0003g0126 others(13): Show |
16 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+10456C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100679561 | |||||||
chr3:100679678 | A | C | 149 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(146): Show |
165 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.2136+10573A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100679678 | |||||||
chr3:100680330 | T | A | 5 | a0001c0001t0003g0108 a0001c0001t0003g0126 a0001c0001t0003g0167 others(2): Show |
5 | HG02258.hp1 HG02559.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2136+11225T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100680330 | |||||||
chr3:100680373 | A | G | 1 | a0003c0003t0001g0147 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2136+11268A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100680373 | |||||||
chr3:100680395 | G | A | 1 | a0001c0001t0005g0072 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2136+11290G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100680395 | |||||||
chr3:100680466 | T | A | 16 | a0001c0001t0003g0033 a0001c0001t0003g0108 a0001c0001t0003g0126 others(13): Show |
16 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+11361T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100680466 | |||||||
chr3:100680607 | G | A | 3 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0005t0008g0106 |
3 | HG00280.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2136+11502G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100680607 | |||||||
chr3:100680608 | C | A | 3 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0005t0008g0106 |
3 | HG00280.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2136+11503C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100680608 | |||||||
chr3:100680613 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2136+11508C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100680613 | |||||||
chr3:100680658 | T | C | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2136+11553T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100680658 | |||||||
chr3:100680668 | G | A | 243 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(240): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.2136+11563G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100680668 | |||||||
chr3:100680751 | C | T | 1 | a0001c0001t0001g0314 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2136+11646C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100680751 | |||||||
chr3:100680752 | G | A | 16 | a0001c0001t0003g0033 a0001c0001t0003g0108 a0001c0001t0003g0126 others(13): Show |
16 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+11647G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100680752 | |||||||
chr3:100680768 | C | T | 64 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(61): Show |
67 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.2136+11663C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100680768 | |||||||
chr3:100680769 | G | A | 16 | a0001c0001t0003g0033 a0001c0001t0003g0108 a0001c0001t0003g0126 others(13): Show |
16 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2136+11664G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100680769 | |||||||
chr3:100680792 | A | G | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2136+11687A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100680792 | |||||||
chr3:100681070 | T | C | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2136+11965T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100681070 | |||||||
chr3:100681190 | T | C | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2136+12085T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100681190 | |||||||
chr3:100681293 | A | ATCTTT | 16 | a0001c0001t0001g0086 a0001c0001t0001g0092 a0001c0001t0001g0103 others(13): Show |
16 | HG02027.hp2 HG02129.hp1 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.2136+12200_2136+12 others(11): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100681293 | ||||||
chr3:100681305 | C | CT | 8 | a0001c0001t0001g0123 a0001c0001t0001g0229 a0001c0001t0005g0072 others(5): Show |
9 | HG00438.hp2 HG00609.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.2136+12214dupT | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100681305 | ||||||
chr3:100681321 | T | C | 9 | a0004c0004t0002g0022 a0004c0004t0002g0037 a0004c0004t0002g0038 others(6): Show |
9 | HG00735.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2136+12216T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100681321 | |||||||
chr3:100681396 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2136+12291C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100681396 | |||||||
chr3:100681410 | A | G | 70 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(67): Show |
75 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.2136+12305A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100681410 | |||||||
chr3:100681438 | G | C | 1 | a0002c0002t0001g0260 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2136+12333G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100681438 | |||||||
chr3:100681784 | A | G | 3 | a0003c0003t0001g0129 a0003c0003t0001g0132 a0003c0003t0001g0133 |
3 | HG01074.hp1 HG01943.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.2136+12679A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100681784 | |||||||
chr3:100681799 | C | G | 1 | a0001c0001t0001g0173 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2136+12694C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100681799 | |||||||
chr3:100681889 | C | T | 148 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(145): Show |
164 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.2136+12784C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100681889 | |||||||
chr3:100682295 | G | A | 214 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(211): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.2137-12449G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100682295 | |||||||
chr3:100682356 | C | T | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2137-12388C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100682356 | |||||||
chr3:100682357 | G | C | 2 | a0002c0002t0001g0270 a0002c0002t0001g0298 |
2 | NA18950.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.2137-12387G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100682357 | |||||||
chr3:100682404 | A | T | 9 | a0004c0004t0002g0022 a0004c0004t0002g0037 a0004c0004t0002g0038 others(6): Show |
9 | HG00735.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2137-12340A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100682404 | |||||||
chr3:100682499 | C | A | 1 | a0001c0001t0001g0092 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2137-12245C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100682499 | |||||||
chr3:100682661 | G | T | 214 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(211): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.2137-12083G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100682661 | |||||||
chr3:100682700 | C | A | 3 | a0005c0006t0001g0006 a0005c0006t0001g0030 a0005c0006t0001g0031 |
4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2137-12044C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100682700 | |||||||
chr3:100682824 | G | T | 1 | a0002c0002t0001g0308 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2137-11920G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100682824 | |||||||
chr3:100682955 | T | C | 235 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(232): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.2137-11789T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100682955 | |||||||
chr3:100682967 | G | A | 1 | a0003c0003t0001g0136 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2137-11777G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100682967 | |||||||
chr3:100683137 | A | G | 8 | a0001c0008t0001g0041 a0002c0002t0001g0071 a0002c0002t0001g0306 others(5): Show |
8 | HG01891.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2137-11607A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100683137 | |||||||
chr3:100683183 | C | T | 51 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0079 others(48): Show |
53 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.2137-11561C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100683183 | |||||||
chr3:100683336 | C | A | 3 | a0005c0006t0001g0006 a0005c0006t0001g0030 a0005c0006t0001g0031 |
4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2137-11408C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100683336 | |||||||
chr3:100683378 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2137-11366C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100683378 | |||||||
chr3:100683528 | C | A | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-11216C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100683528 | |||||||
chr3:100683570 | C | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-11174C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100683570 | |||||||
chr3:100683641 | G | A | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-11103G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100683641 | |||||||
chr3:100683667 | T | G | 2 | a0002c0002t0001g0270 a0002c0002t0001g0298 |
2 | NA18950.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.2137-11077T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100683667 | |||||||
chr3:100683676 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0078 a0001c0001t0001g0229 |
4 | HG00438.hp2 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2137-11068G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100683676 | |||||||
chr3:100683847 | T | C | 9 | a0004c0004t0002g0022 a0004c0004t0002g0037 a0004c0004t0002g0038 others(6): Show |
9 | HG00735.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2137-10897T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100683847 | |||||||
chr3:100684187 | C | G | 2 | a0001c0008t0009g0036 a0001c0010t0001g0039 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2137-10557C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100684187 | |||||||
chr3:100684257 | C | CTATCTAT others(5): Show |
2 | a0001c0001t0001g0066 a0009c0012t0001g0067 |
2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2137-10484_2137-10 others(18): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100684257 | ||||||
chr3:100684257 | C | CTATTTAT others(1): Show |
179 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0032 others(176): Show |
195 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.2137-10470_2137-10 others(14): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100684257 | ||||||
chr3:100684257 | C | CTATTTAT others(5): Show |
13 | a0001c0001t0001g0117 a0001c0001t0001g0160 a0001c0001t0001g0178 others(10): Show |
14 | HG01109.hp2 HG01123.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.2137-10474_2137-10 others(18): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100684257 | ||||||
chr3:100684257 | C | CTATTTAT others(9): Show |
5 | a0001c0001t0001g0166 a0001c0001t0001g0242 a0001c0001t0002g0061 others(2): Show |
5 | HG02080.hp1 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2137-10478_2137-10 others(22): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100684257 | ||||||
chr3:100684257 | C | CTATTTAT others(13): Show |
33 | a0001c0001t0001g0078 a0001c0001t0001g0200 a0001c0001t0001g0205 others(30): Show |
34 | HG00735.hp2 HG01243.hp1 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.2137-10482_2137-10 others(26): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100684257 | ||||||
chr3:100684257 | C | CTATTTAT others(17): Show |
56 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(53): Show |
59 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.2137-10486_2137-10 others(30): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100684257 | ||||||
chr3:100684257 | C | CTATTTAT others(21): Show |
1 | a0001c0001t0001g0315 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2137-10463_2137-10 others(34): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100684257 | ||||||
chr3:100684266 | T | TATTTATT others(6): Show |
1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-10477_2137-10 others(19): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100684266 | ||||||
chr3:100684364 | A | G | 3 | a0005c0006t0001g0006 a0005c0006t0001g0030 a0005c0006t0001g0031 |
4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2137-10380A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100684364 | |||||||
chr3:100684389 | A | C | 18 | a0001c0001t0003g0033 a0001c0001t0003g0108 a0001c0001t0003g0126 others(15): Show |
18 | HG00735.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.2137-10355A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100684389 | |||||||
chr3:100685033 | T | C | 1 | a0004c0004t0002g0022 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2137-9711T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685033 | |||||||
chr3:100685083 | T | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(108): Show |
126 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.2137-9661T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685083 | |||||||
chr3:100685126 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2137-9618C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685126 | |||||||
chr3:100685296 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0158 |
2 | HG03130.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.2137-9448C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685296 | |||||||
chr3:100685354 | T | A | 2 | a0001c0008t0009g0036 a0001c0010t0001g0039 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2137-9390T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685354 | |||||||
chr3:100685422 | C | T | 8 | a0001c0001t0003g0033 a0001c0001t0003g0108 a0001c0001t0003g0126 others(5): Show |
8 | HG00280.hp1 HG02258.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2137-9322C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685422 | |||||||
chr3:100685482 | G | A | 111 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(108): Show |
126 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.2137-9262G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685482 | |||||||
chr3:100685494 | T | G | 1 | a0001c0001t0001g0175 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2137-9250T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685494 | |||||||
chr3:100685580 | T | C | 1 | a0001c0001t0005g0072 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2137-9164T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685580 | |||||||
chr3:100685602 | C | A | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2137-9142C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685602 | |||||||
chr3:100685643 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2137-9101C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685643 | |||||||
chr3:100685660 | T | A | 3 | a0005c0006t0001g0006 a0005c0006t0001g0030 a0005c0006t0001g0031 |
4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2137-9084T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685660 | |||||||
chr3:100685717 | C | T | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2137-9027C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685717 | |||||||
chr3:100685823 | C | T | 4 | a0001c0001t0001g0157 a0001c0001t0001g0173 a0001c0001t0001g0210 others(1): Show |
4 | HG00423.hp1 HG02027.hp1 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.2137-8921C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685823 | |||||||
chr3:100685824 | A | G | 4 | a0001c0001t0001g0157 a0001c0001t0001g0173 a0001c0001t0001g0210 others(1): Show |
4 | HG00423.hp1 HG02027.hp1 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.2137-8920A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685824 | |||||||
chr3:100685982 | G | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-8762G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100685982 | |||||||
chr3:100686020 | A | G | 18 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0003g0033 others(15): Show |
18 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.2137-8724A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100686020 | |||||||
chr3:100686061 | G | A | 1 | a0001c0001t0003g0033 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2137-8683G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100686061 | |||||||
chr3:100686067 | G | C | 136 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(133): Show |
151 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.2137-8677G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100686067 | |||||||
chr3:100686151 | T | C | 2 | a0001c0008t0009g0036 a0001c0010t0001g0039 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2137-8593T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100686151 | |||||||
chr3:100686293 | A | G | 1 | a0003c0003t0001g0149 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2137-8451A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100686293 | |||||||
chr3:100686324 | T | C | 3 | a0006c0007t0004g0042 a0006c0007t0004g0043 a0006c0007t0004g0044 |
3 | HG02109.hp1 HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2137-8420T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100686324 | |||||||
chr3:100686459 | G | A | 207 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(204): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.2137-8285G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100686459 | |||||||
chr3:100686475 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2137-8269C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100686475 | |||||||
chr3:100686581 | G | C | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-8163G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100686581 | |||||||
chr3:100686644 | A | G | 68 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(65): Show |
72 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.2137-8100A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100686644 | |||||||
chr3:100686693 | T | C | 311 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(308): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.2137-8051T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100686693 | |||||||
chr3:100686828 | C | A | 2 | a0001c0008t0009g0036 a0001c0010t0001g0039 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2137-7916C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100686828 | |||||||
chr3:100686852 | G | A | 137 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(134): Show |
152 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.2137-7892G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100686852 | |||||||
chr3:100686857 | G | A | 137 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(134): Show |
152 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.2137-7887G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100686857 | |||||||
chr3:100687014 | A | G | 3 | a0002c0002t0001g0302 a0002c0002t0001g0304 a0002c0002t0001g0305 |
3 | HG02165.hp2 NA18999.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2137-7730A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687014 | |||||||
chr3:100687039 | A | T | 1 | a0001c0001t0003g0033 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2137-7705A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687039 | |||||||
chr3:100687172 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2137-7572C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687172 | |||||||
chr3:100687242 | G | T | 1 | a0001c0001t0001g0053 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2137-7502G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687242 | |||||||
chr3:100687335 | G | A | 118 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(115): Show |
133 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.2137-7409G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687335 | |||||||
chr3:100687431 | C | G | 18 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0003g0033 others(15): Show |
18 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.2137-7313C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687431 | |||||||
chr3:100687510 | C | G | 1 | a0011c0013t0001g0190 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2137-7234C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687510 | |||||||
chr3:100687511 | G | A | 3 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0002c0002t0001g0301 |
3 | HG01358.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2137-7233G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687511 | |||||||
chr3:100687583 | C | T | 207 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(204): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.2137-7161C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687583 | |||||||
chr3:100687616 | C | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-7128C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687616 | |||||||
chr3:100687718 | G | C | 1 | a0001c0001t0001g0220 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2137-7026G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687718 | |||||||
chr3:100687743 | G | T | 1 | a0001c0001t0001g0117 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2137-7001G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687743 | |||||||
chr3:100687771 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2137-6973C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687771 | |||||||
chr3:100687815 | C | A | 2 | a0002c0002t0001g0261 a0002c0002t0001g0262 |
2 | HG01099.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2137-6929C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687815 | |||||||
chr3:100687896 | T | C | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2137-6848T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687896 | |||||||
chr3:100687903 | G | T | 1 | a0001c0008t0001g0041 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2137-6841G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687903 | |||||||
chr3:100687934 | A | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-6810A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687934 | |||||||
chr3:100687950 | T | A | 118 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(115): Show |
133 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.2137-6794T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687950 | |||||||
chr3:100687999 | T | C | 8 | a0001c0008t0001g0041 a0002c0002t0001g0071 a0002c0002t0001g0306 others(5): Show |
8 | HG01891.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2137-6745T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100687999 | |||||||
chr3:100688005 | A | C | 141 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(138): Show |
157 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.2137-6739A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688005 | |||||||
chr3:100688046 | T | A | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-6698T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688046 | |||||||
chr3:100688109 | A | G | 137 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(134): Show |
152 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.2137-6635A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688109 | |||||||
chr3:100688141 | C | G | 1 | a0002c0002t0001g0303 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2137-6603C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688141 | |||||||
chr3:100688181 | T | C | 1 | a0002c0002t0001g0259 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2137-6563T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688181 | |||||||
chr3:100688187 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2137-6557G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688187 | |||||||
chr3:100688191 | C | G | 1 | a0002c0002t0001g0259 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2137-6553C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688191 | |||||||
chr3:100688214 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2137-6530A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688214 | |||||||
chr3:100688245 | T | C | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2137-6499T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688245 | |||||||
chr3:100688246 | G | A | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2137-6498G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688246 | |||||||
chr3:100688264 | T | C | 1 | a0003c0003t0003g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2137-6480T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688264 | |||||||
chr3:100688291 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2137-6453T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688291 | |||||||
chr3:100688292 | G | T | 1 | a0001c0001t0001g0118 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2137-6452G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688292 | |||||||
chr3:100688297 | A | T | 1 | a0001c0001t0001g0118 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2137-6447A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688297 | |||||||
chr3:100688431 | T | A | 5 | a0001c0001t0001g0125 a0001c0001t0001g0195 a0001c0001t0001g0223 others(2): Show |
5 | HG01123.hp2 HG01952.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.2137-6313T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688431 | |||||||
chr3:100688477 | C | A | 137 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(134): Show |
152 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.2137-6267C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688477 | |||||||
chr3:100688576 | G | C | 1 | a0001c0001t0001g0100 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2137-6168G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688576 | |||||||
chr3:100688582 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2137-6162G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688582 | |||||||
chr3:100688588 | A | G | 47 | a0001c0001t0001g0081 a0002c0002t0001g0001 a0002c0002t0001g0004 others(44): Show |
60 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.2137-6156A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688588 | |||||||
chr3:100688593 | C | T | 47 | a0001c0001t0001g0081 a0002c0002t0001g0001 a0002c0002t0001g0004 others(44): Show |
60 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.2137-6151C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688593 | |||||||
chr3:100688622 | A | G | 1 | a0001c0008t0001g0041 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2137-6122A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688622 | |||||||
chr3:100688649 | A | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-6095A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688649 | |||||||
chr3:100688655 | G | A | 136 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(133): Show |
151 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.2137-6089G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688655 | |||||||
chr3:100688738 | C | G | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-6006C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688738 | |||||||
chr3:100688763 | C | G | 2 | a0001c0001t0001g0066 a0009c0012t0001g0067 |
2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2137-5981C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688763 | |||||||
chr3:100688782 | G | A | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-5962G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688782 | |||||||
chr3:100688783 | A | C | 118 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(115): Show |
133 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.2137-5961A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688783 | |||||||
chr3:100688830 | G | A | 1 | a0002c0002t0001g0287 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2137-5914G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688830 | |||||||
chr3:100688862 | G | C | 1 | a0001c0008t0009g0036 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2137-5882G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688862 | |||||||
chr3:100688924 | G | T | 8 | a0001c0008t0001g0041 a0002c0002t0001g0071 a0002c0002t0001g0306 others(5): Show |
8 | HG01891.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2137-5820G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688924 | |||||||
chr3:100688928 | G | T | 137 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(134): Show |
152 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.2137-5816G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688928 | |||||||
chr3:100688971 | G | A | 3 | a0005c0006t0001g0006 a0005c0006t0001g0030 a0005c0006t0001g0031 |
4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2137-5773G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688971 | |||||||
chr3:100688983 | A | C | 110 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(107): Show |
125 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.2137-5761A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688983 | |||||||
chr3:100688999 | T | C | 3 | a0005c0006t0001g0006 a0005c0006t0001g0030 a0005c0006t0001g0031 |
4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2137-5745T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100688999 | |||||||
chr3:100689045 | G | A | 118 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(115): Show |
133 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.2137-5699G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689045 | |||||||
chr3:100689112 | A | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0096 a0001c0001t0001g0180 others(6): Show |
10 | NA18946.hp2 NA18957.hp2 NA18960.hp1 others(7): Show |
intron_variant | MODIFIER | c.2137-5632A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689112 | |||||||
chr3:100689170 | G | A | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2137-5574G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689170 | |||||||
chr3:100689279 | G | A | 15 | a0001c0001t0003g0033 a0001c0001t0003g0108 a0001c0001t0003g0126 others(12): Show |
15 | HG02109.hp1 HG02258.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.2137-5465G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689279 | |||||||
chr3:100689397 | C | T | 118 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(115): Show |
133 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.2137-5347C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689397 | |||||||
chr3:100689403 | A | T | 1 | a0003c0003t0001g0251 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2137-5341A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689403 | |||||||
chr3:100689442 | G | A | 16 | a0001c0001t0003g0033 a0001c0001t0003g0108 a0001c0001t0003g0126 others(13): Show |
16 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2137-5302G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689442 | |||||||
chr3:100689444 | T | C | 8 | a0001c0008t0001g0041 a0002c0002t0001g0071 a0002c0002t0001g0306 others(5): Show |
8 | HG01891.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2137-5300T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689444 | |||||||
chr3:100689447 | T | C | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-5297T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689447 | |||||||
chr3:100689453 | C | T | 18 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0003g0033 others(15): Show |
18 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.2137-5291C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689453 | |||||||
chr3:100689514 | G | A | 3 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0002c0002t0001g0307 |
3 | HG02970.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2137-5230G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689514 | |||||||
chr3:100689682 | T | C | 1 | a0001c0001t0001g0011 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2137-5062T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689682 | |||||||
chr3:100689703 | C | A | 1 | a0004c0004t0002g0038 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2137-5041C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689703 | |||||||
chr3:100689729 | T | G | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2137-5015T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689729 | |||||||
chr3:100689770 | A | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(136): Show |
154 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.2137-4974A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689770 | |||||||
chr3:100689866 | T | A | 9 | a0004c0004t0002g0022 a0004c0004t0002g0037 a0004c0004t0002g0038 others(6): Show |
9 | HG00735.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2137-4878T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689866 | |||||||
chr3:100689887 | C | T | 136 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(133): Show |
151 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.2137-4857C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689887 | |||||||
chr3:100689942 | T | C | 8 | a0001c0008t0001g0041 a0002c0002t0001g0071 a0002c0002t0001g0306 others(5): Show |
8 | HG01891.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2137-4802T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689942 | |||||||
chr3:100689973 | C | G | 3 | a0005c0006t0001g0006 a0005c0006t0001g0030 a0005c0006t0001g0031 |
4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2137-4771C>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100689973 | |||||||
chr3:100690069 | G | A | 9 | a0004c0004t0002g0022 a0004c0004t0002g0037 a0004c0004t0002g0038 others(6): Show |
9 | HG00735.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2137-4675G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100690069 | |||||||
chr3:100690102 | G | A | 2 | a0001c0008t0009g0036 a0001c0010t0001g0039 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2137-4642G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100690102 | |||||||
chr3:100690126 | A | G | 1 | a0001c0001t0005g0072 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2137-4618A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100690126 | |||||||
chr3:100690136 | G | A | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-4608G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100690136 | |||||||
chr3:100690157 | T | C | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2137-4587T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100690157 | |||||||
chr3:100690445 | T | A | 18 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0003g0033 others(15): Show |
18 | HG00735.hp2 HG02109.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.2137-4299T>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100690445 | |||||||
chr3:100690474 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2137-4270C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100690474 | |||||||
chr3:100690551 | G | A | 1 | a0001c0001t0001g0255 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2137-4193G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100690551 | |||||||
chr3:100690628 | G | A | 1 | a0003c0003t0001g0147 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2137-4116G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100690628 | |||||||
chr3:100690844 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2137-3900G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100690844 | |||||||
chr3:100690863 | T | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(136): Show |
154 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.2137-3881T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100690863 | |||||||
chr3:100690925 | G | T | 110 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(107): Show |
125 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.2137-3819G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100690925 | |||||||
chr3:100691027 | C | T | 3 | a0005c0006t0001g0006 a0005c0006t0001g0030 a0005c0006t0001g0031 |
4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2137-3717C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691027 | |||||||
chr3:100691141 | A | G | 2 | a0003c0003t0001g0026 a0003c0003t0001g0028 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2137-3603A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691141 | |||||||
chr3:100691152 | A | C | 8 | a0001c0008t0001g0041 a0002c0002t0001g0071 a0002c0002t0001g0306 others(5): Show |
8 | HG01891.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2137-3592A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691152 | |||||||
chr3:100691159 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2137-3585G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691159 | |||||||
chr3:100691169 | C | T | 8 | a0001c0008t0001g0041 a0002c0002t0001g0071 a0002c0002t0001g0306 others(5): Show |
8 | HG01891.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2137-3575C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691169 | |||||||
chr3:100691230 | G | A | 3 | a0001c0001t0001g0105 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | HG00099.hp1 HG01192.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.2137-3514G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691230 | |||||||
chr3:100691256 | G | A | 9 | a0004c0004t0002g0022 a0004c0004t0002g0037 a0004c0004t0002g0038 others(6): Show |
9 | HG00735.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2137-3488G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691256 | |||||||
chr3:100691313 | G | A | 1 | a0003c0003t0001g0130 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2137-3431G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691313 | |||||||
chr3:100691441 | A | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(136): Show |
154 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.2137-3303A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691441 | |||||||
chr3:100691523 | A | G | 1 | a0002c0002t0001g0261 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2137-3221A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691523 | |||||||
chr3:100691591 | T | G | 1 | a0001c0001t0001g0224 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2137-3153T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691591 | |||||||
chr3:100691608 | C | T | 120 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(117): Show |
135 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.2137-3136C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691608 | |||||||
chr3:100691609 | A | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(136): Show |
154 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.2137-3135A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691609 | |||||||
chr3:100691649 | T | G | 1 | a0001c0001t0001g0111 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2137-3095T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691649 | |||||||
chr3:100691698 | T | TGATGGGC others(320): Show |
4 | a0001c0001t0001g0073 a0001c0001t0001g0098 a0001c0001t0001g0192 others(1): Show |
4 | HG00280.hp2 HG01943.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.2137-3028_2137-302 others(331): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100691698 | ||||||
chr3:100691698 | T | TGATGGGC others(321): Show |
1 | a0001c0001t0001g0078 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2137-3028_2137-302 others(332): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100691698 | ||||||
chr3:100691698 | T | TGATGGGC others(321): Show |
1 | a0001c0001t0001g0200 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2137-3028_2137-302 others(332): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100691698 | ||||||
chr3:100691698 | T | TGATGGGC others(321): Show |
50 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(47): Show |
53 | HG00140.hp2 HG00597.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.2137-3028_2137-302 others(332): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100691698 | ||||||
chr3:100691698 | T | TGATGGGC others(321): Show |
5 | a0001c0008t0009g0036 a0001c0010t0001g0039 a0005c0006t0001g0006 others(2): Show |
6 | HG01975.hp2 HG02257.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2137-3028_2137-302 others(332): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100691698 | ||||||
chr3:100691698 | T | TGATGGGC others(322): Show |
7 | a0001c0001t0001g0105 a0001c0001t0001g0109 a0001c0001t0001g0111 others(4): Show |
7 | HG00099.hp1 HG00438.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.2137-3028_2137-302 others(333): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100691698 | ||||||
chr3:100691698 | T | TGATGGGC others(322): Show |
1 | a0001c0001t0005g0072 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2137-3028_2137-302 others(333): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100691698 | ||||||
chr3:100691698 | T | TGATGGGC others(323): Show |
1 | a0001c0001t0001g0238 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2137-3028_2137-302 others(334): Show |
ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 100691698 | ||||||
chr3:100691740 | C | A | 1 | a0001c0001t0005g0072 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2137-3004C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691740 | |||||||
chr3:100691748 | C | T | 118 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(115): Show |
133 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.2137-2996C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691748 | |||||||
chr3:100691779 | A | T | 110 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(107): Show |
125 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.2137-2965A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691779 | |||||||
chr3:100691880 | C | T | 110 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(107): Show |
125 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.2137-2864C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100691880 | |||||||
chr3:100692021 | C | T | 1 | a0003c0003t0001g0134 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2137-2723C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100692021 | |||||||
chr3:100692081 | T | C | 9 | a0004c0004t0002g0022 a0004c0004t0002g0037 a0004c0004t0002g0038 others(6): Show |
9 | HG00735.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2137-2663T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100692081 | |||||||
chr3:100692112 | A | C | 9 | a0004c0004t0002g0022 a0004c0004t0002g0037 a0004c0004t0002g0038 others(6): Show |
9 | HG00735.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2137-2632A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100692112 | |||||||
chr3:100692138 | A | G | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-2606A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100692138 | |||||||
chr3:100692456 | A | C | 3 | a0005c0006t0001g0006 a0005c0006t0001g0030 a0005c0006t0001g0031 |
4 | HG01975.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2137-2288A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100692456 | |||||||
chr3:100692490 | A | G | 79 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(76): Show |
83 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.2137-2254A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100692490 | |||||||
chr3:100692508 | C | T | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2137-2236C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100692508 | |||||||
chr3:100692517 | G | A | 207 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(204): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.2137-2227G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100692517 | |||||||
chr3:100692589 | C | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-2155C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100692589 | |||||||
chr3:100692738 | G | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0118 |
2 | HG00609.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.2137-2006G>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100692738 | |||||||
chr3:100692794 | T | G | 110 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(107): Show |
125 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.2137-1950T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100692794 | |||||||
chr3:100692851 | A | G | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-1893A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100692851 | |||||||
chr3:100692892 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2137-1852G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100692892 | |||||||
chr3:100692949 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2137-1795C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100692949 | |||||||
chr3:100693033 | A | T | 207 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(204): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.2137-1711A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100693033 | |||||||
chr3:100693050 | G | A | 207 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(204): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.2137-1694G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100693050 | |||||||
chr3:100693266 | G | T | 1 | a0001c0001t0001g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2137-1478G>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100693266 | |||||||
chr3:100693320 | A | C | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | NA18965.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2137-1424A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100693320 | |||||||
chr3:100693320 | A | G | 7 | a0001c0001t0003g0033 a0001c0001t0003g0108 a0001c0001t0003g0126 others(4): Show |
7 | HG02258.hp1 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2137-1424A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100693320 | |||||||
chr3:100693397 | A | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(204): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.2137-1347A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100693397 | |||||||
chr3:100693648 | A | T | 19 | a0001c0001t0001g0010 a0001c0001t0001g0084 a0001c0001t0001g0087 others(16): Show |
20 | HG00544.hp2 HG00558.hp2 HG02071.hp2 others(17): Show |
intron_variant | MODIFIER | c.2137-1096A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100693648 | |||||||
chr3:100693685 | A | T | 1 | a0001c0005t0008g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2137-1059A>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100693685 | |||||||
chr3:100693719 | C | A | 1 | a0001c0001t0001g0250 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2137-1025C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100693719 | |||||||
chr3:100693732 | T | C | 1 | a0001c0001t0001g0164 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2137-1012T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100693732 | |||||||
chr3:100693759 | T | G | 5 | a0001c0001t0003g0108 a0001c0001t0003g0126 a0001c0001t0003g0167 others(2): Show |
5 | HG02258.hp1 HG02559.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2137-985T>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100693759 | |||||||
chr3:100693841 | C | T | 7 | a0001c0001t0001g0012 a0001c0001t0001g0083 a0001c0001t0001g0117 others(4): Show |
8 | HG00735.hp1 HG00738.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.2137-903C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100693841 | |||||||
chr3:100693997 | A | C | 1 | a0001c0001t0001g0128 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2137-747A>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100693997 | |||||||
chr3:100694088 | C | A | 1 | a0002c0002t0001g0279 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2137-656C>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100694088 | |||||||
chr3:100694165 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2137-579G>A | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100694165 | |||||||
chr3:100694297 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2137-447A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100694297 | |||||||
chr3:100694419 | A | G | 7 | a0001c0001t0003g0033 a0001c0001t0003g0108 a0001c0001t0003g0126 others(4): Show |
7 | HG02258.hp1 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2137-325A>G | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100694419 | |||||||
chr3:100694515 | C | T | 8 | a0001c0008t0001g0041 a0002c0002t0001g0071 a0002c0002t0001g0306 others(5): Show |
8 | HG01891.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2137-229C>T | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100694515 | |||||||
chr3:100694641 | T | C | 1 | a0001c0001t0003g0033 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2137-103T>C | ADGRG7 | ENSG00000144820.8 | transcript | ENST00000273352.8 | protein_coding | 15/15 | chr3 | 100694641 |