Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 245973 |
| ensemblid | ENSG00000143882.12 |
| hgncid | 18264 |
| symbol | ATP6V1C2 |
| name | ATPase H+ transporting V1 subunit C2 |
| refseq_nuc | NM_001039362.2 |
| refseq_prot | NP_001034451.1 |
| ensembl_nuc | ENST00000272238.9 |
| ensembl_prot | ENSP00000272238.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 10721630 |
| end | 10785110 |
| strand | + |
| ver | v1.2 |
| region | chr2:10721630-10785110 |
| region5000 | chr2:10716630-10790110 |
| regionname0 | ATP6V1C2_chr2_10721630_10785110 |
| regionname5000 | ATP6V1C2_chr2_10716630_10790110 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 427 | 175 | 29 | 28 | 93 | 5 | 20 | 65 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | MSEFW others(422): Show |
chr2 | 10716630 | 10790110 |
| a0002 | 1/1 | 427 | 172 | 58 | 41 | 44 | 5 | 22 | 34 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | MSEFW others(422): Show |
chr2 | 10716630 | 10790110 |
| a0003 | 0/0 | 427 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | MSEFW others(422): Show |
chr2 | 10716630 | 10790110 |
| a0004 | 0/0 | 427 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | MSEFW others(422): Show |
chr2 | 10716630 | 10790110 |
| a0005 | 0/0 | 427 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | MSEFW others(422): Show |
chr2 | 10716630 | 10790110 |
| a0006 | 0/0 | 427 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | MSEFW others(422): Show |
chr2 | 10716630 | 10790110 |
| a0007 | 0/0 | 427 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | MSEFW others(422): Show |
chr2 | 10716630 | 10790110 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1281 | 170 | 27 | 27 | 93 | 5 | 18 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | ATGTC others(1276): Show |
chr2 | 10716630 | 10790110 | ||
| a0001c0006 | 0/0 | 1281 | 3 | 0 | 1 | 0 | 0 | 2 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | ATGTC others(1276): Show |
chr2 | 10716630 | 10790110 | ||
| a0001c0015 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | ATGTC others(1276): Show |
chr2 | 10716630 | 10790110 | ||
| a0001c0016 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | ATGTC others(1276): Show |
chr2 | 10716630 | 10790110 | ||
| a0002c0002 | 1/1 | 1281 | 124 | 42 | 29 | 40 | 2 | 9 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | ATGTC others(1276): Show |
chr2 | 10716630 | 10790110 | ||
| a0002c0003 | 0/0 | 1281 | 25 | 8 | 7 | 4 | 2 | 4 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | ATGTC others(1276): Show |
chr2 | 10716630 | 10790110 | ||
| a0002c0004 | 0/0 | 1281 | 12 | 2 | 1 | 0 | 1 | 8 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | ATGTC others(1276): Show |
chr2 | 10716630 | 10790110 | ||
| a0002c0005 | 0/0 | 1281 | 4 | 4 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | ATGTC others(1276): Show |
chr2 | 10716630 | 10790110 | ||
| a0002c0007 | 0/0 | 1281 | 3 | 0 | 3 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | ATGTC others(1276): Show |
chr2 | 10716630 | 10790110 | ||
| a0002c0009 | 0/0 | 1281 | 2 | 1 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | ATGTC others(1276): Show |
chr2 | 10716630 | 10790110 | ||
| a0002c0013 | 0/0 | 1281 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | ATGTC others(1276): Show |
chr2 | 10716630 | 10790110 | ||
| a0002c0018 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | ATGTC others(1276): Show |
chr2 | 10716630 | 10790110 | ||
| a0003c0008 | 0/0 | 1281 | 2 | 0 | 2 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | ATGTC others(1276): Show |
chr2 | 10716630 | 10790110 | ||
| a0003c0010 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | ATGTC others(1276): Show |
chr2 | 10716630 | 10790110 | ||
| a0004c0011 | 0/0 | 1281 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | ATGTC others(1276): Show |
chr2 | 10716630 | 10790110 | ||
| a0005c0012 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | ATGTC others(1276): Show |
chr2 | 10716630 | 10790110 | ||
| a0006c0017 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | ATGTC others(1276): Show |
chr2 | 10716630 | 10790110 | ||
| a0007c0014 | 0/0 | 1281 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | ATGTC others(1276): Show |
chr2 | 10716630 | 10790110 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3259 | 70 | 11 | 7 | 48 | 1 | 3 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3254): Show |
chr2 | 10716630 | 10790110 |
| a0001c0001t0002 | 0/0 | 3259 | 84 | 4 | 19 | 43 | 3 | 15 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3254): Show |
chr2 | 10716630 | 10790110 |
| a0001c0001t0004 | 0/0 | 3258 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3253): Show |
chr2 | 10716630 | 10790110 |
| a0001c0001t0006 | 0/0 | 3259 | 4 | 3 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3254): Show |
chr2 | 10716630 | 10790110 |
| a0001c0001t0007 | 0/0 | 3258 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3253): Show |
chr2 | 10716630 | 10790110 |
| a0001c0001t0008 | 0/0 | 3259 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3254): Show |
chr2 | 10716630 | 10790110 |
| a0001c0001t0011 | 0/0 | 3259 | 2 | 0 | 0 | 2 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3254): Show |
chr2 | 10716630 | 10790110 |
| a0001c0001t0013 | 0/0 | 3259 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3254): Show |
chr2 | 10716630 | 10790110 |
| a0001c0001t0016 | 0/0 | 3259 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3254): Show |
chr2 | 10716630 | 10790110 |
| a0001c0001t0020 | 0/0 | 3259 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3254): Show |
chr2 | 10716630 | 10790110 |
| a0001c0001t0026 | 0/0 | 3259 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3254): Show |
chr2 | 10716630 | 10790110 |
| a0001c0006t0005 | 0/0 | 3258 | 3 | 0 | 1 | 0 | 0 | 2 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3253): Show |
chr2 | 10716630 | 10790110 |
| a0001c0015t0006 | 0/0 | 3259 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3254): Show |
chr2 | 10716630 | 10790110 |
| a0001c0016t0001 | 0/0 | 3259 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3254): Show |
chr2 | 10716630 | 10790110 |
| a0002c0002t0001 | 1/1 | 3259 | 60 | 8 | 16 | 27 | 2 | 5 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3254): Show |
chr2 | 10716630 | 10790110 |
| a0002c0002t0002 | 0/0 | 3259 | 23 | 1 | 6 | 12 | 0 | 4 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3254): Show |
chr2 | 10716630 | 10790110 |
| a0002c0002t0003 | 0/0 | 3258 | 15 | 13 | 2 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3253): Show |
chr2 | 10716630 | 10790110 |
| a0002c0002t0004 | 0/0 | 3258 | 7 | 7 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3253): Show |
chr2 | 10716630 | 10790110 |
| a0002c0002t0006 | 0/0 | 3259 | 4 | 4 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3254): Show |
chr2 | 10716630 | 10790110 |
| a0002c0002t0007 | 0/0 | 3258 | 4 | 3 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3253): Show |
chr2 | 10716630 | 10790110 |
| a0002c0002t0008 | 0/0 | 3259 | 2 | 1 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3254): Show |
chr2 | 10716630 | 10790110 |
| a0002c0002t0010 | 0/0 | 3259 | 2 | 1 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3254): Show |
chr2 | 10716630 | 10790110 |
| a0002c0002t0014 | 0/0 | 3259 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3254): Show |
chr2 | 10716630 | 10790110 |
| a0002c0002t0015 | 0/0 | 3259 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3254): Show |
chr2 | 10716630 | 10790110 |
| a0002c0002t0018 | 0/0 | 3259 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3254): Show |
chr2 | 10716630 | 10790110 |
| a0002c0002t0019 | 0/0 | 3259 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3254): Show |
chr2 | 10716630 | 10790110 |
| a0002c0002t0023 | 0/0 | 3259 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3254): Show |
chr2 | 10716630 | 10790110 |
| a0002c0002t0024 | 0/0 | 3259 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3254): Show |
chr2 | 10716630 | 10790110 |
| a0002c0002t0025 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3253): Show |
chr2 | 10716630 | 10790110 |
| a0002c0003t0002 | 0/0 | 3259 | 17 | 0 | 7 | 4 | 2 | 4 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3254): Show |
chr2 | 10716630 | 10790110 |
| a0002c0003t0004 | 0/0 | 3258 | 6 | 6 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3253): Show |
chr2 | 10716630 | 10790110 |
| a0002c0003t0012 | 0/0 | 3259 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3254): Show |
chr2 | 10716630 | 10790110 |
| a0002c0004t0005 | 0/0 | 3258 | 12 | 2 | 1 | 0 | 1 | 8 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3253): Show |
chr2 | 10716630 | 10790110 |
| a0002c0005t0001 | 0/0 | 3259 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3254): Show |
chr2 | 10716630 | 10790110 |
| a0002c0005t0003 | 0/0 | 3258 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3253): Show |
chr2 | 10716630 | 10790110 |
| a0002c0005t0008 | 0/0 | 3259 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3254): Show |
chr2 | 10716630 | 10790110 |
| a0002c0007t0009 | 0/0 | 3258 | 3 | 0 | 3 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3253): Show |
chr2 | 10716630 | 10790110 |
| a0002c0009t0004 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3253): Show |
chr2 | 10716630 | 10790110 |
| a0002c0009t0022 | 0/0 | 3258 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3253): Show |
chr2 | 10716630 | 10790110 |
| a0002c0013t0001 | 0/0 | 3259 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3254): Show |
chr2 | 10716630 | 10790110 |
| a0002c0018t0013 | 0/0 | 3259 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3254): Show |
chr2 | 10716630 | 10790110 |
| a0003c0008t0003 | 0/0 | 3258 | 2 | 0 | 2 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3253): Show |
chr2 | 10716630 | 10790110 |
| a0003c0010t0002 | 0/0 | 3259 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3254): Show |
chr2 | 10716630 | 10790110 |
| a0004c0011t0017 | 0/0 | 3258 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3253): Show |
chr2 | 10716630 | 10790110 |
| a0005c0012t0003 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3253): Show |
chr2 | 10716630 | 10790110 |
| a0006c0017t0001 | 0/0 | 3259 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3254): Show |
chr2 | 10716630 | 10790110 |
| a0007c0014t0021 | 0/0 | 3258 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | GAAGC others(3253): Show |
chr2 | 10716630 | 10790110 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0006g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0007g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0007g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0008g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0008g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0011g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0011g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0013g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0016g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0020g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0026g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0006t0005g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0006t0005g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0006t0005g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0015t0006g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0016t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0235 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0274 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0006g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0006g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0006g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0007g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0007g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0007g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0007g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0008g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0008g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0010g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0010g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0014g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0015g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0018g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0019g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0023g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0024g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0025g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0003t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0003t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0003t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0003t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0003t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0003t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0003t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0003t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0003t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0003t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0003t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0003t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0003t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0003t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0003t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0003t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0003t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0003t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0003t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0003t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0003t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0003t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0003t0012g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0003t0012g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0004t0005g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0004t0005g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0004t0005g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0004t0005g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0004t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0004t0005g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0004t0005g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0004t0005g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0004t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0004t0005g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0004t0005g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0004t0005g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0005t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0005t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0005t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0005t0008g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0007t0009g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0007t0009g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0007t0009g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0009t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0009t0022g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0013t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0018t0013g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0003c0008t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0003c0008t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0003c0010t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0004c0011t0017g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0005c0012t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0006c0017t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0007c0014t0021g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0285 | EUR | GBR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0118 | EUR | GBR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00323 | hp1 | a0001 | c0001 | t0020 | g0056 | EUR | FIN | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00323 | hp2 | a0002 | c0003 | t0002 | g0093 | EUR | FIN | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | CHS | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | CHS | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0328 | EAS | CHS | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | CHS | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | CHS | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00597 | hp2 | a0002 | c0003 | t0002 | g0327 | EAS | CHS | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0184 | EAS | CHS | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | CHS | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00639 | hp1 | a0002 | c0009 | t0022 | g0155 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00639 | hp2 | a0002 | c0002 | t0008 | g0244 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0276 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | CHS | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0304 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00733 | hp2 | a0002 | c0003 | t0002 | g0277 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0315 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0351 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0303 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0261 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0264 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0150 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01069 | hp2 | a0002 | c0007 | t0009 | g0040 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0295 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01070 | hp2 | a0002 | c0002 | t0014 | g0222 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0284 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01071 | hp2 | a0002 | c0007 | t0009 | g0041 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0278 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0268 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0098 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01099 | hp1 | a0001 | c0006 | t0005 | g0038 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01099 | hp2 | a0002 | c0003 | t0002 | g0142 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0169 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01109 | hp1 | a0002 | c0002 | t0003 | g0224 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01109 | hp2 | a0002 | c0002 | t0024 | g0226 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0275 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01167 | hp2 | a0003 | c0008 | t0003 | g0122 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01169 | hp2 | a0003 | c0008 | t0003 | g0146 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0257 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0309 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01192 | hp1 | a0002 | c0007 | t0009 | g0151 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0269 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0283 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01243 | hp2 | a0002 | c0002 | t0003 | g0243 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0166 | AMR | CLM | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01255 | hp2 | a0002 | c0003 | t0002 | g0129 | AMR | CLM | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01256 | hp2 | a0002 | c0003 | t0002 | g0126 | AMR | CLM | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0305 | AMR | CLM | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01258 | hp1 | a0002 | c0003 | t0002 | g0127 | AMR | CLM | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01261 | hp1 | a0002 | c0002 | t0007 | g0234 | AMR | CLM | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0281 | AMR | CLM | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | CLM | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0272 | AMR | CLM | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0035 | AMR | CLM | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01433 | hp2 | a0002 | c0004 | t0005 | g0046 | AMR | CLM | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0164 | AMR | CLM | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01496 | hp2 | a0002 | c0002 | t0010 | g0108 | AMR | CLM | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0130 | EUR | IBS | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01517 | hp2 | a0002 | c0003 | t0002 | g0273 | EUR | IBS | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01884 | hp1 | a0002 | c0003 | t0012 | g0160 | AFR | ACB | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01884 | hp2 | a0002 | c0002 | t0007 | g0106 | AFR | ACB | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0115 | AFR | ACB | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0306 | AMR | PEL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01934 | hp2 | a0004 | c0011 | t0017 | g0149 | AMR | PEL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01978 | hp1 | a0001 | c0001 | t0006 | g0308 | AMR | PEL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0185 | AMR | PEL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0287 | AMR | PEL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01981 | hp2 | a0002 | c0003 | t0002 | g0084 | AMR | PEL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0340 | AMR | PEL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | KHV | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02040 | hp1 | a0001 | c0001 | t0011 | g0342 | EAS | KHV | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | KHV | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0237 | AFR | ACB | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0111 | AFR | ACB | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | KHV | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | KHV | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02074 | hp1 | a0002 | c0003 | t0002 | g0082 | EAS | KHV | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | KHV | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0346 | EAS | KHV | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | KHV | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0079 | EAS | KHV | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | KHV | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0133 | EAS | KHV | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | KHV | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02145 | hp2 | a0002 | c0002 | t0003 | g0231 | AFR | ACB | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0068 | AMR | PEL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0165 | AMR | PEL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | CDX | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | CDX | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CDX | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0072 | AFR | ACB | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02257 | hp2 | a0002 | c0003 | t0004 | g0138 | AFR | ACB | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PEL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0187 | AMR | PEL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02280 | hp1 | a0002 | c0005 | t0001 | g0116 | AFR | ACB | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0161 | AFR | ACB | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0316 | AMR | PEL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0333 | AMR | PEL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | PEL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0314 | AMR | PEL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | KHV | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | KHV | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02572 | hp1 | a0002 | c0002 | t0003 | g0254 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02572 | hp2 | a0002 | c0002 | t0006 | g0241 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02602 | hp1 | a0002 | c0003 | t0002 | g0148 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0317 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02615 | hp2 | a0005 | c0012 | t0003 | g0233 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02622 | hp1 | a0002 | c0002 | t0010 | g0105 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02630 | hp1 | a0002 | c0003 | t0004 | g0152 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02630 | hp2 | a0002 | c0002 | t0003 | g0251 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02647 | hp1 | a0002 | c0002 | t0004 | g0239 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02698 | hp1 | a0001 | c0006 | t0005 | g0321 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0290 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02717 | hp1 | a0002 | c0002 | t0004 | g0238 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0097 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02723 | hp1 | a0001 | c0001 | t0008 | g0245 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0218 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02735 | hp2 | a0001 | c0006 | t0005 | g0323 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02738 | hp1 | a0002 | c0003 | t0002 | g0119 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0330 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02809 | hp1 | a0006 | c0017 | t0001 | g0216 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02809 | hp2 | a0002 | c0003 | t0004 | g0076 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0114 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02886 | hp1 | a0002 | c0002 | t0003 | g0246 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0228 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02895 | hp1 | a0002 | c0009 | t0004 | g0157 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02895 | hp2 | a0002 | c0002 | t0004 | g0103 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02896 | hp1 | a0002 | c0002 | t0003 | g0255 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02896 | hp2 | a0002 | c0003 | t0004 | g0073 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02897 | hp1 | a0002 | c0002 | t0004 | g0107 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02897 | hp2 | a0002 | c0002 | t0003 | g0256 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02922 | hp1 | a0002 | c0002 | t0007 | g0223 | AFR | ESN | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02922 | hp2 | a0002 | c0002 | t0003 | g0258 | AFR | ESN | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0096 | AFR | ESN | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02965 | hp2 | a0001 | c0016 | t0001 | g0156 | AFR | ESN | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02970 | hp1 | a0002 | c0002 | t0006 | g0229 | AFR | ESN | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02970 | hp2 | a0002 | c0002 | t0003 | g0214 | AFR | ESN | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02976 | hp1 | a0002 | c0005 | t0003 | g0159 | AFR | ESN | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0339 | AFR | ESN | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03041 | hp1 | a0002 | c0002 | t0004 | g0123 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0101 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03098 | hp1 | a0001 | c0001 | t0008 | g0259 | AFR | MSL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03098 | hp2 | a0002 | c0003 | t0004 | g0058 | AFR | MSL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03130 | hp1 | a0002 | c0005 | t0003 | g0154 | AFR | ESN | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03130 | hp2 | a0002 | c0005 | t0008 | g0158 | AFR | ESN | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03139 | hp1 | a0002 | c0002 | t0003 | g0249 | AFR | ESN | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03139 | hp2 | a0002 | c0002 | t0025 | g0227 | AFR | ESN | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03195 | hp1 | a0002 | c0002 | t0006 | g0240 | AFR | ESN | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03195 | hp2 | a0002 | c0004 | t0005 | g0109 | AFR | ESN | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03209 | hp1 | a0002 | c0003 | t0012 | g0232 | AFR | MSL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03209 | hp2 | a0002 | c0002 | t0008 | g0236 | AFR | MSL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03225 | hp1 | a0001 | c0001 | t0013 | g0074 | AFR | MSL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03239 | hp1 | a0002 | c0004 | t0005 | g0286 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0124 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0104 | AFR | MSL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03490 | hp1 | a0002 | c0004 | t0005 | g0137 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03491 | hp1 | a0002 | c0004 | t0005 | g0095 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0102 | AFR | ESN | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0088 | AFR | ESN | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03540 | hp1 | a0002 | c0002 | t0003 | g0250 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03540 | hp2 | a0002 | c0002 | t0007 | g0134 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03579 | hp1 | a0001 | c0001 | t0016 | g0220 | AFR | MSL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03579 | hp2 | a0002 | c0002 | t0023 | g0099 | AFR | MSL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03654 | hp1 | a0002 | c0013 | t0001 | g0136 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03654 | hp2 | a0002 | c0004 | t0005 | g0141 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0135 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03688 | hp1 | a0002 | c0004 | t0005 | g0143 | SAS | STU | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0282 | SAS | STU | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0331 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03704 | hp2 | a0002 | c0004 | t0005 | g0311 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0289 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03710 | hp2 | a0002 | c0004 | t0005 | g0085 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03834 | hp1 | a0002 | c0003 | t0002 | g0067 | SAS | BEB | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0011 | SAS | BEB | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | BEB | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0350 | SAS | BEB | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | BEB | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03942 | hp2 | a0002 | c0004 | t0005 | g0177 | SAS | BEB | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0120 | SAS | STU | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | STU | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0326 | SAS | BEB | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG04184 | hp2 | a0002 | c0003 | t0002 | g0086 | SAS | BEB | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | STU | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0267 | SAS | STU | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0343 | SAS | STU | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0140 | SAS | STU | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0225 | AFR | YRI | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18906 | hp1 | a0002 | c0002 | t0003 | g0248 | AFR | YRI | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | YRI | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0288 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18943 | hp1 | a0002 | c0003 | t0002 | g0009 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0335 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0310 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18951 | hp2 | a0001 | c0001 | t0011 | g0080 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18966 | hp1 | a0002 | c0002 | t0019 | g0050 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0312 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18975 | hp2 | a0002 | c0003 | t0002 | g0121 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0332 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0171 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19003 | hp1 | a0002 | c0002 | t0002 | g0344 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19004 | hp1 | a0002 | c0002 | t0002 | g0334 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19005 | hp2 | a0007 | c0014 | t0021 | g0179 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0294 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0318 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0348 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19030 | hp1 | a0001 | c0015 | t0006 | g0247 | AFR | LWK | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19030 | hp2 | a0002 | c0004 | t0005 | g0162 | AFR | LWK | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | LWK | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19043 | hp2 | a0002 | c0002 | t0004 | g0117 | AFR | LWK | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0280 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0329 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0172 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0347 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0319 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0345 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0147 | AFR | ASW | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA20129 | hp2 | a0002 | c0002 | t0003 | g0253 | AFR | ASW | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA20752 | hp1 | a0002 | c0004 | t0005 | g0045 | EUR | TSI | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0279 | EUR | TSI | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0341 | EUR | TSI | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0270 | EUR | TSI | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0324 | SAS | GIH | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0337 | SAS | GIH | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01123 | hp1 | a0002 | c0003 | t0002 | g0063 | AMR | CLM | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0021 | AMR | CLM | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0325 | AFR | ACB | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02109 | hp2 | a0002 | c0002 | t0015 | g0221 | AFR | ACB | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02486 | hp1 | a0002 | c0002 | t0003 | g0252 | AFR | ACB | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02486 | hp2 | a0002 | c0002 | t0004 | g0215 | AFR | ACB | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02559 | hp1 | a0002 | c0018 | t0013 | g0217 | AFR | ACB | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0242 | AFR | ACB | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03471 | hp1 | a0002 | c0002 | t0018 | g0077 | AFR | MSL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03471 | hp2 | a0002 | c0002 | t0006 | g0230 | AFR | MSL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG06807 | hp1 | a0003 | c0010 | t0002 | g0260 | AFR | USA | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG06807 | hp2 | a0002 | c0003 | t0004 | g0125 | AFR | USA | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | USA | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA20300 | hp2 | a0001 | c0001 | t0026 | g0100 | AFR | USA | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0274 | REF | REF | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0235 | REF | REF | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:10754006 | G | A | 2 | a0003 a0004 |
4 | HG01167.hp2 HG01169.hp2 HG01934.hp2 others(1): Show |
missense_variant | MODERATE | c.223G>A | p.Val75Met | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/14 | 351/3259 | 223/1284 | 75/427 | chr2 | 10754006 | |||
| chr2:10768767 | A | G | 2 | a0001 a0004 |
176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
missense_variant | MODERATE | c.427A>G | p.Asn143Asp | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/14 | 555/3259 | 427/1284 | 143/427 | chr2 | 10768767 | |||
| chr2:10771871 | T | C | 1 | a0006 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.503T>C | p.Ile168Thr | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 7/14 | 631/3259 | 503/1284 | 168/427 | chr2 | 10771871 | |||
| chr2:10771912 | G | A | 1 | a0005 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.544G>A | p.Val182Ile | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 7/14 | 672/3259 | 544/1284 | 182/427 | chr2 | 10771912 | |||
| chr2:10777682 | G | A | 1 | a0007 | 1 | NA19005.hp2 | missense_variant | MODERATE | c.923G>A | p.Gly308Glu | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 11/14 | 1051/3259 | 923/1284 | 308/427 | chr2 | 10777682 | |||
| chr2:10778596 | G | A | 1 | a0006 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.988G>A | p.Val330Met | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/14 | 1116/3259 | 988/1284 | 330/427 | chr2 | 10778596 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:10722930 | C | T | 2 | a0002c0018 a0006c0017 |
2 | HG02559.hp1 HG02809.hp1 |
synonymous_variant | LOW | c.81C>T | p.Ser27Ser | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/14 | 209/3259 | 81/1284 | 27/427 | chr2 | 10722930 | |||
| chr2:10726528 | C | T | 3 | a0001c0016 a0002c0005 a0002c0009 |
7 | HG00639.hp1 HG02280.hp1 HG02895.hp1 others(4): Show |
synonymous_variant | LOW | c.156C>T | p.Gly52Gly | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/14 | 284/3259 | 156/1284 | 52/427 | chr2 | 10726528 | |||
| chr2:10754062 | C | T | 1 | a0001c0015 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.279C>T | p.Asn93Asn | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/14 | 407/3259 | 279/1284 | 93/427 | chr2 | 10754062 | |||
| chr2:10764398 | C | T | 1 | a0002c0007 | 3 | HG01069.hp2 HG01071.hp2 HG01192.hp1 |
synonymous_variant | LOW | c.351C>T | p.Leu117Leu | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/14 | 479/3259 | 351/1284 | 117/427 | chr2 | 10764398 | |||
| chr2:10772593 | G | A | 3 | a0002c0003 a0002c0009 a0003c0008 |
29 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(26): Show |
synonymous_variant | LOW | c.621G>A | p.Val207Val | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/14 | 749/3259 | 621/1284 | 207/427 | chr2 | 10772593 | |||
| chr2:10777602 | T | C | 1 | a0002c0013 | 1 | HG03654.hp1 | synonymous_variant | LOW | c.843T>C | p.Ala281Ala | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 11/14 | 971/3259 | 843/1284 | 281/427 | chr2 | 10777602 | |||
| chr2:10783227 | T | C | 3 | a0001c0006 a0002c0004 a0004c0011 |
16 | HG01099.hp1 HG01433.hp2 HG01934.hp2 others(13): Show |
synonymous_variant | LOW | c.1248T>C | p.Tyr416Tyr | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 14/14 | 1376/3259 | 1248/1284 | 416/427 | chr2 | 10783227 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:10721658 | A | T | 4 | a0001c0001t0026 a0002c0002t0023 a0002c0002t0024 others(1): Show |
4 | HG01109.hp2 HG03139.hp2 HG03579.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-100A>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 1/14 | 1192 | chr2 | 10721658 | ||||||
| chr2:10722831 | G | A | 3 | a0001c0001t0016 a0002c0002t0014 a0002c0002t0015 |
3 | HG01070.hp2 HG02109.hp2 HG03579.hp1 |
5_prime_UTR_variant | MODIFIER | c.-19G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/14 | 19 | chr2 | 10722831 | ||||||
| chr2:10783303 | T | G | 1 | a0004c0011t0017 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*40T>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 14/14 | 40 | chr2 | 10783303 | ||||||
| chr2:10783338 | G | A | 1 | a0002c0002t0018 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*75G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 14/14 | 75 | chr2 | 10783338 | ||||||
| chr2:10783455 | C | T | 20 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(17): Show |
53 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*192C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 14/14 | 192 | chr2 | 10783455 | ||||||
| chr2:10783540 | G | A | 4 | a0001c0001t0006 a0001c0015t0006 a0002c0002t0006 others(1): Show |
11 | HG01496.hp2 HG01978.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*277G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 14/14 | 277 | chr2 | 10783540 | ||||||
| chr2:10783565 | T | C | 1 | a0002c0007t0009 | 3 | HG01069.hp2 HG01071.hp2 HG01192.hp1 |
3_prime_UTR_variant | MODIFIER | c.*302T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 14/14 | 302 | chr2 | 10783565 | ||||||
| chr2:10783574 | T | C | 4 | a0001c0001t0006 a0001c0015t0006 a0002c0002t0006 others(1): Show |
11 | HG01496.hp2 HG01978.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*311T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 14/14 | 311 | chr2 | 10783574 | ||||||
| chr2:10783695 | C | T | 15 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(12): Show |
33 | HG00639.hp1 HG00639.hp2 HG01261.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*432C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 14/14 | 432 | chr2 | 10783695 | ||||||
| chr2:10783843 | T | C | 1 | a0001c0001t0011 | 2 | HG02040.hp1 NA18951.hp2 |
3_prime_UTR_variant | MODIFIER | c.*580T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 14/14 | 580 | chr2 | 10783843 | ||||||
| chr2:10783865 | T | C | 15 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(12): Show |
33 | HG00639.hp1 HG00639.hp2 HG01261.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*602T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 14/14 | 602 | chr2 | 10783865 | ||||||
| chr2:10783877 | T | C | 2 | a0001c0001t0013 a0002c0018t0013 |
2 | HG02559.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*614T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 14/14 | 614 | chr2 | 10783877 | ||||||
| chr2:10784050 | C | T | 1 | a0002c0003t0012 | 2 | HG01884.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*787C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 14/14 | 787 | chr2 | 10784050 | ||||||
| chr2:10784186 | TG | T | 5 | a0002c0002t0003 a0002c0002t0025 a0002c0005t0003 others(2): Show |
21 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*924delG | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 14/14 | 924 | chr2 | 10784186 | ||||||
| chr2:10784209 | C | T | 1 | a0001c0001t0020 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*946C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 14/14 | 946 | chr2 | 10784209 | ||||||
| chr2:10784271 | T | C | 1 | a0002c0002t0010 | 2 | HG01496.hp2 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1008T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 14/14 | 1008 | chr2 | 10784271 | ||||||
| chr2:10784398 | T | C | 28 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(25): Show |
184 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*1135T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 14/14 | 1135 | chr2 | 10784398 | ||||||
| chr2:10784458 | C | A | 2 | a0002c0007t0009 a0007c0014t0021 |
4 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1195C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 14/14 | 1195 | chr2 | 10784458 | ||||||
| chr2:10784487 | C | T | 2 | a0002c0007t0009 a0007c0014t0021 |
4 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1224C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 14/14 | 1224 | chr2 | 10784487 | ||||||
| chr2:10784559 | AC | A | 12 | a0001c0001t0004 a0001c0001t0007 a0001c0006t0005 others(9): Show |
43 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1297delC | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 14/14 | 1297 | chr2 | 10784559 | ||||||
| chr2:10784560 | CT | C | 16 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0011 others(13): Show |
141 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*1299delT | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 14/14 | 1299 | INFO_REALIGN_3_PRIME | chr2 | 10784560 | |||||
| chr2:10784567 | G | A | 18 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0013 others(15): Show |
47 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1304G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 14/14 | 1304 | chr2 | 10784567 | ||||||
| chr2:10784983 | G | T | 1 | a0002c0002t0019 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1720G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 14/14 | 1720 | chr2 | 10784983 | ||||||
| chr2:10785003 | C | T | 1 | a0002c0009t0022 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1740C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 14/14 | 1740 | chr2 | 10785003 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:10721950 | T | C | 2 | a0001c0001t0002g0004 a0002c0002t0001g0005 |
2 | HG04199.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-27+219T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 1/13 | chr2 | 10721950 | |||||||
| chr2:10722013 | G | T | 52 | a0001c0001t0001g0302 a0001c0001t0001g0307 a0001c0001t0001g0313 others(49): Show |
52 | HG00544.hp1 HG00597.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.-27+282G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 1/13 | chr2 | 10722013 | |||||||
| chr2:10722062 | G | A | 96 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(93): Show |
98 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-27+331G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 1/13 | chr2 | 10722062 | |||||||
| chr2:10722086 | G | A | 2 | a0001c0001t0026g0100 a0002c0002t0023g0099 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-27+355G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 1/13 | chr2 | 10722086 | |||||||
| chr2:10722150 | T | C | 62 | a0001c0001t0001g0302 a0001c0001t0001g0307 a0001c0001t0001g0313 others(59): Show |
62 | HG00544.hp1 HG00597.hp2 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.-27+419T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 1/13 | chr2 | 10722150 | |||||||
| chr2:10722203 | G | A | 172 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0144 others(169): Show |
173 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.-27+472G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 1/13 | chr2 | 10722203 | |||||||
| chr2:10722220 | C | T | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(1): Show |
4 | NA18960.hp1 NA19009.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27+489C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 1/13 | chr2 | 10722220 | |||||||
| chr2:10722247 | G | C | 1 | a0001c0001t0001g0219 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-27+516G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 1/13 | chr2 | 10722247 | |||||||
| chr2:10722286 | C | T | 1 | a0001c0001t0002g0218 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-26-538C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 1/13 | chr2 | 10722286 | |||||||
| chr2:10722318 | T | A | 1 | a0001c0001t0001g0219 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-26-506T>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 1/13 | chr2 | 10722318 | |||||||
| chr2:10722365 | G | A | 2 | a0001c0001t0001g0112 a0002c0002t0001g0111 |
2 | HG01891.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-26-459G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 1/13 | chr2 | 10722365 | |||||||
| chr2:10722444 | C | T | 34 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0279 others(31): Show |
34 | HG00140.hp1 HG00597.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.-26-380C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 1/13 | chr2 | 10722444 | |||||||
| chr2:10722493 | C | G | 1 | a0003c0010t0002g0260 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-26-331C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 1/13 | chr2 | 10722493 | |||||||
| chr2:10722513 | C | A | 1 | a0001c0001t0001g0113 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-26-311C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 1/13 | chr2 | 10722513 | |||||||
| chr2:10722514 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-26-310T>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 1/13 | chr2 | 10722514 | |||||||
| chr2:10722560 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0007 |
2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-26-264G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 1/13 | chr2 | 10722560 | |||||||
| chr2:10722576 | G | T | 2 | a0002c0018t0013g0217 a0006c0017t0001g0216 |
2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-26-248G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 1/13 | chr2 | 10722576 | |||||||
| chr2:10722673 | G | A | 2 | a0002c0018t0013g0217 a0006c0017t0001g0216 |
2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-26-151G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 1/13 | chr2 | 10722673 | |||||||
| chr2:10722759 | C | G | 1 | a0001c0001t0001g0219 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-26-65C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 1/13 | chr2 | 10722759 | |||||||
| chr2:10722760 | G | T | 1 | a0002c0002t0002g0098 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-26-64G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 1/13 | chr2 | 10722760 | |||||||
| chr2:10723046 | T | C | 1 | a0001c0001t0004g0114 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.129+68T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10723046 | |||||||
| chr2:10723099 | G | A | 8 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0104 others(5): Show |
8 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.129+121G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10723099 | |||||||
| chr2:10723124 | C | T | 15 | a0001c0001t0002g0257 a0001c0001t0008g0245 a0001c0001t0008g0259 others(12): Show |
15 | HG01175.hp1 HG02486.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.129+146C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10723124 | |||||||
| chr2:10723135 | T | G | 3 | a0001c0001t0016g0220 a0002c0002t0014g0222 a0002c0002t0015g0221 |
3 | HG01070.hp2 HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.129+157T>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10723135 | |||||||
| chr2:10723141 | A | G | 202 | a0001c0001t0001g0112 a0001c0001t0001g0144 a0001c0001t0001g0153 others(199): Show |
203 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.129+163A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10723141 | |||||||
| chr2:10723363 | A | G | 8 | a0001c0001t0007g0237 a0002c0002t0001g0242 a0002c0002t0003g0243 others(5): Show |
8 | HG00639.hp2 HG01243.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.129+385A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10723363 | |||||||
| chr2:10723448 | G | A | 16 | a0001c0001t0002g0257 a0001c0001t0008g0245 a0001c0001t0008g0259 others(13): Show |
16 | HG01175.hp1 HG02486.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.129+470G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10723448 | |||||||
| chr2:10723656 | G | A | 3 | a0001c0001t0016g0220 a0002c0002t0014g0222 a0002c0002t0015g0221 |
3 | HG01070.hp2 HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.129+678G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10723656 | |||||||
| chr2:10723821 | C | T | 3 | a0002c0002t0002g0351 a0002c0002t0003g0214 a0002c0002t0004g0215 |
3 | HG00735.hp2 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.129+843C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10723821 | |||||||
| chr2:10723837 | C | CA | 108 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(105): Show |
110 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.129+878dupA | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 10723837 | ||||||
| chr2:10723837 | C | CAA | 6 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0002g0004 others(3): Show |
6 | HG00741.hp1 HG02015.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.129+877_129+878dup others(2): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 10723837 | ||||||
| chr2:10723837 | CAAAAAAA | C | 169 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0144 others(166): Show |
170 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.129+872_129+878del others(7): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 10723837 | ||||||
| chr2:10723873 | AT | A | 169 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0144 others(166): Show |
170 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.129+902delT | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 10723873 | ||||||
| chr2:10724183 | G | T | 2 | a0002c0018t0013g0217 a0006c0017t0001g0216 |
2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.129+1205G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10724183 | |||||||
| chr2:10724316 | T | G | 2 | a0001c0001t0002g0301 a0002c0002t0001g0300 |
2 | NA18965.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.129+1338T>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10724316 | |||||||
| chr2:10724386 | G | A | 7 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0104 others(4): Show |
7 | HG01884.hp2 HG02622.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.129+1408G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10724386 | |||||||
| chr2:10724522 | G | A | 2 | a0002c0018t0013g0217 a0006c0017t0001g0216 |
2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.129+1544G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10724522 | |||||||
| chr2:10724616 | C | T | 1 | a0002c0002t0001g0225 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.129+1638C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10724616 | |||||||
| chr2:10724628 | C | T | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(1): Show |
4 | NA18960.hp1 NA19009.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+1650C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10724628 | |||||||
| chr2:10724674 | CT | C | 328 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(325): Show |
331 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.129+1713delT | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 10724674 | ||||||
| chr2:10724990 | C | T | 15 | a0001c0001t0002g0257 a0001c0001t0008g0245 a0001c0001t0008g0259 others(12): Show |
15 | HG01175.hp1 HG02486.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.130-1512C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10724990 | |||||||
| chr2:10725127 | A | G | 12 | a0001c0001t0002g0257 a0001c0001t0008g0245 a0002c0002t0003g0248 others(9): Show |
12 | HG01175.hp1 HG02486.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.130-1375A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10725127 | |||||||
| chr2:10725304 | ATTTGGGA others(7): Show |
A | 2 | a0002c0002t0024g0226 a0002c0002t0025g0227 |
2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.130-1197_130-1184d others(16): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10725304 | |||||||
| chr2:10725319 | G | A | 2 | a0002c0002t0024g0226 a0002c0002t0025g0227 |
2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.130-1183G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10725319 | |||||||
| chr2:10725403 | C | A | 2 | a0002c0018t0013g0217 a0006c0017t0001g0216 |
2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.130-1099C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10725403 | |||||||
| chr2:10725450 | G | C | 15 | a0001c0001t0002g0257 a0001c0001t0008g0245 a0001c0001t0008g0259 others(12): Show |
15 | HG01175.hp1 HG02486.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.130-1052G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10725450 | |||||||
| chr2:10725489 | A | AT | 110 | a0001c0001t0001g0087 a0001c0001t0001g0089 a0001c0001t0001g0090 others(107): Show |
110 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.130-990dupT | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 10725489 | ||||||
| chr2:10725489 | A | ATT | 66 | a0001c0001t0001g0163 a0001c0001t0001g0168 a0001c0001t0001g0173 others(63): Show |
67 | HG00408.hp2 HG00558.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.130-991_130-990dup others(2): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 10725489 | ||||||
| chr2:10725489 | AT | A | 24 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0296 others(21): Show |
24 | HG00558.hp2 HG01169.hp1 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.130-990delT | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 10725489 | ||||||
| chr2:10725489 | ATTTT | A | 23 | a0001c0001t0001g0279 a0001c0001t0002g0264 a0001c0001t0002g0278 others(20): Show |
23 | HG00140.hp1 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.130-993_130-990del others(4): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 10725489 | ||||||
| chr2:10725557 | C | T | 1 | a0001c0001t0007g0237 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.130-945C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10725557 | |||||||
| chr2:10725586 | C | T | 1 | a0002c0002t0001g0341 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.130-916C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10725586 | |||||||
| chr2:10725650 | A | G | 7 | a0001c0016t0001g0156 a0002c0005t0001g0116 a0002c0005t0003g0154 others(4): Show |
7 | HG00639.hp1 HG02280.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.130-852A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10725650 | |||||||
| chr2:10725723 | G | C | 1 | a0002c0002t0002g0124 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.130-779G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10725723 | |||||||
| chr2:10725771 | A | G | 2 | a0002c0018t0013g0217 a0006c0017t0001g0216 |
2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.130-731A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10725771 | |||||||
| chr2:10725801 | C | T | 2 | a0002c0018t0013g0217 a0006c0017t0001g0216 |
2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.130-701C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10725801 | |||||||
| chr2:10725924 | A | G | 108 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(105): Show |
110 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.130-578A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10725924 | |||||||
| chr2:10726067 | C | T | 1 | a0002c0002t0001g0228 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.130-435C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10726067 | |||||||
| chr2:10726152 | T | C | 2 | a0001c0001t0002g0014 a0001c0001t0002g0015 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.130-350T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10726152 | |||||||
| chr2:10726200 | A | C | 1 | a0001c0001t0002g0340 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.130-302A>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10726200 | |||||||
| chr2:10726394 | A | C | 1 | a0001c0001t0001g0083 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.130-108A>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10726394 | |||||||
| chr2:10726475 | C | T | 8 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0104 others(5): Show |
8 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.130-27C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 2/13 | chr2 | 10726475 | |||||||
| chr2:10726702 | G | A | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(1): Show |
4 | NA18960.hp1 NA19009.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.197+133G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10726702 | |||||||
| chr2:10726870 | T | C | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(1): Show |
4 | NA18960.hp1 NA19009.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.197+301T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10726870 | |||||||
| chr2:10726934 | C | T | 1 | a0002c0003t0002g0082 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.197+365C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10726934 | |||||||
| chr2:10727035 | GCCTT | G | 333 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(330): Show |
336 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.197+482_197+485del others(4): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10727035 | ||||||
| chr2:10727047 | TCCTTCCT others(9): Show |
T | 2 | a0002c0002t0001g0208 a0002c0002t0001g0209 |
2 | NA18990.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.197+482_197+497del others(16): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10727047 | ||||||
| chr2:10727051 | T | C | 21 | a0001c0001t0002g0081 a0001c0001t0006g0101 a0001c0001t0006g0102 others(18): Show |
21 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.197+482T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10727051 | |||||||
| chr2:10727060 | C | T | 23 | a0001c0001t0001g0302 a0001c0001t0001g0313 a0001c0001t0001g0320 others(20): Show |
23 | HG00735.hp1 HG00738.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.197+491C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10727060 | |||||||
| chr2:10727144 | A | G | 190 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(187): Show |
193 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.197+575A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10727144 | |||||||
| chr2:10727204 | G | A | 2 | a0002c0002t0001g0225 a0002c0002t0003g0224 |
2 | HG01109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.197+635G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10727204 | |||||||
| chr2:10727207 | C | G | 2 | a0001c0001t0001g0090 a0001c0001t0011g0080 |
2 | NA18951.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.197+638C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10727207 | |||||||
| chr2:10727223 | C | G | 1 | a0001c0001t0001g0153 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.197+654C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10727223 | |||||||
| chr2:10727261 | G | A | 3 | a0001c0001t0001g0112 a0002c0002t0001g0111 a0002c0003t0004g0125 |
3 | HG01891.hp1 HG02055.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.197+692G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10727261 | |||||||
| chr2:10727321 | C | T | 3 | a0001c0001t0026g0100 a0002c0018t0013g0217 a0006c0017t0001g0216 |
3 | HG02559.hp1 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.197+752C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10727321 | |||||||
| chr2:10727389 | G | GA | 16 | a0001c0001t0002g0128 a0001c0001t0002g0257 a0001c0001t0008g0259 others(13): Show |
16 | HG01175.hp1 HG01256.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.197+838dupA | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10727389 | ||||||
| chr2:10727389 | GA | G | 40 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0210 others(37): Show |
40 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.197+838delA | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10727389 | ||||||
| chr2:10727389 | GAA | G | 22 | a0001c0001t0002g0212 a0001c0001t0006g0101 a0001c0001t0006g0102 others(19): Show |
22 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.197+837_197+838del others(2): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10727389 | ||||||
| chr2:10727419 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.197+850G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10727419 | |||||||
| chr2:10727563 | C | CAAAT | 16 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0104 others(13): Show |
16 | HG00639.hp2 HG01243.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.197+997_197+998ins others(4): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10727563 | ||||||
| chr2:10727605 | G | A | 4 | a0002c0002t0003g0231 a0002c0002t0007g0234 a0002c0003t0012g0232 others(1): Show |
4 | HG01261.hp1 HG02145.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.197+1036G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10727605 | |||||||
| chr2:10727637 | C | G | 333 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(330): Show |
336 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.197+1068C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10727637 | |||||||
| chr2:10727714 | G | C | 344 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(341): Show |
347 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(344): Show |
intron_variant | MODIFIER | c.197+1145G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10727714 | |||||||
| chr2:10727792 | C | G | 6 | a0001c0001t0007g0237 a0002c0002t0001g0242 a0002c0002t0003g0243 others(3): Show |
6 | HG00639.hp2 HG01243.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.197+1223C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10727792 | |||||||
| chr2:10727814 | G | T | 4 | a0002c0002t0001g0150 a0002c0002t0004g0123 a0002c0003t0004g0152 others(1): Show |
4 | HG01069.hp1 HG01192.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.197+1245G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10727814 | |||||||
| chr2:10727821 | C | T | 1 | a0002c0002t0003g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.197+1252C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10727821 | |||||||
| chr2:10727861 | G | A | 3 | a0001c0001t0016g0220 a0002c0002t0014g0222 a0002c0002t0015g0221 |
3 | HG01070.hp2 HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.197+1292G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10727861 | |||||||
| chr2:10727865 | C | G | 88 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0210 others(85): Show |
88 | HG00140.hp2 HG00544.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.197+1296C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10727865 | |||||||
| chr2:10727877 | C | T | 21 | a0001c0001t0001g0307 a0001c0001t0001g0333 a0001c0001t0001g0336 others(18): Show |
21 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.197+1308C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10727877 | |||||||
| chr2:10727899 | G | A | 87 | a0001c0001t0001g0144 a0001c0001t0001g0153 a0001c0001t0001g0163 others(84): Show |
88 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.197+1330G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10727899 | |||||||
| chr2:10727968 | C | G | 1 | a0001c0015t0006g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.197+1399C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10727968 | |||||||
| chr2:10727991 | A | G | 3 | a0001c0001t0002g0291 a0002c0002t0001g0271 a0002c0002t0001g0292 |
3 | HG00597.hp1 HG02523.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.197+1422A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10727991 | |||||||
| chr2:10728007 | G | A | 2 | a0001c0001t0002g0016 a0001c0001t0002g0017 |
2 | HG00544.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.197+1438G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10728007 | |||||||
| chr2:10728184 | C | T | 3 | a0001c0001t0026g0100 a0002c0018t0013g0217 a0006c0017t0001g0216 |
3 | HG02559.hp1 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.197+1615C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10728184 | |||||||
| chr2:10728488 | C | T | 1 | a0001c0001t0001g0010 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.197+1919C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10728488 | |||||||
| chr2:10728525 | C | T | 1 | a0002c0002t0001g0079 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.197+1956C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10728525 | |||||||
| chr2:10728526 | C | G | 7 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(4): Show |
7 | HG02559.hp1 HG02809.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.197+1957C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10728526 | |||||||
| chr2:10728753 | C | T | 1 | a0001c0001t0002g0305 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.197+2184C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10728753 | |||||||
| chr2:10728774 | C | CA | 51 | a0001c0001t0001g0019 a0001c0001t0001g0265 a0001c0001t0001g0302 others(48): Show |
51 | HG00544.hp1 HG00597.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.197+2225dupA | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10728774 | ||||||
| chr2:10728774 | C | CCA | 8 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0104 others(5): Show |
8 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.197+2205_197+2206i others(4): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10728774 | |||||||
| chr2:10728774 | CA | C | 81 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0078 others(78): Show |
82 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.197+2225delA | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10728774 | ||||||
| chr2:10728881 | A | G | 15 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(12): Show |
15 | HG01496.hp2 HG01884.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.197+2312A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10728881 | |||||||
| chr2:10728962 | C | CA | 130 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(127): Show |
132 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.197+2412dupA | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10728962 | ||||||
| chr2:10728962 | CA | C | 100 | a0001c0001t0001g0078 a0001c0001t0001g0144 a0001c0001t0001g0153 others(97): Show |
101 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.197+2412delA | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10728962 | ||||||
| chr2:10728962 | CAA | C | 7 | a0001c0001t0004g0097 a0001c0001t0016g0220 a0002c0002t0001g0096 others(4): Show |
7 | HG01070.hp2 HG01167.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.197+2411_197+2412d others(4): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10728962 | ||||||
| chr2:10728962 | CAAA | C | 7 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(4): Show |
7 | HG02559.hp1 HG02809.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.197+2410_197+2412d others(5): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10728962 | ||||||
| chr2:10729066 | G | T | 1 | a0002c0002t0001g0329 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.197+2497G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10729066 | |||||||
| chr2:10729127 | C | CA | 6 | a0001c0001t0001g0163 a0001c0001t0008g0259 a0002c0002t0001g0161 others(3): Show |
6 | HG02280.hp2 HG03098.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.197+2570dupA | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10729127 | ||||||
| chr2:10729158 | T | A | 1 | a0001c0001t0016g0220 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.197+2589T>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10729158 | |||||||
| chr2:10729172 | C | CTTTTTTT others(1): Show |
7 | a0001c0001t0002g0212 a0002c0002t0002g0171 a0002c0002t0023g0099 others(4): Show |
7 | HG01109.hp2 HG01167.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.197+2606_197+2613d others(10): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10729172 | ||||||
| chr2:10729172 | C | CTTTTTTT others(2): Show |
82 | a0001c0001t0001g0078 a0001c0001t0001g0144 a0001c0001t0001g0153 others(79): Show |
83 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.197+2605_197+2613d others(11): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10729172 | ||||||
| chr2:10729172 | C | CTTTTTTT others(3): Show |
7 | a0001c0001t0002g0170 a0001c0001t0026g0100 a0002c0002t0003g0246 others(4): Show |
7 | HG00673.hp1 HG02559.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.197+2604_197+2613d others(12): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10729172 | ||||||
| chr2:10729172 | C | CTTTTTTT others(4): Show |
11 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(8): Show |
11 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.197+2613_197+2614i others(13): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10729172 | ||||||
| chr2:10729218 | A | G | 8 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0104 others(5): Show |
8 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.197+2649A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10729218 | |||||||
| chr2:10729219 | G | C | 8 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0104 others(5): Show |
8 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.197+2650G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10729219 | |||||||
| chr2:10729235 | G | A | 1 | a0002c0002t0003g0224 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.197+2666G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10729235 | |||||||
| chr2:10729275 | T | C | 3 | a0001c0001t0026g0100 a0002c0018t0013g0217 a0006c0017t0001g0216 |
3 | HG02559.hp1 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.197+2706T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10729275 | |||||||
| chr2:10729288 | C | T | 1 | a0002c0003t0002g0067 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.197+2719C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10729288 | |||||||
| chr2:10729307 | G | A | 144 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(141): Show |
146 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.197+2738G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10729307 | |||||||
| chr2:10729344 | A | G | 2 | a0001c0001t0026g0100 a0002c0018t0013g0217 |
2 | HG02559.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.197+2775A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10729344 | |||||||
| chr2:10729365 | T | C | 8 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0104 others(5): Show |
8 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.197+2796T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10729365 | |||||||
| chr2:10729479 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.197+2910A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10729479 | |||||||
| chr2:10729537 | A | G | 1 | a0002c0003t0002g0121 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.197+2968A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10729537 | |||||||
| chr2:10729648 | T | G | 8 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0104 others(5): Show |
8 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.197+3079T>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10729648 | |||||||
| chr2:10729841 | T | C | 8 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0104 others(5): Show |
8 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.197+3272T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10729841 | |||||||
| chr2:10729882 | G | A | 15 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(12): Show |
15 | HG01496.hp2 HG01884.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.197+3313G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10729882 | |||||||
| chr2:10730230 | T | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(257): Show |
263 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.197+3661T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10730230 | |||||||
| chr2:10730307 | G | A | 1 | a0002c0002t0003g0246 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.197+3738G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10730307 | |||||||
| chr2:10730327 | G | C | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(1): Show |
4 | NA18960.hp1 NA19009.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.197+3758G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10730327 | |||||||
| chr2:10730395 | T | C | 15 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(12): Show |
15 | HG01496.hp2 HG01884.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.197+3826T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10730395 | |||||||
| chr2:10730604 | TG | T | 5 | a0002c0002t0004g0103 a0002c0002t0004g0107 a0002c0002t0007g0106 others(2): Show |
5 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.197+4038delG | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10730604 | ||||||
| chr2:10730606 | GGT | G | 3 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0104 |
3 | HG03041.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.197+4038_197+4039d others(4): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10730606 | |||||||
| chr2:10730607 | G | GT | 10 | a0001c0001t0001g0019 a0001c0001t0002g0118 a0001c0001t0006g0308 others(7): Show |
10 | HG00140.hp2 HG00597.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.197+4056dupT | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10730607 | ||||||
| chr2:10730607 | GT | G | 41 | a0001c0001t0001g0112 a0001c0001t0001g0313 a0001c0001t0002g0257 others(38): Show |
41 | HG00408.hp1 HG00639.hp2 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.197+4056delT | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10730607 | ||||||
| chr2:10730607 | GTT | G | 127 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(124): Show |
129 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.197+4055_197+4056d others(4): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10730607 | ||||||
| chr2:10730653 | C | CT | 7 | a0001c0001t0001g0019 a0001c0001t0002g0132 a0002c0002t0001g0326 others(4): Show |
7 | HG02738.hp1 HG04115.hp2 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.197+4100dupT | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10730653 | ||||||
| chr2:10730653 | CT | C | 154 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
156 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.197+4100delT | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10730653 | ||||||
| chr2:10730653 | CTT | C | 90 | a0001c0001t0001g0066 a0001c0001t0001g0078 a0001c0001t0001g0153 others(87): Show |
91 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.197+4099_197+4100d others(4): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10730653 | ||||||
| chr2:10730653 | CTTT | C | 11 | a0001c0001t0001g0144 a0001c0001t0002g0174 a0001c0001t0002g0175 others(8): Show |
11 | HG01256.hp1 HG01496.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.197+4098_197+4100d others(5): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10730653 | ||||||
| chr2:10730801 | C | T | 1 | a0002c0002t0001g0228 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.197+4232C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10730801 | |||||||
| chr2:10730881 | G | A | 1 | a0001c0001t0002g0176 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.197+4312G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10730881 | |||||||
| chr2:10730957 | A | AT | 10 | a0001c0001t0001g0112 a0001c0001t0007g0237 a0002c0002t0001g0111 others(7): Show |
10 | HG00639.hp2 HG01243.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.197+4398dupT | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10730957 | ||||||
| chr2:10731063 | C | T | 1 | a0002c0002t0007g0223 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.197+4494C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10731063 | |||||||
| chr2:10731459 | G | A | 91 | a0001c0001t0001g0078 a0001c0001t0001g0144 a0001c0001t0001g0153 others(88): Show |
92 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.197+4890G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10731459 | |||||||
| chr2:10731582 | A | G | 1 | a0002c0003t0002g0142 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.197+5013A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10731582 | |||||||
| chr2:10731658 | C | T | 91 | a0001c0001t0001g0078 a0001c0001t0001g0144 a0001c0001t0001g0153 others(88): Show |
92 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.197+5089C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10731658 | |||||||
| chr2:10731688 | A | C | 1 | a0002c0004t0005g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.197+5119A>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10731688 | |||||||
| chr2:10731693 | G | A | 1 | a0002c0002t0001g0329 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.197+5124G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10731693 | |||||||
| chr2:10731836 | T | C | 1 | a0002c0002t0006g0240 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.197+5267T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10731836 | |||||||
| chr2:10731930 | A | G | 2 | a0002c0002t0001g0161 a0002c0002t0007g0134 |
2 | HG02280.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.197+5361A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10731930 | |||||||
| chr2:10732439 | T | C | 1 | a0002c0004t0005g0143 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.197+5870T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10732439 | |||||||
| chr2:10732531 | G | A | 1 | a0001c0006t0005g0321 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.197+5962G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10732531 | |||||||
| chr2:10732561 | T | C | 99 | a0001c0001t0001g0078 a0001c0001t0001g0144 a0001c0001t0001g0153 others(96): Show |
100 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.197+5992T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10732561 | |||||||
| chr2:10732692 | G | T | 2 | a0001c0001t0026g0100 a0002c0018t0013g0217 |
2 | HG02559.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.197+6123G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10732692 | |||||||
| chr2:10732844 | G | A | 99 | a0001c0001t0001g0078 a0001c0001t0001g0144 a0001c0001t0001g0153 others(96): Show |
100 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.197+6275G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10732844 | |||||||
| chr2:10732881 | G | A | 2 | a0002c0002t0003g0248 a0002c0002t0003g0258 |
2 | HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.197+6312G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10732881 | |||||||
| chr2:10732967 | C | CA | 94 | a0001c0001t0001g0022 a0001c0001t0001g0112 a0001c0001t0001g0113 others(91): Show |
94 | HG00140.hp2 HG00544.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.197+6411dupA | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10732967 | ||||||
| chr2:10732967 | C | CAAAA | 90 | a0001c0001t0001g0078 a0001c0001t0001g0144 a0001c0001t0001g0153 others(87): Show |
91 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.197+6408_197+6411d others(6): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10732967 | ||||||
| chr2:10732967 | C | CAAAAA | 7 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0104 others(4): Show |
7 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.197+6407_197+6411d others(7): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10732967 | ||||||
| chr2:10733120 | G | A | 4 | a0001c0001t0001g0070 a0001c0001t0001g0178 a0001c0001t0002g0023 others(1): Show |
4 | HG01358.hp2 HG02135.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.197+6551G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10733120 | |||||||
| chr2:10733159 | CA | C | 3 | a0002c0002t0001g0228 a0002c0002t0003g0214 a0002c0002t0004g0215 |
3 | HG02486.hp2 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.197+6591delA | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10733159 | |||||||
| chr2:10733231 | A | T | 3 | a0001c0001t0016g0220 a0002c0002t0014g0222 a0002c0002t0015g0221 |
3 | HG01070.hp2 HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.197+6662A>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10733231 | |||||||
| chr2:10733485 | A | G | 5 | a0001c0001t0002g0257 a0001c0016t0001g0156 a0002c0005t0008g0158 others(2): Show |
5 | HG00639.hp1 HG01175.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.197+6916A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10733485 | |||||||
| chr2:10733548 | T | A | 8 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0104 others(5): Show |
8 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.197+6979T>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10733548 | |||||||
| chr2:10733636 | T | TA | 93 | a0001c0001t0001g0078 a0001c0001t0001g0144 a0001c0001t0001g0153 others(90): Show |
94 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.197+7079dupA | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10733636 | ||||||
| chr2:10733655 | T | C | 6 | a0001c0001t0004g0097 a0001c0001t0016g0220 a0002c0002t0001g0096 others(3): Show |
6 | HG01070.hp2 HG02109.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.197+7086T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10733655 | |||||||
| chr2:10733707 | G | A | 86 | a0001c0001t0001g0113 a0001c0001t0001g0210 a0001c0001t0001g0211 others(83): Show |
86 | HG00140.hp2 HG00544.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.197+7138G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10733707 | |||||||
| chr2:10733812 | A | AAGTGCTT others(22): Show |
204 | a0001c0001t0001g0078 a0001c0001t0001g0112 a0001c0001t0001g0113 others(201): Show |
205 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(202): Show |
intron_variant | MODIFIER | c.197+7259_197+7287d others(31): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10733812 | ||||||
| chr2:10733812 | A | G | 1 | a0002c0002t0001g0304 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.197+7243A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10733812 | |||||||
| chr2:10734044 | G | T | 1 | a0002c0003t0004g0125 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.197+7475G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10734044 | |||||||
| chr2:10734091 | G | A | 1 | a0007c0014t0021g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.197+7522G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10734091 | |||||||
| chr2:10734386 | G | A | 107 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0210 others(104): Show |
107 | HG00140.hp2 HG00544.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.197+7817G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10734386 | |||||||
| chr2:10734395 | C | T | 2 | a0001c0001t0002g0305 a0001c0001t0002g0325 |
2 | HG01257.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.197+7826C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10734395 | |||||||
| chr2:10734479 | C | A | 8 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0104 others(5): Show |
8 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.197+7910C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10734479 | |||||||
| chr2:10734545 | G | A | 198 | a0001c0001t0001g0078 a0001c0001t0001g0112 a0001c0001t0001g0113 others(195): Show |
199 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(196): Show |
intron_variant | MODIFIER | c.197+7976G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10734545 | |||||||
| chr2:10734556 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.197+7987T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10734556 | |||||||
| chr2:10734611 | A | G | 15 | a0001c0001t0001g0112 a0001c0001t0004g0097 a0001c0001t0016g0220 others(12): Show |
15 | HG00639.hp2 HG01070.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.197+8042A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10734611 | |||||||
| chr2:10734720 | C | T | 90 | a0001c0001t0001g0078 a0001c0001t0001g0144 a0001c0001t0001g0153 others(87): Show |
91 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.197+8151C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10734720 | |||||||
| chr2:10734883 | T | G | 98 | a0001c0001t0001g0078 a0001c0001t0001g0144 a0001c0001t0001g0153 others(95): Show |
99 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.197+8314T>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10734883 | |||||||
| chr2:10734992 | G | A | 8 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0104 others(5): Show |
8 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.197+8423G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10734992 | |||||||
| chr2:10735098 | A | C | 107 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0210 others(104): Show |
107 | HG00140.hp2 HG00544.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.197+8529A>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10735098 | |||||||
| chr2:10735232 | T | A | 8 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0104 others(5): Show |
8 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.197+8663T>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10735232 | |||||||
| chr2:10735338 | T | C | 1 | a0002c0009t0022g0155 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.197+8769T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10735338 | |||||||
| chr2:10735422 | G | A | 106 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0210 others(103): Show |
106 | HG00140.hp2 HG00544.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.197+8853G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10735422 | |||||||
| chr2:10735495 | C | T | 1 | a0002c0002t0003g0224 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.197+8926C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10735495 | |||||||
| chr2:10735536 | G | A | 1 | a0002c0002t0006g0229 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.197+8967G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10735536 | |||||||
| chr2:10735585 | CT | C | 8 | a0001c0001t0001g0070 a0001c0001t0001g0163 a0001c0001t0016g0220 others(5): Show |
8 | HG01070.hp2 HG02109.hp2 HG03540.hp2 others(5): Show |
intron_variant | MODIFIER | c.197+9030delT | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10735585 | ||||||
| chr2:10735598 | T | C | 1 | a0002c0002t0006g0229 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.197+9029T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10735598 | |||||||
| chr2:10735598 | TTC | T | 7 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0104 others(4): Show |
7 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.197+9035_197+9036d others(4): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10735598 | ||||||
| chr2:10735691 | A | T | 1 | a0002c0005t0008g0158 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.197+9122A>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10735691 | |||||||
| chr2:10735743 | AT | A | 197 | a0001c0001t0001g0078 a0001c0001t0001g0112 a0001c0001t0001g0113 others(194): Show |
198 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.197+9186delT | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10735743 | ||||||
| chr2:10735832 | G | C | 207 | a0001c0001t0001g0078 a0001c0001t0001g0112 a0001c0001t0001g0113 others(204): Show |
208 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(205): Show |
intron_variant | MODIFIER | c.197+9263G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10735832 | |||||||
| chr2:10735963 | C | T | 1 | a0002c0003t0002g0063 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.197+9394C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10735963 | |||||||
| chr2:10736011 | C | T | 1 | a0002c0004t0005g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.197+9442C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10736011 | |||||||
| chr2:10736028 | C | T | 1 | a0002c0004t0005g0143 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.197+9459C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10736028 | |||||||
| chr2:10736075 | A | T | 1 | a0002c0002t0001g0345 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.197+9506A>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10736075 | |||||||
| chr2:10736110 | C | T | 90 | a0001c0001t0001g0078 a0001c0001t0001g0144 a0001c0001t0001g0153 others(87): Show |
91 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.197+9541C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10736110 | |||||||
| chr2:10736111 | G | A | 8 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0104 others(5): Show |
8 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.197+9542G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10736111 | |||||||
| chr2:10736128 | G | T | 1 | a0002c0004t0005g0109 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.197+9559G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10736128 | |||||||
| chr2:10736162 | T | TC | 16 | a0001c0001t0001g0112 a0001c0001t0016g0220 a0002c0002t0001g0111 others(13): Show |
16 | HG00639.hp2 HG01070.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.197+9593_197+9594i others(3): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10736162 | |||||||
| chr2:10736164 | C | CCT | 16 | a0001c0001t0001g0112 a0001c0001t0016g0220 a0002c0002t0001g0111 others(13): Show |
16 | HG00639.hp2 HG01070.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.197+9595_197+9596i others(4): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10736164 | |||||||
| chr2:10736295 | C | T | 3 | a0001c0001t0026g0100 a0002c0018t0013g0217 a0006c0017t0001g0216 |
3 | HG02559.hp1 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.197+9726C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10736295 | |||||||
| chr2:10736296 | G | A | 86 | a0001c0001t0001g0113 a0001c0001t0001g0210 a0001c0001t0001g0211 others(83): Show |
86 | HG00140.hp2 HG00544.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.197+9727G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10736296 | |||||||
| chr2:10736396 | C | T | 1 | a0001c0015t0006g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.197+9827C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10736396 | |||||||
| chr2:10736447 | A | T | 1 | a0001c0001t0007g0237 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.197+9878A>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10736447 | |||||||
| chr2:10736464 | A | G | 4 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0104 others(1): Show |
4 | HG01884.hp2 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.197+9895A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10736464 | |||||||
| chr2:10736557 | C | T | 1 | a0006c0017t0001g0216 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.197+9988C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10736557 | |||||||
| chr2:10736574 | A | G | 136 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(133): Show |
138 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.197+10005A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10736574 | |||||||
| chr2:10736593 | G | A | 1 | a0001c0001t0002g0001 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.197+10024G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10736593 | |||||||
| chr2:10736673 | G | A | 89 | a0001c0001t0001g0078 a0001c0001t0001g0144 a0001c0001t0001g0153 others(86): Show |
90 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.197+10104G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10736673 | |||||||
| chr2:10736742 | G | A | 2 | a0002c0002t0006g0229 a0002c0002t0006g0230 |
2 | HG02970.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.197+10173G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10736742 | |||||||
| chr2:10736776 | C | G | 5 | a0001c0001t0001g0089 a0002c0002t0001g0062 a0002c0003t0002g0009 others(2): Show |
5 | HG01981.hp2 HG02071.hp1 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.197+10207C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10736776 | |||||||
| chr2:10736781 | T | C | 3 | a0001c0001t0026g0100 a0002c0018t0013g0217 a0006c0017t0001g0216 |
3 | HG02559.hp1 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.197+10212T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10736781 | |||||||
| chr2:10736801 | CT | C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(133): Show |
138 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.197+10251delT | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10736801 | ||||||
| chr2:10736801 | CTT | C | 137 | a0001c0001t0001g0024 a0001c0001t0001g0078 a0001c0001t0001g0113 others(134): Show |
138 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.197+10250_197+1025 others(6): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10736801 | ||||||
| chr2:10736801 | CTTT | C | 55 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(52): Show |
55 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.197+10249_197+1025 others(7): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10736801 | ||||||
| chr2:10736801 | CTTTT | C | 9 | a0001c0001t0001g0112 a0002c0002t0001g0111 a0002c0002t0001g0242 others(6): Show |
9 | HG00639.hp2 HG01243.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.197+10248_197+1025 others(8): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10736801 | ||||||
| chr2:10736855 | T | G | 1 | a0001c0001t0001g0203 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.197+10286T>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10736855 | |||||||
| chr2:10736901 | C | T | 1 | a0001c0001t0002g0120 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.197+10332C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10736901 | |||||||
| chr2:10737105 | GTTGC | G | 6 | a0001c0001t0007g0237 a0002c0002t0003g0231 a0002c0002t0007g0234 others(3): Show |
6 | HG01261.hp1 HG02055.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.197+10539_197+1054 others(8): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10737105 | ||||||
| chr2:10737197 | T | C | 2 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
2 | NA18964.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.197+10628T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10737197 | |||||||
| chr2:10737260 | CAAA | C | 13 | a0001c0001t0001g0070 a0001c0001t0002g0202 a0001c0001t0006g0101 others(10): Show |
13 | HG01255.hp2 HG01496.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.197+10707_197+1070 others(7): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10737260 | ||||||
| chr2:10737279 | G | C | 104 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0210 others(101): Show |
104 | HG00140.hp2 HG00544.hp1 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.197+10710G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10737279 | |||||||
| chr2:10737331 | G | A | 1 | a0002c0002t0003g0249 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.197+10762G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10737331 | |||||||
| chr2:10737418 | CA | C | 195 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0078 others(192): Show |
196 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(193): Show |
intron_variant | MODIFIER | c.197+10864delA | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10737418 | ||||||
| chr2:10737580 | A | C | 3 | a0001c0001t0002g0324 a0001c0001t0002g0343 a0002c0002t0001g0326 |
3 | HG04184.hp1 HG04204.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.197+11011A>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10737580 | |||||||
| chr2:10737600 | C | A | 1 | a0002c0002t0003g0224 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.197+11031C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10737600 | |||||||
| chr2:10737678 | G | C | 6 | a0001c0001t0007g0237 a0002c0002t0003g0231 a0002c0002t0007g0234 others(3): Show |
6 | HG01261.hp1 HG02055.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.197+11109G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10737678 | |||||||
| chr2:10737736 | C | T | 1 | a0001c0001t0008g0245 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.197+11167C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10737736 | |||||||
| chr2:10737834 | C | T | 19 | a0001c0001t0001g0112 a0001c0001t0016g0220 a0001c0001t0026g0100 others(16): Show |
19 | HG00639.hp2 HG01070.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.197+11265C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10737834 | |||||||
| chr2:10737962 | A | G | 1 | a0002c0002t0001g0317 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.197+11393A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10737962 | |||||||
| chr2:10738201 | C | A | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(1): Show |
4 | NA18960.hp1 NA19009.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.197+11632C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10738201 | |||||||
| chr2:10738385 | G | T | 88 | a0001c0001t0001g0113 a0001c0001t0001g0210 a0001c0001t0001g0211 others(85): Show |
88 | HG00140.hp2 HG00544.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.197+11816G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10738385 | |||||||
| chr2:10738444 | C | T | 1 | a0002c0003t0004g0138 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.197+11875C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10738444 | |||||||
| chr2:10738641 | T | A | 11 | a0001c0001t0001g0112 a0001c0001t0026g0100 a0002c0002t0001g0111 others(8): Show |
11 | HG00639.hp2 HG01243.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.197+12072T>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10738641 | |||||||
| chr2:10738863 | A | G | 1 | a0002c0002t0002g0315 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.197+12294A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10738863 | |||||||
| chr2:10738864 | C | T | 6 | a0001c0001t0001g0153 a0001c0001t0002g0176 a0001c0001t0002g0198 others(3): Show |
6 | HG00438.hp2 HG00621.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.197+12295C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10738864 | |||||||
| chr2:10738893 | C | T | 1 | a0002c0003t0004g0138 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.197+12324C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10738893 | |||||||
| chr2:10738912 | G | C | 10 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(7): Show |
10 | HG02559.hp1 HG02647.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.197+12343G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10738912 | |||||||
| chr2:10738972 | G | T | 2 | a0002c0003t0002g0126 a0002c0003t0002g0127 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.197+12403G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10738972 | |||||||
| chr2:10738994 | G | A | 1 | a0001c0001t0002g0346 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.197+12425G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10738994 | |||||||
| chr2:10739000 | C | T | 1 | a0002c0002t0010g0105 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.197+12431C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10739000 | |||||||
| chr2:10739016 | C | T | 2 | a0002c0002t0004g0103 a0002c0002t0004g0107 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.197+12447C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10739016 | |||||||
| chr2:10739120 | A | G | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | NA18950.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.197+12551A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10739120 | |||||||
| chr2:10739125 | T | C | 146 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(143): Show |
148 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.197+12556T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10739125 | |||||||
| chr2:10739161 | C | T | 36 | a0001c0001t0001g0078 a0001c0001t0002g0075 a0001c0001t0008g0259 others(33): Show |
36 | HG01069.hp1 HG01109.hp2 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.197+12592C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10739161 | |||||||
| chr2:10739189 | A | G | 8 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0104 others(5): Show |
8 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.197+12620A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10739189 | |||||||
| chr2:10739197 | C | A | 4 | a0002c0002t0001g0150 a0002c0002t0001g0225 a0002c0003t0004g0152 others(1): Show |
4 | HG01069.hp1 HG01192.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.197+12628C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10739197 | |||||||
| chr2:10739207 | C | T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0055 a0001c0001t0001g0057 others(1): Show |
4 | HG00323.hp1 HG00738.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.197+12638C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10739207 | |||||||
| chr2:10739214 | C | T | 151 | a0001c0001t0001g0024 a0001c0001t0001g0049 a0001c0001t0001g0051 others(148): Show |
152 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.197+12645C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10739214 | |||||||
| chr2:10739217 | A | T | 1 | a0002c0005t0001g0116 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.197+12648A>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10739217 | |||||||
| chr2:10739223 | C | T | 3 | a0001c0001t0001g0307 a0001c0001t0001g0336 a0002c0002t0001g0335 |
3 | NA18943.hp2 NA18983.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.197+12654C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10739223 | |||||||
| chr2:10739254 | G | C | 1 | a0002c0004t0005g0177 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.197+12685G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10739254 | |||||||
| chr2:10739285 | AAAAT | A | 62 | a0001c0001t0001g0078 a0001c0001t0001g0178 a0001c0001t0001g0204 others(59): Show |
62 | HG00140.hp1 HG00597.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.197+12736_197+1273 others(8): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10739285 | ||||||
| chr2:10739531 | C | T | 3 | a0001c0001t0002g0343 a0002c0002t0001g0326 a0002c0002t0002g0124 |
3 | HG03239.hp2 HG04184.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.197+12962C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10739531 | |||||||
| chr2:10739626 | C | T | 4 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0219 others(1): Show |
4 | HG02723.hp2 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.197+13057C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10739626 | |||||||
| chr2:10739821 | C | T | 1 | a0001c0001t0002g0293 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.197+13252C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10739821 | |||||||
| chr2:10739871 | G | A | 1 | a0002c0004t0005g0177 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.197+13302G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10739871 | |||||||
| chr2:10740044 | C | T | 334 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(331): Show |
337 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.197+13475C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10740044 | |||||||
| chr2:10740087 | C | CA | 109 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(106): Show |
111 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.197+13534dupA | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10740087 | ||||||
| chr2:10740087 | CA | C | 6 | a0001c0001t0001g0054 a0001c0001t0001g0163 a0001c0001t0002g0202 others(3): Show |
6 | HG02523.hp2 HG02922.hp1 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.197+13534delA | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10740087 | ||||||
| chr2:10740481 | A | G | 5 | a0002c0002t0001g0150 a0002c0002t0001g0225 a0002c0002t0004g0123 others(2): Show |
5 | HG01069.hp1 HG01192.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.198-13500A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10740481 | |||||||
| chr2:10740725 | C | T | 1 | a0002c0003t0002g0067 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.198-13256C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10740725 | |||||||
| chr2:10740848 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.198-13133G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10740848 | |||||||
| chr2:10740855 | T | C | 1 | a0001c0001t0002g0185 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.198-13126T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10740855 | |||||||
| chr2:10740876 | G | A | 338 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(335): Show |
341 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.198-13105G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10740876 | |||||||
| chr2:10740953 | C | G | 29 | a0001c0001t0001g0078 a0001c0001t0002g0075 a0001c0001t0008g0245 others(26): Show |
29 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.198-13028C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10740953 | |||||||
| chr2:10740967 | G | A | 1 | a0002c0002t0008g0236 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.198-13014G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10740967 | |||||||
| chr2:10741038 | G | C | 344 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(341): Show |
347 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(344): Show |
intron_variant | MODIFIER | c.198-12943G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10741038 | |||||||
| chr2:10741242 | G | A | 6 | a0002c0002t0001g0242 a0002c0002t0003g0243 a0002c0002t0006g0240 others(3): Show |
6 | HG00639.hp2 HG01243.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.198-12739G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10741242 | |||||||
| chr2:10741434 | AAC | A | 344 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(341): Show |
347 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(344): Show |
intron_variant | MODIFIER | c.198-12543_198-1254 others(6): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10741434 | ||||||
| chr2:10741491 | T | C | 344 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(341): Show |
347 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(344): Show |
intron_variant | MODIFIER | c.198-12490T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10741491 | |||||||
| chr2:10741520 | A | G | 343 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(340): Show |
346 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(343): Show |
intron_variant | MODIFIER | c.198-12461A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10741520 | |||||||
| chr2:10741545 | C | A | 2 | a0001c0001t0002g0014 a0001c0001t0002g0015 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.198-12436C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10741545 | |||||||
| chr2:10741556 | C | T | 2 | a0002c0002t0003g0258 a0002c0009t0022g0155 |
2 | HG00639.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.198-12425C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10741556 | |||||||
| chr2:10741710 | CTG | C | 344 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(341): Show |
347 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(344): Show |
intron_variant | MODIFIER | c.198-12268_198-1226 others(6): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10741710 | ||||||
| chr2:10741741 | C | T | 82 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(79): Show |
84 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.198-12240C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10741741 | |||||||
| chr2:10741891 | C | T | 1 | a0002c0002t0010g0108 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.198-12090C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10741891 | |||||||
| chr2:10741892 | C | CTCCTTCC others(1): Show |
4 | a0002c0002t0001g0150 a0002c0002t0001g0225 a0002c0003t0004g0152 others(1): Show |
4 | HG01069.hp1 HG01192.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.198-12057_198-1205 others(12): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10741892 | ||||||
| chr2:10741892 | CTCCT | C | 28 | a0001c0001t0001g0078 a0001c0001t0002g0075 a0001c0001t0002g0176 others(25): Show |
28 | HG00621.hp2 HG00639.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.198-12053_198-1205 others(8): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10741892 | ||||||
| chr2:10741892 | CTCCTTCC others(1): Show |
C | 311 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(308): Show |
314 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.198-12057_198-1205 others(12): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10741892 | ||||||
| chr2:10741892 | CTCCTTCC others(5): Show |
C | 2 | a0001c0001t0002g0186 a0002c0002t0002g0124 |
2 | HG00408.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.198-12061_198-1205 others(16): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10741892 | ||||||
| chr2:10741942 | G | A | 5 | a0002c0002t0001g0150 a0002c0002t0001g0225 a0002c0002t0004g0123 others(2): Show |
5 | HG01069.hp1 HG01192.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.198-12039G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10741942 | |||||||
| chr2:10742045 | G | C | 2 | a0001c0001t0002g0183 a0002c0002t0001g0184 |
2 | HG00621.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.198-11936G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10742045 | |||||||
| chr2:10742057 | G | A | 11 | a0002c0002t0001g0150 a0002c0002t0001g0225 a0002c0002t0001g0242 others(8): Show |
11 | HG00639.hp2 HG01069.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.198-11924G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10742057 | |||||||
| chr2:10742187 | G | T | 1 | a0002c0002t0002g0337 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.198-11794G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10742187 | |||||||
| chr2:10742202 | G | T | 1 | a0001c0001t0002g0348 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.198-11779G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10742202 | |||||||
| chr2:10742558 | G | A | 1 | a0002c0005t0001g0116 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.198-11423G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10742558 | |||||||
| chr2:10742560 | C | T | 2 | a0002c0002t0001g0304 a0002c0002t0010g0108 |
2 | HG00733.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.198-11421C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10742560 | |||||||
| chr2:10742561 | G | A | 1 | a0002c0002t0006g0230 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.198-11420G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10742561 | |||||||
| chr2:10742569 | C | T | 3 | a0001c0001t0001g0113 a0001c0001t0001g0210 a0001c0001t0001g0211 |
3 | NA18955.hp2 NA18978.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.198-11412C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10742569 | |||||||
| chr2:10742576 | C | G | 1 | a0001c0001t0002g0201 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.198-11405C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10742576 | |||||||
| chr2:10742584 | T | C | 6 | a0002c0002t0001g0150 a0002c0002t0001g0225 a0002c0002t0004g0123 others(3): Show |
6 | HG01069.hp1 HG01192.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.198-11397T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10742584 | |||||||
| chr2:10742632 | G | C | 343 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(340): Show |
346 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(343): Show |
intron_variant | MODIFIER | c.198-11349G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10742632 | |||||||
| chr2:10742640 | G | A | 1 | a0002c0002t0001g0275 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.198-11341G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10742640 | |||||||
| chr2:10742820 | G | A | 7 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0104 others(4): Show |
7 | HG01884.hp2 HG02622.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.198-11161G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10742820 | |||||||
| chr2:10742844 | T | C | 1 | a0001c0001t0002g0198 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.198-11137T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10742844 | |||||||
| chr2:10742860 | C | T | 1 | a0001c0001t0002g0197 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.198-11121C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10742860 | |||||||
| chr2:10742976 | C | A | 1 | a0002c0005t0003g0159 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.198-11005C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10742976 | |||||||
| chr2:10742994 | T | C | 1 | a0002c0002t0001g0304 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.198-10987T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10742994 | |||||||
| chr2:10743161 | G | C | 1 | a0001c0001t0002g0309 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.198-10820G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10743161 | |||||||
| chr2:10743170 | G | A | 1 | a0002c0002t0007g0223 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.198-10811G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10743170 | |||||||
| chr2:10743180 | A | G | 1 | a0002c0002t0001g0275 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.198-10801A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10743180 | |||||||
| chr2:10743181 | A | G | 1 | a0001c0001t0002g0023 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.198-10800A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10743181 | |||||||
| chr2:10743271 | A | G | 5 | a0002c0002t0001g0150 a0002c0002t0001g0225 a0002c0002t0004g0123 others(2): Show |
5 | HG01069.hp1 HG01192.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.198-10710A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10743271 | |||||||
| chr2:10743294 | A | G | 2 | a0002c0004t0005g0045 a0002c0004t0005g0046 |
2 | HG01433.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.198-10687A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10743294 | |||||||
| chr2:10743407 | A | G | 1 | a0002c0002t0007g0134 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.198-10574A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10743407 | |||||||
| chr2:10743667 | C | T | 4 | a0001c0001t0016g0220 a0002c0002t0014g0222 a0002c0002t0015g0221 others(1): Show |
4 | HG01070.hp2 HG02109.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.198-10314C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10743667 | |||||||
| chr2:10743710 | C | A | 216 | a0001c0001t0001g0024 a0001c0001t0001g0049 a0001c0001t0001g0051 others(213): Show |
217 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(214): Show |
intron_variant | MODIFIER | c.198-10271C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10743710 | |||||||
| chr2:10743711 | G | A | 1 | a0002c0002t0003g0246 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.198-10270G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10743711 | |||||||
| chr2:10743797 | T | C | 1 | a0001c0001t0002g0331 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.198-10184T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10743797 | |||||||
| chr2:10743853 | C | G | 1 | a0001c0001t0002g0212 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.198-10128C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10743853 | |||||||
| chr2:10743890 | C | T | 1 | a0002c0002t0006g0230 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.198-10091C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10743890 | |||||||
| chr2:10743968 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.198-10013C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10743968 | |||||||
| chr2:10743981 | CAAA | C | 189 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0051 others(186): Show |
190 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.198-9986_198-9984d others(5): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10743981 | ||||||
| chr2:10743989 | AAAAAAAA others(2): Show |
A | 7 | a0001c0001t0002g0268 a0001c0001t0002g0269 a0001c0001t0002g0270 others(4): Show |
7 | HG00323.hp2 HG01074.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.198-9989_198-9981d others(11): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10743989 | ||||||
| chr2:10743991 | AAAAAAAT | A | 124 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(121): Show |
126 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.198-9987_198-9981d others(9): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10743991 | ||||||
| chr2:10743992 | A | AT | 5 | a0001c0001t0002g0257 a0002c0002t0003g0231 a0002c0005t0001g0116 others(2): Show |
5 | HG00639.hp1 HG01175.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.198-9989_198-9988i others(3): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10743992 | |||||||
| chr2:10743995 | A | T | 81 | a0001c0001t0001g0024 a0001c0001t0001g0144 a0001c0001t0001g0153 others(78): Show |
82 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.198-9986A>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10743995 | |||||||
| chr2:10743995 | AAAT | A | 7 | a0001c0001t0008g0245 a0002c0002t0004g0238 a0002c0002t0004g0239 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.198-9974_198-9972d others(5): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10743995 | ||||||
| chr2:10744001 | T | A | 1 | a0002c0002t0023g0099 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.198-9980T>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10744001 | |||||||
| chr2:10744004 | T | TA | 3 | a0001c0001t0001g0024 a0002c0002t0001g0092 a0002c0002t0008g0236 |
3 | HG03209.hp2 NA18965.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.198-9975dupA | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10744004 | ||||||
| chr2:10744150 | C | T | 4 | a0001c0001t0001g0178 a0001c0001t0001g0204 a0001c0001t0002g0291 others(1): Show |
4 | HG00597.hp1 HG02132.hp2 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.198-9831C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10744150 | |||||||
| chr2:10744583 | C | T | 14 | a0002c0002t0003g0246 a0002c0002t0003g0248 a0002c0002t0003g0249 others(11): Show |
14 | HG02486.hp1 HG02572.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.198-9398C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10744583 | |||||||
| chr2:10744651 | G | T | 1 | a0002c0002t0001g0091 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.198-9330G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10744651 | |||||||
| chr2:10744669 | C | CT | 30 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0024 others(27): Show |
30 | HG00642.hp1 HG00735.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.198-9294dupT | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10744669 | ||||||
| chr2:10744669 | C | CTT | 66 | a0001c0001t0001g0053 a0001c0001t0001g0090 a0001c0001t0001g0163 others(63): Show |
66 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.198-9295_198-9294d others(4): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10744669 | ||||||
| chr2:10744825 | C | T | 3 | a0001c0001t0002g0169 a0001c0001t0002g0213 a0002c0002t0002g0021 |
3 | HG01106.hp2 HG01123.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.198-9156C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10744825 | |||||||
| chr2:10744916 | G | A | 6 | a0001c0001t0002g0282 a0002c0002t0001g0096 a0002c0002t0003g0224 others(3): Show |
6 | HG01109.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.198-9065G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10744916 | |||||||
| chr2:10744958 | C | T | 23 | a0001c0001t0007g0237 a0001c0001t0016g0220 a0002c0002t0001g0096 others(20): Show |
23 | HG00639.hp2 HG01070.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.198-9023C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10744958 | |||||||
| chr2:10745028 | GTTTA | G | 3 | a0002c0007t0009g0040 a0002c0007t0009g0041 a0002c0007t0009g0151 |
3 | HG01069.hp2 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.198-8945_198-8942d others(6): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10745028 | ||||||
| chr2:10745036 | A | C | 22 | a0001c0001t0001g0078 a0001c0001t0002g0075 a0002c0002t0001g0072 others(19): Show |
22 | HG01069.hp1 HG02257.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.198-8945A>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10745036 | |||||||
| chr2:10745041 | C | CT | 217 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(214): Show |
219 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.198-8922dupT | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10745041 | ||||||
| chr2:10745041 | C | CTT | 9 | a0001c0001t0001g0013 a0001c0001t0001g0083 a0001c0001t0002g0014 others(6): Show |
9 | HG00558.hp2 HG00673.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.198-8923_198-8922d others(4): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10745041 | ||||||
| chr2:10745041 | CT | C | 43 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0048 others(40): Show |
44 | HG00639.hp2 HG01069.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.198-8922delT | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10745041 | ||||||
| chr2:10745151 | CTCCTGCC others(22): Show |
C | 1 | a0001c0001t0002g0185 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.198-8829_198-8801d others(31): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10745151 | |||||||
| chr2:10745168 | C | T | 1 | a0002c0002t0001g0068 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.198-8813C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10745168 | |||||||
| chr2:10745179 | A | G | 274 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(271): Show |
277 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.198-8802A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10745179 | |||||||
| chr2:10745358 | G | GT | 89 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0071 others(86): Show |
89 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.198-8612dupT | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10745358 | ||||||
| chr2:10745498 | A | G | 17 | a0002c0002t0001g0150 a0002c0002t0003g0246 a0002c0002t0003g0248 others(14): Show |
17 | HG01069.hp1 HG02486.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.198-8483A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10745498 | |||||||
| chr2:10745632 | C | T | 5 | a0001c0001t0007g0237 a0002c0002t0003g0224 a0002c0002t0004g0103 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.198-8349C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10745632 | |||||||
| chr2:10745693 | T | C | 7 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0039 others(4): Show |
7 | HG00673.hp2 HG02071.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.198-8288T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10745693 | |||||||
| chr2:10745700 | G | A | 2 | a0002c0002t0003g0248 a0002c0002t0003g0258 |
2 | HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.198-8281G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10745700 | |||||||
| chr2:10745775 | T | C | 77 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0071 others(74): Show |
77 | HG00544.hp1 HG00597.hp1 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.198-8206T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10745775 | |||||||
| chr2:10745842 | C | G | 267 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(264): Show |
270 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.198-8139C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10745842 | |||||||
| chr2:10745972 | C | T | 229 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(226): Show |
231 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.198-8009C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10745972 | |||||||
| chr2:10746043 | T | C | 12 | a0001c0001t0007g0237 a0001c0001t0016g0220 a0002c0002t0001g0096 others(9): Show |
12 | HG01070.hp2 HG01109.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.198-7938T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10746043 | |||||||
| chr2:10746125 | G | C | 1 | a0002c0002t0001g0033 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.198-7856G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10746125 | |||||||
| chr2:10746161 | G | A | 10 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0048 others(7): Show |
11 | HG00639.hp2 HG01243.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.198-7820G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10746161 | |||||||
| chr2:10746166 | A | G | 13 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0048 others(10): Show |
14 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.198-7815A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10746166 | |||||||
| chr2:10746196 | C | T | 137 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0019 others(134): Show |
139 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.198-7785C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10746196 | |||||||
| chr2:10746263 | A | G | 33 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0048 others(30): Show |
34 | HG00639.hp2 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.198-7718A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10746263 | |||||||
| chr2:10746320 | C | A | 1 | a0002c0004t0005g0109 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.198-7661C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10746320 | |||||||
| chr2:10746320 | C | T | 122 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0024 others(119): Show |
123 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(120): Show |
intron_variant | MODIFIER | c.198-7661C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10746320 | |||||||
| chr2:10746358 | T | C | 1 | a0002c0002t0002g0337 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.198-7623T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10746358 | |||||||
| chr2:10746398 | CT | C | 6 | a0001c0001t0007g0237 a0002c0002t0001g0096 a0002c0002t0001g0161 others(3): Show |
6 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.198-7573delT | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10746398 | ||||||
| chr2:10746466 | G | T | 1 | a0007c0014t0021g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.198-7515G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10746466 | |||||||
| chr2:10746467 | C | T | 1 | a0007c0014t0021g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.198-7514C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10746467 | |||||||
| chr2:10746557 | C | T | 1 | a0001c0001t0002g0194 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.198-7424C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10746557 | |||||||
| chr2:10746643 | C | T | 1 | a0001c0001t0002g0343 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.198-7338C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10746643 | |||||||
| chr2:10746652 | C | T | 1 | a0002c0004t0005g0046 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.198-7329C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10746652 | |||||||
| chr2:10746657 | G | A | 2 | a0002c0002t0004g0103 a0002c0002t0004g0107 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.198-7324G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10746657 | |||||||
| chr2:10746852 | T | C | 11 | a0001c0001t0007g0237 a0001c0015t0006g0247 a0002c0002t0001g0096 others(8): Show |
11 | HG01109.hp2 HG01261.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.198-7129T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10746852 | |||||||
| chr2:10746908 | T | A | 1 | a0007c0014t0021g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.198-7073T>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10746908 | |||||||
| chr2:10746949 | G | A | 270 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(267): Show |
273 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(270): Show |
intron_variant | MODIFIER | c.198-7032G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10746949 | |||||||
| chr2:10747152 | C | T | 1 | a0002c0002t0006g0230 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.198-6829C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10747152 | |||||||
| chr2:10747383 | C | T | 21 | a0002c0002t0001g0115 a0002c0002t0001g0150 a0002c0002t0003g0246 others(18): Show |
21 | HG01069.hp1 HG01496.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.198-6598C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10747383 | |||||||
| chr2:10747541 | T | G | 87 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0047 others(84): Show |
88 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.198-6440T>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10747541 | |||||||
| chr2:10747583 | G | C | 1 | a0001c0001t0007g0237 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.198-6398G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10747583 | |||||||
| chr2:10747661 | A | T | 1 | a0002c0003t0002g0327 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.198-6320A>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10747661 | |||||||
| chr2:10747663 | C | G | 1 | a0002c0002t0002g0334 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.198-6318C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10747663 | |||||||
| chr2:10747701 | CA | C | 102 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0047 others(99): Show |
103 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.198-6269delA | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10747701 | ||||||
| chr2:10748294 | C | T | 18 | a0002c0002t0001g0115 a0002c0002t0001g0150 a0002c0002t0001g0242 others(15): Show |
18 | HG01069.hp1 HG01891.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.198-5687C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10748294 | |||||||
| chr2:10748295 | G | A | 6 | a0001c0001t0001g0078 a0001c0001t0002g0075 a0002c0002t0001g0072 others(3): Show |
6 | HG02257.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.198-5686G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10748295 | |||||||
| chr2:10748433 | AT | A | 18 | a0002c0002t0001g0052 a0002c0002t0001g0115 a0002c0002t0001g0150 others(15): Show |
18 | HG01069.hp1 HG01891.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.198-5537delT | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10748433 | ||||||
| chr2:10748570 | G | T | 2 | a0002c0002t0007g0234 a0005c0012t0003g0233 |
2 | HG01261.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.198-5411G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10748570 | |||||||
| chr2:10748581 | A | G | 1 | a0001c0015t0006g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.198-5400A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10748581 | |||||||
| chr2:10748722 | C | A | 2 | a0002c0002t0001g0111 a0002c0002t0006g0229 |
2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.198-5259C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10748722 | |||||||
| chr2:10748756 | G | A | 1 | a0002c0002t0004g0117 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.198-5225G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10748756 | |||||||
| chr2:10748766 | G | A | 1 | a0007c0014t0021g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.198-5215G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10748766 | |||||||
| chr2:10748853 | G | A | 1 | a0002c0002t0023g0099 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.198-5128G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10748853 | |||||||
| chr2:10748857 | C | T | 1 | a0002c0002t0001g0242 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.198-5124C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10748857 | |||||||
| chr2:10748884 | C | A | 1 | a0002c0003t0002g0093 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.198-5097C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10748884 | |||||||
| chr2:10748930 | A | G | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | NA18950.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.198-5051A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10748930 | |||||||
| chr2:10748952 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.198-5029C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10748952 | |||||||
| chr2:10748955 | C | T | 1 | a0001c0001t0001g0279 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.198-5026C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10748955 | |||||||
| chr2:10748962 | C | G | 1 | a0002c0002t0001g0242 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.198-5019C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10748962 | |||||||
| chr2:10749054 | C | T | 74 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0047 others(71): Show |
75 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.198-4927C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10749054 | |||||||
| chr2:10749130 | C | CA | 6 | a0001c0001t0001g0028 a0001c0001t0001g0039 a0002c0002t0001g0111 others(3): Show |
6 | HG02055.hp2 HG02970.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.198-4831dupA | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10749130 | ||||||
| chr2:10749130 | CA | C | 158 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(155): Show |
160 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.198-4831delA | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10749130 | ||||||
| chr2:10749130 | CAA | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0047 others(90): Show |
94 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.198-4832_198-4831d others(4): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10749130 | ||||||
| chr2:10749130 | CAAAAA | C | 6 | a0001c0001t0016g0220 a0002c0002t0001g0096 a0002c0002t0001g0161 others(3): Show |
6 | HG01070.hp2 HG02280.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.198-4835_198-4831d others(7): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10749130 | ||||||
| chr2:10749166 | A | G | 8 | a0001c0001t0007g0237 a0001c0015t0006g0247 a0002c0002t0001g0096 others(5): Show |
8 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.198-4815A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10749166 | |||||||
| chr2:10749168 | C | T | 3 | a0001c0001t0007g0237 a0001c0015t0006g0247 a0002c0002t0024g0226 |
3 | HG01109.hp2 HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.198-4813C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10749168 | |||||||
| chr2:10749178 | A | ATTATATA others(8178): Show |
1 | a0001c0001t0001g0196 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.198-3903_198-3902i others(8187): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10749178 | ||||||
| chr2:10749178 | A | ATTATATA others(8179): Show |
1 | a0002c0002t0001g0184 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.198-3903_198-3902i others(8188): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10749178 | ||||||
| chr2:10749178 | A | ATTATATA others(8179): Show |
1 | a0002c0002t0002g0332 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.198-3903_198-3902i others(8188): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10749178 | ||||||
| chr2:10749178 | A | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0047 others(74): Show |
78 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.198-4803A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10749178 | |||||||
| chr2:10749230 | C | G | 8 | a0001c0001t0007g0237 a0001c0015t0006g0247 a0002c0002t0001g0096 others(5): Show |
8 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.198-4751C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10749230 | |||||||
| chr2:10749261 | G | A | 1 | a0001c0001t0007g0237 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.198-4720G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10749261 | |||||||
| chr2:10749422 | A | T | 8 | a0001c0001t0007g0237 a0001c0015t0006g0247 a0002c0002t0001g0096 others(5): Show |
8 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.198-4559A>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10749422 | |||||||
| chr2:10749491 | C | T | 6 | a0001c0001t0001g0078 a0001c0001t0002g0075 a0002c0002t0001g0072 others(3): Show |
6 | HG02257.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.198-4490C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10749491 | |||||||
| chr2:10749498 | T | C | 17 | a0002c0002t0001g0115 a0002c0002t0001g0150 a0002c0002t0003g0246 others(14): Show |
17 | HG01069.hp1 HG01891.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.198-4483T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10749498 | |||||||
| chr2:10749528 | T | G | 4 | a0002c0002t0001g0111 a0002c0002t0004g0117 a0002c0002t0006g0229 others(1): Show |
4 | HG02055.hp2 HG02970.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.198-4453T>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10749528 | |||||||
| chr2:10749583 | T | C | 9 | a0001c0001t0007g0237 a0001c0015t0006g0247 a0002c0002t0001g0096 others(6): Show |
9 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.198-4398T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10749583 | |||||||
| chr2:10749658 | G | A | 7 | a0001c0001t0007g0237 a0001c0015t0006g0247 a0002c0002t0001g0096 others(4): Show |
7 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.198-4323G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10749658 | |||||||
| chr2:10749662 | A | C | 134 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(131): Show |
136 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.198-4319A>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10749662 | |||||||
| chr2:10749664 | ATTC | A | 3 | a0001c0001t0007g0237 a0001c0015t0006g0247 a0002c0002t0024g0226 |
3 | HG01109.hp2 HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.198-4314_198-4312d others(5): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10749664 | ||||||
| chr2:10749823 | GTAT | G | 6 | a0002c0002t0001g0261 a0002c0002t0001g0275 a0002c0002t0001g0276 others(3): Show |
6 | HG00642.hp2 HG00733.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.198-4153_198-4151d others(5): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10749823 | ||||||
| chr2:10749872 | G | A | 16 | a0002c0002t0001g0150 a0002c0002t0003g0246 a0002c0002t0003g0248 others(13): Show |
16 | HG01069.hp1 HG02486.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.198-4109G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10749872 | |||||||
| chr2:10749883 | G | T | 1 | a0001c0001t0001g0054 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.198-4098G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10749883 | |||||||
| chr2:10750079 | G | A | 218 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(215): Show |
220 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.198-3902G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10750079 | |||||||
| chr2:10750172 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.198-3809C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10750172 | |||||||
| chr2:10750282 | C | T | 2 | a0002c0002t0007g0234 a0005c0012t0003g0233 |
2 | HG01261.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.198-3699C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10750282 | |||||||
| chr2:10750311 | G | T | 2 | a0001c0001t0002g0314 a0002c0002t0001g0335 |
2 | HG02300.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.198-3670G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10750311 | |||||||
| chr2:10750460 | A | G | 1 | a0007c0014t0021g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.198-3521A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10750460 | |||||||
| chr2:10750494 | C | T | 1 | a0001c0015t0006g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.198-3487C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10750494 | |||||||
| chr2:10750528 | CA | C | 240 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(237): Show |
242 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.198-3441delA | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10750528 | ||||||
| chr2:10750755 | A | G | 80 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(77): Show |
80 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.198-3226A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10750755 | |||||||
| chr2:10750779 | A | G | 81 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0047 others(78): Show |
82 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.198-3202A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10750779 | |||||||
| chr2:10750872 | T | C | 21 | a0002c0002t0001g0115 a0002c0002t0001g0150 a0002c0002t0003g0246 others(18): Show |
21 | HG01069.hp1 HG01496.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.198-3109T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10750872 | |||||||
| chr2:10750885 | CAGTGCTT others(17): Show |
C | 1 | a0007c0014t0021g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.198-3062_198-3039d others(26): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10750885 | ||||||
| chr2:10750896 | G | A | 1 | a0001c0001t0002g0191 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.198-3085G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10750896 | |||||||
| chr2:10750901 | G | A | 4 | a0002c0002t0003g0243 a0002c0002t0008g0244 a0002c0003t0004g0138 others(1): Show |
4 | HG00639.hp2 HG01243.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.198-3080G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10750901 | |||||||
| chr2:10750920 | GCATAGTA others(17): Show |
G | 1 | a0001c0001t0013g0074 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.198-3037_198-3014d others(26): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10750920 | ||||||
| chr2:10751070 | G | A | 3 | a0001c0001t0002g0316 a0002c0002t0002g0306 a0002c0002t0002g0351 |
3 | HG00735.hp2 HG01934.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.198-2911G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10751070 | |||||||
| chr2:10751090 | A | G | 1 | a0007c0014t0021g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.198-2891A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10751090 | |||||||
| chr2:10751475 | G | A | 1 | a0001c0001t0007g0237 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.198-2506G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10751475 | |||||||
| chr2:10751505 | C | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0047 others(73): Show |
77 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.198-2476C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10751505 | |||||||
| chr2:10751537 | G | T | 4 | a0002c0002t0001g0096 a0002c0002t0001g0161 a0002c0002t0007g0134 others(1): Show |
4 | HG02280.hp2 HG02965.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.198-2444G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10751537 | |||||||
| chr2:10751781 | C | T | 1 | a0001c0001t0007g0237 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.198-2200C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10751781 | |||||||
| chr2:10751813 | C | T | 1 | a0002c0002t0001g0345 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.198-2168C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10751813 | |||||||
| chr2:10751931 | G | C | 1 | a0002c0003t0002g0327 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.198-2050G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10751931 | |||||||
| chr2:10752003 | G | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0047 others(76): Show |
80 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.198-1978G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10752003 | |||||||
| chr2:10752007 | T | C | 335 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(332): Show |
338 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(335): Show |
intron_variant | MODIFIER | c.198-1974T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10752007 | |||||||
| chr2:10752071 | A | C | 90 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0047 others(87): Show |
91 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.198-1910A>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10752071 | |||||||
| chr2:10752080 | C | A | 2 | a0002c0002t0007g0106 a0002c0002t0007g0223 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.198-1901C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10752080 | |||||||
| chr2:10752083 | C | A | 8 | a0001c0001t0001g0061 a0001c0001t0001g0094 a0002c0002t0001g0188 others(5): Show |
8 | HG01884.hp2 HG02602.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.198-1898C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10752083 | |||||||
| chr2:10752199 | A | G | 1 | a0001c0001t0026g0100 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.198-1782A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10752199 | |||||||
| chr2:10752275 | G | C | 345 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(342): Show |
348 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(345): Show |
intron_variant | MODIFIER | c.198-1706G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10752275 | |||||||
| chr2:10752307 | G | A | 2 | a0002c0002t0001g0111 a0002c0002t0004g0117 |
2 | HG02055.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.198-1674G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10752307 | |||||||
| chr2:10752417 | T | C | 2 | a0002c0002t0001g0130 a0002c0002t0001g0304 |
2 | HG00733.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.198-1564T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10752417 | |||||||
| chr2:10752461 | C | T | 1 | a0002c0004t0005g0177 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.198-1520C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10752461 | |||||||
| chr2:10752462 | T | G | 1 | a0004c0011t0017g0149 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.198-1519T>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10752462 | |||||||
| chr2:10752514 | A | G | 1 | a0002c0002t0001g0317 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.198-1467A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10752514 | |||||||
| chr2:10752529 | T | C | 4 | a0002c0002t0003g0243 a0002c0002t0008g0244 a0002c0003t0004g0138 others(1): Show |
4 | HG00639.hp2 HG01243.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.198-1452T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10752529 | |||||||
| chr2:10752543 | C | A | 10 | a0002c0002t0001g0225 a0002c0002t0003g0214 a0002c0002t0003g0243 others(7): Show |
10 | HG00639.hp2 HG01243.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.198-1438C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10752543 | |||||||
| chr2:10752676 | C | T | 4 | a0002c0002t0003g0243 a0002c0002t0008g0244 a0002c0003t0004g0138 others(1): Show |
4 | HG00639.hp2 HG01243.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.198-1305C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10752676 | |||||||
| chr2:10752739 | T | C | 1 | a0002c0002t0001g0111 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.198-1242T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10752739 | |||||||
| chr2:10752882 | G | A | 5 | a0002c0002t0001g0115 a0002c0002t0002g0171 a0002c0007t0009g0040 others(2): Show |
5 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.198-1099G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10752882 | |||||||
| chr2:10752944 | C | T | 1 | a0002c0002t0002g0020 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.198-1037C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10752944 | |||||||
| chr2:10752949 | T | C | 1 | a0002c0002t0002g0124 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.198-1032T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10752949 | |||||||
| chr2:10753069 | A | G | 1 | a0002c0004t0005g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.198-912A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10753069 | |||||||
| chr2:10753173 | A | G | 1 | a0007c0014t0021g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.198-808A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10753173 | |||||||
| chr2:10753380 | C | T | 2 | a0001c0001t0002g0189 a0002c0003t0002g0086 |
2 | HG02015.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.198-601C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10753380 | |||||||
| chr2:10753428 | C | T | 23 | a0001c0001t0001g0042 a0001c0001t0002g0003 a0001c0001t0002g0017 others(20): Show |
24 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.198-553C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10753428 | |||||||
| chr2:10753429 | G | A | 1 | a0002c0002t0001g0242 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.198-552G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10753429 | |||||||
| chr2:10753532 | AT | A | 19 | a0001c0001t0001g0113 a0001c0001t0001g0298 a0001c0001t0001g0339 others(16): Show |
19 | HG00639.hp2 HG01074.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.198-432delT | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10753532 | ||||||
| chr2:10753532 | ATT | A | 6 | a0002c0002t0001g0242 a0002c0002t0003g0214 a0002c0002t0004g0123 others(3): Show |
6 | HG02559.hp2 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.198-433_198-432del others(2): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10753532 | ||||||
| chr2:10753584 | T | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0055 a0001c0001t0020g0056 |
3 | HG00323.hp1 HG01106.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.198-397T>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10753584 | |||||||
| chr2:10753624 | C | T | 1 | a0001c0001t0002g0065 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.198-357C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10753624 | |||||||
| chr2:10753673 | G | A | 1 | a0001c0001t0002g0192 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.198-308G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10753673 | |||||||
| chr2:10753675 | C | T | 2 | a0001c0001t0007g0237 a0002c0002t0024g0226 |
2 | HG01109.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.198-306C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10753675 | |||||||
| chr2:10753830 | G | A | 1 | a0001c0001t0001g0039 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.198-151G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10753830 | |||||||
| chr2:10753851 | C | T | 2 | a0001c0001t0002g0343 a0002c0004t0005g0143 |
2 | HG03688.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.198-130C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10753851 | |||||||
| chr2:10754077 | C | T | 1 | a0002c0002t0001g0317 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.283+11C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10754077 | |||||||
| chr2:10754109 | T | C | 1 | a0001c0001t0002g0202 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.283+43T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10754109 | |||||||
| chr2:10754122 | G | A | 1 | a0001c0001t0002g0283 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.283+56G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10754122 | |||||||
| chr2:10754274 | G | A | 2 | a0002c0002t0003g0231 a0002c0009t0004g0157 |
2 | HG02145.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.283+208G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10754274 | |||||||
| chr2:10754290 | A | G | 1 | a0001c0001t0002g0198 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.283+224A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10754290 | |||||||
| chr2:10754314 | C | T | 1 | a0002c0004t0005g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.283+248C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10754314 | |||||||
| chr2:10754378 | G | A | 82 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0047 others(79): Show |
83 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.283+312G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10754378 | |||||||
| chr2:10754542 | ATTTTCTT others(3): Show |
A | 6 | a0001c0001t0002g0269 a0001c0001t0002g0283 a0002c0002t0001g0284 others(3): Show |
6 | HG01070.hp1 HG01071.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.283+511_283+520del others(10): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 10754542 | ||||||
| chr2:10754542 | ATTTTCTT others(8): Show |
A | 254 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(251): Show |
256 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.283+506_283+520del others(15): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 10754542 | ||||||
| chr2:10754542 | ATTTTCTT others(13): Show |
A | 82 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0047 others(79): Show |
83 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.283+501_283+520del others(20): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 10754542 | ||||||
| chr2:10754563 | TTTTCTTT others(12): Show |
T | 1 | a0002c0002t0001g0335 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.283+501_283+519del others(19): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 10754563 | ||||||
| chr2:10754583 | T | C | 6 | a0001c0015t0006g0247 a0002c0002t0001g0111 a0002c0002t0001g0150 others(3): Show |
6 | HG01069.hp1 HG02055.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+517T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10754583 | |||||||
| chr2:10754609 | G | A | 83 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0047 others(80): Show |
84 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.283+543G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10754609 | |||||||
| chr2:10754653 | A | G | 193 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(190): Show |
194 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.283+587A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10754653 | |||||||
| chr2:10754733 | T | C | 83 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0047 others(80): Show |
84 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.283+667T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10754733 | |||||||
| chr2:10754742 | T | TTG | 3 | a0002c0002t0001g0292 a0002c0002t0001g0335 a0002c0002t0001g0347 |
3 | NA18943.hp2 NA19012.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.283+688_283+689dup others(2): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 10754742 | ||||||
| chr2:10754760 | A | C | 1 | a0001c0001t0002g0190 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.283+694A>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10754760 | |||||||
| chr2:10754761 | A | G | 341 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(338): Show |
344 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(341): Show |
intron_variant | MODIFIER | c.283+695A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10754761 | |||||||
| chr2:10754824 | G | A | 1 | a0002c0002t0002g0133 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.283+758G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10754824 | |||||||
| chr2:10754829 | G | A | 3 | a0001c0001t0002g0023 a0001c0001t0002g0190 a0002c0003t0002g0121 |
3 | HG02056.hp2 NA18975.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.283+763G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10754829 | |||||||
| chr2:10754831 | C | T | 1 | a0002c0002t0002g0035 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.283+765C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10754831 | |||||||
| chr2:10754918 | A | G | 1 | a0002c0002t0010g0108 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.283+852A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10754918 | |||||||
| chr2:10754984 | C | T | 2 | a0002c0002t0001g0208 a0002c0002t0001g0209 |
2 | NA18990.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.283+918C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10754984 | |||||||
| chr2:10755063 | G | T | 2 | a0001c0001t0004g0097 a0001c0001t0004g0114 |
2 | HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.283+997G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10755063 | |||||||
| chr2:10755105 | C | A | 1 | a0002c0002t0001g0111 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.283+1039C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10755105 | |||||||
| chr2:10755141 | A | T | 3 | a0002c0003t0012g0160 a0002c0003t0012g0232 a0002c0004t0005g0162 |
3 | HG01884.hp1 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.283+1075A>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10755141 | |||||||
| chr2:10755276 | T | C | 92 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(89): Show |
93 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.283+1210T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10755276 | |||||||
| chr2:10755357 | T | G | 1 | a0002c0002t0001g0096 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.283+1291T>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10755357 | |||||||
| chr2:10755453 | A | G | 1 | a0002c0002t0024g0226 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.283+1387A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10755453 | |||||||
| chr2:10755510 | G | T | 2 | a0001c0001t0002g0014 a0001c0001t0002g0015 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.283+1444G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10755510 | |||||||
| chr2:10755871 | C | T | 1 | a0002c0002t0001g0111 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.283+1805C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10755871 | |||||||
| chr2:10755923 | G | T | 2 | a0001c0001t0002g0176 a0001c0001t0002g0200 |
2 | NA19010.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.283+1857G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10755923 | |||||||
| chr2:10756065 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.283+1999A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10756065 | |||||||
| chr2:10756105 | C | G | 1 | a0002c0009t0004g0157 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.283+2039C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10756105 | |||||||
| chr2:10756166 | A | G | 80 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0047 others(77): Show |
81 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.283+2100A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10756166 | |||||||
| chr2:10756220 | C | T | 1 | a0002c0003t0002g0148 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.283+2154C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10756220 | |||||||
| chr2:10756309 | G | A | 1 | a0001c0006t0005g0321 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.283+2243G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10756309 | |||||||
| chr2:10756372 | AAAC | A | 87 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(84): Show |
87 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.283+2312_283+2314d others(5): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 10756372 | ||||||
| chr2:10756427 | T | C | 1 | a0002c0002t0001g0096 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.283+2361T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10756427 | |||||||
| chr2:10756441 | C | T | 5 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0104 others(2): Show |
5 | HG02572.hp2 HG03041.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.283+2375C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10756441 | |||||||
| chr2:10756446 | G | A | 1 | a0001c0001t0007g0237 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.283+2380G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10756446 | |||||||
| chr2:10756610 | T | C | 84 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0047 others(81): Show |
85 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.283+2544T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10756610 | |||||||
| chr2:10756657 | G | T | 2 | a0002c0002t0001g0276 a0002c0003t0002g0277 |
2 | HG00642.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.283+2591G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10756657 | |||||||
| chr2:10756672 | C | T | 87 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(84): Show |
87 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.283+2606C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10756672 | |||||||
| chr2:10756733 | G | T | 1 | a0002c0002t0007g0134 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.283+2667G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10756733 | |||||||
| chr2:10756737 | G | T | 50 | a0001c0001t0002g0001 a0001c0001t0002g0189 a0001c0001t0002g0267 others(47): Show |
51 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.283+2671G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10756737 | |||||||
| chr2:10756795 | T | C | 98 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(95): Show |
98 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.283+2729T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10756795 | |||||||
| chr2:10756848 | G | A | 83 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0047 others(80): Show |
84 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.283+2782G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10756848 | |||||||
| chr2:10756904 | C | T | 6 | a0001c0001t0007g0237 a0002c0002t0001g0115 a0002c0002t0007g0234 others(3): Show |
6 | HG01109.hp2 HG01261.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.283+2838C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10756904 | |||||||
| chr2:10756943 | T | A | 1 | a0001c0015t0006g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.283+2877T>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10756943 | |||||||
| chr2:10756987 | T | C | 3 | a0001c0001t0016g0220 a0002c0002t0002g0147 a0002c0002t0015g0221 |
3 | HG02109.hp2 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.283+2921T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10756987 | |||||||
| chr2:10757003 | C | CT | 15 | a0001c0001t0002g0290 a0001c0001t0002g0309 a0001c0001t0006g0308 others(12): Show |
15 | HG01175.hp2 HG01978.hp1 HG02074.hp1 others(12): Show |
intron_variant | MODIFIER | c.283+2966dupT | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 10757003 | ||||||
| chr2:10757003 | CT | C | 12 | a0001c0001t0001g0039 a0001c0001t0001g0051 a0001c0001t0001g0054 others(9): Show |
12 | HG00140.hp2 HG00741.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.283+2966delT | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 10757003 | ||||||
| chr2:10757003 | CTT | C | 79 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(76): Show |
79 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.283+2965_283+2966d others(4): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 10757003 | ||||||
| chr2:10757003 | CTTT | C | 29 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0064 others(26): Show |
29 | HG00639.hp2 HG00642.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.283+2964_283+2966d others(5): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 10757003 | ||||||
| chr2:10757003 | CTTTT | C | 86 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(83): Show |
87 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.283+2963_283+2966d others(6): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 10757003 | ||||||
| chr2:10757003 | CTTTTTTT | C | 8 | a0001c0001t0002g0346 a0002c0002t0001g0092 a0002c0002t0001g0184 others(5): Show |
8 | HG00621.hp1 HG00735.hp1 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.283+2960_283+2966d others(9): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 10757003 | ||||||
| chr2:10757003 | CTTTTTTT others(1): Show |
C | 72 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0047 others(69): Show |
73 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.283+2959_283+2966d others(10): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 10757003 | ||||||
| chr2:10757003 | CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0002g0257 a0002c0009t0022g0155 |
2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.283+2955_283+2966d others(14): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 10757003 | ||||||
| chr2:10757015 | T | G | 8 | a0001c0001t0002g0346 a0002c0002t0001g0092 a0002c0002t0001g0184 others(5): Show |
8 | HG00621.hp1 HG00735.hp1 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.283+2949T>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10757015 | |||||||
| chr2:10757016 | T | G | 72 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0047 others(69): Show |
73 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.283+2950T>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10757016 | |||||||
| chr2:10757162 | G | A | 1 | a0002c0003t0002g0119 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.283+3096G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10757162 | |||||||
| chr2:10757365 | C | T | 1 | a0002c0002t0001g0304 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.283+3299C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10757365 | |||||||
| chr2:10757386 | A | G | 79 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0047 others(76): Show |
80 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.283+3320A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10757386 | |||||||
| chr2:10757412 | CTTA | C | 79 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0047 others(76): Show |
80 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.283+3351_283+3353d others(5): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 10757412 | ||||||
| chr2:10757510 | C | T | 2 | a0001c0001t0002g0174 a0001c0001t0002g0175 |
2 | NA18980.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.283+3444C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10757510 | |||||||
| chr2:10757815 | T | A | 16 | a0001c0001t0001g0078 a0002c0002t0001g0072 a0002c0002t0001g0225 others(13): Show |
16 | HG00639.hp2 HG01243.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.283+3749T>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10757815 | |||||||
| chr2:10757816 | T | A | 2 | a0002c0002t0007g0106 a0002c0002t0007g0223 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.283+3750T>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10757816 | |||||||
| chr2:10757817 | A | T | 2 | a0001c0001t0008g0259 a0002c0002t0006g0230 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.283+3751A>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10757817 | |||||||
| chr2:10758164 | C | G | 4 | a0002c0002t0001g0115 a0002c0002t0007g0234 a0002c0004t0005g0162 others(1): Show |
4 | HG01261.hp1 HG01891.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+4098C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10758164 | |||||||
| chr2:10758174 | A | C | 1 | a0001c0001t0002g0202 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.283+4108A>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10758174 | |||||||
| chr2:10758284 | C | G | 90 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(87): Show |
91 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.283+4218C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10758284 | |||||||
| chr2:10758323 | G | C | 1 | a0001c0001t0002g0017 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.283+4257G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10758323 | |||||||
| chr2:10758412 | C | T | 1 | a0007c0014t0021g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.283+4346C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10758412 | |||||||
| chr2:10758419 | C | T | 1 | a0002c0002t0001g0096 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.283+4353C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10758419 | |||||||
| chr2:10758422 | G | C | 1 | a0002c0002t0001g0242 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.283+4356G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10758422 | |||||||
| chr2:10758519 | G | C | 1 | a0007c0014t0021g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.283+4453G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10758519 | |||||||
| chr2:10758609 | A | G | 16 | a0001c0001t0001g0078 a0002c0002t0001g0072 a0002c0002t0001g0225 others(13): Show |
16 | HG00639.hp2 HG01243.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.283+4543A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10758609 | |||||||
| chr2:10758610 | A | C | 2 | a0001c0001t0002g0270 a0001c0001t0002g0285 |
2 | HG00140.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.283+4544A>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10758610 | |||||||
| chr2:10758712 | G | T | 85 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0047 others(82): Show |
86 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.283+4646G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10758712 | |||||||
| chr2:10758724 | G | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0047 others(83): Show |
87 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.283+4658G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10758724 | |||||||
| chr2:10758742 | A | T | 2 | a0001c0001t0008g0259 a0002c0002t0006g0230 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.283+4676A>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10758742 | |||||||
| chr2:10758961 | C | T | 90 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(87): Show |
90 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.283+4895C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10758961 | |||||||
| chr2:10759143 | G | A | 198 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(195): Show |
199 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.283+5077G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10759143 | |||||||
| chr2:10759397 | G | A | 1 | a0007c0014t0021g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.284-4934G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10759397 | |||||||
| chr2:10759547 | G | A | 1 | a0002c0004t0005g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.284-4784G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10759547 | |||||||
| chr2:10759660 | G | A | 2 | a0001c0001t0008g0259 a0002c0002t0006g0230 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.284-4671G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10759660 | |||||||
| chr2:10759727 | C | T | 203 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(200): Show |
204 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.284-4604C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10759727 | |||||||
| chr2:10759817 | A | G | 79 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0047 others(76): Show |
80 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.284-4514A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10759817 | |||||||
| chr2:10759892 | G | A | 1 | a0007c0014t0021g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.284-4439G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10759892 | |||||||
| chr2:10759949 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0002g0183 |
2 | HG02074.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.284-4382G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10759949 | |||||||
| chr2:10760023 | G | T | 1 | a0001c0001t0006g0308 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.284-4308G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10760023 | |||||||
| chr2:10760030 | G | GT | 246 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(243): Show |
248 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.284-4287dupT | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 10760030 | ||||||
| chr2:10760030 | G | GTT | 30 | a0001c0001t0001g0010 a0001c0001t0001g0307 a0001c0001t0001g0336 others(27): Show |
30 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.284-4288_284-4287d others(4): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 10760030 | ||||||
| chr2:10760030 | G | T | 2 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
2 | NA18964.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.284-4301G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10760030 | |||||||
| chr2:10760037 | T | G | 1 | a0002c0002t0001g0242 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.284-4294T>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10760037 | |||||||
| chr2:10760101 | C | T | 1 | a0002c0002t0006g0229 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.284-4230C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10760101 | |||||||
| chr2:10760129 | C | T | 204 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(201): Show |
205 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.284-4202C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10760129 | |||||||
| chr2:10760170 | C | T | 1 | a0002c0002t0001g0115 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.284-4161C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10760170 | |||||||
| chr2:10760201 | C | T | 204 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(201): Show |
205 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.284-4130C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10760201 | |||||||
| chr2:10760241 | G | A | 1 | a0002c0004t0005g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.284-4090G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10760241 | |||||||
| chr2:10760323 | A | G | 2 | a0001c0001t0008g0259 a0002c0002t0006g0230 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.284-4008A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10760323 | |||||||
| chr2:10760349 | C | T | 204 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(201): Show |
205 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.284-3982C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10760349 | |||||||
| chr2:10760407 | C | T | 1 | a0002c0004t0005g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.284-3924C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10760407 | |||||||
| chr2:10760503 | G | A | 1 | a0002c0002t0001g0242 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.284-3828G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10760503 | |||||||
| chr2:10760579 | G | T | 1 | a0002c0002t0024g0226 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.284-3752G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10760579 | |||||||
| chr2:10760592 | C | G | 1 | a0001c0001t0007g0237 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.284-3739C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10760592 | |||||||
| chr2:10760615 | G | A | 1 | a0002c0002t0006g0229 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.284-3716G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10760615 | |||||||
| chr2:10760869 | G | C | 158 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(155): Show |
159 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.284-3462G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10760869 | |||||||
| chr2:10760903 | A | T | 3 | a0001c0001t0016g0220 a0002c0002t0002g0147 a0002c0002t0015g0221 |
3 | HG02109.hp2 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.284-3428A>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10760903 | |||||||
| chr2:10760933 | C | CG | 19 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0104 others(16): Show |
19 | HG02486.hp1 HG02572.hp1 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.284-3396dupG | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 10760933 | ||||||
| chr2:10760936 | C | G | 208 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(205): Show |
209 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.284-3395C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10760936 | |||||||
| chr2:10760949 | G | A | 1 | a0007c0014t0021g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.284-3382G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10760949 | |||||||
| chr2:10760949 | G | T | 3 | a0001c0001t0016g0220 a0002c0002t0002g0147 a0002c0002t0015g0221 |
3 | HG02109.hp2 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.284-3382G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10760949 | |||||||
| chr2:10761138 | C | T | 1 | a0001c0001t0002g0282 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.284-3193C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10761138 | |||||||
| chr2:10761197 | G | A | 2 | a0002c0003t0002g0126 a0002c0003t0002g0127 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.284-3134G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10761197 | |||||||
| chr2:10761198 | G | T | 1 | a0002c0002t0001g0312 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.284-3133G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10761198 | |||||||
| chr2:10761211 | C | T | 1 | a0004c0011t0017g0149 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.284-3120C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10761211 | |||||||
| chr2:10761309 | A | G | 291 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(288): Show |
293 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.284-3022A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10761309 | |||||||
| chr2:10761366 | A | G | 291 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(288): Show |
293 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.284-2965A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10761366 | |||||||
| chr2:10761418 | C | T | 1 | a0001c0001t0002g0285 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.284-2913C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10761418 | |||||||
| chr2:10761479 | C | T | 1 | a0002c0002t0002g0147 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.284-2852C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10761479 | |||||||
| chr2:10761563 | C | A | 1 | a0001c0001t0002g0343 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.284-2768C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10761563 | |||||||
| chr2:10761664 | C | T | 205 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(202): Show |
206 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.284-2667C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10761664 | |||||||
| chr2:10761665 | G | A | 1 | a0001c0001t0008g0259 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.284-2666G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10761665 | |||||||
| chr2:10761685 | G | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0047 others(76): Show |
80 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.284-2646G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10761685 | |||||||
| chr2:10761706 | G | A | 2 | a0001c0001t0008g0259 a0002c0002t0006g0230 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.284-2625G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10761706 | |||||||
| chr2:10761859 | T | A | 1 | a0002c0002t0001g0228 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.284-2472T>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10761859 | |||||||
| chr2:10761898 | C | T | 1 | a0002c0002t0024g0226 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.284-2433C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10761898 | |||||||
| chr2:10762039 | G | A | 3 | a0001c0001t0016g0220 a0002c0002t0002g0147 a0002c0002t0015g0221 |
3 | HG02109.hp2 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.284-2292G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10762039 | |||||||
| chr2:10762044 | A | G | 205 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(202): Show |
206 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.284-2287A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10762044 | |||||||
| chr2:10762071 | G | C | 1 | a0002c0002t0001g0318 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.284-2260G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10762071 | |||||||
| chr2:10762145 | A | AT | 108 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0047 others(105): Show |
109 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(106): Show |
intron_variant | MODIFIER | c.284-2168dupT | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 10762145 | ||||||
| chr2:10762165 | A | G | 6 | a0001c0001t0007g0237 a0002c0002t0001g0115 a0002c0002t0007g0234 others(3): Show |
6 | HG01109.hp2 HG01261.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.284-2166A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10762165 | |||||||
| chr2:10762167 | A | G | 3 | a0002c0002t0010g0108 a0002c0002t0014g0222 a0002c0002t0023g0099 |
3 | HG01070.hp2 HG01496.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.284-2164A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10762167 | |||||||
| chr2:10762181 | C | T | 3 | a0001c0001t0016g0220 a0002c0002t0002g0147 a0002c0002t0015g0221 |
3 | HG02109.hp2 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.284-2150C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10762181 | |||||||
| chr2:10762199 | G | A | 1 | a0001c0001t0001g0010 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.284-2132G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10762199 | |||||||
| chr2:10762281 | A | G | 204 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(201): Show |
205 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.284-2050A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10762281 | |||||||
| chr2:10762286 | C | T | 1 | a0002c0002t0001g0242 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.284-2045C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10762286 | |||||||
| chr2:10762287 | G | A | 194 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(191): Show |
195 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.284-2044G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10762287 | |||||||
| chr2:10762291 | G | C | 2 | a0001c0001t0008g0259 a0002c0002t0006g0230 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.284-2040G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10762291 | |||||||
| chr2:10762319 | C | T | 204 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(201): Show |
205 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.284-2012C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10762319 | |||||||
| chr2:10762565 | C | T | 12 | a0001c0001t0001g0078 a0002c0002t0001g0072 a0002c0002t0001g0225 others(9): Show |
12 | HG02257.hp1 HG02486.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-1766C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10762565 | |||||||
| chr2:10762574 | T | C | 3 | a0002c0007t0009g0040 a0002c0007t0009g0041 a0002c0007t0009g0151 |
3 | HG01069.hp2 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.284-1757T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10762574 | |||||||
| chr2:10762649 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.284-1682C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10762649 | |||||||
| chr2:10762694 | C | T | 1 | a0001c0001t0001g0265 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.284-1637C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10762694 | |||||||
| chr2:10762695 | T | C | 1 | a0001c0001t0001g0265 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.284-1636T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10762695 | |||||||
| chr2:10762704 | C | A | 1 | a0002c0002t0006g0230 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.284-1627C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10762704 | |||||||
| chr2:10762731 | C | T | 201 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(198): Show |
202 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.284-1600C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10762731 | |||||||
| chr2:10762732 | G | A | 4 | a0002c0002t0001g0242 a0002c0002t0007g0234 a0002c0003t0002g0086 others(1): Show |
4 | HG01261.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-1599G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10762732 | |||||||
| chr2:10762734 | C | T | 3 | a0001c0001t0001g0090 a0001c0001t0001g0163 a0001c0001t0001g0320 |
3 | HG02155.hp2 NA19003.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.284-1597C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10762734 | |||||||
| chr2:10762796 | C | T | 1 | a0002c0002t0001g0096 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.284-1535C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10762796 | |||||||
| chr2:10762834 | GTCC | G | 4 | a0002c0002t0003g0243 a0002c0002t0008g0244 a0002c0003t0004g0138 others(1): Show |
4 | HG00639.hp2 HG01243.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-1491_284-1489d others(5): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 10762834 | ||||||
| chr2:10762846 | C | G | 3 | a0001c0001t0016g0220 a0002c0002t0002g0147 a0002c0002t0015g0221 |
3 | HG02109.hp2 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.284-1485C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10762846 | |||||||
| chr2:10762895 | G | A | 12 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0104 others(9): Show |
12 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.284-1436G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10762895 | |||||||
| chr2:10762935 | C | T | 1 | a0002c0002t0004g0117 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.284-1396C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10762935 | |||||||
| chr2:10763003 | T | G | 7 | a0001c0001t0007g0237 a0001c0001t0016g0220 a0002c0002t0001g0150 others(4): Show |
7 | HG01069.hp1 HG01109.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-1328T>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10763003 | |||||||
| chr2:10763078 | C | G | 1 | a0001c0001t0001g0265 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.284-1253C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10763078 | |||||||
| chr2:10763079 | G | C | 1 | a0001c0001t0001g0265 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.284-1252G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10763079 | |||||||
| chr2:10763113 | C | T | 12 | a0001c0001t0001g0078 a0002c0002t0001g0072 a0002c0002t0001g0225 others(9): Show |
12 | HG02257.hp1 HG02486.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-1218C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10763113 | |||||||
| chr2:10763201 | C | T | 1 | a0001c0001t0002g0212 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.284-1130C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10763201 | |||||||
| chr2:10763202 | G | A | 1 | a0001c0001t0002g0314 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.284-1129G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10763202 | |||||||
| chr2:10763222 | C | T | 1 | a0002c0002t0010g0108 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.284-1109C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10763222 | |||||||
| chr2:10763223 | A | G | 296 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(293): Show |
298 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.284-1108A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10763223 | |||||||
| chr2:10763286 | C | T | 170 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(167): Show |
171 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.284-1045C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10763286 | |||||||
| chr2:10763443 | C | G | 1 | a0002c0002t0001g0275 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.284-888C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10763443 | |||||||
| chr2:10763452 | G | A | 2 | a0002c0002t0002g0147 a0002c0002t0015g0221 |
2 | HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.284-879G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10763452 | |||||||
| chr2:10763502 | A | C | 16 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0104 others(13): Show |
16 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.284-829A>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10763502 | |||||||
| chr2:10763627 | G | A | 1 | a0001c0001t0002g0331 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.284-704G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10763627 | |||||||
| chr2:10763647 | C | T | 2 | a0001c0001t0004g0097 a0001c0001t0004g0114 |
2 | HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.284-684C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10763647 | |||||||
| chr2:10763648 | G | A | 1 | a0002c0002t0004g0117 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.284-683G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10763648 | |||||||
| chr2:10763664 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0094 |
2 | NA19057.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.284-667G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10763664 | |||||||
| chr2:10763699 | GC | G | 3 | a0001c0001t0001g0336 a0002c0002t0001g0005 a0002c0002t0002g0171 |
3 | NA18983.hp2 NA18986.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.284-629delC | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 10763699 | ||||||
| chr2:10763725 | G | A | 1 | a0001c0001t0007g0237 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.284-606G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10763725 | |||||||
| chr2:10763828 | A | C | 1 | a0001c0001t0002g0309 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.284-503A>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10763828 | |||||||
| chr2:10764002 | ATAGCAT | A | 3 | a0001c0001t0001g0336 a0002c0002t0001g0005 a0002c0002t0002g0171 |
3 | NA18983.hp2 NA18986.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.284-328_284-323del others(6): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10764002 | |||||||
| chr2:10764010 | T | G | 3 | a0001c0001t0001g0336 a0002c0002t0001g0005 a0002c0002t0002g0171 |
3 | NA18983.hp2 NA18986.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.284-321T>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10764010 | |||||||
| chr2:10764011 | A | T | 3 | a0001c0001t0001g0336 a0002c0002t0001g0005 a0002c0002t0002g0171 |
3 | NA18983.hp2 NA18986.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.284-320A>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10764011 | |||||||
| chr2:10764070 | T | C | 1 | a0002c0002t0006g0230 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.284-261T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10764070 | |||||||
| chr2:10764147 | C | G | 1 | a0002c0002t0001g0111 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.284-184C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10764147 | |||||||
| chr2:10764167 | C | T | 2 | a0002c0002t0001g0284 a0002c0002t0001g0295 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.284-164C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10764167 | |||||||
| chr2:10764178 | C | T | 11 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0013g0074 others(8): Show |
11 | HG01167.hp2 HG01169.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.284-153C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10764178 | |||||||
| chr2:10764237 | G | A | 1 | a0004c0011t0017g0149 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.284-94G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10764237 | |||||||
| chr2:10764484 | T | G | 2 | a0003c0008t0003g0122 a0003c0008t0003g0146 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.378+59T>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10764484 | |||||||
| chr2:10764489 | A | G | 15 | a0002c0002t0001g0150 a0002c0002t0001g0161 a0002c0002t0003g0224 others(12): Show |
15 | HG00639.hp1 HG01069.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+64A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10764489 | |||||||
| chr2:10764557 | T | TC | 10 | a0001c0001t0001g0078 a0002c0002t0001g0072 a0002c0002t0001g0096 others(7): Show |
10 | HG01934.hp2 HG02257.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.378+134dupC | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 10764557 | ||||||
| chr2:10764630 | C | T | 5 | a0002c0002t0007g0234 a0002c0003t0004g0152 a0002c0004t0005g0109 others(2): Show |
5 | HG00639.hp1 HG01261.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.378+205C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10764630 | |||||||
| chr2:10764649 | C | G | 5 | a0002c0002t0007g0234 a0002c0003t0004g0152 a0002c0004t0005g0109 others(2): Show |
5 | HG00639.hp1 HG01261.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.378+224C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10764649 | |||||||
| chr2:10764690 | G | A | 2 | a0002c0002t0003g0224 a0006c0017t0001g0216 |
2 | HG01109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.378+265G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10764690 | |||||||
| chr2:10764701 | G | A | 1 | a0001c0001t0002g0268 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.378+276G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10764701 | |||||||
| chr2:10764799 | G | A | 1 | a0007c0014t0021g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.378+374G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10764799 | |||||||
| chr2:10764841 | C | T | 7 | a0002c0002t0006g0229 a0002c0002t0006g0230 a0002c0002t0006g0240 others(4): Show |
7 | HG01496.hp2 HG02109.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.378+416C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10764841 | |||||||
| chr2:10764842 | A | G | 347 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(344): Show |
350 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(347): Show |
intron_variant | MODIFIER | c.378+417A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10764842 | |||||||
| chr2:10764920 | G | A | 12 | a0002c0002t0001g0096 a0002c0002t0004g0117 a0002c0003t0004g0058 others(9): Show |
12 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.378+495G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10764920 | |||||||
| chr2:10764976 | CA | C | 177 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(174): Show |
179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.378+564delA | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 10764976 | ||||||
| chr2:10765028 | C | A | 2 | a0002c0002t0001g0130 a0002c0002t0001g0261 |
2 | HG00741.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.378+603C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10765028 | |||||||
| chr2:10765057 | G | A | 2 | a0002c0002t0007g0234 a0002c0004t0005g0162 |
2 | HG01261.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.378+632G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10765057 | |||||||
| chr2:10765070 | G | T | 161 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(158): Show |
163 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.378+645G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10765070 | |||||||
| chr2:10765181 | T | C | 29 | a0002c0002t0001g0115 a0002c0002t0001g0150 a0002c0002t0001g0161 others(26): Show |
29 | HG01069.hp1 HG01069.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.378+756T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10765181 | |||||||
| chr2:10765420 | A | G | 1 | a0002c0002t0001g0225 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.378+995A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10765420 | |||||||
| chr2:10765465 | G | A | 29 | a0002c0002t0001g0096 a0002c0002t0004g0117 a0002c0003t0002g0009 others(26): Show |
29 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.378+1040G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10765465 | |||||||
| chr2:10765563 | C | A | 1 | a0001c0001t0001g0054 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.378+1138C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10765563 | |||||||
| chr2:10765573 | C | T | 1 | a0002c0002t0001g0319 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.378+1148C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10765573 | |||||||
| chr2:10765635 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.378+1210G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10765635 | |||||||
| chr2:10765638 | G | A | 2 | a0002c0002t0014g0222 a0002c0002t0023g0099 |
2 | HG01070.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.378+1213G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10765638 | |||||||
| chr2:10765692 | T | G | 1 | a0002c0002t0001g0079 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.378+1267T>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10765692 | |||||||
| chr2:10765907 | C | T | 16 | a0002c0003t0002g0009 a0002c0003t0002g0063 a0002c0003t0002g0067 others(13): Show |
16 | HG00323.hp2 HG00597.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.378+1482C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10765907 | |||||||
| chr2:10766009 | G | A | 2 | a0002c0003t0012g0160 a0002c0003t0012g0232 |
2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.378+1584G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10766009 | |||||||
| chr2:10766055 | G | A | 2 | a0002c0003t0012g0160 a0002c0003t0012g0232 |
2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.378+1630G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10766055 | |||||||
| chr2:10766065 | C | T | 1 | a0001c0001t0002g0291 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.378+1640C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10766065 | |||||||
| chr2:10766189 | A | G | 30 | a0002c0002t0001g0096 a0002c0002t0004g0117 a0002c0003t0002g0009 others(27): Show |
30 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.378+1764A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10766189 | |||||||
| chr2:10766287 | C | T | 2 | a0001c0001t0001g0173 a0001c0001t0001g0349 |
2 | NA19066.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.378+1862C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10766287 | |||||||
| chr2:10766413 | T | C | 1 | a0002c0002t0004g0117 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.378+1988T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10766413 | |||||||
| chr2:10766563 | G | A | 1 | a0001c0001t0002g0343 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.378+2138G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10766563 | |||||||
| chr2:10766573 | A | AT | 11 | a0001c0001t0002g0282 a0002c0002t0001g0242 a0002c0002t0004g0103 others(8): Show |
11 | HG01109.hp2 HG02559.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.379-2138dupT | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 10766573 | ||||||
| chr2:10766583 | G | A | 11 | a0002c0002t0001g0111 a0002c0002t0003g0249 a0002c0002t0004g0123 others(8): Show |
11 | HG00639.hp2 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.379-2136G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10766583 | |||||||
| chr2:10766674 | C | T | 1 | a0001c0001t0002g0343 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.379-2045C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10766674 | |||||||
| chr2:10766811 | T | TA | 11 | a0002c0002t0001g0111 a0002c0002t0003g0249 a0002c0002t0004g0123 others(8): Show |
11 | HG00639.hp2 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.379-1907dupA | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 10766811 | ||||||
| chr2:10766938 | CTG | C | 3 | a0002c0002t0001g0072 a0002c0002t0018g0077 a0002c0005t0001g0116 |
3 | HG02257.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.379-1778_379-1777d others(4): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 10766938 | ||||||
| chr2:10766963 | T | C | 1 | a0002c0002t0015g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.379-1756T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10766963 | |||||||
| chr2:10767041 | T | A | 19 | a0002c0002t0001g0115 a0002c0002t0003g0214 a0002c0002t0003g0224 others(16): Show |
19 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.379-1678T>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10767041 | |||||||
| chr2:10767096 | TTA | T | 3 | a0001c0001t0001g0313 a0001c0001t0001g0333 a0001c0001t0002g0340 |
3 | HG01993.hp2 HG02273.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.379-1622_379-1621d others(4): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10767096 | |||||||
| chr2:10767135 | A | C | 103 | a0001c0001t0002g0316 a0001c0001t0002g0338 a0002c0002t0001g0005 others(100): Show |
103 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.379-1584A>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10767135 | |||||||
| chr2:10767159 | C | CT | 119 | a0001c0001t0001g0349 a0002c0002t0001g0005 a0002c0002t0001g0030 others(116): Show |
119 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.379-1541dupT | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 10767159 | ||||||
| chr2:10767159 | C | CTT | 123 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(120): Show |
124 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.379-1542_379-1541d others(4): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 10767159 | ||||||
| chr2:10767159 | C | CTTT | 78 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0024 others(75): Show |
80 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.379-1543_379-1541d others(5): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 10767159 | ||||||
| chr2:10767521 | G | A | 172 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(169): Show |
175 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.379-1198G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10767521 | |||||||
| chr2:10767551 | G | A | 33 | a0002c0002t0001g0225 a0002c0002t0004g0117 a0002c0002t0007g0106 others(30): Show |
33 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.379-1168G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10767551 | |||||||
| chr2:10767606 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.379-1113C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10767606 | |||||||
| chr2:10767709 | C | T | 1 | a0002c0004t0005g0085 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.379-1010C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10767709 | |||||||
| chr2:10767808 | ATTTAT | A | 3 | a0002c0007t0009g0040 a0002c0007t0009g0041 a0002c0007t0009g0151 |
3 | HG01069.hp2 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.379-905_379-901del others(5): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 10767808 | ||||||
| chr2:10767932 | A | G | 2 | a0002c0002t0007g0106 a0002c0002t0007g0223 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.379-787A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10767932 | |||||||
| chr2:10768028 | C | G | 1 | a0002c0002t0002g0172 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.379-691C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10768028 | |||||||
| chr2:10768033 | G | A | 312 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(309): Show |
315 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.379-686G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10768033 | |||||||
| chr2:10768071 | A | G | 312 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(309): Show |
315 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.379-648A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10768071 | |||||||
| chr2:10768074 | G | A | 4 | a0002c0002t0001g0225 a0002c0002t0010g0108 a0002c0003t0012g0160 others(1): Show |
4 | HG01496.hp2 HG01884.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-645G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10768074 | |||||||
| chr2:10768107 | A | C | 312 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(309): Show |
315 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.379-612A>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10768107 | |||||||
| chr2:10768110 | G | A | 1 | a0002c0004t0005g0311 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.379-609G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10768110 | |||||||
| chr2:10768111 | C | T | 1 | a0001c0001t0002g0001 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.379-608C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10768111 | |||||||
| chr2:10768126 | G | C | 345 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(342): Show |
348 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(345): Show |
intron_variant | MODIFIER | c.379-593G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10768126 | |||||||
| chr2:10768170 | C | A | 1 | a0002c0002t0001g0300 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.379-549C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10768170 | |||||||
| chr2:10768195 | C | T | 5 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0153 others(2): Show |
5 | HG00438.hp2 NA18949.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.379-524C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10768195 | |||||||
| chr2:10768248 | G | C | 1 | a0002c0002t0001g0115 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.379-471G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10768248 | |||||||
| chr2:10768294 | T | C | 1 | a0002c0002t0001g0228 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.379-425T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10768294 | |||||||
| chr2:10768434 | G | A | 169 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(166): Show |
172 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.379-285G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10768434 | |||||||
| chr2:10768447 | C | T | 16 | a0002c0003t0002g0009 a0002c0003t0002g0063 a0002c0003t0002g0067 others(13): Show |
16 | HG00323.hp2 HG00597.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.379-272C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10768447 | |||||||
| chr2:10768463 | C | T | 1 | a0002c0002t0001g0341 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.379-256C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10768463 | |||||||
| chr2:10768536 | G | A | 40 | a0002c0002t0001g0150 a0002c0002t0001g0161 a0002c0002t0001g0225 others(37): Show |
40 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.379-183G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10768536 | |||||||
| chr2:10768716 | C | T | 2 | a0002c0002t0003g0252 a0002c0002t0003g0253 |
2 | HG02486.hp1 NA20129.hp2 |
splice_region_variant&intron_variant | LOW | c.379-3C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10768716 | |||||||
| chr2:10768966 | C | T | 26 | a0001c0001t0008g0259 a0001c0001t0016g0220 a0002c0002t0007g0106 others(23): Show |
26 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.470+156C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10768966 | |||||||
| chr2:10769062 | C | G | 2 | a0002c0002t0014g0222 a0002c0002t0023g0099 |
2 | HG01070.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.470+252C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10769062 | |||||||
| chr2:10769098 | T | C | 183 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(180): Show |
184 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(181): Show |
intron_variant | MODIFIER | c.470+288T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10769098 | |||||||
| chr2:10769176 | C | T | 11 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0028 others(8): Show |
11 | HG00673.hp2 HG02132.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.470+366C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10769176 | |||||||
| chr2:10769208 | T | C | 113 | a0001c0001t0002g0316 a0002c0002t0001g0005 a0002c0002t0001g0030 others(110): Show |
113 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.470+398T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10769208 | |||||||
| chr2:10769276 | G | A | 1 | a0002c0002t0001g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.470+466G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10769276 | |||||||
| chr2:10769314 | A | G | 40 | a0002c0002t0001g0225 a0002c0002t0004g0117 a0002c0002t0006g0229 others(37): Show |
40 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.470+504A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10769314 | |||||||
| chr2:10769390 | C | T | 1 | a0002c0003t0002g0142 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.470+580C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10769390 | |||||||
| chr2:10769416 | G | A | 1 | a0006c0017t0001g0216 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.470+606G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10769416 | |||||||
| chr2:10769485 | C | T | 1 | a0001c0016t0001g0156 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.470+675C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10769485 | |||||||
| chr2:10769542 | A | G | 1 | a0001c0001t0002g0331 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.470+732A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10769542 | |||||||
| chr2:10769588 | T | C | 65 | a0001c0001t0002g0316 a0002c0002t0001g0005 a0002c0002t0001g0030 others(62): Show |
65 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.470+778T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10769588 | |||||||
| chr2:10769631 | C | A | 2 | a0002c0002t0007g0234 a0002c0004t0005g0162 |
2 | HG01261.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.470+821C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10769631 | |||||||
| chr2:10769658 | C | T | 2 | a0001c0001t0008g0259 a0001c0001t0016g0220 |
2 | HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.470+848C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10769658 | |||||||
| chr2:10769659 | G | T | 1 | a0001c0001t0002g0324 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.470+849G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10769659 | |||||||
| chr2:10769702 | AAAAC | A | 7 | a0002c0002t0001g0062 a0002c0002t0001g0188 a0002c0002t0001g0208 others(4): Show |
7 | NA18949.hp1 NA18955.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.470+908_470+911del others(4): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | 10769702 | ||||||
| chr2:10769860 | C | A | 2 | a0002c0002t0001g0096 a0002c0002t0001g0115 |
2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.470+1050C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10769860 | |||||||
| chr2:10769861 | C | G | 9 | a0001c0001t0013g0074 a0002c0002t0001g0111 a0002c0002t0004g0123 others(6): Show |
9 | HG00639.hp2 HG02055.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.470+1051C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10769861 | |||||||
| chr2:10769884 | A | G | 1 | a0002c0002t0001g0276 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.470+1074A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10769884 | |||||||
| chr2:10769929 | C | A | 41 | a0002c0002t0001g0225 a0002c0002t0004g0117 a0002c0002t0006g0229 others(38): Show |
41 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.470+1119C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10769929 | |||||||
| chr2:10769942 | G | A | 2 | a0002c0003t0012g0160 a0002c0003t0012g0232 |
2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.470+1132G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10769942 | |||||||
| chr2:10769959 | C | G | 1 | a0002c0003t0002g0148 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.470+1149C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10769959 | |||||||
| chr2:10770123 | G | A | 2 | a0002c0002t0001g0096 a0002c0002t0001g0115 |
2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.470+1313G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10770123 | |||||||
| chr2:10770124 | C | T | 2 | a0002c0002t0001g0096 a0002c0002t0001g0115 |
2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.470+1314C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10770124 | |||||||
| chr2:10770148 | C | T | 1 | a0002c0002t0015g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.470+1338C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10770148 | |||||||
| chr2:10770258 | C | T | 1 | a0001c0001t0002g0331 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.470+1448C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10770258 | |||||||
| chr2:10770313 | G | A | 1 | a0002c0002t0010g0108 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.470+1503G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10770313 | |||||||
| chr2:10770355 | G | A | 1 | a0001c0006t0005g0323 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.471-1484G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10770355 | |||||||
| chr2:10770363 | A | C | 3 | a0002c0007t0009g0040 a0002c0007t0009g0041 a0002c0007t0009g0151 |
3 | HG01069.hp2 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.471-1476A>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10770363 | |||||||
| chr2:10770403 | A | G | 2 | a0002c0002t0001g0150 a0002c0002t0001g0161 |
2 | HG01069.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.471-1436A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10770403 | |||||||
| chr2:10770447 | G | A | 2 | a0001c0001t0008g0259 a0001c0001t0016g0220 |
2 | HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.471-1392G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10770447 | |||||||
| chr2:10770581 | C | T | 10 | a0002c0003t0004g0058 a0002c0003t0004g0073 a0002c0003t0004g0076 others(7): Show |
10 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.471-1258C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10770581 | |||||||
| chr2:10770693 | T | G | 1 | a0002c0002t0001g0115 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.471-1146T>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10770693 | |||||||
| chr2:10770725 | T | C | 110 | a0001c0001t0002g0316 a0002c0002t0001g0005 a0002c0002t0001g0030 others(107): Show |
110 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.471-1114T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10770725 | |||||||
| chr2:10770751 | C | T | 41 | a0002c0002t0001g0225 a0002c0002t0004g0117 a0002c0002t0006g0229 others(38): Show |
41 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.471-1088C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10770751 | |||||||
| chr2:10770816 | A | C | 1 | a0001c0001t0002g0269 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.471-1023A>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10770816 | |||||||
| chr2:10770843 | C | T | 192 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(189): Show |
194 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.471-996C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10770843 | |||||||
| chr2:10770869 | C | T | 2 | a0002c0002t0007g0106 a0002c0002t0007g0223 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.471-970C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10770869 | |||||||
| chr2:10770911 | T | C | 1 | a0002c0002t0007g0106 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.471-928T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10770911 | |||||||
| chr2:10771043 | G | T | 8 | a0002c0002t0004g0117 a0002c0002t0006g0229 a0002c0002t0006g0230 others(5): Show |
8 | HG01884.hp2 HG02572.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.471-796G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10771043 | |||||||
| chr2:10771075 | C | T | 30 | a0002c0003t0002g0009 a0002c0003t0002g0063 a0002c0003t0002g0067 others(27): Show |
30 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.471-764C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10771075 | |||||||
| chr2:10771084 | T | C | 1 | a0002c0002t0007g0106 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.471-755T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10771084 | |||||||
| chr2:10771182 | G | A | 1 | a0007c0014t0021g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.471-657G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10771182 | |||||||
| chr2:10771247 | A | G | 3 | a0002c0007t0009g0040 a0002c0007t0009g0041 a0002c0007t0009g0151 |
3 | HG01069.hp2 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.471-592A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10771247 | |||||||
| chr2:10771408 | C | T | 1 | a0002c0002t0003g0248 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.471-431C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10771408 | |||||||
| chr2:10771426 | G | A | 29 | a0001c0006t0005g0038 a0001c0006t0005g0321 a0001c0006t0005g0323 others(26): Show |
29 | HG00642.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.471-413G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10771426 | |||||||
| chr2:10771590 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.471-249C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10771590 | |||||||
| chr2:10771603 | G | A | 1 | a0007c0014t0021g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.471-236G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10771603 | |||||||
| chr2:10771765 | T | C | 318 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(315): Show |
321 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(318): Show |
intron_variant | MODIFIER | c.471-74T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 6/13 | chr2 | 10771765 | |||||||
| chr2:10771966 | C | T | 25 | a0001c0006t0005g0038 a0001c0006t0005g0321 a0001c0006t0005g0323 others(22): Show |
25 | HG00642.hp2 HG00735.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.569+29C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 7/13 | chr2 | 10771966 | |||||||
| chr2:10771998 | G | A | 2 | a0002c0002t0014g0222 a0002c0002t0023g0099 |
2 | HG01070.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.569+61G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 7/13 | chr2 | 10771998 | |||||||
| chr2:10772027 | T | G | 110 | a0001c0001t0002g0316 a0001c0001t0013g0074 a0002c0002t0001g0005 others(107): Show |
110 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.569+90T>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 7/13 | chr2 | 10772027 | |||||||
| chr2:10772256 | C | T | 1 | a0005c0012t0003g0233 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.570-286C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 7/13 | chr2 | 10772256 | |||||||
| chr2:10772273 | G | A | 68 | a0001c0001t0002g0316 a0002c0002t0001g0005 a0002c0002t0001g0030 others(65): Show |
68 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.570-269G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 7/13 | chr2 | 10772273 | |||||||
| chr2:10772315 | G | C | 1 | a0002c0002t0001g0225 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.570-227G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 7/13 | chr2 | 10772315 | |||||||
| chr2:10772322 | C | A | 65 | a0001c0001t0002g0316 a0002c0002t0001g0005 a0002c0002t0001g0030 others(62): Show |
65 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.570-220C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 7/13 | chr2 | 10772322 | |||||||
| chr2:10772397 | C | A | 2 | a0002c0002t0001g0225 a0002c0002t0010g0108 |
2 | HG01496.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.570-145C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 7/13 | chr2 | 10772397 | |||||||
| chr2:10772462 | G | C | 1 | a0007c0014t0021g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.570-80G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 7/13 | chr2 | 10772462 | |||||||
| chr2:10772464 | T | C | 1 | a0002c0002t0001g0115 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.570-78T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 7/13 | chr2 | 10772464 | |||||||
| chr2:10772479 | G | A | 1 | a0002c0002t0003g0249 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.570-63G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 7/13 | chr2 | 10772479 | |||||||
| chr2:10772506 | T | G | 2 | a0002c0003t0004g0058 a0002c0009t0004g0157 |
2 | HG02895.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.570-36T>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 7/13 | chr2 | 10772506 | |||||||
| chr2:10772508 | C | A | 1 | a0002c0002t0002g0315 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.570-34C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 7/13 | chr2 | 10772508 | |||||||
| chr2:10772538 | G | A | 9 | a0001c0001t0013g0074 a0002c0002t0001g0111 a0002c0002t0004g0123 others(6): Show |
9 | HG00639.hp2 HG02055.hp2 HG02486.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.570-4G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 7/13 | chr2 | 10772538 | |||||||
| chr2:10772689 | GC | G | 4 | a0002c0002t0001g0242 a0002c0002t0004g0103 a0002c0002t0004g0107 others(1): Show |
4 | HG01109.hp2 HG02559.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.638+83delC | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 10772689 | ||||||
| chr2:10772836 | G | GGCTGCCC others(9): Show |
137 | a0001c0001t0002g0316 a0001c0001t0002g0338 a0001c0001t0013g0074 others(134): Show |
137 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.638+227_638+242dup others(16): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 10772836 | ||||||
| chr2:10772910 | G | A | 160 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.638+300G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10772910 | |||||||
| chr2:10772918 | G | A | 2 | a0003c0008t0003g0122 a0003c0008t0003g0146 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.638+308G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10772918 | |||||||
| chr2:10772957 | C | T | 35 | a0001c0001t0007g0237 a0002c0002t0001g0096 a0002c0002t0001g0115 others(32): Show |
35 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.638+347C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10772957 | |||||||
| chr2:10772977 | C | T | 4 | a0002c0002t0001g0096 a0002c0002t0001g0115 a0002c0002t0007g0106 others(1): Show |
4 | HG01884.hp2 HG01891.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.638+367C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10772977 | |||||||
| chr2:10772986 | C | T | 2 | a0002c0002t0001g0150 a0002c0002t0001g0161 |
2 | HG01069.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.638+376C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10772986 | |||||||
| chr2:10773023 | T | C | 281 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(278): Show |
284 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.638+413T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10773023 | |||||||
| chr2:10773044 | A | G | 222 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(219): Show |
225 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.638+434A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10773044 | |||||||
| chr2:10773098 | C | T | 3 | a0002c0003t0002g0126 a0002c0003t0002g0127 a0002c0003t0002g0273 |
3 | HG01256.hp2 HG01258.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.638+488C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10773098 | |||||||
| chr2:10773111 | A | G | 131 | a0001c0001t0002g0316 a0001c0001t0002g0338 a0001c0006t0005g0038 others(128): Show |
131 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.638+501A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10773111 | |||||||
| chr2:10773213 | G | A | 3 | a0002c0002t0001g0072 a0002c0002t0018g0077 a0002c0005t0001g0116 |
3 | HG02257.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.638+603G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10773213 | |||||||
| chr2:10773261 | G | A | 1 | a0001c0001t0002g0348 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.638+651G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10773261 | |||||||
| chr2:10773271 | G | A | 28 | a0001c0006t0005g0038 a0001c0006t0005g0321 a0001c0006t0005g0323 others(25): Show |
28 | HG00642.hp2 HG00735.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.638+661G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10773271 | |||||||
| chr2:10773274 | A | ACACT | 22 | a0001c0001t0007g0237 a0002c0002t0003g0214 a0002c0002t0003g0224 others(19): Show |
22 | HG01109.hp1 HG01243.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.638+667_638+670dup others(4): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 10773274 | ||||||
| chr2:10773294 | T | C | 11 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(8): Show |
12 | HG01496.hp2 HG02145.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.638+684T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10773294 | |||||||
| chr2:10773323 | G | C | 4 | a0002c0007t0009g0040 a0002c0007t0009g0041 a0002c0007t0009g0151 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.638+713G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10773323 | |||||||
| chr2:10773391 | T | C | 22 | a0001c0001t0007g0237 a0002c0002t0003g0214 a0002c0002t0003g0224 others(19): Show |
22 | HG01109.hp1 HG01243.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.638+781T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10773391 | |||||||
| chr2:10773444 | C | A | 8 | a0001c0001t0002g0065 a0001c0001t0002g0169 a0001c0001t0002g0181 others(5): Show |
8 | HG01106.hp2 HG01978.hp2 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.638+834C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10773444 | |||||||
| chr2:10773444 | C | G | 340 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(337): Show |
343 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(340): Show |
intron_variant | MODIFIER | c.638+834C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10773444 | |||||||
| chr2:10773571 | TG | T | 10 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(7): Show |
10 | HG00558.hp2 HG01993.hp2 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.638+965delG | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 10773571 | ||||||
| chr2:10773603 | G | A | 1 | a0001c0001t0002g0001 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.638+993G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10773603 | |||||||
| chr2:10773651 | A | G | 347 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(344): Show |
350 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(347): Show |
intron_variant | MODIFIER | c.638+1041A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10773651 | |||||||
| chr2:10773753 | C | T | 2 | a0001c0001t0002g0176 a0001c0001t0002g0200 |
2 | NA19010.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.639-1035C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10773753 | |||||||
| chr2:10773841 | G | A | 1 | a0002c0002t0015g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.639-947G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10773841 | |||||||
| chr2:10773881 | A | G | 2 | a0002c0002t0001g0150 a0002c0002t0001g0161 |
2 | HG01069.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.639-907A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10773881 | |||||||
| chr2:10773882 | T | C | 8 | a0002c0002t0001g0225 a0002c0002t0010g0108 a0002c0002t0014g0222 others(5): Show |
8 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.639-906T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10773882 | |||||||
| chr2:10773916 | G | A | 1 | a0001c0001t0002g0025 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.639-872G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10773916 | |||||||
| chr2:10773965 | G | A | 4 | a0002c0002t0001g0225 a0002c0002t0010g0108 a0002c0002t0014g0222 others(1): Show |
4 | HG01070.hp2 HG01496.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.639-823G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10773965 | |||||||
| chr2:10773981 | A | G | 23 | a0002c0002t0001g0225 a0002c0002t0002g0018 a0002c0002t0010g0108 others(20): Show |
23 | HG00323.hp2 HG00597.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.639-807A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10773981 | |||||||
| chr2:10774025 | G | A | 1 | a0001c0001t0004g0114 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.639-763G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10774025 | |||||||
| chr2:10774044 | G | A | 3 | a0002c0002t0002g0011 a0002c0002t0002g0124 a0002c0002t0004g0117 |
3 | HG03239.hp2 HG03834.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.639-744G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10774044 | |||||||
| chr2:10774089 | C | G | 98 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0055 others(95): Show |
100 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.639-699C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10774089 | |||||||
| chr2:10774119 | T | C | 4 | a0002c0002t0001g0225 a0002c0002t0010g0108 a0002c0002t0014g0222 others(1): Show |
4 | HG01070.hp2 HG01496.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.639-669T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10774119 | |||||||
| chr2:10774263 | T | C | 1 | a0001c0001t0002g0004 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.639-525T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10774263 | |||||||
| chr2:10774276 | T | TCAGAGAT others(1): Show |
15 | a0001c0001t0007g0237 a0001c0001t0013g0074 a0002c0002t0004g0123 others(12): Show |
15 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.639-510_639-503dup others(8): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 10774276 | ||||||
| chr2:10774354 | T | C | 2 | a0002c0003t0012g0160 a0002c0003t0012g0232 |
2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.639-434T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10774354 | |||||||
| chr2:10774484 | T | C | 124 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0055 others(121): Show |
126 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.639-304T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10774484 | |||||||
| chr2:10774491 | G | A | 94 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0055 others(91): Show |
96 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.639-297G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10774491 | |||||||
| chr2:10774531 | C | T | 1 | a0001c0001t0013g0074 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.639-257C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10774531 | |||||||
| chr2:10774604 | G | A | 1 | a0002c0003t0002g0067 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.639-184G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10774604 | |||||||
| chr2:10774741 | A | T | 18 | a0002c0002t0002g0018 a0002c0003t0002g0009 a0002c0003t0002g0063 others(15): Show |
18 | HG00323.hp2 HG00597.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.639-47A>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 8/13 | chr2 | 10774741 | |||||||
| chr2:10774894 | A | G | 133 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(130): Show |
136 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.731+14A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 9/13 | chr2 | 10774894 | |||||||
| chr2:10774911 | C | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0055 a0001c0001t0001g0057 others(2): Show |
5 | HG00323.hp1 HG00738.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.731+31C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 9/13 | chr2 | 10774911 | |||||||
| chr2:10774964 | T | A | 107 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(104): Show |
107 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.732-14T>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 9/13 | chr2 | 10774964 | |||||||
| chr2:10775090 | A | G | 1 | a0007c0014t0021g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.825+19A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10775090 | |||||||
| chr2:10775216 | G | A | 2 | a0001c0001t0002g0270 a0001c0001t0002g0285 |
2 | HG00140.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.825+145G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10775216 | |||||||
| chr2:10775248 | G | A | 1 | a0002c0002t0008g0236 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.825+177G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10775248 | |||||||
| chr2:10775322 | T | G | 1 | a0002c0002t0024g0226 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.825+251T>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10775322 | |||||||
| chr2:10775323 | G | A | 124 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(121): Show |
124 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.825+252G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10775323 | |||||||
| chr2:10775422 | C | A | 1 | a0002c0003t0002g0142 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.825+351C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10775422 | |||||||
| chr2:10775468 | G | A | 2 | a0002c0003t0012g0160 a0002c0003t0012g0232 |
2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.825+397G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10775468 | |||||||
| chr2:10775574 | G | A | 3 | a0002c0007t0009g0040 a0002c0007t0009g0041 a0002c0007t0009g0151 |
3 | HG01069.hp2 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.825+503G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10775574 | |||||||
| chr2:10775582 | T | A | 1 | a0002c0002t0001g0111 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.825+511T>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10775582 | |||||||
| chr2:10775626 | A | G | 81 | a0001c0001t0002g0257 a0001c0001t0007g0237 a0001c0001t0008g0259 others(78): Show |
81 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.825+555A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10775626 | |||||||
| chr2:10775627 | C | T | 221 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(218): Show |
223 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.825+556C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10775627 | |||||||
| chr2:10775672 | AC | A | 21 | a0002c0002t0003g0214 a0002c0002t0003g0224 a0002c0002t0003g0231 others(18): Show |
21 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.825+602delC | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10775672 | |||||||
| chr2:10775676 | T | A | 4 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0104 others(1): Show |
4 | HG03041.hp2 HG03486.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.825+605T>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10775676 | |||||||
| chr2:10775762 | A | G | 212 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(209): Show |
215 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.825+691A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10775762 | |||||||
| chr2:10775816 | G | C | 2 | a0002c0002t0002g0133 a0002c0002t0002g0344 |
2 | HG02132.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.825+745G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10775816 | |||||||
| chr2:10775832 | A | C | 17 | a0001c0006t0005g0038 a0001c0006t0005g0321 a0001c0006t0005g0323 others(14): Show |
17 | HG01081.hp2 HG01099.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.825+761A>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10775832 | |||||||
| chr2:10775884 | A | G | 216 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(213): Show |
219 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.825+813A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10775884 | |||||||
| chr2:10776050 | C | T | 2 | a0002c0003t0012g0160 a0002c0003t0012g0232 |
2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.825+979C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10776050 | |||||||
| chr2:10776107 | A | G | 22 | a0002c0002t0002g0018 a0002c0002t0002g0147 a0002c0003t0002g0009 others(19): Show |
22 | HG00323.hp2 HG00597.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.825+1036A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10776107 | |||||||
| chr2:10776115 | GC | G | 137 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(134): Show |
140 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.825+1047delC | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 10776115 | ||||||
| chr2:10776134 | G | A | 4 | a0002c0007t0009g0040 a0002c0007t0009g0041 a0002c0007t0009g0151 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.825+1063G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10776134 | |||||||
| chr2:10776147 | C | T | 1 | a0006c0017t0001g0216 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.825+1076C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10776147 | |||||||
| chr2:10776217 | AG | A | 107 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(104): Show |
109 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.825+1151delG | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 10776217 | ||||||
| chr2:10776266 | C | CGT | 40 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(37): Show |
41 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.825+1209_825+1210d others(4): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 10776266 | ||||||
| chr2:10776266 | CGT | C | 30 | a0001c0001t0002g0257 a0001c0001t0007g0088 a0001c0001t0007g0237 others(27): Show |
30 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.825+1209_825+1210d others(4): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 10776266 | ||||||
| chr2:10776266 | CGTGT | C | 104 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(101): Show |
106 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.825+1207_825+1210d others(6): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 10776266 | ||||||
| chr2:10776277 | G | C | 10 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0104 others(7): Show |
10 | HG01978.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.825+1206G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10776277 | |||||||
| chr2:10776282 | C | T | 48 | a0001c0001t0008g0259 a0001c0001t0016g0220 a0001c0006t0005g0038 others(45): Show |
48 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.825+1211C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10776282 | |||||||
| chr2:10776286 | C | A | 1 | a0002c0002t0001g0225 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.825+1215C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10776286 | |||||||
| chr2:10776291 | G | A | 12 | a0001c0001t0007g0088 a0001c0001t0007g0237 a0002c0002t0007g0106 others(9): Show |
12 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.825+1220G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10776291 | |||||||
| chr2:10776302 | AGTGT | A | 58 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(55): Show |
59 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.825+1239_825+1242d others(6): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 10776302 | ||||||
| chr2:10776357 | C | T | 2 | a0002c0003t0012g0160 a0002c0003t0012g0232 |
2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.826-1228C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10776357 | |||||||
| chr2:10776370 | C | T | 8 | a0001c0001t0004g0097 a0001c0001t0004g0114 a0002c0003t0004g0073 others(5): Show |
8 | HG00639.hp1 HG02257.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.826-1215C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10776370 | |||||||
| chr2:10776371 | G | A | 1 | a0002c0002t0004g0215 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.826-1214G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10776371 | |||||||
| chr2:10776436 | C | T | 22 | a0001c0001t0002g0257 a0002c0002t0003g0214 a0002c0002t0003g0224 others(19): Show |
22 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.826-1149C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10776436 | |||||||
| chr2:10776437 | A | G | 225 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(222): Show |
228 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.826-1148A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10776437 | |||||||
| chr2:10776458 | T | C | 234 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(231): Show |
237 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.826-1127T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10776458 | |||||||
| chr2:10776484 | C | T | 2 | a0001c0001t0002g0174 a0001c0001t0002g0212 |
2 | NA18968.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.826-1101C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10776484 | |||||||
| chr2:10776495 | A | C | 2 | a0001c0001t0002g0174 a0001c0001t0002g0212 |
2 | NA18968.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.826-1090A>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10776495 | |||||||
| chr2:10776544 | G | A | 64 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(61): Show |
65 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.826-1041G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10776544 | |||||||
| chr2:10776567 | C | T | 133 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(130): Show |
135 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.826-1018C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10776567 | |||||||
| chr2:10776617 | C | G | 17 | a0001c0006t0005g0038 a0001c0006t0005g0321 a0001c0006t0005g0323 others(14): Show |
17 | HG01081.hp2 HG01099.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.826-968C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10776617 | |||||||
| chr2:10776618 | G | A | 8 | a0001c0001t0004g0097 a0001c0001t0004g0114 a0002c0003t0004g0073 others(5): Show |
8 | HG00639.hp1 HG02257.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.826-967G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10776618 | |||||||
| chr2:10776639 | C | T | 1 | a0001c0001t0006g0308 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.826-946C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10776639 | |||||||
| chr2:10776644 | C | T | 22 | a0002c0002t0002g0018 a0002c0002t0002g0147 a0002c0002t0014g0222 others(19): Show |
22 | HG00323.hp2 HG00597.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.826-941C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10776644 | |||||||
| chr2:10776651 | T | A | 9 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(6): Show |
10 | HG01069.hp1 HG02145.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.826-934T>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10776651 | |||||||
| chr2:10776715 | C | T | 6 | a0001c0001t0007g0088 a0001c0001t0007g0237 a0002c0002t0007g0106 others(3): Show |
6 | HG01261.hp1 HG01884.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.826-870C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10776715 | |||||||
| chr2:10776753 | A | G | 1 | a0001c0001t0002g0257 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.826-832A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10776753 | |||||||
| chr2:10776756 | C | T | 5 | a0002c0002t0001g0275 a0002c0002t0001g0276 a0002c0002t0001g0284 others(2): Show |
5 | HG00642.hp2 HG00738.hp1 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.826-829C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10776756 | |||||||
| chr2:10776761 | C | A | 22 | a0001c0001t0002g0257 a0002c0002t0003g0214 a0002c0002t0003g0224 others(19): Show |
22 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.826-824C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10776761 | |||||||
| chr2:10776778 | G | C | 1 | a0001c0001t0002g0194 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.826-807G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10776778 | |||||||
| chr2:10776832 | C | T | 45 | a0001c0001t0002g0257 a0001c0001t0004g0097 a0001c0001t0004g0114 others(42): Show |
45 | HG00639.hp1 HG00639.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.826-753C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10776832 | |||||||
| chr2:10776896 | G | T | 1 | a0002c0002t0008g0236 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.826-689G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10776896 | |||||||
| chr2:10777196 | T | G | 1 | a0001c0001t0002g0257 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.826-389T>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10777196 | |||||||
| chr2:10777345 | A | G | 1 | a0001c0001t0008g0245 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.826-240A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10777345 | |||||||
| chr2:10777429 | C | T | 20 | a0002c0002t0002g0018 a0002c0002t0002g0147 a0002c0003t0002g0009 others(17): Show |
20 | HG00323.hp2 HG00597.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.826-156C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10777429 | |||||||
| chr2:10777468 | G | A | 17 | a0001c0006t0005g0038 a0001c0006t0005g0321 a0001c0006t0005g0323 others(14): Show |
17 | HG01081.hp2 HG01099.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.826-117G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10777468 | |||||||
| chr2:10777578 | C | A | 1 | a0002c0004t0005g0095 | 1 | HG03491.hp1 | splice_region_variant&intron_variant | LOW | c.826-7C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 10/13 | chr2 | 10777578 | |||||||
| chr2:10777856 | G | A | 2 | a0001c0001t0008g0259 a0001c0001t0016g0220 |
2 | HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.963+134G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 11/13 | chr2 | 10777856 | |||||||
| chr2:10777942 | TC | T | 103 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(100): Show |
105 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.963+224delC | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 10777942 | ||||||
| chr2:10777953 | CTGGCTGG others(3): Show |
C | 4 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0104 others(1): Show |
4 | HG03041.hp2 HG03486.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+241_963+250del others(10): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 10777953 | ||||||
| chr2:10778006 | T | C | 2 | a0002c0002t0001g0096 a0002c0002t0001g0115 |
2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.963+284T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 11/13 | chr2 | 10778006 | |||||||
| chr2:10778083 | C | T | 126 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(123): Show |
128 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.963+361C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 11/13 | chr2 | 10778083 | |||||||
| chr2:10778140 | C | T | 1 | a0002c0002t0002g0020 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.963+418C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 11/13 | chr2 | 10778140 | |||||||
| chr2:10778236 | A | G | 44 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(41): Show |
45 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.964-336A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 11/13 | chr2 | 10778236 | |||||||
| chr2:10778258 | A | G | 44 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(41): Show |
45 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.964-314A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 11/13 | chr2 | 10778258 | |||||||
| chr2:10778337 | G | A | 17 | a0001c0006t0005g0038 a0001c0006t0005g0321 a0001c0006t0005g0323 others(14): Show |
17 | HG01081.hp2 HG01099.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.964-235G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 11/13 | chr2 | 10778337 | |||||||
| chr2:10778384 | C | T | 3 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0004g0114 |
3 | HG02818.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.964-188C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 11/13 | chr2 | 10778384 | |||||||
| chr2:10778545 | G | A | 1 | a0002c0002t0001g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.964-27G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 11/13 | chr2 | 10778545 | |||||||
| chr2:10778772 | C | T | 9 | a0002c0002t0001g0072 a0002c0002t0001g0096 a0002c0002t0001g0111 others(6): Show |
9 | HG01109.hp2 HG01891.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1061+103C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10778772 | |||||||
| chr2:10778806 | C | T | 1 | a0002c0003t0002g0119 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1061+137C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10778806 | |||||||
| chr2:10778817 | G | A | 1 | a0002c0005t0001g0116 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1061+148G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10778817 | |||||||
| chr2:10778881 | A | G | 1 | a0002c0002t0002g0280 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1061+212A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10778881 | |||||||
| chr2:10778909 | C | T | 15 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(12): Show |
16 | HG01069.hp1 HG01261.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1061+240C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10778909 | |||||||
| chr2:10779006 | C | T | 129 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(126): Show |
131 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.1061+337C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779006 | |||||||
| chr2:10779021 | C | T | 9 | a0002c0002t0001g0072 a0002c0002t0001g0096 a0002c0002t0001g0111 others(6): Show |
9 | HG01109.hp2 HG01891.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1061+352C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779021 | |||||||
| chr2:10779082 | A | G | 1 | a0002c0002t0002g0018 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1061+413A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779082 | |||||||
| chr2:10779102 | T | C | 213 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(210): Show |
216 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.1061+433T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779102 | |||||||
| chr2:10779105 | C | CT | 19 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0104 others(16): Show |
19 | HG01109.hp2 HG01496.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1061+448dupT | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 10779105 | ||||||
| chr2:10779105 | CT | C | 13 | a0001c0001t0008g0245 a0001c0001t0013g0074 a0001c0001t0026g0100 others(10): Show |
13 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1061+448delT | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 10779105 | ||||||
| chr2:10779105 | CTT | C | 19 | a0001c0001t0008g0259 a0001c0001t0016g0220 a0001c0006t0005g0038 others(16): Show |
19 | HG01081.hp2 HG01099.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.1061+447_1061+448d others(4): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 10779105 | ||||||
| chr2:10779144 | G | A | 1 | a0001c0001t0002g0132 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1061+475G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779144 | |||||||
| chr2:10779253 | C | T | 51 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(48): Show |
52 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.1061+584C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779253 | |||||||
| chr2:10779384 | C | T | 17 | a0001c0006t0005g0038 a0001c0006t0005g0321 a0001c0006t0005g0323 others(14): Show |
17 | HG01081.hp2 HG01099.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.1061+715C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779384 | |||||||
| chr2:10779391 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0094 |
2 | NA19057.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1061+722G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779391 | |||||||
| chr2:10779418 | T | TA | 10 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(7): Show |
11 | HG00140.hp1 HG01069.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1061+760dupA | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 10779418 | ||||||
| chr2:10779418 | TA | T | 64 | a0001c0001t0004g0097 a0001c0001t0004g0114 a0001c0001t0007g0088 others(61): Show |
64 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.1061+760delA | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 10779418 | ||||||
| chr2:10779426 | A | AT | 8 | a0001c0001t0001g0064 a0001c0001t0002g0075 a0001c0001t0002g0176 others(5): Show |
8 | HG01074.hp2 HG02056.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061+757_1061+758i others(3): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779426 | |||||||
| chr2:10779428 | A | AT | 96 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0014 others(93): Show |
98 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.1061+759_1061+760i others(3): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779428 | |||||||
| chr2:10779428 | A | T | 110 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(107): Show |
110 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.1061+759A>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779428 | |||||||
| chr2:10779432 | T | C | 17 | a0001c0006t0005g0038 a0001c0006t0005g0321 a0001c0006t0005g0323 others(14): Show |
17 | HG01081.hp2 HG01099.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.1061+763T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779432 | |||||||
| chr2:10779443 | G | A | 1 | a0002c0002t0002g0021 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1061+774G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779443 | |||||||
| chr2:10779445 | A | G | 1 | a0002c0002t0002g0021 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1061+776A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779445 | |||||||
| chr2:10779447 | G | A | 1 | a0002c0002t0002g0021 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1061+778G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779447 | |||||||
| chr2:10779447 | GTA | G | 179 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(176): Show |
181 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.1061+794_1061+795d others(4): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 10779447 | ||||||
| chr2:10779449 | A | G | 1 | a0002c0002t0002g0021 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1061+780A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779449 | |||||||
| chr2:10779531 | C | T | 17 | a0001c0006t0005g0038 a0001c0006t0005g0321 a0001c0006t0005g0323 others(14): Show |
17 | HG01081.hp2 HG01099.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.1061+862C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779531 | |||||||
| chr2:10779543 | G | T | 1 | a0001c0001t0001g0180 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1061+874G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779543 | |||||||
| chr2:10779618 | G | A | 9 | a0001c0001t0007g0088 a0001c0001t0007g0237 a0002c0002t0007g0106 others(6): Show |
9 | HG00639.hp2 HG01261.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.1061+949G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779618 | |||||||
| chr2:10779650 | C | T | 3 | a0002c0007t0009g0040 a0002c0007t0009g0041 a0002c0007t0009g0151 |
3 | HG01069.hp2 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1061+981C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779650 | |||||||
| chr2:10779685 | TA | T | 25 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(22): Show |
25 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.1061+1017delA | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779685 | |||||||
| chr2:10779686 | A | AG | 27 | a0001c0001t0004g0097 a0001c0001t0004g0114 a0001c0001t0008g0245 others(24): Show |
27 | HG00639.hp1 HG00639.hp2 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.1061+1018dupG | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 10779686 | ||||||
| chr2:10779686 | A | G | 100 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(97): Show |
102 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.1061+1017A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779686 | |||||||
| chr2:10779687 | G | GA | 19 | a0001c0001t0001g0051 a0001c0001t0001g0070 a0001c0001t0001g0089 others(16): Show |
19 | HG01070.hp2 HG01256.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.1061+1038dupA | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 10779687 | ||||||
| chr2:10779688 | A | G | 25 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(22): Show |
25 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.1061+1019A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779688 | |||||||
| chr2:10779689 | A | G | 1 | a0001c0001t0001g0029 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1061+1020A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779689 | |||||||
| chr2:10779707 | A | AAG | 17 | a0001c0006t0005g0038 a0001c0006t0005g0321 a0001c0006t0005g0323 others(14): Show |
17 | HG01081.hp2 HG01099.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.1061+1038_1061+103 others(6): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779707 | |||||||
| chr2:10779712 | A | G | 1 | a0002c0002t0002g0098 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1061+1043A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779712 | |||||||
| chr2:10779801 | C | T | 17 | a0001c0006t0005g0038 a0001c0006t0005g0321 a0001c0006t0005g0323 others(14): Show |
17 | HG01081.hp2 HG01099.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.1061+1132C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779801 | |||||||
| chr2:10779831 | T | G | 49 | a0001c0001t0002g0257 a0001c0001t0004g0097 a0001c0001t0004g0114 others(46): Show |
49 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.1061+1162T>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779831 | |||||||
| chr2:10779857 | C | T | 26 | a0001c0001t0002g0257 a0001c0001t0004g0097 a0001c0001t0004g0114 others(23): Show |
26 | HG00639.hp1 HG00639.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.1061+1188C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779857 | |||||||
| chr2:10779866 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1061+1197T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779866 | |||||||
| chr2:10779899 | C | T | 3 | a0001c0001t0001g0090 a0001c0001t0001g0163 a0001c0001t0001g0320 |
3 | HG02155.hp2 NA19003.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1061+1230C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779899 | |||||||
| chr2:10779906 | G | A | 1 | a0001c0001t0002g0305 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1061+1237G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779906 | |||||||
| chr2:10779912 | C | T | 1 | a0007c0014t0021g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1061+1243C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779912 | |||||||
| chr2:10779962 | C | T | 18 | a0002c0002t0002g0018 a0002c0003t0002g0009 a0002c0003t0002g0063 others(15): Show |
18 | HG00323.hp2 HG00597.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.1061+1293C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779962 | |||||||
| chr2:10779969 | C | T | 1 | a0002c0004t0005g0137 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1061+1300C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779969 | |||||||
| chr2:10779979 | C | T | 17 | a0001c0006t0005g0038 a0001c0006t0005g0321 a0001c0006t0005g0323 others(14): Show |
17 | HG01081.hp2 HG01099.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.1061+1310C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10779979 | |||||||
| chr2:10780078 | C | A | 4 | a0002c0007t0009g0040 a0002c0007t0009g0041 a0002c0007t0009g0151 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1061+1409C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10780078 | |||||||
| chr2:10780132 | T | C | 122 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(119): Show |
124 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1061+1463T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10780132 | |||||||
| chr2:10780157 | G | A | 17 | a0001c0006t0005g0038 a0001c0006t0005g0321 a0001c0006t0005g0323 others(14): Show |
17 | HG01081.hp2 HG01099.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.1061+1488G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10780157 | |||||||
| chr2:10780291 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1061+1622A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10780291 | |||||||
| chr2:10780418 | G | T | 1 | a0002c0002t0025g0227 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1061+1749G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10780418 | |||||||
| chr2:10780464 | T | C | 48 | a0001c0001t0002g0257 a0001c0001t0004g0097 a0001c0001t0004g0114 others(45): Show |
48 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.1062-1779T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10780464 | |||||||
| chr2:10780468 | C | T | 4 | a0002c0007t0009g0040 a0002c0007t0009g0041 a0002c0007t0009g0151 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1062-1775C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10780468 | |||||||
| chr2:10780504 | G | A | 1 | a0001c0001t0006g0308 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1062-1739G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10780504 | |||||||
| chr2:10780513 | C | T | 20 | a0001c0006t0005g0038 a0001c0006t0005g0321 a0001c0006t0005g0323 others(17): Show |
20 | HG01069.hp2 HG01071.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1062-1730C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10780513 | |||||||
| chr2:10780536 | C | T | 1 | a0002c0002t0001g0292 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1062-1707C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10780536 | |||||||
| chr2:10780548 | T | C | 106 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(103): Show |
108 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.1062-1695T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10780548 | |||||||
| chr2:10780656 | C | T | 4 | a0002c0007t0009g0040 a0002c0007t0009g0041 a0002c0007t0009g0151 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1062-1587C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10780656 | |||||||
| chr2:10780688 | C | T | 1 | a0001c0001t0008g0259 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1062-1555C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10780688 | |||||||
| chr2:10780728 | G | A | 3 | a0002c0002t0004g0117 a0002c0003t0004g0058 a0002c0009t0004g0157 |
3 | HG02895.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1062-1515G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10780728 | |||||||
| chr2:10780749 | C | CT | 45 | a0001c0001t0001g0049 a0001c0001t0002g0132 a0001c0001t0002g0257 others(42): Show |
45 | HG00639.hp1 HG00639.hp2 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.1062-1480dupT | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 10780749 | ||||||
| chr2:10780749 | CT | C | 27 | a0001c0001t0001g0094 a0001c0001t0002g0014 a0001c0001t0002g0015 others(24): Show |
27 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.1062-1480delT | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 10780749 | ||||||
| chr2:10780878 | G | A | 6 | a0001c0001t0007g0088 a0001c0001t0007g0237 a0002c0002t0007g0106 others(3): Show |
6 | HG01261.hp1 HG01884.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1062-1365G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10780878 | |||||||
| chr2:10780937 | G | T | 1 | a0001c0001t0002g0190 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1062-1306G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10780937 | |||||||
| chr2:10780947 | G | A | 28 | a0001c0001t0002g0257 a0001c0001t0004g0097 a0001c0001t0004g0114 others(25): Show |
28 | HG00639.hp1 HG00639.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.1062-1296G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10780947 | |||||||
| chr2:10781035 | T | C | 344 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(341): Show |
347 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(344): Show |
intron_variant | MODIFIER | c.1062-1208T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10781035 | |||||||
| chr2:10781041 | C | T | 11 | a0001c0001t0002g0257 a0001c0001t0008g0245 a0001c0001t0008g0259 others(8): Show |
11 | HG00639.hp2 HG01175.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1062-1202C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10781041 | |||||||
| chr2:10781092 | G | T | 1 | a0002c0002t0002g0315 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1062-1151G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10781092 | |||||||
| chr2:10781100 | C | T | 1 | a0002c0004t0005g0085 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1062-1143C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10781100 | |||||||
| chr2:10781108 | G | A | 2 | a0001c0001t0002g0269 a0001c0001t0002g0283 |
2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.1062-1135G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10781108 | |||||||
| chr2:10781128 | A | G | 1 | a0001c0001t0002g0309 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1062-1115A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10781128 | |||||||
| chr2:10781135 | G | A | 21 | a0002c0002t0003g0214 a0002c0002t0003g0224 a0002c0002t0003g0231 others(18): Show |
21 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.1062-1108G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10781135 | |||||||
| chr2:10781192 | C | T | 2 | a0001c0001t0001g0266 a0001c0001t0001g0350 |
2 | HG03669.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1062-1051C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10781192 | |||||||
| chr2:10781213 | G | A | 10 | a0001c0001t0008g0245 a0001c0001t0008g0259 a0001c0001t0013g0074 others(7): Show |
10 | HG00639.hp2 HG02559.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1062-1030G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10781213 | |||||||
| chr2:10781251 | G | A | 20 | a0001c0006t0005g0038 a0001c0006t0005g0321 a0001c0006t0005g0323 others(17): Show |
20 | HG01069.hp2 HG01071.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1062-992G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10781251 | |||||||
| chr2:10781271 | G | A | 2 | a0002c0004t0005g0162 a0004c0011t0017g0149 |
2 | HG01934.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1062-972G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10781271 | |||||||
| chr2:10781350 | C | T | 1 | a0007c0014t0021g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1062-893C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10781350 | |||||||
| chr2:10781370 | T | C | 176 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(173): Show |
178 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.1062-873T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10781370 | |||||||
| chr2:10781375 | G | C | 1 | a0002c0002t0004g0117 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1062-868G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10781375 | |||||||
| chr2:10781416 | T | G | 2 | a0002c0002t0002g0147 a0003c0010t0002g0260 |
2 | HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1062-827T>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10781416 | |||||||
| chr2:10781418 | C | T | 4 | a0002c0007t0009g0040 a0002c0007t0009g0041 a0002c0007t0009g0151 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1062-825C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10781418 | |||||||
| chr2:10781464 | C | T | 1 | a0001c0001t0002g0201 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1062-779C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10781464 | |||||||
| chr2:10781477 | C | CA | 7 | a0001c0001t0007g0088 a0001c0001t0007g0237 a0002c0002t0007g0106 others(4): Show |
7 | HG01261.hp1 HG01884.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1062-755dupA | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 10781477 | ||||||
| chr2:10781544 | A | T | 4 | a0002c0002t0001g0288 a0002c0002t0001g0300 a0002c0002t0001g0329 others(1): Show |
4 | NA18941.hp1 NA18983.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.1062-699A>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10781544 | |||||||
| chr2:10781586 | C | G | 3 | a0002c0002t0001g0062 a0002c0002t0001g0208 a0002c0002t0001g0209 |
3 | NA18955.hp1 NA18990.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1062-657C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10781586 | |||||||
| chr2:10781634 | T | C | 4 | a0002c0007t0009g0040 a0002c0007t0009g0041 a0002c0007t0009g0151 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1062-609T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10781634 | |||||||
| chr2:10781772 | A | C | 1 | a0002c0002t0001g0294 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1062-471A>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10781772 | |||||||
| chr2:10781901 | C | T | 17 | a0001c0006t0005g0038 a0001c0006t0005g0321 a0001c0006t0005g0323 others(14): Show |
17 | HG01099.hp1 HG01433.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.1062-342C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10781901 | |||||||
| chr2:10781905 | C | T | 3 | a0002c0007t0009g0040 a0002c0007t0009g0041 a0002c0007t0009g0151 |
3 | HG01069.hp2 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1062-338C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10781905 | |||||||
| chr2:10781921 | C | A | 10 | a0001c0001t0008g0245 a0001c0001t0008g0259 a0001c0001t0013g0074 others(7): Show |
10 | HG00639.hp2 HG02559.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1062-322C>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10781921 | |||||||
| chr2:10781921 | C | G | 18 | a0001c0001t0002g0257 a0001c0001t0004g0097 a0001c0001t0004g0114 others(15): Show |
18 | HG00639.hp1 HG01175.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1062-322C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10781921 | |||||||
| chr2:10782060 | AATTCTAG others(46): Show |
A | 4 | a0002c0007t0009g0040 a0002c0007t0009g0041 a0002c0007t0009g0151 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1062-182_1062-130d others(55): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10782060 | |||||||
| chr2:10782063 | T | C | 18 | a0002c0002t0003g0214 a0002c0002t0003g0224 a0002c0002t0003g0231 others(15): Show |
18 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1062-180T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10782063 | |||||||
| chr2:10782125 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1062-118T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10782125 | |||||||
| chr2:10782159 | G | A | 1 | a0002c0002t0007g0106 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1062-84G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10782159 | |||||||
| chr2:10782175 | G | C | 28 | a0001c0001t0002g0257 a0001c0001t0004g0097 a0001c0001t0004g0114 others(25): Show |
28 | HG00639.hp1 HG00639.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.1062-68G>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 12/13 | chr2 | 10782175 | |||||||
| chr2:10782390 | A | C | 127 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(124): Show |
129 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1194+15A>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 13/13 | chr2 | 10782390 | |||||||
| chr2:10782456 | A | G | 1 | a0001c0001t0002g0257 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1194+81A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 13/13 | chr2 | 10782456 | |||||||
| chr2:10782570 | C | T | 1 | a0002c0002t0023g0099 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1194+195C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 13/13 | chr2 | 10782570 | |||||||
| chr2:10782571 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1194+196G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 13/13 | chr2 | 10782571 | |||||||
| chr2:10782730 | T | C | 1 | a0001c0001t0002g0325 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1194+355T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 13/13 | chr2 | 10782730 | |||||||
| chr2:10782735 | G | A | 4 | a0002c0007t0009g0040 a0002c0007t0009g0041 a0002c0007t0009g0151 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1194+360G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 13/13 | chr2 | 10782735 | |||||||
| chr2:10782785 | C | T | 10 | a0001c0001t0008g0245 a0001c0001t0008g0259 a0001c0001t0013g0074 others(7): Show |
10 | HG00639.hp2 HG02559.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1195-389C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 13/13 | chr2 | 10782785 | |||||||
| chr2:10782801 | A | C | 32 | a0001c0001t0004g0097 a0001c0001t0004g0114 a0001c0001t0007g0088 others(29): Show |
32 | HG00639.hp1 HG00639.hp2 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.1195-373A>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 13/13 | chr2 | 10782801 | |||||||
| chr2:10782801 | A | T | 1 | a0002c0002t0004g0117 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1195-373A>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 13/13 | chr2 | 10782801 | |||||||
| chr2:10782829 | C | CA | 41 | a0001c0001t0001g0010 a0001c0001t0001g0022 a0001c0001t0001g0027 others(38): Show |
41 | HG00673.hp2 HG01109.hp2 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.1195-311dupA | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 10782829 | ||||||
| chr2:10782829 | C | CAA | 28 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(25): Show |
28 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1195-312_1195-311d others(4): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 10782829 | ||||||
| chr2:10782829 | C | CAAA | 10 | a0001c0001t0001g0024 a0001c0001t0001g0173 a0001c0001t0001g0219 others(7): Show |
10 | HG01070.hp2 HG01978.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1195-313_1195-311d others(5): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 10782829 | ||||||
| chr2:10782829 | C | CAAAA | 10 | a0001c0001t0001g0006 a0001c0001t0001g0047 a0001c0001t0001g0055 others(7): Show |
10 | HG01106.hp1 HG01496.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1195-314_1195-311d others(6): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 10782829 | ||||||
| chr2:10782829 | CA | C | 30 | a0001c0001t0001g0078 a0001c0001t0001g0205 a0002c0002t0001g0005 others(27): Show |
30 | HG00621.hp1 HG00642.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.1195-311delA | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 10782829 | ||||||
| chr2:10782829 | CAA | C | 17 | a0001c0001t0002g0004 a0001c0001t0002g0034 a0001c0001t0002g0037 others(14): Show |
17 | HG00621.hp2 HG00733.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.1195-312_1195-311d others(4): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 10782829 | ||||||
| chr2:10782829 | CAAA | C | 67 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0017 others(64): Show |
69 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.1195-313_1195-311d others(5): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 10782829 | ||||||
| chr2:10782829 | CAAAA | C | 18 | a0001c0001t0001g0048 a0001c0001t0002g0131 a0001c0001t0002g0191 others(15): Show |
18 | HG00597.hp2 HG01099.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.1195-314_1195-311d others(6): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 10782829 | ||||||
| chr2:10782829 | CAAAAAAA others(2): Show |
C | 6 | a0001c0001t0002g0016 a0001c0001t0002g0264 a0001c0001t0002g0324 others(3): Show |
6 | HG00544.hp1 HG00544.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.1195-319_1195-311d others(11): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 10782829 | ||||||
| chr2:10782829 | CAAAAAAA others(3): Show |
C | 35 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0118 others(32): Show |
35 | HG00140.hp2 HG00735.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.1195-320_1195-311d others(12): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 10782829 | ||||||
| chr2:10782829 | CAAAAAAA others(4): Show |
C | 6 | a0002c0002t0002g0011 a0002c0002t0008g0244 a0002c0002t0018g0077 others(3): Show |
6 | HG00639.hp2 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1195-321_1195-311d others(13): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 10782829 | ||||||
| chr2:10782829 | CAAAAAAA others(5): Show |
C | 7 | a0001c0001t0008g0245 a0001c0001t0008g0259 a0001c0001t0013g0074 others(4): Show |
7 | HG02559.hp1 HG02723.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1195-322_1195-311d others(14): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 10782829 | ||||||
| chr2:10782829 | CAAAAAAA others(6): Show |
C | 17 | a0001c0001t0004g0097 a0001c0001t0004g0114 a0001c0001t0007g0237 others(14): Show |
17 | HG00639.hp1 HG02055.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1195-323_1195-311d others(15): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 10782829 | ||||||
| chr2:10782829 | CAAAAAAA others(7): Show |
C | 6 | a0001c0001t0007g0088 a0002c0002t0004g0107 a0002c0002t0007g0106 others(3): Show |
6 | HG01261.hp1 HG01884.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1195-324_1195-311d others(16): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 10782829 | ||||||
| chr2:10783142 | C | T | 6 | a0001c0001t0007g0088 a0001c0001t0007g0237 a0002c0002t0007g0106 others(3): Show |
6 | HG01261.hp1 HG01884.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1195-32C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 13/13 | chr2 | 10783142 | |||||||
| chr2:10783158 | A | G | 33 | a0001c0001t0004g0097 a0001c0001t0004g0114 a0001c0001t0007g0088 others(30): Show |
33 | HG00639.hp1 HG00639.hp2 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.1195-16A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 13/13 | chr2 | 10783158 |