| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 427 | 175 | 29 | 28 | 93 | 5 | 20 | 65 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002 | 1/1 | 427 | 172 | 58 | 41 | 44 | 5 | 22 | 34 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0003 | 0/0 | 427 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0004 | 0/0 | 427 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0005 | 0/0 | 427 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0006 | 0/0 | 427 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0007 | 0/0 | 427 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1284 | 170 | 27 | 27 | 93 | 5 | 18 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| c0002 | 1/1 | 1284 | 124 | 42 | 29 | 40 | 2 | 9 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| c0003 | 0/0 | 1284 | 25 | 8 | 7 | 4 | 2 | 4 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| c0004 | 0/0 | 1284 | 12 | 2 | 1 | 0 | 1 | 8 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| c0005 | 0/0 | 1284 | 4 | 4 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| c0006 | 0/0 | 1284 | 3 | 0 | 1 | 0 | 0 | 2 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| c0007 | 0/0 | 1284 | 3 | 0 | 3 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| c0008 | 0/0 | 1284 | 2 | 0 | 2 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| c0009 | 0/0 | 1284 | 2 | 1 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| c0010 | 0/0 | 1284 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| c0011 | 0/0 | 1284 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| c0012 | 0/0 | 1284 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| c0013 | 0/0 | 1284 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| c0014 | 0/0 | 1284 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| c0015 | 0/0 | 1284 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| c0016 | 0/0 | 1284 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| c0017 | 0/0 | 1284 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| c0018 | 0/0 | 1284 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1976 | 134 | 22 | 23 | 75 | 3 | 9 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| t0002 | 0/0 | 1975 | 125 | 6 | 32 | 59 | 5 | 23 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| t0003 | 0/0 | 1975 | 20 | 16 | 4 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| t0004 | 0/0 | 1975 | 16 | 16 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| t0005 | 0/0 | 1975 | 15 | 2 | 2 | 0 | 1 | 10 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| t0006 | 0/0 | 1976 | 9 | 8 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| t0007 | 0/0 | 1975 | 6 | 5 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| t0008 | 0/0 | 1975 | 5 | 4 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| t0009 | 0/0 | 1975 | 3 | 0 | 3 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| t0010 | 0/0 | 1976 | 2 | 1 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| t0011 | 0/0 | 1975 | 2 | 0 | 0 | 2 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| t0012 | 0/0 | 1975 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| t0013 | 0/0 | 1975 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| t0014 | 0/0 | 1975 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| t0015 | 0/0 | 1976 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| t0016 | 0/0 | 1975 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| t0017 | 0/0 | 1975 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| t0018 | 0/0 | 1975 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| t0019 | 0/0 | 1976 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| t0020 | 0/0 | 1976 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| t0021 | 0/0 | 1975 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| t0022 | 0/0 | 1975 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| t0023 | 0/0 | 1975 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| t0024 | 0/0 | 1976 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| t0025 | 0/0 | 1975 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| t0026 | 0/0 | 1975 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0233 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0275 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1284 | 170 | 27 | 27 | 93 | 5 | 18 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0001c0006 | 0/0 | 1284 | 3 | 0 | 1 | 0 | 0 | 2 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0001c0015 | 0/0 | 1284 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0001c0016 | 0/0 | 1284 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0002 | 1/1 | 1284 | 124 | 42 | 29 | 40 | 2 | 9 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0003 | 0/0 | 1284 | 25 | 8 | 7 | 4 | 2 | 4 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0004 | 0/0 | 1284 | 12 | 2 | 1 | 0 | 1 | 8 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0005 | 0/0 | 1284 | 4 | 4 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0007 | 0/0 | 1284 | 3 | 0 | 3 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0009 | 0/0 | 1284 | 2 | 1 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0013 | 0/0 | 1284 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0018 | 0/0 | 1284 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0003c0008 | 0/0 | 1284 | 2 | 0 | 2 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0003c0010 | 0/0 | 1284 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0004c0011 | 0/0 | 1284 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0005c0012 | 0/0 | 1284 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0006c0014 | 0/0 | 1284 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0007c0017 | 0/0 | 1284 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | 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 | copy fasta | chr2 | 10716630 | 10790110 |
| a0001c0001t0002 | 0/0 | 3258 | 84 | 4 | 19 | 43 | 3 | 15 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0001c0001t0004 | 0/0 | 3258 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0001c0001t0006 | 0/0 | 3259 | 4 | 3 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0001c0001t0007 | 0/0 | 3258 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0001c0001t0008 | 0/0 | 3258 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0001c0001t0011 | 0/0 | 3258 | 2 | 0 | 0 | 2 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0001c0001t0013 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0001c0001t0016 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0001c0001t0020 | 0/0 | 3259 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0001c0001t0026 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0001c0006t0005 | 0/0 | 3258 | 3 | 0 | 1 | 0 | 0 | 2 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0001c0015t0006 | 0/0 | 3259 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0001c0016t0001 | 0/0 | 3259 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0002t0001 | 1/1 | 3259 | 60 | 8 | 16 | 27 | 2 | 5 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0002t0002 | 0/0 | 3258 | 23 | 1 | 6 | 12 | 0 | 4 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0002t0003 | 0/0 | 3258 | 15 | 13 | 2 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0002t0004 | 0/0 | 3258 | 7 | 7 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0002t0006 | 0/0 | 3259 | 4 | 4 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0002t0007 | 0/0 | 3258 | 4 | 3 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0002t0008 | 0/0 | 3258 | 2 | 1 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0002t0010 | 0/0 | 3259 | 2 | 1 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0002t0014 | 0/0 | 3258 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0002t0015 | 0/0 | 3259 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0002t0018 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0002t0019 | 0/0 | 3259 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0002t0023 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0002t0024 | 0/0 | 3259 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0002t0025 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0003t0002 | 0/0 | 3258 | 17 | 0 | 7 | 4 | 2 | 4 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0003t0004 | 0/0 | 3258 | 6 | 6 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0003t0012 | 0/0 | 3258 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0004t0005 | 0/0 | 3258 | 12 | 2 | 1 | 0 | 1 | 8 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0005t0001 | 0/0 | 3259 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0005t0003 | 0/0 | 3258 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0005t0008 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0007t0009 | 0/0 | 3258 | 3 | 0 | 3 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0009t0004 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0009t0022 | 0/0 | 3258 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0013t0001 | 0/0 | 3259 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0002c0018t0013 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0003c0008t0003 | 0/0 | 3258 | 2 | 0 | 2 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0003c0010t0002 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0004c0011t0017 | 0/0 | 3258 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0005c0012t0003 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0006c0014t0021 | 0/0 | 3258 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| a0007c0017t0001 | 0/0 | 3259 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | copy fasta | chr2 | 10716630 | 10790110 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 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 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0030 | 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 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0043 | 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 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0052 | 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 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0079 | 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 |
| a0001c0001t0001g0305 | 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 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0318 | 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 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0001g0324 | 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 |
| a0001c0001t0001g0347 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0044 | 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 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0001c0001t0002g0119 | 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 |
| a0001c0001t0002g0136 | 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 | 1 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0006g0335 | 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 |
| a0001c0001t0011g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0011g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0001t0013g0075 | 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 |
| a0001c0006t0005g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0006t0005g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0001c0006t0005g0337 | 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 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0051 | 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 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0080 | 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 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0141 | 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 |
| a0002c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0233 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0241 | 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 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0275 | 0/1 | 1 | 0 | 0 | 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 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0288 | 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 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0313 | 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 |
| a0002c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0002c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 |
| a0002c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0002c0002t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0002g0342 | 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 |
| a0002c0002t0003g0215 | 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 |
| a0002c0002t0003g0229 | 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 |
| a0002c0002t0004g0214 | 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 |
| a0002c0002t0006g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0006g0228 | 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 |
| a0002c0002t0006g0244 | 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 |
| a0002c0002t0007g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0008g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0008g0242 | 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 |
| a0002c0002t0018g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0019g0049 | 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 |
| a0002c0002t0024g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0002t0025g0236 | 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 |
| a0002c0003t0002g0068 | 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 |
| a0002c0003t0002g0118 | 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 |
| a0002c0003t0002g0312 | 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 |
| a0002c0003t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0003t0004g0077 | 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 |
| a0002c0003t0004g0135 | 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 |
| a0002c0003t0012g0230 | 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 |
| a0002c0004t0005g0140 | 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 |
| a0002c0004t0005g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0004t0005g0327 | 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 |
| a0002c0007t0009g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0002c0007t0009g0029 | 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 |
| a0002c0013t0001g0139 | 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 |
| a0005c0012t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0006c0014t0021g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| a0007c0017t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 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 | g0282 | EUR | GBR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0119 | 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 | g0066 | 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 | g0311 | EAS | CHS | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0017 | 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 | g0312 | 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 | g0242 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0044 | 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 | g0302 | 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 | g0329 | 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 | g0306 | 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 | g0028 | 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 | g0029 | 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 | g0040 | 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 | g0042 | 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 | g0235 | AMR | PUR | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0274 | 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 | g0325 | 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 | g0289 | 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 | g0165 | 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 | g0041 | AMR | CLM | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0303 | 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 | g0038 | AMR | CLM | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG01261 | hp1 | a0002 | c0002 | t0007 | g0232 | 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 | g0039 | 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 | g0304 | 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 | g0335 | 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 | g0286 | 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 | g0067 | 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 | g0348 | EAS | KHV | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0021 | 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 | g0344 | 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 | g0080 | EAS | KHV | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0035 | 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 | g0229 | AFR | ACB | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0069 | AMR | PEL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0166 | 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 | g0336 | 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 | g0073 | AFR | ACB | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02257 | hp2 | a0002 | c0003 | t0004 | g0135 | AFR | ACB | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0324 | 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 | g0330 | AMR | PEL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0318 | 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 | g0326 | 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 | g0244 | 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 | g0331 | 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 | g0231 | 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 | g0076 | 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 | g0309 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02698 | hp1 | a0001 | c0006 | t0005 | g0308 | 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 | g0047 | 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 | g0337 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02738 | hp1 | a0002 | c0003 | t0002 | g0118 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0315 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02809 | hp1 | a0007 | c0017 | t0001 | g0216 | AFR | GWD | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02809 | hp2 | a0002 | c0003 | t0004 | g0077 | 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 | g0226 | 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 | g0074 | 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 | g0227 | AFR | ESN | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02970 | hp2 | a0002 | c0002 | t0003 | g0215 | 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 | g0323 | 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 | g0236 | 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 | g0230 | AFR | MSL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03209 | hp2 | a0002 | c0002 | t0008 | g0234 | AFR | MSL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03225 | hp1 | a0001 | c0001 | t0013 | g0075 | 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 | g0285 | 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 | g0140 | 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 | g0139 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03654 | hp2 | a0002 | c0004 | t0005 | g0137 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0138 | 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 | g0283 | SAS | STU | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0316 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03704 | hp2 | a0002 | c0004 | t0005 | g0327 | SAS | PJL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0288 | 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 | g0068 | 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 | g0016 | 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 | g0026 | 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 | g0020 | SAS | STU | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0339 | 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 | g0349 | SAS | STU | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0141 | 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 | g0048 | AFR | YRI | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0287 | 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 | g0319 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0023 | 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 | g0334 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0050 | 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 | g0034 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18951 | hp2 | a0001 | c0001 | t0011 | g0081 | 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 | g0307 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0032 | 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 | g0025 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18966 | hp1 | a0002 | c0002 | t0019 | g0049 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0328 | 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 | g0053 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0136 | 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 | g0072 | 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 | g0033 | 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 | g0320 | 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 | g0071 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0070 | 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 | g0030 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0305 | 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 | g0317 | 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 | g0342 | 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 | g0314 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19005 | hp2 | a0006 | 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 | g0031 | 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 | g0332 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0346 | 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 | g0079 | 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 | g0024 | 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 | g0313 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0051 | 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 | g0052 | 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 | g0345 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0018 | 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 | g0333 | 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 | g0347 | 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 | g0027 | 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 | g0043 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0343 | EAS | JPT | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0037 | 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 | g0338 | SAS | GIH | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0321 | 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 | g0022 | AMR | CLM | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0310 | 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 | g0214 | 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 | g0241 | AFR | ACB | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03471 | hp1 | a0002 | c0002 | t0018 | g0078 | AFR | MSL | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| HG03471 | hp2 | a0002 | c0002 | t0006 | g0228 | 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 | hp1 | a0002 | c0002 | t0001 | g0275 | REF | REF | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0233 | REF | REF | ATP6V1C2_chr2_10716630_10790110 | ATP6V1C2 | chr2 | 10716630 | 10790110 |
| 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 | a0003a0004 | 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 | a0001a0004 | 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 | a0007 | 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 | a0006 | 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 | a0007 | 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 |
| 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 | a0002c0018a0007c0017 | 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 | a0001c0016a0002c0005a0002c0009 | 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 | a0002c0003a0002c0009a0003c0008 | 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 | a0001c0006a0002c0004a0004c0011 | 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 |
| 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 | a0001c0001t0026a0002c0002t0023a0002c0002t0024others(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 | a0001c0001t0016a0002c0002t0014a0002c0002t0015 | 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 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(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 | a0001c0001t0006a0001c0015t0006a0002c0002t0006others(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 | a0001c0001t0006a0001c0015t0006a0002c0002t0006others(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 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(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 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(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 | a0001c0001t0013a0002c0018t0013 | 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 | a0002c0002t0003a0002c0002t0025a0002c0005t0003others(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 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(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 | a0002c0007t0009a0006c0014t0021 | 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 | a0002c0007t0009a0006c0014t0021 | 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 | a0001c0001t0004a0001c0001t0007a0001c0006t0005others(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 | a0001c0001t0002a0001c0001t0008a0001c0001t0011others(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 | a0001c0001t0004a0001c0001t0008a0001c0001t0013others(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 |
| 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 | a0001c0001t0002g0004a0002c0002t0001g0005 | 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 | a0001c0001t0001g0305a0001c0001t0001g0307a0001c0001t0001g0309others(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 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0026g0100a0002c0002t0023g0099 | 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 | a0001c0001t0001g0305a0001c0001t0001g0307a0001c0001t0001g0309others(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 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0144others(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 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(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 | a0001c0001t0001g0112a0002c0002t0001g0111 | 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 | 35 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0279others(32): Show | 35 | HG00140.hp1 HG00597.hp1 HG00642.hp2 others(32): 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 | a0001c0001t0001g0006a0001c0001t0001g0007 | 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 | a0002c0018t0013g0217a0007c0017t0001g0216 | 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 | a0002c0018t0013g0217a0007c0017t0001g0216 | 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 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0104others(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 | a0001c0001t0002g0257a0001c0001t0008g0245a0001c0001t0008g0259others(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 | a0001c0001t0016g0220a0002c0002t0014g0222a0002c0002t0015g0221 | 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 | a0001c0001t0001g0112a0001c0001t0001g0144a0001c0001t0001g0153others(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 | a0001c0001t0007g0237a0002c0002t0001g0241a0002c0002t0003g0243others(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 | a0001c0001t0002g0257a0001c0001t0008g0245a0001c0001t0008g0259others(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 | a0001c0001t0016g0220a0002c0002t0014g0222a0002c0002t0015g0221 | 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 | a0002c0002t0002g0351a0002c0002t0003g0215a0002c0002t0004g0214 | 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 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0002g0004others(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 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0144others(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 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0144others(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 | a0002c0018t0013g0217a0007c0017t0001g0216 | 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 | a0001c0001t0002g0301a0002c0002t0001g0300 | 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 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0104others(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 | a0002c0018t0013g0217a0007c0017t0001g0216 | 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 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(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 | 329 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(326): Show | 332 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(329): 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 | a0001c0001t0002g0257a0001c0001t0008g0245a0001c0001t0008g0259others(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 | a0001c0001t0002g0257a0001c0001t0008g0245a0002c0002t0003g0248others(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 | a0002c0002t0024g0235a0002c0002t0025g0236 | 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 | a0002c0002t0024g0235a0002c0002t0025g0236 | 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 | a0002c0018t0013g0217a0007c0017t0001g0216 | 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 | a0001c0001t0002g0257a0001c0001t0008g0245a0001c0001t0008g0259others(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 | a0001c0001t0001g0087a0001c0001t0001g0089a0001c0001t0001g0090others(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 | a0001c0001t0001g0163a0001c0001t0001g0168a0001c0001t0001g0173others(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 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0296others(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 | 24 | a0001c0001t0001g0279a0001c0001t0002g0264a0001c0001t0002g0278others(21): Show | 24 | HG00140.hp1 HG00642.hp2 HG00733.hp2 others(21): 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 | a0001c0016t0001g0156a0002c0005t0001g0116a0002c0005t0003g0154others(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 | a0002c0018t0013g0217a0007c0017t0001g0216 | 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 | a0002c0018t0013g0217a0007c0017t0001g0216 | 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 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0002c0002t0001g0226 | 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 | a0001c0001t0002g0014a0001c0001t0002g0015 | 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 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0104others(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 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(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 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(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 | 334 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(331): Show | 337 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(334): 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 | a0002c0002t0001g0208a0002c0002t0001g0209 | 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 | a0001c0001t0002g0016a0001c0001t0006g0101a0001c0001t0006g0102others(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 | a0001c0001t0001g0307a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0002c0002t0001g0225a0002c0002t0003g0224 | 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 | a0001c0001t0001g0090a0001c0001t0011g0081 | 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 | a0001c0001t0001g0112a0002c0002t0001g0111a0002c0003t0004g0125 | 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 | a0001c0001t0026g0100a0002c0018t0013g0217a0007c0017t0001g0216 | 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 | a0001c0001t0002g0128a0001c0001t0002g0257a0001c0001t0008g0259others(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 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0210others(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 | a0001c0001t0002g0212a0001c0001t0006g0101a0001c0001t0006g0102others(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 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0104others(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 | a0002c0002t0003g0229a0002c0002t0007g0232a0002c0003t0012g0230others(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 | 334 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(331): Show | 337 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.197+1068C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10727637 | ||||||
| chr2:10727714
|
G | C | 345 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(342): Show | 348 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(345): 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 | a0001c0001t0007g0237a0002c0002t0001g0241a0002c0002t0003g0243others(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 | a0002c0002t0001g0150a0002c0002t0004g0123a0002c0003t0004g0152others(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 | a0001c0001t0016g0220a0002c0002t0014g0222a0002c0002t0015g0221 | 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 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0210others(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 | a0001c0001t0001g0305a0001c0001t0001g0318a0001c0001t0001g0320others(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 | a0001c0001t0001g0144a0001c0001t0001g0153a0001c0001t0001g0163others(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 | a0001c0001t0002g0291a0002c0002t0001g0271a0002c0002t0001g0292 | 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 | a0001c0001t0002g0017a0001c0001t0002g0018 | 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 | a0001c0001t0026g0100a0002c0018t0013g0217a0007c0017t0001g0216 | 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 | a0002c0002t0001g0080 | 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 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(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 | a0001c0001t0002g0303 | 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 | a0001c0001t0001g0020a0001c0001t0001g0265a0001c0001t0001g0305others(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 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0104others(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 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0079others(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 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(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 | 131 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(128): Show | 133 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(130): 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 | a0001c0001t0001g0079a0001c0001t0001g0144a0001c0001t0001g0153others(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 | a0001c0001t0004g0097a0001c0001t0016g0220a0002c0002t0001g0096others(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 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(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 | a0002c0002t0001g0313 | 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 | a0001c0001t0001g0163a0001c0001t0008g0259a0002c0002t0001g0161others(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 | a0001c0001t0002g0212a0002c0002t0002g0171a0002c0002t0023g0099others(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 | a0001c0001t0001g0079a0001c0001t0001g0144a0001c0001t0001g0153others(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 | a0001c0001t0002g0170a0001c0001t0026g0100a0002c0002t0003g0246others(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 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(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 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0104others(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 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0104others(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 | a0001c0001t0026g0100a0002c0018t0013g0217a0007c0017t0001g0216 | 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 | a0002c0003t0002g0068 | 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 | 145 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(142): Show | 147 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(144): 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 | a0001c0001t0026g0100a0002c0018t0013g0217 | 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 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0104others(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 | a0001c0001t0001g0067 | 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 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0104others(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 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0104others(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 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(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 | 261 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 264 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(261): 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 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(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 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(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 | a0002c0002t0004g0103a0002c0002t0004g0107a0002c0002t0007g0106others(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 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0104 | 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 | a0001c0001t0001g0020a0001c0001t0002g0119a0001c0001t0006g0335others(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 | a0001c0001t0001g0112a0001c0001t0001g0324a0001c0001t0002g0257others(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 | 128 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(125): Show | 130 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(127): 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 | a0001c0001t0001g0020a0001c0001t0002g0132a0002c0002t0001g0339others(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 | 155 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(152): Show | 157 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(154): 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 | a0001c0001t0001g0067a0001c0001t0001g0079a0001c0001t0001g0153others(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 | a0001c0001t0001g0144a0001c0001t0002g0174a0001c0001t0002g0175others(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 | a0002c0002t0001g0226 | 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 | a0001c0001t0001g0112a0001c0001t0007g0237a0002c0002t0001g0111others(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 | a0001c0001t0001g0079a0001c0001t0001g0144a0001c0001t0001g0153others(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 | a0001c0001t0001g0079a0001c0001t0001g0144a0001c0001t0001g0153others(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 | a0002c0002t0001g0313 | 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 | a0002c0002t0001g0161a0002c0002t0007g0134 | 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 | a0001c0006t0005g0308 | 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 | a0001c0001t0001g0079a0001c0001t0001g0144a0001c0001t0001g0153others(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 | a0001c0001t0026g0100a0002c0018t0013g0217 | 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 | a0001c0001t0001g0079a0001c0001t0001g0144a0001c0001t0001g0153others(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 | a0002c0002t0003g0248a0002c0002t0003g0258 | 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 | a0001c0001t0001g0023a0001c0001t0001g0112a0001c0001t0001g0113others(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 | a0001c0001t0001g0079a0001c0001t0001g0144a0001c0001t0001g0153others(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 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0104others(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 | a0001c0001t0001g0071a0001c0001t0001g0178a0001c0001t0002g0024others(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 | a0002c0002t0001g0226a0002c0002t0003g0215a0002c0002t0004g0214 | 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 | a0001c0001t0016g0220a0002c0002t0014g0222a0002c0002t0015g0221 | 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 | a0001c0001t0002g0257a0001c0016t0001g0156a0002c0005t0008g0158others(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 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0104others(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 | a0001c0001t0001g0079a0001c0001t0001g0144a0001c0001t0001g0153others(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 | a0001c0001t0004g0097a0001c0001t0016g0220a0002c0002t0001g0096others(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 | a0001c0001t0001g0113a0001c0001t0001g0210a0001c0001t0001g0211others(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 | a0001c0001t0001g0079a0001c0001t0001g0112a0001c0001t0001g0113others(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 | a0002c0002t0001g0302 | 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 | a0006c0014t0021g0179 | 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 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0210others(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 | a0001c0001t0002g0303a0001c0001t0002g0310 | 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 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0104others(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 | a0001c0001t0001g0079a0001c0001t0001g0112a0001c0001t0001g0113others(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 | a0001c0001t0001g0112a0001c0001t0004g0097a0001c0001t0016g0220others(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 | a0001c0001t0001g0079a0001c0001t0001g0144a0001c0001t0001g0153others(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 | a0001c0001t0001g0079a0001c0001t0001g0144a0001c0001t0001g0153others(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 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0104others(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 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0210others(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 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0104others(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 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0210others(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 | a0002c0002t0006g0227 | 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 | a0001c0001t0001g0071a0001c0001t0001g0163a0001c0001t0016g0220others(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 | a0002c0002t0006g0227 | 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 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0104others(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 | a0001c0001t0001g0079a0001c0001t0001g0112a0001c0001t0001g0113others(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 | a0001c0001t0001g0079a0001c0001t0001g0112a0001c0001t0001g0113others(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 | a0002c0002t0001g0343 | 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 | a0001c0001t0001g0079a0001c0001t0001g0144a0001c0001t0001g0153others(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 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0104others(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 | a0001c0001t0001g0112a0001c0001t0016g0220a0002c0002t0001g0111others(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 | a0001c0001t0001g0112a0001c0001t0016g0220a0002c0002t0001g0111others(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 | a0001c0001t0026g0100a0002c0018t0013g0217a0007c0017t0001g0216 | 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 | a0001c0001t0001g0113a0001c0001t0001g0210a0001c0001t0001g0211others(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 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0104others(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 | a0007c0017t0001g0216 | 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 | 137 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(134): Show | 139 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(136): 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 | a0001c0001t0001g0079a0001c0001t0001g0144a0001c0001t0001g0153others(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 | a0002c0002t0006g0227a0002c0002t0006g0228 | 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 | a0001c0001t0001g0089a0002c0002t0001g0062a0002c0003t0002g0009others(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 | a0001c0001t0026g0100a0002c0018t0013g0217a0007c0017t0001g0216 | 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 | 137 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(134): Show | 139 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(136): 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 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0113others(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 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(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 | a0001c0001t0001g0112a0002c0002t0001g0111a0002c0002t0001g0241others(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 | a0001c0001t0007g0237a0002c0002t0003g0229a0002c0002t0007g0232others(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 | a0001c0001t0002g0181a0001c0001t0002g0182 | 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
|
CAA | C | 333 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(330): Show | 336 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.197+10708_197+1070 others(6): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10737260 | |||||
| chr2:10737260
|
CAAA | C | 13 | a0001c0001t0001g0071a0001c0001t0002g0202a0001c0001t0006g0101others(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 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0210others(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 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0079others(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 | a0001c0001t0002g0338a0001c0001t0002g0349a0002c0002t0001g0339 | 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 | a0001c0001t0007g0237a0002c0002t0003g0229a0002c0002t0007g0232others(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 | a0001c0001t0001g0112a0001c0001t0016g0220a0001c0001t0026g0100others(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 | a0002c0002t0001g0331 | 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 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(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 | a0001c0001t0001g0113a0001c0001t0001g0210a0001c0001t0001g0211others(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 | a0002c0003t0004g0135 | 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 | a0001c0001t0001g0112a0001c0001t0026g0100a0002c0002t0001g0111others(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 | a0002c0002t0002g0329 | 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 | a0001c0001t0001g0153a0001c0001t0002g0176a0001c0001t0002g0198others(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 | a0002c0003t0004g0135 | 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 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(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 | a0002c0003t0002g0126a0002c0003t0002g0127 | 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 | a0001c0001t0002g0344 | 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 | a0002c0002t0004g0103a0002c0002t0004g0107 | 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 | a0001c0001t0002g0206a0001c0001t0002g0207 | 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 | 147 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(144): Show | 149 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(146): 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 | a0001c0001t0001g0079a0001c0001t0002g0076a0001c0001t0008g0259others(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 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0104others(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 | a0002c0002t0001g0150a0002c0002t0001g0225a0002c0003t0004g0152others(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 | a0001c0001t0001g0012a0001c0001t0001g0055a0001c0001t0001g0057others(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 | a0001c0001t0001g0025a0001c0001t0001g0050a0001c0001t0001g0052others(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 | a0001c0001t0001g0305a0001c0001t0001g0320a0002c0002t0001g0319 | 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 | 63 | a0001c0001t0001g0079a0001c0001t0001g0178a0001c0001t0001g0204others(60): Show | 63 | HG00140.hp1 HG00597.hp1 HG00642.hp2 others(60): 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 | |||||
| chr2:10739314
|
T | C | 350 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(347): Show | 353 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(350): Show |
intron_variant | MODIFIER | c.197+12745T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10739314 | ||||||
| chr2:10739386
|
G | A | 350 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(347): Show | 353 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(350): Show |
intron_variant | MODIFIER | c.197+12817G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10739386 | ||||||
| chr2:10739531
|
C | T | 3 | a0001c0001t0002g0349a0002c0002t0001g0339a0002c0002t0002g0124 | 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 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0219others(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 | ||||||
| chr2:10739973
|
G | GCACCTGT others(4): Show |
350 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(347): Show | 353 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(350): Show |
intron_variant | MODIFIER | c.197+13406_197+1340 others(15): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10739973 | |||||
| chr2:10739977
|
G | GCTA | 350 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(347): Show | 353 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(350): Show |
intron_variant | MODIFIER | c.197+13410_197+1341 others(7): Show |
ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 10739977 | |||||
| chr2:10740044
|
C | T | 335 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(332): Show | 338 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(335): 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 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0054a0001c0001t0001g0163a0001c0001t0002g0202others(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 | a0002c0002t0001g0150a0002c0002t0001g0225a0002c0002t0004g0123others(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 | a0002c0003t0002g0068 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.198-13256C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10740725 | ||||||
| chr2:10740751
|
G | A | 350 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(347): Show | 353 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(350): Show |
intron_variant | MODIFIER | c.198-13230G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10740751 | ||||||
| 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 | 339 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(336): Show | 342 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(339): 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 | a0001c0001t0001g0079a0001c0001t0002g0076a0001c0001t0008g0245others(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 | a0002c0002t0008g0234 | 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 | 345 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(342): Show | 348 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(345): 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 | a0002c0002t0001g0241a0002c0002t0003g0243a0002c0002t0006g0240others(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 | 345 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(342): Show | 348 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(345): 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 | 345 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(342): Show | 348 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(345): Show |
intron_variant | MODIFIER | c.198-12490T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10741491 | ||||||
| chr2:10741520
|
A | G | 344 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(341): Show | 347 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(344): 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 | a0001c0001t0002g0014a0001c0001t0002g0015 | 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 | a0002c0002t0003g0258a0002c0009t0022g0155 | 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 | 345 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(342): Show | 348 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(345): 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 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0002c0002t0001g0150a0002c0002t0001g0225a0002c0003t0004g0152others(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 | a0001c0001t0001g0079a0001c0001t0002g0076a0001c0001t0002g0176others(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 | 312 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(309): Show | 315 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(312): 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 | a0001c0001t0002g0186a0002c0002t0002g0124 | 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 | a0002c0002t0001g0150a0002c0002t0001g0225a0002c0002t0004g0123others(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 | ||||||
| chr2:10742041
|
C | T | 350 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(347): Show | 353 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(350): Show |
intron_variant | MODIFIER | c.198-11940C>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10742041 | ||||||
| chr2:10742045
|
G | C | 2 | a0001c0001t0002g0183a0002c0002t0001g0184 | 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 | a0002c0002t0001g0150a0002c0002t0001g0225a0002c0002t0001g0241others(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 | a0002c0002t0002g0321 | 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 | a0001c0001t0002g0346 | 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 | a0002c0002t0001g0302a0002c0002t0010g0108 | 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 | a0002c0002t0006g0228 | 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 | a0001c0001t0001g0113a0001c0001t0001g0210a0001c0001t0001g0211 | 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 | a0002c0002t0001g0150a0002c0002t0001g0225a0002c0002t0004g0123others(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 | 344 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(341): Show | 347 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(344): 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 | a0002c0002t0001g0274 | 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 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0104others(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 | a0002c0002t0001g0302 | 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 | a0001c0001t0002g0325 | 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 | a0002c0002t0001g0274 | 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 | a0001c0001t0002g0024 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.198-10800A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10743181 | ||||||
| chr2:10743200
|
A | T | 350 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(347): Show | 353 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(350): Show |
intron_variant | MODIFIER | c.198-10781A>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10743200 | ||||||
| chr2:10743271
|
A | G | 5 | a0002c0002t0001g0150a0002c0002t0001g0225a0002c0002t0004g0123others(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 | ||||||
| chr2:10743275
|
T | A | 1 | a0002c0002t0001g0275 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.198-10706T>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10743275 | ||||||
| chr2:10743294
|
A | G | 2 | a0002c0004t0005g0045a0002c0004t0005g0046 | 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 | ||||||
| chr2:10743412
|
G | T | 350 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(347): Show | 353 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(350): Show |
intron_variant | MODIFIER | c.198-10569G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10743412 | ||||||
| chr2:10743667
|
C | T | 4 | a0001c0001t0016g0220a0002c0002t0014g0222a0002c0002t0015g0221others(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 | 217 | a0001c0001t0001g0025a0001c0001t0001g0050a0001c0001t0001g0052others(214): Show | 218 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(215): 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 | a0001c0001t0002g0316 | 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 | a0002c0002t0006g0228 | 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 | a0001c0001t0001g0030a0001c0001t0001g0047a0001c0001t0001g0050others(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 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270others(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 | 125 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(122): Show | 127 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(124): 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 | a0001c0001t0002g0257a0002c0002t0003g0229a0002c0005t0001g0116others(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 | a0001c0001t0001g0025a0001c0001t0001g0144a0001c0001t0001g0153others(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 | a0001c0001t0008g0245a0002c0002t0004g0238a0002c0002t0004g0239others(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 | a0001c0001t0001g0025a0002c0002t0001g0092a0002c0002t0008g0234 | 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 | a0001c0001t0001g0178a0001c0001t0001g0204a0001c0001t0002g0291others(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 | a0002c0002t0003g0246a0002c0002t0003g0248a0002c0002t0003g0249others(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 | a0001c0001t0001g0010a0001c0001t0001g0020a0001c0001t0001g0025others(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 | 67 | a0001c0001t0001g0052a0001c0001t0001g0090a0001c0001t0001g0163others(64): Show | 67 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(64): 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 | a0001c0001t0002g0169a0001c0001t0002g0213a0002c0002t0002g0022 | 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 | a0001c0001t0002g0283a0002c0002t0001g0096a0002c0002t0003g0224others(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 | a0001c0001t0007g0237a0001c0001t0016g0220a0002c0002t0001g0096others(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 | a0002c0007t0009g0028a0002c0007t0009g0029a0002c0007t0009g0151 | 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 | a0001c0001t0001g0079a0001c0001t0002g0076a0002c0002t0001g0073others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0013a0001c0001t0001g0083a0001c0001t0002g0014others(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 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0048others(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 | a0002c0002t0001g0069 | 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 | 275 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(272): Show | 278 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.198-8802A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10745179 | ||||||
| chr2:10745358
|
G | GT | 90 | a0001c0001t0001g0025a0001c0001t0001g0052a0001c0001t0001g0072others(87): Show | 90 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(87): 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 | a0002c0002t0001g0150a0002c0002t0003g0246a0002c0002t0003g0248others(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 | a0001c0001t0007g0237a0002c0002t0003g0224a0002c0002t0004g0103others(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 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0043others(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 | a0002c0002t0003g0248a0002c0002t0003g0258 | 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 | 78 | a0001c0001t0001g0025a0001c0001t0001g0052a0001c0001t0001g0072others(75): Show | 78 | HG00544.hp1 HG00597.hp1 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.198-8206T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10745775 | ||||||
| chr2:10745842
|
C | G | 268 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(265): Show | 271 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.198-8139C>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10745842 | ||||||
| chr2:10745972
|
C | T | 230 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(227): Show | 232 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(229): 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 | a0001c0001t0007g0237a0001c0001t0016g0220a0002c0002t0001g0096others(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 | a0002c0002t0001g0066 | 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 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0048others(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 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0048others(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 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0020others(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 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0048others(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 | 123 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0025others(120): Show | 124 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(121): 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 | a0002c0002t0002g0321 | 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 | a0001c0001t0007g0237a0002c0002t0001g0096a0002c0002t0001g0161others(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 | a0006c0014t0021g0179 | 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 | a0006c0014t0021g0179 | 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 | a0001c0001t0002g0349 | 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 | a0002c0002t0004g0103a0002c0002t0004g0107 | 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 | a0001c0001t0007g0237a0001c0015t0006g0247a0002c0002t0001g0096others(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 | a0006c0014t0021g0179 | 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 | 271 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(268): Show | 274 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(271): 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 | a0002c0002t0006g0228 | 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 | a0002c0002t0001g0115a0002c0002t0001g0150a0002c0002t0003g0246others(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 | 88 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0047others(85): Show | 89 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(86): 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 | a0002c0003t0002g0312 | 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 | a0002c0002t0002g0314 | 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 | 103 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0047others(100): Show | 104 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(101): 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 | a0002c0002t0001g0115a0002c0002t0001g0150a0002c0002t0001g0241others(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 | a0001c0001t0001g0079a0001c0001t0002g0076a0002c0002t0001g0073others(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 | a0002c0002t0001g0051a0002c0002t0001g0115a0002c0002t0001g0150others(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 | a0002c0002t0007g0232a0005c0012t0003g0231 | 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 | a0002c0002t0001g0111a0002c0002t0006g0227 | 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 | a0006c0014t0021g0179 | 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 | a0002c0002t0001g0241 | 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 | a0001c0001t0002g0206a0001c0001t0002g0207 | 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 | a0002c0002t0001g0241 | 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 | 75 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0047others(72): Show | 76 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(73): 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 | a0001c0001t0001g0033a0001c0001t0001g0043a0002c0002t0001g0111others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(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 | 94 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0047others(91): Show | 95 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(92): 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 | a0001c0001t0016g0220a0002c0002t0001g0096a0002c0002t0001g0161others(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 | a0001c0001t0007g0237a0001c0015t0006g0247a0002c0002t0001g0096others(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 | a0001c0001t0007g0237a0001c0015t0006g0247a0002c0002t0024g0235 | 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 | a0002c0002t0002g0317 | 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 | 78 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0047others(75): Show | 79 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(76): 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 | a0001c0001t0007g0237a0001c0015t0006g0247a0002c0002t0001g0096others(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 | a0001c0001t0007g0237a0001c0015t0006g0247a0002c0002t0001g0096others(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 | a0001c0001t0001g0079a0001c0001t0002g0076a0002c0002t0001g0073others(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 | a0002c0002t0001g0115a0002c0002t0001g0150a0002c0002t0003g0246others(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 | a0002c0002t0001g0111a0002c0002t0004g0117a0002c0002t0006g0227others(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 | a0001c0001t0007g0237a0001c0015t0006g0247a0002c0002t0001g0096others(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 | a0001c0001t0007g0237a0001c0015t0006g0247a0002c0002t0001g0096others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(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 | a0001c0001t0007g0237a0001c0015t0006g0247a0002c0002t0024g0235 | 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 | a0002c0002t0001g0261a0002c0002t0001g0274a0002c0002t0001g0276others(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 | a0002c0002t0001g0150a0002c0002t0003g0246a0002c0002t0003g0248others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0002g0044 | 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 | a0002c0002t0007g0232a0005c0012t0003g0231 | 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 | a0001c0001t0002g0326a0002c0002t0001g0319 | 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 | a0006c0014t0021g0179 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0013others(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 | 82 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0047others(79): Show | 83 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(80): 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 | a0002c0002t0001g0115a0002c0002t0001g0150a0002c0002t0003g0246others(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 | a0006c0014t0021g0179 | 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 | a0002c0002t0003g0243a0002c0002t0008g0242a0002c0003t0004g0135others(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 | a0001c0001t0013g0075 | 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 | a0001c0001t0002g0330a0002c0002t0002g0304a0002c0002t0002g0351 | 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 | a0006c0014t0021g0179 | 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 | 77 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0047others(74): Show | 78 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(75): 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 | a0002c0002t0001g0096a0002c0002t0001g0161a0002c0002t0007g0134others(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 | a0002c0002t0001g0343 | 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 | a0002c0003t0002g0312 | 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 | 80 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0047others(77): Show | 81 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.198-1978G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10752003 | ||||||
| chr2:10752007
|
T | C | 336 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(333): Show | 339 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.198-1974T>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 3/13 | chr2 | 10752007 | ||||||
| chr2:10752071
|
A | C | 91 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0047others(88): Show | 92 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(89): 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 | a0002c0002t0007g0106a0002c0002t0007g0223 | 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 | a0001c0001t0001g0061a0001c0001t0001g0094a0002c0002t0001g0188others(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 | 346 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(343): Show | 349 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(346): 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 | a0002c0002t0001g0111a0002c0002t0004g0117 | 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 | a0002c0002t0001g0130a0002c0002t0001g0302 | 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 | a0002c0002t0001g0331 | 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 | a0002c0002t0003g0243a0002c0002t0008g0242a0002c0003t0004g0135others(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 | a0002c0002t0001g0225a0002c0002t0003g0215a0002c0002t0003g0243others(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 | a0002c0002t0003g0243a0002c0002t0008g0242a0002c0003t0004g0135others(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 | a0002c0002t0001g0115a0002c0002t0002g0171a0002c0007t0009g0028others(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 | a0002c0002t0002g0021 | 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 | a0006c0014t0021g0179 | 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 | a0001c0001t0002g0189a0002c0003t0002g0086 | 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 | a0001c0001t0001g0030a0001c0001t0002g0003a0001c0001t0002g0018others(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 | a0002c0002t0001g0241 | 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 | 20 | a0001c0001t0001g0113a0001c0001t0001g0298a0001c0001t0001g0323others(17): Show | 20 | HG00639.hp2 HG01074.hp1 HG01109.hp2 others(17): 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 | a0002c0002t0001g0241a0002c0002t0003g0215a0002c0002t0004g0123others(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 | a0001c0001t0001g0012a0001c0001t0001g0055a0001c0001t0020g0056 | 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 | a0001c0001t0007g0237a0002c0002t0024g0235 | 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 | a0001c0001t0001g0043 | 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 | a0001c0001t0002g0349a0002c0004t0005g0143 | 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 | a0002c0002t0001g0331 | 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 | a0001c0001t0002g0289 | 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 | a0002c0002t0003g0229a0002c0009t0004g0157 | 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 | 83 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0047others(80): Show | 84 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(81): 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 | a0001c0001t0002g0269a0001c0001t0002g0289a0002c0002t0001g0284others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(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 | 83 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0047others(80): Show | 84 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(81): 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 | a0002c0002t0001g0319 | 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 | a0001c0015t0006g0247a0002c0002t0001g0111a0002c0002t0001g0150others(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 | 84 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0047others(81): Show | 85 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(82): 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(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 | 84 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0047others(81): Show | 85 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(82): 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 | a0002c0002t0001g0292a0002c0002t0001g0319a0002c0002t0001g0345 | 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 | 342 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(339): Show | 345 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(342): 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 | a0001c0001t0002g0024a0001c0001t0002g0190a0002c0003t0002g0121 | 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 | a0002c0002t0002g0039 | 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 | a0002c0002t0001g0208a0002c0002t0001g0209 | 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 | a0001c0001t0004g0097a0001c0001t0004g0114 | 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 | a0002c0003t0012g0160a0002c0003t0012g0230a0002c0004t0005g0162 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(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 | a0002c0002t0024g0235 | 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 | a0001c0001t0002g0014a0001c0001t0002g0015 | 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 | a0001c0001t0002g0176a0001c0001t0002g0200 | 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 | a0001c0001t0001g0079 | 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 | 81 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0047others(78): Show | 82 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(79): 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 | a0001c0006t0005g0308 | 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 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0013others(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 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0104others(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 | 85 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0047others(82): Show | 86 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(83): 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 | a0002c0002t0001g0276a0002c0003t0002g0277 | 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 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0013others(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 | a0001c0001t0002g0001a0001c0001t0002g0189a0001c0001t0002g0267others(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 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0013others(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 | 84 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0047others(81): Show | 85 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(82): 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 | a0001c0001t0007g0237a0002c0002t0001g0115a0002c0002t0007g0232others(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 | a0001c0001t0016g0220a0002c0002t0002g0147a0002c0002t0015g0221 | 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 | a0001c0001t0002g0290a0001c0001t0002g0325a0001c0001t0006g0335others(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 | a0001c0001t0001g0043a0001c0001t0001g0050a0001c0001t0001g0054others(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 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0013others(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 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0064others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(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 | 9 | a0001c0001t0002g0344a0002c0002t0001g0092a0002c0002t0001g0184others(6): Show | 9 | HG00621.hp1 HG00735.hp1 HG00735.hp2 others(6): 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 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0047others(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 | a0001c0001t0002g0257a0002c0009t0022g0155 | 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 | 9 | a0001c0001t0002g0344a0002c0002t0001g0092a0002c0002t0001g0184others(6): Show | 9 | HG00621.hp1 HG00735.hp1 HG00735.hp2 others(6): 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 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0047others(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 | a0002c0003t0002g0118 | 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 | a0002c0002t0001g0302 | 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 | 80 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0047others(77): Show | 81 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.283+3320A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10757386 | ||||||
| chr2:10757412
|
CTTA | C | 80 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0047others(77): Show | 81 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(78): 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 | a0001c0001t0002g0174a0001c0001t0002g0175 | 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 | a0001c0001t0001g0079a0002c0002t0001g0073a0002c0002t0001g0225others(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 | a0002c0002t0007g0106a0002c0002t0007g0223 | 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 | a0001c0001t0008g0259a0002c0002t0006g0228 | 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 | a0002c0002t0001g0115a0002c0002t0007g0232a0002c0004t0005g0162others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(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 | a0001c0001t0002g0018 | 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 | a0006c0014t0021g0179 | 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 | a0002c0002t0001g0241 | 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 | a0006c0014t0021g0179 | 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 | a0001c0001t0001g0079a0002c0002t0001g0073a0002c0002t0001g0225others(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 | a0001c0001t0002g0270a0001c0001t0002g0282 | 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 | 86 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0047others(83): Show | 87 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.283+4646G>T | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10758712 | ||||||
| chr2:10758724
|
G | A | 87 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0047others(84): Show | 88 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(85): 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 | a0001c0001t0008g0259a0002c0002t0006g0228 | 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 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0013others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0006c0014t0021g0179 | 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 | a0001c0001t0008g0259a0002c0002t0006g0228 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(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 | 80 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0047others(77): Show | 81 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(78): 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 | a0006c0014t0021g0179 | 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 | a0001c0001t0001g0072a0001c0001t0002g0183 | 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 | a0001c0001t0006g0335 | 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 | 247 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(244): Show | 249 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(246): 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 | a0001c0001t0001g0010a0001c0001t0001g0305a0001c0001t0001g0320others(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 | a0001c0001t0002g0181a0001c0001t0002g0182 | 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 | a0002c0002t0001g0241 | 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 | a0002c0002t0006g0227 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0008g0259a0002c0002t0006g0228 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0002c0002t0001g0241 | 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 | a0002c0002t0024g0235 | 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 | a0002c0002t0006g0227 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0016g0220a0002c0002t0002g0147a0002c0002t0015g0221 | 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 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0104others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0006c0014t0021g0179 | 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 | a0001c0001t0016g0220a0002c0002t0002g0147a0002c0002t0015g0221 | 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 | a0001c0001t0002g0283 | 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 | a0002c0003t0002g0126a0002c0003t0002g0127 | 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 | a0002c0002t0001g0328 | 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 | 292 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(289): Show | 294 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.284-3022A>G | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 4/13 | chr2 | 10761309 | ||||||
| chr2:10761366
|
A | G | 292 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(289): Show | 294 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(291): 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 | a0001c0001t0002g0282 | 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 | a0001c0001t0002g0349 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(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 | 80 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0047others(77): Show | 81 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(78): 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 | a0001c0001t0008g0259a0002c0002t0006g0228 | 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 | a0002c0002t0001g0226 | 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 | a0002c0002t0024g0235 | 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 | a0001c0001t0016g0220a0002c0002t0002g0147a0002c0002t0015g0221 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0002c0002t0001g0332 | 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 | 109 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0047others(106): Show | 110 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(107): 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 | a0001c0001t0007g0237a0002c0002t0001g0115a0002c0002t0007g0232others(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 | a0002c0002t0010g0108a0002c0002t0014g0222a0002c0002t0023g0099 | 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 | a0001c0001t0016g0220a0002c0002t0002g0147a0002c0002t0015g0221 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0002c0002t0001g0241 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0008g0259a0002c0002t0006g0228 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0079a0002c0002t0001g0073a0002c0002t0001g0225others(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 | a0002c0007t0009g0028a0002c0007t0009g0029a0002c0007t0009g0151 | 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 | a0001c0001t0002g0044 | 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 | a0002c0002t0006g0228 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0002c0002t0001g0241a0002c0002t0007g0232a0002c0003t0002g0086others(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 | a0001c0001t0001g0090a0001c0001t0001g0163a0001c0001t0001g0336 | 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 | a0002c0002t0003g0243a0002c0002t0008g0242a0002c0003t0004g0135others(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 | a0001c0001t0016g0220a0002c0002t0002g0147a0002c0002t0015g0221 | 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 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0104others(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 | a0001c0001t0007g0237a0001c0001t0016g0220a0002c0002t0001g0150others(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 | a0001c0001t0001g0079a0002c0002t0001g0073a0002c0002t0001g0225others(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 | a0001c0001t0002g0326 | 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 | 297 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(294): Show | 299 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(296): 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0002c0002t0001g0274 | 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 | a0002c0002t0002g0147a0002c0002t0015g0221 | 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 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0104others(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 | a0001c0001t0002g0316 | 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 | a0001c0001t0004g0097a0001c0001t0004g0114 | 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 | a0001c0001t0001g0061a0001c0001t0001g0094 | 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 | a0001c0001t0001g0320a0002c0002t0001g0005a0002c0002t0002g0171 | 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 | a0001c0001t0002g0325 | 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 | a0001c0001t0001g0320a0002c0002t0001g0005a0002c0002t0002g0171 | 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 | a0001c0001t0001g0320a0002c0002t0001g0005a0002c0002t0002g0171 | 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 | a0001c0001t0001g0320a0002c0002t0001g0005a0002c0002t0002g0171 | 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 | a0002c0002t0006g0228 | 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 | a0002c0002t0001g0284a0002c0002t0001g0295 | 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 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0013g0075others(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 | a0003c0008t0003g0122a0003c0008t0003g0146 | 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 | a0002c0002t0001g0150a0002c0002t0001g0161a0002c0002t0003g0224others(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 | a0001c0001t0001g0079a0002c0002t0001g0073a0002c0002t0001g0096others(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 | a0002c0002t0007g0232a0002c0003t0004g0152a0002c0004t0005g0109others(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 | a0002c0002t0007g0232a0002c0003t0004g0152a0002c0004t0005g0109others(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 | a0002c0002t0003g0224a0007c0017t0001g0216 | 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 | a0006c0014t0021g0179 | 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 | a0002c0002t0006g0227a0002c0002t0006g0228a0002c0002t0006g0240others(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 | 348 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(345): Show | 351 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(348): 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 | a0002c0002t0001g0096a0002c0002t0004g0117a0002c0003t0004g0058others(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 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(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 | a0002c0002t0001g0130a0002c0002t0001g0261 | 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 | a0002c0002t0007g0232a0002c0004t0005g0162 | 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 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(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 | a0002c0002t0001g0115a0002c0002t0001g0150a0002c0002t0001g0161others(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 | a0002c0002t0001g0096a0002c0002t0004g0117a0002c0003t0002g0009others(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 | a0002c0002t0001g0333 | 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 | a0001c0001t0002g0040 | 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 | a0002c0002t0014g0222a0002c0002t0023g0099 | 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 | a0002c0002t0001g0080 | 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 | a0002c0003t0002g0009a0002c0003t0002g0063a0002c0003t0002g0068others(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 | a0002c0003t0012g0160a0002c0003t0012g0230 | 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 | a0002c0003t0012g0160a0002c0003t0012g0230 | 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 | a0002c0002t0001g0096a0002c0002t0004g0117a0002c0003t0002g0009others(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 | a0001c0001t0001g0173a0001c0001t0001g0347 | 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 | a0001c0001t0002g0349 | 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 | a0001c0001t0002g0283a0002c0002t0001g0241a0002c0002t0004g0103others(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 | a0002c0002t0001g0111a0002c0002t0003g0249a0002c0002t0004g0123others(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 | a0001c0001t0002g0349 | 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 | a0002c0002t0001g0111a0002c0002t0003g0249a0002c0002t0004g0123others(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 | a0002c0002t0001g0073a0002c0002t0018g0078a0002c0005t0001g0116 | 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 | a0002c0002t0001g0115a0002c0002t0003g0215a0002c0002t0003g0224others(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 | a0001c0001t0001g0318a0001c0001t0001g0324a0001c0001t0002g0340 | 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 | 104 | a0001c0001t0002g0322a0001c0001t0002g0330a0002c0002t0001g0005others(101): Show | 104 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.379-1584A>C | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10767135 | ||||||
| chr2:10767159
|
C | CT | 120 | a0001c0001t0001g0347a0002c0002t0001g0005a0002c0002t0001g0035others(117): Show | 120 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(117): 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 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0025others(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 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0002c0002t0001g0225a0002c0002t0004g0117a0002c0002t0007g0106others(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 | a0001c0001t0001g0079 | 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 | a0002c0007t0009g0028a0002c0007t0009g0029a0002c0007t0009g0151 | 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 | a0002c0002t0007g0106a0002c0002t0007g0223 | 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 | 313 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(310): Show | 316 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.379-686G>A | ATP6V1C2 | ENSG00000143882.12 | transcript | ENST00000272238.9 | protein_coding | 5/13 | chr2 | 10768033 | ||||||
| chr2:10768071
|
A | G | 313 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(310): Show | 316 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(313): 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 | a0002c0002t0001g0225a0002c0002t0010g0108a0002c0003t0012g0160others(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 | 313 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(310): Show | 316 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(313): 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 | a0002c0004t0005g0327 | 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 | 346 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(343): Show | 349 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(346): 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 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0153others(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 | a0002c0002t0001g0226 | 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 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0002c0003t0002g0009a0002c0003t0002g0063a0002c0003t0002g0068others(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 | a0002c0002t0001g0150a0002c0002t0001g0161a0002c0002t0001g0225others(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 | a0002c0002t0003g0252a0002c0002t0003g0253 | 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 | a0001c0001t0008g0259a0001c0001t0016g0220a0002c0002t0007g0106others(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 | a0002c0002t0014g0222a0002c0002t0023g0099 | 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 | 184 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(181): Show | 185 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(182): 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 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(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 | 114 | a0001c0001t0002g0330a0002c0002t0001g0005a0002c0002t0001g0035others(111): Show | 114 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(111): 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 | a0002c0002t0001g0073 | 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 | a0002c0002t0001g0225a0002c0002t0004g0117a0002c0002t0006g0227others(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 | a0007c0017t0001g0216 | 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 | a0001c0001t0002g0316 | 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 | 66 | a0001c0001t0002g0330a0002c0002t0001g0005a0002c0002t0001g0035others(63): Show | 66 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(63): 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 | a0002c0002t0007g0232a0002c0004t0005g0162 | 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 | a0001c0001t0008g0259a0001c0001t0016g0220 | 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 | a0001c0001t0002g0338 | 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 | a0002c0002t0001g0062a0002c0002t0001g0188a0002c0002t0001g0208others(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 | a0002c0002t0001g0096a0002c0002t0001g0115 | 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 | a0001c0001t0013g0075a0002c0002t0001g0111a0002c0002t0004g0123others(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 | a0002c0002t0001g0225a0002c0002t0004g0117a0002c0002t0006g0227others(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 | a0002c0003t0012g0160a0002c0003t0012g0230 | 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 | a0002c0002t0001g0096a0002c0002t0001g0115 | 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 | a0002c0002t0001g0096a0002c0002t0001g0115 | 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 | a0001c0001t0002g0316 | 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 | a0001c0006t0005g0337 | 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 | a0002c0007t0009g0028a0002c0007t0009g0029a0002c0007t0009g0151 | 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 | a0002c0002t0001g0150a0002c0002t0001g0161 | 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 | a0001c0001t0008g0259a0001c0001t0016g0220 | 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 | a0002c0003t0004g0058a0002c0003t0004g0074a0002c0003t0004g0077others(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 | 111 | a0001c0001t0002g0330a0002c0002t0001g0005a0002c0002t0001g0035others(108): Show | 111 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(108): 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 | a0002c0002t0001g0225a0002c0002t0004g0117a0002c0002t0006g0227others(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 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(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 | a0002c0002t0007g0106a0002c0002t0007g0223 | 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 | a0002c0002t0004g0117a0002c0002t0006g0227a0002c0002t0006g0228others(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 | a0002c0003t0002g0009a0002c0003t0002g0063a0002c0003t0002g0068others(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 | a0006c0014t0021g0179 | 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 | a0002c0007t0009g0028a0002c0007t0009g0029a0002c0007t0009g0151 | 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 | a0001c0006t0005g0042a0001c0006t0005g0308a0001c0006t0005g0337others(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 | a0006c0014t0021g0179 | 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 | 319 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(316): Show | 322 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(319): 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 | a0001c0006t0005g0042a0001c0006t0005g0308a0001c0006t0005g0337others(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 | a0002c0002t0014g0222a0002c0002t0023g0099 | 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 | 111 | a0001c0001t0002g0330a0001c0001t0013g0075a0002c0002t0001g0005others(108): Show | 111 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(108): 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 | a0005c0012t0003g0231 | 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 | 69 | a0001c0001t0002g0330a0002c0002t0001g0005a0002c0002t0001g0035others(66): Show | 69 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(66): 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 | 66 | a0001c0001t0002g0330a0002c0002t0001g0005a0002c0002t0001g0035others(63): Show | 66 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(63): 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 | a0002c0002t0001g0225a0002c0002t0010g0108 | 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 | a0006c0014t0021g0179 | 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 | a0002c0003t0004g0058a0002c0009t0004g0157 | 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 | a0002c0002t0002g0329 | 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 | a0001c0001t0013g0075a0002c0002t0001g0111a0002c0002t0004g0123others(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 | a0002c0002t0001g0241a0002c0002t0004g0103a0002c0002t0004g0107others(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 |
138 | a0001c0001t0002g0322a0001c0001t0002g0330a0001c0001t0013g0075others(135): Show | 138 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(135): 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 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(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 | a0003c0008t0003g0122a0003c0008t0003g0146 | 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 | a0001c0001t0007g0237a0002c0002t0001g0096a0002c0002t0001g0115others(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 | a0002c0002t0001g0096a0002c0002t0001g0115a0002c0002t0007g0106others(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 | a0002c0002t0001g0150a0002c0002t0001g0161 | 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 | 282 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(279): Show | 285 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(282): 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 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0002c0003t0002g0126a0002c0003t0002g0127a0002c0003t0002g0273 | 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 | 132 | a0001c0001t0002g0322a0001c0001t0002g0330a0001c0006t0005g0042others(129): Show | 132 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(129): 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 | a0002c0002t0001g0073a0002c0002t0018g0078a0002c0005t0001g0116 | 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 | a0001c0001t0002g0346 | 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 | a0001c0006t0005g0042a0001c0006t0005g0308a0001c0006t0005g0337others(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 | a0001c0001t0007g0237a0002c0002t0003g0215a0002c0002t0003g0224others(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 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0002c0007t0009g0028a0002c0007t0009g0029a0002c0007t0009g0151others(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 | a0001c0001t0007g0237a0002c0002t0003g0215a0002c0002t0003g0224others(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 | a0001c0001t0002g0065a0001c0001t0002g0169a0001c0001t0002g0181others(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 | 341 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(338): Show | 344 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(341): 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 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0013others(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 | 348 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(345): Show | 351 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(348): 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 | a0001c0001t0002g0176a0001c0001t0002g0200 | 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 | a0002c0002t0001g0150a0002c0002t0001g0161 | 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 | a0002c0002t0001g0225a0002c0002t0010g0108a0002c0002t0014g0222others(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 | a0001c0001t0002g0026 | 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 | a0002c0002t0001g0225a0002c0002t0010g0108a0002c0002t0014g0222others(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 | a0002c0002t0001g0225a0002c0002t0002g0019a0002c0002t0010g0108others(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 | a0002c0002t0002g0011a0002c0002t0002g0124a0002c0002t0004g0117 | 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 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0055others(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 | a0002c0002t0001g0225a0002c0002t0010g0108a0002c0002t0014g0222others(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 | a0001c0001t0007g0237a0001c0001t0013g0075a0002c0002t0004g0123others(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 | a0002c0003t0012g0160a0002c0003t0012g0230 | 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 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0055others(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 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0055others(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 | a0001c0001t0013g0075 | 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 | a0002c0003t0002g0068 | 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 | a0002c0002t0002g0019a0002c0003t0002g0009a0002c0003t0002g0063others(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 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0012a0001c0001t0001g0055a0001c0001t0001g0057others(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 | 108 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0013others(105): Show | 108 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(105): 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 | a0006c0014t0021g0179 | 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 | a0001c0001t0002g0270a0001c0001t0002g0282 | 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 | a0002c0002t0008g0234 | 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 | a0002c0002t0024g0235 | 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 | 125 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(122): Show | 125 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(122): 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 | a0002c0003t0012g0160a0002c0003t0012g0230 | 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 | a0002c0007t0009g0028a0002c0007t0009g0029a0002c0007t0009g0151 | 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 | a0001c0001t0002g0257a0001c0001t0007g0237a0001c0001t0008g0259others(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 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(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 | a0002c0002t0003g0215a0002c0002t0003g0224a0002c0002t0003g0229others(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 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0104others(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 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0002c0002t0002g0133a0002c0002t0002g0342 | 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 | a0001c0006t0005g0042a0001c0006t0005g0308a0001c0006t0005g0337others(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 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0002c0003t0012g0160a0002c0003t0012g0230 | 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 | a0002c0002t0002g0019a0002c0002t0002g0147a0002c0003t0002g0009others(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 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0002c0007t0009g0028a0002c0007t0009g0029a0002c0007t0009g0151others(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 | a0007c0017t0001g0216 | 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 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(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 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0002g0257a0001c0001t0007g0088a0001c0001t0007g0237others(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 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(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 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0104others(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 | a0001c0001t0008g0259a0001c0001t0016g0220a0001c0006t0005g0042others(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 | a0001c0001t0007g0088a0001c0001t0007g0237a0002c0002t0007g0106others(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 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0002c0003t0012g0160a0002c0003t0012g0230 | 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 | a0001c0001t0004g0097a0001c0001t0004g0114a0002c0003t0004g0074others(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 | a0002c0002t0004g0214 | 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 | a0001c0001t0002g0257a0002c0002t0003g0215a0002c0002t0003g0224others(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 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0002g0174a0001c0001t0002g0212 | 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 | a0001c0001t0002g0174a0001c0001t0002g0212 | 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 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(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 | a0001c0006t0005g0042a0001c0006t0005g0308a0001c0006t0005g0337others(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 | a0001c0001t0004g0097a0001c0001t0004g0114a0002c0003t0004g0074others(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 | a0001c0001t0006g0335 | 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 | a0002c0002t0002g0019a0002c0002t0002g0147a0002c0002t0014g0222others(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 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0007g0088a0001c0001t0007g0237a0002c0002t0007g0106others(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 | a0002c0002t0001g0274a0002c0002t0001g0276a0002c0002t0001g0284others(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 | a0001c0001t0002g0257a0002c0002t0003g0215a0002c0002t0003g0224others(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 | a0001c0001t0002g0257a0001c0001t0004g0097a0001c0001t0004g0114others(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 | a0002c0002t0008g0234 | 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 | a0002c0002t0002g0019a0002c0002t0002g0147a0002c0003t0002g0009others(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 | a0001c0006t0005g0042a0001c0006t0005g0308a0001c0006t0005g0337others(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 | a0001c0001t0008g0259a0001c0001t0016g0220 | 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 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(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 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0104others(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 | a0002c0002t0001g0096a0002c0002t0001g0115 | 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 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(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 | a0002c0002t0002g0021 | 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 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0006t0005g0042a0001c0006t0005g0308a0001c0006t0005g0337others(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 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0004g0114 | 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 | a0002c0002t0001g0073 | 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 | a0002c0002t0001g0073a0002c0002t0001g0096a0002c0002t0001g0111others(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 | a0002c0003t0002g0118 | 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 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(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 | a0002c0002t0001g0073a0002c0002t0001g0096a0002c0002t0001g0111others(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 | a0002c0002t0002g0019 | 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 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0104others(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 | a0001c0001t0008g0245a0001c0001t0013g0075a0001c0001t0026g0100others(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 | a0001c0001t0008g0259a0001c0001t0016g0220a0001c0006t0005g0042others(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 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0006t0005g0042a0001c0006t0005g0308a0001c0006t0005g0337others(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 | a0001c0001t0001g0061a0001c0001t0001g0094 | 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 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0004g0097a0001c0001t0004g0114a0001c0001t0007g0088others(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 | a0001c0001t0001g0064a0001c0001t0002g0076a0001c0001t0002g0176others(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 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0014others(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 | 111 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(108): Show | 111 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(108): 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 | a0001c0006t0005g0042a0001c0006t0005g0308a0001c0006t0005g0337others(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 | a0002c0002t0002g0022 | 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 | a0002c0002t0002g0022 | 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 | a0002c0002t0002g0022 | 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 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(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 | a0002c0002t0002g0022 | 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 | a0001c0006t0005g0042a0001c0006t0005g0308a0001c0006t0005g0337others(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 | a0001c0001t0007g0088a0001c0001t0007g0237a0002c0002t0007g0106others(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 | a0002c0007t0009g0028a0002c0007t0009g0029a0002c0007t0009g0151 | 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 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0017others(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 | a0001c0001t0004g0097a0001c0001t0004g0114a0001c0001t0008g0245others(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 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(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 | a0001c0001t0001g0050a0001c0001t0001g0071a0001c0001t0001g0089others(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 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0017others(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 | a0001c0001t0001g0034 | 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 | a0001c0006t0005g0042a0001c0006t0005g0308a0001c0006t0005g0337others(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 | a0001c0006t0005g0042a0001c0006t0005g0308a0001c0006t0005g0337others(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 | a0001c0001t0002g0257a0001c0001t0004g0097a0001c0001t0004g0114others(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 | a0001c0001t0002g0257a0001c0001t0004g0097a0001c0001t0004g0114others(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 | a0001c0001t0001g0090a0001c0001t0001g0163a0001c0001t0001g0336 | 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 | a0001c0001t0002g0303 | 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 | a0006c0014t0021g0179 | 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 | a0002c0002t0002g0019a0002c0003t0002g0009a0002c0003t0002g0063others(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 | a0002c0004t0005g0140 | 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 | a0001c0006t0005g0042a0001c0006t0005g0308a0001c0006t0005g0337others(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 | a0002c0007t0009g0028a0002c0007t0009g0029a0002c0007t0009g0151others(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 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(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 | a0001c0006t0005g0042a0001c0006t0005g0308a0001c0006t0005g0337others(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 | a0002c0002t0025g0236 | 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 | a0001c0001t0002g0257a0001c0001t0004g0097a0001c0001t0004g0114others(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 | a0002c0007t0009g0028a0002c0007t0009g0029a0002c0007t0009g0151others(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 | a0001c0001t0006g0335 | 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 | a0001c0006t0005g0042a0001c0006t0005g0308a0001c0006t0005g0337others(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 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(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 | a0002c0007t0009g0028a0002c0007t0009g0029a0002c0007t0009g0151others(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 | a0002c0002t0004g0117a0002c0003t0004g0058a0002c0009t0004g0157 | 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 | a0001c0001t0001g0053a0001c0001t0002g0132a0001c0001t0002g0257others(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 | a0001c0001t0001g0094a0001c0001t0002g0014a0001c0001t0002g0015others(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 | a0001c0001t0007g0088a0001c0001t0007g0237a0002c0002t0007g0106others(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 | a0001c0001t0002g0257a0001c0001t0004g0097a0001c0001t0004g0114others(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 | 345 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(342): Show | 348 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(345): 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 | a0001c0001t0002g0257a0001c0001t0008g0245a0001c0001t0008g0259others(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 | a0002c0002t0002g0329 | 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 | a0001c0001t0002g0269a0001c0001t0002g0289 | 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 | a0001c0001t0002g0325 | 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 | a0002c0002t0003g0215a0002c0002t0003g0224a0002c0002t0003g0229others(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 | a0001c0001t0001g0266a0001c0001t0001g0350 | 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 | a0001c0001t0008g0245a0001c0001t0008g0259a0001c0001t0013g0075others(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 | a0001c0006t0005g0042a0001c0006t0005g0308a0001c0006t0005g0337others(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 | a0002c0004t0005g0162a0004c0011t0017g0149 | 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 | a0006c0014t0021g0179 | 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 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(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 | a0002c0002t0002g0147a0003c0010t0002g0260 | 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 | a0002c0007t0009g0028a0002c0007t0009g0029a0002c0007t0009g0151others(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 | a0001c0001t0007g0088a0001c0001t0007g0237a0002c0002t0007g0106others(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 | a0002c0002t0001g0287a0002c0002t0001g0300a0002c0002t0001g0313others(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 | a0002c0002t0001g0062a0002c0002t0001g0208a0002c0002t0001g0209 | 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 | a0002c0007t0009g0028a0002c0007t0009g0029a0002c0007t0009g0151others(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 | a0001c0006t0005g0042a0001c0006t0005g0308a0001c0006t0005g0337others(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 | a0002c0007t0009g0028a0002c0007t0009g0029a0002c0007t0009g0151 | 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 | a0001c0001t0008g0245a0001c0001t0008g0259a0001c0001t0013g0075others(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 | a0001c0001t0002g0257a0001c0001t0004g0097a0001c0001t0004g0114others(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 | a0002c0007t0009g0028a0002c0007t0009g0029a0002c0007t0009g0151others(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 | a0002c0002t0003g0215a0002c0002t0003g0224a0002c0002t0003g0229others(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 | a0001c0001t0002g0257a0001c0001t0004g0097a0001c0001t0004g0114others(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 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(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 | a0001c0001t0002g0040 | 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 | a0001c0001t0002g0310 | 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 | a0002c0007t0009g0028a0002c0007t0009g0029a0002c0007t0009g0151others(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 | a0001c0001t0008g0245a0001c0001t0008g0259a0001c0001t0013g0075others(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 | a0001c0001t0004g0097a0001c0001t0004g0114a0001c0001t0007g0088others(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 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0032others(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 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0025a0001c0001t0001g0173a0001c0001t0001g0219others(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 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0055others(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 | 31 | a0001c0001t0001g0079a0001c0001t0001g0205a0002c0002t0001g0005others(28): Show | 31 | HG00621.hp1 HG00642.hp2 HG00738.hp1 others(28): 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 | a0001c0001t0002g0004a0001c0001t0002g0038a0001c0001t0002g0041others(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 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0016others(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 | a0001c0001t0001g0047a0001c0001t0002g0131a0001c0001t0002g0191others(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 | a0001c0001t0002g0017a0001c0001t0002g0264a0001c0001t0002g0338others(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 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0119others(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 | a0002c0002t0002g0011a0002c0002t0008g0242a0002c0002t0018g0078others(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 | a0001c0001t0008g0245a0001c0001t0008g0259a0001c0001t0013g0075others(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 | a0001c0001t0004g0097a0001c0001t0004g0114a0001c0001t0007g0237others(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 | a0001c0001t0007g0088a0002c0002t0004g0107a0002c0002t0007g0106others(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 | a0001c0001t0007g0088a0001c0001t0007g0237a0002c0002t0007g0106others(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 | a0001c0001t0004g0097a0001c0001t0004g0114a0001c0001t0007g0088others(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 |