Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 535 |
| ensemblid | ENSG00000033627.18 |
| hgncid | 865 |
| symbol | ATP6V0A1 |
| name | ATPase H+ transporting V0 subunit a1 |
| refseq_nuc | NM_001130021.3 |
| refseq_prot | NP_001123493.1 |
| ensembl_nuc | ENST00000343619.9 |
| ensembl_prot | ENSP00000342951.3 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 42458878 |
| end | 42522579 |
| strand | + |
| ver | v1.2 |
| region | chr17:42458878-42522579 |
| region5000 | chr17:42453878-42527579 |
| regionname0 | ATP6V0A1_chr17_42458878_42522579 |
| regionname5000 | ATP6V0A1_chr17_42453878_42527579 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 837 | 316 | 88 | 65 | 114 | 12 | 35 | 82 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | MGELF others(832): Show |
chr17 | 42453878 | 42527579 |
| a0002 | 0/0 | 837 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | MGELF others(832): Show |
chr17 | 42453878 | 42527579 |
| a0003 | 0/0 | 837 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | MGELF others(832): Show |
chr17 | 42453878 | 42527579 |
| a0004 | 0/0 | 837 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | MGELF others(832): Show |
chr17 | 42453878 | 42527579 |
| a0005 | 0/0 | 837 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | MGELF others(832): Show |
chr17 | 42453878 | 42527579 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2511 | 309 | 86 | 62 | 114 | 11 | 34 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ATGGG others(2506): Show |
chr17 | 42453878 | 42527579 | ||
| a0001c0002 | 0/0 | 2511 | 4 | 0 | 2 | 0 | 1 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ATGGG others(2506): Show |
chr17 | 42453878 | 42527579 | ||
| a0001c0003 | 0/0 | 2511 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ATGGG others(2506): Show |
chr17 | 42453878 | 42527579 | ||
| a0001c0006 | 0/0 | 2511 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ATGGG others(2506): Show |
chr17 | 42453878 | 42527579 | ||
| a0001c0009 | 0/0 | 2511 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ATGGG others(2506): Show |
chr17 | 42453878 | 42527579 | ||
| a0002c0005 | 0/0 | 2511 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ATGGG others(2506): Show |
chr17 | 42453878 | 42527579 | ||
| a0003c0007 | 0/0 | 2511 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ATGGG others(2506): Show |
chr17 | 42453878 | 42527579 | ||
| a0004c0008 | 0/0 | 2511 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ATGGG others(2506): Show |
chr17 | 42453878 | 42527579 | ||
| a0005c0004 | 0/0 | 2511 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ATGGG others(2506): Show |
chr17 | 42453878 | 42527579 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4106 | 197 | 42 | 49 | 72 | 7 | 25 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ACGTC others(4101): Show |
chr17 | 42453878 | 42527579 |
| a0001c0001t0002 | 0/0 | 4106 | 62 | 9 | 8 | 37 | 4 | 4 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ACGTC others(4101): Show |
chr17 | 42453878 | 42527579 |
| a0001c0001t0003 | 0/0 | 4106 | 14 | 10 | 4 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ACGTC others(4101): Show |
chr17 | 42453878 | 42527579 |
| a0001c0001t0004 | 0/0 | 4106 | 8 | 8 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ACGTC others(4101): Show |
chr17 | 42453878 | 42527579 |
| a0001c0001t0005 | 0/0 | 4106 | 7 | 0 | 0 | 4 | 0 | 3 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ACGTC others(4101): Show |
chr17 | 42453878 | 42527579 |
| a0001c0001t0006 | 0/0 | 4106 | 6 | 6 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ACGTC others(4101): Show |
chr17 | 42453878 | 42527579 |
| a0001c0001t0007 | 0/0 | 4106 | 5 | 5 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ACGTC others(4101): Show |
chr17 | 42453878 | 42527579 |
| a0001c0001t0008 | 0/0 | 4106 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ACGTC others(4101): Show |
chr17 | 42453878 | 42527579 |
| a0001c0001t0009 | 0/0 | 4106 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ACGTC others(4101): Show |
chr17 | 42453878 | 42527579 |
| a0001c0001t0010 | 0/0 | 4106 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ACGTC others(4101): Show |
chr17 | 42453878 | 42527579 |
| a0001c0001t0011 | 0/0 | 4106 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ACGTC others(4101): Show |
chr17 | 42453878 | 42527579 |
| a0001c0001t0012 | 0/0 | 4106 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ACGTC others(4101): Show |
chr17 | 42453878 | 42527579 |
| a0001c0001t0013 | 0/0 | 4106 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ACGTC others(4101): Show |
chr17 | 42453878 | 42527579 |
| a0001c0001t0014 | 0/0 | 4106 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ACGTC others(4101): Show |
chr17 | 42453878 | 42527579 |
| a0001c0001t0015 | 0/0 | 4106 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ACGTC others(4101): Show |
chr17 | 42453878 | 42527579 |
| a0001c0001t0016 | 0/0 | 4106 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ACGTC others(4101): Show |
chr17 | 42453878 | 42527579 |
| a0001c0002t0001 | 0/0 | 4106 | 4 | 0 | 2 | 0 | 1 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ACGTC others(4101): Show |
chr17 | 42453878 | 42527579 |
| a0001c0003t0001 | 0/0 | 4106 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ACGTC others(4101): Show |
chr17 | 42453878 | 42527579 |
| a0001c0006t0001 | 0/0 | 4106 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ACGTC others(4101): Show |
chr17 | 42453878 | 42527579 |
| a0001c0009t0001 | 0/0 | 4106 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ACGTC others(4101): Show |
chr17 | 42453878 | 42527579 |
| a0002c0005t0001 | 0/0 | 4106 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ACGTC others(4101): Show |
chr17 | 42453878 | 42527579 |
| a0003c0007t0003 | 0/0 | 4106 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ACGTC others(4101): Show |
chr17 | 42453878 | 42527579 |
| a0004c0008t0001 | 0/0 | 4106 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ACGTC others(4101): Show |
chr17 | 42453878 | 42527579 |
| a0005c0004t0001 | 0/0 | 4106 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | ACGTC others(4101): Show |
chr17 | 42453878 | 42527579 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 9 | 1 | 1 | 7 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0034 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0193 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0007 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0003g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0004g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0004g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0005g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0006g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0006g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0006g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0007g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0007g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0007g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0007g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0008g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0009g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0010g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0011g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0012g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0013g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0014g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0015g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0001t0016g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0006t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0001c0009t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0002c0005t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0003c0007t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0004c0008t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| a0005c0004t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0007 | EUR | GBR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | GBR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0188 | EUR | GBR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0246 | EUR | FIN | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0143 | EUR | FIN | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0141 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | CHS | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG00733 | hp2 | a0001 | c0006 | t0001 | g0009 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0029 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0040 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01243 | hp2 | a0001 | c0001 | t0009 | g0078 | AMR | PUR | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | CLM | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | CLM | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0140 | AMR | CLM | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01496 | hp1 | a0002 | c0005 | t0001 | g0002 | AMR | CLM | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | IBS | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0112 | EUR | IBS | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0113 | EUR | IBS | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0059 | EUR | IBS | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | ACB | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0004 | AFR | ACB | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PEL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | KHV | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | KHV | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | KHV | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | KHV | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | KHV | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0137 | AFR | ACB | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PEL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CDX | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | CDX | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | ACB | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02257 | hp2 | a0003 | c0007 | t0003 | g0107 | AFR | ACB | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0069 | AFR | ACB | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | ACB | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | PEL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | ACB | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | ACB | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | KHV | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02572 | hp1 | a0001 | c0001 | t0008 | g0032 | AFR | GWD | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0038 | AFR | GWD | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | GWD | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0079 | AFR | GWD | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0036 | AFR | GWD | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | GWD | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0111 | SAS | PJL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0091 | AFR | GWD | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0016 | AFR | GWD | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0108 | AFR | ESN | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | ESN | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | ESN | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0004 | AFR | GWD | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0068 | AFR | ESN | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ESN | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03139 | hp2 | a0001 | c0001 | t0011 | g0100 | AFR | ESN | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ESN | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03209 | hp1 | a0001 | c0009 | t0001 | g0192 | AFR | MSL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0031 | AFR | MSL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | MSL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03540 | hp2 | a0001 | c0001 | t0014 | g0219 | AFR | GWD | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | MSL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0039 | AFR | MSL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | STU | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | STU | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0177 | SAS | PJL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0173 | SAS | PJL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | BEB | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03831 | hp2 | a0001 | c0001 | t0015 | g0097 | SAS | BEB | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03942 | hp1 | a0004 | c0008 | t0001 | g0263 | SAS | BEB | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | STU | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | STU | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG04199 | hp1 | a0001 | c0001 | t0016 | g0148 | SAS | STU | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | STU | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | STU | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0142 | SAS | STU | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG04228 | hp1 | a0001 | c0001 | t0005 | g0186 | SAS | STU | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | STU | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | CHB | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | CHB | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHB | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18906 | hp1 | a0001 | c0001 | t0010 | g0164 | AFR | YRI | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | YRI | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18939 | hp2 | a0001 | c0001 | t0013 | g0117 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18982 | hp2 | a0001 | c0001 | t0005 | g0098 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18984 | hp2 | a0001 | c0001 | t0005 | g0174 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18989 | hp1 | a0001 | c0001 | t0005 | g0170 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19010 | hp1 | a0001 | c0001 | t0005 | g0176 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | LWK | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0094 | AFR | LWK | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | LWK | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0004 | AFR | LWK | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | YRI | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0016 | AFR | YRI | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA20129 | hp1 | a0005 | c0004 | t0001 | g0024 | AFR | ASW | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ASW | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0247 | EUR | TSI | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0254 | EUR | TSI | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | ACB | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0075 | AFR | ACB | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | MSL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | MSL | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0090 | AFR | USA | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | USA | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0076 | AFR | USA | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA21309 | hp1 | a0001 | c0001 | t0012 | g0180 | AFR | LWK | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | LWK | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0193 | REF | REF | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0034 | REF | REF | ATP6V0A1_chr17_42453878_42527579 | ATP6V0A1 | chr17 | 42453878 | 42527579 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:42501222 | T | C | 1 | a0005 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.1922T>C | p.Val641Ala | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/22 | 2055/4106 | 1922/2514 | 641/837 | chr17 | 42501222 | |||
| chr17:42507556 | G | A | 1 | a0002 | 1 | HG01496.hp1 | missense_variant | MODERATE | c.2041G>A | p.Gly681Arg | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 18/22 | 2174/4106 | 2041/2514 | 681/837 | chr17 | 42507556 | |||
| chr17:42507604 | A | G | 1 | a0004 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.2089A>G | p.Thr697Ala | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 18/22 | 2222/4106 | 2089/2514 | 697/837 | chr17 | 42507604 | |||
| chr17:42514349 | C | T | 1 | a0003 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.2309C>T | p.Ala770Val | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/22 | 2442/4106 | 2309/2514 | 770/837 | chr17 | 42514349 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:42480711 | C | T | 1 | a0001c0002 | 4 | HG00323.hp2 HG00642.hp1 HG01361.hp1 others(1): Show |
synonymous_variant | LOW | c.678C>T | p.Gly226Gly | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 8/22 | 811/4106 | 678/2514 | 226/837 | chr17 | 42480711 | |||
| chr17:42483101 | A | G | 1 | a0001c0009 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.780A>G | p.Gly260Gly | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/22 | 913/4106 | 780/2514 | 260/837 | chr17 | 42483101 | |||
| chr17:42498953 | G | A | 1 | a0001c0003 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.1590G>A | p.Thr530Thr | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 15/22 | 1723/4106 | 1590/2514 | 530/837 | chr17 | 42498953 | |||
| chr17:42514431 | G | A | 1 | a0001c0006 | 1 | HG00733.hp2 | synonymous_variant | LOW | c.2391G>A | p.Ser797Ser | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/22 | 2524/4106 | 2391/2514 | 797/837 | chr17 | 42514431 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:42458922 | C | G | 1 | a0001c0001t0006 | 6 | HG01891.hp1 HG02572.hp2 HG03041.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-89C>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 1/22 | 1973 | chr17 | 42458922 | ||||||
| chr17:42521136 | G | A | 5 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(2): Show |
24 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*16G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 22/22 | 16 | chr17 | 42521136 | ||||||
| chr17:42521210 | G | A | 1 | a0001c0001t0010 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*90G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 22/22 | 90 | chr17 | 42521210 | ||||||
| chr17:42521448 | C | T | 1 | a0001c0001t0016 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*328C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 22/22 | 328 | chr17 | 42521448 | ||||||
| chr17:42521449 | G | A | 2 | a0001c0001t0011 a0001c0001t0012 |
2 | HG03139.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*329G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 22/22 | 329 | chr17 | 42521449 | ||||||
| chr17:42521518 | G | A | 1 | a0001c0001t0011 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*398G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 22/22 | 398 | chr17 | 42521518 | ||||||
| chr17:42521544 | G | T | 1 | a0001c0001t0005 | 7 | HG03704.hp1 HG03710.hp2 HG04228.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*424G>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 22/22 | 424 | chr17 | 42521544 | ||||||
| chr17:42521558 | C | T | 1 | a0001c0001t0015 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*438C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 22/22 | 438 | chr17 | 42521558 | ||||||
| chr17:42521703 | T | C | 2 | a0001c0001t0002 a0001c0001t0013 |
63 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*583T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 22/22 | 583 | chr17 | 42521703 | ||||||
| chr17:42521898 | C | A | 4 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(1): Show |
23 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*778C>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 22/22 | 778 | chr17 | 42521898 | ||||||
| chr17:42521924 | G | A | 1 | a0001c0001t0007 | 5 | HG02809.hp2 HG02818.hp1 HG06807.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*804G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 22/22 | 804 | chr17 | 42521924 | ||||||
| chr17:42521947 | A | G | 2 | a0001c0001t0007 a0001c0001t0016 |
6 | HG02809.hp2 HG02818.hp1 HG04199.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*827A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 22/22 | 827 | chr17 | 42521947 | ||||||
| chr17:42522273 | G | A | 1 | a0001c0001t0008 | 2 | HG02572.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1153G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 22/22 | 1153 | chr17 | 42522273 | ||||||
| chr17:42522290 | C | T | 1 | a0001c0001t0014 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1170C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 22/22 | 1170 | chr17 | 42522290 | ||||||
| chr17:42522326 | G | T | 1 | a0001c0001t0013 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1206G>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 22/22 | 1206 | chr17 | 42522326 | ||||||
| chr17:42522576 | C | T | 1 | a0001c0001t0004 | 8 | HG02258.hp1 HG02451.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1456C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 22/22 | 1456 | chr17 | 42522576 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:42459035 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-48+72C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 1/21 | chr17 | 42459035 | |||||||
| chr17:42459270 | C | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(87): Show |
105 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.-48+307C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 1/21 | chr17 | 42459270 | |||||||
| chr17:42459346 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-48+383G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 1/21 | chr17 | 42459346 | |||||||
| chr17:42459525 | A | AGAGATAT others(6): Show |
1 | a0001c0001t0001g0274 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-48+567_-48+579dup others(13): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr17 | 42459525 | ||||||
| chr17:42459629 | C | T | 5 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(2): Show |
5 | HG01175.hp2 HG01255.hp2 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+666C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 1/21 | chr17 | 42459629 | |||||||
| chr17:42459635 | T | G | 1 | a0001c0001t0001g0028 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-48+672T>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 1/21 | chr17 | 42459635 | |||||||
| chr17:42460386 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-47-462G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 1/21 | chr17 | 42460386 | |||||||
| chr17:42460583 | A | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(258): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.-47-265A>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 1/21 | chr17 | 42460583 | |||||||
| chr17:42461084 | A | G | 1 | a0001c0009t0001g0192 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.117+73A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42461084 | |||||||
| chr17:42461327 | A | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG01123.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.117+316A>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42461327 | |||||||
| chr17:42461396 | A | C | 1 | a0001c0001t0001g0189 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.117+385A>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42461396 | |||||||
| chr17:42461423 | T | C | 46 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(43): Show |
56 | HG00140.hp1 HG00639.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.117+412T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42461423 | |||||||
| chr17:42461545 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.117+534C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42461545 | |||||||
| chr17:42462044 | C | CA | 68 | a0001c0001t0001g0028 a0001c0001t0001g0041 a0001c0001t0001g0042 others(65): Show |
69 | HG00438.hp2 HG00597.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.117+1056dupA | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 42462044 | ||||||
| chr17:42462147 | C | T | 1 | a0001c0001t0002g0188 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.117+1136C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42462147 | |||||||
| chr17:42462217 | A | C | 1 | a0001c0001t0001g0187 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.117+1206A>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42462217 | |||||||
| chr17:42462275 | A | G | 1 | a0001c0001t0005g0186 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.117+1264A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42462275 | |||||||
| chr17:42462683 | G | A | 1 | a0001c0001t0002g0049 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.117+1672G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42462683 | |||||||
| chr17:42462761 | T | A | 2 | a0001c0001t0002g0104 a0001c0001t0002g0105 |
2 | HG02080.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.117+1750T>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42462761 | |||||||
| chr17:42462837 | T | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0041 a0001c0001t0001g0050 others(2): Show |
7 | HG01891.hp2 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.117+1826T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42462837 | |||||||
| chr17:42462855 | C | A | 1 | a0001c0001t0009g0078 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.117+1844C>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42462855 | |||||||
| chr17:42462922 | A | G | 2 | a0001c0001t0002g0103 a0001c0001t0002g0185 |
2 | HG02027.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.117+1911A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42462922 | |||||||
| chr17:42462998 | C | CT | 117 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(114): Show |
137 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.117+2011dupT | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 42462998 | ||||||
| chr17:42462998 | C | CTT | 28 | a0001c0001t0001g0028 a0001c0001t0001g0053 a0001c0001t0001g0101 others(25): Show |
28 | HG00140.hp2 HG00438.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.117+2010_117+2011d others(4): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 42462998 | ||||||
| chr17:42462998 | C | CTTT | 35 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(32): Show |
45 | HG00140.hp1 HG00639.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.117+2009_117+2011d others(5): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 42462998 | ||||||
| chr17:42462998 | C | CTTTT | 11 | a0001c0001t0001g0041 a0001c0001t0001g0045 a0001c0001t0001g0046 others(8): Show |
11 | HG00741.hp1 HG01074.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.117+2008_117+2011d others(6): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 42462998 | ||||||
| chr17:42463099 | G | A | 1 | a0001c0001t0002g0106 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.117+2088G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42463099 | |||||||
| chr17:42463151 | CACCGCCG others(23): Show |
C | 55 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(52): Show |
60 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.117+2142_117+2171d others(32): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 42463151 | ||||||
| chr17:42463213 | C | G | 3 | a0001c0001t0007g0016 a0001c0001t0007g0090 a0001c0001t0007g0091 |
4 | HG02809.hp2 HG02818.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+2202C>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42463213 | |||||||
| chr17:42463496 | T | C | 1 | a0001c0001t0001g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.117+2485T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42463496 | |||||||
| chr17:42463554 | C | T | 4 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0070 others(1): Show |
4 | HG00140.hp1 HG00741.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.117+2543C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42463554 | |||||||
| chr17:42463743 | C | T | 4 | a0001c0002t0001g0140 a0001c0002t0001g0141 a0001c0002t0001g0142 others(1): Show |
4 | HG00323.hp2 HG00642.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-2686C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42463743 | |||||||
| chr17:42463847 | T | C | 56 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(53): Show |
61 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.118-2582T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42463847 | |||||||
| chr17:42464013 | G | C | 1 | a0003c0007t0003g0107 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.118-2416G>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42464013 | |||||||
| chr17:42464013 | G | T | 1 | a0001c0001t0007g0094 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.118-2416G>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42464013 | |||||||
| chr17:42464071 | C | T | 1 | a0001c0003t0001g0137 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.118-2358C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42464071 | |||||||
| chr17:42464597 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.118-1832G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42464597 | |||||||
| chr17:42465026 | T | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(194): Show |
227 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.118-1403T>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42465026 | |||||||
| chr17:42465063 | G | C | 1 | a0001c0001t0004g0014 | 2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.118-1366G>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42465063 | |||||||
| chr17:42465194 | ATGT | A | 9 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0209 others(6): Show |
9 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.118-1231_118-1229d others(5): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 42465194 | ||||||
| chr17:42465224 | G | A | 6 | a0001c0001t0001g0027 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.118-1205G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42465224 | |||||||
| chr17:42465284 | G | A | 4 | a0001c0001t0003g0017 a0001c0001t0003g0079 a0001c0001t0003g0108 others(1): Show |
5 | HG02257.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-1145G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42465284 | |||||||
| chr17:42465579 | C | T | 1 | a0001c0003t0001g0137 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.118-850C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42465579 | |||||||
| chr17:42465802 | A | G | 1 | a0001c0001t0016g0148 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.118-627A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42465802 | |||||||
| chr17:42465812 | G | A | 1 | a0001c0001t0002g0109 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.118-617G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42465812 | |||||||
| chr17:42465977 | A | G | 1 | a0001c0001t0007g0091 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.118-452A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42465977 | |||||||
| chr17:42466233 | C | T | 55 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(52): Show |
60 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.118-196C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 2/21 | chr17 | 42466233 | |||||||
| chr17:42467066 | G | C | 4 | a0001c0001t0003g0017 a0001c0001t0003g0079 a0001c0001t0003g0108 others(1): Show |
5 | HG02257.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+559G>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 3/21 | chr17 | 42467066 | |||||||
| chr17:42467071 | C | T | 3 | a0001c0001t0002g0089 a0001c0001t0002g0136 a0001c0001t0016g0148 |
3 | HG04199.hp1 NA18997.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.196+564C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 3/21 | chr17 | 42467071 | |||||||
| chr17:42467146 | CA | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(255): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.196+652delA | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr17 | 42467146 | ||||||
| chr17:42467320 | A | G | 1 | a0001c0001t0011g0100 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.197-690A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 3/21 | chr17 | 42467320 | |||||||
| chr17:42467802 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.197-208G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 3/21 | chr17 | 42467802 | |||||||
| chr17:42467874 | T | TTA | 54 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0018 others(51): Show |
61 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.197-123_197-122dup others(2): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr17 | 42467874 | ||||||
| chr17:42467910 | C | A | 2 | a0001c0001t0001g0196 a0001c0001t0001g0223 |
2 | HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.197-100C>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 3/21 | chr17 | 42467910 | |||||||
| chr17:42468311 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.294+204T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 4/21 | chr17 | 42468311 | |||||||
| chr17:42468606 | T | C | 1 | a0001c0009t0001g0192 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.294+499T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 4/21 | chr17 | 42468606 | |||||||
| chr17:42468843 | C | CTATTT | 8 | a0001c0001t0001g0027 a0001c0001t0001g0149 a0001c0001t0001g0150 others(5): Show |
8 | HG00642.hp1 HG01361.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.294+758_294+762dup others(5): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr17 | 42468843 | ||||||
| chr17:42468843 | CTATTT | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(76): Show |
94 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.294+758_294+762del others(5): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr17 | 42468843 | ||||||
| chr17:42469071 | C | T | 3 | a0001c0001t0003g0013 a0001c0001t0003g0033 a0001c0001t0003g0040 |
4 | HG01243.hp1 HG02451.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+964C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 4/21 | chr17 | 42469071 | |||||||
| chr17:42469149 | A | G | 1 | a0001c0001t0011g0100 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.295-941A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 4/21 | chr17 | 42469149 | |||||||
| chr17:42469241 | G | GAAAGTTA others(6): Show |
1 | a0001c0001t0001g0211 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.295-847_295-835dup others(13): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr17 | 42469241 | ||||||
| chr17:42469323 | C | CT | 33 | a0001c0001t0001g0041 a0001c0001t0001g0046 a0001c0001t0001g0047 others(30): Show |
33 | HG01106.hp2 HG01175.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.295-743dupT | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr17 | 42469323 | ||||||
| chr17:42469323 | C | CTT | 8 | a0001c0001t0004g0014 a0001c0001t0004g0015 a0001c0001t0004g0068 others(5): Show |
10 | HG02258.hp1 HG02451.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.295-744_295-743dup others(2): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr17 | 42469323 | ||||||
| chr17:42469323 | CT | C | 51 | a0001c0001t0001g0050 a0001c0001t0001g0262 a0001c0001t0002g0006 others(48): Show |
59 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.295-743delT | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr17 | 42469323 | ||||||
| chr17:42469416 | C | T | 1 | a0001c0001t0011g0100 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.295-674C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 4/21 | chr17 | 42469416 | |||||||
| chr17:42469524 | G | A | 1 | a0001c0001t0005g0170 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.295-566G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 4/21 | chr17 | 42469524 | |||||||
| chr17:42469830 | C | T | 1 | a0001c0001t0016g0148 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.295-260C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 4/21 | chr17 | 42469830 | |||||||
| chr17:42470255 | A | T | 1 | a0001c0001t0001g0255 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.423+37A>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42470255 | |||||||
| chr17:42470457 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.423+239A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42470457 | |||||||
| chr17:42470520 | G | A | 4 | a0001c0002t0001g0140 a0001c0002t0001g0141 a0001c0002t0001g0142 others(1): Show |
4 | HG00323.hp2 HG00642.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.423+302G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42470520 | |||||||
| chr17:42470735 | A | T | 1 | a0001c0001t0001g0211 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.423+517A>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42470735 | |||||||
| chr17:42470737 | T | G | 1 | a0001c0001t0001g0211 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.423+519T>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42470737 | |||||||
| chr17:42470764 | G | A | 1 | a0001c0001t0011g0100 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.423+546G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42470764 | |||||||
| chr17:42470894 | A | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(88): Show |
106 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.423+676A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42470894 | |||||||
| chr17:42470950 | C | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0214 a0001c0001t0001g0251 others(3): Show |
8 | HG01099.hp1 HG01169.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.423+732C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42470950 | |||||||
| chr17:42470973 | A | G | 55 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0018 others(52): Show |
62 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.423+755A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42470973 | |||||||
| chr17:42470980 | G | A | 1 | a0001c0003t0001g0137 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.423+762G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42470980 | |||||||
| chr17:42471256 | T | TA | 55 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0018 others(52): Show |
62 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.423+1045dupA | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 42471256 | ||||||
| chr17:42471349 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.423+1131G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42471349 | |||||||
| chr17:42471421 | C | CA | 35 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0044 others(32): Show |
38 | HG00140.hp1 HG00639.hp1 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.423+1221dupA | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 42471421 | ||||||
| chr17:42471421 | CA | C | 60 | a0001c0001t0001g0169 a0001c0001t0001g0211 a0001c0001t0001g0250 others(57): Show |
68 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.423+1221delA | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 42471421 | ||||||
| chr17:42471524 | A | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(89): Show |
107 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.423+1306A>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42471524 | |||||||
| chr17:42471878 | C | A | 1 | a0001c0001t0002g0111 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.423+1660C>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42471878 | |||||||
| chr17:42471948 | C | T | 1 | a0001c0001t0015g0097 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.423+1730C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42471948 | |||||||
| chr17:42471996 | C | A | 3 | a0001c0001t0007g0016 a0001c0001t0007g0090 a0001c0001t0007g0091 |
4 | HG02809.hp2 HG02818.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.423+1778C>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42471996 | |||||||
| chr17:42472051 | C | CT | 156 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(153): Show |
178 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.423+1850dupT | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 42472051 | ||||||
| chr17:42472051 | C | CTT | 6 | a0001c0001t0001g0028 a0001c0001t0001g0168 a0001c0001t0001g0171 others(3): Show |
6 | HG01074.hp1 HG01175.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.423+1849_423+1850d others(4): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 42472051 | ||||||
| chr17:42472052 | T | C | 1 | a0001c0001t0002g0080 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.423+1834T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42472052 | |||||||
| chr17:42472068 | T | C | 1 | a0001c0001t0004g0068 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.423+1850T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42472068 | |||||||
| chr17:42472214 | C | T | 3 | a0001c0001t0007g0016 a0001c0001t0007g0090 a0001c0001t0007g0091 |
4 | HG02809.hp2 HG02818.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.423+1996C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42472214 | |||||||
| chr17:42472450 | C | T | 2 | a0001c0001t0003g0030 a0001c0001t0003g0037 |
2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.423+2232C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42472450 | |||||||
| chr17:42472583 | G | C | 1 | a0001c0001t0001g0230 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.423+2365G>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42472583 | |||||||
| chr17:42472592 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.423+2374C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42472592 | |||||||
| chr17:42472593 | G | A | 4 | a0001c0001t0003g0017 a0001c0001t0003g0079 a0001c0001t0003g0108 others(1): Show |
5 | HG02257.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.423+2375G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42472593 | |||||||
| chr17:42472638 | C | T | 54 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(51): Show |
59 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.423+2420C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42472638 | |||||||
| chr17:42472647 | C | T | 1 | a0001c0001t0007g0094 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.423+2429C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42472647 | |||||||
| chr17:42472702 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.423+2484C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42472702 | |||||||
| chr17:42473071 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.423+2853G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42473071 | |||||||
| chr17:42473074 | A | G | 1 | a0001c0001t0001g0211 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.423+2856A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42473074 | |||||||
| chr17:42473158 | C | T | 4 | a0001c0001t0003g0017 a0001c0001t0003g0079 a0001c0001t0003g0108 others(1): Show |
5 | HG02257.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.423+2940C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42473158 | |||||||
| chr17:42473217 | G | A | 3 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0003t0001g0137 |
3 | HG02145.hp2 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.423+2999G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42473217 | |||||||
| chr17:42473310 | C | T | 1 | a0001c0001t0001g0220 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.423+3092C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42473310 | |||||||
| chr17:42473393 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.423+3175C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42473393 | |||||||
| chr17:42473578 | A | T | 1 | a0001c0001t0001g0071 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.423+3360A>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42473578 | |||||||
| chr17:42473747 | C | T | 4 | a0001c0001t0003g0017 a0001c0001t0003g0079 a0001c0001t0003g0108 others(1): Show |
5 | HG02257.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.423+3529C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42473747 | |||||||
| chr17:42473817 | G | T | 4 | a0001c0001t0007g0016 a0001c0001t0007g0090 a0001c0001t0007g0091 others(1): Show |
5 | HG02809.hp2 HG02818.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.423+3599G>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42473817 | |||||||
| chr17:42473859 | T | C | 1 | a0001c0001t0016g0148 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.423+3641T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42473859 | |||||||
| chr17:42473985 | TG | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0050 a0001c0001t0001g0051 others(1): Show |
4 | HG03195.hp2 HG03471.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.424-3671delG | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 42473985 | ||||||
| chr17:42474006 | A | AT | 7 | a0001c0001t0001g0165 a0001c0001t0001g0210 a0001c0001t0001g0260 others(4): Show |
7 | HG02055.hp2 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.424-3640dupT | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 42474006 | ||||||
| chr17:42474034 | G | A | 4 | a0001c0001t0003g0017 a0001c0001t0003g0079 a0001c0001t0003g0108 others(1): Show |
5 | HG02257.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.424-3626G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42474034 | |||||||
| chr17:42474088 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.424-3572C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42474088 | |||||||
| chr17:42474105 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.424-3555C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42474105 | |||||||
| chr17:42474305 | C | T | 1 | a0001c0002t0001g0143 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.424-3355C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42474305 | |||||||
| chr17:42474324 | C | CT | 11 | a0001c0001t0001g0154 a0001c0001t0001g0196 a0001c0001t0001g0197 others(8): Show |
11 | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.424-3323dupT | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr17 | 42474324 | ||||||
| chr17:42474425 | G | A | 4 | a0001c0001t0007g0016 a0001c0001t0007g0090 a0001c0001t0007g0091 others(1): Show |
5 | HG02809.hp2 HG02818.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.424-3235G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42474425 | |||||||
| chr17:42474438 | A | T | 1 | a0001c0001t0002g0188 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.424-3222A>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42474438 | |||||||
| chr17:42474501 | G | A | 1 | a0001c0001t0016g0148 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.424-3159G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42474501 | |||||||
| chr17:42474589 | G | A | 7 | a0001c0001t0002g0007 a0001c0001t0002g0081 a0001c0001t0002g0112 others(4): Show |
9 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.424-3071G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42474589 | |||||||
| chr17:42474751 | A | G | 7 | a0001c0001t0002g0020 a0001c0001t0002g0086 a0001c0001t0002g0128 others(4): Show |
8 | NA18962.hp2 NA18968.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.424-2909A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42474751 | |||||||
| chr17:42474833 | T | C | 1 | a0001c0001t0016g0148 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.424-2827T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42474833 | |||||||
| chr17:42475127 | T | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0053 a0001c0001t0001g0074 |
3 | HG01074.hp2 HG01433.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.424-2533T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42475127 | |||||||
| chr17:42475266 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.424-2394A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42475266 | |||||||
| chr17:42475504 | A | G | 1 | a0001c0002t0001g0143 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.424-2156A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42475504 | |||||||
| chr17:42475627 | C | A | 1 | a0001c0001t0001g0231 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.424-2033C>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42475627 | |||||||
| chr17:42475702 | G | A | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.424-1958G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42475702 | |||||||
| chr17:42475785 | T | C | 1 | a0001c0001t0012g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.424-1875T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42475785 | |||||||
| chr17:42476071 | G | T | 1 | a0001c0001t0001g0063 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.424-1589G>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42476071 | |||||||
| chr17:42476192 | A | G | 1 | a0001c0001t0016g0148 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.424-1468A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42476192 | |||||||
| chr17:42476692 | C | T | 4 | a0001c0001t0003g0030 a0001c0001t0003g0037 a0001c0001t0008g0032 others(1): Show |
4 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.424-968C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42476692 | |||||||
| chr17:42477060 | C | T | 1 | a0001c0009t0001g0192 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.424-600C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42477060 | |||||||
| chr17:42477245 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.424-415T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42477245 | |||||||
| chr17:42477328 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.424-332G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42477328 | |||||||
| chr17:42477564 | A | G | 2 | a0001c0001t0001g0154 a0001c0001t0001g0187 |
2 | HG01192.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.424-96A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42477564 | |||||||
| chr17:42477570 | C | T | 1 | a0001c0001t0003g0035 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.424-90C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 5/21 | chr17 | 42477570 | |||||||
| chr17:42477765 | G | A | 3 | a0001c0001t0007g0016 a0001c0001t0007g0090 a0001c0001t0007g0091 |
4 | HG02809.hp2 HG02818.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.506+23G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 6/21 | chr17 | 42477765 | |||||||
| chr17:42477783 | G | A | 1 | a0001c0001t0016g0148 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.506+41G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 6/21 | chr17 | 42477783 | |||||||
| chr17:42478218 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.507-245G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 6/21 | chr17 | 42478218 | |||||||
| chr17:42478225 | G | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0067 |
2 | HG02698.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.507-238G>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 6/21 | chr17 | 42478225 | |||||||
| chr17:42478368 | G | GAT | 7 | a0001c0001t0001g0023 a0001c0001t0001g0095 a0001c0001t0001g0096 others(4): Show |
8 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.507-85_507-84dupTA | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr17 | 42478368 | ||||||
| chr17:42478805 | A | G | 1 | a0001c0001t0006g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.633+216A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 7/21 | chr17 | 42478805 | |||||||
| chr17:42478928 | T | TA | 6 | a0001c0001t0001g0046 a0001c0001t0001g0055 a0001c0001t0001g0062 others(3): Show |
6 | HG02698.hp1 HG02738.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.633+339_633+340ins others(1): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 7/21 | chr17 | 42478928 | |||||||
| chr17:42479030 | C | T | 2 | a0001c0001t0004g0015 a0001c0001t0004g0075 |
3 | HG02451.hp1 HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.633+441C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 7/21 | chr17 | 42479030 | |||||||
| chr17:42479693 | G | A | 2 | a0001c0001t0005g0098 a0001c0001t0005g0176 |
2 | NA18982.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.634-974G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 7/21 | chr17 | 42479693 | |||||||
| chr17:42479705 | G | A | 1 | a0001c0003t0001g0137 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.634-962G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 7/21 | chr17 | 42479705 | |||||||
| chr17:42479750 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.634-917A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 7/21 | chr17 | 42479750 | |||||||
| chr17:42479821 | G | C | 2 | a0001c0001t0001g0199 a0001c0001t0001g0222 |
2 | HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.634-846G>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 7/21 | chr17 | 42479821 | |||||||
| chr17:42479831 | T | A | 1 | a0001c0001t0006g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.634-836T>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 7/21 | chr17 | 42479831 | |||||||
| chr17:42479877 | A | T | 1 | a0001c0001t0009g0078 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.634-790A>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 7/21 | chr17 | 42479877 | |||||||
| chr17:42479927 | G | A | 3 | a0001c0001t0007g0016 a0001c0001t0007g0090 a0001c0001t0007g0091 |
4 | HG02809.hp2 HG02818.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.634-740G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 7/21 | chr17 | 42479927 | |||||||
| chr17:42480090 | T | G | 1 | a0001c0009t0001g0192 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.634-577T>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 7/21 | chr17 | 42480090 | |||||||
| chr17:42480252 | C | T | 2 | a0001c0001t0002g0127 a0001c0001t0002g0133 |
2 | HG02615.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.634-415C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 7/21 | chr17 | 42480252 | |||||||
| chr17:42480343 | C | T | 1 | a0001c0001t0005g0170 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.634-324C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 7/21 | chr17 | 42480343 | |||||||
| chr17:42480491 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.634-176C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 7/21 | chr17 | 42480491 | |||||||
| chr17:42480873 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.716+124G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 8/21 | chr17 | 42480873 | |||||||
| chr17:42480947 | G | C | 3 | a0001c0001t0002g0106 a0001c0001t0002g0115 a0001c0001t0002g0145 |
3 | HG02129.hp2 NA18940.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.716+198G>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 8/21 | chr17 | 42480947 | |||||||
| chr17:42481341 | G | A | 1 | a0001c0001t0016g0148 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.716+592G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 8/21 | chr17 | 42481341 | |||||||
| chr17:42481341 | G | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(87): Show |
105 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.716+592G>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 8/21 | chr17 | 42481341 | |||||||
| chr17:42481344 | T | G | 1 | a0001c0001t0002g0188 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.716+595T>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 8/21 | chr17 | 42481344 | |||||||
| chr17:42481584 | C | T | 1 | a0001c0001t0001g0247 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.716+835C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 8/21 | chr17 | 42481584 | |||||||
| chr17:42481712 | A | G | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG00323.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.716+963A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 8/21 | chr17 | 42481712 | |||||||
| chr17:42481967 | G | A | 54 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0018 others(51): Show |
61 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.717-1071G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 8/21 | chr17 | 42481967 | |||||||
| chr17:42482154 | G | A | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(193): Show |
226 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.717-884G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 8/21 | chr17 | 42482154 | |||||||
| chr17:42482195 | A | G | 2 | a0001c0001t0004g0014 a0001c0001t0004g0069 |
3 | HG02258.hp1 HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.717-843A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 8/21 | chr17 | 42482195 | |||||||
| chr17:42482221 | ACTGCAGC others(9): Show |
A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0064 |
5 | HG02559.hp2 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.717-813_717-798del others(16): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr17 | 42482221 | ||||||
| chr17:42482386 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.717-652A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 8/21 | chr17 | 42482386 | |||||||
| chr17:42482421 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.717-617A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 8/21 | chr17 | 42482421 | |||||||
| chr17:42482623 | A | G | 1 | a0001c0001t0001g0245 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.717-415A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 8/21 | chr17 | 42482623 | |||||||
| chr17:42482822 | A | G | 3 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0003t0001g0137 |
3 | HG02145.hp2 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.717-216A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 8/21 | chr17 | 42482822 | |||||||
| chr17:42482850 | C | T | 5 | a0001c0001t0001g0061 a0001c0001t0007g0016 a0001c0001t0007g0090 others(2): Show |
6 | HG02683.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.717-188C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 8/21 | chr17 | 42482850 | |||||||
| chr17:42482855 | C | T | 2 | a0001c0001t0002g0114 a0001c0001t0002g0132 |
2 | HG00741.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.717-183C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 8/21 | chr17 | 42482855 | |||||||
| chr17:42482895 | C | CA | 20 | a0001c0001t0001g0028 a0001c0001t0001g0048 a0001c0001t0001g0066 others(17): Show |
21 | HG00741.hp1 HG01175.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.717-122dupA | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr17 | 42482895 | ||||||
| chr17:42482895 | CA | C | 55 | a0001c0001t0001g0003 a0001c0001t0001g0064 a0001c0001t0001g0207 others(52): Show |
65 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.717-122delA | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr17 | 42482895 | ||||||
| chr17:42482975 | G | C | 1 | a0001c0001t0006g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.717-63G>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 8/21 | chr17 | 42482975 | |||||||
| chr17:42483383 | C | T | 26 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0044 others(23): Show |
29 | HG00140.hp1 HG00639.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.810+252C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | chr17 | 42483383 | |||||||
| chr17:42483411 | A | AT | 9 | a0001c0001t0001g0060 a0001c0001t0004g0076 a0001c0001t0007g0016 others(6): Show |
10 | HG00323.hp2 HG00642.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.810+294dupT | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr17 | 42483411 | ||||||
| chr17:42483494 | G | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(194): Show |
227 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.810+363G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | chr17 | 42483494 | |||||||
| chr17:42483625 | A | C | 1 | a0001c0001t0001g0191 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.810+494A>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | chr17 | 42483625 | |||||||
| chr17:42483684 | C | T | 1 | a0001c0002t0001g0140 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.810+553C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | chr17 | 42483684 | |||||||
| chr17:42483716 | G | T | 1 | a0001c0001t0006g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.810+585G>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | chr17 | 42483716 | |||||||
| chr17:42483754 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0101 a0001c0001t0001g0172 |
5 | NA18964.hp1 NA18999.hp2 NA19067.hp2 others(2): Show |
intron_variant | MODIFIER | c.810+623G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | chr17 | 42483754 | |||||||
| chr17:42483937 | T | G | 1 | a0001c0001t0001g0252 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.810+806T>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | chr17 | 42483937 | |||||||
| chr17:42484108 | A | G | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.810+977A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | chr17 | 42484108 | |||||||
| chr17:42484150 | C | T | 45 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(42): Show |
55 | HG00140.hp1 HG00639.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.810+1019C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | chr17 | 42484150 | |||||||
| chr17:42484157 | A | G | 2 | a0001c0001t0011g0100 a0001c0001t0012g0180 |
2 | HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.810+1026A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | chr17 | 42484157 | |||||||
| chr17:42484217 | C | T | 1 | a0001c0009t0001g0192 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.810+1086C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | chr17 | 42484217 | |||||||
| chr17:42484258 | C | T | 1 | a0001c0001t0014g0219 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.810+1127C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | chr17 | 42484258 | |||||||
| chr17:42484634 | C | T | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.810+1503C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | chr17 | 42484634 | |||||||
| chr17:42484670 | A | G | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG01123.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.810+1539A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | chr17 | 42484670 | |||||||
| chr17:42484839 | TTTCTTTT others(6): Show |
T | 1 | a0001c0003t0001g0137 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.810+1711_810+1723d others(15): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr17 | 42484839 | ||||||
| chr17:42484852 | CT | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(249): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.810+1736delT | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr17 | 42484852 | ||||||
| chr17:42484853 | T | C | 1 | a0001c0003t0001g0137 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.810+1722T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | chr17 | 42484853 | |||||||
| chr17:42484931 | C | T | 1 | a0001c0001t0002g0111 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.810+1800C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | chr17 | 42484931 | |||||||
| chr17:42484953 | A | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.810+1822A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | chr17 | 42484953 | |||||||
| chr17:42484959 | C | T | 4 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0033 others(1): Show |
6 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.810+1828C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | chr17 | 42484959 | |||||||
| chr17:42485108 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.810+1977C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | chr17 | 42485108 | |||||||
| chr17:42485185 | A | G | 1 | a0001c0001t0006g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.811-1970A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | chr17 | 42485185 | |||||||
| chr17:42485347 | T | C | 3 | a0001c0001t0007g0016 a0001c0001t0007g0090 a0001c0001t0007g0091 |
4 | HG02809.hp2 HG02818.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.811-1808T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | chr17 | 42485347 | |||||||
| chr17:42485530 | GT | G | 20 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0027 others(17): Show |
22 | HG00438.hp1 HG00597.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.811-1621delT | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr17 | 42485530 | ||||||
| chr17:42485539 | G | GTTTGT | 59 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0018 others(56): Show |
67 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.811-1587_811-1583d others(7): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr17 | 42485539 | ||||||
| chr17:42485539 | G | GTTTGTTT others(3): Show |
1 | a0001c0001t0016g0148 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.811-1592_811-1583d others(12): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr17 | 42485539 | ||||||
| chr17:42485539 | GTTTGT | G | 4 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0013g0117 others(1): Show |
4 | HG02145.hp2 HG02630.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.811-1587_811-1583d others(7): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr17 | 42485539 | ||||||
| chr17:42485539 | GTTTGTTT others(3): Show |
G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0223 |
2 | HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.811-1592_811-1583d others(12): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr17 | 42485539 | ||||||
| chr17:42485643 | C | T | 1 | a0001c0001t0002g0131 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.811-1512C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | chr17 | 42485643 | |||||||
| chr17:42486052 | T | C | 1 | a0001c0001t0001g0270 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.811-1103T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | chr17 | 42486052 | |||||||
| chr17:42486135 | G | A | 4 | a0001c0002t0001g0140 a0001c0002t0001g0141 a0001c0002t0001g0142 others(1): Show |
4 | HG00323.hp2 HG00642.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.811-1020G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | chr17 | 42486135 | |||||||
| chr17:42486223 | C | G | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.811-932C>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | chr17 | 42486223 | |||||||
| chr17:42486280 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.811-875G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | chr17 | 42486280 | |||||||
| chr17:42486281 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.811-874C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | chr17 | 42486281 | |||||||
| chr17:42486452 | G | GTAAAATG others(1): Show |
3 | a0001c0001t0001g0027 a0001c0001t0001g0150 a0001c0001t0001g0153 |
3 | HG03139.hp1 HG03540.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.811-701_811-694dup others(8): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr17 | 42486452 | ||||||
| chr17:42486555 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.811-600C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | chr17 | 42486555 | |||||||
| chr17:42486699 | G | C | 1 | a0001c0001t0002g0133 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.811-456G>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | chr17 | 42486699 | |||||||
| chr17:42486807 | A | G | 5 | a0001c0001t0001g0023 a0001c0001t0001g0096 a0001c0001t0001g0163 others(2): Show |
6 | HG02559.hp1 HG02615.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.811-348A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 9/21 | chr17 | 42486807 | |||||||
| chr17:42487396 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1023+29C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 10/21 | chr17 | 42487396 | |||||||
| chr17:42487404 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(76): Show |
94 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1023+37G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 10/21 | chr17 | 42487404 | |||||||
| chr17:42487584 | C | T | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1023+217C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 10/21 | chr17 | 42487584 | |||||||
| chr17:42487589 | G | A | 6 | a0001c0001t0003g0029 a0001c0001t0003g0035 a0001c0001t0006g0004 others(3): Show |
8 | HG01109.hp2 HG01891.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1023+222G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 10/21 | chr17 | 42487589 | |||||||
| chr17:42487684 | C | T | 1 | a0001c0003t0001g0137 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1023+317C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 10/21 | chr17 | 42487684 | |||||||
| chr17:42487738 | A | T | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(256): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1023+371A>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 10/21 | chr17 | 42487738 | |||||||
| chr17:42487758 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1023+391A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 10/21 | chr17 | 42487758 | |||||||
| chr17:42488048 | A | C | 1 | a0001c0001t0001g0051 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1023+681A>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 10/21 | chr17 | 42488048 | |||||||
| chr17:42488195 | G | A | 1 | a0001c0001t0016g0148 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1023+828G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 10/21 | chr17 | 42488195 | |||||||
| chr17:42488517 | G | T | 3 | a0001c0001t0002g0006 a0001c0001t0002g0110 a0001c0001t0002g0144 |
5 | HG00735.hp2 HG02109.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1023+1150G>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 10/21 | chr17 | 42488517 | |||||||
| chr17:42488633 | G | T | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | NA18612.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.1023+1266G>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 10/21 | chr17 | 42488633 | |||||||
| chr17:42488805 | G | T | 1 | a0001c0009t0001g0192 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1023+1438G>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 10/21 | chr17 | 42488805 | |||||||
| chr17:42488971 | T | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1024-1516T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 10/21 | chr17 | 42488971 | |||||||
| chr17:42488972 | G | T | 1 | a0001c0001t0002g0147 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1024-1515G>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 10/21 | chr17 | 42488972 | |||||||
| chr17:42488985 | A | G | 54 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0018 others(51): Show |
61 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.1024-1502A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 10/21 | chr17 | 42488985 | |||||||
| chr17:42489005 | ACT | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(194): Show |
227 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.1024-1479_1024-147 others(6): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr17 | 42489005 | ||||||
| chr17:42489014 | C | CA | 13 | a0001c0001t0001g0102 a0001c0001t0001g0167 a0001c0001t0001g0196 others(10): Show |
13 | HG01243.hp1 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1024-1458dupA | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr17 | 42489014 | ||||||
| chr17:42489076 | G | GT | 38 | a0001c0001t0001g0027 a0001c0001t0001g0059 a0001c0001t0001g0066 others(35): Show |
38 | HG00597.hp2 HG01361.hp2 HG01517.hp2 others(35): Show |
intron_variant | MODIFIER | c.1024-1398dupT | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr17 | 42489076 | ||||||
| chr17:42489154 | C | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(71): Show |
89 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1024-1333C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 10/21 | chr17 | 42489154 | |||||||
| chr17:42489303 | A | G | 1 | a0001c0001t0002g0129 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1024-1184A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 10/21 | chr17 | 42489303 | |||||||
| chr17:42489493 | AATG | A | 58 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0018 others(55): Show |
66 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.1024-991_1024-989d others(5): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr17 | 42489493 | ||||||
| chr17:42489604 | GAA | G | 4 | a0001c0001t0007g0016 a0001c0001t0007g0090 a0001c0001t0007g0091 others(1): Show |
5 | HG02809.hp2 HG02818.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1024-881_1024-880d others(4): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr17 | 42489604 | ||||||
| chr17:42490355 | T | C | 3 | a0001c0001t0007g0016 a0001c0001t0007g0090 a0001c0001t0007g0091 |
4 | HG02809.hp2 HG02818.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024-132T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 10/21 | chr17 | 42490355 | |||||||
| chr17:42490381 | A | C | 1 | a0001c0001t0001g0214 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1024-106A>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 10/21 | chr17 | 42490381 | |||||||
| chr17:42490434 | T | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(258): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1024-53T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 10/21 | chr17 | 42490434 | |||||||
| chr17:42490476 | A | C | 1 | a0001c0001t0001g0058 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1024-11A>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 10/21 | chr17 | 42490476 | |||||||
| chr17:42490834 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1174+197G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42490834 | |||||||
| chr17:42490929 | G | A | 1 | a0001c0009t0001g0192 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1174+292G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42490929 | |||||||
| chr17:42491077 | A | C | 1 | a0001c0009t0001g0192 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1174+440A>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42491077 | |||||||
| chr17:42491197 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1174+560A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42491197 | |||||||
| chr17:42491200 | A | G | 3 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 |
3 | HG01884.hp2 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1174+563A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42491200 | |||||||
| chr17:42491307 | A | T | 1 | a0001c0001t0001g0179 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1174+670A>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42491307 | |||||||
| chr17:42491342 | G | A | 2 | a0001c0001t0002g0127 a0001c0001t0002g0133 |
2 | HG02615.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1174+705G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42491342 | |||||||
| chr17:42491579 | G | A | 3 | a0001c0001t0007g0016 a0001c0001t0007g0090 a0001c0001t0007g0091 |
4 | HG02809.hp2 HG02818.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174+942G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42491579 | |||||||
| chr17:42491683 | A | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1174+1046A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42491683 | |||||||
| chr17:42491725 | T | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0205 a0005c0004t0001g0024 |
3 | HG00597.hp2 HG03239.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1174+1088T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42491725 | |||||||
| chr17:42491726 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0205 a0005c0004t0001g0024 |
3 | HG00597.hp2 HG03239.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1174+1089G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42491726 | |||||||
| chr17:42491728 | C | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0205 a0005c0004t0001g0024 |
3 | HG00597.hp2 HG03239.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1174+1091C>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42491728 | |||||||
| chr17:42491735 | T | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0205 a0005c0004t0001g0024 |
3 | HG00597.hp2 HG03239.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1174+1098T>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42491735 | |||||||
| chr17:42491743 | C | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0205 a0005c0004t0001g0024 |
3 | HG00597.hp2 HG03239.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1174+1106C>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42491743 | |||||||
| chr17:42492046 | C | T | 53 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0018 others(50): Show |
60 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1174+1409C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42492046 | |||||||
| chr17:42492230 | T | G | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.1174+1593T>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42492230 | |||||||
| chr17:42492277 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1174+1640G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42492277 | |||||||
| chr17:42492324 | A | G | 2 | a0001c0001t0011g0100 a0001c0001t0012g0180 |
2 | HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1174+1687A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42492324 | |||||||
| chr17:42492444 | C | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0050 a0001c0001t0001g0051 others(1): Show |
4 | HG03195.hp2 HG03471.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174+1807C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42492444 | |||||||
| chr17:42492535 | C | A | 4 | a0001c0001t0003g0030 a0001c0001t0003g0037 a0001c0001t0008g0032 others(1): Show |
4 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1175-1799C>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42492535 | |||||||
| chr17:42492551 | A | C | 55 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0018 others(52): Show |
62 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1175-1783A>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42492551 | |||||||
| chr17:42492579 | G | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0187 |
2 | HG01192.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1175-1755G>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42492579 | |||||||
| chr17:42492593 | C | T | 45 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(42): Show |
55 | HG00140.hp1 HG00639.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1175-1741C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42492593 | |||||||
| chr17:42492599 | G | A | 2 | a0001c0001t0004g0014 a0001c0001t0004g0069 |
3 | HG02258.hp1 HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1175-1735G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42492599 | |||||||
| chr17:42492612 | A | G | 2 | a0001c0001t0001g0210 a0001c0001t0001g0261 |
2 | HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1175-1722A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42492612 | |||||||
| chr17:42492656 | A | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0044 others(17): Show |
23 | HG00140.hp1 HG00639.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.1175-1678A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42492656 | |||||||
| chr17:42492706 | CA | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(240): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1175-1608delA | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr17 | 42492706 | ||||||
| chr17:42492733 | C | T | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1175-1601C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42492733 | |||||||
| chr17:42492789 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(258): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1175-1545A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42492789 | |||||||
| chr17:42492803 | G | A | 4 | a0001c0001t0002g0083 a0001c0001t0002g0093 a0001c0001t0002g0119 others(1): Show |
4 | NA18941.hp1 NA18956.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.1175-1531G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42492803 | |||||||
| chr17:42492941 | C | G | 1 | a0001c0001t0001g0160 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1175-1393C>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42492941 | |||||||
| chr17:42493027 | G | A | 4 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0033 others(1): Show |
6 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.1175-1307G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42493027 | |||||||
| chr17:42493093 | C | A | 1 | a0001c0001t0001g0155 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1175-1241C>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42493093 | |||||||
| chr17:42493199 | A | T | 2 | a0001c0001t0005g0098 a0001c0001t0005g0176 |
2 | NA18982.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1175-1135A>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42493199 | |||||||
| chr17:42493456 | A | G | 1 | a0001c0009t0001g0192 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1175-878A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42493456 | |||||||
| chr17:42493509 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1175-825A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42493509 | |||||||
| chr17:42493780 | C | T | 1 | a0001c0001t0002g0133 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1175-554C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42493780 | |||||||
| chr17:42493941 | A | G | 3 | a0001c0001t0001g0207 a0001c0001t0001g0266 a0001c0001t0001g0274 |
3 | HG00639.hp2 HG01081.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.1175-393A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42493941 | |||||||
| chr17:42494010 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1175-324G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42494010 | |||||||
| chr17:42494039 | C | T | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1175-295C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 11/21 | chr17 | 42494039 | |||||||
| chr17:42494600 | A | G | 6 | a0001c0001t0001g0196 a0001c0001t0001g0209 a0001c0001t0001g0223 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1314+127A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 12/21 | chr17 | 42494600 | |||||||
| chr17:42494683 | G | C | 1 | a0001c0001t0001g0057 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1314+210G>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 12/21 | chr17 | 42494683 | |||||||
| chr17:42494785 | G | A | 46 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(43): Show |
56 | HG00140.hp1 HG00639.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1315-249G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 12/21 | chr17 | 42494785 | |||||||
| chr17:42495381 | T | C | 3 | a0001c0001t0007g0016 a0001c0001t0007g0090 a0001c0001t0007g0091 |
4 | HG02809.hp2 HG02818.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1469+193T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 13/21 | chr17 | 42495381 | |||||||
| chr17:42495822 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1560+106A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42495822 | |||||||
| chr17:42496061 | C | CA | 8 | a0001c0001t0001g0158 a0001c0001t0001g0161 a0001c0001t0002g0111 others(5): Show |
8 | HG00642.hp1 HG01109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1560+365dupA | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr17 | 42496061 | ||||||
| chr17:42496061 | CA | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
162 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1560+365delA | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr17 | 42496061 | ||||||
| chr17:42496078 | A | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(86): Show |
104 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.1560+362A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42496078 | |||||||
| chr17:42496094 | G | C | 8 | a0001c0001t0001g0011 a0001c0001t0001g0207 a0001c0001t0001g0214 others(5): Show |
10 | HG00639.hp2 HG01099.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1560+378G>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42496094 | |||||||
| chr17:42496222 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1560+506G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42496222 | |||||||
| chr17:42496422 | G | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1560+706G>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42496422 | |||||||
| chr17:42496718 | G | T | 1 | a0001c0001t0001g0074 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1560+1002G>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42496718 | |||||||
| chr17:42496756 | C | T | 1 | a0001c0001t0001g0243 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1560+1040C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42496756 | |||||||
| chr17:42496773 | T | C | 55 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0018 others(52): Show |
62 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1560+1057T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42496773 | |||||||
| chr17:42497040 | G | A | 5 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(2): Show |
5 | HG01175.hp2 HG01255.hp2 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.1560+1324G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42497040 | |||||||
| chr17:42497067 | C | T | 4 | a0001c0001t0003g0030 a0001c0001t0003g0037 a0001c0001t0008g0032 others(1): Show |
4 | HG01884.hp1 HG02258.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1560+1351C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42497067 | |||||||
| chr17:42497300 | C | CA | 60 | a0001c0001t0001g0092 a0001c0001t0001g0156 a0001c0001t0001g0161 others(57): Show |
68 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.1561-1603dupA | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr17 | 42497300 | ||||||
| chr17:42497300 | C | CAA | 9 | a0001c0001t0002g0082 a0001c0001t0002g0083 a0001c0001t0002g0084 others(6): Show |
9 | HG00735.hp2 HG02027.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.1560+1604_1561-160 others(6): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr17 | 42497300 | ||||||
| chr17:42497300 | CA | C | 8 | a0001c0001t0001g0064 a0001c0001t0001g0139 a0001c0001t0001g0178 others(5): Show |
8 | HG02630.hp1 HG02965.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1561-1603delA | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr17 | 42497300 | ||||||
| chr17:42497304 | A | AC | 3 | a0001c0001t0007g0016 a0001c0001t0007g0090 a0001c0001t0007g0091 |
4 | HG02809.hp2 HG02818.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1560+1588_1560+158 others(5): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42497304 | |||||||
| chr17:42497342 | G | T | 30 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0028 others(27): Show |
33 | HG00642.hp1 HG01074.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.1561-1582G>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42497342 | |||||||
| chr17:42497455 | G | A | 1 | a0001c0001t0004g0068 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1561-1469G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42497455 | |||||||
| chr17:42497496 | T | C | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1561-1428T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42497496 | |||||||
| chr17:42497545 | G | A | 1 | a0001c0001t0005g0186 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1561-1379G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42497545 | |||||||
| chr17:42497676 | G | GA | 9 | a0001c0001t0001g0021 a0001c0001t0001g0102 a0001c0001t0001g0156 others(6): Show |
10 | HG00438.hp1 HG00597.hp1 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.1561-1234dupA | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr17 | 42497676 | ||||||
| chr17:42497722 | A | G | 3 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0003t0001g0137 |
3 | HG02145.hp2 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1561-1202A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42497722 | |||||||
| chr17:42497727 | A | G | 4 | a0001c0001t0007g0016 a0001c0001t0007g0090 a0001c0001t0007g0091 others(1): Show |
5 | HG02809.hp2 HG02818.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1561-1197A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42497727 | |||||||
| chr17:42497733 | G | T | 1 | a0001c0001t0004g0076 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1561-1191G>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42497733 | |||||||
| chr17:42497764 | G | A | 2 | a0001c0001t0008g0032 a0001c0001t0008g0036 |
2 | HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1561-1160G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42497764 | |||||||
| chr17:42497776 | G | A | 6 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0209 others(3): Show |
6 | HG02717.hp1 HG02896.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1561-1148G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42497776 | |||||||
| chr17:42497918 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1561-1006C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42497918 | |||||||
| chr17:42497942 | G | GA | 4 | a0001c0001t0006g0004 a0001c0001t0006g0031 a0001c0001t0006g0038 others(1): Show |
6 | HG01891.hp1 HG02572.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1561-969dupA | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr17 | 42497942 | ||||||
| chr17:42498008 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1561-916G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42498008 | |||||||
| chr17:42498130 | A | G | 1 | a0001c0002t0001g0142 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1561-794A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42498130 | |||||||
| chr17:42498136 | G | T | 1 | a0001c0001t0002g0124 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1561-788G>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42498136 | |||||||
| chr17:42498404 | C | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(193): Show |
226 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.1561-520C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42498404 | |||||||
| chr17:42498554 | G | A | 1 | a0001c0001t0002g0126 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1561-370G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42498554 | |||||||
| chr17:42498590 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1561-334G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42498590 | |||||||
| chr17:42498645 | T | G | 2 | a0001c0001t0011g0100 a0001c0001t0012g0180 |
2 | HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1561-279T>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42498645 | |||||||
| chr17:42498787 | C | T | 40 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(37): Show |
48 | HG00140.hp1 HG00639.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.1561-137C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42498787 | |||||||
| chr17:42498804 | T | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0025 others(30): Show |
43 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.1561-120T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42498804 | |||||||
| chr17:42498911 | C | G | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1561-13C>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42498911 | |||||||
| chr17:42498911 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1561-13C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 14/21 | chr17 | 42498911 | |||||||
| chr17:42499099 | TA | T | 54 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0018 others(51): Show |
61 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.1679+60delA | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr17 | 42499099 | ||||||
| chr17:42499185 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1679+143G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 15/21 | chr17 | 42499185 | |||||||
| chr17:42499253 | C | T | 1 | a0001c0003t0001g0137 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1679+211C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 15/21 | chr17 | 42499253 | |||||||
| chr17:42499409 | C | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(258): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1679+367C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 15/21 | chr17 | 42499409 | |||||||
| chr17:42499425 | G | A | 1 | a0001c0009t0001g0192 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1679+383G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 15/21 | chr17 | 42499425 | |||||||
| chr17:42499439 | C | A | 1 | a0001c0001t0001g0253 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1679+397C>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 15/21 | chr17 | 42499439 | |||||||
| chr17:42499479 | T | A | 56 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(53): Show |
61 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.1679+437T>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 15/21 | chr17 | 42499479 | |||||||
| chr17:42499483 | T | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0161 |
2 | HG02074.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1679+441T>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 15/21 | chr17 | 42499483 | |||||||
| chr17:42499510 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1679+468G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 15/21 | chr17 | 42499510 | |||||||
| chr17:42499573 | G | C | 3 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0003t0001g0137 |
3 | HG02145.hp2 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1679+531G>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 15/21 | chr17 | 42499573 | |||||||
| chr17:42499707 | G | A | 1 | a0001c0001t0002g0125 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1679+665G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 15/21 | chr17 | 42499707 | |||||||
| chr17:42499787 | C | CA | 7 | a0001c0001t0001g0172 a0001c0001t0001g0224 a0001c0001t0001g0238 others(4): Show |
8 | HG02809.hp2 HG02818.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1679+759dupA | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr17 | 42499787 | ||||||
| chr17:42500004 | G | A | 1 | a0001c0001t0007g0094 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1680-703G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 15/21 | chr17 | 42500004 | |||||||
| chr17:42500066 | C | T | 1 | a0001c0001t0001g0220 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1680-641C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 15/21 | chr17 | 42500066 | |||||||
| chr17:42500074 | C | CA | 30 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0027 others(27): Show |
32 | HG00438.hp1 HG00597.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.1680-613dupA | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr17 | 42500074 | ||||||
| chr17:42500074 | CAAAAAA | C | 54 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0018 others(51): Show |
61 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.1680-618_1680-613d others(8): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr17 | 42500074 | ||||||
| chr17:42500349 | G | A | 1 | a0001c0003t0001g0137 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1680-358G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 15/21 | chr17 | 42500349 | |||||||
| chr17:42500353 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0002g0049 |
2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1680-354G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 15/21 | chr17 | 42500353 | |||||||
| chr17:42500531 | G | A | 1 | a0001c0009t0001g0192 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1680-176G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 15/21 | chr17 | 42500531 | |||||||
| chr17:42500565 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1680-142C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 15/21 | chr17 | 42500565 | |||||||
| chr17:42501013 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1896+90C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 16/21 | chr17 | 42501013 | |||||||
| chr17:42501083 | T | G | 4 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0033 others(1): Show |
6 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.1897-114T>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 16/21 | chr17 | 42501083 | |||||||
| chr17:42501338 | CTTTTG | C | 15 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0201 others(12): Show |
18 | HG00099.hp2 HG00639.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.2004+42_2004+46del others(5): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr17 | 42501338 | ||||||
| chr17:42501516 | G | A | 39 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(36): Show |
47 | HG00140.hp1 HG00639.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.2004+212G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42501516 | |||||||
| chr17:42501634 | C | T | 1 | a0001c0001t0002g0049 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2004+330C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42501634 | |||||||
| chr17:42501635 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2004+331G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42501635 | |||||||
| chr17:42501656 | G | A | 9 | a0001c0001t0001g0154 a0001c0001t0001g0187 a0001c0001t0005g0098 others(6): Show |
9 | HG01192.hp2 HG02738.hp2 HG03704.hp1 others(6): Show |
intron_variant | MODIFIER | c.2004+352G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42501656 | |||||||
| chr17:42501903 | G | A | 1 | a0001c0001t0001g0273 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2004+599G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42501903 | |||||||
| chr17:42501904 | C | T | 1 | a0001c0001t0002g0123 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2004+600C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42501904 | |||||||
| chr17:42501958 | T | C | 3 | a0001c0001t0003g0017 a0001c0001t0003g0079 a0001c0001t0003g0108 |
4 | HG02622.hp2 HG02630.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2004+654T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42501958 | |||||||
| chr17:42502108 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2004+804A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42502108 | |||||||
| chr17:42502494 | G | GCA | 13 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0017 others(10): Show |
16 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.2004+1191_2004+119 others(6): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr17 | 42502494 | ||||||
| chr17:42502494 | G | GCACA | 6 | a0001c0001t0003g0029 a0001c0001t0003g0035 a0001c0001t0006g0004 others(3): Show |
8 | HG01109.hp2 HG01891.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2004+1191_2004+119 others(8): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr17 | 42502494 | ||||||
| chr17:42502495 | C | T | 6 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0209 others(3): Show |
6 | HG02717.hp1 HG02896.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2004+1191C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42502495 | |||||||
| chr17:42502496 | G | A | 73 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0018 others(70): Show |
85 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.2004+1192G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42502496 | |||||||
| chr17:42502496 | G | GCA | 5 | a0001c0001t0004g0076 a0001c0001t0007g0016 a0001c0001t0007g0090 others(2): Show |
6 | HG02809.hp2 HG02818.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.2004+1211_2004+121 others(6): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr17 | 42502496 | ||||||
| chr17:42502498 | A | G | 1 | a0001c0001t0001g0206 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2004+1194A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42502498 | |||||||
| chr17:42502506 | A | G | 20 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0092 others(17): Show |
23 | HG00642.hp1 HG01074.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.2004+1202A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42502506 | |||||||
| chr17:42502740 | T | C | 1 | a0001c0001t0002g0049 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2004+1436T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42502740 | |||||||
| chr17:42502899 | A | G | 3 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0003t0001g0137 |
3 | HG02145.hp2 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2004+1595A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42502899 | |||||||
| chr17:42503434 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2004+2130G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42503434 | |||||||
| chr17:42503603 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0010g0164 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2004+2299C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42503603 | |||||||
| chr17:42503773 | GGTCATCC others(17): Show |
G | 1 | a0001c0001t0001g0203 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2004+2494_2004+251 others(28): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr17 | 42503773 | ||||||
| chr17:42503889 | C | A | 1 | a0001c0001t0001g0238 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2004+2585C>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42503889 | |||||||
| chr17:42503956 | A | T | 1 | a0001c0001t0001g0270 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2004+2652A>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42503956 | |||||||
| chr17:42504025 | T | G | 79 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0018 others(76): Show |
92 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(89): Show |
intron_variant | MODIFIER | c.2004+2721T>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42504025 | |||||||
| chr17:42504420 | A | G | 2 | a0001c0001t0001g0210 a0001c0001t0001g0261 |
2 | HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2005-3100A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42504420 | |||||||
| chr17:42504568 | G | A | 1 | a0001c0001t0002g0115 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2005-2952G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42504568 | |||||||
| chr17:42504827 | T | C | 1 | a0001c0001t0007g0094 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2005-2693T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42504827 | |||||||
| chr17:42505036 | C | CT | 6 | a0001c0001t0001g0182 a0001c0001t0002g0083 a0001c0001t0003g0017 others(3): Show |
7 | HG00438.hp1 HG02257.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2005-2468dupT | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr17 | 42505036 | ||||||
| chr17:42505036 | CT | C | 11 | a0001c0001t0001g0225 a0001c0001t0001g0251 a0001c0001t0002g0007 others(8): Show |
14 | HG00099.hp1 HG00642.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.2005-2468delT | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr17 | 42505036 | ||||||
| chr17:42505083 | T | G | 40 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(37): Show |
48 | HG00140.hp1 HG00639.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.2005-2437T>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42505083 | |||||||
| chr17:42505116 | A | C | 2 | a0001c0001t0002g0085 a0001c0001t0002g0109 |
2 | HG02083.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.2005-2404A>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42505116 | |||||||
| chr17:42505145 | C | T | 2 | a0001c0001t0011g0100 a0001c0001t0012g0180 |
2 | HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2005-2375C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42505145 | |||||||
| chr17:42505315 | C | T | 2 | a0001c0001t0001g0229 a0004c0008t0001g0263 |
2 | HG03831.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.2005-2205C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42505315 | |||||||
| chr17:42505522 | G | T | 49 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0018 others(46): Show |
56 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.2005-1998G>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42505522 | |||||||
| chr17:42505559 | C | T | 62 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(59): Show |
75 | HG00140.hp1 HG00639.hp1 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.2005-1961C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42505559 | |||||||
| chr17:42505737 | A | G | 1 | a0001c0001t0011g0100 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2005-1783A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42505737 | |||||||
| chr17:42505787 | CT | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(74): Show |
92 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.2005-1718delT | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr17 | 42505787 | ||||||
| chr17:42505898 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2005-1622C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42505898 | |||||||
| chr17:42505913 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2005-1607G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42505913 | |||||||
| chr17:42505976 | C | T | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2005-1544C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42505976 | |||||||
| chr17:42506488 | G | A | 1 | a0001c0001t0003g0029 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2005-1032G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42506488 | |||||||
| chr17:42506515 | C | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
59 | HG00140.hp1 HG00639.hp1 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.2005-1005C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42506515 | |||||||
| chr17:42506639 | T | C | 4 | a0001c0001t0007g0016 a0001c0001t0007g0090 a0001c0001t0007g0091 others(1): Show |
5 | HG02809.hp2 HG02818.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.2005-881T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42506639 | |||||||
| chr17:42506642 | C | T | 1 | a0001c0001t0003g0040 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2005-878C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42506642 | |||||||
| chr17:42506665 | T | G | 1 | a0001c0001t0001g0203 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2005-855T>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42506665 | |||||||
| chr17:42506706 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2005-814T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42506706 | |||||||
| chr17:42507078 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2005-442G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42507078 | |||||||
| chr17:42507177 | A | G | 2 | a0001c0001t0008g0032 a0001c0001t0008g0036 |
2 | HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2005-343A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42507177 | |||||||
| chr17:42507198 | A | G | 79 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0018 others(76): Show |
92 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(89): Show |
intron_variant | MODIFIER | c.2005-322A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42507198 | |||||||
| chr17:42507314 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2005-206A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42507314 | |||||||
| chr17:42507390 | A | T | 11 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0200 others(8): Show |
12 | HG00438.hp2 HG00597.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.2005-130A>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 17/21 | chr17 | 42507390 | |||||||
| chr17:42507637 | C | T | 1 | a0001c0001t0002g0088 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2112+10C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 18/21 | chr17 | 42507637 | |||||||
| chr17:42507725 | T | G | 21 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0027 others(18): Show |
23 | HG00438.hp1 HG00597.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.2112+98T>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 18/21 | chr17 | 42507725 | |||||||
| chr17:42507869 | G | A | 1 | a0001c0001t0005g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2112+242G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 18/21 | chr17 | 42507869 | |||||||
| chr17:42507938 | C | G | 3 | a0001c0001t0007g0016 a0001c0001t0007g0090 a0001c0001t0007g0091 |
4 | HG02809.hp2 HG02818.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2112+311C>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 18/21 | chr17 | 42507938 | |||||||
| chr17:42508034 | A | T | 1 | a0001c0001t0001g0225 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2112+407A>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 18/21 | chr17 | 42508034 | |||||||
| chr17:42508350 | G | A | 2 | a0001c0001t0006g0004 a0001c0001t0006g0031 |
4 | HG01891.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2113-222G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 18/21 | chr17 | 42508350 | |||||||
| chr17:42508785 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2130+196G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 19/21 | chr17 | 42508785 | |||||||
| chr17:42509242 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2130+653G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 19/21 | chr17 | 42509242 | |||||||
| chr17:42509669 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2130+1080C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 19/21 | chr17 | 42509669 | |||||||
| chr17:42510044 | AT | A | 20 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0017 others(17): Show |
25 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.2130+1458delT | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr17 | 42510044 | ||||||
| chr17:42510642 | G | A | 1 | a0001c0001t0001g0023 | 2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2130+2053G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 19/21 | chr17 | 42510642 | |||||||
| chr17:42511309 | C | T | 20 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0017 others(17): Show |
25 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.2131-2552C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 19/21 | chr17 | 42511309 | |||||||
| chr17:42511515 | A | G | 1 | a0001c0001t0002g0104 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2131-2346A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 19/21 | chr17 | 42511515 | |||||||
| chr17:42511702 | C | G | 2 | a0001c0001t0002g0112 a0001c0001t0002g0113 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2131-2159C>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 19/21 | chr17 | 42511702 | |||||||
| chr17:42511795 | T | C | 20 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0017 others(17): Show |
25 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.2131-2066T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 19/21 | chr17 | 42511795 | |||||||
| chr17:42511820 | G | A | 1 | a0001c0001t0015g0097 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2131-2041G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 19/21 | chr17 | 42511820 | |||||||
| chr17:42512271 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2131-1590G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 19/21 | chr17 | 42512271 | |||||||
| chr17:42512282 | C | T | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0216 others(1): Show |
4 | NA18964.hp2 NA18981.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.2131-1579C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 19/21 | chr17 | 42512282 | |||||||
| chr17:42512594 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2131-1267C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 19/21 | chr17 | 42512594 | |||||||
| chr17:42512595 | G | C | 2 | a0001c0001t0001g0003 a0001c0001t0001g0064 |
5 | HG02559.hp2 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2131-1266G>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 19/21 | chr17 | 42512595 | |||||||
| chr17:42512662 | G | A | 1 | a0001c0001t0002g0124 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2131-1199G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 19/21 | chr17 | 42512662 | |||||||
| chr17:42512722 | C | A | 1 | a0001c0001t0002g0121 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2131-1139C>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 19/21 | chr17 | 42512722 | |||||||
| chr17:42512776 | C | T | 1 | a0001c0001t0016g0148 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2131-1085C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 19/21 | chr17 | 42512776 | |||||||
| chr17:42512800 | G | A | 1 | a0001c0001t0015g0097 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2131-1061G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 19/21 | chr17 | 42512800 | |||||||
| chr17:42512965 | A | G | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2131-896A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 19/21 | chr17 | 42512965 | |||||||
| chr17:42513079 | T | C | 3 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0011g0100 |
3 | HG02630.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2131-782T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 19/21 | chr17 | 42513079 | |||||||
| chr17:42513704 | T | C | 4 | a0001c0001t0002g0006 a0001c0001t0002g0049 a0001c0001t0002g0110 others(1): Show |
6 | HG00735.hp2 HG02109.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2131-157T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 19/21 | chr17 | 42513704 | |||||||
| chr17:42513986 | C | T | 1 | a0001c0001t0002g0147 | 1 | NA19087.hp2 | splice_region_variant&intron_variant | LOW | c.2248+8C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 20/21 | chr17 | 42513986 | |||||||
| chr17:42514662 | CTTCCCTA others(6): Show |
C | 1 | a0001c0001t0001g0265 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2420+203_2420+215d others(15): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42514662 | |||||||
| chr17:42514760 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2420+300C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42514760 | |||||||
| chr17:42514859 | A | G | 1 | a0001c0001t0002g0125 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2420+399A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42514859 | |||||||
| chr17:42514931 | C | T | 1 | a0001c0001t0002g0019 | 2 | NA18957.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.2420+471C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42514931 | |||||||
| chr17:42514953 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2420+493C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42514953 | |||||||
| chr17:42515115 | C | G | 2 | a0001c0001t0003g0017 a0001c0001t0003g0079 |
3 | HG02622.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2420+655C>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42515115 | |||||||
| chr17:42515225 | G | T | 1 | a0001c0001t0001g0265 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2420+765G>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42515225 | |||||||
| chr17:42515228 | A | G | 1 | a0001c0001t0001g0265 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2420+768A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42515228 | |||||||
| chr17:42515229 | G | A | 1 | a0001c0001t0001g0265 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2420+769G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42515229 | |||||||
| chr17:42515308 | T | C | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG02896.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2420+848T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42515308 | |||||||
| chr17:42515337 | C | T | 1 | a0001c0001t0002g0145 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2420+877C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42515337 | |||||||
| chr17:42515357 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2420+897C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42515357 | |||||||
| chr17:42515468 | C | CA | 65 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(62): Show |
70 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.2420+1027dupA | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 42515468 | ||||||
| chr17:42515468 | CA | C | 26 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0002g0006 others(23): Show |
32 | HG00735.hp2 HG01167.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.2420+1027delA | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 42515468 | ||||||
| chr17:42515468 | CAA | C | 45 | a0001c0001t0002g0007 a0001c0001t0002g0018 a0001c0001t0002g0019 others(42): Show |
50 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.2420+1026_2420+102 others(6): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 42515468 | ||||||
| chr17:42515554 | G | A | 54 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0018 others(51): Show |
61 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.2420+1094G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42515554 | |||||||
| chr17:42515644 | C | T | 2 | a0001c0001t0001g0249 a0001c0001t0002g0088 |
2 | HG01952.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.2420+1184C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42515644 | |||||||
| chr17:42515790 | A | G | 2 | a0001c0001t0002g0103 a0001c0001t0002g0185 |
2 | HG02027.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.2420+1330A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42515790 | |||||||
| chr17:42516331 | C | T | 1 | a0001c0001t0009g0078 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2420+1871C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42516331 | |||||||
| chr17:42516372 | A | G | 1 | a0001c0009t0001g0192 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2420+1912A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42516372 | |||||||
| chr17:42516493 | C | T | 1 | a0001c0001t0003g0012 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2420+2033C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42516493 | |||||||
| chr17:42516609 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2420+2149C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42516609 | |||||||
| chr17:42516641 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2420+2181G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42516641 | |||||||
| chr17:42516971 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0077 |
2 | HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.2420+2511C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42516971 | |||||||
| chr17:42517128 | A | T | 1 | a0001c0001t0001g0239 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2420+2668A>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42517128 | |||||||
| chr17:42517219 | G | T | 1 | a0001c0001t0002g0111 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2420+2759G>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42517219 | |||||||
| chr17:42517281 | AAAC | A | 3 | a0001c0001t0007g0016 a0001c0001t0007g0090 a0001c0001t0007g0091 |
4 | HG02809.hp2 HG02818.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2420+2845_2420+284 others(7): Show |
ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr17 | 42517281 | ||||||
| chr17:42517302 | C | A | 6 | a0001c0001t0002g0122 a0001c0001t0002g0133 a0001c0001t0007g0016 others(3): Show |
7 | HG02273.hp1 HG02615.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2420+2842C>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42517302 | |||||||
| chr17:42517305 | C | A | 71 | a0001c0001t0001g0074 a0001c0001t0001g0092 a0001c0001t0001g0178 others(68): Show |
80 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.2420+2845C>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42517305 | |||||||
| chr17:42517308 | A | C | 2 | a0001c0001t0011g0100 a0001c0001t0012g0180 |
2 | HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2420+2848A>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42517308 | |||||||
| chr17:42517321 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2420+2861G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42517321 | |||||||
| chr17:42517537 | C | G | 1 | a0001c0001t0001g0218 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2420+3077C>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42517537 | |||||||
| chr17:42517672 | C | G | 1 | a0001c0001t0007g0094 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2420+3212C>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42517672 | |||||||
| chr17:42517988 | A | C | 1 | a0001c0001t0001g0212 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2421-3039A>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42517988 | |||||||
| chr17:42518124 | G | A | 1 | a0001c0001t0001g0025 | 2 | NA18997.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.2421-2903G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42518124 | |||||||
| chr17:42518157 | C | T | 3 | a0001c0001t0007g0016 a0001c0001t0007g0090 a0001c0001t0007g0091 |
4 | HG02809.hp2 HG02818.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2421-2870C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42518157 | |||||||
| chr17:42518212 | C | G | 30 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0028 others(27): Show |
33 | HG00642.hp1 HG01074.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.2421-2815C>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42518212 | |||||||
| chr17:42518224 | C | T | 4 | a0001c0001t0001g0214 a0001c0001t0001g0251 a0001c0001t0001g0253 others(1): Show |
4 | HG01169.hp1 HG01433.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.2421-2803C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42518224 | |||||||
| chr17:42518471 | C | G | 1 | a0001c0001t0005g0186 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2421-2556C>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42518471 | |||||||
| chr17:42518534 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2421-2493C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42518534 | |||||||
| chr17:42518928 | A | G | 1 | a0001c0001t0002g0088 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2421-2099A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42518928 | |||||||
| chr17:42519300 | T | A | 1 | a0001c0001t0006g0038 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2421-1727T>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42519300 | |||||||
| chr17:42519336 | G | T | 3 | a0001c0001t0007g0016 a0001c0001t0007g0090 a0001c0001t0007g0091 |
4 | HG02809.hp2 HG02818.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2421-1691G>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42519336 | |||||||
| chr17:42519366 | G | A | 1 | a0001c0001t0002g0128 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2421-1661G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42519366 | |||||||
| chr17:42519418 | G | A | 2 | a0001c0001t0002g0146 a0001c0001t0013g0117 |
2 | NA18939.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.2421-1609G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42519418 | |||||||
| chr17:42519747 | C | A | 2 | a0001c0001t0002g0103 a0001c0001t0002g0185 |
2 | HG02027.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.2421-1280C>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42519747 | |||||||
| chr17:42519943 | C | T | 14 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0029 others(11): Show |
18 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.2421-1084C>T | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42519943 | |||||||
| chr17:42520023 | A | G | 3 | a0001c0001t0001g0231 a0001c0001t0011g0100 a0001c0001t0012g0180 |
3 | HG03130.hp2 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2421-1004A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42520023 | |||||||
| chr17:42520124 | G | C | 4 | a0001c0001t0007g0016 a0001c0001t0007g0090 a0001c0001t0007g0091 others(1): Show |
5 | HG02809.hp2 HG02818.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.2421-903G>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42520124 | |||||||
| chr17:42520244 | T | C | 1 | a0001c0009t0001g0192 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2421-783T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42520244 | |||||||
| chr17:42520292 | A | G | 1 | a0001c0009t0001g0192 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2421-735A>G | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42520292 | |||||||
| chr17:42520520 | T | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0211 a0001c0001t0001g0257 others(1): Show |
6 | HG00558.hp1 HG02523.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.2421-507T>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42520520 | |||||||
| chr17:42520643 | G | C | 1 | a0001c0001t0011g0100 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2421-384G>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42520643 | |||||||
| chr17:42520700 | G | A | 1 | a0001c0001t0001g0273 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2421-327G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42520700 | |||||||
| chr17:42520721 | G | A | 53 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0018 others(50): Show |
60 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.2421-306G>A | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42520721 | |||||||
| chr17:42520904 | T | C | 20 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0017 others(17): Show |
25 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.2421-123T>C | ATP6V0A1 | ENSG00000033627.18 | transcript | ENST00000343619.9 | protein_coding | 21/21 | chr17 | 42520904 |