Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10159 |
| ensemblid | ENSG00000182220.15 |
| hgncid | 18305 |
| symbol | ATP6AP2 |
| name | ATPase H+ transporting accessory protein 2 |
| refseq_nuc | NM_005765.3 |
| refseq_prot | NP_005756.2 |
| ensembl_nuc | ENST00000636580.2 |
| ensembl_prot | ENSP00000490083.1 |
| mane_status | MANE Select |
| chr | chrX |
| start | 40580970 |
| end | 40606848 |
| strand | + |
| ver | v1.2 |
| region | chrX:40580970-40606848 |
| region5000 | chrX:40575970-40611848 |
| regionname0 | ATP6AP2_chrX_40580970_40606848 |
| regionname5000 | ATP6AP2_chrX_40575970_40611848 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 350 | 286 | 70 | 48 | 136 | 9 | 21 | 105 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | MAVFV others(345): Show |
chrX | 40575970 | 40611848 |
| a0002 | 0/0 | 350 | 5 | 0 | 4 | 0 | 0 | 1 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | MAVFV others(345): Show |
chrX | 40575970 | 40611848 |
| a0003 | 0/0 | 350 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | MAVFV others(345): Show |
chrX | 40575970 | 40611848 |
| a0004 | 0/0 | 350 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | MAVFV others(345): Show |
chrX | 40575970 | 40611848 |
| a0005 | 0/0 | 350 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | MAVFV others(345): Show |
chrX | 40575970 | 40611848 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1050 | 222 | 42 | 36 | 112 | 9 | 21 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | ATGGC others(1045): Show |
chrX | 40575970 | 40611848 | ||
| a0001c0002 | 0/0 | 1050 | 55 | 20 | 11 | 24 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | ATGGC others(1045): Show |
chrX | 40575970 | 40611848 | ||
| a0001c0003 | 0/0 | 1050 | 7 | 6 | 1 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | ATGGC others(1045): Show |
chrX | 40575970 | 40611848 | ||
| a0001c0006 | 0/0 | 1050 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | ATGGC others(1045): Show |
chrX | 40575970 | 40611848 | ||
| a0002c0005 | 0/0 | 1050 | 5 | 0 | 4 | 0 | 0 | 1 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | ATGGC others(1045): Show |
chrX | 40575970 | 40611848 | ||
| a0003c0004 | 0/0 | 1050 | 5 | 5 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | ATGGC others(1045): Show |
chrX | 40575970 | 40611848 | ||
| a0004c0007 | 0/0 | 1050 | 2 | 0 | 2 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | ATGGC others(1045): Show |
chrX | 40575970 | 40611848 | ||
| a0005c0008 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | ATGGC others(1045): Show |
chrX | 40575970 | 40611848 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2242 | 217 | 38 | 36 | 112 | 9 | 20 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | GAGTC others(2237): Show |
chrX | 40575970 | 40611848 |
| a0001c0001t0003 | 0/0 | 2242 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | GAGTC others(2237): Show |
chrX | 40575970 | 40611848 |
| a0001c0001t0004 | 0/0 | 2242 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | GAGTC others(2237): Show |
chrX | 40575970 | 40611848 |
| a0001c0001t0005 | 0/0 | 2242 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | GAGTC others(2237): Show |
chrX | 40575970 | 40611848 |
| a0001c0001t0008 | 0/0 | 2242 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | GAGTC others(2237): Show |
chrX | 40575970 | 40611848 |
| a0001c0002t0002 | 0/0 | 2242 | 41 | 7 | 11 | 23 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | GAGTC others(2237): Show |
chrX | 40575970 | 40611848 |
| a0001c0002t0003 | 0/0 | 2242 | 12 | 12 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | GAGTC others(2237): Show |
chrX | 40575970 | 40611848 |
| a0001c0002t0006 | 0/0 | 2242 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | GAGTC others(2237): Show |
chrX | 40575970 | 40611848 |
| a0001c0002t0007 | 0/0 | 2242 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | GAGTC others(2237): Show |
chrX | 40575970 | 40611848 |
| a0001c0003t0003 | 0/0 | 2242 | 7 | 6 | 1 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | GAGTC others(2237): Show |
chrX | 40575970 | 40611848 |
| a0001c0006t0003 | 0/0 | 2242 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | GAGTC others(2237): Show |
chrX | 40575970 | 40611848 |
| a0002c0005t0001 | 0/0 | 2242 | 5 | 0 | 4 | 0 | 0 | 1 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | GAGTC others(2237): Show |
chrX | 40575970 | 40611848 |
| a0003c0004t0003 | 0/0 | 2242 | 5 | 5 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | GAGTC others(2237): Show |
chrX | 40575970 | 40611848 |
| a0004c0007t0001 | 0/0 | 2242 | 2 | 0 | 2 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | GAGTC others(2237): Show |
chrX | 40575970 | 40611848 |
| a0005c0008t0003 | 0/0 | 2242 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | GAGTC others(2237): Show |
chrX | 40575970 | 40611848 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 30 | 0 | 6 | 14 | 4 | 6 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0002 | 0/0 | 10 | 0 | 5 | 4 | 0 | 1 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0004 | 0/0 | 7 | 3 | 0 | 4 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0014 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0026 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0112 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0003g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0001t0008g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0002g0005 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0002g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0002g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0003g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0003g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0003g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0002t0007g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0003t0003g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0003t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0003t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0003t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0003t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0006t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0001c0006t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0002c0005t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0002c0005t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0002c0005t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0002c0005t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0002c0005t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0003c0004t0003g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0003c0004t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0003c0004t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0004c0007t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| a0005c0008t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0106 | EUR | FIN | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | FIN | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | CHS | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0159 | EAS | CHS | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0166 | AMR | PUR | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG00642 | hp1 | a0002 | c0005 | t0001 | g0009 | AMR | PUR | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG00741 | hp1 | a0002 | c0005 | t0001 | g0002 | AMR | PUR | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01069 | hp1 | a0002 | c0005 | t0001 | g0035 | AMR | PUR | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01071 | hp1 | a0002 | c0005 | t0001 | g0001 | AMR | PUR | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01081 | hp2 | a0001 | c0003 | t0003 | g0028 | AMR | PUR | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01167 | hp1 | a0004 | c0007 | t0001 | g0034 | AMR | PUR | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01169 | hp2 | a0004 | c0007 | t0001 | g0034 | AMR | PUR | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0154 | AMR | CLM | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0016 | AMR | CLM | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0016 | AMR | CLM | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0158 | AMR | CLM | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0163 | AMR | CLM | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0164 | AMR | PEL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0016 | AMR | PEL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0156 | AMR | PEL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02145 | hp1 | a0001 | c0003 | t0003 | g0029 | AFR | ACB | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CDX | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | CDX | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CDX | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0180 | AFR | ACB | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02280 | hp2 | a0001 | c0003 | t0003 | g0074 | AFR | ACB | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0147 | AFR | ACB | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02615 | hp1 | a0001 | c0002 | t0003 | g0149 | AFR | GWD | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0131 | AFR | GWD | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02630 | hp2 | a0001 | c0003 | t0003 | g0077 | AFR | GWD | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02698 | hp1 | a0001 | c0001 | t0008 | g0026 | SAS | PJL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02717 | hp1 | a0001 | c0002 | t0003 | g0184 | AFR | GWD | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02723 | hp1 | a0001 | c0003 | t0003 | g0029 | AFR | GWD | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02723 | hp2 | a0001 | c0006 | t0003 | g0072 | AFR | GWD | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0040 | AFR | GWD | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02818 | hp1 | a0001 | c0002 | t0003 | g0040 | AFR | GWD | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0178 | AFR | GWD | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02896 | hp1 | a0001 | c0002 | t0003 | g0042 | AFR | GWD | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02896 | hp2 | a0001 | c0006 | t0003 | g0073 | AFR | GWD | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02897 | hp1 | a0001 | c0002 | t0003 | g0042 | AFR | GWD | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0152 | AFR | ESN | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02970 | hp1 | a0001 | c0002 | t0003 | g0043 | AFR | ESN | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02970 | hp2 | a0003 | c0004 | t0003 | g0015 | AFR | ESN | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02976 | hp2 | a0003 | c0004 | t0003 | g0162 | AFR | ESN | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG03041 | hp1 | a0001 | c0002 | t0003 | g0172 | AFR | GWD | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG03041 | hp2 | a0001 | c0002 | t0002 | g0148 | AFR | GWD | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG03130 | hp1 | a0003 | c0004 | t0003 | g0015 | AFR | ESN | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG03195 | hp1 | a0003 | c0004 | t0003 | g0015 | AFR | ESN | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG03516 | hp2 | a0001 | c0002 | t0003 | g0043 | AFR | ESN | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG03540 | hp1 | a0001 | c0003 | t0003 | g0075 | AFR | GWD | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG03540 | hp2 | a0001 | c0003 | t0003 | g0028 | AFR | GWD | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0146 | AFR | MSL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG03654 | hp1 | a0002 | c0005 | t0001 | g0105 | SAS | PJL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | STU | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | STU | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18522 | hp1 | a0005 | c0008 | t0003 | g0168 | AFR | YRI | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18941 | hp2 | a0001 | c0002 | t0002 | g0089 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18946 | hp2 | a0001 | c0002 | t0007 | g0005 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0139 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18989 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0160 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0175 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19006 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0153 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19030 | hp1 | a0001 | c0002 | t0003 | g0143 | AFR | LWK | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19030 | hp2 | a0001 | c0002 | t0006 | g0144 | AFR | LWK | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19043 | hp1 | a0003 | c0004 | t0003 | g0181 | AFR | LWK | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19055 | hp1 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19063 | hp1 | a0001 | c0002 | t0002 | g0165 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19064 | hp1 | a0001 | c0002 | t0002 | g0161 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19078 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0118 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19240 | hp1 | a0001 | c0002 | t0003 | g0151 | AFR | YRI | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | YRI | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ASW | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ASW | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | TSI | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0167 | AFR | MSL | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG06807 | hp1 | a0001 | c0002 | t0003 | g0150 | AFR | USA | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | USA | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | USA | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0155 | AFR | USA | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | LWK | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | LWK | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0112 | REF | REF | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0026 | REF | REF | ATP6AP2_chrX_40575970_40611848 | ATP6AP2 | chrX | 40575970 | 40611848 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:40591282 | C | T | 1 | a0005 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.217C>T | p.Arg73Trp | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/9 | 313/2242 | 217/1053 | 73/350 | chrX | 40591282 | |||
| chrX:40591333 | C | G | 1 | a0002 | 5 | HG00642.hp1 HG00741.hp1 HG01069.hp1 others(2): Show |
missense_variant | MODERATE | c.268C>G | p.Pro90Ala | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/9 | 364/2242 | 268/1053 | 90/350 | chrX | 40591333 | |||
| chrX:40597620 | G | A | 1 | a0004 | 2 | HG01167.hp1 HG01169.hp2 |
missense_variant | MODERATE | c.490G>A | p.Val164Ile | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 5/9 | 586/2242 | 490/1053 | 164/350 | chrX | 40597620 | |||
| chrX:40605570 | G | C | 1 | a0003 | 5 | HG02970.hp2 HG02976.hp2 HG03130.hp1 others(2): Show |
missense_variant | MODERATE | c.868G>C | p.Ala290Pro | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 9/9 | 964/2242 | 868/1053 | 290/350 | chrX | 40605570 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:40591350 | G | A | 2 | a0001c0003 a0001c0006 |
9 | HG01081.hp2 HG02145.hp1 HG02280.hp2 others(6): Show |
synonymous_variant | LOW | c.285G>A | p.Ser95Ser | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/9 | 381/2242 | 285/1053 | 95/350 | chrX | 40591350 | |||
| chrX:40600788 | T | C | 3 | a0001c0002 a0003c0004 a0005c0008 |
61 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(58): Show |
synonymous_variant | LOW | c.765T>C | p.Tyr255Tyr | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/9 | 861/2242 | 765/1053 | 255/350 | chrX | 40600788 | |||
| chrX:40605752 | T | C | 1 | a0001c0006 | 2 | HG02723.hp2 HG02896.hp2 |
synonymous_variant | LOW | c.1050T>C | p.Asp350Asp | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 9/9 | 1146/2242 | 1050/1053 | 350/350 | chrX | 40605752 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:40581020 | C | A | 1 | a0001c0001t0004 | 1 | HG02622.hp1 | 5_prime_UTR_variant | MODIFIER | c.-46C>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/9 | 46 | chrX | 40581020 | ||||||
| chrX:40581031 | G | C | 1 | a0001c0001t0005 | 1 | HG02257.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-35G>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/9 | chrX | 40581031 | |||||||
| chrX:40605932 | C | T | 1 | a0001c0001t0008 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*177C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 9/9 | 177 | chrX | 40605932 | ||||||
| chrX:40605940 | C | T | 1 | a0001c0002t0007 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*185C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 9/9 | 185 | chrX | 40605940 | ||||||
| chrX:40606021 | A | T | 9 | a0001c0001t0003 a0001c0002t0002 a0001c0002t0003 others(6): Show |
72 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*266A>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 9/9 | 266 | chrX | 40606021 | ||||||
| chrX:40606113 | A | G | 2 | a0001c0002t0002 a0001c0002t0007 |
42 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*358A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 9/9 | 358 | chrX | 40606113 | ||||||
| chrX:40606261 | G | A | 1 | a0001c0002t0006 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*506G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 9/9 | 506 | chrX | 40606261 | ||||||
| chrX:40606516 | A | G | 9 | a0001c0001t0003 a0001c0002t0002 a0001c0002t0003 others(6): Show |
72 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*761A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 9/9 | 761 | chrX | 40606516 | ||||||
| chrX:40606564 | T | C | 9 | a0001c0001t0003 a0001c0002t0002 a0001c0002t0003 others(6): Show |
72 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*809T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 9/9 | 809 | chrX | 40606564 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:40581224 | C | T | 1 | a0001c0002t0003g0184 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.37+122C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40581224 | |||||||
| chrX:40581344 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.37+242C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40581344 | |||||||
| chrX:40581345 | C | A | 1 | a0001c0001t0001g0183 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.37+243C>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40581345 | |||||||
| chrX:40581551 | T | C | 5 | a0001c0001t0001g0019 a0001c0001t0001g0044 a0001c0001t0001g0045 others(2): Show |
6 | HG01255.hp1 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.37+449T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40581551 | |||||||
| chrX:40581675 | G | C | 1 | a0001c0001t0003g0020 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.37+573G>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40581675 | |||||||
| chrX:40581824 | A | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0182 |
4 | HG00323.hp2 HG01515.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.37+722A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40581824 | |||||||
| chrX:40582100 | G | A | 1 | a0001c0001t0003g0020 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.37+998G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40582100 | |||||||
| chrX:40582101 | G | T | 1 | a0003c0004t0003g0181 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.37+999G>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40582101 | |||||||
| chrX:40582223 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0048 |
3 | HG00741.hp2 HG02738.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.37+1121T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40582223 | |||||||
| chrX:40582297 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.37+1195G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40582297 | |||||||
| chrX:40582352 | C | T | 2 | a0001c0001t0001g0179 a0001c0001t0005g0180 |
2 | HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.37+1250C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40582352 | |||||||
| chrX:40582388 | A | G | 1 | a0001c0002t0002g0178 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.37+1286A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40582388 | |||||||
| chrX:40582487 | G | A | 2 | a0001c0001t0001g0179 a0001c0001t0005g0180 |
2 | HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.37+1385G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40582487 | |||||||
| chrX:40582606 | C | T | 1 | a0001c0001t0001g0017 | 3 | HG02809.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.37+1504C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40582606 | |||||||
| chrX:40582773 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.37+1671A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40582773 | |||||||
| chrX:40582977 | A | G | 2 | a0001c0001t0001g0047 a0001c0001t0001g0176 |
2 | HG00733.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.37+1875A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40582977 | |||||||
| chrX:40582992 | G | A | 1 | a0001c0001t0003g0020 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.37+1890G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40582992 | |||||||
| chrX:40582997 | A | G | 1 | a0001c0002t0002g0175 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.37+1895A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40582997 | |||||||
| chrX:40583080 | G | A | 1 | a0001c0001t0003g0020 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.37+1978G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40583080 | |||||||
| chrX:40583106 | G | A | 7 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0050 others(4): Show |
9 | HG01099.hp1 HG01943.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.37+2004G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40583106 | |||||||
| chrX:40583198 | A | G | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG03669.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.37+2096A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40583198 | |||||||
| chrX:40583251 | T | C | 1 | a0001c0001t0003g0020 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.37+2149T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40583251 | |||||||
| chrX:40583261 | T | C | 8 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0055 others(5): Show |
10 | HG00558.hp1 HG01169.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.37+2159T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40583261 | |||||||
| chrX:40583460 | A | C | 1 | a0001c0002t0003g0172 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.37+2358A>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40583460 | |||||||
| chrX:40583527 | C | T | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(169): Show |
273 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.37+2425C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40583527 | |||||||
| chrX:40583566 | C | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.37+2464C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40583566 | |||||||
| chrX:40584260 | G | T | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 |
3 | NA18974.hp1 NA19012.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.37+3158G>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40584260 | |||||||
| chrX:40584263 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0176 |
2 | HG00733.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.37+3161G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40584263 | |||||||
| chrX:40584364 | C | CT | 40 | a0001c0001t0001g0145 a0001c0001t0001g0157 a0001c0002t0002g0005 others(37): Show |
57 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.37+3279dupT | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 40584364 | ||||||
| chrX:40584364 | CT | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(102): Show |
186 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.37+3279delT | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 40584364 | ||||||
| chrX:40584571 | T | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
272 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.37+3469T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40584571 | |||||||
| chrX:40584664 | T | C | 1 | a0001c0002t0006g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.37+3562T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40584664 | |||||||
| chrX:40584769 | T | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
272 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.37+3667T>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40584769 | |||||||
| chrX:40584864 | C | T | 1 | a0005c0008t0003g0168 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.37+3762C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40584864 | |||||||
| chrX:40584889 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
272 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.37+3787A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40584889 | |||||||
| chrX:40584903 | C | A | 5 | a0001c0001t0001g0145 a0001c0002t0003g0040 a0001c0002t0003g0184 others(2): Show |
8 | HG02572.hp1 HG02717.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.37+3801C>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40584903 | |||||||
| chrX:40584935 | A | G | 1 | a0001c0001t0003g0020 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.37+3833A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40584935 | |||||||
| chrX:40584941 | C | T | 1 | a0001c0001t0003g0020 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.37+3839C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40584941 | |||||||
| chrX:40585097 | G | C | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.38-3889G>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40585097 | |||||||
| chrX:40585179 | C | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
268 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.38-3807C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40585179 | |||||||
| chrX:40585537 | G | A | 1 | a0003c0004t0003g0181 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.38-3449G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40585537 | |||||||
| chrX:40585620 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0176 |
2 | HG00733.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.38-3366G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40585620 | |||||||
| chrX:40585628 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.38-3358C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40585628 | |||||||
| chrX:40585670 | G | A | 1 | a0001c0001t0003g0020 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.38-3316G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40585670 | |||||||
| chrX:40585682 | T | C | 1 | a0001c0001t0003g0020 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.38-3304T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40585682 | |||||||
| chrX:40585683 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.38-3303G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40585683 | |||||||
| chrX:40585786 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.38-3200G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40585786 | |||||||
| chrX:40585876 | T | A | 1 | a0001c0001t0003g0020 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.38-3110T>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40585876 | |||||||
| chrX:40586053 | C | T | 1 | a0001c0001t0003g0020 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.38-2933C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40586053 | |||||||
| chrX:40586182 | C | T | 2 | a0001c0002t0003g0043 a0001c0002t0003g0143 |
3 | HG02970.hp1 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.38-2804C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40586182 | |||||||
| chrX:40586275 | A | G | 1 | a0001c0001t0003g0020 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.38-2711A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40586275 | |||||||
| chrX:40586326 | C | T | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.38-2660C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40586326 | |||||||
| chrX:40586419 | G | C | 5 | a0001c0001t0001g0012 a0001c0001t0001g0079 a0001c0001t0001g0080 others(2): Show |
7 | HG02257.hp1 HG02622.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.38-2567G>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40586419 | |||||||
| chrX:40586688 | T | C | 1 | a0001c0001t0003g0020 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.38-2298T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40586688 | |||||||
| chrX:40586747 | T | C | 8 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(5): Show |
8 | HG02258.hp1 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.38-2239T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40586747 | |||||||
| chrX:40586849 | A | C | 1 | a0001c0001t0001g0078 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.38-2137A>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40586849 | |||||||
| chrX:40586869 | C | T | 1 | a0001c0001t0003g0020 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.38-2117C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40586869 | |||||||
| chrX:40587184 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
268 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.38-1802T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40587184 | |||||||
| chrX:40587308 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0133 |
2 | HG01074.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.38-1678G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40587308 | |||||||
| chrX:40587386 | C | T | 9 | a0001c0001t0001g0179 a0001c0001t0005g0180 a0001c0003t0003g0028 others(6): Show |
11 | HG01081.hp2 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.38-1600C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40587386 | |||||||
| chrX:40587387 | A | G | 9 | a0001c0001t0001g0179 a0001c0001t0005g0180 a0001c0003t0003g0028 others(6): Show |
11 | HG01081.hp2 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.38-1599A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40587387 | |||||||
| chrX:40587445 | C | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
272 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.38-1541C>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40587445 | |||||||
| chrX:40587823 | G | A | 2 | a0001c0006t0003g0072 a0001c0006t0003g0073 |
2 | HG02723.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.38-1163G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40587823 | |||||||
| chrX:40587862 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.38-1124A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40587862 | |||||||
| chrX:40587884 | A | G | 1 | a0001c0001t0001g0017 | 3 | HG02809.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.38-1102A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40587884 | |||||||
| chrX:40587886 | T | G | 1 | a0001c0002t0002g0041 | 2 | NA18963.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.38-1100T>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40587886 | |||||||
| chrX:40588098 | G | T | 1 | a0001c0001t0003g0020 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.38-888G>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40588098 | |||||||
| chrX:40588119 | A | C | 2 | a0001c0002t0003g0040 a0001c0002t0003g0184 |
3 | HG02717.hp1 HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.38-867A>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40588119 | |||||||
| chrX:40588161 | A | T | 1 | a0001c0001t0001g0130 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.38-825A>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40588161 | |||||||
| chrX:40588276 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.38-710T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40588276 | |||||||
| chrX:40588303 | G | A | 17 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0032 others(14): Show |
29 | HG00423.hp1 HG00438.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.38-683G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40588303 | |||||||
| chrX:40588334 | G | GCC | 8 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0059 others(5): Show |
13 | HG00408.hp2 HG01884.hp2 NA18946.hp1 others(10): Show |
intron_variant | MODIFIER | c.38-638_38-637dupCC | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 40588334 | ||||||
| chrX:40588337 | C | CCA | 56 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0014 others(53): Show |
81 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.38-648_38-647insAC | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 40588337 | ||||||
| chrX:40588338 | C | CA | 90 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(87): Show |
160 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.38-648_38-647insA | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40588338 | |||||||
| chrX:40588339 | C | A | 14 | a0001c0001t0001g0134 a0001c0001t0001g0145 a0001c0002t0003g0040 others(11): Show |
19 | HG00738.hp1 HG02572.hp1 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.38-647C>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40588339 | |||||||
| chrX:40588340 | C | A | 10 | a0001c0001t0001g0082 a0001c0001t0001g0179 a0001c0001t0005g0180 others(7): Show |
12 | HG01081.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.38-646C>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40588340 | |||||||
| chrX:40588345 | C | A | 3 | a0001c0002t0002g0146 a0001c0002t0002g0147 a0001c0002t0002g0148 |
3 | HG02451.hp2 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.38-641C>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40588345 | |||||||
| chrX:40588567 | A | G | 1 | a0001c0001t0004g0131 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.38-419A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40588567 | |||||||
| chrX:40588610 | C | T | 1 | a0001c0001t0003g0020 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.38-376C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40588610 | |||||||
| chrX:40588704 | T | TTTTG | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
271 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.38-274_38-271dupGT others(2): Show |
ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 40588704 | ||||||
| chrX:40588742 | C | G | 1 | a0001c0001t0001g0037 | 2 | HG00735.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.38-244C>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40588742 | |||||||
| chrX:40588894 | G | C | 1 | a0001c0001t0001g0097 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.38-92G>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 1/8 | chrX | 40588894 | |||||||
| chrX:40589185 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.168+69C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 2/8 | chrX | 40589185 | |||||||
| chrX:40589268 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.168+152C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 2/8 | chrX | 40589268 | |||||||
| chrX:40589299 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.168+183G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 2/8 | chrX | 40589299 | |||||||
| chrX:40589558 | G | GT | 18 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0032 others(15): Show |
30 | HG00423.hp1 HG00438.hp1 HG01981.hp2 others(27): Show |
intron_variant | MODIFIER | c.168+454dupT | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 40589558 | ||||||
| chrX:40589931 | A | G | 1 | a0001c0001t0003g0020 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.168+815A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 2/8 | chrX | 40589931 | |||||||
| chrX:40590010 | G | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
268 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.168+894G>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 2/8 | chrX | 40590010 | |||||||
| chrX:40590116 | C | T | 3 | a0001c0001t0001g0145 a0003c0004t0003g0015 a0003c0004t0003g0181 |
5 | HG02572.hp1 HG02970.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+1000C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 2/8 | chrX | 40590116 | |||||||
| chrX:40590122 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.168+1006C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 2/8 | chrX | 40590122 | |||||||
| chrX:40590185 | G | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(113): Show |
197 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.169-1049G>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 2/8 | chrX | 40590185 | |||||||
| chrX:40590330 | A | G | 1 | a0001c0002t0002g0148 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.169-904A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 2/8 | chrX | 40590330 | |||||||
| chrX:40590415 | A | G | 2 | a0001c0002t0003g0043 a0001c0002t0003g0143 |
3 | HG02970.hp1 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.169-819A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 2/8 | chrX | 40590415 | |||||||
| chrX:40590672 | C | G | 2 | a0001c0001t0001g0179 a0001c0001t0005g0180 |
2 | HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.169-562C>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 2/8 | chrX | 40590672 | |||||||
| chrX:40590710 | T | C | 1 | a0001c0001t0003g0020 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.169-524T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 2/8 | chrX | 40590710 | |||||||
| chrX:40590794 | T | G | 1 | a0001c0001t0003g0020 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.169-440T>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 2/8 | chrX | 40590794 | |||||||
| chrX:40591674 | G | C | 1 | a0001c0001t0003g0020 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.300+309G>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40591674 | |||||||
| chrX:40592029 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.300+664T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40592029 | |||||||
| chrX:40592110 | T | G | 1 | a0001c0001t0003g0020 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.300+745T>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40592110 | |||||||
| chrX:40592220 | A | G | 2 | a0001c0003t0003g0029 a0001c0003t0003g0075 |
3 | HG02145.hp1 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.300+855A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40592220 | |||||||
| chrX:40592523 | G | C | 1 | a0001c0001t0001g0098 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.300+1158G>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40592523 | |||||||
| chrX:40592688 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.300+1323T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40592688 | |||||||
| chrX:40592809 | T | C | 1 | a0001c0001t0003g0020 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.300+1444T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40592809 | |||||||
| chrX:40592818 | C | G | 1 | a0001c0001t0005g0180 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.300+1453C>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40592818 | |||||||
| chrX:40592883 | G | T | 8 | a0001c0002t0003g0151 a0001c0003t0003g0028 a0001c0003t0003g0029 others(5): Show |
10 | HG01081.hp2 HG02145.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.300+1518G>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40592883 | |||||||
| chrX:40592942 | A | G | 1 | a0001c0001t0003g0020 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.300+1577A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40592942 | |||||||
| chrX:40592970 | C | T | 12 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0038 others(9): Show |
15 | HG00408.hp1 HG00609.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.300+1605C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40592970 | |||||||
| chrX:40593305 | C | G | 1 | a0001c0001t0005g0180 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.300+1940C>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40593305 | |||||||
| chrX:40593310 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.300+1945G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40593310 | |||||||
| chrX:40593325 | T | C | 1 | a0001c0001t0001g0013 | 3 | NA18945.hp1 NA18964.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.300+1960T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40593325 | |||||||
| chrX:40593411 | T | C | 40 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0016 others(37): Show |
57 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.300+2046T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40593411 | |||||||
| chrX:40593450 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.300+2085C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40593450 | |||||||
| chrX:40593451 | G | A | 2 | a0001c0002t0003g0043 a0001c0002t0003g0143 |
3 | HG02970.hp1 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.300+2086G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40593451 | |||||||
| chrX:40593452 | C | T | 2 | a0001c0001t0001g0179 a0001c0001t0005g0180 |
2 | HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.300+2087C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40593452 | |||||||
| chrX:40593717 | A | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(72): Show |
141 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.300+2352A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40593717 | |||||||
| chrX:40593972 | G | C | 3 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0004c0007t0001g0034 |
5 | HG00280.hp1 HG00735.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+2607G>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40593972 | |||||||
| chrX:40594066 | A | AT | 7 | a0001c0003t0003g0028 a0001c0003t0003g0029 a0001c0003t0003g0074 others(4): Show |
9 | HG01081.hp2 HG02145.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.300+2705dupT | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 40594066 | ||||||
| chrX:40594085 | C | CA | 8 | a0001c0001t0003g0020 a0001c0003t0003g0028 a0001c0003t0003g0029 others(5): Show |
11 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.300+2728dupA | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 40594085 | ||||||
| chrX:40594092 | AATATAAG others(1): Show |
A | 14 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0032 others(11): Show |
25 | HG00423.hp1 HG00438.hp1 HG02027.hp1 others(22): Show |
intron_variant | MODIFIER | c.300+2730_300+2737d others(10): Show |
ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 40594092 | ||||||
| chrX:40594093 | AT | A | 4 | a0001c0001t0001g0047 a0001c0001t0001g0176 a0001c0001t0001g0179 others(1): Show |
4 | HG00733.hp1 HG02257.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.300+2729delT | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40594093 | |||||||
| chrX:40594111 | A | G | 14 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0032 others(11): Show |
25 | HG00423.hp1 HG00438.hp1 HG02027.hp1 others(22): Show |
intron_variant | MODIFIER | c.300+2746A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40594111 | |||||||
| chrX:40594260 | C | A | 1 | a0001c0001t0001g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.300+2895C>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40594260 | |||||||
| chrX:40594652 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
272 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.301-2597A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40594652 | |||||||
| chrX:40594855 | T | C | 6 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 others(3): Show |
6 | HG02258.hp1 HG02615.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.301-2394T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40594855 | |||||||
| chrX:40595012 | A | C | 1 | a0001c0001t0001g0113 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.301-2237A>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40595012 | |||||||
| chrX:40595321 | T | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(111): Show |
194 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.301-1928T>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40595321 | |||||||
| chrX:40595340 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0176 |
2 | HG00733.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.301-1909G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40595340 | |||||||
| chrX:40595433 | A | G | 4 | a0001c0001t0001g0047 a0001c0001t0001g0176 a0001c0001t0001g0179 others(1): Show |
4 | HG00733.hp1 HG02257.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.301-1816A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40595433 | |||||||
| chrX:40595562 | C | G | 8 | a0001c0001t0003g0020 a0001c0003t0003g0028 a0001c0003t0003g0029 others(5): Show |
11 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.301-1687C>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40595562 | |||||||
| chrX:40595792 | C | G | 2 | a0001c0001t0001g0025 a0002c0005t0001g0105 |
3 | HG01169.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.301-1457C>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40595792 | |||||||
| chrX:40595968 | C | A | 1 | a0001c0001t0001g0031 | 2 | NA18955.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.301-1281C>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40595968 | |||||||
| chrX:40596008 | G | A | 8 | a0001c0001t0003g0020 a0001c0003t0003g0028 a0001c0003t0003g0029 others(5): Show |
11 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.301-1241G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40596008 | |||||||
| chrX:40596093 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.301-1156C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40596093 | |||||||
| chrX:40596134 | G | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | HG02071.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.301-1115G>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40596134 | |||||||
| chrX:40596178 | C | CA | 8 | a0001c0001t0001g0093 a0001c0001t0003g0020 a0001c0002t0002g0089 others(5): Show |
11 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.301-1058dupA | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 40596178 | ||||||
| chrX:40596469 | T | C | 8 | a0001c0001t0003g0020 a0001c0003t0003g0028 a0001c0003t0003g0029 others(5): Show |
11 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.301-780T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40596469 | |||||||
| chrX:40596479 | T | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
270 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.301-770T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40596479 | |||||||
| chrX:40596774 | A | C | 2 | a0001c0002t0003g0150 a0005c0008t0003g0168 |
2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.301-475A>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40596774 | |||||||
| chrX:40596868 | C | CCTT | 8 | a0001c0001t0003g0020 a0001c0003t0003g0028 a0001c0003t0003g0029 others(5): Show |
11 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.301-379_301-378ins others(3): Show |
ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 40596868 | ||||||
| chrX:40596954 | G | A | 1 | a0001c0001t0005g0180 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.301-295G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40596954 | |||||||
| chrX:40596954 | G | C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.301-295G>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40596954 | |||||||
| chrX:40597043 | T | C | 8 | a0001c0001t0003g0020 a0001c0003t0003g0028 a0001c0003t0003g0029 others(5): Show |
11 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.301-206T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40597043 | |||||||
| chrX:40597045 | A | T | 8 | a0001c0001t0003g0020 a0001c0003t0003g0028 a0001c0003t0003g0029 others(5): Show |
11 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.301-204A>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40597045 | |||||||
| chrX:40597062 | G | A | 2 | a0001c0002t0003g0040 a0001c0002t0003g0184 |
3 | HG02717.hp1 HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.301-187G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40597062 | |||||||
| chrX:40597215 | A | T | 3 | a0001c0003t0003g0028 a0001c0003t0003g0074 a0001c0003t0003g0077 |
4 | HG01081.hp2 HG02280.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.301-34A>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40597215 | |||||||
| chrX:40597227 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0104 |
2 | HG02080.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.301-22C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 3/8 | chrX | 40597227 | |||||||
| chrX:40597709 | G | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
272 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.534+45G>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 5/8 | chrX | 40597709 | |||||||
| chrX:40597833 | T | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
270 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.534+169T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 5/8 | chrX | 40597833 | |||||||
| chrX:40597855 | C | A | 1 | a0001c0001t0003g0020 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.534+191C>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 5/8 | chrX | 40597855 | |||||||
| chrX:40597894 | G | A | 8 | a0001c0001t0003g0020 a0001c0003t0003g0028 a0001c0003t0003g0029 others(5): Show |
11 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.534+230G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 5/8 | chrX | 40597894 | |||||||
| chrX:40598014 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.534+350G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 5/8 | chrX | 40598014 | |||||||
| chrX:40598100 | A | G | 8 | a0001c0001t0003g0020 a0001c0003t0003g0028 a0001c0003t0003g0029 others(5): Show |
11 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.534+436A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 5/8 | chrX | 40598100 | |||||||
| chrX:40598256 | G | C | 8 | a0001c0001t0003g0020 a0001c0003t0003g0028 a0001c0003t0003g0029 others(5): Show |
11 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.535-425G>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 5/8 | chrX | 40598256 | |||||||
| chrX:40598325 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.535-356A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 5/8 | chrX | 40598325 | |||||||
| chrX:40598369 | G | A | 1 | a0001c0002t0002g0146 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.535-312G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 5/8 | chrX | 40598369 | |||||||
| chrX:40598994 | G | A | 8 | a0001c0001t0003g0020 a0001c0003t0003g0028 a0001c0003t0003g0029 others(5): Show |
11 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.588+260G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 6/8 | chrX | 40598994 | |||||||
| chrX:40599794 | C | T | 2 | a0001c0001t0001g0179 a0001c0001t0005g0180 |
2 | HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.738+53C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 7/8 | chrX | 40599794 | |||||||
| chrX:40599833 | T | C | 5 | a0001c0002t0003g0042 a0001c0002t0003g0149 a0001c0002t0003g0151 others(2): Show |
6 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.738+92T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 7/8 | chrX | 40599833 | |||||||
| chrX:40600121 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.738+380A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 7/8 | chrX | 40600121 | |||||||
| chrX:40600128 | C | T | 7 | a0001c0003t0003g0028 a0001c0003t0003g0029 a0001c0003t0003g0074 others(4): Show |
9 | HG01081.hp2 HG02145.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.738+387C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 7/8 | chrX | 40600128 | |||||||
| chrX:40600313 | T | TTTC | 51 | a0001c0001t0003g0020 a0001c0002t0002g0005 a0001c0002t0002g0006 others(48): Show |
72 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.739-448_739-446dup others(3): Show |
ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 40600313 | ||||||
| chrX:40600379 | G | A | 8 | a0001c0001t0003g0020 a0001c0003t0003g0028 a0001c0003t0003g0029 others(5): Show |
11 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.739-383G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 7/8 | chrX | 40600379 | |||||||
| chrX:40600597 | A | C | 51 | a0001c0001t0003g0020 a0001c0002t0002g0005 a0001c0002t0002g0006 others(48): Show |
72 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.739-165A>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 7/8 | chrX | 40600597 | |||||||
| chrX:40600931 | T | TA | 45 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0017 others(42): Show |
62 | HG00408.hp1 HG00558.hp1 HG01099.hp1 others(59): Show |
intron_variant | MODIFIER | c.858+63dupA | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 40600931 | ||||||
| chrX:40600931 | T | TAA | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(64): Show |
131 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.858+62_858+63dupAA | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 40600931 | ||||||
| chrX:40600964 | A | T | 8 | a0001c0001t0003g0020 a0001c0003t0003g0028 a0001c0003t0003g0029 others(5): Show |
11 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.858+83A>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40600964 | |||||||
| chrX:40601197 | C | T | 2 | a0001c0002t0002g0016 a0001c0002t0002g0166 |
4 | HG00639.hp1 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.858+316C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40601197 | |||||||
| chrX:40601254 | A | T | 1 | a0001c0001t0001g0051 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.858+373A>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40601254 | |||||||
| chrX:40601283 | C | T | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.858+402C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40601283 | |||||||
| chrX:40601307 | C | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
271 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.858+426C>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40601307 | |||||||
| chrX:40601390 | G | A | 1 | a0001c0002t0002g0158 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.858+509G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40601390 | |||||||
| chrX:40601391 | G | A | 3 | a0001c0001t0001g0082 a0001c0001t0001g0145 a0001c0001t0001g0177 |
3 | HG02572.hp1 HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.858+510G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40601391 | |||||||
| chrX:40601442 | G | T | 3 | a0001c0001t0001g0082 a0001c0001t0001g0145 a0001c0001t0001g0177 |
3 | HG02572.hp1 HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.858+561G>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40601442 | |||||||
| chrX:40601451 | A | G | 1 | a0001c0001t0003g0020 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.858+570A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40601451 | |||||||
| chrX:40601706 | T | C | 1 | a0001c0001t0001g0107 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.858+825T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40601706 | |||||||
| chrX:40601856 | T | C | 1 | a0004c0007t0001g0034 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.858+975T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40601856 | |||||||
| chrX:40601962 | A | G | 51 | a0001c0001t0003g0020 a0001c0002t0002g0005 a0001c0002t0002g0006 others(48): Show |
72 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.858+1081A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40601962 | |||||||
| chrX:40602003 | TGGGTGTG others(496): Show |
T | 51 | a0001c0001t0003g0020 a0001c0002t0002g0005 a0001c0002t0002g0006 others(48): Show |
72 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.858+1126_858+1628d others(2): Show |
ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 40602003 | ||||||
| chrX:40602147 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.858+1266T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40602147 | |||||||
| chrX:40602275 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.858+1394C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40602275 | |||||||
| chrX:40602378 | C | T | 4 | a0001c0001t0001g0047 a0001c0001t0001g0176 a0001c0001t0001g0179 others(1): Show |
4 | HG00733.hp1 HG02257.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.858+1497C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40602378 | |||||||
| chrX:40602519 | G | T | 51 | a0001c0001t0003g0020 a0001c0002t0002g0005 a0001c0002t0002g0006 others(48): Show |
72 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.858+1638G>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40602519 | |||||||
| chrX:40602554 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0124 |
2 | NA18944.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.858+1673G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40602554 | |||||||
| chrX:40602649 | C | CA | 34 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(31): Show |
49 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.858+1785dupA | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 40602649 | ||||||
| chrX:40602649 | CA | C | 63 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(60): Show |
92 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.858+1785delA | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 40602649 | ||||||
| chrX:40602662 | A | C | 1 | a0001c0001t0003g0020 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.858+1781A>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40602662 | |||||||
| chrX:40602666 | A | C | 51 | a0001c0001t0003g0020 a0001c0002t0002g0005 a0001c0002t0002g0006 others(48): Show |
72 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.858+1785A>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40602666 | |||||||
| chrX:40602754 | T | C | 51 | a0001c0001t0003g0020 a0001c0002t0002g0005 a0001c0002t0002g0006 others(48): Show |
72 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.858+1873T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40602754 | |||||||
| chrX:40602843 | A | G | 51 | a0001c0001t0003g0020 a0001c0002t0002g0005 a0001c0002t0002g0006 others(48): Show |
72 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.858+1962A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40602843 | |||||||
| chrX:40602913 | C | CT | 36 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0060 others(33): Show |
51 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.858+2060dupT | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 40602913 | ||||||
| chrX:40602913 | C | CTT | 6 | a0001c0001t0001g0067 a0001c0002t0002g0030 a0001c0002t0002g0041 others(3): Show |
8 | HG01952.hp1 NA18940.hp1 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.858+2059_858+2060d others(4): Show |
ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 40602913 | ||||||
| chrX:40602913 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0179 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.858+2051_858+2060d others(12): Show |
ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 40602913 | ||||||
| chrX:40602931 | TTTTTTTT others(4): Show |
T | 3 | a0001c0001t0001g0080 a0001c0001t0001g0091 a0001c0001t0001g0111 |
3 | HG02895.hp1 NA18943.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.858+2051_858+2061d others(13): Show |
ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40602931 | |||||||
| chrX:40602932 | TTTTTTTT others(3): Show |
T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(102): Show |
184 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.858+2052_858+2061d others(12): Show |
ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40602932 | |||||||
| chrX:40602941 | TG | T | 8 | a0001c0001t0003g0020 a0001c0002t0003g0040 a0001c0002t0003g0150 others(5): Show |
11 | HG02055.hp1 HG02717.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.858+2062delG | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 40602941 | ||||||
| chrX:40602942 | G | T | 67 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(64): Show |
92 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.858+2061G>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40602942 | |||||||
| chrX:40603256 | A | T | 4 | a0001c0002t0003g0042 a0001c0002t0003g0149 a0001c0002t0003g0151 others(1): Show |
5 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.859-2305A>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40603256 | |||||||
| chrX:40603264 | G | A | 1 | a0001c0002t0002g0153 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.859-2297G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40603264 | |||||||
| chrX:40603284 | T | C | 51 | a0001c0001t0003g0020 a0001c0002t0002g0005 a0001c0002t0002g0006 others(48): Show |
72 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.859-2277T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40603284 | |||||||
| chrX:40603355 | C | CAAAA | 12 | a0001c0002t0002g0147 a0001c0002t0002g0154 a0001c0002t0002g0163 others(9): Show |
15 | HG01081.hp2 HG01256.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.859-2196_859-2193d others(6): Show |
ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 40603355 | ||||||
| chrX:40603355 | C | CAAAAA | 36 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0016 others(33): Show |
53 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.859-2197_859-2193d others(7): Show |
ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 40603355 | ||||||
| chrX:40603355 | CA | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(109): Show |
192 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.859-2193delA | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 40603355 | ||||||
| chrX:40603404 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0048 |
3 | HG00741.hp2 HG02738.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.859-2157C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40603404 | |||||||
| chrX:40603778 | T | C | 44 | a0001c0001t0003g0020 a0001c0002t0002g0005 a0001c0002t0002g0006 others(41): Show |
63 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.859-1783T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40603778 | |||||||
| chrX:40603797 | G | A | 1 | a0001c0001t0003g0020 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.859-1764G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40603797 | |||||||
| chrX:40603949 | T | A | 51 | a0001c0001t0003g0020 a0001c0002t0002g0005 a0001c0002t0002g0006 others(48): Show |
72 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.859-1612T>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40603949 | |||||||
| chrX:40603979 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.859-1582A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40603979 | |||||||
| chrX:40604137 | A | G | 2 | a0001c0001t0001g0047 a0001c0001t0001g0176 |
2 | HG00733.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.859-1424A>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40604137 | |||||||
| chrX:40604162 | TA | T | 43 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0016 others(40): Show |
61 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.859-1391delA | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 40604162 | ||||||
| chrX:40604265 | T | C | 51 | a0001c0001t0003g0020 a0001c0002t0002g0005 a0001c0002t0002g0006 others(48): Show |
72 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.859-1296T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40604265 | |||||||
| chrX:40604453 | G | T | 51 | a0001c0001t0003g0020 a0001c0002t0002g0005 a0001c0002t0002g0006 others(48): Show |
72 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.859-1108G>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40604453 | |||||||
| chrX:40604579 | A | T | 1 | a0001c0001t0001g0036 | 2 | HG02559.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.859-982A>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40604579 | |||||||
| chrX:40604620 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
269 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.859-941T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40604620 | |||||||
| chrX:40604642 | C | T | 2 | a0001c0001t0001g0179 a0001c0001t0005g0180 |
2 | HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.859-919C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40604642 | |||||||
| chrX:40604685 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.859-876T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40604685 | |||||||
| chrX:40604700 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.859-861G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40604700 | |||||||
| chrX:40604724 | T | C | 4 | a0001c0002t0003g0042 a0001c0002t0003g0149 a0001c0002t0003g0151 others(1): Show |
5 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.859-837T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40604724 | |||||||
| chrX:40604931 | A | AT | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(104): Show |
188 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.859-611dupT | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 40604931 | ||||||
| chrX:40604980 | C | CTGGA | 51 | a0001c0001t0003g0020 a0001c0002t0002g0005 a0001c0002t0002g0006 others(48): Show |
72 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.859-580_859-577dup others(4): Show |
ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 40604980 | ||||||
| chrX:40605026 | T | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
270 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.859-535T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40605026 | |||||||
| chrX:40605058 | C | T | 3 | a0001c0003t0003g0028 a0001c0003t0003g0074 a0001c0003t0003g0077 |
4 | HG01081.hp2 HG02280.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.859-503C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40605058 | |||||||
| chrX:40605088 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.859-473G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40605088 | |||||||
| chrX:40605101 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.859-460C>T | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40605101 | |||||||
| chrX:40605332 | T | G | 1 | a0001c0002t0002g0164 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.859-229T>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40605332 | |||||||
| chrX:40605411 | G | A | 7 | a0001c0003t0003g0028 a0001c0003t0003g0029 a0001c0003t0003g0074 others(4): Show |
9 | HG01081.hp2 HG02145.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.859-150G>A | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40605411 | |||||||
| chrX:40605424 | T | G | 1 | a0001c0001t0001g0109 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.859-137T>G | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40605424 | |||||||
| chrX:40605457 | T | C | 2 | a0001c0001t0001g0136 a0001c0001t0001g0140 |
2 | NA18982.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.859-104T>C | ATP6AP2 | ENSG00000182220.15 | transcript | ENST00000636580.2 | protein_coding | 8/8 | chrX | 40605457 |