Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23400 |
| ensemblid | ENSG00000159363.19 |
| hgncid | 30213 |
| symbol | ATP13A2 |
| name | ATPase cation transporting 13A2 |
| refseq_nuc | NM_022089.4 |
| refseq_prot | NP_071372.1 |
| ensembl_nuc | ENST00000326735.13 |
| ensembl_prot | ENSP00000327214.8 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 16985958 |
| end | 17011928 |
| strand | - |
| ver | v1.2 |
| region | chr1:16985958-17011928 |
| region5000 | chr1:16980958-17016928 |
| regionname0 | ATP13A2_chr1_16985958_17011928 |
| regionname5000 | ATP13A2_chr1_16980958_17016928 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1180 | 349 | 89 | 56 | 156 | 10 | 36 | 121 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | MSADS others(1175): Show |
chr1 | 16980958 | 17016928 |
| a0002 | 0/0 | 1180 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | MSADS others(1175): Show |
chr1 | 16980958 | 17016928 |
| a0003 | 0/0 | 1180 | 4 | 0 | 2 | 0 | 2 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | MSADS others(1175): Show |
chr1 | 16980958 | 17016928 |
| a0004 | 0/0 | 1180 | 2 | 0 | 1 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | MSADS others(1175): Show |
chr1 | 16980958 | 17016928 |
| a0005 | 0/0 | 1180 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | MSADS others(1175): Show |
chr1 | 16980958 | 17016928 |
| a0006 | 0/0 | 1180 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | MSADS others(1175): Show |
chr1 | 16980958 | 17016928 |
| a0007 | 0/0 | 1180 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | MSADS others(1175): Show |
chr1 | 16980958 | 17016928 |
| a0008 | 0/0 | 1180 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | MSADS others(1175): Show |
chr1 | 16980958 | 17016928 |
| a0009 | 0/0 | 1180 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | MSADS others(1175): Show |
chr1 | 16980958 | 17016928 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3540 | 121 | 8 | 23 | 81 | 3 | 6 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | ATGAG others(3535): Show |
chr1 | 16980958 | 17016928 | ||
| a0001c0002 | 0/1 | 3540 | 95 | 11 | 18 | 44 | 6 | 15 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | ATGAG others(3535): Show |
chr1 | 16980958 | 17016928 | ||
| a0001c0003 | 1/0 | 3540 | 57 | 17 | 2 | 28 | 0 | 9 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | ATGAG others(3535): Show |
chr1 | 16980958 | 17016928 | ||
| a0001c0004 | 0/0 | 3540 | 31 | 24 | 7 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | ATGAG others(3535): Show |
chr1 | 16980958 | 17016928 | ||
| a0001c0005 | 0/0 | 3540 | 13 | 11 | 2 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | ATGAG others(3535): Show |
chr1 | 16980958 | 17016928 | ||
| a0001c0006 | 0/0 | 3540 | 6 | 0 | 2 | 1 | 0 | 3 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | ATGAG others(3535): Show |
chr1 | 16980958 | 17016928 | ||
| a0001c0007 | 0/0 | 3540 | 6 | 3 | 1 | 0 | 1 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | ATGAG others(3535): Show |
chr1 | 16980958 | 17016928 | ||
| a0001c0008 | 0/0 | 3540 | 5 | 5 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | ATGAG others(3535): Show |
chr1 | 16980958 | 17016928 | ||
| a0001c0013 | 0/0 | 3540 | 2 | 2 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | ATGAG others(3535): Show |
chr1 | 16980958 | 17016928 | ||
| a0001c0014 | 0/0 | 3540 | 2 | 2 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | ATGAG others(3535): Show |
chr1 | 16980958 | 17016928 | ||
| a0001c0016 | 0/0 | 3540 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | ATGAG others(3535): Show |
chr1 | 16980958 | 17016928 | ||
| a0001c0018 | 0/0 | 3540 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | ATGAG others(3535): Show |
chr1 | 16980958 | 17016928 | ||
| a0001c0019 | 0/0 | 3540 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | ATGAG others(3535): Show |
chr1 | 16980958 | 17016928 | ||
| a0001c0021 | 0/0 | 3540 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | ATGAG others(3535): Show |
chr1 | 16980958 | 17016928 | ||
| a0001c0022 | 0/0 | 3540 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | ATGAG others(3535): Show |
chr1 | 16980958 | 17016928 | ||
| a0001c0024 | 0/0 | 3540 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | ATGAG others(3535): Show |
chr1 | 16980958 | 17016928 | ||
| a0001c0025 | 0/0 | 3540 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | ATGAG others(3535): Show |
chr1 | 16980958 | 17016928 | ||
| a0001c0026 | 0/0 | 3540 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | ATGAG others(3535): Show |
chr1 | 16980958 | 17016928 | ||
| a0001c0027 | 0/0 | 3540 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | ATGAG others(3535): Show |
chr1 | 16980958 | 17016928 | ||
| a0001c0029 | 0/0 | 3540 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | ATGAG others(3535): Show |
chr1 | 16980958 | 17016928 | ||
| a0001c0030 | 0/0 | 3540 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | ATGAG others(3535): Show |
chr1 | 16980958 | 17016928 | ||
| a0002c0009 | 0/0 | 3540 | 4 | 3 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | ATGAG others(3535): Show |
chr1 | 16980958 | 17016928 | ||
| a0003c0010 | 0/0 | 3540 | 4 | 0 | 2 | 0 | 2 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | ATGAG others(3535): Show |
chr1 | 16980958 | 17016928 | ||
| a0004c0017 | 0/0 | 3540 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | ATGAG others(3535): Show |
chr1 | 16980958 | 17016928 | ||
| a0004c0020 | 0/0 | 3540 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | ATGAG others(3535): Show |
chr1 | 16980958 | 17016928 | ||
| a0005c0012 | 0/0 | 3540 | 2 | 2 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | ATGAG others(3535): Show |
chr1 | 16980958 | 17016928 | ||
| a0006c0011 | 0/0 | 3540 | 2 | 2 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | ATGAG others(3535): Show |
chr1 | 16980958 | 17016928 | ||
| a0007c0023 | 0/0 | 3540 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | ATGAG others(3535): Show |
chr1 | 16980958 | 17016928 | ||
| a0008c0028 | 0/0 | 3540 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | ATGAG others(3535): Show |
chr1 | 16980958 | 17016928 | ||
| a0009c0015 | 0/0 | 3540 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | ATGAG others(3535): Show |
chr1 | 16980958 | 17016928 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3996 | 120 | 8 | 23 | 80 | 3 | 6 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0001c0001t0005 | 0/0 | 3996 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0001c0002t0001 | 0/1 | 3996 | 92 | 10 | 17 | 43 | 6 | 15 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0001c0002t0002 | 0/0 | 3996 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0001c0002t0006 | 0/0 | 3996 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0001c0002t0007 | 0/0 | 3996 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0001c0003t0001 | 1/0 | 3996 | 54 | 15 | 1 | 28 | 0 | 9 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0001c0003t0004 | 0/0 | 3996 | 2 | 2 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0001c0003t0008 | 0/0 | 3996 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0001c0004t0001 | 0/0 | 3996 | 31 | 24 | 7 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0001c0005t0001 | 0/0 | 3996 | 11 | 9 | 2 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0001c0005t0003 | 0/0 | 3996 | 2 | 2 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0001c0006t0001 | 0/0 | 3996 | 4 | 0 | 0 | 1 | 0 | 3 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0001c0006t0002 | 0/0 | 3996 | 2 | 0 | 2 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0001c0007t0001 | 0/0 | 3996 | 6 | 3 | 1 | 0 | 1 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0001c0008t0001 | 0/0 | 3996 | 5 | 5 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0001c0013t0001 | 0/0 | 3996 | 2 | 2 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0001c0014t0001 | 0/0 | 3996 | 2 | 2 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0001c0016t0001 | 0/0 | 3996 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0001c0018t0001 | 0/0 | 3996 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0001c0019t0001 | 0/0 | 3996 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0001c0021t0001 | 0/0 | 3996 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0001c0022t0001 | 0/0 | 3996 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0001c0024t0001 | 0/0 | 3996 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0001c0025t0001 | 0/0 | 3996 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0001c0026t0001 | 0/0 | 3996 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0001c0027t0001 | 0/0 | 3996 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0001c0029t0001 | 0/0 | 3996 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0001c0030t0001 | 0/0 | 3996 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0002c0009t0001 | 0/0 | 3996 | 4 | 3 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0003c0010t0001 | 0/0 | 3996 | 4 | 0 | 2 | 0 | 2 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0004c0017t0001 | 0/0 | 3996 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0004c0020t0001 | 0/0 | 3996 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0005c0012t0001 | 0/0 | 3996 | 2 | 2 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0006c0011t0001 | 0/0 | 3996 | 2 | 2 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0007c0023t0001 | 0/0 | 3996 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0008c0028t0001 | 0/0 | 3996 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| a0009c0015t0001 | 0/0 | 3996 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | AGTGT others(3991): Show |
chr1 | 16980958 | 17016928 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 11 | 1 | 2 | 7 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 1 | 3 | 1 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0006 | 0/0 | 5 | 1 | 1 | 3 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0012 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0019 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0036 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0001 | 0/0 | 27 | 5 | 6 | 11 | 2 | 3 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0003 | 0/0 | 9 | 0 | 2 | 6 | 1 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0014 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0024 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0082 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0006g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0002t0007g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0004 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0009 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0028 | 1/0 | 2 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0003t0008g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0004t0001g0013 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0004t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0004t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0004t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0004t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0004t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0004t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0004t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0004t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0004t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0004t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0004t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0004t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0004t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0004t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0004t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0004t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0004t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0004t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0004t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0004t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0004t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0004t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0004t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0005t0001g0017 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0005t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0005t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0005t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0005t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0005t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0005t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0005t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0005t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0005t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0005t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0006t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0006t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0006t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0006t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0006t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0007t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0007t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0007t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0007t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0007t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0007t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0008t0001g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0008t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0013t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0013t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0014t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0014t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0016t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0018t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0019t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0021t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0022t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0024t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0025t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0026t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0027t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0029t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0001c0030t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0002c0009t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0002c0009t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0002c0009t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0002c0009t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0003c0010t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0003c0010t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0003c0010t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0004c0017t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0004c0020t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0005c0012t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0006c0011t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0006c0011t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0007c0023t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0008c0028t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| a0009c0015t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0201 | EUR | GBR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | GBR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0022 | EUR | FIN | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG00408 | hp1 | a0001 | c0022 | t0001 | g0069 | EAS | CHS | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | CHS | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG00544 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | CHS | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0147 | EAS | CHS | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG00642 | hp1 | a0002 | c0009 | t0001 | g0238 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG00642 | hp2 | a0001 | c0004 | t0001 | g0223 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG00673 | hp1 | a0001 | c0003 | t0001 | g0009 | EAS | CHS | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG00733 | hp1 | a0003 | c0010 | t0001 | g0030 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG00733 | hp2 | a0001 | c0003 | t0008 | g0254 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0052 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01069 | hp1 | a0001 | c0004 | t0001 | g0013 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01070 | hp1 | a0001 | c0002 | t0007 | g0094 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01070 | hp2 | a0001 | c0005 | t0001 | g0017 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01071 | hp1 | a0001 | c0004 | t0001 | g0013 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01071 | hp2 | a0001 | c0005 | t0001 | g0017 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01074 | hp2 | a0004 | c0020 | t0001 | g0047 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01099 | hp1 | a0001 | c0025 | t0001 | g0229 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0089 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01106 | hp1 | a0001 | c0004 | t0001 | g0222 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01106 | hp2 | a0001 | c0007 | t0001 | g0097 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01109 | hp1 | a0001 | c0004 | t0001 | g0044 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01109 | hp2 | a0001 | c0004 | t0001 | g0224 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01167 | hp2 | a0001 | c0006 | t0002 | g0025 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0063 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01169 | hp2 | a0001 | c0006 | t0002 | g0025 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01175 | hp2 | a0003 | c0010 | t0001 | g0119 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0150 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0065 | AMR | PUR | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01346 | hp1 | a0001 | c0004 | t0001 | g0225 | AMR | CLM | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0087 | AMR | CLM | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | IBS | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01515 | hp2 | a0003 | c0010 | t0001 | g0141 | EUR | IBS | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0003 | EUR | IBS | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01517 | hp2 | a0003 | c0010 | t0001 | g0030 | EUR | IBS | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01891 | hp1 | a0001 | c0008 | t0001 | g0007 | AFR | ACB | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01891 | hp2 | a0005 | c0012 | t0001 | g0021 | AFR | ACB | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0035 | AMR | PEL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0061 | AMR | PEL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02015 | hp1 | a0001 | c0003 | t0001 | g0009 | EAS | KHV | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02055 | hp1 | a0001 | c0003 | t0001 | g0143 | AFR | ACB | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02055 | hp2 | a0001 | c0003 | t0001 | g0029 | AFR | ACB | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | KHV | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | KHV | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02074 | hp2 | a0001 | c0003 | t0001 | g0148 | EAS | KHV | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02083 | hp2 | a0004 | c0017 | t0001 | g0179 | EAS | KHV | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | KHV | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | KHV | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02145 | hp1 | a0001 | c0003 | t0004 | g0128 | AFR | ACB | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02145 | hp2 | a0002 | c0009 | t0001 | g0239 | AFR | ACB | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02155 | hp1 | a0001 | c0003 | t0001 | g0010 | EAS | CDX | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CDX | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CDX | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CDX | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02257 | hp2 | a0001 | c0004 | t0001 | g0105 | AFR | ACB | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02258 | hp2 | a0001 | c0003 | t0001 | g0140 | AFR | ACB | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0077 | AMR | PEL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02280 | hp1 | a0001 | c0004 | t0001 | g0020 | AFR | ACB | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0080 | AFR | ACB | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02451 | hp1 | a0001 | c0013 | t0001 | g0227 | AFR | ACB | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0066 | AFR | ACB | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02572 | hp1 | a0001 | c0014 | t0001 | g0099 | AFR | GWD | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02572 | hp2 | a0001 | c0004 | t0001 | g0231 | AFR | GWD | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0014 | SAS | PJL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02615 | hp1 | a0001 | c0004 | t0001 | g0243 | AFR | GWD | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02622 | hp1 | a0001 | c0004 | t0001 | g0016 | AFR | GWD | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02622 | hp2 | a0001 | c0013 | t0001 | g0228 | AFR | GWD | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02630 | hp1 | a0001 | c0029 | t0001 | g0043 | AFR | GWD | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0117 | AFR | GWD | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02647 | hp2 | a0001 | c0003 | t0001 | g0108 | AFR | GWD | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0074 | SAS | PJL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0026 | SAS | PJL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02723 | hp1 | a0001 | c0008 | t0001 | g0007 | AFR | GWD | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02723 | hp2 | a0001 | c0004 | t0001 | g0104 | AFR | GWD | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0075 | SAS | PJL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02738 | hp1 | a0001 | c0030 | t0001 | g0093 | SAS | PJL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02738 | hp2 | a0001 | c0006 | t0001 | g0068 | SAS | PJL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02809 | hp1 | a0001 | c0005 | t0001 | g0017 | AFR | GWD | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02809 | hp2 | a0001 | c0027 | t0001 | g0220 | AFR | GWD | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02818 | hp1 | a0001 | c0005 | t0001 | g0236 | AFR | GWD | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02818 | hp2 | a0001 | c0004 | t0001 | g0240 | AFR | GWD | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02886 | hp1 | a0001 | c0007 | t0001 | g0100 | AFR | GWD | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02886 | hp2 | a0001 | c0005 | t0003 | g0109 | AFR | GWD | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02895 | hp1 | a0006 | c0011 | t0001 | g0131 | AFR | GWD | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02895 | hp2 | a0001 | c0004 | t0001 | g0103 | AFR | GWD | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02896 | hp2 | a0001 | c0004 | t0001 | g0247 | AFR | GWD | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02897 | hp1 | a0006 | c0011 | t0001 | g0124 | AFR | GWD | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02897 | hp2 | a0001 | c0004 | t0001 | g0013 | AFR | GWD | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0132 | AFR | ESN | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02922 | hp2 | a0001 | c0007 | t0001 | g0098 | AFR | ESN | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02965 | hp1 | a0001 | c0004 | t0001 | g0245 | AFR | ESN | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02965 | hp2 | a0001 | c0005 | t0001 | g0235 | AFR | ESN | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02970 | hp1 | a0001 | c0004 | t0001 | g0230 | AFR | ESN | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02970 | hp2 | a0001 | c0008 | t0001 | g0086 | AFR | ESN | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02976 | hp1 | a0001 | c0004 | t0001 | g0151 | AFR | ESN | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0035 | SAS | PJL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03041 | hp1 | a0001 | c0005 | t0001 | g0050 | AFR | GWD | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03098 | hp1 | a0001 | c0004 | t0001 | g0244 | AFR | MSL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | MSL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03130 | hp2 | a0001 | c0004 | t0001 | g0020 | AFR | ESN | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0149 | AFR | ESN | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03139 | hp2 | a0001 | c0004 | t0001 | g0016 | AFR | ESN | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0083 | AFR | ESN | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03195 | hp2 | a0001 | c0005 | t0001 | g0107 | AFR | ESN | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03209 | hp1 | a0001 | c0005 | t0001 | g0241 | AFR | MSL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0203 | AFR | MSL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03225 | hp1 | a0001 | c0004 | t0001 | g0237 | AFR | MSL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03225 | hp2 | a0001 | c0005 | t0003 | g0110 | AFR | MSL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03239 | hp1 | a0001 | c0003 | t0001 | g0057 | SAS | PJL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03453 | hp1 | a0001 | c0004 | t0001 | g0020 | AFR | MSL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03453 | hp2 | a0001 | c0016 | t0001 | g0114 | AFR | MSL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03486 | hp1 | a0001 | c0005 | t0001 | g0234 | AFR | MSL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03486 | hp2 | a0001 | c0008 | t0001 | g0007 | AFR | MSL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0064 | SAS | PJL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0173 | SAS | PJL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0112 | AFR | ESN | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0118 | AFR | GWD | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03540 | hp2 | a0001 | c0004 | t0001 | g0186 | AFR | GWD | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0029 | AFR | MSL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03579 | hp2 | a0001 | c0008 | t0001 | g0007 | AFR | MSL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03669 | hp1 | a0001 | c0003 | t0001 | g0121 | SAS | PJL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03669 | hp2 | a0007 | c0023 | t0001 | g0070 | SAS | PJL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0122 | SAS | PJL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03704 | hp2 | a0001 | c0003 | t0001 | g0009 | SAS | PJL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0022 | SAS | PJL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0026 | SAS | PJL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03831 | hp1 | a0001 | c0003 | t0001 | g0059 | SAS | BEB | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03831 | hp2 | a0001 | c0003 | t0001 | g0142 | SAS | BEB | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0071 | SAS | BEB | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG04115 | hp1 | a0001 | c0003 | t0001 | g0004 | SAS | STU | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG04115 | hp2 | a0008 | c0028 | t0001 | g0152 | SAS | STU | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG04184 | hp1 | a0001 | c0007 | t0001 | g0048 | SAS | BEB | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG04184 | hp2 | a0001 | c0003 | t0001 | g0134 | SAS | BEB | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0160 | SAS | STU | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0133 | SAS | STU | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG04228 | hp1 | a0001 | c0026 | t0001 | g0129 | SAS | STU | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG04228 | hp2 | a0001 | c0006 | t0001 | g0088 | SAS | STU | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18522 | hp1 | a0001 | c0024 | t0001 | g0242 | AFR | YRI | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18522 | hp2 | a0001 | c0004 | t0001 | g0013 | AFR | YRI | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHB | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHB | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18906 | hp2 | a0002 | c0009 | t0001 | g0233 | AFR | YRI | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18942 | hp2 | a0001 | c0003 | t0001 | g0106 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18944 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18945 | hp1 | a0001 | c0003 | t0001 | g0031 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18946 | hp2 | a0001 | c0003 | t0001 | g0032 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18947 | hp1 | a0001 | c0003 | t0001 | g0055 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18947 | hp2 | a0001 | c0002 | t0006 | g0042 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18950 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18951 | hp1 | a0001 | c0003 | t0001 | g0031 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18952 | hp1 | a0001 | c0003 | t0001 | g0010 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18954 | hp1 | a0001 | c0003 | t0001 | g0123 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18956 | hp2 | a0001 | c0003 | t0001 | g0135 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18963 | hp2 | a0001 | c0003 | t0001 | g0130 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18979 | hp1 | a0001 | c0003 | t0001 | g0028 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18981 | hp2 | a0001 | c0003 | t0001 | g0032 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18982 | hp2 | a0001 | c0003 | t0001 | g0101 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18990 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18997 | hp2 | a0001 | c0003 | t0001 | g0120 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19005 | hp2 | a0009 | c0015 | t0001 | g0145 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19007 | hp1 | a0001 | c0003 | t0001 | g0010 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0060 | AFR | LWK | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19030 | hp2 | a0005 | c0012 | t0001 | g0021 | AFR | LWK | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19043 | hp1 | a0001 | c0004 | t0001 | g0246 | AFR | LWK | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0073 | AFR | LWK | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19055 | hp1 | a0001 | c0003 | t0001 | g0146 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19055 | hp2 | a0001 | c0021 | t0001 | g0067 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19057 | hp1 | a0001 | c0003 | t0001 | g0010 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19060 | hp1 | a0001 | c0001 | t0005 | g0041 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19060 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19067 | hp1 | a0001 | c0003 | t0001 | g0153 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19086 | hp1 | a0001 | c0003 | t0001 | g0144 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19090 | hp2 | a0001 | c0006 | t0001 | g0078 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19240 | hp1 | a0001 | c0003 | t0001 | g0045 | AFR | YRI | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA19240 | hp2 | a0002 | c0009 | t0001 | g0232 | AFR | YRI | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | ASW | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA20129 | hp2 | a0001 | c0003 | t0004 | g0046 | AFR | ASW | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA20752 | hp1 | a0001 | c0007 | t0001 | g0102 | EUR | TSI | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | TSI | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0126 | EUR | TSI | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0024 | EUR | TSI | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA20905 | hp1 | a0001 | c0006 | t0001 | g0076 | SAS | GIH | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA20905 | hp2 | a0001 | c0003 | t0001 | g0058 | SAS | GIH | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0079 | AMR | CLM | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02109 | hp1 | a0001 | c0004 | t0001 | g0016 | AFR | ACB | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0113 | AFR | ACB | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02486 | hp2 | a0001 | c0005 | t0001 | g0226 | AFR | ACB | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG02559 | hp2 | a0001 | c0007 | t0001 | g0096 | AFR | ACB | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0127 | AFR | MSL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG03471 | hp2 | a0001 | c0004 | t0001 | g0248 | AFR | MSL | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG06807 | hp1 | a0001 | c0004 | t0001 | g0116 | AFR | USA | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0154 | AFR | USA | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18955 | hp1 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA20300 | hp1 | a0001 | c0014 | t0001 | g0095 | AFR | USA | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA20300 | hp2 | a0001 | c0018 | t0001 | g0206 | AFR | USA | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA21309 | hp1 | a0001 | c0005 | t0001 | g0111 | AFR | LWK | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| NA21309 | hp2 | a0001 | c0019 | t0001 | g0115 | AFR | LWK | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0082 | REF | REF | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0001 | g0028 | REF | REF | ATP13A2_chr1_16980958_17016928 | ATP13A2 | chr1 | 16980958 | 17016928 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:16987089 | C | T | 1 | a0004 | 2 | HG01074.hp2 HG02083.hp2 |
missense_variant | MODERATE | c.3040G>A | p.Gly1014Ser | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 26/29 | 3230/3996 | 3040/3543 | 1014/1180 | chr1 | 16987089 | |||
| chr1:16988161 | T | A | 1 | a0007 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.2836A>T | p.Ile946Phe | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 25/29 | 3026/3996 | 2836/3543 | 946/1180 | chr1 | 16988161 | |||
| chr1:16992042 | A | G | 1 | a0005 | 2 | HG01891.hp2 NA19030.hp2 |
missense_variant | MODERATE | c.2093T>C | p.Val698Ala | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 19/29 | 2283/3996 | 2093/3543 | 698/1180 | chr1 | 16992042 | |||
| chr1:16992115 | C | T | 1 | a0006 | 2 | HG02895.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.2020G>A | p.Ala674Thr | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 19/29 | 2210/3996 | 2020/3543 | 674/1180 | chr1 | 16992115 | |||
| chr1:17000272 | C | T | 1 | a0003 | 4 | HG00733.hp1 HG01175.hp2 HG01515.hp2 others(1): Show |
missense_variant | MODERATE | c.881G>A | p.Arg294Gln | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 10/29 | 1071/3996 | 881/3543 | 294/1180 | chr1 | 17000272 | |||
| chr1:17000309 | T | A | 1 | a0008 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.844A>T | p.Ser282Cys | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 10/29 | 1034/3996 | 844/3543 | 282/1180 | chr1 | 17000309 | |||
| chr1:17005505 | C | T | 1 | a0009 | 1 | NA19005.hp2 | missense_variant | MODERATE | c.157G>A | p.Val53Met | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 3/29 | 347/3996 | 157/3543 | 53/1180 | chr1 | 17005505 | |||
| chr1:17005517 | C | T | 1 | a0002 | 4 | HG00642.hp1 HG02145.hp2 NA18906.hp2 others(1): Show |
missense_variant | MODERATE | c.145G>A | p.Gly49Ser | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 3/29 | 335/3996 | 145/3543 | 49/1180 | chr1 | 17005517 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:16986233 | G | C | 1 | a0001c0021 | 1 | NA19055.hp2 | synonymous_variant | LOW | c.3531C>G | p.Gly1177Gly | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 29/29 | 3721/3996 | 3531/3543 | 1177/1180 | chr1 | 16986233 | |||
| chr1:16986248 | C | T | 6 | a0001c0002 a0001c0008 a0001c0021 others(3): Show |
103 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(100): Show |
synonymous_variant | LOW | c.3516G>A | p.Pro1172Pro | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 29/29 | 3706/3996 | 3516/3543 | 1172/1180 | chr1 | 16986248 | |||
| chr1:16986335 | G | A | 1 | a0001c0018 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.3429C>T | p.Pro1143Pro | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 29/29 | 3619/3996 | 3429/3543 | 1143/1180 | chr1 | 16986335 | |||
| chr1:16986848 | G | A | 7 | a0001c0002 a0001c0006 a0001c0008 others(4): Show |
109 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(106): Show |
synonymous_variant | LOW | c.3192C>T | p.Ala1064Ala | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 27/29 | 3382/3996 | 3192/3543 | 1064/1180 | chr1 | 16986848 | |||
| chr1:16986896 | G | C | 3 | a0001c0005 a0001c0014 a0002c0009 |
19 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(16): Show |
synonymous_variant | LOW | c.3144C>G | p.Thr1048Thr | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 27/29 | 3334/3996 | 3144/3543 | 1048/1180 | chr1 | 16986896 | |||
| chr1:16987159 | C | T | 8 | a0001c0002 a0001c0006 a0001c0008 others(5): Show |
111 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(108): Show |
synonymous_variant | LOW | c.2970G>A | p.Val990Val | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 26/29 | 3160/3996 | 2970/3543 | 990/1180 | chr1 | 16987159 | |||
| chr1:16988207 | C | T | 5 | a0001c0001 a0001c0016 a0001c0018 others(2): Show |
125 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(122): Show |
synonymous_variant | LOW | c.2790G>A | p.Ser930Ser | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 25/29 | 2980/3996 | 2790/3543 | 930/1180 | chr1 | 16988207 | |||
| chr1:16988360 | C | T | 1 | a0001c0013 | 2 | HG02451.hp1 HG02622.hp2 |
synonymous_variant | LOW | c.2724G>A | p.Ser908Ser | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 24/29 | 2914/3996 | 2724/3543 | 908/1180 | chr1 | 16988360 | |||
| chr1:16988447 | G | A | 7 | a0001c0002 a0001c0006 a0001c0008 others(4): Show |
109 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(106): Show |
synonymous_variant | LOW | c.2637C>T | p.Gly879Gly | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 24/29 | 2827/3996 | 2637/3543 | 879/1180 | chr1 | 16988447 | |||
| chr1:16990172 | G | A | 1 | a0001c0024 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.2367C>T | p.Leu789Leu | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 21/29 | 2557/3996 | 2367/3543 | 789/1180 | chr1 | 16990172 | |||
| chr1:16992516 | G | A | 14 | a0001c0002 a0001c0004 a0001c0006 others(11): Show |
153 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(150): Show |
synonymous_variant | LOW | c.1815C>T | p.Pro605Pro | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 17/29 | 2005/3996 | 1815/3543 | 605/1180 | chr1 | 16992516 | |||
| chr1:16993761 | C | A | 1 | a0001c0008 | 5 | HG01891.hp1 HG02723.hp1 HG02970.hp2 others(2): Show |
synonymous_variant | LOW | c.1617G>T | p.Leu539Leu | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 16/29 | 1807/3996 | 1617/3543 | 539/1180 | chr1 | 16993761 | |||
| chr1:16993764 | G | A | 1 | a0001c0025 | 1 | HG01099.hp1 | synonymous_variant | LOW | c.1614C>T | p.Pro538Pro | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 16/29 | 1804/3996 | 1614/3543 | 538/1180 | chr1 | 16993764 | |||
| chr1:16993806 | G | A | 1 | a0001c0016 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.1572C>T | p.Asp524Asp | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 16/29 | 1762/3996 | 1572/3543 | 524/1180 | chr1 | 16993806 | |||
| chr1:16995982 | G | A | 1 | a0001c0026 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.1536C>T | p.Phe512Phe | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 15/29 | 1726/3996 | 1536/3543 | 512/1180 | chr1 | 16995982 | |||
| chr1:16997084 | C | T | 1 | a0001c0016 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.1131G>A | p.Gly377Gly | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 12/29 | 1321/3996 | 1131/3543 | 377/1180 | chr1 | 16997084 | |||
| chr1:17000045 | G | A | 3 | a0001c0007 a0001c0014 a0001c0027 |
9 | HG01106.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
synonymous_variant | LOW | c.1005C>T | p.Ala335Ala | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/29 | 1195/3996 | 1005/3543 | 335/1180 | chr1 | 17000045 | |||
| chr1:17004716 | G | A | 1 | a0001c0029 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.453C>T | p.Ser151Ser | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 5/29 | 643/3996 | 453/3543 | 151/1180 | chr1 | 17004716 | |||
| chr1:17005548 | G | A | 1 | a0001c0030 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.114C>T | p.Ser38Ser | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 3/29 | 304/3996 | 114/3543 | 38/1180 | chr1 | 17005548 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:16985990 | C | T | 1 | a0001c0005t0003 | 2 | HG02886.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*231G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 29/29 | 231 | chr1 | 16985990 | ||||||
| chr1:16986081 | G | C | 1 | a0001c0003t0004 | 2 | HG02145.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*140C>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 29/29 | 140 | chr1 | 16986081 | ||||||
| chr1:16986091 | G | A | 1 | a0001c0001t0001 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*130C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 29/29 | 130 | chr1 | 16986091 | ||||||
| chr1:16986097 | G | A | 2 | a0001c0002t0002 a0001c0006t0002 |
3 | HG01167.hp2 HG01169.hp2 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*124C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 29/29 | 124 | chr1 | 16986097 | ||||||
| chr1:16986101 | T | A | 1 | a0001c0002t0007 | 1 | HG01070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*120A>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 29/29 | 120 | chr1 | 16986101 | ||||||
| chr1:17011837 | C | G | 1 | a0001c0002t0006 | 1 | NA18947.hp2 | 5_prime_UTR_variant | MODIFIER | c.-99G>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/29 | 99 | chr1 | 17011837 | ||||||
| chr1:17011859 | G | A | 1 | a0001c0003t0008 | 1 | HG00733.hp2 | 5_prime_UTR_variant | MODIFIER | c.-121C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/29 | 121 | chr1 | 17011859 | ||||||
| chr1:17011909 | C | G | 1 | a0001c0001t0005 | 1 | NA19060.hp1 | 5_prime_UTR_variant | MODIFIER | c.-171G>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/29 | 171 | chr1 | 17011909 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:16986662 | G | A | 60 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0008 others(57): Show |
112 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.3236-30C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 27/28 | chr1 | 16986662 | |||||||
| chr1:16986714 | C | T | 1 | a0001c0004t0001g0240 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3236-82G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 27/28 | chr1 | 16986714 | |||||||
| chr1:16986718 | C | A | 1 | a0001c0001t0001g0181 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3236-86G>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 27/28 | chr1 | 16986718 | |||||||
| chr1:16986719 | G | A | 6 | a0001c0003t0001g0118 a0001c0003t0001g0132 a0001c0003t0001g0140 others(3): Show |
6 | HG02055.hp1 HG02258.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.3235+86C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 27/28 | chr1 | 16986719 | |||||||
| chr1:16986749 | C | A | 1 | a0001c0029t0001g0043 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3235+56G>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 27/28 | chr1 | 16986749 | |||||||
| chr1:16986749 | CCCCAGGG others(5): Show |
C | 92 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
127 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.3235+44_3235+55del others(12): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 27/28 | chr1 | 16986749 | |||||||
| chr1:16986788 | C | T | 3 | a0001c0004t0001g0222 a0001c0024t0001g0242 a0001c0025t0001g0229 |
3 | HG01099.hp1 HG01106.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3235+17G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 27/28 | chr1 | 16986788 | |||||||
| chr1:16986959 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
129 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(126): Show |
splice_region_variant&intron_variant | LOW | c.3084-3C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 26/28 | chr1 | 16986959 | |||||||
| chr1:16987022 | G | A | 3 | a0001c0004t0001g0222 a0001c0024t0001g0242 a0001c0025t0001g0229 |
3 | HG01099.hp1 HG01106.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3083+24C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 26/28 | chr1 | 16987022 | |||||||
| chr1:16987440 | G | T | 1 | a0001c0004t0001g0103 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2860-171C>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 25/28 | chr1 | 16987440 | |||||||
| chr1:16987491 | G | A | 2 | a0001c0003t0004g0046 a0001c0003t0004g0128 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2860-222C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 25/28 | chr1 | 16987491 | |||||||
| chr1:16987578 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
129 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.2860-309T>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 25/28 | chr1 | 16987578 | |||||||
| chr1:16987747 | G | C | 2 | a0001c0003t0004g0046 a0001c0003t0004g0128 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2859+391C>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 25/28 | chr1 | 16987747 | |||||||
| chr1:16987800 | G | A | 1 | a0001c0003t0001g0059 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2859+338C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 25/28 | chr1 | 16987800 | |||||||
| chr1:16987829 | G | A | 2 | a0001c0003t0004g0046 a0001c0003t0004g0128 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2859+309C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 25/28 | chr1 | 16987829 | |||||||
| chr1:16987888 | G | T | 2 | a0001c0003t0004g0046 a0001c0003t0004g0128 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2859+250C>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 25/28 | chr1 | 16987888 | |||||||
| chr1:16988056 | A | G | 1 | a0001c0029t0001g0043 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2859+82T>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 25/28 | chr1 | 16988056 | |||||||
| chr1:16988091 | C | T | 1 | a0001c0003t0001g0057 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2859+47G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 25/28 | chr1 | 16988091 | |||||||
| chr1:16988105 | C | T | 1 | a0001c0004t0001g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2859+33G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 25/28 | chr1 | 16988105 | |||||||
| chr1:16988250 | C | T | 2 | a0001c0003t0004g0046 a0001c0003t0004g0128 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2763-16G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 24/28 | chr1 | 16988250 | |||||||
| chr1:16988291 | G | A | 2 | a0001c0003t0004g0046 a0001c0003t0004g0128 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2762+31C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 24/28 | chr1 | 16988291 | |||||||
| chr1:16988293 | C | T | 2 | a0001c0003t0004g0046 a0001c0003t0004g0128 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2762+29G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 24/28 | chr1 | 16988293 | |||||||
| chr1:16988594 | C | T | 2 | a0001c0003t0004g0046 a0001c0003t0004g0128 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2610-120G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 23/28 | chr1 | 16988594 | |||||||
| chr1:16988595 | G | A | 1 | a0001c0002t0001g0062 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2610-121C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 23/28 | chr1 | 16988595 | |||||||
| chr1:16988615 | TATTATTA others(8): Show |
T | 1 | a0001c0029t0001g0043 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2610-156_2610-142d others(17): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 23/28 | chr1 | 16988615 | |||||||
| chr1:16988628 | A | G | 4 | a0001c0004t0001g0230 a0001c0004t0001g0237 a0001c0013t0001g0227 others(1): Show |
4 | HG02451.hp1 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2610-154T>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 23/28 | chr1 | 16988628 | |||||||
| chr1:16988725 | T | C | 2 | a0001c0003t0004g0046 a0001c0003t0004g0128 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2610-251A>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 23/28 | chr1 | 16988725 | |||||||
| chr1:16988747 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
129 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.2610-273A>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 23/28 | chr1 | 16988747 | |||||||
| chr1:16988789 | C | T | 12 | a0001c0002t0001g0008 a0001c0002t0001g0027 a0001c0002t0001g0051 others(9): Show |
16 | HG01123.hp2 HG02056.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.2610-315G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 23/28 | chr1 | 16988789 | |||||||
| chr1:16988930 | G | A | 67 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0008 others(64): Show |
119 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2610-456C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 23/28 | chr1 | 16988930 | |||||||
| chr1:16989057 | T | C | 2 | a0001c0003t0004g0046 a0001c0003t0004g0128 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2610-583A>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 23/28 | chr1 | 16989057 | |||||||
| chr1:16989225 | T | C | 2 | a0001c0005t0001g0050 a0001c0005t0001g0107 |
2 | HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2609+466A>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 23/28 | chr1 | 16989225 | |||||||
| chr1:16989235 | G | A | 3 | a0001c0003t0004g0046 a0001c0003t0004g0128 a0005c0012t0001g0021 |
4 | HG01891.hp2 HG02145.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.2609+456C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 23/28 | chr1 | 16989235 | |||||||
| chr1:16989293 | C | A | 1 | a0001c0029t0001g0043 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2609+398G>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 23/28 | chr1 | 16989293 | |||||||
| chr1:16989295 | G | A | 1 | a0005c0012t0001g0021 | 2 | HG01891.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2609+396C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 23/28 | chr1 | 16989295 | |||||||
| chr1:16989341 | AGCTGG | A | 3 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0217 |
3 | HG00099.hp1 HG01074.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.2609+345_2609+349d others(7): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 23/28 | chr1 | 16989341 | |||||||
| chr1:16989388 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2609+303A>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 23/28 | chr1 | 16989388 | |||||||
| chr1:16989573 | T | C | 2 | a0001c0003t0001g0117 a0001c0003t0001g0127 |
2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2609+118A>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 23/28 | chr1 | 16989573 | |||||||
| chr1:16989878 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2529+9G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 22/28 | chr1 | 16989878 | |||||||
| chr1:16990082 | G | T | 1 | a0005c0012t0001g0021 | 2 | HG01891.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2412+45C>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 21/28 | chr1 | 16990082 | |||||||
| chr1:16990472 | G | C | 4 | a0001c0003t0001g0010 a0001c0003t0001g0055 a0001c0003t0001g0123 others(1): Show |
7 | HG02074.hp2 HG02155.hp1 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.2252-185C>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 20/28 | chr1 | 16990472 | |||||||
| chr1:16990685 | A | AT | 92 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
127 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.2252-399dupA | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 20/28 | chr1 | 16990685 | |||||||
| chr1:16990713 | G | T | 1 | a0001c0003t0001g0108 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2252-426C>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 20/28 | chr1 | 16990713 | |||||||
| chr1:16990832 | C | T | 1 | a0001c0004t0001g0116 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2252-545G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 20/28 | chr1 | 16990832 | |||||||
| chr1:16990857 | A | G | 5 | a0001c0003t0001g0029 a0001c0003t0001g0112 a0001c0003t0001g0113 others(2): Show |
6 | HG02055.hp2 HG02109.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2252-570T>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 20/28 | chr1 | 16990857 | |||||||
| chr1:16991045 | G | C | 1 | a0001c0001t0001g0192 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2251+689C>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 20/28 | chr1 | 16991045 | |||||||
| chr1:16991048 | G | C | 2 | a0001c0003t0004g0046 a0001c0003t0004g0128 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2251+686C>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 20/28 | chr1 | 16991048 | |||||||
| chr1:16991101 | C | G | 1 | a0001c0001t0001g0189 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2251+633G>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 20/28 | chr1 | 16991101 | |||||||
| chr1:16991220 | G | C | 2 | a0001c0003t0004g0046 a0001c0003t0004g0128 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2251+514C>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 20/28 | chr1 | 16991220 | |||||||
| chr1:16991273 | C | T | 3 | a0001c0004t0001g0151 a0001c0007t0001g0097 a0001c0007t0001g0098 |
3 | HG01106.hp2 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2251+461G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 20/28 | chr1 | 16991273 | |||||||
| chr1:16991374 | C | T | 1 | a0001c0004t0001g0222 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2251+360G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 20/28 | chr1 | 16991374 | |||||||
| chr1:16991570 | T | C | 91 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(88): Show |
126 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.2251+164A>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 20/28 | chr1 | 16991570 | |||||||
| chr1:16991576 | G | C | 1 | a0001c0007t0001g0100 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2251+158C>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 20/28 | chr1 | 16991576 | |||||||
| chr1:16991581 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2251+153T>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 20/28 | chr1 | 16991581 | |||||||
| chr1:16991598 | G | A | 1 | a0001c0003t0001g0045 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2251+136C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 20/28 | chr1 | 16991598 | |||||||
| chr1:16991672 | C | T | 1 | a0001c0003t0004g0046 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2251+62G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 20/28 | chr1 | 16991672 | |||||||
| chr1:16991689 | G | A | 3 | a0001c0004t0001g0020 a0001c0004t0001g0240 a0001c0004t0001g0245 |
5 | HG02280.hp1 HG02818.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2251+45C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 20/28 | chr1 | 16991689 | |||||||
| chr1:16991953 | G | A | 4 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
4 | HG02083.hp1 HG03654.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.2126+56C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 19/28 | chr1 | 16991953 | |||||||
| chr1:16992430 | G | A | 1 | a0001c0029t0001g0043 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1846-28C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 17/28 | chr1 | 16992430 | |||||||
| chr1:16992745 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1750-164G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 16/28 | chr1 | 16992745 | |||||||
| chr1:16992792 | C | T | 94 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0008 others(91): Show |
153 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.1750-211G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 16/28 | chr1 | 16992792 | |||||||
| chr1:16992868 | G | A | 1 | a0001c0004t0001g0237 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1750-287C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 16/28 | chr1 | 16992868 | |||||||
| chr1:16992878 | G | A | 1 | a0005c0012t0001g0021 | 2 | HG01891.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1750-297C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 16/28 | chr1 | 16992878 | |||||||
| chr1:16993072 | G | A | 1 | a0007c0023t0001g0070 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1750-491C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 16/28 | chr1 | 16993072 | |||||||
| chr1:16993309 | G | A | 1 | a0001c0019t0001g0115 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1749+320C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 16/28 | chr1 | 16993309 | |||||||
| chr1:16993844 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1543-9C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 15/28 | chr1 | 16993844 | |||||||
| chr1:16993861 | G | C | 1 | a0001c0002t0001g0027 | 2 | NA19012.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1543-26C>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 15/28 | chr1 | 16993861 | |||||||
| chr1:16993880 | G | T | 1 | a0001c0002t0001g0065 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1543-45C>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 15/28 | chr1 | 16993880 | |||||||
| chr1:16994013 | G | T | 1 | a0001c0001t0001g0164 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1543-178C>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 15/28 | chr1 | 16994013 | |||||||
| chr1:16994174 | C | T | 17 | a0001c0005t0001g0017 a0001c0005t0001g0050 a0001c0005t0001g0107 others(14): Show |
19 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1543-339G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 15/28 | chr1 | 16994174 | |||||||
| chr1:16994184 | G | GCGCTCTC others(9): Show |
1 | a0001c0029t0001g0043 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1543-350_1543-349i others(18): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 15/28 | chr1 | 16994184 | |||||||
| chr1:16994188 | T | G | 1 | a0001c0007t0001g0097 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1543-353A>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 15/28 | chr1 | 16994188 | |||||||
| chr1:16994197 | C | CTCTCTCA others(3): Show |
2 | a0001c0001t0001g0157 a0001c0001t0001g0214 |
2 | HG00735.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1543-363_1543-362i others(12): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 15/28 | chr1 | 16994197 | |||||||
| chr1:16994197 | C | CTCTCTCT others(5): Show |
2 | a0001c0001t0001g0162 a0001c0016t0001g0114 |
2 | HG01167.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1543-363_1543-362i others(14): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 15/28 | chr1 | 16994197 | |||||||
| chr1:16994197 | C | CTCTCTCT others(7): Show |
80 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(77): Show |
115 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.1543-363_1543-362i others(16): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 15/28 | chr1 | 16994197 | |||||||
| chr1:16994197 | C | CTCTCTCT others(11): Show |
7 | a0001c0001t0001g0159 a0001c0001t0001g0175 a0001c0001t0001g0185 others(4): Show |
7 | NA18948.hp1 NA18948.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.1543-363_1543-362i others(20): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 15/28 | chr1 | 16994197 | |||||||
| chr1:16994293 | C | T | 2 | a0001c0003t0001g0133 a0001c0003t0001g0134 |
2 | HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1543-458G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 15/28 | chr1 | 16994293 | |||||||
| chr1:16994345 | G | A | 1 | a0001c0002t0001g0079 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1543-510C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 15/28 | chr1 | 16994345 | |||||||
| chr1:16994379 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1543-544G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 15/28 | chr1 | 16994379 | |||||||
| chr1:16994480 | G | A | 1 | a0001c0002t0001g0073 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1543-645C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 15/28 | chr1 | 16994480 | |||||||
| chr1:16994538 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1543-703T>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 15/28 | chr1 | 16994538 | |||||||
| chr1:16994675 | T | A | 1 | a0001c0003t0004g0046 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1543-840A>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 15/28 | chr1 | 16994675 | |||||||
| chr1:16994713 | A | G | 33 | a0001c0004t0001g0013 a0001c0004t0001g0016 a0001c0004t0001g0020 others(30): Show |
40 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.1543-878T>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 15/28 | chr1 | 16994713 | |||||||
| chr1:16994776 | C | A | 17 | a0001c0005t0001g0017 a0001c0005t0001g0050 a0001c0005t0001g0107 others(14): Show |
19 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1543-941G>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 15/28 | chr1 | 16994776 | |||||||
| chr1:16994933 | A | T | 90 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(87): Show |
125 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.1542+1043T>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 15/28 | chr1 | 16994933 | |||||||
| chr1:16994954 | G | C | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1542+1022C>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 15/28 | chr1 | 16994954 | |||||||
| chr1:16995017 | G | A | 9 | a0001c0001t0001g0018 a0001c0001t0001g0037 a0001c0001t0001g0155 others(6): Show |
12 | HG00423.hp2 HG01943.hp1 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1542+959C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 15/28 | chr1 | 16995017 | |||||||
| chr1:16995127 | G | A | 3 | a0001c0001t0001g0217 a0001c0005t0001g0234 a0001c0005t0001g0241 |
3 | HG01081.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1542+849C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 15/28 | chr1 | 16995127 | |||||||
| chr1:16995175 | G | A | 1 | a0001c0001t0001g0251 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1542+801C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 15/28 | chr1 | 16995175 | |||||||
| chr1:16995325 | C | T | 1 | a0001c0003t0004g0046 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1542+651G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 15/28 | chr1 | 16995325 | |||||||
| chr1:16995445 | A | G | 2 | a0001c0001t0001g0208 a0001c0001t0001g0253 |
2 | HG02602.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1542+531T>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 15/28 | chr1 | 16995445 | |||||||
| chr1:16995493 | T | C | 1 | a0001c0003t0004g0046 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1542+483A>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 15/28 | chr1 | 16995493 | |||||||
| chr1:16995572 | C | T | 1 | a0001c0003t0004g0046 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1542+404G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 15/28 | chr1 | 16995572 | |||||||
| chr1:16995737 | C | T | 1 | a0001c0002t0001g0064 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1542+239G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 15/28 | chr1 | 16995737 | |||||||
| chr1:16996188 | G | A | 1 | a0001c0004t0001g0243 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1354-24C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 14/28 | chr1 | 16996188 | |||||||
| chr1:16996519 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1196-23T>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 12/28 | chr1 | 16996519 | |||||||
| chr1:16996658 | T | C | 1 | a0001c0002t0001g0071 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1196-162A>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 12/28 | chr1 | 16996658 | |||||||
| chr1:16996703 | A | T | 90 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(87): Show |
125 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.1196-207T>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 12/28 | chr1 | 16996703 | |||||||
| chr1:16996773 | G | A | 22 | a0001c0004t0001g0013 a0001c0004t0001g0016 a0001c0004t0001g0020 others(19): Show |
29 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1195+247C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 12/28 | chr1 | 16996773 | |||||||
| chr1:16996821 | G | C | 2 | a0001c0007t0001g0048 a0001c0007t0001g0102 |
2 | HG04184.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1195+199C>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 12/28 | chr1 | 16996821 | |||||||
| chr1:16996871 | T | TG | 90 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(87): Show |
125 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.1195+148dupC | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 12/28 | chr1 | 16996871 | |||||||
| chr1:16996938 | C | T | 17 | a0001c0005t0001g0017 a0001c0005t0001g0050 a0001c0005t0001g0107 others(14): Show |
19 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1195+82G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 12/28 | chr1 | 16996938 | |||||||
| chr1:16996954 | T | C | 199 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(196): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.1195+66A>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 12/28 | chr1 | 16996954 | |||||||
| chr1:16997011 | G | A | 6 | a0001c0001t0001g0072 a0001c0001t0001g0170 a0001c0001t0001g0180 others(3): Show |
6 | HG00544.hp1 HG02015.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.1195+9C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 12/28 | chr1 | 16997011 | |||||||
| chr1:16997232 | C | G | 1 | a0001c0007t0001g0097 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1040-57G>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16997232 | |||||||
| chr1:16997298 | C | T | 1 | a0001c0007t0001g0096 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1040-123G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16997298 | |||||||
| chr1:16997414 | C | CGGGGG | 16 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0158 others(13): Show |
20 | HG00642.hp1 HG02040.hp2 HG02148.hp1 others(17): Show |
intron_variant | MODIFIER | c.1040-244_1040-240d others(7): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16997414 | |||||||
| chr1:16997414 | C | CGGGGGG | 32 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0039 others(29): Show |
44 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.1040-245_1040-240d others(8): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16997414 | |||||||
| chr1:16997414 | C | CGGGGGGG | 23 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0034 others(20): Show |
29 | HG00597.hp1 HG00621.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1040-246_1040-240d others(9): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16997414 | |||||||
| chr1:16997414 | C | CGGGGGGG others(1): Show |
19 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0038 others(16): Show |
25 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.1040-247_1040-240d others(10): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16997414 | |||||||
| chr1:16997414 | C | CGGGGGGG others(3): Show |
2 | a0001c0001t0001g0036 a0004c0017t0001g0179 |
3 | HG02083.hp2 NA18906.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1040-240_1040-239i others(12): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16997414 | |||||||
| chr1:16997414 | C | CGGGGGGG others(4): Show |
1 | a0001c0001t0001g0200 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1040-240_1040-239i others(13): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16997414 | |||||||
| chr1:16997414 | C | CGGGGGGG others(5): Show |
1 | a0001c0001t0001g0217 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1040-240_1040-239i others(14): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16997414 | |||||||
| chr1:16997414 | C | CGGGGGGG others(6): Show |
1 | a0001c0001t0001g0187 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1040-240_1040-239i others(15): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16997414 | |||||||
| chr1:16997417 | G | C | 4 | a0001c0003t0001g0118 a0001c0003t0001g0140 a0001c0003t0001g0149 others(1): Show |
4 | HG02258.hp2 HG03139.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1040-242C>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16997417 | |||||||
| chr1:16997424 | T | G | 147 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(144): Show |
190 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.1040-249A>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16997424 | |||||||
| chr1:16997434 | A | G | 1 | a0001c0002t0001g0024 | 2 | NA20129.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1040-259T>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16997434 | |||||||
| chr1:16997483 | T | C | 6 | a0001c0002t0001g0026 a0001c0002t0001g0063 a0001c0002t0001g0073 others(3): Show |
7 | HG01070.hp1 HG01169.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1040-308A>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16997483 | |||||||
| chr1:16997598 | T | C | 1 | a0001c0004t0001g0103 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1040-423A>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16997598 | |||||||
| chr1:16997601 | G | A | 1 | a0001c0029t0001g0043 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1040-426C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16997601 | |||||||
| chr1:16997698 | G | A | 1 | a0001c0024t0001g0242 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1040-523C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16997698 | |||||||
| chr1:16997702 | G | A | 2 | a0001c0003t0004g0046 a0001c0004t0001g0116 |
2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1040-527C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16997702 | |||||||
| chr1:16997773 | G | A | 4 | a0001c0004t0001g0016 a0001c0004t0001g0103 a0001c0004t0001g0104 others(1): Show |
6 | HG02109.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1040-598C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16997773 | |||||||
| chr1:16998039 | C | A | 1 | a0001c0002t0001g0074 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1040-864G>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16998039 | |||||||
| chr1:16998042 | G | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(86): Show |
124 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1040-867C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16998042 | |||||||
| chr1:16998139 | T | C | 4 | a0001c0004t0001g0016 a0001c0004t0001g0103 a0001c0004t0001g0104 others(1): Show |
6 | HG02109.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1040-964A>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16998139 | |||||||
| chr1:16998172 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1040-997C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16998172 | |||||||
| chr1:16998251 | C | T | 2 | a0001c0003t0004g0046 a0001c0004t0001g0116 |
2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1040-1076G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16998251 | |||||||
| chr1:16998263 | G | C | 47 | a0001c0003t0001g0004 a0001c0003t0001g0009 a0001c0003t0001g0010 others(44): Show |
62 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.1040-1088C>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16998263 | |||||||
| chr1:16998300 | G | A | 2 | a0001c0003t0001g0031 a0001c0003t0001g0146 |
3 | NA18945.hp1 NA18951.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1040-1125C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16998300 | |||||||
| chr1:16998509 | G | A | 5 | a0001c0007t0001g0096 a0001c0007t0001g0097 a0001c0007t0001g0098 others(2): Show |
5 | HG01106.hp2 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1040-1334C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16998509 | |||||||
| chr1:16998595 | A | G | 1 | a0001c0004t0001g0104 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1039+1416T>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16998595 | |||||||
| chr1:16998755 | G | A | 1 | a0001c0003t0001g0130 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1039+1256C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16998755 | |||||||
| chr1:16998791 | A | G | 1 | a0001c0006t0001g0088 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1039+1220T>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16998791 | |||||||
| chr1:16998902 | C | T | 1 | a0001c0003t0001g0045 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1039+1109G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16998902 | |||||||
| chr1:16998937 | C | T | 1 | a0001c0003t0001g0150 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1039+1074G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16998937 | |||||||
| chr1:16999001 | G | A | 1 | a0001c0003t0004g0046 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1039+1010C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999001 | |||||||
| chr1:16999063 | T | C | 1 | a0001c0004t0001g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1039+948A>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999063 | |||||||
| chr1:16999239 | G | T | 1 | a0001c0024t0001g0242 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1039+772C>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999239 | |||||||
| chr1:16999332 | A | T | 1 | a0009c0015t0001g0145 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1039+679T>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999332 | |||||||
| chr1:16999375 | C | T | 2 | a0001c0003t0001g0133 a0001c0003t0001g0134 |
2 | HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1039+636G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999375 | |||||||
| chr1:16999380 | C | CA | 103 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(100): Show |
144 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.1039+630dupT | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999380 | |||||||
| chr1:16999380 | C | CAA | 10 | a0001c0001t0001g0168 a0001c0001t0001g0187 a0001c0001t0001g0188 others(7): Show |
10 | HG00408.hp2 HG00741.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1039+629_1039+630d others(4): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999380 | |||||||
| chr1:16999380 | CA | C | 5 | a0001c0002t0001g0063 a0001c0003t0001g0106 a0001c0004t0001g0016 others(2): Show |
7 | HG01169.hp1 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1039+630delT | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999380 | |||||||
| chr1:16999380 | CAAAAA | C | 51 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(48): Show |
66 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.1039+626_1039+630d others(7): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999380 | |||||||
| chr1:16999405 | AG | A | 41 | a0001c0001t0001g0072 a0001c0002t0001g0001 a0001c0002t0001g0003 others(38): Show |
79 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.1039+605delC | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999405 | |||||||
| chr1:16999406 | G | A | 6 | a0001c0002t0001g0001 a0001c0002t0001g0014 a0001c0002t0001g0023 others(3): Show |
8 | HG00597.hp2 HG02135.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1039+605C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999406 | |||||||
| chr1:16999460 | G | A | 91 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(88): Show |
114 | HG00544.hp2 HG00642.hp2 HG00673.hp1 others(111): Show |
intron_variant | MODIFIER | c.1039+551C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999460 | |||||||
| chr1:16999496 | G | A | 1 | a0001c0003t0001g0130 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1039+515C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999496 | |||||||
| chr1:16999636 | A | T | 244 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(241): Show |
353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.1039+375T>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999636 | |||||||
| chr1:16999675 | G | GTCAACAA others(5): Show |
1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+335_1039+336i others(14): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999675 | |||||||
| chr1:16999676 | C | T | 243 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(240): Show |
352 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.1039+335G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999676 | |||||||
| chr1:16999678 | G | T | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+333C>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999678 | |||||||
| chr1:16999684 | C | A | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+327G>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999684 | |||||||
| chr1:16999686 | G | A | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+325C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999686 | |||||||
| chr1:16999687 | A | C | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+324T>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999687 | |||||||
| chr1:16999689 | G | A | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+322C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999689 | |||||||
| chr1:16999691 | C | A | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+320G>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999691 | |||||||
| chr1:16999693 | G | A | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+318C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999693 | |||||||
| chr1:16999694 | G | A | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+317C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999694 | |||||||
| chr1:16999695 | A | T | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+316T>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999695 | |||||||
| chr1:16999702 | G | C | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+309C>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999702 | |||||||
| chr1:16999704 | C | T | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+307G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999704 | |||||||
| chr1:16999707 | G | A | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+304C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999707 | |||||||
| chr1:16999709 | C | A | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+302G>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999709 | |||||||
| chr1:16999709 | C | T | 2 | a0001c0003t0001g0031 a0001c0003t0001g0146 |
3 | NA18945.hp1 NA18951.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1039+302G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999709 | |||||||
| chr1:16999710 | T | A | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+301A>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999710 | |||||||
| chr1:16999711 | G | A | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+300C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999711 | |||||||
| chr1:16999714 | C | A | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+297G>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999714 | |||||||
| chr1:16999722 | T | A | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+289A>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999722 | |||||||
| chr1:16999723 | G | A | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+288C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999723 | |||||||
| chr1:16999726 | A | AAATTAGA others(6): Show |
1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+284_1039+285i others(15): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999726 | |||||||
| chr1:16999728 | T | A | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+283A>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999728 | |||||||
| chr1:16999730 | C | T | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+281G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999730 | |||||||
| chr1:16999731 | A | T | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+280T>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999731 | |||||||
| chr1:16999732 | T | G | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+279A>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999732 | |||||||
| chr1:16999735 | C | T | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+276G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999735 | |||||||
| chr1:16999738 | C | T | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+273G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999738 | |||||||
| chr1:16999741 | A | G | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+270T>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999741 | |||||||
| chr1:16999743 | A | G | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+268T>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999743 | |||||||
| chr1:16999764 | G | A | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+247C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999764 | |||||||
| chr1:16999772 | G | T | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+239C>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999772 | |||||||
| chr1:16999773 | C | G | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+238G>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999773 | |||||||
| chr1:16999781 | G | C | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+230C>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999781 | |||||||
| chr1:16999783 | C | T | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+228G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999783 | |||||||
| chr1:16999787 | G | A | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+224C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999787 | |||||||
| chr1:16999788 | C | G | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+223G>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999788 | |||||||
| chr1:16999790 | A | T | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+221T>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999790 | |||||||
| chr1:16999791 | C | T | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+220G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999791 | |||||||
| chr1:16999793 | C | T | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+218G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999793 | |||||||
| chr1:16999794 | A | G | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+217T>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999794 | |||||||
| chr1:16999795 | G | T | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+216C>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999795 | |||||||
| chr1:16999799 | G | A | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+212C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999799 | |||||||
| chr1:16999800 | C | T | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+211G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999800 | |||||||
| chr1:16999801 | T | G | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+210A>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999801 | |||||||
| chr1:16999804 | G | T | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+207C>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999804 | |||||||
| chr1:16999805 | G | A | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+206C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999805 | |||||||
| chr1:16999807 | A | G | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+204T>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999807 | |||||||
| chr1:16999810 | A | T | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+201T>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999810 | |||||||
| chr1:16999811 | G | T | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+200C>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999811 | |||||||
| chr1:16999813 | A | T | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+198T>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999813 | |||||||
| chr1:16999814 | T | A | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+197A>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999814 | |||||||
| chr1:16999823 | C | G | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+188G>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999823 | |||||||
| chr1:16999833 | GGAGGCTG others(8): Show |
G | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+163_1039+177d others(17): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999833 | |||||||
| chr1:16999849 | T | A | 1 | a0001c0006t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039+162A>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 11/28 | chr1 | 16999849 | |||||||
| chr1:17000196 | C | T | 4 | a0002c0009t0001g0232 a0002c0009t0001g0233 a0002c0009t0001g0238 others(1): Show |
4 | HG00642.hp1 HG02145.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.907+50G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 10/28 | chr1 | 17000196 | |||||||
| chr1:17000217 | C | A | 5 | a0001c0003t0001g0029 a0001c0003t0001g0112 a0001c0003t0001g0113 others(2): Show |
6 | HG02055.hp2 HG02109.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.907+29G>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 10/28 | chr1 | 17000217 | |||||||
| chr1:17000602 | T | A | 8 | a0001c0007t0001g0048 a0001c0007t0001g0096 a0001c0007t0001g0097 others(5): Show |
8 | HG01106.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.706-68A>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 8/28 | chr1 | 17000602 | |||||||
| chr1:17000603 | C | T | 8 | a0001c0007t0001g0048 a0001c0007t0001g0096 a0001c0007t0001g0097 others(5): Show |
8 | HG01106.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.706-69G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 8/28 | chr1 | 17000603 | |||||||
| chr1:17000614 | G | T | 1 | a0001c0025t0001g0229 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.706-80C>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 8/28 | chr1 | 17000614 | |||||||
| chr1:17000760 | G | A | 1 | a0001c0025t0001g0229 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.706-226C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 8/28 | chr1 | 17000760 | |||||||
| chr1:17000771 | A | G | 1 | a0001c0027t0001g0220 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.706-237T>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 8/28 | chr1 | 17000771 | |||||||
| chr1:17000881 | G | A | 4 | a0001c0004t0001g0016 a0001c0004t0001g0103 a0001c0004t0001g0104 others(1): Show |
6 | HG02109.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.706-347C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 8/28 | chr1 | 17000881 | |||||||
| chr1:17000898 | C | T | 4 | a0001c0004t0001g0230 a0001c0004t0001g0237 a0001c0013t0001g0227 others(1): Show |
4 | HG02451.hp1 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.706-364G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 8/28 | chr1 | 17000898 | |||||||
| chr1:17000934 | C | T | 53 | a0001c0001t0001g0072 a0001c0002t0001g0001 a0001c0002t0001g0003 others(50): Show |
103 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.706-400G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 8/28 | chr1 | 17000934 | |||||||
| chr1:17001024 | T | C | 7 | a0001c0003t0001g0118 a0001c0003t0001g0132 a0001c0003t0001g0140 others(4): Show |
7 | HG02055.hp1 HG02258.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.706-490A>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 8/28 | chr1 | 17001024 | |||||||
| chr1:17001161 | T | C | 1 | a0001c0002t0001g0077 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.706-627A>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 8/28 | chr1 | 17001161 | |||||||
| chr1:17001247 | G | A | 1 | a0001c0002t0001g0089 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.706-713C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 8/28 | chr1 | 17001247 | |||||||
| chr1:17001263 | C | CAAAAAA | 13 | a0001c0001t0001g0169 a0001c0001t0001g0172 a0001c0001t0001g0174 others(10): Show |
13 | HG01943.hp2 HG01993.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.706-735_706-730dup others(6): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 8/28 | chr1 | 17001263 | |||||||
| chr1:17001263 | C | CAAAAAAA | 151 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(148): Show |
210 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.706-736_706-730dup others(7): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 8/28 | chr1 | 17001263 | |||||||
| chr1:17001263 | C | CAAAAAAA others(1): Show |
17 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(14): Show |
17 | HG01243.hp1 HG02083.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.706-737_706-730dup others(8): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 8/28 | chr1 | 17001263 | |||||||
| chr1:17001289 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.705+745C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 8/28 | chr1 | 17001289 | |||||||
| chr1:17001347 | G | A | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG00408.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.705+687C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 8/28 | chr1 | 17001347 | |||||||
| chr1:17001365 | T | A | 2 | a0001c0002t0001g0015 a0001c0002t0001g0090 |
4 | HG00438.hp1 NA18939.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.705+669A>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 8/28 | chr1 | 17001365 | |||||||
| chr1:17001384 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.705+650G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 8/28 | chr1 | 17001384 | |||||||
| chr1:17001705 | A | T | 53 | a0001c0001t0001g0072 a0001c0002t0001g0001 a0001c0002t0001g0003 others(50): Show |
103 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.705+329T>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 8/28 | chr1 | 17001705 | |||||||
| chr1:17001715 | G | A | 12 | a0001c0002t0001g0008 a0001c0002t0001g0027 a0001c0002t0001g0051 others(9): Show |
16 | HG01123.hp2 HG02056.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.705+319C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 8/28 | chr1 | 17001715 | |||||||
| chr1:17001775 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.705+259G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 8/28 | chr1 | 17001775 | |||||||
| chr1:17001806 | T | C | 191 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(188): Show |
250 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(247): Show |
intron_variant | MODIFIER | c.705+228A>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 8/28 | chr1 | 17001806 | |||||||
| chr1:17001820 | A | G | 7 | a0001c0001t0001g0034 a0001c0001t0001g0156 a0001c0001t0001g0169 others(4): Show |
10 | HG01496.hp1 HG01928.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.705+214T>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 8/28 | chr1 | 17001820 | |||||||
| chr1:17001902 | T | G | 1 | a0001c0003t0001g0029 | 2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.705+132A>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 8/28 | chr1 | 17001902 | |||||||
| chr1:17001906 | G | A | 4 | a0001c0004t0001g0016 a0001c0004t0001g0103 a0001c0004t0001g0104 others(1): Show |
6 | HG02109.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.705+128C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 8/28 | chr1 | 17001906 | |||||||
| chr1:17002202 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.635+94G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 7/28 | chr1 | 17002202 | |||||||
| chr1:17002225 | A | G | 1 | a0001c0002t0001g0062 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.635+71T>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 7/28 | chr1 | 17002225 | |||||||
| chr1:17002236 | T | C | 2 | a0001c0002t0001g0080 a0001c0002t0007g0094 |
2 | HG01070.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.635+60A>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 7/28 | chr1 | 17002236 | |||||||
| chr1:17002398 | G | A | 1 | a0001c0002t0001g0081 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.558-25C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17002398 | |||||||
| chr1:17002498 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.558-125C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17002498 | |||||||
| chr1:17002686 | C | T | 1 | a0001c0005t0001g0017 | 3 | HG01070.hp2 HG01071.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.558-313G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17002686 | |||||||
| chr1:17002690 | A | G | 3 | a0003c0010t0001g0030 a0003c0010t0001g0119 a0003c0010t0001g0141 |
4 | HG00733.hp1 HG01175.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.558-317T>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17002690 | |||||||
| chr1:17002807 | C | A | 2 | a0001c0002t0001g0053 a0001c0002t0001g0092 |
2 | HG02056.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.558-434G>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17002807 | |||||||
| chr1:17003126 | G | A | 1 | a0001c0003t0001g0135 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.558-753C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17003126 | |||||||
| chr1:17003135 | C | A | 1 | a0001c0004t0001g0245 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.558-762G>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17003135 | |||||||
| chr1:17003193 | TG | T | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 |
3 | HG00408.hp2 HG03239.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.558-821delC | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17003193 | |||||||
| chr1:17003329 | G | A | 4 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
4 | HG02083.hp1 HG03654.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.558-956C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17003329 | |||||||
| chr1:17003401 | T | C | 1 | a0001c0004t0001g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.557+931A>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17003401 | |||||||
| chr1:17003473 | G | A | 5 | a0001c0007t0001g0096 a0001c0007t0001g0097 a0001c0007t0001g0098 others(2): Show |
5 | HG01106.hp2 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.557+859C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17003473 | |||||||
| chr1:17003513 | C | A | 1 | a0001c0029t0001g0043 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.557+819G>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17003513 | |||||||
| chr1:17003531 | C | T | 1 | a0001c0002t0001g0087 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.557+801G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17003531 | |||||||
| chr1:17003579 | A | C | 1 | a0001c0002t0001g0122 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.557+753T>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17003579 | |||||||
| chr1:17003581 | A | C | 1 | a0001c0002t0001g0122 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.557+751T>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17003581 | |||||||
| chr1:17003583 | A | C | 1 | a0001c0002t0001g0122 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.557+749T>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17003583 | |||||||
| chr1:17003585 | C | A | 1 | a0006c0011t0001g0131 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.557+747G>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17003585 | |||||||
| chr1:17003585 | C | CACACACA | 3 | a0001c0001t0001g0019 a0001c0001t0001g0218 a0001c0003t0001g0135 |
3 | NA18956.hp2 NA18959.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.557+746_557+747ins others(7): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17003585 | |||||||
| chr1:17003585 | C | CCA | 30 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0019 others(27): Show |
33 | HG00642.hp2 HG00673.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.557+745_557+746dup others(2): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17003585 | |||||||
| chr1:17003585 | C | CCACA | 49 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0037 others(46): Show |
63 | HG00597.hp2 HG00673.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.557+743_557+746dup others(4): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17003585 | |||||||
| chr1:17003585 | C | CCACACA | 68 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(65): Show |
80 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.557+741_557+746dup others(6): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17003585 | |||||||
| chr1:17003585 | C | CCACACAC others(1): Show |
23 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(20): Show |
24 | HG00099.hp1 HG00597.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.557+739_557+746dup others(8): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17003585 | |||||||
| chr1:17003585 | C | CCACACAC others(3): Show |
25 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(22): Show |
35 | HG00609.hp2 HG01928.hp1 HG01975.hp2 others(32): Show |
intron_variant | MODIFIER | c.557+737_557+746dup others(10): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17003585 | |||||||
| chr1:17003585 | C | CCACACAC others(5): Show |
3 | a0001c0001t0001g0011 a0001c0001t0001g0194 a0001c0002t0001g0035 |
3 | HG01934.hp1 HG01934.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.557+735_557+746dup others(12): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17003585 | |||||||
| chr1:17003585 | C | CCACACAC others(7): Show |
1 | a0001c0001t0001g0005 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.557+733_557+746dup others(14): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17003585 | |||||||
| chr1:17003585 | CCA | C | 16 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0027 others(13): Show |
17 | HG01099.hp1 HG01106.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.557+745_557+746del others(2): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17003585 | |||||||
| chr1:17003585 | CCACA | C | 2 | a0001c0007t0001g0096 a0005c0012t0001g0021 |
3 | HG01891.hp2 HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.557+743_557+746del others(4): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17003585 | |||||||
| chr1:17003585 | CCACACAC others(5): Show |
C | 1 | a0001c0002t0001g0024 | 2 | NA20129.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.557+735_557+746del others(12): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17003585 | |||||||
| chr1:17003624 | T | C | 2 | a0001c0001t0001g0191 a0001c0001t0001g0250 |
2 | HG01993.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.557+708A>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17003624 | |||||||
| chr1:17003654 | G | C | 1 | a0001c0003t0001g0029 | 2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.557+678C>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17003654 | |||||||
| chr1:17003666 | CT | C | 67 | a0001c0001t0001g0038 a0001c0001t0001g0072 a0001c0002t0001g0001 others(64): Show |
116 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.557+665delA | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17003666 | |||||||
| chr1:17003666 | CTT | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(173): Show |
234 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.557+664_557+665del others(2): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17003666 | |||||||
| chr1:17003872 | C | A | 1 | a0001c0007t0001g0100 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.557+460G>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17003872 | |||||||
| chr1:17003953 | C | T | 1 | a0001c0002t0001g0061 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.557+379G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17003953 | |||||||
| chr1:17003958 | A | G | 190 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(187): Show |
249 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.557+374T>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17003958 | |||||||
| chr1:17004025 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.557+307A>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 6/28 | chr1 | 17004025 | |||||||
| chr1:17004558 | G | C | 1 | a0001c0001t0001g0192 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.477+134C>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 5/28 | chr1 | 17004558 | |||||||
| chr1:17004660 | G | A | 3 | a0001c0003t0001g0118 a0001c0003t0001g0140 a0001c0003t0001g0154 |
3 | HG02258.hp2 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.477+32C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 5/28 | chr1 | 17004660 | |||||||
| chr1:17004912 | G | T | 1 | a0001c0008t0001g0086 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.348-91C>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 4/28 | chr1 | 17004912 | |||||||
| chr1:17004918 | G | C | 1 | a0001c0003t0004g0046 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.347+96C>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 4/28 | chr1 | 17004918 | |||||||
| chr1:17004936 | G | C | 1 | a0001c0001t0001g0216 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.347+78C>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 4/28 | chr1 | 17004936 | |||||||
| chr1:17004941 | G | C | 11 | a0001c0004t0001g0230 a0001c0004t0001g0237 a0001c0007t0001g0048 others(8): Show |
11 | HG01106.hp2 HG02451.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.347+73C>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 4/28 | chr1 | 17004941 | |||||||
| chr1:17005132 | C | T | 1 | a0001c0002t0001g0060 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.289-60G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 3/28 | chr1 | 17005132 | |||||||
| chr1:17005181 | A | G | 179 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(176): Show |
238 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(235): Show |
intron_variant | MODIFIER | c.289-109T>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 3/28 | chr1 | 17005181 | |||||||
| chr1:17005223 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.288+151C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 3/28 | chr1 | 17005223 | |||||||
| chr1:17005322 | G | A | 2 | a0001c0003t0001g0144 a0009c0015t0001g0145 |
2 | NA19005.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.288+52C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 3/28 | chr1 | 17005322 | |||||||
| chr1:17005347 | T | C | 1 | a0001c0004t0001g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.288+27A>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 3/28 | chr1 | 17005347 | |||||||
| chr1:17005561 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA18980.hp1 | splice_region_variant&intron_variant | LOW | c.106-5C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 2/28 | chr1 | 17005561 | |||||||
| chr1:17005586 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.106-30G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 2/28 | chr1 | 17005586 | |||||||
| chr1:17005601 | G | A | 1 | a0005c0012t0001g0021 | 2 | HG01891.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.106-45C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 2/28 | chr1 | 17005601 | |||||||
| chr1:17005807 | G | A | 5 | a0001c0007t0001g0096 a0001c0007t0001g0097 a0001c0007t0001g0098 others(2): Show |
5 | HG01106.hp2 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.11-29C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17005807 | |||||||
| chr1:17005900 | C | T | 1 | a0001c0004t0001g0237 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.11-122G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17005900 | |||||||
| chr1:17005912 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.11-134T>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17005912 | |||||||
| chr1:17006005 | C | T | 2 | a0001c0004t0001g0222 a0001c0007t0001g0102 |
2 | HG01106.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.11-227G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17006005 | |||||||
| chr1:17006016 | T | C | 1 | a0001c0002t0007g0094 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.11-238A>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17006016 | |||||||
| chr1:17006248 | C | A | 12 | a0001c0003t0004g0046 a0001c0004t0001g0230 a0001c0004t0001g0237 others(9): Show |
12 | HG01106.hp2 HG02451.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.11-470G>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17006248 | |||||||
| chr1:17006249 | C | A | 12 | a0001c0003t0004g0046 a0001c0004t0001g0230 a0001c0004t0001g0237 others(9): Show |
12 | HG01106.hp2 HG02451.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.11-471G>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17006249 | |||||||
| chr1:17006254 | C | CT | 171 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(168): Show |
230 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(227): Show |
intron_variant | MODIFIER | c.11-477dupA | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17006254 | |||||||
| chr1:17006353 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.11-575G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17006353 | |||||||
| chr1:17006391 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.11-613A>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17006391 | |||||||
| chr1:17006395 | CATGCACC others(5): Show |
C | 1 | a0001c0001t0001g0198 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.11-629_11-618delAT others(10): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17006395 | |||||||
| chr1:17006418 | T | G | 1 | a0001c0001t0001g0198 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.11-640A>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17006418 | |||||||
| chr1:17006430 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.11-652A>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17006430 | |||||||
| chr1:17006439 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.11-661A>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17006439 | |||||||
| chr1:17006471 | G | A | 1 | a0001c0002t0001g0083 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.11-693C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17006471 | |||||||
| chr1:17006678 | G | T | 1 | a0005c0012t0001g0021 | 2 | HG01891.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.11-900C>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17006678 | |||||||
| chr1:17007051 | G | C | 2 | a0001c0005t0001g0235 a0001c0005t0001g0236 |
2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.11-1273C>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17007051 | |||||||
| chr1:17007172 | C | G | 1 | a0001c0001t0001g0199 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.11-1394G>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17007172 | |||||||
| chr1:17007173 | G | C | 1 | a0001c0001t0001g0199 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.11-1395C>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17007173 | |||||||
| chr1:17007372 | C | A | 1 | a0001c0002t0001g0084 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.11-1594G>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17007372 | |||||||
| chr1:17007402 | G | C | 3 | a0001c0003t0001g0032 a0001c0003t0001g0120 a0001c0003t0001g0153 |
4 | NA18946.hp2 NA18981.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.11-1624C>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17007402 | |||||||
| chr1:17007489 | GGCT | G | 3 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0217 |
3 | HG00099.hp1 HG01074.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.11-1714_11-1712del others(3): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17007489 | |||||||
| chr1:17007526 | A | G | 1 | a0001c0003t0001g0121 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.11-1748T>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17007526 | |||||||
| chr1:17007530 | G | C | 1 | a0001c0001t0001g0202 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.11-1752C>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17007530 | |||||||
| chr1:17007550 | CT | C | 222 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(219): Show |
331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.11-1773delA | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17007550 | |||||||
| chr1:17007654 | C | A | 4 | a0001c0004t0001g0013 a0001c0004t0001g0044 a0001c0004t0001g0247 others(1): Show |
7 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.11-1876G>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17007654 | |||||||
| chr1:17007700 | C | T | 1 | a0001c0004t0001g0244 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.11-1922G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17007700 | |||||||
| chr1:17008038 | T | TTTCA | 3 | a0001c0001t0001g0204 a0001c0003t0001g0203 a0001c0004t0001g0244 |
3 | HG02056.hp2 HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.11-2264_11-2261dup others(4): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17008038 | |||||||
| chr1:17008224 | C | G | 11 | a0001c0004t0001g0230 a0001c0004t0001g0237 a0001c0007t0001g0048 others(8): Show |
11 | HG01106.hp2 HG02451.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.11-2446G>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17008224 | |||||||
| chr1:17008295 | C | G | 3 | a0003c0010t0001g0030 a0003c0010t0001g0119 a0003c0010t0001g0141 |
4 | HG00733.hp1 HG01175.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.11-2517G>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17008295 | |||||||
| chr1:17008297 | A | C | 1 | a0001c0004t0001g0116 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.11-2519T>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17008297 | |||||||
| chr1:17008298 | T | A | 1 | a0001c0004t0001g0116 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.11-2520A>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17008298 | |||||||
| chr1:17008319 | A | G | 1 | a0001c0002t0001g0052 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.11-2541T>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17008319 | |||||||
| chr1:17008419 | A | G | 1 | a0001c0001t0001g0033 | 2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.11-2641T>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17008419 | |||||||
| chr1:17008488 | T | C | 4 | a0001c0004t0001g0013 a0001c0004t0001g0044 a0001c0004t0001g0247 others(1): Show |
7 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.11-2710A>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17008488 | |||||||
| chr1:17008496 | T | A | 1 | a0001c0002t0001g0085 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.11-2718A>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17008496 | |||||||
| chr1:17008616 | G | A | 1 | a0001c0007t0001g0100 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.11-2838C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17008616 | |||||||
| chr1:17008673 | G | A | 1 | a0001c0003t0001g0154 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.11-2895C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17008673 | |||||||
| chr1:17008828 | G | T | 1 | a0001c0001t0001g0218 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.10+2901C>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17008828 | |||||||
| chr1:17008939 | G | A | 1 | a0001c0004t0001g0244 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.10+2790C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17008939 | |||||||
| chr1:17008957 | C | CA | 51 | a0001c0001t0001g0125 a0001c0001t0001g0136 a0001c0001t0001g0137 others(48): Show |
71 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.10+2771dupT | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17008957 | |||||||
| chr1:17008957 | C | CAA | 20 | a0001c0002t0001g0147 a0001c0003t0001g0004 a0001c0003t0001g0029 others(17): Show |
26 | HG00544.hp2 HG00597.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.10+2770_10+2771dup others(2): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17008957 | |||||||
| chr1:17008957 | CA | C | 78 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(75): Show |
109 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.10+2771delT | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17008957 | |||||||
| chr1:17009387 | C | CT | 71 | a0001c0001t0001g0072 a0001c0001t0001g0155 a0001c0001t0001g0156 others(68): Show |
121 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.10+2341dupA | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17009387 | |||||||
| chr1:17009387 | C | CTT | 9 | a0001c0002t0001g0014 a0001c0002t0001g0023 a0001c0002t0001g0051 others(6): Show |
12 | HG00642.hp2 HG00735.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.10+2340_10+2341dup others(2): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17009387 | |||||||
| chr1:17009387 | CT | C | 20 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0003t0001g0045 others(17): Show |
22 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.10+2341delA | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17009387 | |||||||
| chr1:17009387 | CTT | C | 45 | a0001c0001t0001g0125 a0001c0001t0001g0136 a0001c0001t0001g0137 others(42): Show |
60 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.10+2340_10+2341del others(2): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17009387 | |||||||
| chr1:17009399 | T | TC | 6 | a0001c0003t0004g0046 a0001c0004t0001g0013 a0001c0004t0001g0044 others(3): Show |
9 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.10+2329_10+2330ins others(1): Show |
ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17009399 | |||||||
| chr1:17009411 | A | T | 1 | a0001c0002t0001g0022 | 2 | HG00280.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.10+2318T>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17009411 | |||||||
| chr1:17009703 | C | T | 3 | a0001c0003t0001g0029 a0001c0003t0001g0112 a0001c0003t0001g0113 |
4 | HG02055.hp2 HG02109.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.10+2026G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17009703 | |||||||
| chr1:17009758 | C | T | 88 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
124 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.10+1971G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17009758 | |||||||
| chr1:17009824 | A | C | 60 | a0001c0001t0001g0125 a0001c0001t0001g0136 a0001c0001t0001g0137 others(57): Show |
75 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.10+1905T>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17009824 | |||||||
| chr1:17010026 | G | T | 58 | a0001c0001t0001g0072 a0001c0002t0001g0001 a0001c0002t0001g0003 others(55): Show |
108 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.10+1703C>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17010026 | |||||||
| chr1:17010048 | A | T | 1 | a0001c0005t0001g0050 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.10+1681T>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17010048 | |||||||
| chr1:17010050 | G | C | 52 | a0001c0001t0001g0125 a0001c0001t0001g0136 a0001c0001t0001g0137 others(49): Show |
67 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.10+1679C>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17010050 | |||||||
| chr1:17010096 | C | T | 1 | a0001c0002t0001g0049 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.10+1633G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17010096 | |||||||
| chr1:17010100 | C | G | 88 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
124 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.10+1629G>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17010100 | |||||||
| chr1:17010333 | C | T | 1 | a0001c0007t0001g0048 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.10+1396G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17010333 | |||||||
| chr1:17010472 | A | G | 1 | a0004c0020t0001g0047 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.10+1257T>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17010472 | |||||||
| chr1:17010732 | C | A | 1 | a0001c0001t0001g0249 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.10+997G>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17010732 | |||||||
| chr1:17010797 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.10+932A>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17010797 | |||||||
| chr1:17010896 | G | A | 121 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(118): Show |
163 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.10+833C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17010896 | |||||||
| chr1:17010988 | A | T | 1 | a0001c0003t0004g0046 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.10+741T>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17010988 | |||||||
| chr1:17011096 | A | G | 1 | a0001c0003t0001g0045 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.10+633T>C | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17011096 | |||||||
| chr1:17011115 | T | C | 1 | a0001c0001t0001g0251 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.10+614A>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17011115 | |||||||
| chr1:17011182 | C | T | 1 | a0001c0004t0001g0044 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.10+547G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17011182 | |||||||
| chr1:17011331 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.10+398C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17011331 | |||||||
| chr1:17011453 | C | T | 2 | a0001c0029t0001g0043 a0005c0012t0001g0021 |
3 | HG01891.hp2 HG02630.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.10+276G>A | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17011453 | |||||||
| chr1:17011638 | G | C | 1 | a0001c0001t0001g0253 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.10+91C>G | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17011638 | |||||||
| chr1:17011688 | G | A | 1 | a0001c0003t0008g0254 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.10+41C>T | ATP13A2 | ENSG00000159363.19 | transcript | ENST00000326735.13 | protein_coding | 1/28 | chr1 | 17011688 |