Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 479 |
| ensemblid | ENSG00000075673.12 |
| hgncid | 13816 |
| symbol | ATP12A |
| name | ATPase H+/K+ transporting non-gastric alpha2 subunit |
| refseq_nuc | NM_001676.7 |
| refseq_prot | NP_001667.4 |
| ensembl_nuc | ENST00000381946.5 |
| ensembl_prot | ENSP00000371372.3 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 24680408 |
| end | 24712472 |
| strand | + |
| ver | v1.2 |
| region | chr13:24680408-24712472 |
| region5000 | chr13:24675408-24717472 |
| regionname0 | ATP12A_chr13_24680408_24712472 |
| regionname5000 | ATP12A_chr13_24675408_24717472 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1039 | 331 | 88 | 55 | 139 | 13 | 34 | 104 | ATP12A_chr13_24675408_24717472 | ATP12A | MHQKT others(1034): Show |
chr13 | 24675408 | 24717472 |
| a0002 | 0/0 | 1039 | 27 | 0 | 7 | 11 | 1 | 8 | 9 | ATP12A_chr13_24675408_24717472 | ATP12A | MHQKT others(1034): Show |
chr13 | 24675408 | 24717472 |
| a0003 | 0/0 | 1039 | 6 | 3 | 1 | 2 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | MHQKT others(1034): Show |
chr13 | 24675408 | 24717472 |
| a0004 | 0/0 | 1039 | 5 | 1 | 3 | 0 | 0 | 1 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | MHQKT others(1034): Show |
chr13 | 24675408 | 24717472 |
| a0005 | 0/0 | 1039 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | MHQKT others(1034): Show |
chr13 | 24675408 | 24717472 |
| a0006 | 0/0 | 1039 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | MHQKT others(1034): Show |
chr13 | 24675408 | 24717472 |
| a0007 | 0/0 | 1039 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | MHQKT others(1034): Show |
chr13 | 24675408 | 24717472 |
| a0008 | 0/0 | 1039 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | MHQKT others(1034): Show |
chr13 | 24675408 | 24717472 |
| a0009 | 0/0 | 1039 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | MHQKT others(1034): Show |
chr13 | 24675408 | 24717472 |
| a0010 | 0/0 | 1039 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | MHQKT others(1034): Show |
chr13 | 24675408 | 24717472 |
| a0011 | 0/0 | 1039 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | MHQKT others(1034): Show |
chr13 | 24675408 | 24717472 |
| a0012 | 0/0 | 1039 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | MHQKT others(1034): Show |
chr13 | 24675408 | 24717472 |
| a0013 | 0/0 | 1039 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | MHQKT others(1034): Show |
chr13 | 24675408 | 24717472 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3117 | 103 | 20 | 24 | 45 | 4 | 9 | ATP12A_chr13_24675408_24717472 | ATP12A | ATGCA others(3112): Show |
chr13 | 24675408 | 24717472 | ||
| a0001c0002 | 0/0 | 3117 | 97 | 14 | 12 | 60 | 2 | 9 | ATP12A_chr13_24675408_24717472 | ATP12A | ATGCA others(3112): Show |
chr13 | 24675408 | 24717472 | ||
| a0001c0003 | 0/1 | 3117 | 78 | 30 | 9 | 26 | 3 | 9 | ATP12A_chr13_24675408_24717472 | ATP12A | ATGCA others(3112): Show |
chr13 | 24675408 | 24717472 | ||
| a0001c0005 | 0/0 | 3117 | 19 | 7 | 7 | 3 | 1 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | ATGCA others(3112): Show |
chr13 | 24675408 | 24717472 | ||
| a0001c0006 | 0/0 | 3117 | 12 | 8 | 2 | 0 | 1 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | ATGCA others(3112): Show |
chr13 | 24675408 | 24717472 | ||
| a0001c0007 | 0/0 | 3117 | 8 | 5 | 0 | 3 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | ATGCA others(3112): Show |
chr13 | 24675408 | 24717472 | ||
| a0001c0008 | 0/0 | 3117 | 6 | 0 | 1 | 1 | 1 | 3 | ATP12A_chr13_24675408_24717472 | ATP12A | ATGCA others(3112): Show |
chr13 | 24675408 | 24717472 | ||
| a0001c0010 | 0/0 | 3117 | 3 | 3 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | ATGCA others(3112): Show |
chr13 | 24675408 | 24717472 | ||
| a0001c0014 | 0/0 | 3117 | 2 | 0 | 0 | 0 | 0 | 2 | ATP12A_chr13_24675408_24717472 | ATP12A | ATGCA others(3112): Show |
chr13 | 24675408 | 24717472 | ||
| a0001c0021 | 0/0 | 3117 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | ATGCA others(3112): Show |
chr13 | 24675408 | 24717472 | ||
| a0001c0022 | 0/0 | 3117 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | ATGCA others(3112): Show |
chr13 | 24675408 | 24717472 | ||
| a0001c0027 | 0/0 | 3117 | 1 | 0 | 0 | 0 | 1 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | ATGCA others(3112): Show |
chr13 | 24675408 | 24717472 | ||
| a0002c0004 | 0/0 | 3117 | 22 | 0 | 5 | 9 | 1 | 7 | ATP12A_chr13_24675408_24717472 | ATP12A | ATGCA others(3112): Show |
chr13 | 24675408 | 24717472 | ||
| a0002c0011 | 0/0 | 3117 | 3 | 0 | 2 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | ATGCA others(3112): Show |
chr13 | 24675408 | 24717472 | ||
| a0002c0020 | 0/0 | 3117 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | ATGCA others(3112): Show |
chr13 | 24675408 | 24717472 | ||
| a0002c0028 | 0/0 | 3117 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | ATGCA others(3112): Show |
chr13 | 24675408 | 24717472 | ||
| a0003c0012 | 0/0 | 3117 | 2 | 2 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | ATGCA others(3112): Show |
chr13 | 24675408 | 24717472 | ||
| a0003c0015 | 0/0 | 3117 | 2 | 0 | 0 | 2 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | ATGCA others(3112): Show |
chr13 | 24675408 | 24717472 | ||
| a0003c0016 | 0/0 | 3117 | 2 | 1 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | ATGCA others(3112): Show |
chr13 | 24675408 | 24717472 | ||
| a0004c0009 | 0/0 | 3117 | 5 | 1 | 3 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | ATGCA others(3112): Show |
chr13 | 24675408 | 24717472 | ||
| a0005c0018 | 0/0 | 3117 | 2 | 1 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | ATGCA others(3112): Show |
chr13 | 24675408 | 24717472 | ||
| a0006c0017 | 0/0 | 3117 | 2 | 0 | 2 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | ATGCA others(3112): Show |
chr13 | 24675408 | 24717472 | ||
| a0007c0019 | 0/0 | 3117 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | ATGCA others(3112): Show |
chr13 | 24675408 | 24717472 | ||
| a0007c0024 | 0/0 | 3117 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | ATGCA others(3112): Show |
chr13 | 24675408 | 24717472 | ||
| a0008c0013 | 0/0 | 3117 | 2 | 2 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | ATGCA others(3112): Show |
chr13 | 24675408 | 24717472 | ||
| a0009c0023 | 0/0 | 3117 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | ATGCA others(3112): Show |
chr13 | 24675408 | 24717472 | ||
| a0010c0025 | 0/0 | 3117 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | ATGCA others(3112): Show |
chr13 | 24675408 | 24717472 | ||
| a0011c0026 | 0/0 | 3117 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | ATGCA others(3112): Show |
chr13 | 24675408 | 24717472 | ||
| a0012c0030 | 0/0 | 3117 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | ATGCA others(3112): Show |
chr13 | 24675408 | 24717472 | ||
| a0013c0029 | 0/0 | 3117 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | ATGCA others(3112): Show |
chr13 | 24675408 | 24717472 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4406 | 85 | 16 | 21 | 35 | 4 | 8 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0001t0004 | 0/0 | 4406 | 9 | 2 | 0 | 6 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0001t0005 | 0/0 | 4406 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0001t0007 | 0/0 | 4406 | 2 | 0 | 0 | 2 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0001t0008 | 0/0 | 4406 | 3 | 0 | 3 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0001t0012 | 0/0 | 4406 | 2 | 0 | 0 | 2 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0001t0014 | 0/0 | 4406 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0002t0001 | 0/0 | 4406 | 92 | 14 | 12 | 55 | 2 | 9 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0002t0004 | 0/0 | 4406 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0002t0005 | 0/0 | 4406 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0002t0007 | 0/0 | 4406 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0002t0011 | 0/0 | 4406 | 2 | 0 | 0 | 2 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0003t0001 | 0/0 | 4406 | 7 | 7 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0003t0002 | 0/1 | 4406 | 26 | 6 | 2 | 10 | 1 | 6 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0003t0004 | 0/0 | 4406 | 10 | 3 | 4 | 1 | 1 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0003t0005 | 0/0 | 4406 | 20 | 4 | 0 | 13 | 1 | 2 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0003t0006 | 0/0 | 4406 | 11 | 10 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0003t0007 | 0/0 | 4406 | 2 | 0 | 0 | 2 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0003t0013 | 0/0 | 4406 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0003t0016 | 0/0 | 4406 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0005t0001 | 0/0 | 4406 | 13 | 1 | 7 | 3 | 1 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0005t0004 | 0/0 | 4406 | 3 | 3 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0005t0009 | 0/0 | 4406 | 3 | 3 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0006t0001 | 0/0 | 4406 | 12 | 8 | 2 | 0 | 1 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0007t0001 | 0/0 | 4406 | 3 | 0 | 0 | 3 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0007t0006 | 0/0 | 4406 | 4 | 4 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0007t0015 | 0/0 | 4406 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0008t0001 | 0/0 | 4406 | 6 | 0 | 1 | 1 | 1 | 3 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0010t0001 | 0/0 | 4406 | 3 | 3 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0014t0001 | 0/0 | 4406 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0014t0004 | 0/0 | 4406 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0021t0001 | 0/0 | 4406 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0022t0007 | 0/0 | 4406 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0001c0027t0001 | 0/0 | 4406 | 1 | 0 | 0 | 0 | 1 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0002c0004t0003 | 0/0 | 4406 | 22 | 0 | 5 | 9 | 1 | 7 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0002c0011t0003 | 0/0 | 4406 | 2 | 0 | 2 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0002c0011t0010 | 0/0 | 4406 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0002c0020t0010 | 0/0 | 4406 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0002c0028t0003 | 0/0 | 4406 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0003c0012t0001 | 0/0 | 4406 | 2 | 2 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0003c0015t0001 | 0/0 | 4406 | 2 | 0 | 0 | 2 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0003c0016t0001 | 0/0 | 4406 | 2 | 1 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0004c0009t0001 | 0/0 | 4406 | 5 | 1 | 3 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0005c0018t0005 | 0/0 | 4406 | 2 | 1 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0006c0017t0001 | 0/0 | 4406 | 2 | 0 | 2 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0007c0019t0001 | 0/0 | 4406 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0007c0024t0001 | 0/0 | 4406 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0008c0013t0006 | 0/0 | 4406 | 2 | 2 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0009c0023t0001 | 0/0 | 4406 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0010c0025t0001 | 0/0 | 4406 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0011c0026t0001 | 0/0 | 4406 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0012c0030t0001 | 0/0 | 4406 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| a0013c0029t0001 | 0/0 | 4406 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | CTCAA others(4401): Show |
chr13 | 24675408 | 24717472 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0023 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0007g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0008g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0008g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0008g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0012g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0012g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0001t0014g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0001 | 0/0 | 21 | 1 | 6 | 10 | 2 | 2 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0002 | 0/0 | 12 | 1 | 1 | 8 | 0 | 2 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0008 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0007g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0011g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0002t0011g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0002g0003 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0002g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0002g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0002g0253 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0004g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0004g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0004g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0004g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0004g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0004g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0004g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0005g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0005g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0005g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0005g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0005g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0005g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0005g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0005g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0006g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0006g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0006g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0006g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0007g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0007g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0013g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0003t0016g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0005t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0005t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0005t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0005t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0005t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0005t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0005t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0005t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0005t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0005t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0005t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0005t0004g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0005t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0005t0009g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0005t0009g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0005t0009g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0006t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0006t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0006t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0006t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0006t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0006t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0006t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0006t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0006t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0006t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0006t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0007t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0007t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0007t0006g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0007t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0007t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0007t0015g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0008t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0008t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0008t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0008t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0008t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0010t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0010t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0010t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0014t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0014t0004g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0021t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0022t0007g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0001c0027t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0002c0004t0003g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0002c0004t0003g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0002c0004t0003g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0002c0004t0003g0038 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0002c0004t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0002c0004t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0002c0004t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0002c0004t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0002c0004t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0002c0004t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0002c0004t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0002c0004t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0002c0004t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0002c0004t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0002c0004t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0002c0011t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0002c0011t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0002c0011t0010g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0002c0020t0010g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0002c0028t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0003c0012t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0003c0012t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0003c0015t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0003c0015t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0003c0016t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0003c0016t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0004c0009t0001g0005 | 0/0 | 5 | 1 | 3 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0005c0018t0005g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0005c0018t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0006c0017t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0006c0017t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0007c0019t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0007c0024t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0008c0013t0006g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0009c0023t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0010c0025t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0011c0026t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0012c0030t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| a0013c0029t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0005 | g0085 | EUR | GBR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00099 | hp2 | a0001 | c0027 | t0001 | g0169 | EUR | GBR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00140 | hp1 | a0001 | c0008 | t0001 | g0182 | EUR | GBR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00140 | hp2 | a0002 | c0004 | t0003 | g0236 | EUR | GBR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | FIN | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00323 | hp2 | a0001 | c0006 | t0001 | g0149 | EUR | FIN | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00408 | hp1 | a0001 | c0002 | t0007 | g0114 | EAS | CHS | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00408 | hp2 | a0009 | c0023 | t0001 | g0101 | EAS | CHS | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00423 | hp2 | a0001 | c0003 | t0005 | g0077 | EAS | CHS | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | CHS | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00438 | hp2 | a0001 | c0003 | t0002 | g0042 | EAS | CHS | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00544 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | CHS | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00558 | hp1 | a0002 | c0028 | t0003 | g0249 | EAS | CHS | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | CHS | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00609 | hp2 | a0001 | c0001 | t0012 | g0071 | EAS | CHS | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00621 | hp2 | a0001 | c0003 | t0007 | g0175 | EAS | CHS | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00639 | hp1 | a0004 | c0009 | t0001 | g0005 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00639 | hp2 | a0001 | c0003 | t0004 | g0278 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00642 | hp1 | a0001 | c0005 | t0001 | g0016 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00733 | hp2 | a0001 | c0001 | t0008 | g0217 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00735 | hp1 | a0001 | c0006 | t0001 | g0143 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00738 | hp2 | a0001 | c0006 | t0001 | g0141 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01069 | hp1 | a0001 | c0003 | t0004 | g0266 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01070 | hp2 | a0001 | c0005 | t0001 | g0054 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01074 | hp1 | a0003 | c0016 | t0001 | g0181 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01081 | hp1 | a0002 | c0004 | t0003 | g0237 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0127 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01106 | hp2 | a0002 | c0004 | t0003 | g0035 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01109 | hp2 | a0005 | c0018 | t0005 | g0215 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01167 | hp1 | a0001 | c0003 | t0002 | g0257 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01167 | hp2 | a0001 | c0008 | t0001 | g0228 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01168 | hp1 | a0006 | c0017 | t0001 | g0209 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01168 | hp2 | a0001 | c0005 | t0001 | g0240 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01169 | hp1 | a0006 | c0017 | t0001 | g0210 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01169 | hp2 | a0001 | c0003 | t0002 | g0256 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01175 | hp2 | a0001 | c0003 | t0006 | g0154 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01192 | hp1 | a0002 | c0011 | t0003 | g0171 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01192 | hp2 | a0001 | c0003 | t0004 | g0003 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01243 | hp1 | a0001 | c0003 | t0004 | g0275 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01243 | hp2 | a0001 | c0003 | t0016 | g0283 | AMR | PUR | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01255 | hp1 | a0001 | c0005 | t0001 | g0177 | AMR | CLM | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0102 | AMR | CLM | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01256 | hp1 | a0001 | c0005 | t0001 | g0057 | AMR | CLM | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01256 | hp2 | a0002 | c0004 | t0003 | g0227 | AMR | CLM | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01257 | hp2 | a0004 | c0009 | t0001 | g0005 | AMR | CLM | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01258 | hp2 | a0001 | c0005 | t0001 | g0056 | AMR | CLM | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01261 | hp1 | a0001 | c0003 | t0013 | g0269 | AMR | CLM | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01496 | hp1 | a0002 | c0004 | t0003 | g0035 | AMR | CLM | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | IBS | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01515 | hp2 | a0001 | c0005 | t0001 | g0179 | EUR | IBS | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01516 | hp1 | a0001 | c0003 | t0004 | g0258 | EUR | IBS | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0221 | EUR | IBS | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01884 | hp1 | a0001 | c0007 | t0006 | g0026 | AFR | ACB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01891 | hp1 | a0001 | c0005 | t0004 | g0287 | AFR | ACB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | ACB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01934 | hp1 | a0002 | c0011 | t0003 | g0184 | AMR | PEL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0111 | AMR | PEL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01952 | hp1 | a0002 | c0004 | t0003 | g0232 | AMR | PEL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01978 | hp1 | a0001 | c0001 | t0008 | g0222 | AMR | PEL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01981 | hp1 | a0007 | c0024 | t0001 | g0206 | AMR | PEL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01981 | hp2 | a0001 | c0005 | t0001 | g0055 | AMR | PEL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | KHV | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02015 | hp2 | a0010 | c0025 | t0001 | g0060 | EAS | KHV | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0243 | EAS | KHV | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02040 | hp2 | a0001 | c0001 | t0007 | g0029 | EAS | KHV | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02055 | hp1 | a0001 | c0010 | t0001 | g0147 | AFR | ACB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0165 | AFR | ACB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | KHV | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | KHV | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0205 | EAS | KHV | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02074 | hp1 | a0003 | c0015 | t0001 | g0117 | EAS | KHV | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02083 | hp1 | a0002 | c0011 | t0010 | g0288 | EAS | KHV | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02129 | hp2 | a0001 | c0005 | t0001 | g0100 | EAS | KHV | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02132 | hp1 | a0001 | c0003 | t0002 | g0003 | EAS | KHV | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | KHV | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02135 | hp1 | a0001 | c0003 | t0002 | g0042 | EAS | KHV | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | KHV | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02145 | hp1 | a0001 | c0003 | t0006 | g0025 | AFR | ACB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02145 | hp2 | a0001 | c0005 | t0004 | g0043 | AFR | ACB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CDX | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02165 | hp2 | a0001 | c0001 | t0012 | g0078 | EAS | CDX | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02257 | hp1 | a0001 | c0003 | t0002 | g0276 | AFR | ACB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02257 | hp2 | a0001 | c0003 | t0006 | g0009 | AFR | ACB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02258 | hp1 | a0001 | c0001 | t0014 | g0284 | AFR | ACB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02258 | hp2 | a0001 | c0003 | t0005 | g0083 | AFR | ACB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02280 | hp1 | a0005 | c0018 | t0005 | g0216 | AFR | ACB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0059 | AFR | ACB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02300 | hp1 | a0001 | c0001 | t0008 | g0034 | AMR | PEL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0103 | AMR | PEL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0282 | AFR | ACB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0135 | AFR | ACB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | KHV | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02523 | hp2 | a0001 | c0001 | t0007 | g0029 | EAS | KHV | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02572 | hp1 | a0001 | c0003 | t0001 | g0163 | AFR | GWD | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0212 | AFR | GWD | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02602 | hp1 | a0001 | c0003 | t0005 | g0044 | SAS | PJL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02602 | hp2 | a0004 | c0009 | t0001 | g0005 | SAS | PJL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02615 | hp1 | a0001 | c0007 | t0006 | g0159 | AFR | GWD | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02615 | hp2 | a0001 | c0003 | t0002 | g0007 | AFR | GWD | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02622 | hp1 | a0001 | c0003 | t0006 | g0155 | AFR | GWD | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02622 | hp2 | a0001 | c0003 | t0002 | g0277 | AFR | GWD | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02647 | hp1 | a0001 | c0003 | t0006 | g0152 | AFR | GWD | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02647 | hp2 | a0001 | c0006 | t0001 | g0024 | AFR | GWD | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02683 | hp1 | a0002 | c0004 | t0003 | g0226 | SAS | PJL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0116 | AFR | GWD | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02717 | hp2 | a0001 | c0006 | t0001 | g0144 | AFR | GWD | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | GWD | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0061 | AFR | GWD | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02738 | hp2 | a0002 | c0004 | t0003 | g0235 | SAS | PJL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02809 | hp2 | a0001 | c0006 | t0001 | g0142 | AFR | GWD | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02818 | hp1 | a0001 | c0006 | t0001 | g0024 | AFR | GWD | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02818 | hp2 | a0001 | c0003 | t0006 | g0010 | AFR | GWD | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02886 | hp1 | a0001 | c0005 | t0009 | g0133 | AFR | GWD | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02886 | hp2 | a0001 | c0007 | t0015 | g0158 | AFR | GWD | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02895 | hp2 | a0001 | c0003 | t0001 | g0214 | AFR | GWD | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02896 | hp1 | a0001 | c0003 | t0006 | g0156 | AFR | GWD | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0173 | AFR | GWD | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02897 | hp2 | a0001 | c0003 | t0006 | g0025 | AFR | GWD | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02922 | hp1 | a0001 | c0003 | t0006 | g0010 | AFR | ESN | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02922 | hp2 | a0001 | c0021 | t0001 | g0176 | AFR | ESN | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02965 | hp1 | a0001 | c0006 | t0001 | g0150 | AFR | ESN | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02965 | hp2 | a0001 | c0003 | t0005 | g0081 | AFR | ESN | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02970 | hp2 | a0001 | c0003 | t0004 | g0040 | AFR | ESN | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | ESN | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02976 | hp2 | a0001 | c0003 | t0005 | g0080 | AFR | ESN | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03017 | hp1 | a0011 | c0026 | t0001 | g0160 | SAS | PJL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03041 | hp1 | a0001 | c0007 | t0006 | g0157 | AFR | GWD | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | ESN | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03130 | hp2 | a0001 | c0003 | t0004 | g0040 | AFR | ESN | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03139 | hp1 | a0001 | c0007 | t0006 | g0026 | AFR | ESN | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | ESN | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0224 | AFR | ESN | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03209 | hp1 | a0001 | c0003 | t0004 | g0286 | AFR | MSL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0082 | AFR | MSL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03225 | hp1 | a0001 | c0005 | t0004 | g0043 | AFR | MSL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03239 | hp2 | a0001 | c0008 | t0001 | g0233 | SAS | PJL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03453 | hp1 | a0003 | c0016 | t0001 | g0180 | AFR | MSL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03453 | hp2 | a0001 | c0005 | t0009 | g0132 | AFR | MSL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03490 | hp1 | a0001 | c0008 | t0001 | g0036 | SAS | PJL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03490 | hp2 | a0001 | c0006 | t0001 | g0151 | SAS | PJL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03491 | hp1 | a0002 | c0004 | t0003 | g0241 | SAS | PJL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03491 | hp2 | a0001 | c0003 | t0002 | g0041 | SAS | PJL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03492 | hp1 | a0001 | c0008 | t0001 | g0036 | SAS | PJL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03492 | hp2 | a0001 | c0003 | t0002 | g0003 | SAS | PJL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03516 | hp1 | a0001 | c0010 | t0001 | g0136 | AFR | ESN | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03516 | hp2 | a0001 | c0006 | t0001 | g0145 | AFR | ESN | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03540 | hp1 | a0008 | c0013 | t0006 | g0009 | AFR | GWD | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03579 | hp2 | a0001 | c0003 | t0006 | g0010 | AFR | MSL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03654 | hp1 | a0001 | c0003 | t0005 | g0220 | SAS | PJL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03654 | hp2 | a0001 | c0005 | t0001 | g0016 | SAS | PJL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03669 | hp1 | a0001 | c0003 | t0002 | g0003 | SAS | PJL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0021 | SAS | PJL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03688 | hp1 | a0002 | c0004 | t0003 | g0037 | SAS | STU | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0008 | SAS | STU | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03704 | hp1 | a0001 | c0003 | t0004 | g0264 | SAS | PJL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03831 | hp1 | a0007 | c0019 | t0001 | g0148 | SAS | BEB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0281 | SAS | BEB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03834 | hp1 | a0001 | c0014 | t0004 | g0274 | SAS | BEB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03834 | hp2 | a0001 | c0003 | t0002 | g0268 | SAS | BEB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0110 | SAS | BEB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03927 | hp2 | a0002 | c0004 | t0003 | g0234 | SAS | BEB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03942 | hp1 | a0002 | c0004 | t0003 | g0038 | SAS | BEB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03942 | hp2 | a0013 | c0029 | t0001 | g0021 | SAS | BEB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | STU | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG04115 | hp2 | a0002 | c0020 | t0010 | g0272 | SAS | STU | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG04184 | hp2 | a0001 | c0014 | t0001 | g0259 | SAS | BEB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0106 | SAS | STU | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG04199 | hp2 | a0001 | c0003 | t0002 | g0273 | SAS | STU | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0122 | SAS | STU | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG04204 | hp2 | a0001 | c0003 | t0002 | g0254 | SAS | STU | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG04228 | hp1 | a0002 | c0004 | t0003 | g0238 | SAS | STU | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | STU | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18522 | hp1 | a0001 | c0006 | t0001 | g0140 | AFR | YRI | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18522 | hp2 | a0008 | c0013 | t0006 | g0009 | AFR | YRI | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18612 | hp2 | a0001 | c0002 | t0005 | g0112 | EAS | CHB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | YRI | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18906 | hp2 | a0001 | c0003 | t0005 | g0084 | AFR | YRI | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18943 | hp2 | a0001 | c0008 | t0001 | g0230 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18944 | hp1 | a0001 | c0002 | t0004 | g0260 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18946 | hp1 | a0001 | c0002 | t0011 | g0245 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18946 | hp2 | a0001 | c0003 | t0002 | g0263 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18948 | hp2 | a0001 | c0002 | t0011 | g0039 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18951 | hp2 | a0001 | c0003 | t0002 | g0251 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18952 | hp1 | a0001 | c0007 | t0001 | g0018 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18954 | hp2 | a0001 | c0003 | t0005 | g0048 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18957 | hp1 | a0001 | c0003 | t0005 | g0046 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0280 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18960 | hp1 | a0001 | c0003 | t0007 | g0129 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18964 | hp2 | a0001 | c0003 | t0005 | g0015 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18966 | hp1 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0279 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18970 | hp2 | a0001 | c0003 | t0004 | g0265 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18983 | hp1 | a0001 | c0003 | t0005 | g0015 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18985 | hp1 | a0001 | c0022 | t0007 | g0248 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18985 | hp2 | a0001 | c0003 | t0005 | g0050 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18986 | hp1 | a0002 | c0004 | t0003 | g0229 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18986 | hp2 | a0001 | c0003 | t0005 | g0242 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18988 | hp1 | a0002 | c0004 | t0003 | g0006 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18988 | hp2 | a0001 | c0003 | t0002 | g0255 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18989 | hp2 | a0001 | c0003 | t0002 | g0041 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18990 | hp2 | a0002 | c0004 | t0003 | g0006 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18993 | hp2 | a0001 | c0001 | t0004 | g0262 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18994 | hp1 | a0001 | c0003 | t0005 | g0076 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18995 | hp1 | a0001 | c0003 | t0005 | g0051 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18995 | hp2 | a0001 | c0007 | t0001 | g0018 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19006 | hp2 | a0001 | c0003 | t0005 | g0049 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19011 | hp1 | a0002 | c0004 | t0003 | g0006 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | LWK | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | LWK | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19043 | hp1 | a0001 | c0006 | t0001 | g0146 | AFR | LWK | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | LWK | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19054 | hp2 | a0001 | c0003 | t0005 | g0062 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19058 | hp2 | a0002 | c0004 | t0003 | g0006 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19060 | hp1 | a0002 | c0004 | t0003 | g0037 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19060 | hp2 | a0001 | c0005 | t0001 | g0022 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19062 | hp1 | a0002 | c0004 | t0003 | g0038 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19062 | hp2 | a0001 | c0007 | t0001 | g0207 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19063 | hp2 | a0001 | c0005 | t0001 | g0022 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19064 | hp2 | a0002 | c0004 | t0003 | g0231 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0261 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19066 | hp2 | a0003 | c0015 | t0001 | g0118 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19080 | hp2 | a0001 | c0003 | t0002 | g0267 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19088 | hp1 | a0001 | c0003 | t0005 | g0047 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19088 | hp2 | a0002 | c0004 | t0003 | g0006 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | YRI | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | YRI | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA20129 | hp1 | a0001 | c0005 | t0001 | g0178 | AFR | ASW | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA20129 | hp2 | a0001 | c0003 | t0006 | g0153 | AFR | ASW | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | TSI | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA20752 | hp2 | a0001 | c0003 | t0002 | g0271 | EUR | TSI | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01123 | hp1 | a0004 | c0009 | t0001 | g0005 | AMR | CLM | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0105 | AMR | CLM | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0124 | AFR | ACB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0285 | AFR | ACB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02486 | hp2 | a0001 | c0003 | t0002 | g0007 | AFR | ACB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02559 | hp1 | a0003 | c0012 | t0001 | g0138 | AFR | ACB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03471 | hp1 | a0012 | c0030 | t0001 | g0250 | AFR | MSL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG03471 | hp2 | a0001 | c0003 | t0002 | g0007 | AFR | MSL | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG06807 | hp1 | a0001 | c0003 | t0001 | g0252 | AFR | USA | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| HG06807 | hp2 | a0004 | c0009 | t0001 | g0005 | AFR | USA | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18955 | hp1 | a0001 | c0003 | t0005 | g0045 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA20300 | hp1 | a0003 | c0012 | t0001 | g0137 | AFR | USA | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA20300 | hp2 | a0001 | c0010 | t0001 | g0139 | AFR | USA | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA21309 | hp1 | a0001 | c0005 | t0009 | g0131 | AFR | LWK | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| NA21309 | hp2 | a0001 | c0003 | t0002 | g0007 | AFR | LWK | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0002 | g0253 | REF | REF | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0023 | REF | REF | ATP12A_chr13_24675408_24717472 | ATP12A | chr13 | 24675408 | 24717472 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:24681660 | C | G | 1 | a0012 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.108C>G | p.Asn36Lys | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/23 | 444/4406 | 108/3120 | 36/1039 | chr13 | 24681660 | |||
| chr13:24690347 | G | A | 1 | a0008 | 2 | HG03540.hp1 NA18522.hp2 |
missense_variant | MODERATE | c.556G>A | p.Val186Ile | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 6/23 | 892/4406 | 556/3120 | 186/1039 | chr13 | 24690347 | |||
| chr13:24690623 | C | T | 1 | a0013 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.701C>T | p.Thr234Met | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 7/23 | 1037/4406 | 701/3120 | 234/1039 | chr13 | 24690623 | |||
| chr13:24692538 | C | T | 1 | a0005 | 2 | HG01109.hp2 HG02280.hp1 |
missense_variant | MODERATE | c.1178C>T | p.Thr393Ile | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 9/23 | 1514/4406 | 1178/3120 | 393/1039 | chr13 | 24692538 | |||
| chr13:24692541 | G | A | 1 | a0005 | 2 | HG01109.hp2 HG02280.hp1 |
missense_variant | MODERATE | c.1181G>A | p.Gly394Glu | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 9/23 | 1517/4406 | 1181/3120 | 394/1039 | chr13 | 24692541 | |||
| chr13:24692879 | A | C | 1 | a0004 | 5 | HG00639.hp1 HG01123.hp1 HG01257.hp2 others(2): Show |
missense_variant | MODERATE | c.1360A>C | p.Asn454His | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 10/23 | 1696/4406 | 1360/3120 | 454/1039 | chr13 | 24692879 | |||
| chr13:24698688 | G | A | 1 | a0007 | 2 | HG01981.hp1 HG03831.hp1 |
missense_variant | MODERATE | c.1543G>A | p.Gly515Ser | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/23 | 1879/4406 | 1543/3120 | 515/1039 | chr13 | 24698688 | |||
| chr13:24698694 | C | T | 1 | a0003 | 2 | HG02074.hp1 NA19066.hp2 |
missense_variant | MODERATE | c.1549C>T | p.Arg517Cys | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/23 | 1885/4406 | 1549/3120 | 517/1039 | chr13 | 24698694 | |||
| chr13:24698695 | G | A | 1 | a0003 | 4 | HG01074.hp1 HG02559.hp1 HG03453.hp1 others(1): Show |
missense_variant | MODERATE | c.1550G>A | p.Arg517His | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/23 | 1886/4406 | 1550/3120 | 517/1039 | chr13 | 24698695 | |||
| chr13:24706321 | A | G | 1 | a0011 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.2027A>G | p.Lys676Arg | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 15/23 | 2363/4406 | 2027/3120 | 676/1039 | chr13 | 24706321 | |||
| chr13:24706425 | C | A | 1 | a0007 | 2 | HG01981.hp1 HG03831.hp1 |
missense_variant | MODERATE | c.2131C>A | p.Gln711Lys | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 15/23 | 2467/4406 | 2131/3120 | 711/1039 | chr13 | 24706425 | |||
| chr13:24707356 | C | G | 1 | a0006 | 2 | HG01168.hp1 HG01169.hp1 |
missense_variant | MODERATE | c.2416C>G | p.Leu806Val | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/23 | 2752/4406 | 2416/3120 | 806/1039 | chr13 | 24707356 | |||
| chr13:24709458 | C | T | 1 | a0002 | 27 | HG00140.hp2 HG00558.hp1 HG01081.hp1 others(24): Show |
missense_variant | MODERATE | c.2588C>T | p.Pro863Leu | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 18/23 | 2924/4406 | 2588/3120 | 863/1039 | chr13 | 24709458 | |||
| chr13:24709744 | T | G | 1 | a0010 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.2679T>G | p.Phe893Leu | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 19/23 | 3015/4406 | 2679/3120 | 893/1039 | chr13 | 24709744 | |||
| chr13:24709767 | T | A | 1 | a0010 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.2702T>A | p.Leu901Gln | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 19/23 | 3038/4406 | 2702/3120 | 901/1039 | chr13 | 24709767 | |||
| chr13:24709777 | A | T | 1 | a0010 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.2712A>T | p.Glu904Asp | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 19/23 | 3048/4406 | 2712/3120 | 904/1039 | chr13 | 24709777 | |||
| chr13:24709825 | A | T | 1 | a0010 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.2760A>T | p.Glu920Asp | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 19/23 | 3096/4406 | 2760/3120 | 920/1039 | chr13 | 24709825 | |||
| chr13:24709826 | T | G | 1 | a0010 | 1 | HG02015.hp2 | missense_variant&splice_region_variant | MODERATE | c.2761T>G | p.Trp921Gly | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 19/23 | 3097/4406 | 2761/3120 | 921/1039 | chr13 | 24709826 | |||
| chr13:24711379 | C | T | 1 | a0009 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.3061C>T | p.Arg1021Trp | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 22/23 | 3397/4406 | 3061/3120 | 1021/1039 | chr13 | 24711379 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:24681567 | C | A | 5 | a0001c0006 a0001c0010 a0003c0012 others(2): Show |
23 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(20): Show |
synonymous_variant | LOW | c.15C>A | p.Thr5Thr | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/23 | 351/4406 | 15/3120 | 5/1039 | chr13 | 24681567 | |||
| chr13:24690618 | T | G | 2 | a0001c0014 a0002c0020 |
3 | HG03834.hp1 HG04115.hp2 HG04184.hp2 |
synonymous_variant | LOW | c.696T>G | p.Ser232Ser | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 7/23 | 1032/4406 | 696/3120 | 232/1039 | chr13 | 24690618 | |||
| chr13:24691001 | T | C | 7 | a0001c0002 a0001c0005 a0001c0021 others(4): Show |
122 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
synonymous_variant | LOW | c.819T>C | p.Val273Val | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 8/23 | 1155/4406 | 819/3120 | 273/1039 | chr13 | 24691001 | |||
| chr13:24691043 | A | C | 1 | a0012c0030 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.861A>C | p.Ser287Ser | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 8/23 | 1197/4406 | 861/3120 | 287/1039 | chr13 | 24691043 | |||
| chr13:24691094 | G | A | 1 | a0001c0021 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.912G>A | p.Glu304Glu | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 8/23 | 1248/4406 | 912/3120 | 304/1039 | chr13 | 24691094 | |||
| chr13:24691133 | C | T | 2 | a0001c0008 a0002c0004 |
28 | HG00140.hp1 HG00140.hp2 HG01081.hp1 others(25): Show |
synonymous_variant | LOW | c.951C>T | p.Ile317Ile | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 8/23 | 1287/4406 | 951/3120 | 317/1039 | chr13 | 24691133 | |||
| chr13:24692539 | T | G | 1 | a0005c0018 | 2 | HG01109.hp2 HG02280.hp1 |
synonymous_variant | LOW | c.1179T>G | p.Thr393Thr | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 9/23 | 1515/4406 | 1179/3120 | 393/1039 | chr13 | 24692539 | |||
| chr13:24692794 | C | A | 5 | a0001c0002 a0001c0007 a0001c0022 others(2): Show |
109 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(106): Show |
synonymous_variant | LOW | c.1275C>A | p.Val425Val | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 10/23 | 1611/4406 | 1275/3120 | 425/1039 | chr13 | 24692794 | |||
| chr13:24698732 | C | T | 8 | a0001c0003 a0001c0010 a0001c0022 others(5): Show |
89 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(86): Show |
synonymous_variant | LOW | c.1587C>T | p.Ile529Ile | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/23 | 1923/4406 | 1587/3120 | 529/1039 | chr13 | 24698732 | |||
| chr13:24700775 | C | T | 1 | a0001c0027 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.1734C>T | p.Asp578Asp | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 13/23 | 2070/4406 | 1734/3120 | 578/1039 | chr13 | 24700775 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:24680420 | C | T | 1 | a0001c0003t0016 | 1 | HG01243.hp2 | 5_prime_UTR_variant | MODIFIER | c.-324C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 1/23 | 324 | chr13 | 24680420 | ||||||
| chr13:24680426 | C | T | 1 | a0001c0005t0009 | 3 | HG02886.hp1 HG03453.hp2 NA21309.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-318C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 1/23 | chr13 | 24680426 | |||||||
| chr13:24680529 | G | A | 11 | a0001c0001t0004 a0001c0001t0014 a0001c0002t0004 others(8): Show |
54 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(51): Show |
5_prime_UTR_variant | MODIFIER | c.-215G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 1/23 | 215 | chr13 | 24680529 | ||||||
| chr13:24680558 | C | A | 4 | a0001c0003t0006 a0001c0007t0006 a0001c0007t0015 others(1): Show |
18 | HG01175.hp2 HG01884.hp1 HG02145.hp1 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-186C>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 1/23 | 186 | chr13 | 24680558 | ||||||
| chr13:24711555 | C | T | 1 | a0001c0003t0016 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*33C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 23/23 | 33 | chr13 | 24711555 | ||||||
| chr13:24711630 | G | T | 17 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0012 others(14): Show |
86 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*108G>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 23/23 | 108 | chr13 | 24711630 | ||||||
| chr13:24711673 | C | T | 7 | a0001c0001t0007 a0001c0001t0012 a0001c0002t0007 others(4): Show |
34 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*151C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 23/23 | 151 | chr13 | 24711673 | ||||||
| chr13:24711776 | G | A | 6 | a0001c0001t0007 a0001c0002t0007 a0001c0003t0002 others(3): Show |
32 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*254G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 23/23 | 254 | chr13 | 24711776 | ||||||
| chr13:24712121 | C | T | 1 | a0001c0001t0014 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*599C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 23/23 | 599 | chr13 | 24712121 | ||||||
| chr13:24712237 | A | G | 1 | a0001c0002t0011 | 2 | NA18946.hp1 NA18948.hp2 |
3_prime_UTR_variant | MODIFIER | c.*715A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 23/23 | 715 | chr13 | 24712237 | ||||||
| chr13:24712426 | G | A | 7 | a0001c0001t0008 a0001c0003t0013 a0002c0004t0003 others(4): Show |
31 | HG00140.hp2 HG00558.hp1 HG00733.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*904G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 23/23 | 904 | chr13 | 24712426 | ||||||
| chr13:24712452 | A | G | 1 | a0001c0001t0014 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*930A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 23/23 | 930 | chr13 | 24712452 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:24680914 | A | C | 44 | a0001c0001t0004g0261 a0001c0001t0004g0262 a0001c0001t0004g0270 others(41): Show |
55 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.9+162A>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 1/22 | chr13 | 24680914 | |||||||
| chr13:24681074 | G | T | 45 | a0001c0001t0004g0261 a0001c0001t0004g0262 a0001c0001t0004g0270 others(42): Show |
56 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.9+322G>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 1/22 | chr13 | 24681074 | |||||||
| chr13:24681195 | GAGGAAAC others(31): Show |
G | 1 | a0001c0003t0002g0251 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.10-356_10-319delGA others(36): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 24681195 | ||||||
| chr13:24681273 | T | TG | 10 | a0001c0001t0001g0052 a0001c0003t0005g0015 a0001c0003t0005g0044 others(7): Show |
11 | HG00735.hp2 HG02602.hp1 NA18954.hp2 others(8): Show |
intron_variant | MODIFIER | c.10-282dupG | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 24681273 | ||||||
| chr13:24681284 | C | G | 44 | a0001c0001t0004g0261 a0001c0001t0004g0262 a0001c0001t0004g0270 others(41): Show |
55 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.10-278C>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 1/22 | chr13 | 24681284 | |||||||
| chr13:24681317 | C | T | 45 | a0001c0001t0004g0261 a0001c0001t0004g0262 a0001c0001t0004g0270 others(42): Show |
56 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.10-245C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 1/22 | chr13 | 24681317 | |||||||
| chr13:24681327 | GCTGGCTG others(11): Show |
G | 1 | a0001c0001t0001g0053 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.10-233_10-216delTG others(16): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 24681327 | ||||||
| chr13:24681365 | G | A | 45 | a0001c0001t0004g0261 a0001c0001t0004g0262 a0001c0001t0004g0270 others(42): Show |
56 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.10-197G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 1/22 | chr13 | 24681365 | |||||||
| chr13:24681411 | A | G | 9 | a0001c0002t0001g0039 a0001c0002t0001g0243 a0001c0002t0001g0244 others(6): Show |
9 | HG00558.hp1 HG02040.hp1 NA18946.hp1 others(6): Show |
intron_variant | MODIFIER | c.10-151A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 1/22 | chr13 | 24681411 | |||||||
| chr13:24681437 | A | G | 44 | a0001c0001t0004g0261 a0001c0001t0004g0262 a0001c0001t0004g0270 others(41): Show |
54 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.10-125A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 1/22 | chr13 | 24681437 | |||||||
| chr13:24681515 | C | T | 1 | a0001c0003t0005g0242 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.10-47C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 1/22 | chr13 | 24681515 | |||||||
| chr13:24681728 | G | A | 1 | a0001c0003t0001g0252 | 1 | HG06807.hp1 | splice_region_variant&intron_variant | LOW | c.168+8G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24681728 | |||||||
| chr13:24681876 | T | C | 5 | a0001c0005t0001g0016 a0001c0005t0001g0054 a0001c0005t0001g0055 others(2): Show |
6 | HG00642.hp1 HG01070.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+156T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24681876 | |||||||
| chr13:24681902 | T | C | 45 | a0001c0001t0004g0261 a0001c0001t0004g0262 a0001c0001t0004g0270 others(42): Show |
56 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.168+182T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24681902 | |||||||
| chr13:24681906 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.168+186G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24681906 | |||||||
| chr13:24681933 | A | G | 184 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(181): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.168+213A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24681933 | |||||||
| chr13:24681939 | T | G | 31 | a0001c0003t0006g0009 a0001c0003t0006g0010 a0001c0003t0006g0025 others(28): Show |
41 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.168+219T>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24681939 | |||||||
| chr13:24681940 | G | GGT | 11 | a0001c0001t0004g0282 a0001c0001t0004g0285 a0001c0001t0014g0284 others(8): Show |
13 | HG01243.hp2 HG01891.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.168+231_168+232dup others(2): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 24681940 | ||||||
| chr13:24681940 | G | T | 31 | a0001c0003t0006g0009 a0001c0003t0006g0010 a0001c0003t0006g0025 others(28): Show |
41 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.168+220G>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24681940 | |||||||
| chr13:24681959 | GGTGTGTG others(49): Show |
G | 18 | a0001c0006t0001g0024 a0001c0006t0001g0140 a0001c0006t0001g0141 others(15): Show |
23 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.168+246_168+301del others(56): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 24681959 | ||||||
| chr13:24681960 | G | A | 45 | a0001c0001t0004g0261 a0001c0001t0004g0262 a0001c0001t0004g0270 others(42): Show |
56 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.168+240G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24681960 | |||||||
| chr13:24681980 | G | T | 121 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(118): Show |
150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.168+260G>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24681980 | |||||||
| chr13:24682034 | GTGTA | G | 139 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(136): Show |
173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.168+318_168+321del others(4): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 24682034 | ||||||
| chr13:24682087 | G | GGT | 44 | a0001c0001t0004g0261 a0001c0001t0004g0262 a0001c0001t0004g0270 others(41): Show |
55 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.168+375_168+376dup others(2): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 24682087 | ||||||
| chr13:24682106 | T | G | 1 | a0012c0030t0001g0250 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.168+386T>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682106 | |||||||
| chr13:24682107 | G | T | 1 | a0012c0030t0001g0250 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.168+387G>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682107 | |||||||
| chr13:24682108 | A | G | 1 | a0012c0030t0001g0250 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.168+388A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682108 | |||||||
| chr13:24682108 | A | T | 44 | a0001c0001t0004g0261 a0001c0001t0004g0262 a0001c0001t0004g0270 others(41): Show |
55 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.168+388A>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682108 | |||||||
| chr13:24682109 | T | G | 44 | a0001c0001t0004g0261 a0001c0001t0004g0262 a0001c0001t0004g0270 others(41): Show |
55 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.168+389T>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682109 | |||||||
| chr13:24682113 | TGTGTG | T | 44 | a0001c0001t0004g0261 a0001c0001t0004g0262 a0001c0001t0004g0270 others(41): Show |
55 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.168+399_168+403del others(5): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 24682113 | ||||||
| chr13:24682114 | G | T | 1 | a0012c0030t0001g0250 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.168+394G>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682114 | |||||||
| chr13:24682116 | G | A | 1 | a0012c0030t0001g0250 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.168+396G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682116 | |||||||
| chr13:24682122 | T | A | 1 | a0001c0002t0001g0059 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.168+402T>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682122 | |||||||
| chr13:24682123 | G | A | 44 | a0001c0001t0004g0261 a0001c0001t0004g0262 a0001c0001t0004g0270 others(41): Show |
55 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.168+403G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682123 | |||||||
| chr13:24682136 | GTATA | G | 44 | a0001c0001t0004g0261 a0001c0001t0004g0262 a0001c0001t0004g0270 others(41): Show |
55 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.168+418_168+421del others(4): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 24682136 | ||||||
| chr13:24682144 | G | T | 44 | a0001c0001t0004g0261 a0001c0001t0004g0262 a0001c0001t0004g0270 others(41): Show |
55 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.168+424G>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682144 | |||||||
| chr13:24682146 | G | A | 44 | a0001c0001t0004g0261 a0001c0001t0004g0262 a0001c0001t0004g0270 others(41): Show |
55 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.168+426G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682146 | |||||||
| chr13:24682151 | GTGTGTGT others(10): Show |
G | 14 | a0001c0003t0006g0009 a0001c0003t0006g0010 a0001c0003t0006g0025 others(11): Show |
19 | HG01175.hp2 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.168+459_168+475del others(17): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 24682151 | ||||||
| chr13:24682155 | GTGTGGTG others(36): Show |
G | 1 | a0012c0030t0001g0250 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.168+437_168+479del others(43): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 24682155 | ||||||
| chr13:24682165 | T | TGTGTGTG others(17): Show |
18 | a0001c0006t0001g0024 a0001c0006t0001g0140 a0001c0006t0001g0141 others(15): Show |
23 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.168+447_168+448ins others(24): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 24682165 | ||||||
| chr13:24682166 | G | A | 44 | a0001c0001t0004g0261 a0001c0001t0004g0262 a0001c0001t0004g0270 others(41): Show |
55 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.168+446G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682166 | |||||||
| chr13:24682168 | A | G | 18 | a0001c0006t0001g0024 a0001c0006t0001g0140 a0001c0006t0001g0141 others(15): Show |
23 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.168+448A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682168 | |||||||
| chr13:24682174 | G | A | 39 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0064 others(36): Show |
46 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.168+454G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682174 | |||||||
| chr13:24682257 | G | A | 1 | a0001c0001t0004g0282 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.168+537G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682257 | |||||||
| chr13:24682258 | T | G | 13 | a0001c0003t0006g0009 a0001c0003t0006g0010 a0001c0003t0006g0025 others(10): Show |
18 | HG01175.hp2 HG01884.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.168+538T>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682258 | |||||||
| chr13:24682332 | G | A | 46 | a0001c0001t0001g0161 a0001c0001t0004g0261 a0001c0001t0004g0262 others(43): Show |
57 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.168+612G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682332 | |||||||
| chr13:24682336 | GGT | G | 45 | a0001c0001t0004g0261 a0001c0001t0004g0262 a0001c0001t0004g0270 others(42): Show |
56 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.168+625_168+626del others(2): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 24682336 | ||||||
| chr13:24682359 | A | G | 46 | a0001c0001t0004g0261 a0001c0001t0004g0262 a0001c0001t0004g0270 others(43): Show |
57 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.168+639A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682359 | |||||||
| chr13:24682361 | A | ATGTGTGG others(11): Show |
1 | a0001c0005t0001g0240 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.168+663_168+680dup others(18): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 24682361 | ||||||
| chr13:24682381 | G | A | 75 | a0001c0001t0001g0128 a0001c0002t0001g0001 a0001c0002t0001g0002 others(72): Show |
116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.168+661G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682381 | |||||||
| chr13:24682381 | G | GTGTGGTG others(219): Show |
1 | a0002c0004t0003g0241 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.168+672_168+673ins others(226): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 24682381 | ||||||
| chr13:24682392 | G | GGTGTGTG others(15): Show |
10 | a0001c0001t0004g0279 a0001c0001t0004g0280 a0001c0001t0004g0281 others(7): Show |
13 | HG00639.hp2 HG01243.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.168+680_168+681ins others(22): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 24682392 | ||||||
| chr13:24682392 | G | GGTGTGTG others(17): Show |
23 | a0001c0001t0004g0261 a0001c0001t0004g0262 a0001c0001t0004g0270 others(20): Show |
30 | HG00438.hp2 HG00544.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.168+680_168+681ins others(24): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 24682392 | ||||||
| chr13:24682392 | G | GGTGTGTG others(19): Show |
11 | a0001c0001t0004g0282 a0001c0001t0004g0285 a0001c0001t0014g0284 others(8): Show |
12 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.168+680_168+681ins others(26): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 24682392 | ||||||
| chr13:24682392 | G | GGTGTGTG others(21): Show |
1 | a0012c0030t0001g0250 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.168+680_168+681ins others(28): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 24682392 | ||||||
| chr13:24682401 | A | ATG | 3 | a0001c0003t0006g0152 a0001c0003t0006g0153 a0001c0003t0006g0154 |
3 | HG01175.hp2 HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.168+695_168+696dup others(2): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 24682401 | ||||||
| chr13:24682401 | A | G | 45 | a0001c0001t0004g0261 a0001c0001t0004g0262 a0001c0001t0004g0270 others(42): Show |
56 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.168+681A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682401 | |||||||
| chr13:24682431 | T | C | 1 | a0001c0003t0005g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.168+711T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682431 | |||||||
| chr13:24682499 | A | G | 1 | a0001c0002t0001g0059 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.168+779A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682499 | |||||||
| chr13:24682557 | C | G | 1 | a0001c0003t0001g0135 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.168+837C>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682557 | |||||||
| chr13:24682557 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.168+837C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682557 | |||||||
| chr13:24682558 | G | C | 287 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(284): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.168+838G>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682558 | |||||||
| chr13:24682559 | C | A | 57 | a0001c0001t0004g0261 a0001c0001t0004g0262 a0001c0001t0004g0270 others(54): Show |
73 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.168+839C>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682559 | |||||||
| chr13:24682569 | A | G | 1 | a0002c0004t0003g0238 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.168+849A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682569 | |||||||
| chr13:24682598 | T | C | 45 | a0001c0001t0004g0261 a0001c0001t0004g0262 a0001c0001t0004g0270 others(42): Show |
56 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.168+878T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682598 | |||||||
| chr13:24682625 | C | G | 45 | a0001c0001t0004g0261 a0001c0001t0004g0262 a0001c0001t0004g0270 others(42): Show |
56 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.168+905C>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682625 | |||||||
| chr13:24682647 | C | T | 1 | a0012c0030t0001g0250 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.168+927C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682647 | |||||||
| chr13:24682742 | G | A | 45 | a0001c0001t0004g0261 a0001c0001t0004g0262 a0001c0001t0004g0270 others(42): Show |
56 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.168+1022G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682742 | |||||||
| chr13:24682753 | G | C | 1 | a0002c0011t0010g0288 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.168+1033G>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682753 | |||||||
| chr13:24682758 | C | G | 45 | a0001c0001t0004g0261 a0001c0001t0004g0262 a0001c0001t0004g0270 others(42): Show |
56 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.168+1038C>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24682758 | |||||||
| chr13:24682959 | C | CTTTTTTT others(3): Show |
9 | a0001c0001t0004g0282 a0001c0001t0004g0285 a0001c0001t0014g0284 others(6): Show |
11 | HG01243.hp2 HG01516.hp1 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.168+1244_168+1253d others(12): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 24682959 | ||||||
| chr13:24682959 | C | CTTTTTTT others(4): Show |
30 | a0001c0001t0001g0128 a0001c0001t0004g0261 a0001c0001t0004g0262 others(27): Show |
38 | HG00544.hp2 HG00639.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.168+1243_168+1253d others(13): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 24682959 | ||||||
| chr13:24682959 | C | CTTTTTTT others(5): Show |
6 | a0001c0001t0004g0281 a0001c0003t0002g0042 a0001c0003t0002g0256 others(3): Show |
7 | HG00438.hp2 HG01169.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.168+1242_168+1253d others(14): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 24682959 | ||||||
| chr13:24682959 | C | CTTTTTTT others(6): Show |
1 | a0001c0003t0002g0257 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.168+1241_168+1253d others(15): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 24682959 | ||||||
| chr13:24682959 | CT | C | 94 | a0001c0001t0001g0027 a0001c0001t0001g0130 a0001c0001t0001g0162 others(91): Show |
136 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.168+1253delT | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 24682959 | ||||||
| chr13:24682959 | CTT | C | 13 | a0001c0003t0006g0009 a0001c0003t0006g0010 a0001c0003t0006g0025 others(10): Show |
18 | HG01175.hp2 HG01884.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.168+1252_168+1253d others(4): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 24682959 | ||||||
| chr13:24683139 | G | GT | 20 | a0001c0001t0001g0225 a0001c0008t0001g0036 a0001c0008t0001g0228 others(17): Show |
28 | HG00140.hp2 HG00597.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.168+1420dupT | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 24683139 | ||||||
| chr13:24683264 | G | C | 2 | a0001c0002t0001g0086 a0001c0002t0001g0087 |
2 | NA18954.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.168+1544G>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24683264 | |||||||
| chr13:24683372 | C | T | 1 | a0001c0002t0001g0224 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.168+1652C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24683372 | |||||||
| chr13:24683433 | A | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0174 |
4 | NA19002.hp2 NA19004.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+1713A>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24683433 | |||||||
| chr13:24683582 | T | C | 65 | a0001c0001t0001g0128 a0001c0001t0004g0261 a0001c0001t0004g0262 others(62): Show |
81 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.169-1732T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24683582 | |||||||
| chr13:24683584 | T | C | 65 | a0001c0001t0001g0128 a0001c0001t0004g0261 a0001c0001t0004g0262 others(62): Show |
81 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.169-1730T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24683584 | |||||||
| chr13:24683586 | C | A | 65 | a0001c0001t0001g0128 a0001c0001t0004g0261 a0001c0001t0004g0262 others(62): Show |
81 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.169-1728C>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24683586 | |||||||
| chr13:24683603 | G | GT | 11 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0218 others(8): Show |
11 | HG00733.hp2 HG01433.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.169-1710dupT | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 24683603 | ||||||
| chr13:24683722 | C | T | 1 | a0001c0003t0001g0135 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.169-1592C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24683722 | |||||||
| chr13:24683779 | C | T | 42 | a0001c0001t0001g0128 a0001c0001t0001g0161 a0001c0001t0004g0261 others(39): Show |
51 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.169-1535C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24683779 | |||||||
| chr13:24683787 | G | A | 3 | a0001c0003t0006g0025 a0001c0003t0006g0155 a0001c0003t0006g0156 |
4 | HG02145.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-1527G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24683787 | |||||||
| chr13:24683794 | C | A | 42 | a0001c0001t0001g0128 a0001c0001t0001g0161 a0001c0001t0004g0261 others(39): Show |
51 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.169-1520C>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24683794 | |||||||
| chr13:24683818 | C | T | 1 | a0012c0030t0001g0250 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.169-1496C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24683818 | |||||||
| chr13:24683898 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.169-1416C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24683898 | |||||||
| chr13:24683913 | C | A | 13 | a0001c0005t0001g0016 a0001c0005t0001g0054 a0001c0005t0001g0055 others(10): Show |
14 | HG00642.hp1 HG01070.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-1401C>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24683913 | |||||||
| chr13:24683967 | A | C | 2 | a0001c0003t0006g0153 a0001c0003t0006g0154 |
2 | HG01175.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.169-1347A>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24683967 | |||||||
| chr13:24683987 | G | T | 1 | a0001c0005t0001g0179 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.169-1327G>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24683987 | |||||||
| chr13:24684005 | T | C | 42 | a0001c0001t0001g0128 a0001c0001t0001g0161 a0001c0001t0004g0261 others(39): Show |
51 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.169-1309T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24684005 | |||||||
| chr13:24684095 | C | A | 47 | a0001c0001t0001g0128 a0001c0001t0001g0161 a0001c0001t0004g0261 others(44): Show |
56 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.169-1219C>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24684095 | |||||||
| chr13:24684114 | TC | T | 167 | a0001c0001t0001g0128 a0001c0001t0001g0161 a0001c0001t0001g0225 others(164): Show |
228 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.169-1197delC | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 24684114 | ||||||
| chr13:24684164 | A | G | 1 | a0001c0002t0001g0173 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.169-1150A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24684164 | |||||||
| chr13:24684184 | G | C | 81 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(78): Show |
102 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.169-1130G>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24684184 | |||||||
| chr13:24684215 | T | C | 66 | a0001c0001t0001g0128 a0001c0001t0001g0161 a0001c0001t0001g0225 others(63): Show |
83 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.169-1099T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24684215 | |||||||
| chr13:24684254 | A | C | 4 | a0001c0010t0001g0136 a0001c0010t0001g0139 a0003c0012t0001g0137 others(1): Show |
4 | HG02559.hp1 HG03516.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-1060A>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24684254 | |||||||
| chr13:24684431 | T | C | 4 | a0001c0002t0001g0088 a0001c0002t0001g0089 a0001c0002t0001g0090 others(1): Show |
4 | HG00597.hp1 NA18951.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-883T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24684431 | |||||||
| chr13:24684547 | G | A | 1 | a0001c0002t0001g0092 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.169-767G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24684547 | |||||||
| chr13:24684673 | T | G | 25 | a0001c0001t0001g0225 a0001c0003t0001g0135 a0001c0008t0001g0036 others(22): Show |
33 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.169-641T>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24684673 | |||||||
| chr13:24684678 | G | A | 25 | a0001c0001t0001g0225 a0001c0003t0001g0135 a0001c0008t0001g0036 others(22): Show |
33 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.169-636G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24684678 | |||||||
| chr13:24684706 | C | A | 31 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0072 others(28): Show |
33 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.169-608C>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24684706 | |||||||
| chr13:24684753 | C | T | 3 | a0001c0014t0001g0259 a0001c0014t0004g0274 a0002c0020t0010g0272 |
3 | HG03834.hp1 HG04115.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.169-561C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24684753 | |||||||
| chr13:24684981 | C | T | 44 | a0001c0001t0001g0128 a0001c0001t0004g0261 a0001c0001t0004g0262 others(41): Show |
53 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.169-333C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24684981 | |||||||
| chr13:24685085 | C | T | 45 | a0001c0001t0001g0128 a0001c0001t0001g0161 a0001c0001t0004g0261 others(42): Show |
54 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.169-229C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24685085 | |||||||
| chr13:24685207 | C | G | 1 | a0001c0001t0001g0213 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.169-107C>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24685207 | |||||||
| chr13:24685210 | A | C | 1 | a0001c0022t0007g0248 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.169-104A>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | chr13 | 24685210 | |||||||
| chr13:24685442 | C | T | 13 | a0001c0005t0001g0016 a0001c0005t0001g0054 a0001c0005t0001g0055 others(10): Show |
14 | HG00642.hp1 HG01070.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.228+69C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24685442 | |||||||
| chr13:24685591 | A | G | 44 | a0001c0001t0001g0128 a0001c0001t0004g0261 a0001c0001t0004g0262 others(41): Show |
53 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.228+218A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24685591 | |||||||
| chr13:24685665 | T | C | 14 | a0001c0005t0001g0016 a0001c0005t0001g0054 a0001c0005t0001g0055 others(11): Show |
15 | HG00642.hp1 HG01070.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.228+292T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24685665 | |||||||
| chr13:24685687 | G | A | 1 | a0001c0021t0001g0176 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.228+314G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24685687 | |||||||
| chr13:24685819 | G | T | 14 | a0001c0003t0001g0212 a0001c0003t0006g0009 a0001c0003t0006g0010 others(11): Show |
19 | HG01175.hp2 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.228+446G>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24685819 | |||||||
| chr13:24685915 | A | C | 43 | a0001c0001t0001g0128 a0001c0001t0004g0261 a0001c0001t0004g0262 others(40): Show |
52 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.228+542A>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24685915 | |||||||
| chr13:24686236 | T | C | 1 | a0001c0006t0001g0142 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.228+863T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24686236 | |||||||
| chr13:24686267 | C | T | 2 | a0001c0005t0004g0043 a0001c0005t0004g0287 |
3 | HG01891.hp1 HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.228+894C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24686267 | |||||||
| chr13:24686440 | C | CAAA | 30 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0072 others(27): Show |
32 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.228+1082_228+1084d others(5): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr13 | 24686440 | ||||||
| chr13:24686440 | C | CAAAA | 15 | a0001c0002t0001g0068 a0001c0003t0005g0085 a0001c0005t0001g0016 others(12): Show |
17 | HG00099.hp1 HG00558.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.228+1081_228+1084d others(6): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr13 | 24686440 | ||||||
| chr13:24686440 | CA | C | 142 | a0001c0001t0001g0128 a0001c0001t0001g0172 a0001c0001t0001g0225 others(139): Show |
204 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.228+1084delA | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr13 | 24686440 | ||||||
| chr13:24686440 | CAA | C | 8 | a0001c0001t0004g0282 a0001c0001t0004g0285 a0001c0002t0001g0126 others(5): Show |
9 | HG02109.hp2 HG02451.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.228+1083_228+1084d others(4): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr13 | 24686440 | ||||||
| chr13:24686463 | G | A | 2 | a0001c0002t0001g0088 a0001c0002t0001g0089 |
2 | HG00597.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.228+1090G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24686463 | |||||||
| chr13:24686499 | A | G | 111 | a0001c0001t0001g0225 a0001c0001t0004g0282 a0001c0001t0004g0285 others(108): Show |
165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.228+1126A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24686499 | |||||||
| chr13:24686552 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.228+1179A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24686552 | |||||||
| chr13:24686600 | A | G | 6 | a0001c0003t0001g0061 a0001c0003t0001g0082 a0001c0003t0005g0080 others(3): Show |
6 | HG02258.hp2 HG02723.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.228+1227A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24686600 | |||||||
| chr13:24686601 | C | T | 6 | a0001c0003t0001g0061 a0001c0003t0001g0082 a0001c0003t0005g0080 others(3): Show |
6 | HG02258.hp2 HG02723.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.228+1228C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24686601 | |||||||
| chr13:24686608 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.228+1235G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24686608 | |||||||
| chr13:24686632 | G | A | 1 | a0001c0002t0001g0096 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.228+1259G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24686632 | |||||||
| chr13:24686652 | T | A | 15 | a0001c0005t0001g0016 a0001c0005t0001g0054 a0001c0005t0001g0055 others(12): Show |
17 | HG00642.hp1 HG01070.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.228+1279T>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24686652 | |||||||
| chr13:24686655 | C | G | 111 | a0001c0001t0001g0225 a0001c0001t0004g0282 a0001c0001t0004g0285 others(108): Show |
165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.228+1282C>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24686655 | |||||||
| chr13:24686670 | C | T | 1 | a0001c0002t0001g0125 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.228+1297C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24686670 | |||||||
| chr13:24686733 | T | C | 1 | a0001c0006t0001g0143 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.228+1360T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24686733 | |||||||
| chr13:24686777 | G | GGAAA | 108 | a0001c0001t0001g0225 a0001c0001t0004g0282 a0001c0001t0004g0285 others(105): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.228+1417_228+1420d others(6): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr13 | 24686777 | ||||||
| chr13:24686807 | C | A | 15 | a0001c0005t0001g0016 a0001c0005t0001g0054 a0001c0005t0001g0055 others(12): Show |
17 | HG00642.hp1 HG01070.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.228+1434C>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24686807 | |||||||
| chr13:24686823 | C | A | 111 | a0001c0001t0001g0225 a0001c0001t0004g0282 a0001c0001t0004g0285 others(108): Show |
165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.228+1450C>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24686823 | |||||||
| chr13:24686907 | G | C | 1 | a0001c0001t0001g0161 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.229-1412G>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24686907 | |||||||
| chr13:24687150 | C | T | 7 | a0001c0001t0001g0161 a0001c0001t0004g0285 a0001c0003t0001g0252 others(4): Show |
8 | HG01109.hp2 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.229-1169C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24687150 | |||||||
| chr13:24687200 | T | C | 150 | a0001c0001t0001g0128 a0001c0001t0001g0161 a0001c0001t0004g0261 others(147): Show |
207 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(204): Show |
intron_variant | MODIFIER | c.229-1119T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24687200 | |||||||
| chr13:24687240 | C | G | 121 | a0001c0001t0001g0128 a0001c0001t0004g0261 a0001c0001t0004g0262 others(118): Show |
172 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.229-1079C>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24687240 | |||||||
| chr13:24687259 | G | C | 7 | a0001c0001t0001g0161 a0001c0001t0004g0285 a0001c0003t0001g0252 others(4): Show |
8 | HG01109.hp2 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.229-1060G>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24687259 | |||||||
| chr13:24687277 | G | A | 3 | a0001c0014t0001g0259 a0001c0014t0004g0274 a0002c0020t0010g0272 |
3 | HG03834.hp1 HG04115.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.229-1042G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24687277 | |||||||
| chr13:24687333 | C | T | 119 | a0001c0001t0001g0128 a0001c0001t0004g0270 a0001c0001t0004g0279 others(116): Show |
170 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.229-986C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24687333 | |||||||
| chr13:24687412 | C | T | 7 | a0001c0001t0001g0161 a0001c0001t0004g0285 a0001c0003t0001g0252 others(4): Show |
8 | HG01109.hp2 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.229-907C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24687412 | |||||||
| chr13:24687463 | CA | C | 129 | a0001c0001t0001g0161 a0001c0001t0004g0285 a0001c0001t0014g0284 others(126): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.229-846delA | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr13 | 24687463 | ||||||
| chr13:24687520 | G | A | 1 | a0001c0003t0002g0263 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.229-799G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24687520 | |||||||
| chr13:24687605 | T | C | 2 | a0001c0003t0006g0009 a0008c0013t0006g0009 |
3 | HG02257.hp2 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.229-714T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24687605 | |||||||
| chr13:24687690 | T | C | 80 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(77): Show |
122 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.229-629T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24687690 | |||||||
| chr13:24687726 | G | A | 1 | a0001c0003t0001g0135 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.229-593G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24687726 | |||||||
| chr13:24687839 | T | C | 80 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(77): Show |
122 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.229-480T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24687839 | |||||||
| chr13:24687876 | A | G | 276 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(273): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.229-443A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24687876 | |||||||
| chr13:24687960 | C | T | 2 | a0005c0018t0005g0215 a0005c0018t0005g0216 |
2 | HG01109.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.229-359C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24687960 | |||||||
| chr13:24688031 | G | A | 81 | a0001c0001t0008g0217 a0001c0002t0001g0001 a0001c0002t0001g0002 others(78): Show |
123 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.229-288G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24688031 | |||||||
| chr13:24688148 | A | G | 33 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0072 others(30): Show |
35 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.229-171A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24688148 | |||||||
| chr13:24688204 | C | G | 128 | a0001c0001t0001g0161 a0001c0001t0004g0285 a0001c0001t0014g0284 others(125): Show |
184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.229-115C>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24688204 | |||||||
| chr13:24688237 | A | G | 1 | a0001c0003t0002g0271 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.229-82A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24688237 | |||||||
| chr13:24688275 | C | T | 1 | a0001c0002t0001g0122 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.229-44C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 3/22 | chr13 | 24688275 | |||||||
| chr13:24688804 | A | G | 100 | a0001c0001t0014g0284 a0001c0002t0001g0001 a0001c0002t0001g0002 others(97): Show |
147 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.432+282A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 4/22 | chr13 | 24688804 | |||||||
| chr13:24688866 | G | A | 80 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(77): Show |
122 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.432+344G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 4/22 | chr13 | 24688866 | |||||||
| chr13:24688986 | T | C | 80 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(77): Show |
122 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.433-276T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 4/22 | chr13 | 24688986 | |||||||
| chr13:24689012 | G | C | 1 | a0001c0003t0002g0271 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.433-250G>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 4/22 | chr13 | 24689012 | |||||||
| chr13:24689089 | C | T | 32 | a0001c0001t0001g0128 a0001c0001t0004g0270 a0001c0001t0004g0279 others(29): Show |
41 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.433-173C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 4/22 | chr13 | 24689089 | |||||||
| chr13:24689091 | T | TA | 80 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(77): Show |
122 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.433-160dupA | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr13 | 24689091 | ||||||
| chr13:24689140 | G | T | 1 | a0001c0001t0001g0223 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.433-122G>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 4/22 | chr13 | 24689140 | |||||||
| chr13:24689161 | G | A | 128 | a0001c0001t0001g0161 a0001c0001t0004g0285 a0001c0001t0014g0284 others(125): Show |
184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.433-101G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 4/22 | chr13 | 24689161 | |||||||
| chr13:24689401 | G | T | 21 | a0001c0003t0001g0135 a0001c0008t0001g0036 a0001c0008t0001g0182 others(18): Show |
29 | HG00140.hp1 HG00140.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.546+26G>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 5/22 | chr13 | 24689401 | |||||||
| chr13:24689586 | C | G | 128 | a0001c0001t0001g0161 a0001c0001t0004g0285 a0001c0001t0014g0284 others(125): Show |
184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.546+211C>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 5/22 | chr13 | 24689586 | |||||||
| chr13:24689714 | C | A | 80 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(77): Show |
122 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.546+339C>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 5/22 | chr13 | 24689714 | |||||||
| chr13:24689744 | A | T | 1 | a0001c0005t0001g0022 | 2 | NA19060.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.546+369A>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 5/22 | chr13 | 24689744 | |||||||
| chr13:24689754 | T | C | 80 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(77): Show |
122 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.546+379T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 5/22 | chr13 | 24689754 | |||||||
| chr13:24689760 | A | G | 7 | a0001c0001t0001g0161 a0001c0001t0004g0285 a0001c0003t0001g0252 others(4): Show |
8 | HG01109.hp2 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.546+385A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 5/22 | chr13 | 24689760 | |||||||
| chr13:24689791 | C | G | 56 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(53): Show |
72 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.546+416C>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 5/22 | chr13 | 24689791 | |||||||
| chr13:24689858 | C | T | 39 | a0001c0001t0001g0128 a0001c0001t0004g0270 a0001c0001t0004g0279 others(36): Show |
48 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.547-480C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 5/22 | chr13 | 24689858 | |||||||
| chr13:24689861 | C | T | 7 | a0001c0001t0001g0161 a0001c0001t0004g0285 a0001c0003t0001g0252 others(4): Show |
8 | HG01109.hp2 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.547-477C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 5/22 | chr13 | 24689861 | |||||||
| chr13:24689892 | C | T | 2 | a0006c0017t0001g0209 a0006c0017t0001g0210 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.547-446C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 5/22 | chr13 | 24689892 | |||||||
| chr13:24689899 | A | G | 80 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(77): Show |
122 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.547-439A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 5/22 | chr13 | 24689899 | |||||||
| chr13:24689914 | G | A | 80 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(77): Show |
122 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.547-424G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 5/22 | chr13 | 24689914 | |||||||
| chr13:24689927 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.547-411C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 5/22 | chr13 | 24689927 | |||||||
| chr13:24689982 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.547-356C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 5/22 | chr13 | 24689982 | |||||||
| chr13:24689999 | T | G | 1 | a0001c0002t0001g0243 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.547-339T>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 5/22 | chr13 | 24689999 | |||||||
| chr13:24690156 | T | A | 3 | a0001c0014t0001g0259 a0001c0014t0004g0274 a0002c0020t0010g0272 |
3 | HG03834.hp1 HG04115.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.547-182T>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 5/22 | chr13 | 24690156 | |||||||
| chr13:24690156 | T | C | 125 | a0001c0001t0001g0161 a0001c0001t0004g0285 a0001c0001t0014g0284 others(122): Show |
181 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.547-182T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 5/22 | chr13 | 24690156 | |||||||
| chr13:24690231 | T | C | 80 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(77): Show |
122 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.547-107T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 5/22 | chr13 | 24690231 | |||||||
| chr13:24690263 | C | T | 5 | a0001c0001t0001g0034 a0001c0001t0001g0221 a0001c0001t0008g0034 others(2): Show |
5 | HG00733.hp2 HG01515.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.547-75C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 5/22 | chr13 | 24690263 | |||||||
| chr13:24690271 | C | T | 1 | a0001c0003t0002g0254 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.547-67C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 5/22 | chr13 | 24690271 | |||||||
| chr13:24690491 | C | A | 16 | a0001c0001t0014g0284 a0001c0003t0001g0212 a0001c0003t0006g0009 others(13): Show |
21 | HG01175.hp2 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.681+19C>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 6/22 | chr13 | 24690491 | |||||||
| chr13:24690506 | T | A | 20 | a0001c0001t0014g0284 a0001c0003t0001g0212 a0001c0003t0006g0009 others(17): Show |
25 | HG01175.hp2 HG01243.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.681+34T>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 6/22 | chr13 | 24690506 | |||||||
| chr13:24690528 | G | T | 80 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(77): Show |
122 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.681+56G>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 6/22 | chr13 | 24690528 | |||||||
| chr13:24690555 | G | T | 1 | a0001c0002t0001g0247 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.682-49G>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 6/22 | chr13 | 24690555 | |||||||
| chr13:24690577 | G | A | 80 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(77): Show |
122 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.682-27G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 6/22 | chr13 | 24690577 | |||||||
| chr13:24690585 | C | T | 80 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(77): Show |
122 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.682-19C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 6/22 | chr13 | 24690585 | |||||||
| chr13:24690737 | C | T | 21 | a0001c0003t0001g0135 a0001c0008t0001g0036 a0001c0008t0001g0182 others(18): Show |
29 | HG00140.hp1 HG00140.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.799+16C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 7/22 | chr13 | 24690737 | |||||||
| chr13:24690744 | C | G | 2 | a0002c0004t0003g0236 a0002c0004t0003g0237 |
2 | HG00140.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.799+23C>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 7/22 | chr13 | 24690744 | |||||||
| chr13:24690870 | T | C | 128 | a0001c0001t0001g0161 a0001c0001t0004g0285 a0001c0001t0014g0284 others(125): Show |
184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.800-112T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 7/22 | chr13 | 24690870 | |||||||
| chr13:24690890 | C | T | 1 | a0010c0025t0001g0060 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.800-92C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 7/22 | chr13 | 24690890 | |||||||
| chr13:24690963 | G | A | 2 | a0001c0005t0004g0043 a0001c0005t0004g0287 |
3 | HG01891.hp1 HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.800-19G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 7/22 | chr13 | 24690963 | |||||||
| chr13:24690963 | G | C | 2 | a0001c0001t0001g0162 a0001c0001t0001g0172 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.800-19G>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 7/22 | chr13 | 24690963 | |||||||
| chr13:24690965 | A | G | 80 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(77): Show |
122 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.800-17A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 7/22 | chr13 | 24690965 | |||||||
| chr13:24691316 | G | A | 20 | a0001c0001t0014g0284 a0001c0003t0001g0212 a0001c0003t0006g0009 others(17): Show |
25 | HG01175.hp2 HG01243.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.1068+66G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 8/22 | chr13 | 24691316 | |||||||
| chr13:24691357 | G | A | 20 | a0001c0008t0001g0036 a0001c0008t0001g0182 a0001c0008t0001g0228 others(17): Show |
28 | HG00140.hp1 HG00140.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1068+107G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 8/22 | chr13 | 24691357 | |||||||
| chr13:24691394 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1068+144T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 8/22 | chr13 | 24691394 | |||||||
| chr13:24691430 | T | G | 4 | a0001c0001t0004g0285 a0001c0003t0001g0252 a0001c0003t0004g0040 others(1): Show |
5 | HG02109.hp2 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1068+180T>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 8/22 | chr13 | 24691430 | |||||||
| chr13:24691481 | A | T | 2 | a0001c0002t0001g0121 a0001c0002t0001g0126 |
2 | HG02056.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.1068+231A>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 8/22 | chr13 | 24691481 | |||||||
| chr13:24691579 | G | T | 2 | a0001c0003t0005g0044 a0001c0003t0005g0085 |
2 | HG00099.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1068+329G>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 8/22 | chr13 | 24691579 | |||||||
| chr13:24691604 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1068+354G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 8/22 | chr13 | 24691604 | |||||||
| chr13:24691636 | C | G | 80 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(77): Show |
122 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1068+386C>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 8/22 | chr13 | 24691636 | |||||||
| chr13:24691637 | G | GA | 161 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0072 others(158): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.1068+398dupA | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 24691637 | ||||||
| chr13:24691668 | C | T | 80 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(77): Show |
122 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1068+418C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 8/22 | chr13 | 24691668 | |||||||
| chr13:24691766 | C | G | 80 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(77): Show |
122 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1068+516C>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 8/22 | chr13 | 24691766 | |||||||
| chr13:24691838 | G | A | 2 | a0001c0003t0005g0044 a0001c0003t0005g0085 |
2 | HG00099.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1068+588G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 8/22 | chr13 | 24691838 | |||||||
| chr13:24692029 | A | G | 84 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(81): Show |
127 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1069-400A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 8/22 | chr13 | 24692029 | |||||||
| chr13:24692111 | G | A | 3 | a0001c0001t0001g0161 a0005c0018t0005g0215 a0005c0018t0005g0216 |
3 | HG01109.hp2 HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1069-318G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 8/22 | chr13 | 24692111 | |||||||
| chr13:24692114 | G | A | 1 | a0001c0001t0001g0223 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1069-315G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 8/22 | chr13 | 24692114 | |||||||
| chr13:24692131 | C | T | 1 | a0001c0001t0004g0282 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1069-298C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 8/22 | chr13 | 24692131 | |||||||
| chr13:24692132 | G | A | 83 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(80): Show |
124 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1069-297G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 8/22 | chr13 | 24692132 | |||||||
| chr13:24692144 | C | T | 15 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0218 others(12): Show |
16 | HG00733.hp2 HG01433.hp2 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.1069-285C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 8/22 | chr13 | 24692144 | |||||||
| chr13:24692208 | A | G | 84 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(81): Show |
127 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1069-221A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 8/22 | chr13 | 24692208 | |||||||
| chr13:24692250 | C | T | 26 | a0001c0001t0004g0285 a0001c0003t0001g0135 a0001c0003t0001g0252 others(23): Show |
35 | HG00140.hp1 HG00140.hp2 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.1069-179C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 8/22 | chr13 | 24692250 | |||||||
| chr13:24692258 | G | A | 83 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(80): Show |
126 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1069-171G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 8/22 | chr13 | 24692258 | |||||||
| chr13:24692261 | G | A | 3 | a0001c0002t0001g0097 a0001c0002t0001g0098 a0001c0002t0001g0099 |
3 | NA18940.hp2 NA19006.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1069-168G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 8/22 | chr13 | 24692261 | |||||||
| chr13:24692261 | G | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0064 a0001c0001t0001g0065 others(2): Show |
6 | NA18940.hp1 NA18952.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.1069-168G>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 8/22 | chr13 | 24692261 | |||||||
| chr13:24692263 | A | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0064 a0001c0001t0001g0065 others(2): Show |
6 | NA18940.hp1 NA18952.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.1069-166A>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 8/22 | chr13 | 24692263 | |||||||
| chr13:24692264 | TA | T | 11 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0218 others(8): Show |
11 | HG00733.hp2 HG01433.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.1069-163delA | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 24692264 | ||||||
| chr13:24692288 | C | T | 1 | a0001c0002t0001g0119 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1069-141C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 8/22 | chr13 | 24692288 | |||||||
| chr13:24692748 | C | T | 81 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(78): Show |
123 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.1268-39C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 9/22 | chr13 | 24692748 | |||||||
| chr13:24692948 | T | C | 1 | a0002c0004t0003g0226 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1377+52T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 10/22 | chr13 | 24692948 | |||||||
| chr13:24692950 | C | T | 84 | a0001c0001t0001g0079 a0001c0002t0001g0001 a0001c0002t0001g0002 others(81): Show |
127 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1377+54C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 10/22 | chr13 | 24692950 | |||||||
| chr13:24693105 | T | C | 1 | a0002c0011t0003g0184 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1377+209T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 10/22 | chr13 | 24693105 | |||||||
| chr13:24693185 | A | G | 2 | a0007c0019t0001g0148 a0007c0024t0001g0206 |
2 | HG01981.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1377+289A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 10/22 | chr13 | 24693185 | |||||||
| chr13:24693397 | C | T | 87 | a0001c0001t0001g0079 a0001c0001t0001g0161 a0001c0002t0001g0001 others(84): Show |
130 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.1377+501C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 10/22 | chr13 | 24693397 | |||||||
| chr13:24693596 | T | C | 90 | a0001c0001t0001g0079 a0001c0001t0001g0128 a0001c0001t0001g0161 others(87): Show |
133 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1377+700T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 10/22 | chr13 | 24693596 | |||||||
| chr13:24693841 | A | C | 1 | a0001c0005t0001g0178 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1378-603A>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 10/22 | chr13 | 24693841 | |||||||
| chr13:24693842 | G | C | 1 | a0001c0005t0001g0178 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1378-602G>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 10/22 | chr13 | 24693842 | |||||||
| chr13:24693969 | T | G | 9 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0219 others(6): Show |
9 | HG00733.hp2 HG01433.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.1378-475T>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 10/22 | chr13 | 24693969 | |||||||
| chr13:24693976 | T | G | 14 | a0001c0003t0001g0212 a0001c0003t0002g0276 a0001c0003t0006g0009 others(11): Show |
18 | HG01175.hp2 HG01243.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1378-468T>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 10/22 | chr13 | 24693976 | |||||||
| chr13:24693988 | C | T | 87 | a0001c0001t0001g0079 a0001c0001t0001g0161 a0001c0002t0001g0001 others(84): Show |
130 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.1378-456C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 10/22 | chr13 | 24693988 | |||||||
| chr13:24693998 | C | T | 1 | a0001c0003t0006g0154 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1378-446C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 10/22 | chr13 | 24693998 | |||||||
| chr13:24694075 | C | A | 3 | a0001c0014t0001g0259 a0001c0014t0004g0274 a0002c0020t0010g0272 |
3 | HG03834.hp1 HG04115.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1378-369C>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 10/22 | chr13 | 24694075 | |||||||
| chr13:24694098 | G | C | 47 | a0001c0003t0001g0135 a0001c0003t0001g0212 a0001c0003t0001g0214 others(44): Show |
60 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1378-346G>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 10/22 | chr13 | 24694098 | |||||||
| chr13:24694127 | C | T | 1 | a0001c0003t0013g0269 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1378-317C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 10/22 | chr13 | 24694127 | |||||||
| chr13:24694230 | C | T | 4 | a0001c0006t0001g0024 a0001c0006t0001g0140 a0001c0006t0001g0141 others(1): Show |
5 | HG00735.hp1 HG00738.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1378-214C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 10/22 | chr13 | 24694230 | |||||||
| chr13:24694279 | G | A | 87 | a0001c0001t0001g0079 a0001c0001t0001g0161 a0001c0002t0001g0001 others(84): Show |
130 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.1378-165G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 10/22 | chr13 | 24694279 | |||||||
| chr13:24694307 | G | A | 85 | a0001c0001t0001g0079 a0001c0001t0001g0161 a0001c0002t0001g0001 others(82): Show |
128 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1378-137G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 10/22 | chr13 | 24694307 | |||||||
| chr13:24694375 | G | T | 3 | a0001c0014t0001g0259 a0001c0014t0004g0274 a0002c0020t0010g0272 |
3 | HG03834.hp1 HG04115.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1378-69G>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 10/22 | chr13 | 24694375 | |||||||
| chr13:24694598 | C | T | 2 | a0001c0010t0001g0136 a0001c0010t0001g0139 |
2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1512+20C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24694598 | |||||||
| chr13:24694614 | C | T | 1 | a0001c0003t0001g0135 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1512+36C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24694614 | |||||||
| chr13:24694638 | A | G | 87 | a0001c0001t0001g0079 a0001c0001t0001g0161 a0001c0002t0001g0001 others(84): Show |
130 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.1512+60A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24694638 | |||||||
| chr13:24694691 | C | T | 3 | a0001c0005t0009g0131 a0001c0005t0009g0132 a0001c0005t0009g0133 |
3 | HG02886.hp1 HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1512+113C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24694691 | |||||||
| chr13:24694710 | A | G | 172 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0079 others(169): Show |
237 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.1512+132A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24694710 | |||||||
| chr13:24694796 | T | C | 87 | a0001c0001t0001g0079 a0001c0001t0001g0161 a0001c0002t0001g0001 others(84): Show |
130 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.1512+218T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24694796 | |||||||
| chr13:24694859 | TCTCA | T | 11 | a0001c0002t0001g0102 a0001c0003t0001g0135 a0001c0003t0006g0155 others(8): Show |
11 | HG01243.hp2 HG01255.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1512+283_1512+286d others(6): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr13 | 24694859 | ||||||
| chr13:24694859 | TCTCACA | T | 161 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0079 others(158): Show |
226 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.1512+283_1512+288d others(8): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr13 | 24694859 | ||||||
| chr13:24694861 | T | TCA | 37 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0072 others(34): Show |
38 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1512+307_1512+308d others(4): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr13 | 24694861 | ||||||
| chr13:24694863 | A | T | 2 | a0001c0001t0004g0279 a0001c0001t0004g0280 |
2 | NA18959.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.1512+285A>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24694863 | |||||||
| chr13:24694944 | C | T | 87 | a0001c0001t0001g0079 a0001c0001t0001g0161 a0001c0002t0001g0001 others(84): Show |
130 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.1512+366C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24694944 | |||||||
| chr13:24694967 | G | C | 35 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0072 others(32): Show |
36 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.1512+389G>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24694967 | |||||||
| chr13:24695020 | G | A | 87 | a0001c0001t0001g0079 a0001c0001t0001g0161 a0001c0002t0001g0001 others(84): Show |
130 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.1512+442G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24695020 | |||||||
| chr13:24695027 | T | C | 207 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0069 others(204): Show |
273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.1512+449T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24695027 | |||||||
| chr13:24695045 | G | A | 1 | a0001c0002t0001g0244 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1512+467G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24695045 | |||||||
| chr13:24695045 | G | C | 85 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0219 others(82): Show |
107 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.1512+467G>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24695045 | |||||||
| chr13:24695055 | G | A | 87 | a0001c0001t0001g0079 a0001c0001t0001g0161 a0001c0002t0001g0001 others(84): Show |
130 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.1512+477G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24695055 | |||||||
| chr13:24695190 | G | A | 21 | a0001c0008t0001g0036 a0001c0008t0001g0182 a0001c0008t0001g0228 others(18): Show |
29 | HG00140.hp1 HG00140.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.1512+612G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24695190 | |||||||
| chr13:24695209 | G | A | 1 | a0001c0003t0001g0135 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1512+631G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24695209 | |||||||
| chr13:24695238 | G | A | 3 | a0001c0003t0016g0283 a0001c0007t0006g0026 a0001c0007t0006g0157 |
4 | HG01243.hp2 HG01884.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1512+660G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24695238 | |||||||
| chr13:24695269 | G | A | 85 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0219 others(82): Show |
107 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.1512+691G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24695269 | |||||||
| chr13:24695376 | C | A | 1 | a0001c0003t0004g0264 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1512+798C>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24695376 | |||||||
| chr13:24695436 | C | T | 2 | a0006c0017t0001g0209 a0006c0017t0001g0210 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1512+858C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24695436 | |||||||
| chr13:24695572 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | NA18944.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1512+994G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24695572 | |||||||
| chr13:24695600 | C | CT | 10 | a0001c0001t0001g0052 a0001c0001t0001g0063 a0001c0001t0001g0134 others(7): Show |
11 | HG00735.hp2 HG01169.hp2 HG03491.hp2 others(8): Show |
intron_variant | MODIFIER | c.1512+1046dupT | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr13 | 24695600 | ||||||
| chr13:24695600 | C | CTT | 28 | a0001c0001t0004g0205 a0001c0003t0001g0135 a0001c0003t0001g0212 others(25): Show |
36 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.1512+1045_1512+104 others(6): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr13 | 24695600 | ||||||
| chr13:24695600 | C | CTTT | 30 | a0001c0001t0004g0285 a0001c0003t0001g0214 a0001c0003t0002g0273 others(27): Show |
39 | HG00140.hp1 HG00140.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1512+1044_1512+104 others(7): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr13 | 24695600 | ||||||
| chr13:24695600 | CT | C | 45 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0072 others(42): Show |
50 | HG00099.hp1 HG00423.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.1512+1046delT | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr13 | 24695600 | ||||||
| chr13:24695600 | CTT | C | 9 | a0001c0002t0001g0095 a0001c0002t0001g0099 a0001c0002t0001g0122 others(6): Show |
9 | HG00558.hp1 HG02074.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1512+1045_1512+104 others(6): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr13 | 24695600 | ||||||
| chr13:24695600 | CTTT | C | 58 | a0001c0001t0001g0079 a0001c0001t0001g0161 a0001c0002t0001g0001 others(55): Show |
99 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.1512+1044_1512+104 others(7): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr13 | 24695600 | ||||||
| chr13:24695600 | CTTTT | C | 19 | a0001c0002t0001g0090 a0001c0002t0001g0103 a0001c0002t0001g0104 others(16): Show |
21 | HG00642.hp1 HG01070.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.1512+1043_1512+104 others(8): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr13 | 24695600 | ||||||
| chr13:24695717 | C | A | 27 | a0001c0001t0004g0285 a0001c0003t0001g0135 a0001c0003t0001g0252 others(24): Show |
36 | HG00140.hp1 HG00140.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.1512+1139C>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24695717 | |||||||
| chr13:24695731 | C | T | 9 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0219 others(6): Show |
9 | HG00733.hp2 HG01433.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.1512+1153C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24695731 | |||||||
| chr13:24696088 | G | A | 21 | a0001c0008t0001g0036 a0001c0008t0001g0182 a0001c0008t0001g0228 others(18): Show |
29 | HG00140.hp1 HG00140.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.1512+1510G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24696088 | |||||||
| chr13:24696224 | C | T | 21 | a0001c0008t0001g0036 a0001c0008t0001g0182 a0001c0008t0001g0228 others(18): Show |
29 | HG00140.hp1 HG00140.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.1512+1646C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24696224 | |||||||
| chr13:24696312 | A | T | 171 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0079 others(168): Show |
236 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.1512+1734A>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24696312 | |||||||
| chr13:24696408 | TAGAAAGG others(330): Show |
T | 6 | a0001c0001t0001g0161 a0001c0002t0001g0119 a0001c0003t0001g0252 others(3): Show |
7 | HG01109.hp2 HG02280.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1512+1847_1513-189 others(4): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr13 | 24696408 | ||||||
| chr13:24696421 | GGGGGGCC others(329): Show |
G | 107 | a0001c0001t0001g0079 a0001c0002t0001g0001 a0001c0002t0001g0002 others(104): Show |
158 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.1512+1848_1513-189 others(4): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr13 | 24696421 | ||||||
| chr13:24696429 | G | A | 9 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0219 others(6): Show |
9 | HG00733.hp2 HG01433.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.1512+1851G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24696429 | |||||||
| chr13:24696575 | G | A | 1 | a0001c0003t0002g0273 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1512+1997G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24696575 | |||||||
| chr13:24696605 | G | C | 1 | a0001c0003t0001g0163 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1512+2027G>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24696605 | |||||||
| chr13:24696685 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1513-1973G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24696685 | |||||||
| chr13:24696705 | C | T | 3 | a0001c0014t0001g0259 a0001c0014t0004g0274 a0002c0020t0010g0272 |
3 | HG03834.hp1 HG04115.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1513-1953C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24696705 | |||||||
| chr13:24696718 | C | CA | 53 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(50): Show |
64 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1513-1912dupA | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr13 | 24696718 | ||||||
| chr13:24696718 | C | CAA | 16 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0028 others(13): Show |
17 | HG00738.hp1 HG01109.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.1513-1913_1513-191 others(6): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr13 | 24696718 | ||||||
| chr13:24696718 | CAAAAAAA others(4): Show |
C | 1 | a0001c0003t0001g0061 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1513-1922_1513-191 others(15): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr13 | 24696718 | ||||||
| chr13:24696718 | CAAAAAAA others(5): Show |
C | 33 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0072 others(30): Show |
34 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1513-1923_1513-191 others(16): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr13 | 24696718 | ||||||
| chr13:24696718 | CAAAAAAA others(6): Show |
C | 12 | a0001c0003t0005g0048 a0001c0003t0006g0009 a0001c0003t0006g0010 others(9): Show |
16 | HG01175.hp2 HG01243.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1513-1924_1513-191 others(17): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr13 | 24696718 | ||||||
| chr13:24696728 | A | AAAG | 34 | a0001c0003t0001g0212 a0001c0003t0001g0214 a0001c0003t0002g0003 others(31): Show |
43 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.1513-1928_1513-192 others(7): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr13 | 24696728 | ||||||
| chr13:24696738 | A | G | 1 | a0011c0026t0001g0160 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1513-1920A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24696738 | |||||||
| chr13:24696761 | G | C | 107 | a0001c0001t0001g0079 a0001c0002t0001g0001 a0001c0002t0001g0002 others(104): Show |
158 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.1513-1897G>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24696761 | |||||||
| chr13:24696761 | G | GC | 64 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0161 others(61): Show |
78 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1513-1896dupC | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr13 | 24696761 | ||||||
| chr13:24697115 | C | G | 1 | a0001c0003t0001g0135 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1513-1543C>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24697115 | |||||||
| chr13:24697216 | T | C | 1 | a0001c0001t0001g0185 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1513-1442T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24697216 | |||||||
| chr13:24697296 | T | C | 171 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0079 others(168): Show |
236 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.1513-1362T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24697296 | |||||||
| chr13:24697300 | A | G | 2 | a0001c0002t0001g0121 a0001c0002t0001g0126 |
2 | HG02056.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.1513-1358A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24697300 | |||||||
| chr13:24697399 | C | T | 2 | a0001c0003t0006g0009 a0008c0013t0006g0009 |
3 | HG02257.hp2 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1513-1259C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24697399 | |||||||
| chr13:24697484 | A | C | 1 | a0001c0003t0002g0271 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1513-1174A>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24697484 | |||||||
| chr13:24697562 | C | A | 1 | a0001c0002t0001g0096 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1513-1096C>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24697562 | |||||||
| chr13:24697571 | T | G | 3 | a0001c0014t0001g0259 a0001c0014t0004g0274 a0002c0020t0010g0272 |
3 | HG03834.hp1 HG04115.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1513-1087T>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24697571 | |||||||
| chr13:24697617 | G | A | 1 | a0001c0003t0001g0135 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1513-1041G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24697617 | |||||||
| chr13:24697639 | C | CA | 46 | a0001c0001t0001g0028 a0001c0001t0001g0034 a0001c0001t0001g0053 others(43): Show |
52 | HG00558.hp2 HG00621.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.1513-1000dupA | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr13 | 24697639 | ||||||
| chr13:24697639 | CA | C | 35 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0072 others(32): Show |
36 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.1513-1000delA | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr13 | 24697639 | ||||||
| chr13:24697639 | CAA | C | 92 | a0001c0001t0001g0079 a0001c0001t0012g0078 a0001c0002t0001g0001 others(89): Show |
136 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1513-1001_1513-100 others(6): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr13 | 24697639 | ||||||
| chr13:24697639 | CAAAAA | C | 21 | a0001c0008t0001g0036 a0001c0008t0001g0182 a0001c0008t0001g0228 others(18): Show |
29 | HG00140.hp1 HG00140.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.1513-1004_1513-100 others(9): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr13 | 24697639 | ||||||
| chr13:24697658 | A | T | 5 | a0001c0003t0001g0135 a0001c0003t0001g0252 a0001c0003t0004g0040 others(2): Show |
6 | HG02055.hp1 HG02451.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1513-1000A>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24697658 | |||||||
| chr13:24697714 | G | GTGATAAT others(1): Show |
171 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0079 others(168): Show |
236 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.1513-944_1513-943i others(10): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24697714 | |||||||
| chr13:24697729 | C | T | 171 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0079 others(168): Show |
236 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.1513-929C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24697729 | |||||||
| chr13:24697755 | G | A | 1 | a0001c0003t0001g0135 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1513-903G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24697755 | |||||||
| chr13:24697758 | G | T | 1 | a0001c0002t0001g0116 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1513-900G>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24697758 | |||||||
| chr13:24697911 | A | G | 3 | a0001c0005t0009g0131 a0001c0005t0009g0132 a0001c0005t0009g0133 |
3 | HG02886.hp1 HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1513-747A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24697911 | |||||||
| chr13:24698117 | C | G | 22 | a0001c0002t0001g0107 a0001c0008t0001g0036 a0001c0008t0001g0182 others(19): Show |
30 | HG00140.hp1 HG00140.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.1513-541C>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24698117 | |||||||
| chr13:24698126 | C | T | 36 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0072 others(33): Show |
41 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1513-532C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24698126 | |||||||
| chr13:24698147 | A | T | 1 | a0012c0030t0001g0250 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1513-511A>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24698147 | |||||||
| chr13:24698203 | G | A | 2 | a0005c0018t0005g0215 a0005c0018t0005g0216 |
2 | HG01109.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1513-455G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24698203 | |||||||
| chr13:24698292 | C | T | 8 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0219 others(5): Show |
8 | HG00733.hp2 HG01433.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.1513-366C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24698292 | |||||||
| chr13:24698404 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1513-254C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24698404 | |||||||
| chr13:24698470 | G | C | 117 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0079 others(114): Show |
168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.1513-188G>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24698470 | |||||||
| chr13:24698594 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1513-64A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24698594 | |||||||
| chr13:24698619 | C | A | 2 | a0001c0005t0004g0043 a0001c0005t0004g0287 |
3 | HG01891.hp1 HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1513-39C>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24698619 | |||||||
| chr13:24698637 | G | C | 2 | a0001c0001t0001g0162 a0001c0001t0001g0172 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1513-21G>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 11/22 | chr13 | 24698637 | |||||||
| chr13:24698862 | G | A | 2 | a0001c0005t0004g0043 a0001c0005t0004g0287 |
3 | HG01891.hp1 HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1705+12G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24698862 | |||||||
| chr13:24698908 | G | A | 3 | a0001c0005t0009g0131 a0001c0005t0009g0132 a0001c0005t0009g0133 |
3 | HG02886.hp1 HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1705+58G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24698908 | |||||||
| chr13:24698950 | C | T | 23 | a0001c0003t0001g0061 a0001c0003t0001g0082 a0001c0003t0001g0163 others(20): Show |
24 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.1705+100C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24698950 | |||||||
| chr13:24698956 | G | T | 5 | a0001c0003t0002g0007 a0001c0003t0002g0276 a0001c0003t0002g0277 others(2): Show |
8 | HG00639.hp2 HG01243.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1705+106G>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24698956 | |||||||
| chr13:24698997 | G | C | 4 | a0001c0003t0001g0252 a0001c0003t0004g0040 a0001c0003t0004g0286 others(1): Show |
5 | HG02055.hp1 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1705+147G>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24698997 | |||||||
| chr13:24699002 | T | C | 82 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0219 others(79): Show |
97 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1705+152T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24699002 | |||||||
| chr13:24699019 | A | G | 83 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0219 others(80): Show |
98 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1705+169A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24699019 | |||||||
| chr13:24699179 | G | A | 1 | a0001c0003t0001g0135 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1705+329G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24699179 | |||||||
| chr13:24699204 | A | G | 3 | a0001c0014t0001g0259 a0001c0014t0004g0274 a0002c0020t0010g0272 |
3 | HG03834.hp1 HG04115.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1705+354A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24699204 | |||||||
| chr13:24699277 | T | C | 23 | a0001c0003t0001g0061 a0001c0003t0001g0082 a0001c0003t0001g0163 others(20): Show |
24 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.1705+427T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24699277 | |||||||
| chr13:24699299 | A | T | 9 | a0001c0003t0006g0009 a0001c0003t0006g0010 a0001c0003t0006g0025 others(6): Show |
13 | HG01175.hp2 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1705+449A>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24699299 | |||||||
| chr13:24699312 | T | C | 23 | a0001c0003t0001g0061 a0001c0003t0001g0082 a0001c0003t0001g0163 others(20): Show |
24 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.1705+462T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24699312 | |||||||
| chr13:24699356 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1705+506G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24699356 | |||||||
| chr13:24699419 | C | T | 4 | a0001c0003t0001g0252 a0001c0003t0004g0040 a0001c0003t0004g0286 others(1): Show |
5 | HG02055.hp1 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1705+569C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24699419 | |||||||
| chr13:24699489 | G | A | 4 | a0001c0003t0001g0252 a0001c0003t0004g0040 a0001c0003t0004g0286 others(1): Show |
5 | HG02055.hp1 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1705+639G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24699489 | |||||||
| chr13:24699548 | G | A | 1 | a0001c0003t0001g0135 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1705+698G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24699548 | |||||||
| chr13:24699565 | T | G | 1 | a0001c0002t0001g0019 | 2 | NA18967.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1705+715T>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24699565 | |||||||
| chr13:24699619 | C | T | 23 | a0001c0003t0001g0061 a0001c0003t0001g0082 a0001c0003t0001g0163 others(20): Show |
24 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.1705+769C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24699619 | |||||||
| chr13:24699697 | G | T | 1 | a0001c0002t0001g0106 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1705+847G>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24699697 | |||||||
| chr13:24699752 | G | A | 4 | a0001c0003t0001g0252 a0001c0003t0004g0040 a0001c0003t0004g0286 others(1): Show |
5 | HG02055.hp1 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1705+902G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24699752 | |||||||
| chr13:24699941 | A | T | 1 | a0001c0001t0001g0079 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1706-806A>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24699941 | |||||||
| chr13:24699980 | G | C | 3 | a0001c0014t0001g0259 a0001c0014t0004g0274 a0002c0020t0010g0272 |
3 | HG03834.hp1 HG04115.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1706-767G>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24699980 | |||||||
| chr13:24700035 | T | C | 74 | a0001c0003t0001g0061 a0001c0003t0001g0082 a0001c0003t0001g0135 others(71): Show |
89 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1706-712T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24700035 | |||||||
| chr13:24700037 | G | T | 35 | a0001c0002t0001g0001 a0001c0002t0001g0019 a0001c0002t0001g0039 others(32): Show |
57 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.1706-710G>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24700037 | |||||||
| chr13:24700112 | C | G | 1 | a0012c0030t0001g0250 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1706-635C>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24700112 | |||||||
| chr13:24700157 | C | G | 4 | a0001c0003t0001g0252 a0001c0003t0004g0040 a0001c0003t0004g0286 others(1): Show |
5 | HG02055.hp1 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1706-590C>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24700157 | |||||||
| chr13:24700193 | T | G | 1 | a0001c0003t0001g0135 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1706-554T>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24700193 | |||||||
| chr13:24700388 | A | G | 202 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0079 others(199): Show |
268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.1706-359A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24700388 | |||||||
| chr13:24700452 | T | C | 2 | a0001c0002t0001g0059 a0001c0002t0001g0116 |
2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1706-295T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24700452 | |||||||
| chr13:24700538 | G | C | 69 | a0001c0001t0001g0079 a0001c0002t0001g0001 a0001c0002t0001g0002 others(66): Show |
110 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.1706-209G>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24700538 | |||||||
| chr13:24700551 | A | G | 1 | a0001c0003t0013g0269 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1706-196A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24700551 | |||||||
| chr13:24700594 | T | C | 1 | a0001c0008t0001g0230 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1706-153T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 12/22 | chr13 | 24700594 | |||||||
| chr13:24700995 | C | A | 3 | a0001c0014t0001g0259 a0001c0014t0004g0274 a0002c0020t0010g0272 |
3 | HG03834.hp1 HG04115.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1881+73C>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 13/22 | chr13 | 24700995 | |||||||
| chr13:24701129 | A | C | 23 | a0001c0003t0001g0061 a0001c0003t0001g0082 a0001c0003t0001g0163 others(20): Show |
24 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.1881+207A>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 13/22 | chr13 | 24701129 | |||||||
| chr13:24701132 | G | A | 1 | a0001c0003t0005g0242 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1881+210G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 13/22 | chr13 | 24701132 | |||||||
| chr13:24701313 | A | C | 88 | a0001c0001t0001g0028 a0001c0001t0001g0079 a0001c0001t0001g0161 others(85): Show |
132 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1881+391A>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 13/22 | chr13 | 24701313 | |||||||
| chr13:24701328 | G | A | 1 | a0001c0010t0001g0139 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1881+406G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 13/22 | chr13 | 24701328 | |||||||
| chr13:24701394 | G | A | 3 | a0001c0001t0001g0164 a0001c0001t0001g0167 a0011c0026t0001g0160 |
3 | HG03017.hp1 HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1881+472G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 13/22 | chr13 | 24701394 | |||||||
| chr13:24701487 | G | C | 9 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0219 others(6): Show |
9 | HG00733.hp2 HG01433.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.1882-448G>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 13/22 | chr13 | 24701487 | |||||||
| chr13:24701501 | C | CA | 8 | a0001c0001t0001g0166 a0001c0001t0001g0168 a0001c0001t0001g0186 others(5): Show |
8 | HG01109.hp1 HG01884.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1882-415dupA | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 24701501 | ||||||
| chr13:24701501 | CA | C | 60 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0058 others(57): Show |
74 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.1882-415delA | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 24701501 | ||||||
| chr13:24701501 | CAA | C | 131 | a0001c0001t0001g0028 a0001c0001t0001g0079 a0001c0001t0001g0161 others(128): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.1882-416_1882-415d others(4): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 24701501 | ||||||
| chr13:24701517 | A | G | 10 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0219 others(7): Show |
11 | HG00733.hp2 HG01433.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.1882-418A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 13/22 | chr13 | 24701517 | |||||||
| chr13:24701669 | C | T | 23 | a0001c0003t0001g0061 a0001c0003t0001g0082 a0001c0003t0001g0163 others(20): Show |
24 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.1882-266C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 13/22 | chr13 | 24701669 | |||||||
| chr13:24701707 | G | T | 1 | a0001c0003t0005g0083 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1882-228G>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 13/22 | chr13 | 24701707 | |||||||
| chr13:24701799 | G | C | 11 | a0001c0003t0006g0009 a0001c0003t0006g0010 a0001c0003t0006g0025 others(8): Show |
15 | HG01175.hp2 HG01243.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1882-136G>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 13/22 | chr13 | 24701799 | |||||||
| chr13:24701840 | C | T | 23 | a0001c0003t0001g0061 a0001c0003t0001g0082 a0001c0003t0001g0163 others(20): Show |
24 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.1882-95C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 13/22 | chr13 | 24701840 | |||||||
| chr13:24701891 | G | A | 1 | a0001c0001t0001g0223 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1882-44G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 13/22 | chr13 | 24701891 | |||||||
| chr13:24702426 | C | T | 1 | a0001c0002t0001g0211 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2018+355C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24702426 | |||||||
| chr13:24702427 | G | A | 1 | a0001c0010t0001g0139 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2018+356G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24702427 | |||||||
| chr13:24702431 | G | A | 1 | a0001c0002t0001g0108 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2018+360G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24702431 | |||||||
| chr13:24702546 | T | C | 3 | a0001c0014t0001g0259 a0001c0014t0004g0274 a0002c0020t0010g0272 |
3 | HG03834.hp1 HG04115.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.2018+475T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24702546 | |||||||
| chr13:24702769 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2018+698C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24702769 | |||||||
| chr13:24702879 | T | G | 2 | a0001c0001t0001g0162 a0001c0001t0001g0172 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2018+808T>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24702879 | |||||||
| chr13:24702955 | G | A | 23 | a0001c0003t0001g0061 a0001c0003t0001g0082 a0001c0003t0001g0163 others(20): Show |
24 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.2018+884G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24702955 | |||||||
| chr13:24703073 | C | T | 23 | a0001c0003t0001g0061 a0001c0003t0001g0082 a0001c0003t0001g0163 others(20): Show |
24 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.2018+1002C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24703073 | |||||||
| chr13:24703181 | G | A | 1 | a0003c0015t0001g0117 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2018+1110G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24703181 | |||||||
| chr13:24703234 | T | TTTTG | 33 | a0001c0001t0001g0164 a0001c0001t0001g0167 a0001c0003t0001g0212 others(30): Show |
42 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.2018+1183_2018+118 others(8): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 24703234 | ||||||
| chr13:24703292 | T | G | 186 | a0001c0001t0001g0028 a0001c0001t0001g0034 a0001c0001t0001g0058 others(183): Show |
249 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.2018+1221T>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24703292 | |||||||
| chr13:24703352 | C | G | 9 | a0001c0003t0006g0009 a0001c0003t0006g0010 a0001c0003t0006g0025 others(6): Show |
13 | HG01175.hp2 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2018+1281C>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24703352 | |||||||
| chr13:24703374 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2018+1303C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24703374 | |||||||
| chr13:24703385 | G | A | 4 | a0001c0006t0001g0024 a0001c0006t0001g0140 a0001c0006t0001g0141 others(1): Show |
5 | HG00735.hp1 HG00738.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2018+1314G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24703385 | |||||||
| chr13:24703387 | C | T | 3 | a0004c0009t0001g0005 a0007c0019t0001g0148 a0007c0024t0001g0206 |
7 | HG00639.hp1 HG01123.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2018+1316C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24703387 | |||||||
| chr13:24703391 | C | T | 21 | a0001c0008t0001g0036 a0001c0008t0001g0182 a0001c0008t0001g0228 others(18): Show |
29 | HG00140.hp1 HG00140.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.2018+1320C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24703391 | |||||||
| chr13:24703416 | A | G | 1 | a0001c0002t0001g0115 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2018+1345A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24703416 | |||||||
| chr13:24703550 | A | T | 92 | a0001c0001t0001g0028 a0001c0001t0001g0079 a0001c0001t0001g0161 others(89): Show |
137 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.2018+1479A>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24703550 | |||||||
| chr13:24703620 | T | G | 1 | a0001c0002t0001g0109 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2018+1549T>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24703620 | |||||||
| chr13:24703657 | A | G | 46 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0164 others(43): Show |
55 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.2018+1586A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24703657 | |||||||
| chr13:24703750 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2018+1679C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24703750 | |||||||
| chr13:24703832 | CATTTTAG others(150): Show |
C | 23 | a0001c0003t0001g0061 a0001c0003t0001g0082 a0001c0003t0001g0163 others(20): Show |
24 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.2018+1872_2018+202 others(4): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 24703832 | ||||||
| chr13:24703843 | A | AT | 57 | a0001c0001t0001g0164 a0001c0001t0001g0167 a0001c0003t0001g0212 others(54): Show |
74 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.2018+1785dupT | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 24703843 | ||||||
| chr13:24704000 | A | AT | 38 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0167 others(35): Show |
47 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.2018+1942dupT | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 24704000 | ||||||
| chr13:24704088 | C | T | 1 | a0001c0005t0001g0100 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2018+2017C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24704088 | |||||||
| chr13:24704159 | G | A | 2 | a0001c0014t0001g0259 a0001c0014t0004g0274 |
2 | HG03834.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.2018+2088G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24704159 | |||||||
| chr13:24704186 | C | T | 11 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0219 others(8): Show |
11 | HG00733.hp2 HG01433.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.2018+2115C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24704186 | |||||||
| chr13:24704267 | A | G | 197 | a0001c0001t0001g0028 a0001c0001t0001g0034 a0001c0001t0001g0058 others(194): Show |
264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.2019-2046A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24704267 | |||||||
| chr13:24704292 | C | T | 1 | a0002c0011t0010g0288 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2019-2021C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24704292 | |||||||
| chr13:24704413 | T | G | 1 | a0001c0003t0001g0135 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2019-1900T>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24704413 | |||||||
| chr13:24704486 | C | G | 2 | a0001c0002t0001g0021 a0013c0029t0001g0021 |
2 | HG03669.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.2019-1827C>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24704486 | |||||||
| chr13:24704518 | C | A | 1 | a0001c0010t0001g0147 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2019-1795C>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24704518 | |||||||
| chr13:24704716 | G | A | 4 | a0002c0004t0003g0035 a0002c0004t0003g0226 a0002c0004t0003g0227 others(1): Show |
5 | HG01106.hp2 HG01256.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.2019-1597G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24704716 | |||||||
| chr13:24704740 | G | A | 1 | a0001c0002t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2019-1573G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24704740 | |||||||
| chr13:24704859 | A | G | 89 | a0001c0001t0001g0028 a0001c0001t0001g0079 a0001c0002t0001g0001 others(86): Show |
133 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.2019-1454A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24704859 | |||||||
| chr13:24704907 | C | T | 21 | a0001c0008t0001g0036 a0001c0008t0001g0182 a0001c0008t0001g0228 others(18): Show |
29 | HG00140.hp1 HG00140.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.2019-1406C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24704907 | |||||||
| chr13:24704998 | CT | C | 25 | a0001c0003t0001g0061 a0001c0003t0001g0082 a0001c0003t0001g0163 others(22): Show |
27 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.2019-1311delT | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 24704998 | ||||||
| chr13:24705246 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2019-1067C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24705246 | |||||||
| chr13:24705253 | C | T | 1 | a0001c0003t0002g0267 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2019-1060C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24705253 | |||||||
| chr13:24705254 | G | A | 1 | a0001c0002t0001g0125 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2019-1059G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24705254 | |||||||
| chr13:24705272 | A | G | 2 | a0001c0014t0001g0259 a0001c0014t0004g0274 |
2 | HG03834.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.2019-1041A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24705272 | |||||||
| chr13:24705630 | C | A | 3 | a0001c0008t0001g0233 a0002c0004t0003g0234 a0002c0004t0003g0235 |
3 | HG02738.hp2 HG03239.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2019-683C>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24705630 | |||||||
| chr13:24705757 | C | T | 1 | a0001c0003t0006g0153 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2019-556C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24705757 | |||||||
| chr13:24705845 | A | G | 23 | a0001c0003t0001g0061 a0001c0003t0001g0082 a0001c0003t0001g0163 others(20): Show |
24 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.2019-468A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24705845 | |||||||
| chr13:24705948 | C | T | 22 | a0001c0008t0001g0036 a0001c0008t0001g0182 a0001c0008t0001g0228 others(19): Show |
30 | HG00140.hp1 HG00140.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.2019-365C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24705948 | |||||||
| chr13:24705986 | T | C | 2 | a0001c0005t0004g0043 a0001c0005t0004g0287 |
3 | HG01891.hp1 HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2019-327T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24705986 | |||||||
| chr13:24706031 | G | T | 1 | a0001c0002t0001g0089 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2019-282G>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24706031 | |||||||
| chr13:24706164 | G | A | 1 | a0001c0003t0005g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2019-149G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 14/22 | chr13 | 24706164 | |||||||
| chr13:24706615 | C | T | 70 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(67): Show |
86 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.2169+152C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 15/22 | chr13 | 24706615 | |||||||
| chr13:24706622 | G | T | 2 | a0003c0012t0001g0137 a0003c0012t0001g0138 |
2 | HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2169+159G>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 15/22 | chr13 | 24706622 | |||||||
| chr13:24706624 | T | C | 3 | a0001c0001t0012g0078 a0001c0014t0001g0259 a0001c0014t0004g0274 |
3 | HG02165.hp2 HG03834.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.2169+161T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 15/22 | chr13 | 24706624 | |||||||
| chr13:24706707 | G | A | 9 | a0001c0005t0001g0016 a0001c0005t0001g0054 a0001c0005t0001g0055 others(6): Show |
10 | HG00642.hp1 HG01070.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.2169+244G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 15/22 | chr13 | 24706707 | |||||||
| chr13:24706740 | A | G | 3 | a0001c0001t0012g0078 a0001c0014t0001g0259 a0001c0014t0004g0274 |
3 | HG02165.hp2 HG03834.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.2169+277A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 15/22 | chr13 | 24706740 | |||||||
| chr13:24706830 | C | T | 2 | a0001c0005t0004g0043 a0001c0005t0004g0287 |
3 | HG01891.hp1 HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2170-193C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 15/22 | chr13 | 24706830 | |||||||
| chr13:24706978 | C | T | 22 | a0001c0003t0001g0061 a0001c0003t0001g0082 a0001c0003t0001g0163 others(19): Show |
23 | HG00099.hp1 HG00423.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.2170-45C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 15/22 | chr13 | 24706978 | |||||||
| chr13:24707239 | G | A | 3 | a0001c0003t0001g0252 a0001c0003t0004g0286 a0001c0010t0001g0147 |
3 | HG02055.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2339-40G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 16/22 | chr13 | 24707239 | |||||||
| chr13:24707713 | C | T | 96 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(93): Show |
114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.2493+280C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24707713 | |||||||
| chr13:24707851 | G | A | 2 | a0001c0014t0001g0259 a0001c0014t0004g0274 |
2 | HG03834.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.2493+418G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24707851 | |||||||
| chr13:24707899 | C | T | 1 | a0001c0003t0002g0273 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2493+466C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24707899 | |||||||
| chr13:24707964 | C | T | 2 | a0001c0014t0001g0259 a0001c0014t0004g0274 |
2 | HG03834.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.2493+531C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24707964 | |||||||
| chr13:24707985 | CA | C | 35 | a0001c0001t0001g0130 a0001c0001t0004g0282 a0001c0002t0001g0173 others(32): Show |
43 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.2493+564delA | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24707985 | ||||||
| chr13:24708006 | A | G | 22 | a0001c0008t0001g0182 a0001c0008t0001g0228 a0002c0004t0003g0006 others(19): Show |
29 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.2493+573A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708006 | |||||||
| chr13:24708026 | G | A | 1 | a0003c0016t0001g0181 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2493+593G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708026 | |||||||
| chr13:24708204 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2493+771A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708204 | |||||||
| chr13:24708272 | G | A | 1 | a0001c0010t0001g0136 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2493+839G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708272 | |||||||
| chr13:24708302 | G | A | 1 | a0001c0003t0001g0082 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2493+869G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708302 | |||||||
| chr13:24708554 | G | A | 1 | a0001c0002t0001g0088 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2494-810G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708554 | |||||||
| chr13:24708667 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2494-697G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708667 | |||||||
| chr13:24708681 | C | T | 26 | a0001c0001t0007g0029 a0001c0002t0001g0110 a0001c0002t0007g0114 others(23): Show |
36 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.2494-683C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708681 | |||||||
| chr13:24708686 | T | G | 1 | a0001c0001t0001g0069 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2494-678T>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708686 | |||||||
| chr13:24708708 | C | T | 2 | a0001c0002t0001g0121 a0001c0002t0001g0126 |
2 | HG02056.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.2494-656C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708708 | |||||||
| chr13:24708868 | A | AAGAGAAA others(3): Show |
1 | a0001c0010t0001g0136 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2494-484_2494-475d others(12): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708868 | ||||||
| chr13:24708868 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2494-496A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708868 | |||||||
| chr13:24708874 | AAG | A | 57 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0030 others(54): Show |
67 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.2494-482_2494-481d others(4): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708874 | ||||||
| chr13:24708878 | G | GAGAA | 6 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0004g0270 others(3): Show |
6 | HG03831.hp2 NA18952.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.2494-483_2494-482i others(6): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708878 | ||||||
| chr13:24708880 | G | GAAAGAGA others(1): Show |
3 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0067 |
4 | NA18940.hp1 NA18961.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.2494-483_2494-482i others(10): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708880 | ||||||
| chr13:24708880 | G | GAAAGAGA others(5): Show |
1 | a0001c0001t0001g0190 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2494-483_2494-482i others(14): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708880 | ||||||
| chr13:24708881 | A | AAAGAGAA others(6): Show |
1 | a0001c0001t0001g0064 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2494-483_2494-482i others(15): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708881 | |||||||
| chr13:24708884 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2494-480A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708884 | |||||||
| chr13:24708886 | G | GGAA | 4 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0067 others(1): Show |
5 | HG00741.hp2 NA18940.hp1 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.2494-478_2494-477i others(5): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708886 | |||||||
| chr13:24708886 | GAGAA | G | 11 | a0001c0003t0005g0048 a0001c0003t0005g0051 a0001c0003t0005g0220 others(8): Show |
12 | HG00140.hp1 HG01109.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.2494-467_2494-464d others(6): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708886 | ||||||
| chr13:24708886 | GAGAAAGA others(10): Show |
G | 1 | a0001c0021t0001g0176 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2494-463_2494-447d others(19): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708886 | ||||||
| chr13:24708887 | A | AAAG | 6 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0004g0270 others(3): Show |
6 | HG03831.hp2 NA18952.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.2494-477_2494-476i others(5): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708887 | |||||||
| chr13:24708888 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2494-476G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708888 | |||||||
| chr13:24708896 | GAAAGGAA others(1): Show |
G | 7 | a0002c0004t0003g0038 a0002c0004t0003g0227 a0002c0004t0003g0235 others(4): Show |
8 | HG00558.hp1 HG01081.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.2494-467_2494-460d others(10): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708896 | |||||||
| chr13:24708896 | GAAAGGAA others(5): Show |
G | 3 | a0002c0004t0003g0226 a0002c0004t0003g0232 a0002c0020t0010g0272 |
3 | HG01952.hp1 HG02683.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.2494-467_2494-456d others(14): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708896 | |||||||
| chr13:24708897 | A | G | 23 | a0001c0001t0005g0165 a0001c0002t0005g0112 a0001c0003t0005g0015 others(20): Show |
26 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.2494-467A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708897 | |||||||
| chr13:24708899 | AG | A | 3 | a0001c0001t0001g0221 a0001c0001t0004g0270 a0001c0001t0004g0281 |
3 | HG01517.hp1 HG03831.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.2494-463delG | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708899 | ||||||
| chr13:24708900 | G | A | 23 | a0001c0001t0005g0165 a0001c0002t0005g0112 a0001c0003t0005g0015 others(20): Show |
26 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.2494-464G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708900 | |||||||
| chr13:24708900 | G | GAAA | 11 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0064 others(8): Show |
14 | HG00741.hp2 HG02258.hp2 NA18940.hp1 others(11): Show |
intron_variant | MODIFIER | c.2494-464_2494-463i others(5): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708900 | |||||||
| chr13:24708900 | G | GAAAGAAA others(28): Show |
1 | a0001c0001t0001g0200 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2494-464_2494-463i others(37): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708900 | |||||||
| chr13:24708900 | G | GGAAA | 39 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0079 others(36): Show |
47 | HG00408.hp2 HG00597.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.2494-404_2494-401d others(6): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708900 | ||||||
| chr13:24708900 | G | GGAAAGAA others(1): Show |
12 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(9): Show |
13 | HG01891.hp2 HG02602.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.2494-408_2494-401d others(10): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708900 | ||||||
| chr13:24708900 | G | GGAAAGAA others(5): Show |
3 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0003t0001g0135 |
3 | HG02451.hp2 NA18969.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2494-412_2494-401d others(14): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708900 | ||||||
| chr13:24708900 | G | GGAAAGAA others(9): Show |
1 | a0001c0001t0001g0167 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2494-416_2494-401d others(18): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708900 | ||||||
| chr13:24708900 | GGAAA | G | 26 | a0001c0001t0001g0134 a0001c0001t0001g0195 a0001c0001t0008g0034 others(23): Show |
33 | HG00544.hp1 HG00733.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.2494-404_2494-401d others(6): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708900 | ||||||
| chr13:24708900 | GGAAAGAA others(1): Show |
G | 23 | a0001c0001t0001g0027 a0001c0001t0001g0069 a0001c0001t0001g0070 others(20): Show |
27 | HG00323.hp1 HG00438.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.2494-408_2494-401d others(10): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708900 | ||||||
| chr13:24708900 | GGAAAGAA others(5): Show |
G | 3 | a0001c0002t0001g0001 a0001c0002t0001g0095 a0008c0013t0006g0009 |
3 | HG03540.hp1 NA18961.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.2494-412_2494-401d others(14): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708900 | ||||||
| chr13:24708900 | GGAAAGAA others(9): Show |
G | 3 | a0001c0002t0001g0002 a0001c0005t0004g0043 a0001c0005t0004g0287 |
4 | HG01891.hp1 HG02145.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2494-416_2494-401d others(18): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708900 | ||||||
| chr13:24708900 | GGAAAGAA others(17): Show |
G | 1 | a0001c0003t0006g0025 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2494-424_2494-401d others(26): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708900 | ||||||
| chr13:24708908 | A | G | 1 | a0001c0021t0001g0176 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2494-456A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708908 | |||||||
| chr13:24708917 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2494-447G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708917 | |||||||
| chr13:24708918 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2494-446A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708918 | |||||||
| chr13:24708926 | A | G | 1 | a0001c0005t0009g0133 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2494-438A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708926 | |||||||
| chr13:24708930 | A | G | 1 | a0001c0005t0009g0133 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2494-434A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708930 | |||||||
| chr13:24708941 | G | GAAAGAAA others(7): Show |
1 | a0001c0001t0014g0284 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2494-421_2494-408d others(16): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708941 | ||||||
| chr13:24708942 | A | AAAGAAAG others(17): Show |
1 | a0001c0006t0001g0149 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2494-401_2494-400i others(26): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708942 | ||||||
| chr13:24708942 | A | AAAGAAAG others(5): Show |
1 | a0001c0010t0001g0136 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2494-411_2494-410i others(14): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708942 | ||||||
| chr13:24708942 | A | AAAGG | 4 | a0001c0001t0004g0282 a0001c0003t0001g0252 a0001c0003t0004g0286 others(1): Show |
4 | HG02451.hp1 HG03209.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2494-419_2494-418i others(6): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708942 | ||||||
| chr13:24708942 | A | G | 3 | a0001c0001t0001g0161 a0001c0001t0001g0166 a0001c0005t0009g0132 |
3 | HG03098.hp2 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2494-422A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708942 | |||||||
| chr13:24708946 | A | AAAGAAAG others(29): Show |
1 | a0001c0005t0001g0054 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2494-401_2494-400i others(38): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708946 | ||||||
| chr13:24708946 | A | AAAGAAAG others(17): Show |
4 | a0001c0001t0001g0030 a0001c0001t0001g0196 a0001c0001t0001g0203 others(1): Show |
5 | HG00738.hp1 HG01993.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.2494-401_2494-400i others(26): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708946 | ||||||
| chr13:24708946 | A | AAAGAAAG others(21): Show |
1 | a0001c0001t0001g0197 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2494-401_2494-400i others(30): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708946 | ||||||
| chr13:24708946 | A | AAAGAAAG others(13): Show |
8 | a0001c0001t0001g0031 a0001c0001t0001g0198 a0001c0001t0001g0201 others(5): Show |
9 | HG00099.hp2 HG00423.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.2494-401_2494-400i others(22): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708946 | ||||||
| chr13:24708946 | A | AAAGAAAG others(17): Show |
1 | a0001c0001t0004g0285 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2494-401_2494-400i others(26): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708946 | ||||||
| chr13:24708946 | A | AAAGAAAG others(21): Show |
1 | a0001c0005t0001g0055 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2494-401_2494-400i others(30): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708946 | ||||||
| chr13:24708946 | A | AAAGAAAG others(9): Show |
14 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0052 others(11): Show |
17 | HG00597.hp2 HG00621.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.2494-403_2494-402i others(18): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708946 | ||||||
| chr13:24708946 | A | AAAGAAAG others(13): Show |
6 | a0001c0001t0001g0073 a0001c0003t0001g0061 a0001c0003t0001g0163 others(3): Show |
7 | HG02572.hp1 HG02723.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.2494-403_2494-402i others(22): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708946 | ||||||
| chr13:24708946 | A | AAAGAAAG others(17): Show |
1 | a0001c0002t0001g0111 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2494-403_2494-402i others(26): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708946 | ||||||
| chr13:24708946 | A | AAAGAAAG others(5): Show |
8 | a0001c0001t0001g0013 a0001c0001t0001g0128 a0001c0002t0001g0124 others(5): Show |
10 | HG01074.hp1 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2494-407_2494-406i others(14): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708946 | ||||||
| chr13:24708946 | A | AAAGAAAG others(9): Show |
1 | a0001c0006t0001g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2494-407_2494-406i others(18): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708946 | ||||||
| chr13:24708946 | A | AAAGAAAG others(13): Show |
3 | a0001c0002t0001g0103 a0001c0005t0001g0016 a0001c0005t0001g0240 |
4 | HG00642.hp1 HG01168.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.2494-407_2494-406i others(22): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708946 | ||||||
| chr13:24708946 | A | AAAGAAAG others(1): Show |
10 | a0001c0001t0001g0075 a0001c0001t0001g0168 a0001c0001t0001g0193 others(7): Show |
11 | HG01433.hp1 HG01884.hp2 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.2494-411_2494-410i others(10): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708946 | ||||||
| chr13:24708946 | A | AAAGAAAG others(5): Show |
5 | a0001c0005t0001g0177 a0001c0006t0001g0024 a0001c0006t0001g0142 others(2): Show |
6 | HG00735.hp1 HG01255.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.2494-411_2494-410i others(14): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708946 | ||||||
| chr13:24708946 | A | AAAGAAAG others(9): Show |
2 | a0001c0005t0001g0056 a0001c0005t0001g0057 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2494-411_2494-410i others(18): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708946 | ||||||
| chr13:24708946 | A | AAAGG | 3 | a0001c0001t0001g0186 a0001c0001t0001g0188 a0001c0002t0001g0020 |
4 | HG00558.hp2 HG02559.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2494-415_2494-414i others(6): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708946 | ||||||
| chr13:24708946 | A | AAAGGAAG others(1): Show |
4 | a0001c0001t0001g0130 a0001c0003t0001g0082 a0001c0006t0001g0141 others(1): Show |
4 | HG00738.hp2 HG01496.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.2494-415_2494-414i others(10): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708946 | ||||||
| chr13:24708946 | A | G | 23 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0053 others(20): Show |
25 | HG00642.hp2 HG00733.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.2494-418A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708946 | |||||||
| chr13:24708948 | AGAAAGAA others(9): Show |
A | 5 | a0001c0001t0012g0078 a0001c0003t0002g0271 a0001c0003t0004g0258 others(2): Show |
5 | HG01069.hp1 HG01516.hp1 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.2494-409_2494-394d others(18): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708948 | ||||||
| chr13:24708950 | A | AAAGAAAG others(5): Show |
1 | a0001c0008t0001g0233 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2494-403_2494-402i others(14): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708950 | ||||||
| chr13:24708952 | AGAAAGAA others(5): Show |
A | 5 | a0001c0001t0012g0071 a0001c0003t0002g0042 a0001c0003t0002g0263 others(2): Show |
5 | HG00438.hp2 HG00609.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.2494-405_2494-394d others(14): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708952 | ||||||
| chr13:24708954 | A | AAAGAAAG others(17): Show |
1 | a0001c0005t0001g0178 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2494-401_2494-400i others(26): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708954 | ||||||
| chr13:24708956 | AGAAAGAA others(1): Show |
A | 13 | a0001c0001t0007g0029 a0001c0003t0002g0003 a0001c0003t0002g0007 others(10): Show |
14 | HG00621.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.2494-401_2494-394d others(10): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708956 | ||||||
| chr13:24708960 | AGAAG | A | 6 | a0001c0003t0002g0003 a0001c0003t0002g0007 a0001c0003t0002g0268 others(3): Show |
7 | HG02257.hp1 HG02615.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2494-400_2494-397d others(6): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708960 | ||||||
| chr13:24708961 | G | GA | 7 | a0001c0003t0005g0044 a0001c0003t0005g0046 a0001c0003t0005g0049 others(4): Show |
7 | HG02258.hp2 HG02602.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.2494-401dupA | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708961 | ||||||
| chr13:24708961 | G | GAAAGA | 3 | a0001c0002t0005g0112 a0001c0003t0005g0047 a0001c0003t0005g0242 |
3 | NA18612.hp2 NA18986.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2494-401_2494-400i others(7): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708961 | ||||||
| chr13:24708962 | AAGG | A | 13 | a0001c0001t0005g0165 a0001c0003t0005g0015 a0001c0003t0005g0045 others(10): Show |
14 | HG00099.hp1 HG00423.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2494-400_2494-398d others(5): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24708962 | ||||||
| chr13:24708964 | G | A | 134 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(131): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.2494-400G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708964 | |||||||
| chr13:24708965 | G | A | 10 | a0001c0002t0005g0112 a0001c0003t0005g0044 a0001c0003t0005g0046 others(7): Show |
10 | HG02258.hp2 HG02602.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.2494-399G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708965 | |||||||
| chr13:24708967 | A | G | 1 | a0001c0001t0014g0284 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2494-397A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24708967 | |||||||
| chr13:24709036 | TG | T | 16 | a0001c0002t0005g0112 a0001c0003t0005g0015 a0001c0003t0005g0044 others(13): Show |
17 | HG00099.hp1 HG00423.hp2 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.2494-324delG | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 24709036 | ||||||
| chr13:24709166 | A | G | 1 | a0001c0005t0009g0131 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2494-198A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24709166 | |||||||
| chr13:24709218 | G | A | 1 | a0001c0002t0001g0122 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2494-146G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24709218 | |||||||
| chr13:24709356 | C | T | 27 | a0001c0001t0007g0029 a0001c0001t0012g0071 a0001c0001t0012g0078 others(24): Show |
37 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(34): Show |
splice_region_variant&intron_variant | LOW | c.2494-8C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 17/22 | chr13 | 24709356 | |||||||
| chr13:24709518 | C | T | 1 | a0001c0003t0001g0163 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2617+31C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 18/22 | chr13 | 24709518 | |||||||
| chr13:24709519 | G | C | 118 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(115): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.2617+32G>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 18/22 | chr13 | 24709519 | |||||||
| chr13:24709521 | GGGCCTGC others(14): Show |
G | 1 | a0010c0025t0001g0060 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2617+37_2617+57del others(21): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr13 | 24709521 | ||||||
| chr13:24709606 | G | A | 65 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(62): Show |
75 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.2618-77G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 18/22 | chr13 | 24709606 | |||||||
| chr13:24709837 | C | T | 1 | a0001c0005t0001g0178 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2763+9C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 19/22 | chr13 | 24709837 | |||||||
| chr13:24710045 | C | T | 45 | a0001c0001t0005g0165 a0001c0001t0014g0284 a0001c0002t0005g0112 others(42): Show |
53 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.2763+217C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 19/22 | chr13 | 24710045 | |||||||
| chr13:24710126 | C | T | 1 | a0012c0030t0001g0250 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2763+298C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 19/22 | chr13 | 24710126 | |||||||
| chr13:24710147 | A | G | 45 | a0001c0001t0005g0165 a0001c0001t0014g0284 a0001c0002t0005g0112 others(42): Show |
53 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.2764-313A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 19/22 | chr13 | 24710147 | |||||||
| chr13:24710194 | C | T | 1 | a0001c0003t0001g0212 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2764-266C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 19/22 | chr13 | 24710194 | |||||||
| chr13:24710198 | A | G | 2 | a0001c0001t0012g0071 a0001c0001t0012g0078 |
2 | HG00609.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.2764-262A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 19/22 | chr13 | 24710198 | |||||||
| chr13:24710269 | A | T | 57 | a0001c0001t0001g0012 a0001c0001t0001g0052 a0001c0001t0001g0130 others(54): Show |
70 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.2764-191A>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 19/22 | chr13 | 24710269 | |||||||
| chr13:24710398 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2764-62T>C | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 19/22 | chr13 | 24710398 | |||||||
| chr13:24710441 | C | T | 1 | a0001c0003t0001g0212 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2764-19C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 19/22 | chr13 | 24710441 | |||||||
| chr13:24710605 | G | T | 1 | a0001c0003t0016g0283 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2897+12G>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 20/22 | chr13 | 24710605 | |||||||
| chr13:24710637 | G | A | 1 | a0001c0001t0014g0284 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2897+44G>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 20/22 | chr13 | 24710637 | |||||||
| chr13:24710762 | C | CAAGTCTG others(4): Show |
1 | a0001c0001t0001g0193 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2898-29_2898-19dup others(11): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 24710762 | ||||||
| chr13:24711090 | C | T | 1 | a0001c0002t0001g0113 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2999+197C>T | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 21/22 | chr13 | 24711090 | |||||||
| chr13:24711223 | C | A | 87 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0027 others(84): Show |
133 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.3000-95C>A | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 21/22 | chr13 | 24711223 | |||||||
| chr13:24711421 | A | G | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0196 others(3): Show |
8 | HG00423.hp1 HG01261.hp2 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.3091+12A>G | ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 22/22 | chr13 | 24711421 |