Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 490 |
| ensemblid | ENSG00000070961.17 |
| hgncid | 814 |
| symbol | ATP2B1 |
| name | ATPase plasma membrane Ca2+ transporting 1 |
| refseq_nuc | NM_001366521.1 |
| refseq_prot | NP_001353450.1 |
| ensembl_nuc | ENST00000428670.8 |
| ensembl_prot | ENSP00000392043.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 89588049 |
| end | 89708838 |
| strand | - |
| ver | v1.2 |
| region | chr12:89588049-89708838 |
| region5000 | chr12:89583049-89713838 |
| regionname0 | ATP2B1_chr12_89588049_89708838 |
| regionname5000 | ATP2B1_chr12_89583049_89713838 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1220 | 329 | 86 | 59 | 128 | 14 | 40 | 92 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | MGDMA others(1215): Show |
chr12 | 89583049 | 89713838 |
| a0002 | 0/0 | 1220 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | MGDMA others(1215): Show |
chr12 | 89583049 | 89713838 |
| a0003 | 0/0 | 1220 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | MGDMA others(1215): Show |
chr12 | 89583049 | 89713838 |
| a0004 | 0/0 | 1220 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | MGDMA others(1215): Show |
chr12 | 89583049 | 89713838 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3660 | 285 | 65 | 44 | 126 | 13 | 36 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | ATGGG others(3655): Show |
chr12 | 89583049 | 89713838 | ||
| a0001c0002 | 0/1 | 3660 | 26 | 8 | 11 | 1 | 1 | 4 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | ATGGG others(3655): Show |
chr12 | 89583049 | 89713838 | ||
| a0001c0003 | 0/0 | 3660 | 5 | 4 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | ATGGG others(3655): Show |
chr12 | 89583049 | 89713838 | ||
| a0001c0004 | 0/0 | 3660 | 5 | 4 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | ATGGG others(3655): Show |
chr12 | 89583049 | 89713838 | ||
| a0001c0005 | 0/0 | 3660 | 3 | 1 | 2 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | ATGGG others(3655): Show |
chr12 | 89583049 | 89713838 | ||
| a0001c0006 | 0/0 | 3660 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | ATGGG others(3655): Show |
chr12 | 89583049 | 89713838 | ||
| a0001c0007 | 0/0 | 3660 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | ATGGG others(3655): Show |
chr12 | 89583049 | 89713838 | ||
| a0001c0009 | 0/0 | 3660 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | ATGGG others(3655): Show |
chr12 | 89583049 | 89713838 | ||
| a0002c0011 | 0/0 | 3660 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | ATGGG others(3655): Show |
chr12 | 89583049 | 89713838 | ||
| a0003c0010 | 0/0 | 3660 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | ATGGG others(3655): Show |
chr12 | 89583049 | 89713838 | ||
| a0004c0008 | 0/0 | 3660 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | ATGGG others(3655): Show |
chr12 | 89583049 | 89713838 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7062 | 216 | 32 | 36 | 106 | 12 | 30 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7057): Show |
chr12 | 89583049 | 89713838 |
| a0001c0001t0002 | 0/0 | 7062 | 18 | 2 | 3 | 11 | 0 | 2 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7057): Show |
chr12 | 89583049 | 89713838 |
| a0001c0001t0003 | 1/0 | 7062 | 9 | 8 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7057): Show |
chr12 | 89583049 | 89713838 |
| a0001c0001t0004 | 0/0 | 7061 | 9 | 8 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7056): Show |
chr12 | 89583049 | 89713838 |
| a0001c0001t0005 | 0/0 | 7062 | 9 | 9 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7057): Show |
chr12 | 89583049 | 89713838 |
| a0001c0001t0006 | 0/0 | 7061 | 5 | 0 | 1 | 3 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7056): Show |
chr12 | 89583049 | 89713838 |
| a0001c0001t0007 | 0/0 | 7061 | 3 | 3 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7056): Show |
chr12 | 89583049 | 89713838 |
| a0001c0001t0008 | 0/0 | 7062 | 3 | 0 | 0 | 2 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7057): Show |
chr12 | 89583049 | 89713838 |
| a0001c0001t0009 | 0/0 | 7062 | 2 | 0 | 1 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7057): Show |
chr12 | 89583049 | 89713838 |
| a0001c0001t0011 | 0/0 | 7062 | 2 | 0 | 0 | 1 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7057): Show |
chr12 | 89583049 | 89713838 |
| a0001c0001t0013 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7057): Show |
chr12 | 89583049 | 89713838 |
| a0001c0001t0014 | 0/0 | 7062 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7057): Show |
chr12 | 89583049 | 89713838 |
| a0001c0001t0016 | 0/0 | 7062 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7057): Show |
chr12 | 89583049 | 89713838 |
| a0001c0001t0017 | 0/0 | 7062 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7057): Show |
chr12 | 89583049 | 89713838 |
| a0001c0001t0018 | 0/0 | 7062 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7057): Show |
chr12 | 89583049 | 89713838 |
| a0001c0001t0019 | 0/0 | 7062 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7057): Show |
chr12 | 89583049 | 89713838 |
| a0001c0001t0020 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7057): Show |
chr12 | 89583049 | 89713838 |
| a0001c0001t0022 | 0/0 | 7062 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7057): Show |
chr12 | 89583049 | 89713838 |
| a0001c0001t0023 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7057): Show |
chr12 | 89583049 | 89713838 |
| a0001c0002t0001 | 0/1 | 7062 | 22 | 6 | 11 | 0 | 0 | 4 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7057): Show |
chr12 | 89583049 | 89713838 |
| a0001c0002t0003 | 0/0 | 7062 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7057): Show |
chr12 | 89583049 | 89713838 |
| a0001c0002t0012 | 0/0 | 7061 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7056): Show |
chr12 | 89583049 | 89713838 |
| a0001c0002t0015 | 0/0 | 7062 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7057): Show |
chr12 | 89583049 | 89713838 |
| a0001c0003t0001 | 0/0 | 7062 | 4 | 3 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7057): Show |
chr12 | 89583049 | 89713838 |
| a0001c0003t0021 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7057): Show |
chr12 | 89583049 | 89713838 |
| a0001c0004t0001 | 0/0 | 7062 | 5 | 4 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7057): Show |
chr12 | 89583049 | 89713838 |
| a0001c0005t0001 | 0/0 | 7062 | 3 | 1 | 2 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7057): Show |
chr12 | 89583049 | 89713838 |
| a0001c0006t0001 | 0/0 | 7062 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7057): Show |
chr12 | 89583049 | 89713838 |
| a0001c0007t0010 | 0/0 | 7062 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7057): Show |
chr12 | 89583049 | 89713838 |
| a0001c0009t0001 | 0/0 | 7062 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7057): Show |
chr12 | 89583049 | 89713838 |
| a0002c0011t0001 | 0/0 | 7062 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7057): Show |
chr12 | 89583049 | 89713838 |
| a0003c0010t0001 | 0/0 | 7062 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7057): Show |
chr12 | 89583049 | 89713838 |
| a0004c0008t0001 | 0/0 | 7062 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | GCAGT others(7057): Show |
chr12 | 89583049 | 89713838 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0003g0016 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0004g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0005g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0005g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0005g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0005g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0005g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0005g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0005g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0006g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0006g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0006g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0006g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0006g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0007g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0007g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0008g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0008g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0008g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0009g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0009g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0011g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0011g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0013g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0014g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0016g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0017g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0018g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0019g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0020g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0022g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0023g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0002t0001g0038 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0002t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0002t0012g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0002t0015g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0003t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0003t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0003t0021g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0004t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0004t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0004t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0004t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0004t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0005t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0005t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0005t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0006t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0006t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0007t0010g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0007t0010g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0009t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0002c0011t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0003c0010t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0004c0008t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | GBR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0286 | EUR | GBR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0289 | EUR | GBR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0240 | EUR | GBR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0238 | EUR | FIN | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00544 | hp2 | a0001 | c0001 | t0019 | g0197 | EAS | CHS | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00597 | hp1 | a0001 | c0001 | t0018 | g0182 | EAS | CHS | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0111 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00735 | hp1 | a0001 | c0001 | t0016 | g0274 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00735 | hp2 | a0001 | c0001 | t0009 | g0013 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0043 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00738 | hp2 | a0001 | c0001 | t0014 | g0014 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00741 | hp2 | a0001 | c0001 | t0006 | g0142 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0041 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0044 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0328 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0045 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0046 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0112 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01167 | hp1 | a0001 | c0004 | t0001 | g0031 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0223 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0229 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0054 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0020 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0055 | AMR | CLM | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01257 | hp2 | a0001 | c0005 | t0001 | g0101 | AMR | CLM | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01261 | hp1 | a0002 | c0011 | t0001 | g0228 | AMR | CLM | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0137 | AMR | CLM | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0290 | EUR | IBS | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01515 | hp2 | a0001 | c0001 | t0009 | g0012 | EUR | IBS | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0250 | EUR | IBS | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01884 | hp1 | a0001 | c0003 | t0001 | g0050 | AFR | ACB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01884 | hp2 | a0001 | c0002 | t0012 | g0002 | AFR | ACB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PEL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PEL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | KHV | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | KHV | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02074 | hp2 | a0001 | c0001 | t0006 | g0217 | EAS | KHV | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02080 | hp2 | a0001 | c0001 | t0017 | g0302 | EAS | KHV | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0047 | AFR | ACB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CDX | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CDX | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0321 | AFR | ACB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | ACB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0323 | AFR | ACB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PEL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PEL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02300 | hp2 | a0001 | c0005 | t0001 | g0084 | AMR | PEL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | ACB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02451 | hp2 | a0001 | c0005 | t0001 | g0083 | AFR | ACB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | KHV | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0117 | AFR | GWD | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0134 | SAS | PJL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0021 | AFR | GWD | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0325 | AFR | GWD | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0113 | AFR | GWD | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02647 | hp1 | a0001 | c0004 | t0001 | g0030 | AFR | GWD | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0116 | AFR | GWD | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0026 | AFR | GWD | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0326 | AFR | GWD | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02723 | hp1 | a0001 | c0006 | t0001 | g0032 | AFR | GWD | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0276 | SAS | PJL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02809 | hp2 | a0001 | c0001 | t0013 | g0003 | AFR | GWD | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | GWD | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02922 | hp1 | a0001 | c0003 | t0021 | g0049 | AFR | ESN | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | ESN | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | ESN | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0322 | AFR | ESN | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0110 | AFR | ESN | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03017 | hp1 | a0001 | c0001 | t0006 | g0246 | SAS | PJL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0118 | AFR | GWD | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03098 | hp1 | a0001 | c0007 | t0010 | g0232 | AFR | MSL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | MSL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | ESN | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03139 | hp2 | a0001 | c0002 | t0012 | g0002 | AFR | ESN | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ESN | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03209 | hp1 | a0001 | c0004 | t0001 | g0035 | AFR | MSL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03209 | hp2 | a0001 | c0007 | t0010 | g0135 | AFR | MSL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | MSL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0051 | AFR | MSL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0324 | AFR | MSL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | MSL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | MSL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | MSL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0243 | SAS | PJL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03516 | hp2 | a0001 | c0004 | t0001 | g0119 | AFR | ESN | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0115 | AFR | GWD | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | STU | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | STU | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03704 | hp2 | a0001 | c0001 | t0011 | g0125 | SAS | PJL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | BEB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03831 | hp2 | a0001 | c0001 | t0008 | g0212 | SAS | BEB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | BEB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0040 | SAS | BEB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | BEB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | BEB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0039 | SAS | STU | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | STU | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | STU | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0136 | SAS | STU | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | STU | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | STU | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18522 | hp1 | a0001 | c0006 | t0001 | g0033 | AFR | YRI | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | YRI | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | CHB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | YRI | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18943 | hp1 | a0001 | c0001 | t0006 | g0282 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18981 | hp2 | a0001 | c0001 | t0011 | g0190 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18986 | hp1 | a0001 | c0009 | t0001 | g0220 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18998 | hp2 | a0003 | c0010 | t0001 | g0306 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19003 | hp2 | a0001 | c0002 | t0015 | g0042 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19010 | hp2 | a0004 | c0008 | t0001 | g0208 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19030 | hp1 | a0001 | c0001 | t0007 | g0022 | AFR | LWK | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0052 | AFR | LWK | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19066 | hp1 | a0001 | c0001 | t0008 | g0210 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19075 | hp1 | a0001 | c0001 | t0006 | g0056 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19075 | hp2 | a0001 | c0001 | t0008 | g0161 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | YRI | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | YRI | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0319 | AFR | ASW | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0114 | AFR | ASW | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0242 | EUR | TSI | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0157 | EUR | TSI | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA20805 | hp1 | a0001 | c0002 | t0003 | g0025 | EUR | TSI | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0236 | EUR | TSI | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA20905 | hp1 | a0001 | c0001 | t0022 | g0239 | SAS | GIH | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | GIH | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02109 | hp2 | a0001 | c0004 | t0001 | g0034 | AFR | ACB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02559 | hp1 | a0001 | c0001 | t0020 | g0048 | AFR | ACB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0023 | AFR | ACB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG06807 | hp1 | a0001 | c0001 | t0023 | g0329 | AFR | USA | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | USA | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | USA | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | USA | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | LWK | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0038 | REF | REF | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0016 | REF | REF | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:89603241 | A | T | 1 | a0003 | 1 | NA18998.hp2 | missense_variant | MODERATE | c.2862T>A | p.Phe954Leu | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 18/21 | 3326/7062 | 2862/3663 | 954/1220 | chr12 | 89603241 | |||
| chr12:89655798 | G | A | 1 | a0002 | 1 | HG01261.hp1 | missense_variant | MODERATE | c.89C>T | p.Thr30Met | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/21 | 553/7062 | 89/3663 | 30/1220 | chr12 | 89655798 | |||
| chr12:89655807 | A | T | 1 | a0004 | 1 | NA19010.hp2 | missense_variant | MODERATE | c.80T>A | p.Phe27Tyr | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/21 | 544/7062 | 80/3663 | 27/1220 | chr12 | 89655807 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:89591227 | C | A | 1 | a0001c0004 | 5 | HG01167.hp1 HG02109.hp2 HG02647.hp1 others(2): Show |
synonymous_variant | LOW | c.3420G>T | p.Ser1140Ser | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 21/21 | 3884/7062 | 3420/3663 | 1140/1220 | chr12 | 89591227 | |||
| chr12:89604242 | A | G | 1 | a0001c0005 | 3 | HG01257.hp2 HG02300.hp2 HG02451.hp2 |
synonymous_variant | LOW | c.2547T>C | p.Tyr849Tyr | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 16/21 | 3011/7062 | 2547/3663 | 849/1220 | chr12 | 89604242 | |||
| chr12:89616817 | A | G | 2 | a0001c0006 a0001c0007 |
4 | HG02723.hp1 HG03098.hp1 HG03209.hp2 others(1): Show |
synonymous_variant | LOW | c.2052T>C | p.Asp684Asp | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/21 | 2516/7062 | 2052/3663 | 684/1220 | chr12 | 89616817 | |||
| chr12:89620168 | A | G | 1 | a0001c0009 | 1 | NA18986.hp1 | synonymous_variant | LOW | c.1660T>C | p.Leu554Leu | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 11/21 | 2124/7062 | 1660/3663 | 554/1220 | chr12 | 89620168 | |||
| chr12:89626608 | G | T | 1 | a0001c0003 | 5 | HG01192.hp1 HG01884.hp1 HG02922.hp1 others(2): Show |
synonymous_variant | LOW | c.975C>A | p.Ala325Ala | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 8/21 | 1439/7062 | 975/3663 | 325/1220 | chr12 | 89626608 | |||
| chr12:89635124 | T | C | 3 | a0001c0002 a0001c0007 a0002c0011 |
28 | HG00639.hp1 HG00738.hp1 HG01070.hp1 others(25): Show |
synonymous_variant | LOW | c.534A>G | p.Glu178Glu | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 4/21 | 998/7062 | 534/3663 | 178/1220 | chr12 | 89635124 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:89588156 | T | C | 1 | a0001c0001t0016 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2828A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 21/21 | 2828 | chr12 | 89588156 | ||||||
| chr12:89588189 | T | G | 1 | a0001c0001t0017 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2795A>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 21/21 | 2795 | chr12 | 89588189 | ||||||
| chr12:89588267 | C | A | 1 | a0001c0001t0018 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2717G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 21/21 | 2717 | chr12 | 89588267 | ||||||
| chr12:89588634 | T | A | 1 | a0001c0001t0005 | 9 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2350A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 21/21 | 2350 | chr12 | 89588634 | ||||||
| chr12:89589333 | A | G | 1 | a0001c0001t0009 | 2 | HG00735.hp2 HG01515.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1651T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 21/21 | 1651 | chr12 | 89589333 | ||||||
| chr12:89589365 | T | A | 1 | a0001c0001t0002 | 18 | HG01243.hp2 HG01943.hp2 HG02027.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1619A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 21/21 | 1619 | chr12 | 89589365 | ||||||
| chr12:89589399 | T | C | 1 | a0001c0002t0012 | 2 | HG01884.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1585A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 21/21 | 1585 | chr12 | 89589399 | ||||||
| chr12:89589538 | G | A | 1 | a0001c0001t0019 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1446C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 21/21 | 1446 | chr12 | 89589538 | ||||||
| chr12:89589606 | T | C | 1 | a0001c0001t0014 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1378A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 21/21 | 1378 | chr12 | 89589606 | ||||||
| chr12:89589845 | A | G | 1 | a0001c0002t0015 | 1 | NA19003.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1139T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 21/21 | 1139 | chr12 | 89589845 | ||||||
| chr12:89590118 | A | G | 1 | a0001c0001t0007 | 3 | HG02622.hp1 HG02717.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*866T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 21/21 | 866 | chr12 | 89590118 | ||||||
| chr12:89590416 | CT | C | 4 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(1): Show |
19 | HG00741.hp2 HG01243.hp1 HG01884.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*567delA | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 21/21 | 567 | chr12 | 89590416 | ||||||
| chr12:89590443 | C | A | 1 | a0001c0001t0020 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*541G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 21/21 | 541 | chr12 | 89590443 | ||||||
| chr12:89590483 | G | C | 1 | a0001c0003t0021 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*501C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 21/21 | 501 | chr12 | 89590483 | ||||||
| chr12:89590790 | C | T | 1 | a0001c0001t0011 | 2 | HG03704.hp2 NA18981.hp2 |
3_prime_UTR_variant | MODIFIER | c.*194G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 21/21 | 194 | chr12 | 89590790 | ||||||
| chr12:89590836 | T | A | 1 | a0001c0001t0008 | 3 | HG03831.hp2 NA19066.hp1 NA19075.hp2 |
3_prime_UTR_variant | MODIFIER | c.*148A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 21/21 | 148 | chr12 | 89590836 | ||||||
| chr12:89590953 | T | C | 1 | a0001c0001t0022 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*31A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 21/21 | 31 | chr12 | 89590953 | ||||||
| chr12:89656047 | G | T | 1 | a0001c0007t0010 | 2 | HG03098.hp1 HG03209.hp2 |
5_prime_UTR_variant | MODIFIER | c.-161C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/21 | 161 | chr12 | 89656047 | ||||||
| chr12:89708626 | G | A | 1 | a0001c0001t0023 | 1 | HG06807.hp1 | 5_prime_UTR_variant | MODIFIER | c.-252C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/21 | 52740 | chr12 | 89708626 | ||||||
| chr12:89708664 | T | G | 27 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(24): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
5_prime_UTR_variant | MODIFIER | c.-290A>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/21 | 52778 | chr12 | 89708664 | ||||||
| chr12:89708770 | G | T | 1 | a0001c0001t0013 | 1 | HG02809.hp2 | 5_prime_UTR_variant | MODIFIER | c.-396C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/21 | 52884 | chr12 | 89708770 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:89591473 | C | T | 1 | a0001c0001t0005g0117 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3352-178G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89591473 | |||||||
| chr12:89591515 | AAAGT | A | 65 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0066 others(62): Show |
65 | HG00099.hp1 HG00642.hp1 HG01167.hp1 others(62): Show |
intron_variant | MODIFIER | c.3352-224_3352-221d others(6): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89591515 | |||||||
| chr12:89591685 | A | G | 1 | a0001c0007t0010g0232 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3352-390T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89591685 | |||||||
| chr12:89591750 | A | C | 1 | a0001c0001t0005g0324 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3352-455T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89591750 | |||||||
| chr12:89591898 | T | C | 1 | a0001c0001t0003g0015 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3352-603A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89591898 | |||||||
| chr12:89592011 | A | G | 1 | a0001c0001t0002g0243 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.3352-716T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89592011 | |||||||
| chr12:89592230 | A | T | 1 | a0001c0001t0001g0126 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3352-935T>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89592230 | |||||||
| chr12:89592387 | C | T | 4 | a0001c0003t0001g0050 a0001c0003t0001g0051 a0001c0003t0001g0054 others(1): Show |
4 | HG01192.hp1 HG01884.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.3352-1092G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89592387 | |||||||
| chr12:89592440 | A | C | 1 | a0001c0001t0001g0308 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3352-1145T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89592440 | |||||||
| chr12:89592559 | C | T | 23 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(20): Show |
23 | HG00423.hp2 HG01070.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.3352-1264G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89592559 | |||||||
| chr12:89592676 | A | C | 5 | a0001c0003t0001g0050 a0001c0003t0001g0051 a0001c0003t0001g0052 others(2): Show |
5 | HG01192.hp1 HG01884.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.3352-1381T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89592676 | |||||||
| chr12:89592746 | T | C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0180 a0001c0001t0001g0278 others(18): Show |
23 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.3352-1451A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89592746 | |||||||
| chr12:89593013 | G | T | 1 | a0001c0001t0001g0291 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.3352-1718C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89593013 | |||||||
| chr12:89593080 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3352-1785A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89593080 | |||||||
| chr12:89593107 | A | G | 2 | a0001c0001t0005g0116 a0001c0001t0005g0117 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.3352-1812T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89593107 | |||||||
| chr12:89593470 | G | A | 1 | a0001c0001t0003g0006 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3352-2175C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89593470 | |||||||
| chr12:89593568 | G | A | 1 | a0001c0002t0012g0002 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3352-2273C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89593568 | |||||||
| chr12:89593794 | A | G | 28 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(25): Show |
30 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(27): Show |
intron_variant | MODIFIER | c.3352-2499T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89593794 | |||||||
| chr12:89593951 | A | T | 4 | a0001c0002t0001g0110 a0001c0002t0001g0111 a0001c0002t0001g0112 others(1): Show |
4 | HG00639.hp1 HG01109.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.3352-2656T>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89593951 | |||||||
| chr12:89593988 | A | G | 1 | a0001c0002t0003g0025 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3352-2693T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89593988 | |||||||
| chr12:89594064 | T | A | 312 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.3352-2769A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89594064 | |||||||
| chr12:89594261 | C | T | 1 | a0001c0001t0003g0006 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3352-2966G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89594261 | |||||||
| chr12:89594479 | A | T | 312 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.3352-3184T>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89594479 | |||||||
| chr12:89594594 | G | GA | 301 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(298): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.3352-3300dupT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89594594 | |||||||
| chr12:89594606 | C | A | 4 | a0001c0002t0001g0110 a0001c0002t0001g0111 a0001c0002t0001g0112 others(1): Show |
4 | HG00639.hp1 HG01109.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.3352-3311G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89594606 | |||||||
| chr12:89594912 | T | A | 1 | a0001c0001t0001g0209 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3352-3617A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89594912 | |||||||
| chr12:89594974 | A | G | 2 | a0001c0001t0009g0012 a0001c0001t0009g0013 |
2 | HG00735.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.3352-3679T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89594974 | |||||||
| chr12:89595170 | C | T | 312 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.3352-3875G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89595170 | |||||||
| chr12:89595258 | T | C | 1 | a0001c0001t0001g0269 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.3351+3859A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89595258 | |||||||
| chr12:89595476 | A | C | 1 | a0001c0001t0006g0217 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3351+3641T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89595476 | |||||||
| chr12:89595488 | TC | T | 4 | a0001c0002t0001g0110 a0001c0002t0001g0111 a0001c0002t0001g0112 others(1): Show |
4 | HG00639.hp1 HG01109.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.3351+3628delG | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89595488 | |||||||
| chr12:89595510 | T | C | 312 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.3351+3607A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89595510 | |||||||
| chr12:89595708 | T | G | 1 | a0001c0001t0003g0006 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3351+3409A>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89595708 | |||||||
| chr12:89595822 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(173): Show |
178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.3351+3295C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89595822 | |||||||
| chr12:89595846 | A | G | 8 | a0001c0002t0001g0110 a0001c0002t0001g0111 a0001c0002t0001g0112 others(5): Show |
8 | HG00639.hp1 HG01109.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.3351+3271T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89595846 | |||||||
| chr12:89596520 | A | G | 5 | a0001c0003t0001g0050 a0001c0003t0001g0051 a0001c0003t0001g0052 others(2): Show |
5 | HG01192.hp1 HG01884.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.3351+2597T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89596520 | |||||||
| chr12:89596621 | C | T | 6 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0213 others(3): Show |
6 | HG02280.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3351+2496G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89596621 | |||||||
| chr12:89596845 | C | A | 3 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0300 |
3 | NA18950.hp2 NA18966.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.3351+2272G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89596845 | |||||||
| chr12:89597307 | A | G | 312 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.3351+1810T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89597307 | |||||||
| chr12:89597381 | A | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(303): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.3351+1736T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89597381 | |||||||
| chr12:89597513 | T | C | 3 | a0001c0001t0001g0286 a0001c0001t0001g0293 a0001c0001t0001g0309 |
3 | HG00099.hp2 HG00639.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.3351+1604A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89597513 | |||||||
| chr12:89597528 | G | A | 278 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(275): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.3351+1589C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89597528 | |||||||
| chr12:89597532 | A | C | 320 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(317): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.3351+1585T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89597532 | |||||||
| chr12:89597536 | C | T | 62 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0067 others(59): Show |
62 | HG00099.hp1 HG00642.hp1 HG01256.hp1 others(59): Show |
intron_variant | MODIFIER | c.3351+1581G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89597536 | |||||||
| chr12:89597538 | G | C | 278 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(275): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.3351+1579C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89597538 | |||||||
| chr12:89597539 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3351+1578C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89597539 | |||||||
| chr12:89597807 | A | T | 7 | a0001c0001t0005g0319 a0001c0001t0005g0321 a0001c0001t0005g0322 others(4): Show |
7 | HG02257.hp1 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3351+1310T>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89597807 | |||||||
| chr12:89597962 | A | C | 311 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(308): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.3351+1155T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89597962 | |||||||
| chr12:89597996 | A | T | 1 | a0001c0001t0001g0294 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3351+1121T>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89597996 | |||||||
| chr12:89598014 | C | G | 1 | a0001c0001t0001g0219 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3351+1103G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89598014 | |||||||
| chr12:89598016 | C | A | 1 | a0001c0001t0001g0219 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3351+1101G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89598016 | |||||||
| chr12:89598039 | C | CAA | 7 | a0001c0001t0001g0069 a0001c0001t0006g0217 a0001c0002t0001g0110 others(4): Show |
7 | HG00639.hp1 HG02074.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.3351+1076_3351+107 others(6): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89598039 | |||||||
| chr12:89598039 | C | CAAA | 138 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0067 others(135): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.3351+1075_3351+107 others(7): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89598039 | |||||||
| chr12:89598039 | C | CAAAA | 121 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(118): Show |
123 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.3351+1074_3351+107 others(8): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89598039 | |||||||
| chr12:89598039 | C | CAAAAA | 34 | a0001c0001t0001g0076 a0001c0001t0001g0093 a0001c0001t0001g0094 others(31): Show |
34 | HG00423.hp1 HG00558.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.3351+1073_3351+107 others(9): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89598039 | |||||||
| chr12:89598039 | C | CAAAAAA | 7 | a0001c0001t0005g0322 a0001c0002t0001g0046 a0001c0002t0001g0047 others(4): Show |
7 | HG01109.hp1 HG01192.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3351+1072_3351+107 others(10): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89598039 | |||||||
| chr12:89598039 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0108 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.3351+1068_3351+107 others(14): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89598039 | |||||||
| chr12:89598120 | AACTTGTC others(7): Show |
A | 5 | a0001c0001t0001g0283 a0001c0001t0001g0288 a0001c0001t0001g0291 others(2): Show |
5 | HG02015.hp2 HG02293.hp2 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.3351+983_3351+996d others(16): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89598120 | |||||||
| chr12:89598735 | T | C | 1 | a0001c0002t0001g0111 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3351+382A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89598735 | |||||||
| chr12:89599088 | T | C | 1 | a0001c0001t0003g0006 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3351+29A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89599088 | |||||||
| chr12:89599517 | A | G | 8 | a0001c0002t0001g0110 a0001c0002t0001g0111 a0001c0002t0001g0112 others(5): Show |
8 | HG00639.hp1 HG01109.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.3169-218T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 19/20 | chr12 | 89599517 | |||||||
| chr12:89599539 | AT | A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0218 a0001c0001t0001g0273 |
3 | HG02602.hp2 HG03239.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.3169-241delA | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 19/20 | chr12 | 89599539 | |||||||
| chr12:89599729 | TA | T | 4 | a0001c0006t0001g0032 a0001c0006t0001g0033 a0001c0007t0010g0135 others(1): Show |
4 | HG02723.hp1 HG03098.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3169-431delT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 19/20 | chr12 | 89599729 | |||||||
| chr12:89599730 | A | T | 86 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(83): Show |
86 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.3169-431T>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 19/20 | chr12 | 89599730 | |||||||
| chr12:89599772 | A | G | 1 | a0001c0001t0001g0204 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.3169-473T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 19/20 | chr12 | 89599772 | |||||||
| chr12:89599790 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3169-491G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 19/20 | chr12 | 89599790 | |||||||
| chr12:89599824 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3169-525G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 19/20 | chr12 | 89599824 | |||||||
| chr12:89600396 | C | A | 1 | a0001c0001t0006g0217 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3168+930G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 19/20 | chr12 | 89600396 | |||||||
| chr12:89600645 | T | C | 1 | a0001c0001t0002g0176 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3168+681A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 19/20 | chr12 | 89600645 | |||||||
| chr12:89600648 | A | AT | 7 | a0001c0001t0005g0116 a0001c0001t0005g0117 a0001c0001t0005g0319 others(4): Show |
7 | HG02257.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3168+677dupA | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 19/20 | chr12 | 89600648 | |||||||
| chr12:89600648 | AT | A | 24 | a0001c0001t0001g0162 a0001c0001t0001g0320 a0001c0002t0001g0039 others(21): Show |
24 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.3168+677delA | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 19/20 | chr12 | 89600648 | |||||||
| chr12:89600875 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3168+451G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 19/20 | chr12 | 89600875 | |||||||
| chr12:89600983 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3168+343G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 19/20 | chr12 | 89600983 | |||||||
| chr12:89601019 | C | T | 2 | a0001c0002t0001g0114 a0001c0002t0001g0115 |
2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3168+307G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 19/20 | chr12 | 89601019 | |||||||
| chr12:89601116 | A | G | 2 | a0001c0002t0001g0114 a0001c0002t0001g0115 |
2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3168+210T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 19/20 | chr12 | 89601116 | |||||||
| chr12:89601300 | TAAAC | T | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 |
3 | HG02258.hp1 HG02896.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3168+22_3168+25del others(4): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 19/20 | chr12 | 89601300 | |||||||
| chr12:89601498 | A | C | 1 | a0001c0001t0001g0205 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3061-65T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 18/20 | chr12 | 89601498 | |||||||
| chr12:89601689 | G | A | 56 | a0001c0001t0001g0097 a0001c0001t0001g0103 a0001c0001t0001g0108 others(53): Show |
56 | HG00140.hp2 HG00280.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.3061-256C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 18/20 | chr12 | 89601689 | |||||||
| chr12:89601762 | C | T | 2 | a0001c0001t0002g0053 a0001c0001t0002g0160 |
2 | HG02886.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3061-329G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 18/20 | chr12 | 89601762 | |||||||
| chr12:89601955 | A | G | 312 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.3061-522T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 18/20 | chr12 | 89601955 | |||||||
| chr12:89602313 | T | C | 311 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(308): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.3060+730A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 18/20 | chr12 | 89602313 | |||||||
| chr12:89602417 | A | G | 1 | a0001c0001t0001g0297 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3060+626T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 18/20 | chr12 | 89602417 | |||||||
| chr12:89602604 | C | T | 18 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(15): Show |
18 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.3060+439G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 18/20 | chr12 | 89602604 | |||||||
| chr12:89602968 | T | C | 2 | a0001c0002t0001g0114 a0001c0002t0001g0115 |
2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3060+75A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 18/20 | chr12 | 89602968 | |||||||
| chr12:89603009 | G | C | 5 | a0001c0003t0001g0050 a0001c0003t0001g0051 a0001c0003t0001g0052 others(2): Show |
5 | HG01192.hp1 HG01884.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.3060+34C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 18/20 | chr12 | 89603009 | |||||||
| chr12:89603701 | T | C | 1 | a0001c0002t0001g0137 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2848+11A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 17/20 | chr12 | 89603701 | |||||||
| chr12:89604750 | G | T | 1 | a0001c0001t0001g0120 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2443-404C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89604750 | |||||||
| chr12:89604759 | C | T | 1 | a0001c0003t0021g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2443-413G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89604759 | |||||||
| chr12:89605106 | C | T | 1 | a0001c0002t0012g0002 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2443-760G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89605106 | |||||||
| chr12:89605191 | C | A | 1 | a0001c0001t0001g0260 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2443-845G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89605191 | |||||||
| chr12:89605512 | T | C | 312 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.2443-1166A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89605512 | |||||||
| chr12:89605597 | A | C | 1 | a0001c0001t0001g0247 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2443-1251T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89605597 | |||||||
| chr12:89605702 | AAAG | A | 3 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0003g0028 |
3 | HG02486.hp2 HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2443-1359_2443-135 others(7): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89605702 | |||||||
| chr12:89605819 | A | C | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2443-1473T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89605819 | |||||||
| chr12:89606076 | C | T | 311 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(308): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.2443-1730G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89606076 | |||||||
| chr12:89606095 | CAGTCACA others(3): Show |
C | 312 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.2443-1759_2443-175 others(14): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89606095 | |||||||
| chr12:89606304 | T | C | 312 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.2443-1958A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89606304 | |||||||
| chr12:89606443 | C | T | 1 | a0001c0001t0001g0311 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2443-2097G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89606443 | |||||||
| chr12:89606571 | A | AC | 9 | a0001c0001t0005g0116 a0001c0001t0005g0117 a0001c0001t0005g0319 others(6): Show |
9 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2443-2226dupG | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89606571 | |||||||
| chr12:89606572 | C | CT | 281 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(278): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.2443-2227dupA | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89606572 | |||||||
| chr12:89606572 | C | CTT | 17 | a0001c0001t0001g0127 a0001c0001t0001g0143 a0001c0001t0001g0163 others(14): Show |
18 | HG01192.hp1 HG01261.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.2443-2228_2443-222 others(6): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89606572 | |||||||
| chr12:89606783 | C | T | 18 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(15): Show |
18 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.2443-2437G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89606783 | |||||||
| chr12:89606827 | C | T | 8 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(5): Show |
8 | HG02109.hp1 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2443-2481G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89606827 | |||||||
| chr12:89606906 | C | T | 18 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(15): Show |
18 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.2443-2560G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89606906 | |||||||
| chr12:89606984 | C | A | 303 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(300): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.2443-2638G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89606984 | |||||||
| chr12:89607038 | T | C | 41 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0102 others(38): Show |
41 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.2443-2692A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89607038 | |||||||
| chr12:89607199 | T | A | 4 | a0001c0006t0001g0032 a0001c0006t0001g0033 a0001c0007t0010g0135 others(1): Show |
4 | HG02723.hp1 HG03098.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2442+2738A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89607199 | |||||||
| chr12:89607461 | G | A | 2 | a0001c0001t0001g0304 a0001c0001t0001g0305 |
2 | HG02293.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.2442+2476C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89607461 | |||||||
| chr12:89607537 | T | C | 302 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(299): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.2442+2400A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89607537 | |||||||
| chr12:89607546 | C | T | 6 | a0001c0001t0002g0122 a0001c0001t0002g0174 a0001c0001t0002g0176 others(3): Show |
6 | HG01243.hp2 HG01943.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.2442+2391G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89607546 | |||||||
| chr12:89607593 | G | T | 1 | a0001c0001t0002g0160 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2442+2344C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89607593 | |||||||
| chr12:89607680 | C | A | 2 | a0001c0001t0001g0286 a0001c0001t0001g0293 |
2 | HG00099.hp2 HG00639.hp2 |
intron_variant | MODIFIER | c.2442+2257G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89607680 | |||||||
| chr12:89607931 | T | C | 3 | a0001c0001t0007g0021 a0001c0001t0007g0022 a0001c0001t0007g0026 |
3 | HG02622.hp1 HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2442+2006A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89607931 | |||||||
| chr12:89608140 | C | T | 303 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(300): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.2442+1797G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89608140 | |||||||
| chr12:89608288 | A | C | 312 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.2442+1649T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89608288 | |||||||
| chr12:89608378 | G | A | 1 | a0001c0002t0012g0002 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2442+1559C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89608378 | |||||||
| chr12:89608396 | G | C | 1 | a0001c0002t0001g0118 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2442+1541C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89608396 | |||||||
| chr12:89608455 | C | T | 302 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(299): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.2442+1482G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89608455 | |||||||
| chr12:89608514 | T | TA | 11 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(8): Show |
11 | HG01081.hp2 HG01192.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.2442+1422dupT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89608514 | |||||||
| chr12:89608651 | A | G | 5 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(2): Show |
5 | HG02280.hp2 HG02809.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2442+1286T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89608651 | |||||||
| chr12:89608931 | G | A | 1 | a0001c0002t0012g0002 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2442+1006C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89608931 | |||||||
| chr12:89609008 | T | C | 2 | a0001c0002t0001g0114 a0001c0002t0001g0115 |
2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2442+929A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89609008 | |||||||
| chr12:89609193 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2442+744T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89609193 | |||||||
| chr12:89609224 | C | T | 8 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0299 others(5): Show |
8 | HG02074.hp1 HG02080.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.2442+713G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89609224 | |||||||
| chr12:89609441 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2442+496T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89609441 | |||||||
| chr12:89609536 | T | C | 1 | a0001c0001t0020g0048 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2442+401A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89609536 | |||||||
| chr12:89609540 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2442+397T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89609540 | |||||||
| chr12:89609615 | T | C | 1 | a0001c0001t0001g0301 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2442+322A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89609615 | |||||||
| chr12:89609677 | A | C | 1 | a0001c0001t0001g0259 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2442+260T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89609677 | |||||||
| chr12:89609819 | G | A | 3 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 |
3 | HG00558.hp1 HG00621.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.2442+118C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89609819 | |||||||
| chr12:89609888 | A | C | 1 | a0001c0001t0001g0106 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2442+49T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89609888 | |||||||
| chr12:89610116 | C | T | 2 | a0001c0001t0001g0143 a0001c0001t0003g0028 |
2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2336-73G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 14/20 | chr12 | 89610116 | |||||||
| chr12:89610330 | T | G | 27 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(24): Show |
29 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(26): Show |
intron_variant | MODIFIER | c.2335+91A>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 14/20 | chr12 | 89610330 | |||||||
| chr12:89610344 | A | G | 1 | a0001c0001t0002g0179 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2335+77T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 14/20 | chr12 | 89610344 | |||||||
| chr12:89610372 | A | G | 2 | a0001c0001t0001g0209 a0004c0008t0001g0208 |
2 | NA18951.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2335+49T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 14/20 | chr12 | 89610372 | |||||||
| chr12:89610546 | T | C | 9 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(6): Show |
9 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(6): Show |
intron_variant | MODIFIER | c.2248-38A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 13/20 | chr12 | 89610546 | |||||||
| chr12:89610666 | C | A | 1 | a0001c0001t0001g0191 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2248-158G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 13/20 | chr12 | 89610666 | |||||||
| chr12:89610678 | T | A | 1 | a0001c0003t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2248-170A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 13/20 | chr12 | 89610678 | |||||||
| chr12:89610788 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2248-280G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 13/20 | chr12 | 89610788 | |||||||
| chr12:89611147 | T | C | 8 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(5): Show |
8 | HG02109.hp1 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2247+46A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 13/20 | chr12 | 89611147 | |||||||
| chr12:89611599 | T | G | 1 | a0001c0001t0001g0191 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2068-227A>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89611599 | |||||||
| chr12:89611729 | T | C | 312 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.2068-357A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89611729 | |||||||
| chr12:89611968 | A | G | 1 | a0001c0001t0004g0020 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2068-596T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89611968 | |||||||
| chr12:89612363 | T | C | 9 | a0001c0001t0005g0116 a0001c0001t0005g0117 a0001c0001t0005g0319 others(6): Show |
9 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2068-991A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89612363 | |||||||
| chr12:89612381 | T | C | 2 | a0001c0001t0001g0258 a0001c0001t0001g0328 |
2 | HG01081.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.2068-1009A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89612381 | |||||||
| chr12:89612448 | G | A | 27 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(24): Show |
29 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(26): Show |
intron_variant | MODIFIER | c.2068-1076C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89612448 | |||||||
| chr12:89612716 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2068-1344C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89612716 | |||||||
| chr12:89612749 | T | C | 3 | a0001c0001t0001g0106 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG00423.hp1 HG02004.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.2068-1377A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89612749 | |||||||
| chr12:89612917 | C | T | 1 | a0001c0001t0005g0319 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2068-1545G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89612917 | |||||||
| chr12:89613071 | C | T | 1 | a0001c0002t0012g0002 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2068-1699G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89613071 | |||||||
| chr12:89613128 | C | T | 19 | a0001c0001t0001g0107 a0001c0002t0001g0039 a0001c0002t0001g0040 others(16): Show |
19 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2068-1756G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89613128 | |||||||
| chr12:89613235 | C | G | 1 | a0001c0001t0004g0007 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2068-1863G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89613235 | |||||||
| chr12:89613320 | A | C | 1 | a0001c0001t0001g0102 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2068-1948T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89613320 | |||||||
| chr12:89613380 | C | T | 1 | a0001c0001t0001g0299 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2068-2008G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89613380 | |||||||
| chr12:89613443 | C | A | 1 | a0001c0001t0001g0165 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2068-2071G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89613443 | |||||||
| chr12:89613665 | C | T | 2 | a0001c0003t0001g0051 a0001c0003t0001g0054 |
2 | HG01192.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2068-2293G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89613665 | |||||||
| chr12:89613679 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0328 |
2 | HG01081.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2068-2307G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89613679 | |||||||
| chr12:89614472 | A | T | 1 | a0001c0001t0001g0087 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2067+2330T>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89614472 | |||||||
| chr12:89614523 | C | A | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG03927.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.2067+2279G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89614523 | |||||||
| chr12:89614600 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2067+2202A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89614600 | |||||||
| chr12:89614834 | T | C | 312 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.2067+1968A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89614834 | |||||||
| chr12:89615182 | A | G | 92 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(89): Show |
92 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.2067+1620T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89615182 | |||||||
| chr12:89615270 | T | C | 1 | a0001c0001t0001g0309 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2067+1532A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89615270 | |||||||
| chr12:89615388 | A | G | 18 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(15): Show |
18 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.2067+1414T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89615388 | |||||||
| chr12:89615755 | C | G | 1 | a0001c0001t0001g0081 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2067+1047G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89615755 | |||||||
| chr12:89615946 | TA | T | 298 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(295): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.2067+855delT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89615946 | |||||||
| chr12:89615988 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2067+814G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89615988 | |||||||
| chr12:89616120 | G | A | 1 | a0001c0002t0012g0002 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2067+682C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89616120 | |||||||
| chr12:89616367 | T | C | 3 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 |
3 | HG00558.hp1 HG00621.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.2067+435A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89616367 | |||||||
| chr12:89616396 | G | C | 7 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(4): Show |
7 | HG01433.hp2 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.2067+406C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89616396 | |||||||
| chr12:89616465 | C | G | 3 | a0001c0005t0001g0083 a0001c0005t0001g0084 a0001c0005t0001g0101 |
3 | HG01257.hp2 HG02300.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2067+337G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89616465 | |||||||
| chr12:89616491 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2067+311A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89616491 | |||||||
| chr12:89616492 | G | A | 3 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0222 |
3 | HG00741.hp1 HG01257.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.2067+310C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89616492 | |||||||
| chr12:89616595 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2067+207A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89616595 | |||||||
| chr12:89617318 | T | C | 13 | a0001c0002t0001g0039 a0001c0002t0001g0041 a0001c0002t0001g0044 others(10): Show |
13 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.1830-279A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 11/20 | chr12 | 89617318 | |||||||
| chr12:89617579 | C | T | 1 | a0001c0001t0006g0282 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1830-540G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 11/20 | chr12 | 89617579 | |||||||
| chr12:89617621 | T | A | 1 | a0001c0001t0001g0284 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1830-582A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 11/20 | chr12 | 89617621 | |||||||
| chr12:89617949 | A | C | 1 | a0001c0001t0003g0006 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1830-910T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 11/20 | chr12 | 89617949 | |||||||
| chr12:89618090 | AT | A | 7 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(4): Show |
7 | HG02109.hp1 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1830-1052delA | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 11/20 | chr12 | 89618090 | |||||||
| chr12:89618369 | C | T | 312 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1830-1330G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 11/20 | chr12 | 89618369 | |||||||
| chr12:89618471 | A | G | 1 | a0001c0001t0001g0077 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1830-1432T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 11/20 | chr12 | 89618471 | |||||||
| chr12:89619167 | T | C | 9 | a0001c0001t0005g0116 a0001c0001t0005g0117 a0001c0001t0005g0319 others(6): Show |
9 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1829+832A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 11/20 | chr12 | 89619167 | |||||||
| chr12:89619268 | A | G | 1 | a0001c0001t0002g0276 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1829+731T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 11/20 | chr12 | 89619268 | |||||||
| chr12:89619312 | T | C | 93 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(90): Show |
93 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.1829+687A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 11/20 | chr12 | 89619312 | |||||||
| chr12:89619378 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1829+621C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 11/20 | chr12 | 89619378 | |||||||
| chr12:89619403 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0105 |
2 | HG01081.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.1829+596C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 11/20 | chr12 | 89619403 | |||||||
| chr12:89619550 | G | A | 18 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(15): Show |
18 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1829+449C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 11/20 | chr12 | 89619550 | |||||||
| chr12:89619566 | G | A | 3 | a0001c0004t0001g0034 a0001c0004t0001g0035 a0001c0004t0001g0119 |
3 | HG02109.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1829+433C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 11/20 | chr12 | 89619566 | |||||||
| chr12:89619570 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1829+429G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 11/20 | chr12 | 89619570 | |||||||
| chr12:89619618 | T | TA | 131 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0066 others(128): Show |
131 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.1829+380dupT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 11/20 | chr12 | 89619618 | |||||||
| chr12:89619618 | T | TAA | 86 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(83): Show |
86 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.1829+379_1829+380d others(4): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 11/20 | chr12 | 89619618 | |||||||
| chr12:89619618 | TA | T | 6 | a0001c0002t0001g0055 a0001c0002t0001g0110 a0001c0002t0001g0111 others(3): Show |
6 | HG00639.hp1 HG01109.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.1829+380delT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 11/20 | chr12 | 89619618 | |||||||
| chr12:89619683 | A | T | 1 | a0001c0001t0001g0196 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1829+316T>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 11/20 | chr12 | 89619683 | |||||||
| chr12:89620274 | C | T | 1 | a0001c0007t0010g0232 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1588-34G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 10/20 | chr12 | 89620274 | |||||||
| chr12:89620289 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1588-49C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 10/20 | chr12 | 89620289 | |||||||
| chr12:89620743 | T | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0108 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1588-503A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 10/20 | chr12 | 89620743 | |||||||
| chr12:89620883 | T | C | 1 | a0001c0003t0021g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1588-643A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 10/20 | chr12 | 89620883 | |||||||
| chr12:89621470 | G | A | 8 | a0001c0002t0001g0110 a0001c0002t0001g0111 a0001c0002t0001g0112 others(5): Show |
8 | HG00639.hp1 HG01109.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1587+79C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 10/20 | chr12 | 89621470 | |||||||
| chr12:89621493 | G | A | 18 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(15): Show |
18 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1587+56C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 10/20 | chr12 | 89621493 | |||||||
| chr12:89621802 | C | CA | 303 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(300): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1345-12dupT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 9/20 | chr12 | 89621802 | |||||||
| chr12:89621847 | A | T | 2 | a0001c0001t0001g0267 a0001c0001t0001g0300 |
2 | NA18950.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.1345-56T>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 9/20 | chr12 | 89621847 | |||||||
| chr12:89621951 | T | A | 4 | a0001c0003t0001g0050 a0001c0003t0001g0051 a0001c0003t0001g0054 others(1): Show |
4 | HG01192.hp1 HG01884.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1345-160A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 9/20 | chr12 | 89621951 | |||||||
| chr12:89622003 | G | A | 1 | a0001c0001t0005g0116 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1345-212C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 9/20 | chr12 | 89622003 | |||||||
| chr12:89622097 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1345-306G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 9/20 | chr12 | 89622097 | |||||||
| chr12:89622185 | T | C | 1 | a0001c0001t0001g0317 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1345-394A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 9/20 | chr12 | 89622185 | |||||||
| chr12:89622299 | A | AT | 243 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(240): Show |
246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.1345-509dupA | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 9/20 | chr12 | 89622299 | |||||||
| chr12:89622447 | A | C | 1 | a0001c0001t0001g0295 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1345-656T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 9/20 | chr12 | 89622447 | |||||||
| chr12:89622506 | T | C | 1 | a0001c0003t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1345-715A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 9/20 | chr12 | 89622506 | |||||||
| chr12:89622679 | T | C | 1 | a0001c0001t0006g0246 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1345-888A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 9/20 | chr12 | 89622679 | |||||||
| chr12:89623025 | A | C | 312 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1344+1158T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 9/20 | chr12 | 89623025 | |||||||
| chr12:89623073 | T | TACC | 312 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1344+1109_1344+111 others(7): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 9/20 | chr12 | 89623073 | |||||||
| chr12:89623354 | CT | C | 14 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0250 others(11): Show |
14 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1344+828delA | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 9/20 | chr12 | 89623354 | |||||||
| chr12:89623400 | T | C | 1 | a0001c0001t0007g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1344+783A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 9/20 | chr12 | 89623400 | |||||||
| chr12:89623895 | T | C | 1 | a0001c0002t0012g0002 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1344+288A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 9/20 | chr12 | 89623895 | |||||||
| chr12:89623959 | G | T | 134 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0097 others(131): Show |
134 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.1344+224C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 9/20 | chr12 | 89623959 | |||||||
| chr12:89623982 | G | A | 2 | a0001c0002t0001g0114 a0001c0002t0001g0115 |
2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1344+201C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 9/20 | chr12 | 89623982 | |||||||
| chr12:89624061 | T | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1344+122A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 9/20 | chr12 | 89624061 | |||||||
| chr12:89624457 | C | A | 20 | a0001c0001t0001g0001 a0001c0001t0001g0278 a0001c0001t0001g0279 others(17): Show |
22 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.1130-60G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 8/20 | chr12 | 89624457 | |||||||
| chr12:89624683 | C | T | 6 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0186 others(3): Show |
6 | HG02280.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1130-286G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 8/20 | chr12 | 89624683 | |||||||
| chr12:89624965 | A | G | 1 | a0001c0001t0001g0280 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1130-568T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 8/20 | chr12 | 89624965 | |||||||
| chr12:89624982 | G | C | 1 | a0001c0001t0001g0266 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1130-585C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 8/20 | chr12 | 89624982 | |||||||
| chr12:89624994 | G | T | 307 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(304): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1130-597C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 8/20 | chr12 | 89624994 | |||||||
| chr12:89625081 | A | G | 312 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1130-684T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 8/20 | chr12 | 89625081 | |||||||
| chr12:89625269 | C | T | 1 | a0001c0001t0020g0048 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1130-872G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 8/20 | chr12 | 89625269 | |||||||
| chr12:89625401 | C | G | 68 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0066 others(65): Show |
68 | HG00099.hp1 HG00642.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1130-1004G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 8/20 | chr12 | 89625401 | |||||||
| chr12:89625452 | C | T | 200 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(197): Show |
202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.1129+1002G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 8/20 | chr12 | 89625452 | |||||||
| chr12:89625584 | CA | C | 52 | a0001c0001t0001g0066 a0001c0001t0001g0143 a0001c0001t0001g0155 others(49): Show |
53 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.1129+869delT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 8/20 | chr12 | 89625584 | |||||||
| chr12:89625584 | CAA | C | 266 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(263): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1129+868_1129+869d others(4): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 8/20 | chr12 | 89625584 | |||||||
| chr12:89625830 | A | C | 1 | a0001c0003t0001g0050 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1129+624T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 8/20 | chr12 | 89625830 | |||||||
| chr12:89625831 | C | A | 1 | a0001c0003t0001g0050 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1129+623G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 8/20 | chr12 | 89625831 | |||||||
| chr12:89625935 | C | T | 2 | a0001c0002t0001g0114 a0001c0002t0001g0115 |
2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1129+519G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 8/20 | chr12 | 89625935 | |||||||
| chr12:89625999 | A | T | 14 | a0001c0001t0001g0120 a0001c0001t0001g0128 a0001c0001t0001g0129 others(11): Show |
14 | HG01346.hp2 HG01433.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1129+455T>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 8/20 | chr12 | 89625999 | |||||||
| chr12:89626028 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1129+426G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 8/20 | chr12 | 89626028 | |||||||
| chr12:89626038 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1129+416G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 8/20 | chr12 | 89626038 | |||||||
| chr12:89626265 | T | C | 2 | a0001c0002t0001g0114 a0001c0002t0001g0115 |
2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1129+189A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 8/20 | chr12 | 89626265 | |||||||
| chr12:89626316 | A | G | 2 | a0001c0003t0001g0051 a0001c0003t0001g0054 |
2 | HG01192.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1129+138T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 8/20 | chr12 | 89626316 | |||||||
| chr12:89626782 | T | C | 1 | a0001c0002t0001g0040 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.968-167A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 7/20 | chr12 | 89626782 | |||||||
| chr12:89626914 | C | T | 303 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(300): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.968-299G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 7/20 | chr12 | 89626914 | |||||||
| chr12:89626960 | A | G | 5 | a0001c0003t0001g0050 a0001c0003t0001g0051 a0001c0003t0001g0052 others(2): Show |
5 | HG01192.hp1 HG01884.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.968-345T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 7/20 | chr12 | 89626960 | |||||||
| chr12:89626968 | T | C | 19 | a0001c0001t0001g0124 a0001c0001t0001g0198 a0001c0001t0001g0199 others(16): Show |
19 | HG00408.hp1 HG01099.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.968-353A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 7/20 | chr12 | 89626968 | |||||||
| chr12:89627319 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.967+359A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 7/20 | chr12 | 89627319 | |||||||
| chr12:89627337 | T | C | 2 | a0001c0002t0001g0114 a0001c0002t0001g0115 |
2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.967+341A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 7/20 | chr12 | 89627337 | |||||||
| chr12:89627396 | C | CA | 21 | a0001c0001t0001g0080 a0001c0001t0001g0089 a0001c0001t0001g0138 others(18): Show |
21 | HG01192.hp1 HG01257.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.967+281dupT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 7/20 | chr12 | 89627396 | |||||||
| chr12:89627396 | CA | C | 22 | a0001c0001t0001g0199 a0001c0001t0001g0234 a0001c0001t0001g0248 others(19): Show |
23 | HG01070.hp2 HG01099.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.967+281delT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 7/20 | chr12 | 89627396 | |||||||
| chr12:89627444 | A | C | 19 | a0001c0001t0001g0124 a0001c0001t0001g0198 a0001c0001t0001g0199 others(16): Show |
19 | HG00408.hp1 HG01099.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.967+234T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 7/20 | chr12 | 89627444 | |||||||
| chr12:89627533 | G | A | 1 | a0001c0004t0001g0034 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.967+145C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 7/20 | chr12 | 89627533 | |||||||
| chr12:89627541 | G | A | 1 | a0001c0001t0001g0320 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.967+137C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 7/20 | chr12 | 89627541 | |||||||
| chr12:89627768 | A | C | 1 | a0001c0001t0001g0102 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.929-52T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 6/20 | chr12 | 89627768 | |||||||
| chr12:89627825 | G | T | 1 | a0001c0001t0001g0211 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.929-109C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 6/20 | chr12 | 89627825 | |||||||
| chr12:89627876 | T | C | 1 | a0001c0001t0001g0205 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.929-160A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 6/20 | chr12 | 89627876 | |||||||
| chr12:89627897 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.929-181G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 6/20 | chr12 | 89627897 | |||||||
| chr12:89627909 | G | A | 1 | a0001c0002t0001g0040 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.929-193C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 6/20 | chr12 | 89627909 | |||||||
| chr12:89628157 | T | C | 312 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.929-441A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 6/20 | chr12 | 89628157 | |||||||
| chr12:89628289 | C | A | 22 | a0001c0001t0001g0097 a0001c0001t0001g0103 a0001c0001t0001g0108 others(19): Show |
22 | HG00140.hp2 HG00280.hp2 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.929-573G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 6/20 | chr12 | 89628289 | |||||||
| chr12:89628315 | T | C | 2 | a0001c0001t0001g0281 a0001c0001t0001g0287 |
2 | NA18962.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.929-599A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 6/20 | chr12 | 89628315 | |||||||
| chr12:89628401 | CA | C | 7 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0017 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.929-686delT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 6/20 | chr12 | 89628401 | |||||||
| chr12:89628401 | CAA | C | 7 | a0001c0001t0004g0007 a0001c0001t0004g0019 a0001c0001t0006g0142 others(4): Show |
7 | HG00741.hp2 HG02074.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.929-687_929-686del others(2): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 6/20 | chr12 | 89628401 | |||||||
| chr12:89628401 | CAAAAAAA others(4): Show |
C | 12 | a0001c0001t0001g0143 a0001c0001t0001g0155 a0001c0001t0001g0258 others(9): Show |
12 | HG01433.hp1 HG02258.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.929-696_929-686del others(11): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 6/20 | chr12 | 89628401 | |||||||
| chr12:89628401 | CAAAAAAA others(5): Show |
C | 265 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(262): Show |
268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.929-697_929-686del others(12): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 6/20 | chr12 | 89628401 | |||||||
| chr12:89628401 | CAAAAAAA others(6): Show |
C | 28 | a0001c0001t0001g0095 a0001c0001t0001g0203 a0001c0001t0001g0225 others(25): Show |
28 | HG00099.hp1 HG00558.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.929-698_929-686del others(13): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 6/20 | chr12 | 89628401 | |||||||
| chr12:89628401 | CAAAAAAA others(7): Show |
C | 2 | a0001c0002t0001g0118 a0001c0002t0001g0134 |
2 | HG02602.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.929-699_929-686del others(14): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 6/20 | chr12 | 89628401 | |||||||
| chr12:89628401 | CAAAAAAA others(18): Show |
C | 5 | a0001c0003t0001g0050 a0001c0003t0001g0051 a0001c0003t0001g0052 others(2): Show |
5 | HG01192.hp1 HG01884.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.929-710_929-686del others(25): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 6/20 | chr12 | 89628401 | |||||||
| chr12:89628440 | C | A | 4 | a0001c0003t0001g0050 a0001c0003t0001g0051 a0001c0003t0001g0054 others(1): Show |
4 | HG01192.hp1 HG01884.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.929-724G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 6/20 | chr12 | 89628440 | |||||||
| chr12:89628599 | A | G | 312 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.929-883T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 6/20 | chr12 | 89628599 | |||||||
| chr12:89629001 | A | T | 307 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(304): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.929-1285T>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 6/20 | chr12 | 89629001 | |||||||
| chr12:89629032 | G | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0108 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.929-1316C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 6/20 | chr12 | 89629032 | |||||||
| chr12:89629078 | T | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0036 a0001c0001t0001g0037 |
3 | HG02615.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.929-1362A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 6/20 | chr12 | 89629078 | |||||||
| chr12:89629092 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.929-1376C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 6/20 | chr12 | 89629092 | |||||||
| chr12:89629273 | T | C | 3 | a0001c0002t0001g0041 a0001c0002t0001g0044 a0001c0002t0001g0055 |
3 | HG01070.hp1 HG01071.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.928+1232A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 6/20 | chr12 | 89629273 | |||||||
| chr12:89629275 | A | G | 4 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0098 others(1): Show |
4 | HG00544.hp1 HG01081.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.928+1230T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 6/20 | chr12 | 89629275 | |||||||
| chr12:89629516 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.928+989G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 6/20 | chr12 | 89629516 | |||||||
| chr12:89629807 | G | C | 6 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(3): Show |
6 | HG02280.hp2 HG02809.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.928+698C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 6/20 | chr12 | 89629807 | |||||||
| chr12:89629991 | T | C | 9 | a0001c0001t0005g0116 a0001c0001t0005g0117 a0001c0001t0005g0319 others(6): Show |
9 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.928+514A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 6/20 | chr12 | 89629991 | |||||||
| chr12:89630057 | G | T | 1 | a0001c0001t0002g0160 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.928+448C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 6/20 | chr12 | 89630057 | |||||||
| chr12:89630070 | G | A | 18 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(15): Show |
18 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.928+435C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 6/20 | chr12 | 89630070 | |||||||
| chr12:89630449 | T | C | 9 | a0001c0001t0005g0116 a0001c0001t0005g0117 a0001c0001t0005g0319 others(6): Show |
9 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.928+56A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 6/20 | chr12 | 89630449 | |||||||
| chr12:89630772 | A | AATATATA others(5): Show |
280 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(277): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.788-139_788-128dup others(12): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89630772 | |||||||
| chr12:89630772 | A | AATATATA others(22): Show |
31 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(28): Show |
31 | HG00639.hp1 HG00738.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.788-128_788-127ins others(29): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89630772 | |||||||
| chr12:89630773 | A | ATATATAA others(10): Show |
1 | a0001c0002t0012g0002 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.788-145_788-129dup others(17): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89630773 | |||||||
| chr12:89630809 | C | G | 1 | a0001c0001t0001g0140 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.788-164G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89630809 | |||||||
| chr12:89630892 | C | T | 1 | a0001c0001t0019g0197 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.788-247G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89630892 | |||||||
| chr12:89630942 | A | T | 2 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
2 | NA18941.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.788-297T>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89630942 | |||||||
| chr12:89631070 | A | G | 17 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(14): Show |
17 | HG00423.hp2 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.788-425T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89631070 | |||||||
| chr12:89631089 | T | C | 279 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(276): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.788-444A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89631089 | |||||||
| chr12:89631298 | G | C | 1 | a0001c0001t0003g0027 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.788-653C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89631298 | |||||||
| chr12:89631693 | T | C | 18 | a0001c0001t0001g0180 a0001c0001t0002g0053 a0001c0001t0002g0122 others(15): Show |
18 | HG01243.hp2 HG01943.hp2 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.788-1048A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89631693 | |||||||
| chr12:89631758 | G | C | 312 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.788-1113C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89631758 | |||||||
| chr12:89631845 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(173): Show |
178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.788-1200C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89631845 | |||||||
| chr12:89631913 | G | A | 1 | a0001c0001t0011g0190 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.788-1268C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89631913 | |||||||
| chr12:89631927 | G | A | 7 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(4): Show |
7 | HG02109.hp1 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.788-1282C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89631927 | |||||||
| chr12:89632018 | T | C | 4 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0292 others(1): Show |
4 | HG02080.hp1 NA18989.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.788-1373A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89632018 | |||||||
| chr12:89632141 | CT | C | 24 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(21): Show |
24 | HG00639.hp1 HG00738.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.788-1497delA | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89632141 | |||||||
| chr12:89632236 | T | C | 1 | a0001c0001t0001g0299 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.788-1591A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89632236 | |||||||
| chr12:89632245 | T | C | 2 | a0001c0002t0001g0040 a0001c0002t0015g0042 |
2 | HG03927.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.788-1600A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89632245 | |||||||
| chr12:89632395 | T | C | 1 | a0001c0001t0001g0279 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.788-1750A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89632395 | |||||||
| chr12:89632638 | C | T | 18 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(15): Show |
18 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.788-1993G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89632638 | |||||||
| chr12:89632685 | G | A | 94 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(91): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.788-2040C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89632685 | |||||||
| chr12:89632686 | C | A | 94 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(91): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.788-2041G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89632686 | |||||||
| chr12:89632746 | A | G | 94 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(91): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.787+2032T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89632746 | |||||||
| chr12:89632869 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.787+1909C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89632869 | |||||||
| chr12:89633426 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.787+1352T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89633426 | |||||||
| chr12:89633480 | AT | A | 308 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(305): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.787+1297delA | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89633480 | |||||||
| chr12:89633546 | T | G | 2 | a0001c0001t0005g0325 a0001c0001t0005g0326 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.787+1232A>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89633546 | |||||||
| chr12:89633605 | A | G | 1 | a0001c0001t0001g0327 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.787+1173T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89633605 | |||||||
| chr12:89633628 | A | G | 5 | a0001c0003t0001g0050 a0001c0003t0001g0051 a0001c0003t0001g0052 others(2): Show |
5 | HG01192.hp1 HG01884.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.787+1150T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89633628 | |||||||
| chr12:89633738 | A | G | 1 | a0001c0001t0001g0309 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.787+1040T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89633738 | |||||||
| chr12:89634319 | A | G | 2 | a0001c0002t0001g0041 a0001c0002t0001g0044 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.787+459T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89634319 | |||||||
| chr12:89635318 | G | A | 1 | a0004c0008t0001g0208 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.407-67C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89635318 | |||||||
| chr12:89635643 | T | G | 1 | a0001c0001t0001g0095 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.407-392A>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89635643 | |||||||
| chr12:89635732 | C | T | 3 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0287 |
3 | NA18962.hp2 NA18970.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.407-481G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89635732 | |||||||
| chr12:89635960 | G | A | 303 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(300): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.407-709C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89635960 | |||||||
| chr12:89636092 | T | G | 1 | a0001c0001t0020g0048 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.407-841A>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89636092 | |||||||
| chr12:89636182 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.407-931G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89636182 | |||||||
| chr12:89636203 | G | C | 303 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(300): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.407-952C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89636203 | |||||||
| chr12:89636234 | G | C | 312 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.407-983C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89636234 | |||||||
| chr12:89636371 | C | G | 18 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(15): Show |
18 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.407-1120G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89636371 | |||||||
| chr12:89636376 | CAA | C | 36 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(33): Show |
38 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.407-1127_407-1126d others(4): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89636376 | |||||||
| chr12:89636413 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.407-1162A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89636413 | |||||||
| chr12:89636739 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.407-1488G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89636739 | |||||||
| chr12:89636866 | A | C | 1 | a0001c0001t0001g0120 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.407-1615T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89636866 | |||||||
| chr12:89636888 | T | C | 312 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.407-1637A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89636888 | |||||||
| chr12:89637010 | G | T | 1 | a0001c0001t0001g0218 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.407-1759C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89637010 | |||||||
| chr12:89637416 | A | ATT | 309 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(306): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.407-2167_407-2166d others(4): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89637416 | |||||||
| chr12:89637423 | C | T | 312 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.407-2172G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89637423 | |||||||
| chr12:89637618 | C | T | 133 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0102 others(130): Show |
133 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.407-2367G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89637618 | |||||||
| chr12:89638059 | T | TCCTA | 305 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(302): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.407-2812_407-2809d others(6): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89638059 | |||||||
| chr12:89638351 | A | T | 4 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0250 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.407-3100T>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89638351 | |||||||
| chr12:89638505 | A | T | 1 | a0001c0002t0001g0136 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.407-3254T>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89638505 | |||||||
| chr12:89638774 | A | T | 9 | a0001c0001t0005g0116 a0001c0001t0005g0117 a0001c0001t0005g0319 others(6): Show |
9 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.406+3384T>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89638774 | |||||||
| chr12:89638798 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.406+3360A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89638798 | |||||||
| chr12:89638805 | A | C | 1 | a0001c0007t0010g0135 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.406+3353T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89638805 | |||||||
| chr12:89638821 | C | T | 3 | a0001c0001t0007g0021 a0001c0001t0007g0022 a0001c0001t0007g0026 |
3 | HG02622.hp1 HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.406+3337G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89638821 | |||||||
| chr12:89638866 | C | A | 5 | a0001c0003t0001g0050 a0001c0003t0001g0051 a0001c0003t0001g0052 others(2): Show |
5 | HG01192.hp1 HG01884.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.406+3292G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89638866 | |||||||
| chr12:89639166 | T | C | 13 | a0001c0002t0001g0039 a0001c0002t0001g0041 a0001c0002t0001g0044 others(10): Show |
13 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.406+2992A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89639166 | |||||||
| chr12:89639171 | C | G | 4 | a0001c0003t0001g0050 a0001c0003t0001g0051 a0001c0003t0001g0054 others(1): Show |
4 | HG01192.hp1 HG01884.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.406+2987G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89639171 | |||||||
| chr12:89639223 | G | C | 4 | a0001c0001t0001g0181 a0001c0001t0001g0183 a0001c0001t0001g0219 others(1): Show |
4 | HG00597.hp1 HG02129.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.406+2935C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89639223 | |||||||
| chr12:89639275 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0105 |
2 | HG01081.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.406+2883C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89639275 | |||||||
| chr12:89639391 | C | G | 9 | a0001c0001t0005g0116 a0001c0001t0005g0117 a0001c0001t0005g0319 others(6): Show |
9 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.406+2767G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89639391 | |||||||
| chr12:89639453 | G | A | 2 | a0001c0001t0009g0012 a0001c0001t0009g0013 |
2 | HG00735.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.406+2705C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89639453 | |||||||
| chr12:89639524 | C | A | 1 | a0001c0001t0020g0048 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.406+2634G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89639524 | |||||||
| chr12:89639747 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.406+2411T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89639747 | |||||||
| chr12:89640086 | T | C | 6 | a0001c0002t0001g0110 a0001c0002t0001g0111 a0001c0002t0001g0112 others(3): Show |
6 | HG00639.hp1 HG01109.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.406+2072A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89640086 | |||||||
| chr12:89640507 | A | C | 9 | a0001c0001t0005g0116 a0001c0001t0005g0117 a0001c0001t0005g0319 others(6): Show |
9 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.406+1651T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89640507 | |||||||
| chr12:89640625 | G | GC | 201 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(198): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.406+1532_406+1533i others(3): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89640625 | |||||||
| chr12:89640630 | T | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(198): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.406+1528A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89640630 | |||||||
| chr12:89640774 | GA | G | 5 | a0001c0003t0001g0050 a0001c0003t0001g0051 a0001c0003t0001g0052 others(2): Show |
5 | HG01192.hp1 HG01884.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.406+1383delT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89640774 | |||||||
| chr12:89640821 | T | C | 2 | a0001c0001t0002g0123 a0001c0001t0002g0175 |
2 | NA19056.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.406+1337A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89640821 | |||||||
| chr12:89640904 | G | A | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.406+1254C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89640904 | |||||||
| chr12:89640935 | A | G | 2 | a0001c0001t0001g0278 a0003c0010t0001g0306 |
2 | NA18942.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.406+1223T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89640935 | |||||||
| chr12:89640985 | C | T | 1 | a0001c0001t0007g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.406+1173G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89640985 | |||||||
| chr12:89640988 | A | C | 1 | a0001c0001t0001g0263 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.406+1170T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89640988 | |||||||
| chr12:89641256 | T | C | 297 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(294): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.406+902A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89641256 | |||||||
| chr12:89641479 | T | TACACCTT others(14): Show |
1 | a0001c0001t0001g0082 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.406+658_406+678dup others(21): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89641479 | |||||||
| chr12:89641564 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.406+594G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89641564 | |||||||
| chr12:89642439 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.209-84T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89642439 | |||||||
| chr12:89642485 | A | G | 1 | a0001c0001t0004g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.209-130T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89642485 | |||||||
| chr12:89642629 | G | C | 1 | a0001c0002t0012g0002 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.209-274C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89642629 | |||||||
| chr12:89642700 | G | GT | 7 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0275 others(4): Show |
7 | HG00140.hp2 HG00280.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.209-346dupA | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89642700 | |||||||
| chr12:89642729 | C | T | 3 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0092 |
3 | HG00597.hp2 NA18945.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.209-374G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89642729 | |||||||
| chr12:89642766 | G | A | 3 | a0001c0001t0001g0244 a0001c0001t0001g0264 a0001c0001t0001g0265 |
3 | HG01168.hp1 HG02293.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.209-411C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89642766 | |||||||
| chr12:89642833 | G | GA | 18 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(15): Show |
18 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.209-479dupT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89642833 | |||||||
| chr12:89642933 | C | T | 312 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.209-578G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89642933 | |||||||
| chr12:89643020 | G | C | 1 | a0001c0003t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.209-665C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89643020 | |||||||
| chr12:89643052 | A | C | 9 | a0001c0001t0005g0116 a0001c0001t0005g0117 a0001c0001t0005g0319 others(6): Show |
9 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.209-697T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89643052 | |||||||
| chr12:89643065 | T | TAC | 10 | a0001c0001t0001g0063 a0001c0001t0001g0140 a0001c0001t0001g0148 others(7): Show |
11 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(8): Show |
intron_variant | MODIFIER | c.209-712_209-711dup others(2): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89643065 | |||||||
| chr12:89643065 | T | TACACAC | 90 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(87): Show |
90 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.209-716_209-711dup others(6): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89643065 | |||||||
| chr12:89643065 | T | TACACACA others(1): Show |
3 | a0001c0001t0001g0159 a0001c0004t0001g0034 a0001c0004t0001g0119 |
3 | HG02109.hp2 HG03516.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.209-718_209-711dup others(8): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89643065 | |||||||
| chr12:89643065 | T | TACACACA others(3): Show |
6 | a0001c0002t0001g0110 a0001c0002t0001g0112 a0001c0002t0001g0113 others(3): Show |
6 | HG01109.hp2 HG02630.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-720_209-711dup others(10): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89643065 | |||||||
| chr12:89643065 | T | TACACACA others(5): Show |
5 | a0001c0002t0001g0111 a0001c0002t0001g0114 a0001c0002t0001g0115 others(2): Show |
5 | HG00639.hp1 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-722_209-711dup others(12): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89643065 | |||||||
| chr12:89643065 | T | TACACACA others(7): Show |
1 | a0001c0002t0003g0025 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.209-724_209-711dup others(14): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89643065 | |||||||
| chr12:89643065 | T | TACACACA others(9): Show |
12 | a0001c0002t0001g0039 a0001c0002t0001g0041 a0001c0002t0001g0043 others(9): Show |
12 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.209-726_209-711dup others(16): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89643065 | |||||||
| chr12:89643065 | T | TACACACA others(11): Show |
1 | a0001c0002t0001g0134 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.209-728_209-711dup others(18): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89643065 | |||||||
| chr12:89643065 | T | TACACACA others(13): Show |
2 | a0001c0002t0001g0040 a0001c0002t0001g0118 |
2 | HG03041.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.209-730_209-711dup others(20): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89643065 | |||||||
| chr12:89643065 | T | TATACACA others(1): Show |
4 | a0001c0003t0001g0050 a0001c0003t0001g0051 a0001c0003t0001g0054 others(1): Show |
4 | HG01192.hp1 HG01884.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-711_209-710ins others(8): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89643065 | |||||||
| chr12:89643065 | TAC | T | 10 | a0001c0001t0001g0283 a0001c0001t0005g0116 a0001c0001t0005g0117 others(7): Show |
10 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.209-712_209-711del others(2): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89643065 | |||||||
| chr12:89643065 | TACAC | T | 27 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(24): Show |
29 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(26): Show |
intron_variant | MODIFIER | c.209-714_209-711del others(4): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89643065 | |||||||
| chr12:89643091 | C | T | 7 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0275 others(4): Show |
7 | HG00140.hp2 HG00280.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.209-736G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89643091 | |||||||
| chr12:89643093 | T | C | 9 | a0001c0001t0020g0048 a0001c0002t0001g0110 a0001c0002t0001g0111 others(6): Show |
9 | HG00639.hp1 HG01109.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.209-738A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89643093 | |||||||
| chr12:89643097 | T | C | 1 | a0001c0001t0004g0007 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.209-742A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89643097 | |||||||
| chr12:89643160 | GTATGTAT others(11): Show |
G | 1 | a0001c0002t0001g0055 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.209-823_209-806del others(18): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89643160 | |||||||
| chr12:89643178 | ATATG | A | 4 | a0001c0003t0001g0050 a0001c0003t0001g0051 a0001c0003t0001g0054 others(1): Show |
4 | HG01192.hp1 HG01884.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-827_209-824del others(4): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89643178 | |||||||
| chr12:89643279 | G | T | 1 | a0001c0001t0001g0066 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.209-924C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89643279 | |||||||
| chr12:89643283 | A | C | 1 | a0001c0001t0003g0015 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.209-928T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89643283 | |||||||
| chr12:89643286 | T | A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0203 |
2 | NA18953.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.209-931A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89643286 | |||||||
| chr12:89643464 | G | C | 1 | a0001c0004t0001g0030 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.209-1109C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89643464 | |||||||
| chr12:89643565 | C | T | 302 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(299): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.209-1210G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89643565 | |||||||
| chr12:89643729 | T | C | 2 | a0001c0001t0001g0082 a0001c0001t0001g0095 |
2 | HG00099.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.209-1374A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89643729 | |||||||
| chr12:89643808 | A | C | 3 | a0001c0004t0001g0034 a0001c0004t0001g0035 a0001c0004t0001g0119 |
3 | HG02109.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.209-1453T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89643808 | |||||||
| chr12:89644023 | G | C | 1 | a0001c0003t0001g0050 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.209-1668C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89644023 | |||||||
| chr12:89644057 | G | C | 1 | a0001c0001t0001g0141 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.209-1702C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89644057 | |||||||
| chr12:89644072 | C | A | 312 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.209-1717G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89644072 | |||||||
| chr12:89644259 | T | C | 1 | a0001c0001t0001g0266 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.209-1904A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89644259 | |||||||
| chr12:89644399 | A | T | 1 | a0001c0001t0016g0274 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.209-2044T>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89644399 | |||||||
| chr12:89644445 | A | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(34): Show |
39 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.209-2090T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89644445 | |||||||
| chr12:89644524 | T | C | 1 | a0001c0003t0001g0051 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.209-2169A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89644524 | |||||||
| chr12:89644651 | T | C | 6 | a0001c0001t0002g0122 a0001c0001t0002g0174 a0001c0001t0002g0176 others(3): Show |
6 | HG01243.hp2 HG01943.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-2296A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89644651 | |||||||
| chr12:89644777 | T | C | 312 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.209-2422A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89644777 | |||||||
| chr12:89644907 | T | C | 1 | a0001c0001t0001g0299 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.209-2552A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89644907 | |||||||
| chr12:89644942 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.209-2587C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89644942 | |||||||
| chr12:89644958 | C | T | 4 | a0001c0003t0001g0050 a0001c0003t0001g0051 a0001c0003t0001g0054 others(1): Show |
4 | HG01192.hp1 HG01884.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-2603G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89644958 | |||||||
| chr12:89645035 | T | C | 1 | a0001c0003t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.209-2680A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89645035 | |||||||
| chr12:89645058 | C | T | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | NA18950.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.209-2703G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89645058 | |||||||
| chr12:89645067 | T | G | 3 | a0001c0001t0007g0021 a0001c0001t0007g0022 a0001c0001t0007g0026 |
3 | HG02622.hp1 HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.209-2712A>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89645067 | |||||||
| chr12:89645109 | G | C | 1 | a0001c0001t0001g0263 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.209-2754C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89645109 | |||||||
| chr12:89645201 | C | G | 5 | a0001c0001t0002g0169 a0001c0001t0002g0170 a0001c0001t0002g0171 others(2): Show |
5 | HG02027.hp2 NA18612.hp1 NA19057.hp2 others(2): Show |
intron_variant | MODIFIER | c.209-2846G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89645201 | |||||||
| chr12:89645309 | T | G | 1 | a0001c0001t0004g0020 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.209-2954A>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89645309 | |||||||
| chr12:89645352 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.209-2997G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89645352 | |||||||
| chr12:89645441 | T | C | 7 | a0001c0001t0005g0319 a0001c0001t0005g0321 a0001c0001t0005g0322 others(4): Show |
7 | HG02257.hp1 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.209-3086A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89645441 | |||||||
| chr12:89645549 | C | T | 17 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(14): Show |
17 | HG00423.hp2 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.209-3194G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89645549 | |||||||
| chr12:89645625 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.209-3270T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89645625 | |||||||
| chr12:89645850 | C | A | 1 | a0001c0001t0001g0222 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.209-3495G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89645850 | |||||||
| chr12:89645934 | T | C | 1 | a0001c0001t0001g0209 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.209-3579A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89645934 | |||||||
| chr12:89645996 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.209-3641C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89645996 | |||||||
| chr12:89646095 | T | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(34): Show |
39 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.209-3740A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89646095 | |||||||
| chr12:89646107 | G | A | 125 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0102 others(122): Show |
125 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.209-3752C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89646107 | |||||||
| chr12:89646132 | G | A | 1 | a0001c0001t0003g0006 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.209-3777C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89646132 | |||||||
| chr12:89646241 | G | C | 1 | a0001c0001t0001g0094 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.209-3886C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89646241 | |||||||
| chr12:89646243 | G | A | 296 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(293): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.209-3888C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89646243 | |||||||
| chr12:89646718 | G | A | 7 | a0001c0001t0005g0319 a0001c0001t0005g0321 a0001c0001t0005g0322 others(4): Show |
7 | HG02257.hp1 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.209-4363C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89646718 | |||||||
| chr12:89646724 | T | G | 1 | a0001c0001t0001g0297 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.209-4369A>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89646724 | |||||||
| chr12:89646843 | A | T | 19 | a0001c0001t0001g0091 a0001c0002t0001g0039 a0001c0002t0001g0040 others(16): Show |
19 | HG00544.hp1 HG00738.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.209-4488T>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89646843 | |||||||
| chr12:89646996 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.209-4641T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89646996 | |||||||
| chr12:89647044 | T | G | 1 | a0001c0001t0001g0221 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.209-4689A>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89647044 | |||||||
| chr12:89647168 | C | T | 14 | a0001c0001t0001g0060 a0001c0001t0001g0079 a0001c0001t0001g0080 others(11): Show |
14 | HG02027.hp1 HG02040.hp1 NA18941.hp2 others(11): Show |
intron_variant | MODIFIER | c.209-4813G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89647168 | |||||||
| chr12:89647207 | C | T | 1 | a0001c0001t0011g0125 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.209-4852G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89647207 | |||||||
| chr12:89647230 | C | G | 296 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(293): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.209-4875G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89647230 | |||||||
| chr12:89647231 | T | A | 296 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(293): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.209-4876A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89647231 | |||||||
| chr12:89647349 | A | G | 6 | a0001c0002t0001g0110 a0001c0002t0001g0111 a0001c0002t0001g0112 others(3): Show |
6 | HG00639.hp1 HG01109.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.209-4994T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89647349 | |||||||
| chr12:89647383 | T | C | 2 | a0001c0001t0001g0224 a0001c0001t0001g0231 |
2 | NA19056.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.209-5028A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89647383 | |||||||
| chr12:89647393 | A | G | 9 | a0001c0001t0005g0116 a0001c0001t0005g0117 a0001c0001t0005g0319 others(6): Show |
9 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.209-5038T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89647393 | |||||||
| chr12:89647425 | G | A | 5 | a0001c0003t0001g0050 a0001c0003t0001g0051 a0001c0003t0001g0052 others(2): Show |
5 | HG01192.hp1 HG01884.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-5070C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89647425 | |||||||
| chr12:89647555 | C | T | 5 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(2): Show |
5 | HG02280.hp2 HG02809.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-5200G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89647555 | |||||||
| chr12:89647618 | G | T | 1 | a0001c0003t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.209-5263C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89647618 | |||||||
| chr12:89647917 | G | A | 4 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(1): Show |
4 | HG01081.hp2 HG01192.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-5562C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89647917 | |||||||
| chr12:89648006 | T | C | 305 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(302): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.209-5651A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89648006 | |||||||
| chr12:89648054 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.209-5699A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89648054 | |||||||
| chr12:89648120 | G | A | 1 | a0001c0001t0001g0268 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.209-5765C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89648120 | |||||||
| chr12:89648365 | C | G | 203 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(200): Show |
205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.209-6010G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89648365 | |||||||
| chr12:89648485 | C | G | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | NA19058.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.209-6130G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89648485 | |||||||
| chr12:89648635 | C | T | 1 | a0001c0001t0004g0007 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.209-6280G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89648635 | |||||||
| chr12:89648639 | T | C | 4 | a0001c0002t0001g0110 a0001c0002t0001g0111 a0001c0002t0001g0112 others(1): Show |
4 | HG00639.hp1 HG01109.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.209-6284A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89648639 | |||||||
| chr12:89648694 | G | C | 1 | a0001c0002t0012g0002 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.209-6339C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89648694 | |||||||
| chr12:89648728 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.209-6373C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89648728 | |||||||
| chr12:89648836 | G | C | 1 | a0001c0002t0012g0002 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.209-6481C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89648836 | |||||||
| chr12:89649067 | C | T | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG02145.hp2 HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.208+6612G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89649067 | |||||||
| chr12:89649082 | C | G | 13 | a0001c0002t0001g0039 a0001c0002t0001g0041 a0001c0002t0001g0044 others(10): Show |
13 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.208+6597G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89649082 | |||||||
| chr12:89649238 | C | T | 2 | a0001c0002t0001g0114 a0001c0002t0001g0115 |
2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.208+6441G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89649238 | |||||||
| chr12:89649247 | A | C | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG03017.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.208+6432T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89649247 | |||||||
| chr12:89649307 | T | G | 1 | a0001c0001t0001g0062 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.208+6372A>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89649307 | |||||||
| chr12:89649321 | C | T | 4 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0222 others(1): Show |
4 | HG00741.hp1 HG01257.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+6358G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89649321 | |||||||
| chr12:89649567 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.208+6112C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89649567 | |||||||
| chr12:89649602 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.208+6077A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89649602 | |||||||
| chr12:89649826 | T | C | 1 | a0001c0004t0001g0119 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.208+5853A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89649826 | |||||||
| chr12:89649902 | A | G | 13 | a0001c0002t0001g0039 a0001c0002t0001g0041 a0001c0002t0001g0044 others(10): Show |
13 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.208+5777T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89649902 | |||||||
| chr12:89650116 | T | C | 1 | a0001c0002t0012g0002 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.208+5563A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89650116 | |||||||
| chr12:89650324 | A | C | 1 | a0001c0001t0001g0029 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.208+5355T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89650324 | |||||||
| chr12:89650325 | C | A | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+5354G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89650325 | |||||||
| chr12:89650350 | A | T | 6 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(3): Show |
6 | HG02280.hp2 HG02809.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+5329T>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89650350 | |||||||
| chr12:89650599 | T | C | 1 | a0001c0001t0008g0212 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.208+5080A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89650599 | |||||||
| chr12:89650635 | G | C | 2 | a0001c0001t0005g0116 a0001c0001t0005g0117 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.208+5044C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89650635 | |||||||
| chr12:89650853 | G | C | 2 | a0001c0001t0001g0202 a0001c0001t0001g0206 |
2 | HG02155.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.208+4826C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89650853 | |||||||
| chr12:89650885 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.208+4794T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89650885 | |||||||
| chr12:89651348 | GGCGATCC others(12): Show |
G | 4 | a0001c0001t0001g0189 a0001c0001t0001g0219 a0001c0001t0008g0161 others(1): Show |
4 | HG02129.hp2 HG02132.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+4312_208+4330d others(21): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89651348 | |||||||
| chr12:89651367 | A | G | 17 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(14): Show |
17 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.208+4312T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89651367 | |||||||
| chr12:89651367 | A | T | 1 | a0001c0001t0001g0187 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.208+4312T>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89651367 | |||||||
| chr12:89651608 | A | T | 1 | a0001c0001t0004g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.208+4071T>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89651608 | |||||||
| chr12:89651653 | T | C | 3 | a0001c0001t0001g0192 a0001c0001t0001g0194 a0001c0009t0001g0220 |
3 | HG02523.hp2 NA18986.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.208+4026A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89651653 | |||||||
| chr12:89652027 | A | G | 1 | a0001c0001t0001g0327 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.208+3652T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89652027 | |||||||
| chr12:89652036 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.208+3643G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89652036 | |||||||
| chr12:89652037 | G | A | 3 | a0001c0001t0001g0104 a0001c0001t0001g0211 a0001c0001t0011g0190 |
3 | HG06807.hp2 NA18951.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.208+3642C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89652037 | |||||||
| chr12:89652081 | T | A | 1 | a0001c0001t0001g0249 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.208+3598A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89652081 | |||||||
| chr12:89652114 | TTGTGAAC others(10): Show |
T | 1 | a0001c0001t0001g0069 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.208+3548_208+3564d others(19): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89652114 | |||||||
| chr12:89652211 | G | A | 2 | a0001c0001t0006g0246 a0001c0007t0010g0232 |
2 | HG03017.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.208+3468C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89652211 | |||||||
| chr12:89652320 | TC | T | 312 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.208+3358delG | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89652320 | |||||||
| chr12:89652352 | T | C | 1 | a0001c0001t0023g0329 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.208+3327A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89652352 | |||||||
| chr12:89652589 | T | C | 1 | a0001c0001t0004g0007 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.208+3090A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89652589 | |||||||
| chr12:89652741 | G | GT | 93 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(90): Show |
93 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.208+2937dupA | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89652741 | |||||||
| chr12:89653055 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.208+2624T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89653055 | |||||||
| chr12:89653132 | C | T | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | NA18953.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.208+2547G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89653132 | |||||||
| chr12:89653217 | G | A | 312 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.208+2462C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89653217 | |||||||
| chr12:89653269 | C | T | 1 | a0001c0001t0005g0319 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.208+2410G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89653269 | |||||||
| chr12:89653273 | G | T | 1 | a0001c0001t0006g0142 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.208+2406C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89653273 | |||||||
| chr12:89653283 | CT | C | 13 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(10): Show |
14 | HG00639.hp1 HG01109.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.208+2395delA | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89653283 | |||||||
| chr12:89653283 | CTT | C | 34 | a0001c0001t0001g0036 a0001c0001t0001g0070 a0001c0001t0001g0129 others(31): Show |
34 | HG01192.hp1 HG01884.hp1 HG01934.hp1 others(31): Show |
intron_variant | MODIFIER | c.208+2394_208+2395d others(4): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89653283 | |||||||
| chr12:89653283 | CTTT | C | 264 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0037 others(261): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.208+2393_208+2395d others(5): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89653283 | |||||||
| chr12:89653320 | C | T | 18 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(15): Show |
18 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.208+2359G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89653320 | |||||||
| chr12:89653328 | C | T | 1 | a0001c0002t0001g0112 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.208+2351G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89653328 | |||||||
| chr12:89653357 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.208+2322G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89653357 | |||||||
| chr12:89653400 | T | C | 5 | a0001c0003t0001g0050 a0001c0003t0001g0051 a0001c0003t0001g0052 others(2): Show |
5 | HG01192.hp1 HG01884.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.208+2279A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89653400 | |||||||
| chr12:89653519 | G | C | 1 | a0001c0001t0001g0138 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.208+2160C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89653519 | |||||||
| chr12:89653549 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.208+2130C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89653549 | |||||||
| chr12:89653922 | G | T | 9 | a0001c0001t0005g0116 a0001c0001t0005g0117 a0001c0001t0005g0319 others(6): Show |
9 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.208+1757C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89653922 | |||||||
| chr12:89654464 | T | C | 1 | a0001c0001t0004g0007 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.208+1215A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89654464 | |||||||
| chr12:89655132 | A | G | 1 | a0001c0001t0001g0327 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.208+547T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89655132 | |||||||
| chr12:89655357 | T | C | 8 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0299 others(5): Show |
8 | HG02074.hp1 HG02080.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.208+322A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89655357 | |||||||
| chr12:89655387 | T | C | 1 | a0001c0001t0002g0053 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.208+292A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89655387 | |||||||
| chr12:89655590 | C | T | 18 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(15): Show |
18 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.208+89G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89655590 | |||||||
| chr12:89655591 | G | A | 1 | a0001c0001t0006g0217 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.208+88C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89655591 | |||||||
| chr12:89656726 | A | G | 94 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(91): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.-221-619T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89656726 | |||||||
| chr12:89656864 | T | C | 1 | a0001c0001t0001g0281 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-221-757A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89656864 | |||||||
| chr12:89656878 | G | C | 18 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(15): Show |
18 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-221-771C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89656878 | |||||||
| chr12:89656886 | T | A | 1 | a0001c0002t0001g0046 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-221-779A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89656886 | |||||||
| chr12:89656914 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-221-807T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89656914 | |||||||
| chr12:89656948 | T | C | 1 | a0001c0001t0001g0133 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-221-841A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89656948 | |||||||
| chr12:89657137 | T | G | 16 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(13): Show |
16 | NA18950.hp1 NA18951.hp2 NA18965.hp2 others(13): Show |
intron_variant | MODIFIER | c.-221-1030A>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89657137 | |||||||
| chr12:89657230 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-221-1123C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89657230 | |||||||
| chr12:89657232 | C | G | 1 | a0001c0001t0014g0014 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-221-1125G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89657232 | |||||||
| chr12:89657304 | G | T | 5 | a0001c0003t0001g0050 a0001c0003t0001g0051 a0001c0003t0001g0052 others(2): Show |
5 | HG01192.hp1 HG01884.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-221-1197C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89657304 | |||||||
| chr12:89657395 | T | C | 7 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0244 others(4): Show |
7 | HG01106.hp1 HG01168.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.-221-1288A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89657395 | |||||||
| chr12:89657680 | A | C | 1 | a0001c0001t0002g0276 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-221-1573T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89657680 | |||||||
| chr12:89657770 | G | A | 84 | a0001c0001t0001g0103 a0001c0001t0001g0108 a0001c0001t0001g0138 others(81): Show |
84 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.-221-1663C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89657770 | |||||||
| chr12:89657853 | G | A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0081 |
2 | HG02155.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.-221-1746C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89657853 | |||||||
| chr12:89657938 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-221-1831A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89657938 | |||||||
| chr12:89658432 | T | C | 9 | a0001c0001t0005g0116 a0001c0001t0005g0117 a0001c0001t0005g0319 others(6): Show |
9 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-221-2325A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89658432 | |||||||
| chr12:89658598 | G | GAGAGAGA others(6): Show |
1 | a0001c0002t0001g0047 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-221-2492_-221-249 others(17): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89658598 | |||||||
| chr12:89658598 | G | GAGAGAGA others(14): Show |
1 | a0001c0001t0001g0207 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-221-2492_-221-249 others(25): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89658598 | |||||||
| chr12:89658598 | G | GGA | 35 | a0001c0001t0001g0060 a0001c0001t0001g0076 a0001c0001t0001g0081 others(32): Show |
35 | HG00558.hp1 HG00621.hp2 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.-221-2493_-221-249 others(6): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89658598 | |||||||
| chr12:89658598 | G | GGAGA | 39 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0069 others(36): Show |
39 | HG00280.hp2 HG00642.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.-221-2495_-221-249 others(8): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89658598 | |||||||
| chr12:89658598 | G | GGAGAGA | 52 | a0001c0001t0001g0036 a0001c0001t0001g0063 a0001c0001t0001g0065 others(49): Show |
52 | HG00099.hp1 HG00621.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.-221-2497_-221-249 others(10): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89658598 | |||||||
| chr12:89658598 | G | GGAGAGAG others(1): Show |
37 | a0001c0001t0001g0037 a0001c0001t0001g0066 a0001c0001t0001g0073 others(34): Show |
37 | HG00099.hp2 HG00639.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.-221-2499_-221-249 others(12): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89658598 | |||||||
| chr12:89658598 | G | GGAGAGAG others(3): Show |
18 | a0001c0001t0001g0029 a0001c0001t0001g0078 a0001c0001t0001g0091 others(15): Show |
18 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(15): Show |
intron_variant | MODIFIER | c.-221-2501_-221-249 others(14): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89658598 | |||||||
| chr12:89658598 | G | GGAGAGAG others(5): Show |
11 | a0001c0001t0001g0099 a0001c0001t0001g0108 a0001c0001t0001g0127 others(8): Show |
11 | HG00597.hp1 HG01106.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.-221-2503_-221-249 others(16): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89658598 | |||||||
| chr12:89658598 | G | GGAGAGAG others(7): Show |
11 | a0001c0001t0001g0074 a0001c0001t0001g0124 a0001c0001t0001g0206 others(8): Show |
11 | HG00140.hp2 HG02015.hp1 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.-221-2505_-221-249 others(18): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89658598 | |||||||
| chr12:89658598 | G | GGAGAGAG others(9): Show |
4 | a0001c0001t0001g0164 a0001c0001t0001g0199 a0001c0001t0001g0200 others(1): Show |
4 | HG01099.hp1 HG01934.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.-221-2507_-221-249 others(20): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89658598 | |||||||
| chr12:89658598 | G | GGAGAGAG others(11): Show |
7 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0237 others(4): Show |
7 | HG01346.hp1 HG01978.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.-221-2509_-221-249 others(22): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89658598 | |||||||
| chr12:89658598 | G | GGAGAGAG others(13): Show |
5 | a0001c0001t0001g0203 a0001c0001t0001g0284 a0001c0001t0001g0304 others(2): Show |
6 | HG01884.hp2 HG02300.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-2511_-221-249 others(24): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89658598 | |||||||
| chr12:89658598 | G | GGAGAGAG others(19): Show |
1 | a0001c0001t0001g0285 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-221-2517_-221-249 others(30): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89658598 | |||||||
| chr12:89658598 | G | GGAGAGAG others(25): Show |
1 | a0001c0001t0001g0292 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-221-2523_-221-249 others(36): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89658598 | |||||||
| chr12:89658598 | GGA | G | 29 | a0001c0001t0001g0001 a0001c0001t0001g0139 a0001c0001t0001g0141 others(26): Show |
31 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.-221-2493_-221-249 others(6): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89658598 | |||||||
| chr12:89658598 | GGAGA | G | 14 | a0001c0001t0001g0097 a0001c0001t0001g0107 a0001c0001t0001g0138 others(11): Show |
14 | HG00738.hp1 HG00738.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-221-2495_-221-249 others(8): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89658598 | |||||||
| chr12:89658598 | GGAGAGA | G | 9 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0250 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.-221-2497_-221-249 others(10): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89658598 | |||||||
| chr12:89658598 | GGAGAGAG others(1): Show |
G | 4 | a0001c0001t0001g0085 a0001c0002t0001g0110 a0001c0002t0001g0111 others(1): Show |
4 | HG00639.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-221-2499_-221-249 others(12): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89658598 | |||||||
| chr12:89658598 | GGAGAGAG others(5): Show |
G | 1 | a0001c0001t0003g0006 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-221-2503_-221-249 others(16): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89658598 | |||||||
| chr12:89658598 | GGAGAGAG others(13): Show |
G | 1 | a0001c0001t0001g0314 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-221-2511_-221-249 others(24): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89658598 | |||||||
| chr12:89658639 | G | GAGAGAGA others(13): Show |
1 | a0001c0001t0001g0162 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-221-2533_-221-253 others(24): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89658639 | |||||||
| chr12:89658641 | G | GAGAGAGA others(11): Show |
1 | a0004c0008t0001g0208 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-221-2535_-221-253 others(22): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89658641 | |||||||
| chr12:89658641 | G | GAGAGAGA others(7): Show |
1 | a0001c0001t0001g0209 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-221-2535_-221-253 others(18): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89658641 | |||||||
| chr12:89658641 | G | GAGAGAGA others(3): Show |
1 | a0001c0001t0001g0082 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-221-2535_-221-253 others(14): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89658641 | |||||||
| chr12:89658649 | T | G | 4 | a0001c0001t0001g0095 a0001c0001t0001g0187 a0001c0001t0001g0288 others(1): Show |
5 | HG00099.hp1 HG01884.hp2 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.-221-2542A>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89658649 | |||||||
| chr12:89659357 | A | AAC | 34 | a0001c0001t0001g0067 a0001c0001t0001g0163 a0001c0001t0001g0165 others(31): Show |
35 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.-221-3252_-221-325 others(6): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89659357 | |||||||
| chr12:89659357 | A | AACAC | 10 | a0001c0001t0001g0078 a0001c0001t0001g0098 a0001c0001t0001g0269 others(7): Show |
10 | HG00639.hp1 HG01109.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.-221-3254_-221-325 others(8): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89659357 | |||||||
| chr12:89659357 | A | AACACAC | 84 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(81): Show |
84 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.-221-3256_-221-325 others(10): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89659357 | |||||||
| chr12:89659357 | A | AACACACA others(1): Show |
3 | a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0001g0127 |
3 | HG00408.hp2 HG01261.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-221-3258_-221-325 others(12): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89659357 | |||||||
| chr12:89659357 | A | AACACACA others(3): Show |
1 | a0001c0001t0001g0093 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-221-3260_-221-325 others(14): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89659357 | |||||||
| chr12:89659357 | AAC | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(30): Show |
35 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.-221-3252_-221-325 others(6): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89659357 | |||||||
| chr12:89659395 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-221-3288G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89659395 | |||||||
| chr12:89659578 | T | C | 305 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(302): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.-221-3471A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89659578 | |||||||
| chr12:89659704 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-221-3597G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89659704 | |||||||
| chr12:89659816 | G | A | 1 | a0001c0001t0002g0174 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-221-3709C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89659816 | |||||||
| chr12:89659908 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-221-3801G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89659908 | |||||||
| chr12:89659915 | C | CA | 21 | a0001c0001t0001g0059 a0001c0001t0001g0063 a0001c0001t0001g0075 others(18): Show |
21 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.-221-3809dupT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89659915 | |||||||
| chr12:89659931 | C | A | 3 | a0001c0001t0001g0082 a0001c0001t0001g0128 a0001c0001t0001g0221 |
3 | HG02055.hp1 HG03654.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.-221-3824G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89659931 | |||||||
| chr12:89659931 | C | CA | 12 | a0001c0001t0001g0085 a0001c0001t0001g0126 a0001c0001t0001g0129 others(9): Show |
12 | HG01433.hp2 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-221-3825dupT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89659931 | |||||||
| chr12:89659941 | C | A | 25 | a0001c0001t0001g0085 a0001c0001t0001g0124 a0001c0001t0001g0198 others(22): Show |
25 | HG00408.hp1 HG00741.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.-221-3834G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89659941 | |||||||
| chr12:89660294 | C | T | 1 | a0001c0001t0003g0006 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-221-4187G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89660294 | |||||||
| chr12:89660678 | A | C | 1 | a0001c0001t0001g0314 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-221-4571T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89660678 | |||||||
| chr12:89660684 | T | G | 2 | a0001c0002t0001g0114 a0001c0002t0001g0115 |
2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-221-4577A>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89660684 | |||||||
| chr12:89660814 | T | G | 4 | a0001c0002t0001g0110 a0001c0002t0001g0111 a0001c0002t0001g0112 others(1): Show |
4 | HG00639.hp1 HG01109.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-221-4707A>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89660814 | |||||||
| chr12:89660842 | T | C | 70 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0066 others(67): Show |
70 | HG00099.hp1 HG00642.hp1 HG01167.hp1 others(67): Show |
intron_variant | MODIFIER | c.-221-4735A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89660842 | |||||||
| chr12:89661239 | C | T | 1 | a0001c0002t0012g0002 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-221-5132G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89661239 | |||||||
| chr12:89661330 | A | C | 1 | a0001c0003t0001g0050 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-221-5223T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89661330 | |||||||
| chr12:89661369 | A | T | 1 | a0001c0005t0001g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-221-5262T>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89661369 | |||||||
| chr12:89661379 | T | G | 21 | a0001c0001t0001g0001 a0001c0001t0001g0277 a0001c0001t0001g0278 others(18): Show |
23 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.-221-5272A>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89661379 | |||||||
| chr12:89661500 | T | G | 7 | a0001c0001t0001g0094 a0001c0001t0001g0099 a0001c0001t0001g0100 others(4): Show |
7 | HG00558.hp2 NA18955.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.-221-5393A>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89661500 | |||||||
| chr12:89661718 | G | C | 8 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(5): Show |
8 | HG02109.hp1 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-221-5611C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89661718 | |||||||
| chr12:89662010 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-221-5903A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89662010 | |||||||
| chr12:89662052 | C | A | 9 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 others(6): Show |
9 | HG02015.hp2 HG02080.hp1 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.-221-5945G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89662052 | |||||||
| chr12:89662093 | C | A | 1 | a0001c0001t0003g0010 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-221-5986G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89662093 | |||||||
| chr12:89662137 | C | CT | 8 | a0001c0001t0005g0116 a0001c0001t0005g0117 a0001c0001t0005g0319 others(5): Show |
8 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.-221-6031dupA | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89662137 | |||||||
| chr12:89662137 | CT | C | 12 | a0001c0001t0001g0080 a0001c0001t0001g0121 a0001c0001t0001g0133 others(9): Show |
12 | HG01192.hp1 HG01256.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.-221-6031delA | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89662137 | |||||||
| chr12:89662318 | T | C | 2 | a0001c0002t0001g0114 a0001c0002t0001g0115 |
2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-221-6211A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89662318 | |||||||
| chr12:89662349 | A | G | 302 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(299): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.-221-6242T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89662349 | |||||||
| chr12:89662391 | A | G | 1 | a0001c0004t0001g0119 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-221-6284T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89662391 | |||||||
| chr12:89662451 | A | G | 1 | a0004c0008t0001g0208 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-221-6344T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89662451 | |||||||
| chr12:89662457 | T | C | 6 | a0001c0002t0001g0110 a0001c0002t0001g0111 a0001c0002t0001g0112 others(3): Show |
6 | HG00639.hp1 HG01109.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-6350A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89662457 | |||||||
| chr12:89662464 | G | A | 6 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(3): Show |
6 | HG02280.hp2 HG02809.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-221-6357C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89662464 | |||||||
| chr12:89662916 | G | T | 7 | a0001c0001t0005g0319 a0001c0001t0005g0321 a0001c0001t0005g0322 others(4): Show |
7 | HG02257.hp1 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-221-6809C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89662916 | |||||||
| chr12:89663071 | T | C | 1 | a0001c0004t0001g0035 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-221-6964A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89663071 | |||||||
| chr12:89663442 | A | G | 1 | a0001c0001t0011g0190 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-221-7335T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89663442 | |||||||
| chr12:89663475 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-221-7368G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89663475 | |||||||
| chr12:89663513 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-221-7406T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89663513 | |||||||
| chr12:89663525 | G | A | 1 | a0001c0001t0002g0179 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-221-7418C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89663525 | |||||||
| chr12:89663655 | C | G | 2 | a0001c0001t0001g0120 a0001c0001t0001g0191 |
2 | HG01346.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-221-7548G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89663655 | |||||||
| chr12:89663687 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-221-7580C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89663687 | |||||||
| chr12:89663704 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-221-7597T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89663704 | |||||||
| chr12:89663884 | C | CTGTT | 319 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(316): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.-221-7778_-221-777 others(8): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89663884 | |||||||
| chr12:89664052 | T | C | 1 | a0001c0001t0001g0242 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-221-7945A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89664052 | |||||||
| chr12:89664318 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-221-8211G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89664318 | |||||||
| chr12:89664463 | T | G | 1 | a0001c0001t0001g0138 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-221-8356A>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89664463 | |||||||
| chr12:89664851 | C | CT | 36 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(33): Show |
38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-221-8745dupA | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89664851 | |||||||
| chr12:89664945 | C | T | 5 | a0001c0003t0001g0050 a0001c0003t0001g0051 a0001c0003t0001g0052 others(2): Show |
5 | HG01192.hp1 HG01884.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-221-8838G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89664945 | |||||||
| chr12:89665065 | G | A | 94 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(91): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.-221-8958C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89665065 | |||||||
| chr12:89665071 | T | C | 296 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(293): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-221-8964A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89665071 | |||||||
| chr12:89665124 | C | T | 1 | a0001c0001t0020g0048 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-221-9017G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89665124 | |||||||
| chr12:89665956 | C | T | 3 | a0001c0001t0001g0157 a0001c0001t0001g0218 a0001c0001t0001g0273 |
3 | HG02602.hp2 HG03239.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-221-9849G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89665956 | |||||||
| chr12:89666173 | T | C | 1 | a0001c0001t0014g0014 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-221-10066A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89666173 | |||||||
| chr12:89666222 | CA | C | 6 | a0001c0002t0001g0110 a0001c0002t0001g0111 a0001c0002t0001g0112 others(3): Show |
6 | HG00639.hp1 HG01109.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-10116delT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89666222 | |||||||
| chr12:89666318 | C | T | 8 | a0001c0001t0001g0121 a0001c0001t0001g0127 a0001c0001t0001g0150 others(5): Show |
8 | HG00642.hp1 HG01256.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.-221-10211G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89666318 | |||||||
| chr12:89666414 | A | G | 4 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0098 others(1): Show |
4 | HG00544.hp1 HG01081.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.-221-10307T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89666414 | |||||||
| chr12:89666560 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-221-10453G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89666560 | |||||||
| chr12:89666570 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-221-10463C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89666570 | |||||||
| chr12:89666745 | G | A | 1 | a0001c0002t0012g0002 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-221-10638C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89666745 | |||||||
| chr12:89666809 | G | A | 95 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(92): Show |
95 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.-221-10702C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89666809 | |||||||
| chr12:89666956 | C | A | 2 | a0001c0001t0001g0277 a0001c0001t0016g0274 |
2 | HG00735.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.-221-10849G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89666956 | |||||||
| chr12:89667038 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-221-10931T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89667038 | |||||||
| chr12:89667407 | C | A | 1 | a0001c0001t0001g0102 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-221-11300G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89667407 | |||||||
| chr12:89667452 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-221-11345A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89667452 | |||||||
| chr12:89667748 | A | T | 1 | a0001c0002t0012g0002 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-221-11641T>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89667748 | |||||||
| chr12:89667782 | G | A | 17 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(14): Show |
17 | HG00423.hp2 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.-221-11675C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89667782 | |||||||
| chr12:89668089 | T | C | 3 | a0001c0001t0007g0021 a0001c0001t0007g0022 a0001c0001t0007g0026 |
3 | HG02622.hp1 HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-221-11982A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89668089 | |||||||
| chr12:89668337 | A | T | 6 | a0001c0002t0001g0110 a0001c0002t0001g0111 a0001c0002t0001g0112 others(3): Show |
6 | HG00639.hp1 HG01109.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-12230T>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89668337 | |||||||
| chr12:89668599 | G | A | 95 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(92): Show |
95 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.-221-12492C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89668599 | |||||||
| chr12:89668696 | C | T | 6 | a0001c0002t0001g0110 a0001c0002t0001g0111 a0001c0002t0001g0112 others(3): Show |
6 | HG00639.hp1 HG01109.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-12589G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89668696 | |||||||
| chr12:89668718 | A | G | 7 | a0001c0002t0001g0040 a0001c0002t0015g0042 a0001c0003t0001g0050 others(4): Show |
7 | HG01192.hp1 HG01884.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-221-12611T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89668718 | |||||||
| chr12:89668773 | T | C | 1 | a0001c0001t0006g0246 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-221-12666A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89668773 | |||||||
| chr12:89668885 | A | G | 34 | a0001c0001t0001g0103 a0001c0001t0001g0108 a0001c0001t0001g0181 others(31): Show |
34 | HG00140.hp2 HG00280.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.-221-12778T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89668885 | |||||||
| chr12:89669037 | A | AACACACT others(25): Show |
1 | a0001c0001t0011g0190 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-221-12962_-221-12 others(38): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89669037 | |||||||
| chr12:89669149 | T | C | 1 | a0001c0002t0012g0002 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-221-13042A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89669149 | |||||||
| chr12:89669178 | T | C | 1 | a0001c0002t0012g0002 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-221-13071A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89669178 | |||||||
| chr12:89669333 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-221-13226C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89669333 | |||||||
| chr12:89669383 | CA | C | 3 | a0001c0001t0002g0123 a0001c0001t0002g0175 a0001c0001t0002g0184 |
3 | NA18941.hp1 NA19056.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-221-13277delT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89669383 | |||||||
| chr12:89669549 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-221-13442C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89669549 | |||||||
| chr12:89669551 | A | C | 1 | a0001c0001t0020g0048 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-221-13444T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89669551 | |||||||
| chr12:89669616 | T | C | 1 | a0001c0002t0001g0137 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-221-13509A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89669616 | |||||||
| chr12:89669751 | A | C | 2 | a0001c0001t0005g0325 a0001c0001t0005g0326 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-221-13644T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89669751 | |||||||
| chr12:89670294 | C | T | 1 | a0001c0001t0003g0006 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-221-14187G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89670294 | |||||||
| chr12:89670295 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-221-14188C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89670295 | |||||||
| chr12:89670308 | T | C | 18 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(15): Show |
18 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-221-14201A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89670308 | |||||||
| chr12:89670371 | A | AT | 177 | a0001c0001t0001g0063 a0001c0001t0001g0102 a0001c0001t0001g0103 others(174): Show |
177 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.-221-14265dupA | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89670371 | |||||||
| chr12:89670477 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-221-14370G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89670477 | |||||||
| chr12:89670631 | G | T | 1 | a0001c0002t0012g0002 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-221-14524C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89670631 | |||||||
| chr12:89670743 | C | CA | 6 | a0001c0002t0001g0110 a0001c0002t0001g0111 a0001c0002t0001g0112 others(3): Show |
6 | HG00639.hp1 HG01109.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-14637dupT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89670743 | |||||||
| chr12:89670827 | T | G | 311 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(308): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.-221-14720A>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89670827 | |||||||
| chr12:89670833 | T | C | 1 | a0001c0002t0012g0002 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-221-14726A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89670833 | |||||||
| chr12:89670929 | A | G | 3 | a0001c0001t0001g0157 a0001c0001t0001g0218 a0001c0001t0001g0273 |
3 | HG02602.hp2 HG03239.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-221-14822T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89670929 | |||||||
| chr12:89670952 | T | TA | 296 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(293): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-221-14846dupT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89670952 | |||||||
| chr12:89670952 | T | TAA | 9 | a0001c0001t0001g0128 a0001c0001t0001g0143 a0001c0001t0001g0187 others(6): Show |
9 | HG01346.hp1 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.-221-14847_-221-14 others(8): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89670952 | |||||||
| chr12:89670973 | G | T | 1 | a0001c0001t0001g0263 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-221-14866C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89670973 | |||||||
| chr12:89671005 | T | A | 1 | a0001c0001t0001g0139 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-221-14898A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89671005 | |||||||
| chr12:89671205 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-221-15098G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89671205 | |||||||
| chr12:89671312 | G | C | 1 | a0001c0001t0001g0140 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-221-15205C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89671312 | |||||||
| chr12:89671468 | T | C | 1 | a0001c0001t0003g0015 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-221-15361A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89671468 | |||||||
| chr12:89671517 | C | T | 1 | a0001c0001t0005g0325 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-221-15410G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89671517 | |||||||
| chr12:89671522 | C | T | 1 | a0001c0001t0003g0006 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-221-15415G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89671522 | |||||||
| chr12:89671527 | A | G | 305 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(302): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.-221-15420T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89671527 | |||||||
| chr12:89671598 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-221-15491G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89671598 | |||||||
| chr12:89671696 | C | A | 2 | a0001c0002t0001g0114 a0001c0002t0001g0115 |
2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-221-15589G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89671696 | |||||||
| chr12:89671771 | G | GT | 115 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(112): Show |
116 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.-221-15665dupA | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89671771 | |||||||
| chr12:89671771 | G | GTT | 160 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(157): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.-221-15666_-221-15 others(8): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89671771 | |||||||
| chr12:89671771 | G | GTTT | 22 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0213 others(19): Show |
22 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.-221-15667_-221-15 others(9): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89671771 | |||||||
| chr12:89672130 | A | G | 2 | a0001c0001t0005g0116 a0001c0001t0005g0117 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-221-16023T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89672130 | |||||||
| chr12:89672150 | T | C | 2 | a0001c0001t0001g0308 a0001c0001t0001g0309 |
2 | HG02015.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-221-16043A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89672150 | |||||||
| chr12:89672160 | A | G | 9 | a0001c0001t0005g0116 a0001c0001t0005g0117 a0001c0001t0005g0319 others(6): Show |
9 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-221-16053T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89672160 | |||||||
| chr12:89672370 | C | T | 1 | a0001c0001t0003g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-221-16263G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89672370 | |||||||
| chr12:89672511 | T | C | 2 | a0001c0001t0001g0188 a0001c0001t0001g0313 |
2 | NA18943.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.-221-16404A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89672511 | |||||||
| chr12:89672558 | C | T | 271 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(268): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.-221-16451G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89672558 | |||||||
| chr12:89672633 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-221-16526G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89672633 | |||||||
| chr12:89673084 | T | G | 1 | a0001c0001t0006g0246 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-221-16977A>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89673084 | |||||||
| chr12:89673230 | G | T | 6 | a0001c0001t0005g0319 a0001c0001t0005g0321 a0001c0001t0005g0322 others(3): Show |
6 | HG02257.hp1 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-17123C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89673230 | |||||||
| chr12:89673644 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-221-17537C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89673644 | |||||||
| chr12:89673723 | C | T | 4 | a0001c0001t0001g0103 a0001c0001t0001g0108 a0001c0001t0009g0012 others(1): Show |
4 | HG00735.hp2 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.-221-17616G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89673723 | |||||||
| chr12:89673811 | G | C | 5 | a0001c0003t0001g0050 a0001c0003t0001g0051 a0001c0003t0001g0052 others(2): Show |
5 | HG01192.hp1 HG01884.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-221-17704C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89673811 | |||||||
| chr12:89673999 | G | A | 2 | a0001c0001t0005g0116 a0001c0001t0005g0117 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-221-17892C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89673999 | |||||||
| chr12:89674069 | T | C | 4 | a0001c0002t0001g0110 a0001c0002t0001g0111 a0001c0002t0001g0112 others(1): Show |
4 | HG00639.hp1 HG01109.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-221-17962A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89674069 | |||||||
| chr12:89674105 | G | C | 1 | a0001c0001t0002g0243 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-221-17998C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89674105 | |||||||
| chr12:89674161 | T | C | 18 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(15): Show |
18 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-221-18054A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89674161 | |||||||
| chr12:89674570 | C | G | 6 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(3): Show |
6 | HG02280.hp2 HG02809.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-221-18463G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89674570 | |||||||
| chr12:89674578 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-221-18471C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89674578 | |||||||
| chr12:89674591 | T | C | 1 | a0001c0001t0001g0327 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-221-18484A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89674591 | |||||||
| chr12:89674647 | A | G | 5 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(2): Show |
5 | HG02280.hp2 HG02809.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-221-18540T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89674647 | |||||||
| chr12:89674675 | T | C | 1 | a0001c0001t0014g0014 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-221-18568A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89674675 | |||||||
| chr12:89674860 | C | A | 2 | a0001c0001t0004g0008 a0001c0001t0004g0024 |
2 | HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-221-18753G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89674860 | |||||||
| chr12:89675194 | A | G | 18 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(15): Show |
18 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-221-19087T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89675194 | |||||||
| chr12:89675272 | A | G | 1 | a0001c0001t0004g0004 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-221-19165T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89675272 | |||||||
| chr12:89675319 | T | A | 1 | a0001c0001t0001g0068 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-221-19212A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89675319 | |||||||
| chr12:89675476 | T | C | 296 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(293): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-221-19369A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89675476 | |||||||
| chr12:89675499 | T | G | 94 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(91): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.-221-19392A>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89675499 | |||||||
| chr12:89675532 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-221-19425C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89675532 | |||||||
| chr12:89675553 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-221-19446T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89675553 | |||||||
| chr12:89675622 | T | C | 1 | a0001c0001t0003g0006 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-221-19515A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89675622 | |||||||
| chr12:89675768 | T | C | 2 | a0001c0001t0001g0090 a0001c0001t0001g0105 |
2 | HG01081.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.-221-19661A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89675768 | |||||||
| chr12:89675785 | A | G | 1 | a0001c0001t0020g0048 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-221-19678T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89675785 | |||||||
| chr12:89675858 | G | T | 2 | a0001c0001t0003g0005 a0001c0001t0003g0011 |
2 | HG02895.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-221-19751C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89675858 | |||||||
| chr12:89676261 | C | T | 270 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(267): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.-221-20154G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89676261 | |||||||
| chr12:89676324 | G | C | 1 | a0001c0001t0001g0241 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-221-20217C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89676324 | |||||||
| chr12:89676743 | C | A | 296 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(293): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-221-20636G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89676743 | |||||||
| chr12:89676854 | T | A | 1 | a0001c0001t0001g0093 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-221-20747A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89676854 | |||||||
| chr12:89677030 | A | G | 1 | a0001c0001t0001g0317 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-221-20923T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677030 | |||||||
| chr12:89677042 | CAAAG | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(172): Show |
177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.-221-20939_-221-20 others(10): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677042 | |||||||
| chr12:89677046 | G | C | 1 | a0001c0002t0001g0043 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-221-20939C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677046 | |||||||
| chr12:89677115 | C | T | 2 | a0001c0001t0001g0304 a0001c0001t0001g0305 |
2 | HG02293.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.-221-21008G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677115 | |||||||
| chr12:89677132 | T | C | 5 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(2): Show |
5 | HG02280.hp2 HG02809.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-221-21025A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677132 | |||||||
| chr12:89677470 | T | C | 1 | a0001c0001t0001g0273 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-221-21363A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677470 | |||||||
| chr12:89677476 | A | C | 1 | a0001c0001t0001g0187 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-221-21369T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677476 | |||||||
| chr12:89677638 | A | G | 1 | a0001c0003t0021g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-221-21531T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677638 | |||||||
| chr12:89677954 | T | TTATATAT others(3): Show |
1 | a0001c0007t0010g0232 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-221-21857_-221-21 others(16): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677954 | |||||||
| chr12:89677954 | T | TTATATAT others(5): Show |
1 | a0001c0002t0001g0111 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-221-21859_-221-21 others(18): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677954 | |||||||
| chr12:89677954 | T | TTATATAT others(7): Show |
2 | a0001c0002t0001g0113 a0001c0003t0021g0049 |
2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-221-21861_-221-21 others(20): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677954 | |||||||
| chr12:89677954 | T | TTATATAT others(13): Show |
1 | a0001c0002t0001g0110 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-221-21848_-221-21 others(26): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677954 | |||||||
| chr12:89677954 | T | TTATATAT others(15): Show |
1 | a0001c0002t0001g0112 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-221-21848_-221-21 others(28): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677954 | |||||||
| chr12:89677954 | T | TTATATAT others(25): Show |
1 | a0001c0007t0010g0135 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-221-21848_-221-21 others(38): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677954 | |||||||
| chr12:89677954 | T | TTATATAT others(87): Show |
1 | a0001c0001t0005g0116 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-221-21848_-221-21 others(100): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677954 | |||||||
| chr12:89677954 | T | TTATATAT others(7): Show |
32 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(29): Show |
32 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.-221-21848_-221-21 others(20): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677954 | |||||||
| chr12:89677954 | T | TTATATAT others(9): Show |
5 | a0001c0001t0001g0075 a0001c0001t0001g0085 a0001c0001t0001g0087 others(2): Show |
5 | HG03017.hp2 HG03195.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.-221-21848_-221-21 others(22): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677954 | |||||||
| chr12:89677954 | T | TTATATAT others(11): Show |
4 | a0001c0001t0001g0069 a0001c0001t0020g0048 a0001c0002t0001g0114 others(1): Show |
4 | HG01167.hp1 HG02559.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.-221-21848_-221-21 others(24): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677954 | |||||||
| chr12:89677954 | T | TTATATAT others(13): Show |
15 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0070 others(12): Show |
15 | HG02976.hp2 HG03540.hp1 HG03654.hp2 others(12): Show |
intron_variant | MODIFIER | c.-221-21848_-221-21 others(26): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677954 | |||||||
| chr12:89677954 | T | TTATATAT others(15): Show |
4 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0006g0056 others(1): Show |
4 | HG03041.hp2 NA18950.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.-221-21848_-221-21 others(28): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677954 | |||||||
| chr12:89677954 | T | TTATATAT others(17): Show |
6 | a0001c0001t0001g0077 a0001c0002t0001g0136 a0001c0002t0001g0137 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.-221-21848_-221-21 others(30): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677954 | |||||||
| chr12:89677954 | T | TTATATAT others(19): Show |
7 | a0001c0002t0001g0039 a0001c0002t0001g0041 a0001c0002t0001g0044 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.-221-21848_-221-21 others(32): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677954 | |||||||
| chr12:89677954 | T | TTATATAT others(21): Show |
1 | a0001c0002t0001g0045 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-221-21848_-221-21 others(34): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677954 | |||||||
| chr12:89677954 | T | TTATATAT others(91): Show |
1 | a0001c0001t0005g0326 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-221-21848_-221-21 others(104): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677954 | |||||||
| chr12:89677954 | T | TTATATAT others(87): Show |
1 | a0001c0001t0005g0321 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-221-21848_-221-21 others(100): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677954 | |||||||
| chr12:89677954 | T | TTATATAT others(63): Show |
1 | a0001c0001t0001g0150 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-221-21848_-221-21 others(76): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677954 | |||||||
| chr12:89677954 | T | TTATATAT others(65): Show |
1 | a0001c0001t0001g0065 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-221-21848_-221-21 others(78): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677954 | |||||||
| chr12:89677954 | T | TTATATAT others(35): Show |
1 | a0001c0001t0001g0311 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-221-21848_-221-21 others(48): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677954 | |||||||
| chr12:89677954 | T | TTATATAT others(33): Show |
2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG01361.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-221-21848_-221-21 others(46): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677954 | |||||||
| chr12:89677954 | TTA | T | 24 | a0001c0001t0001g0063 a0001c0001t0001g0143 a0001c0001t0001g0144 others(21): Show |
24 | HG00140.hp2 HG00621.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.-221-21849_-221-21 others(8): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677954 | |||||||
| chr12:89677954 | TTATA | T | 31 | a0001c0001t0001g0102 a0001c0001t0001g0128 a0001c0001t0001g0129 others(28): Show |
31 | HG00408.hp1 HG00597.hp1 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.-221-21851_-221-21 others(10): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677954 | |||||||
| chr12:89677954 | TTATATA | T | 20 | a0001c0001t0001g0124 a0001c0001t0001g0145 a0001c0001t0001g0163 others(17): Show |
20 | HG01099.hp1 HG02027.hp2 HG02155.hp2 others(17): Show |
intron_variant | MODIFIER | c.-221-21853_-221-21 others(12): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677954 | |||||||
| chr12:89677956 | A | ATATATAT others(5): Show |
19 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0066 others(16): Show |
19 | HG00408.hp2 HG00423.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-221-21850_-221-21 others(18): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677956 | |||||||
| chr12:89677958 | A | ATATATAT others(3): Show |
10 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0097 others(7): Show |
10 | HG00558.hp2 HG00642.hp2 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.-221-21852_-221-21 others(16): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677958 | |||||||
| chr12:89677958 | A | ATATATAT others(29): Show |
1 | a0001c0001t0001g0121 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-221-21852_-221-21 others(42): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677958 | |||||||
| chr12:89677960 | A | ATATATAT others(1): Show |
3 | a0001c0001t0001g0076 a0001c0001t0001g0089 a0001c0006t0001g0032 |
3 | HG02071.hp1 HG02723.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.-221-21854_-221-21 others(14): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677960 | |||||||
| chr12:89677963 | TATATATA others(5): Show |
T | 1 | a0001c0001t0001g0264 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-221-21868_-221-21 others(18): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677963 | |||||||
| chr12:89677963 | TATATATA others(9): Show |
T | 2 | a0001c0001t0001g0245 a0001c0001t0001g0307 |
2 | HG01106.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.-221-21872_-221-21 others(22): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677963 | |||||||
| chr12:89677965 | T | C | 4 | a0001c0001t0001g0193 a0001c0001t0001g0204 a0001c0001t0001g0294 others(1): Show |
4 | HG03704.hp1 HG03704.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-221-21858A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677965 | |||||||
| chr12:89677965 | T | TAC | 5 | a0001c0001t0001g0064 a0001c0001t0001g0164 a0001c0001t0001g0195 others(2): Show |
5 | HG02071.hp2 HG02809.hp1 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-221-21859_-221-21 others(8): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677965 | |||||||
| chr12:89677965 | T | TACAC | 3 | a0001c0001t0001g0133 a0001c0001t0008g0212 a0001c0001t0019g0197 |
3 | HG00544.hp2 HG03831.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.-221-21859_-221-21 others(10): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677965 | |||||||
| chr12:89677965 | T | TACACAC | 5 | a0001c0001t0001g0126 a0001c0001t0001g0185 a0001c0001t0001g0192 others(2): Show |
5 | NA18747.hp1 NA18998.hp1 NA19068.hp2 others(2): Show |
intron_variant | MODIFIER | c.-221-21859_-221-21 others(12): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677965 | |||||||
| chr12:89677965 | TATATATA others(1): Show |
T | 8 | a0001c0001t0001g0225 a0001c0001t0001g0227 a0001c0001t0002g0122 others(5): Show |
8 | HG00558.hp1 HG00621.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.-221-21866_-221-21 others(14): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677965 | |||||||
| chr12:89677965 | TATATATA others(3): Show |
T | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | NA18972.hp2 NA19058.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-221-21868_-221-21 others(16): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677965 | |||||||
| chr12:89677965 | TATATATA others(7): Show |
T | 3 | a0001c0001t0001g0187 a0001c0001t0001g0248 a0001c0001t0001g0249 |
3 | HG01070.hp2 HG01071.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-221-21872_-221-21 others(20): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677965 | |||||||
| chr12:89677965 | TATATATA others(9): Show |
T | 18 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(15): Show |
18 | HG00423.hp2 HG01099.hp2 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.-221-21874_-221-21 others(22): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677965 | |||||||
| chr12:89677965 | TATATATA others(13): Show |
T | 1 | a0001c0001t0001g0180 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-221-21878_-221-21 others(26): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677965 | |||||||
| chr12:89677965 | TATATATA others(17): Show |
T | 4 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(1): Show |
4 | HG01081.hp2 HG01192.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.-221-21882_-221-21 others(30): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677965 | |||||||
| chr12:89677967 | T | C | 30 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0103 others(27): Show |
30 | HG00544.hp2 HG00621.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.-221-21860A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677967 | |||||||
| chr12:89677967 | TATATAC | T | 5 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(2): Show |
5 | HG02280.hp2 HG02809.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-221-21866_-221-21 others(12): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677967 | |||||||
| chr12:89677967 | TATATACA others(1): Show |
T | 22 | a0001c0001t0001g0029 a0001c0001t0001g0036 a0001c0001t0001g0037 others(19): Show |
22 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.-221-21868_-221-21 others(14): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677967 | |||||||
| chr12:89677967 | TATATACA others(5): Show |
T | 1 | a0001c0001t0002g0276 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-221-21872_-221-21 others(18): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677967 | |||||||
| chr12:89677968 | A | G | 9 | a0001c0001t0005g0319 a0001c0001t0005g0322 a0001c0001t0005g0323 others(6): Show |
9 | HG00738.hp1 HG01109.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-221-21861T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677968 | |||||||
| chr12:89677969 | T | C | 53 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0102 others(50): Show |
53 | HG00140.hp2 HG00544.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.-221-21862A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677969 | |||||||
| chr12:89677969 | TATACACA others(1): Show |
T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0238 a0001c0001t0001g0289 others(1): Show |
5 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-221-21870_-221-21 others(14): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677969 | |||||||
| chr12:89677971 | T | C | 91 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0102 others(88): Show |
91 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.-221-21864A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677971 | |||||||
| chr12:89677971 | T | TACACAC | 7 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0017 others(4): Show |
7 | HG02559.hp2 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-221-21870_-221-21 others(12): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677971 | |||||||
| chr12:89677971 | T | TACACACA others(1): Show |
4 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0006g0246 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-221-21872_-221-21 others(14): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677971 | |||||||
| chr12:89677971 | T | TATATACA others(5): Show |
1 | a0001c0001t0006g0142 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-221-21865_-221-21 others(18): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677971 | |||||||
| chr12:89677971 | T | TATATATA others(7): Show |
1 | a0001c0003t0001g0054 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-221-21865_-221-21 others(20): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677971 | |||||||
| chr12:89677971 | T | TATATATA others(7): Show |
1 | a0001c0003t0001g0051 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-221-21865_-221-21 others(20): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677971 | |||||||
| chr12:89677971 | T | TATATATA others(9): Show |
1 | a0001c0003t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-221-21865_-221-21 others(22): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677971 | |||||||
| chr12:89677971 | T | TATATATA others(13): Show |
1 | a0001c0002t0012g0002 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-221-21865_-221-21 others(26): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677971 | |||||||
| chr12:89677971 | T | TATATATA others(19): Show |
1 | a0001c0002t0001g0043 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-221-21865_-221-21 others(32): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677971 | |||||||
| chr12:89677971 | T | TATATATA others(21): Show |
1 | a0001c0002t0015g0042 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-221-21865_-221-21 others(34): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677971 | |||||||
| chr12:89677971 | T | TATATATA others(23): Show |
2 | a0001c0002t0001g0040 a0001c0002t0001g0046 |
2 | HG01109.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-221-21865_-221-21 others(36): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677971 | |||||||
| chr12:89677971 | T | TATATATA others(123): Show |
1 | a0001c0001t0005g0322 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-221-21865_-221-21 others(136): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677971 | |||||||
| chr12:89677971 | T | TATATATA others(93): Show |
1 | a0001c0001t0005g0323 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-221-21865_-221-21 others(106): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677971 | |||||||
| chr12:89677971 | T | TATATATA others(65): Show |
1 | a0001c0001t0005g0325 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-221-21865_-221-21 others(78): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677971 | |||||||
| chr12:89677971 | T | TATATATA others(85): Show |
1 | a0001c0001t0005g0319 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-221-21865_-221-21 others(98): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677971 | |||||||
| chr12:89677971 | T | TATATATA others(113): Show |
1 | a0001c0001t0005g0324 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-221-21865_-221-21 others(126): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677971 | |||||||
| chr12:89677971 | T | TATATATA others(79): Show |
1 | a0001c0001t0005g0117 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-221-21865_-221-21 others(92): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677971 | |||||||
| chr12:89677973 | C | T | 102 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(99): Show |
102 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.-221-21866G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677973 | |||||||
| chr12:89677975 | C | T | 99 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(96): Show |
99 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.-221-21868G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677975 | |||||||
| chr12:89677977 | C | T | 97 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(94): Show |
97 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.-221-21870G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677977 | |||||||
| chr12:89677979 | C | T | 94 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(91): Show |
94 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.-221-21872G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677979 | |||||||
| chr12:89677981 | C | T | 93 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(90): Show |
93 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.-221-21874G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677981 | |||||||
| chr12:89677983 | C | T | 85 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(82): Show |
85 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.-221-21876G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677983 | |||||||
| chr12:89677985 | C | T | 26 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(23): Show |
26 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.-221-21878G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677985 | |||||||
| chr12:89677987 | C | T | 4 | a0001c0001t0001g0097 a0001c0001t0001g0317 a0001c0007t0010g0135 others(1): Show |
4 | HG02735.hp2 HG03098.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-221-21880G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677987 | |||||||
| chr12:89677989 | C | T | 3 | a0001c0001t0001g0097 a0001c0007t0010g0135 a0001c0007t0010g0232 |
3 | HG02735.hp2 HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-221-21882G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677989 | |||||||
| chr12:89677991 | C | T | 2 | a0001c0007t0010g0135 a0001c0007t0010g0232 |
2 | HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-221-21884G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677991 | |||||||
| chr12:89677993 | C | T | 2 | a0001c0007t0010g0135 a0001c0007t0010g0232 |
2 | HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-221-21886G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677993 | |||||||
| chr12:89677995 | C | T | 1 | a0001c0007t0010g0135 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-221-21888G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89677995 | |||||||
| chr12:89678017 | C | T | 1 | a0001c0004t0001g0031 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-221-21910G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89678017 | |||||||
| chr12:89678019 | T | C | 6 | a0001c0002t0001g0110 a0001c0002t0001g0111 a0001c0002t0001g0112 others(3): Show |
6 | HG00639.hp1 HG01109.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-21912A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89678019 | |||||||
| chr12:89678021 | T | C | 1 | a0001c0007t0010g0135 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-221-21914A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89678021 | |||||||
| chr12:89678238 | G | A | 296 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(293): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-221-22131C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89678238 | |||||||
| chr12:89678299 | G | A | 95 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(92): Show |
95 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.-221-22192C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89678299 | |||||||
| chr12:89678379 | G | T | 2 | a0001c0002t0001g0114 a0001c0002t0001g0115 |
2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-221-22272C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89678379 | |||||||
| chr12:89678477 | C | A | 1 | a0001c0001t0002g0053 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-221-22370G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89678477 | |||||||
| chr12:89678667 | A | T | 2 | a0001c0002t0001g0114 a0001c0002t0001g0115 |
2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-221-22560T>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89678667 | |||||||
| chr12:89678685 | A | G | 1 | a0001c0001t0004g0007 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-221-22578T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89678685 | |||||||
| chr12:89679129 | A | G | 9 | a0001c0001t0005g0116 a0001c0001t0005g0117 a0001c0001t0005g0319 others(6): Show |
9 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-221-23022T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89679129 | |||||||
| chr12:89679198 | C | T | 8 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(5): Show |
8 | HG02109.hp1 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-221-23091G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89679198 | |||||||
| chr12:89679200 | G | C | 1 | a0001c0001t0001g0263 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-221-23093C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89679200 | |||||||
| chr12:89679524 | C | T | 26 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(23): Show |
26 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.-221-23417G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89679524 | |||||||
| chr12:89679566 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-221-23459C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89679566 | |||||||
| chr12:89679782 | C | T | 7 | a0001c0001t0005g0319 a0001c0001t0005g0321 a0001c0001t0005g0322 others(4): Show |
7 | HG02257.hp1 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-221-23675G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89679782 | |||||||
| chr12:89679808 | T | C | 305 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(302): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.-221-23701A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89679808 | |||||||
| chr12:89680115 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-221-24008T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89680115 | |||||||
| chr12:89680215 | A | C | 3 | a0001c0001t0001g0189 a0001c0001t0008g0161 a0001c0001t0008g0210 |
3 | HG02132.hp2 NA19066.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.-221-24108T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89680215 | |||||||
| chr12:89680229 | C | T | 6 | a0001c0002t0001g0110 a0001c0002t0001g0111 a0001c0002t0001g0112 others(3): Show |
6 | HG00639.hp1 HG01109.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-221-24122G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89680229 | |||||||
| chr12:89680310 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-221-24203A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89680310 | |||||||
| chr12:89680424 | T | C | 3 | a0001c0001t0001g0209 a0001c0002t0001g0113 a0004c0008t0001g0208 |
3 | HG02630.hp2 NA18951.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-221-24317A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89680424 | |||||||
| chr12:89680551 | T | C | 1 | a0001c0003t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-221-24444A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89680551 | |||||||
| chr12:89680575 | G | C | 1 | a0001c0001t0001g0183 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-221-24468C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89680575 | |||||||
| chr12:89680651 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-221-24544G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89680651 | |||||||
| chr12:89680664 | G | C | 95 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(92): Show |
95 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.-221-24557C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89680664 | |||||||
| chr12:89680700 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-221-24593A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89680700 | |||||||
| chr12:89680775 | T | A | 1 | a0001c0001t0001g0313 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-221-24668A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89680775 | |||||||
| chr12:89680829 | C | T | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG03927.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-221-24722G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89680829 | |||||||
| chr12:89681284 | C | T | 3 | a0001c0001t0005g0322 a0001c0001t0005g0323 a0001c0001t0005g0324 |
3 | HG02258.hp2 HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-221-25177G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89681284 | |||||||
| chr12:89681381 | A | AT | 170 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(167): Show |
172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.-221-25275_-221-25 others(7): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89681381 | |||||||
| chr12:89681381 | A | ATT | 4 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(1): Show |
4 | HG00558.hp1 HG00621.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.-221-25275_-221-25 others(8): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89681381 | |||||||
| chr12:89681382 | A | T | 295 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(292): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.-221-25275T>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89681382 | |||||||
| chr12:89681466 | C | T | 95 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(92): Show |
95 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.-221-25359G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89681466 | |||||||
| chr12:89681834 | T | G | 1 | a0001c0001t0002g0243 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-221-25727A>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89681834 | |||||||
| chr12:89681909 | T | C | 18 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(15): Show |
18 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-221-25802A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89681909 | |||||||
| chr12:89682355 | T | C | 1 | a0001c0001t0001g0314 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-222+26241A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89682355 | |||||||
| chr12:89682516 | G | T | 18 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(15): Show |
18 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-222+26080C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89682516 | |||||||
| chr12:89682829 | G | A | 1 | a0001c0002t0012g0002 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-222+25767C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89682829 | |||||||
| chr12:89682857 | T | C | 5 | a0001c0001t0002g0169 a0001c0001t0002g0170 a0001c0001t0002g0171 others(2): Show |
5 | HG02027.hp2 NA18612.hp1 NA19057.hp2 others(2): Show |
intron_variant | MODIFIER | c.-222+25739A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89682857 | |||||||
| chr12:89682955 | T | C | 6 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0186 others(3): Show |
6 | HG02280.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-222+25641A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89682955 | |||||||
| chr12:89683121 | T | C | 4 | a0001c0003t0001g0050 a0001c0003t0001g0051 a0001c0003t0001g0054 others(1): Show |
4 | HG01192.hp1 HG01884.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-222+25475A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89683121 | |||||||
| chr12:89683188 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-222+25408C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89683188 | |||||||
| chr12:89683262 | T | C | 9 | a0001c0001t0005g0116 a0001c0001t0005g0117 a0001c0001t0005g0319 others(6): Show |
9 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-222+25334A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89683262 | |||||||
| chr12:89683385 | T | A | 1 | a0001c0001t0001g0315 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-222+25211A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89683385 | |||||||
| chr12:89683437 | C | G | 1 | a0001c0001t0001g0298 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-222+25159G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89683437 | |||||||
| chr12:89683441 | C | T | 1 | a0001c0001t0005g0321 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-222+25155G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89683441 | |||||||
| chr12:89683517 | C | T | 9 | a0001c0001t0005g0116 a0001c0001t0005g0117 a0001c0001t0005g0319 others(6): Show |
9 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-222+25079G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89683517 | |||||||
| chr12:89683620 | T | C | 302 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(299): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.-222+24976A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89683620 | |||||||
| chr12:89683675 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-222+24921G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89683675 | |||||||
| chr12:89683706 | A | G | 1 | a0001c0001t0001g0289 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-222+24890T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89683706 | |||||||
| chr12:89684051 | T | A | 1 | a0001c0001t0004g0007 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-222+24545A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89684051 | |||||||
| chr12:89684254 | T | A | 312 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.-222+24342A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89684254 | |||||||
| chr12:89684273 | T | G | 312 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.-222+24323A>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89684273 | |||||||
| chr12:89684289 | C | G | 1 | a0001c0001t0001g0076 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-222+24307G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89684289 | |||||||
| chr12:89684316 | C | T | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 |
3 | HG02258.hp1 HG02896.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-222+24280G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89684316 | |||||||
| chr12:89684591 | C | T | 6 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0186 others(3): Show |
6 | HG02280.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-222+24005G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89684591 | |||||||
| chr12:89684612 | C | G | 1 | a0001c0001t0020g0048 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-222+23984G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89684612 | |||||||
| chr12:89684704 | T | C | 9 | a0001c0001t0005g0116 a0001c0001t0005g0117 a0001c0001t0005g0319 others(6): Show |
9 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-222+23892A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89684704 | |||||||
| chr12:89684758 | C | T | 1 | a0001c0003t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-222+23838G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89684758 | |||||||
| chr12:89684782 | C | T | 2 | a0001c0002t0001g0114 a0001c0002t0001g0115 |
2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-222+23814G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89684782 | |||||||
| chr12:89684845 | C | T | 270 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(267): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.-222+23751G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89684845 | |||||||
| chr12:89685041 | A | G | 1 | a0001c0002t0012g0002 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-222+23555T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89685041 | |||||||
| chr12:89685047 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-222+23549A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89685047 | |||||||
| chr12:89685181 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-222+23415T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89685181 | |||||||
| chr12:89685207 | T | TA | 306 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(303): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.-222+23388dupT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89685207 | |||||||
| chr12:89685239 | T | C | 5 | a0001c0003t0001g0050 a0001c0003t0001g0051 a0001c0003t0001g0052 others(2): Show |
5 | HG01192.hp1 HG01884.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-222+23357A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89685239 | |||||||
| chr12:89685294 | C | G | 1 | a0001c0001t0001g0162 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-222+23302G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89685294 | |||||||
| chr12:89685309 | C | T | 1 | a0001c0002t0012g0002 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-222+23287G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89685309 | |||||||
| chr12:89685422 | C | G | 1 | a0001c0002t0001g0055 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-222+23174G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89685422 | |||||||
| chr12:89685483 | G | C | 1 | a0001c0001t0001g0255 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-222+23113C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89685483 | |||||||
| chr12:89685707 | T | C | 2 | a0001c0001t0002g0053 a0001c0001t0002g0160 |
2 | HG02886.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-222+22889A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89685707 | |||||||
| chr12:89685877 | C | T | 2 | a0001c0001t0001g0248 a0001c0001t0001g0249 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-222+22719G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89685877 | |||||||
| chr12:89685894 | A | G | 1 | a0001c0001t0001g0315 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-222+22702T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89685894 | |||||||
| chr12:89685898 | G | A | 1 | a0001c0001t0001g0244 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-222+22698C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89685898 | |||||||
| chr12:89685981 | G | A | 3 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0222 |
3 | HG00741.hp1 HG01257.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.-222+22615C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89685981 | |||||||
| chr12:89686066 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-222+22530G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89686066 | |||||||
| chr12:89686288 | C | G | 2 | a0001c0002t0001g0114 a0001c0002t0001g0115 |
2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-222+22308G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89686288 | |||||||
| chr12:89686327 | T | C | 5 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(2): Show |
5 | HG02109.hp1 HG02258.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-222+22269A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89686327 | |||||||
| chr12:89686435 | C | T | 1 | a0001c0001t0002g0122 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-222+22161G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89686435 | |||||||
| chr12:89686443 | C | A | 294 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(291): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-222+22153G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89686443 | |||||||
| chr12:89686513 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-222+22083C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89686513 | |||||||
| chr12:89686638 | T | C | 1 | a0001c0007t0010g0135 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-222+21958A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89686638 | |||||||
| chr12:89686842 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-222+21754G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89686842 | |||||||
| chr12:89687040 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-222+21556G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89687040 | |||||||
| chr12:89687116 | G | C | 1 | a0001c0002t0012g0002 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-222+21480C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89687116 | |||||||
| chr12:89687162 | A | G | 15 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(12): Show |
15 | NA18950.hp1 NA18951.hp2 NA18966.hp1 others(12): Show |
intron_variant | MODIFIER | c.-222+21434T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89687162 | |||||||
| chr12:89687166 | C | T | 1 | a0001c0001t0001g0236 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-222+21430G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89687166 | |||||||
| chr12:89687411 | T | A | 1 | a0001c0001t0001g0303 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-222+21185A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89687411 | |||||||
| chr12:89687411 | T | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(172): Show |
177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.-222+21185A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89687411 | |||||||
| chr12:89687536 | G | A | 2 | a0001c0001t0008g0161 a0001c0001t0008g0210 |
2 | NA19066.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.-222+21060C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89687536 | |||||||
| chr12:89687727 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-222+20869C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89687727 | |||||||
| chr12:89688389 | T | C | 42 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0102 others(39): Show |
42 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.-222+20207A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89688389 | |||||||
| chr12:89688480 | G | C | 1 | a0001c0001t0003g0015 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-222+20116C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89688480 | |||||||
| chr12:89688523 | T | C | 1 | a0001c0002t0012g0002 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-222+20073A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89688523 | |||||||
| chr12:89688744 | T | G | 1 | a0001c0001t0001g0297 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-222+19852A>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89688744 | |||||||
| chr12:89689132 | C | A | 292 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(289): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-222+19464G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89689132 | |||||||
| chr12:89689139 | C | G | 1 | a0001c0001t0001g0162 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-222+19457G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89689139 | |||||||
| chr12:89689237 | A | C | 2 | a0001c0001t0005g0116 a0001c0001t0005g0117 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-222+19359T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89689237 | |||||||
| chr12:89689294 | A | C | 1 | a0001c0007t0010g0135 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-222+19302T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89689294 | |||||||
| chr12:89689510 | T | A | 2 | a0001c0002t0001g0114 a0001c0002t0001g0115 |
2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-222+19086A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89689510 | |||||||
| chr12:89689641 | T | C | 6 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(3): Show |
6 | HG02280.hp2 HG02809.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-222+18955A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89689641 | |||||||
| chr12:89689648 | C | T | 7 | a0001c0001t0001g0277 a0001c0002t0001g0110 a0001c0002t0001g0111 others(4): Show |
7 | HG00639.hp1 HG01109.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-222+18948G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89689648 | |||||||
| chr12:89689649 | G | A | 1 | a0001c0002t0012g0002 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-222+18947C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89689649 | |||||||
| chr12:89689656 | T | G | 3 | a0001c0005t0001g0083 a0001c0005t0001g0084 a0001c0005t0001g0101 |
3 | HG01257.hp2 HG02300.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-222+18940A>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89689656 | |||||||
| chr12:89689689 | T | C | 1 | a0001c0003t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-222+18907A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89689689 | |||||||
| chr12:89689837 | G | A | 1 | a0001c0001t0005g0117 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-222+18759C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89689837 | |||||||
| chr12:89690017 | G | A | 312 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.-222+18579C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89690017 | |||||||
| chr12:89690039 | T | A | 5 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(2): Show |
5 | HG01433.hp2 HG02055.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.-222+18557A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89690039 | |||||||
| chr12:89690043 | G | A | 4 | a0001c0002t0001g0110 a0001c0002t0001g0111 a0001c0002t0001g0112 others(1): Show |
4 | HG00639.hp1 HG01109.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-222+18553C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89690043 | |||||||
| chr12:89690327 | C | CT | 90 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(87): Show |
90 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.-222+18268dupA | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89690327 | |||||||
| chr12:89690580 | T | A | 1 | a0001c0001t0001g0320 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-222+18016A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89690580 | |||||||
| chr12:89690581 | A | T | 1 | a0001c0002t0012g0002 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-222+18015T>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89690581 | |||||||
| chr12:89690638 | T | C | 3 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 |
3 | HG02040.hp1 NA18977.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-222+17958A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89690638 | |||||||
| chr12:89690909 | A | G | 4 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0250 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.-222+17687T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89690909 | |||||||
| chr12:89690910 | G | C | 1 | a0001c0001t0001g0180 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-222+17686C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89690910 | |||||||
| chr12:89691087 | G | C | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG02145.hp2 HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-222+17509C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89691087 | |||||||
| chr12:89691338 | C | T | 3 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 |
3 | HG00558.hp1 HG00621.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.-222+17258G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89691338 | |||||||
| chr12:89691384 | G | T | 1 | a0001c0001t0001g0126 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-222+17212C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89691384 | |||||||
| chr12:89691392 | T | C | 5 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(2): Show |
5 | HG02280.hp2 HG02809.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-222+17204A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89691392 | |||||||
| chr12:89691395 | G | C | 1 | a0001c0001t0001g0288 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-222+17201C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89691395 | |||||||
| chr12:89691667 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-222+16929T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89691667 | |||||||
| chr12:89691803 | A | C | 9 | a0001c0001t0005g0116 a0001c0001t0005g0117 a0001c0001t0005g0319 others(6): Show |
9 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-222+16793T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89691803 | |||||||
| chr12:89691903 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-222+16693A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89691903 | |||||||
| chr12:89691909 | G | A | 2 | a0001c0002t0001g0114 a0001c0002t0001g0115 |
2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-222+16687C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89691909 | |||||||
| chr12:89692384 | C | A | 1 | a0001c0001t0001g0211 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-222+16212G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89692384 | |||||||
| chr12:89692816 | T | G | 1 | a0001c0002t0001g0118 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-222+15780A>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89692816 | |||||||
| chr12:89693288 | T | C | 1 | a0001c0001t0001g0107 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-222+15308A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89693288 | |||||||
| chr12:89693399 | T | C | 4 | a0001c0002t0001g0110 a0001c0002t0001g0111 a0001c0002t0001g0112 others(1): Show |
4 | HG00639.hp1 HG01109.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-222+15197A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89693399 | |||||||
| chr12:89693524 | A | G | 1 | a0001c0001t0006g0246 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-222+15072T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89693524 | |||||||
| chr12:89693557 | C | G | 1 | a0001c0001t0002g0173 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-222+15039G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89693557 | |||||||
| chr12:89693613 | TC | T | 304 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(301): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.-222+14982delG | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89693613 | |||||||
| chr12:89693855 | C | T | 9 | a0001c0001t0005g0116 a0001c0001t0005g0117 a0001c0001t0005g0319 others(6): Show |
9 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-222+14741G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89693855 | |||||||
| chr12:89693873 | T | C | 1 | a0001c0001t0008g0212 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-222+14723A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89693873 | |||||||
| chr12:89693900 | T | C | 6 | a0001c0002t0001g0110 a0001c0002t0001g0111 a0001c0002t0001g0112 others(3): Show |
6 | HG00639.hp1 HG01109.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-222+14696A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89693900 | |||||||
| chr12:89694142 | T | C | 1 | a0001c0001t0003g0006 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-222+14454A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89694142 | |||||||
| chr12:89694401 | T | C | 1 | a0001c0001t0002g0053 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-222+14195A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89694401 | |||||||
| chr12:89694531 | G | A | 2 | a0001c0002t0001g0114 a0001c0002t0001g0115 |
2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-222+14065C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89694531 | |||||||
| chr12:89694803 | T | A | 92 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(89): Show |
92 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.-222+13793A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89694803 | |||||||
| chr12:89694991 | G | A | 83 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(80): Show |
83 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.-222+13605C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89694991 | |||||||
| chr12:89695013 | G | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(199): Show |
204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.-222+13583C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89695013 | |||||||
| chr12:89695052 | C | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(178): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.-222+13544G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89695052 | |||||||
| chr12:89695058 | C | CAAAAAA | 32 | a0001c0001t0001g0068 a0001c0001t0001g0090 a0001c0001t0001g0091 others(29): Show |
32 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.-222+13532_-222+13 others(12): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89695058 | |||||||
| chr12:89695058 | C | CAAAAAAA | 162 | a0001c0001t0001g0029 a0001c0001t0001g0036 a0001c0001t0001g0037 others(159): Show |
163 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.-222+13531_-222+13 others(13): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89695058 | |||||||
| chr12:89695058 | C | CAAAAAAA others(1): Show |
47 | a0001c0001t0001g0001 a0001c0001t0001g0085 a0001c0001t0001g0086 others(44): Show |
49 | HG00140.hp1 HG00280.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.-222+13530_-222+13 others(14): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89695058 | |||||||
| chr12:89695067 | A | AAAAAAAA others(1): Show |
34 | a0001c0001t0001g0103 a0001c0001t0001g0108 a0001c0001t0001g0181 others(31): Show |
34 | HG00140.hp2 HG00280.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.-222+13528_-222+13 others(14): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89695067 | |||||||
| chr12:89695067 | A | AAAAAAAG | 23 | a0001c0001t0001g0180 a0001c0001t0001g0214 a0001c0001t0001g0224 others(20): Show |
23 | HG01167.hp2 HG01243.hp2 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.-222+13528_-222+13 others(13): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89695067 | |||||||
| chr12:89695149 | C | T | 4 | a0001c0001t0002g0169 a0001c0001t0002g0170 a0001c0001t0002g0171 others(1): Show |
4 | NA18612.hp1 NA19057.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.-222+13447G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89695149 | |||||||
| chr12:89695218 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-222+13378C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89695218 | |||||||
| chr12:89695395 | C | T | 5 | a0001c0003t0001g0050 a0001c0003t0001g0051 a0001c0003t0001g0052 others(2): Show |
5 | HG01192.hp1 HG01884.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-222+13201G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89695395 | |||||||
| chr12:89695461 | A | G | 1 | a0001c0001t0001g0066 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-222+13135T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89695461 | |||||||
| chr12:89695641 | T | G | 1 | a0001c0001t0001g0263 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-222+12955A>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89695641 | |||||||
| chr12:89695735 | T | C | 1 | a0001c0001t0001g0292 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-222+12861A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89695735 | |||||||
| chr12:89696104 | C | T | 304 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(301): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.-222+12492G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89696104 | |||||||
| chr12:89696509 | CAA | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(206): Show |
211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.-222+12085_-222+12 others(8): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89696509 | |||||||
| chr12:89696524 | G | A | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | NA18972.hp2 NA19058.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-222+12072C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89696524 | |||||||
| chr12:89696620 | C | G | 2 | a0001c0001t0001g0222 a0001c0001t0001g0236 |
2 | HG00741.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-222+11976G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89696620 | |||||||
| chr12:89696781 | G | C | 2 | a0001c0001t0001g0264 a0001c0001t0001g0265 |
2 | HG01168.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.-222+11815C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89696781 | |||||||
| chr12:89696964 | C | T | 91 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(88): Show |
91 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.-222+11632G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89696964 | |||||||
| chr12:89697064 | C | CA | 10 | a0001c0001t0005g0116 a0001c0001t0005g0117 a0001c0001t0005g0319 others(7): Show |
10 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-222+11531dupT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89697064 | |||||||
| chr12:89697064 | CA | C | 9 | a0001c0001t0001g0089 a0001c0001t0001g0098 a0001c0001t0001g0099 others(6): Show |
9 | HG01106.hp1 HG02071.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-222+11531delT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89697064 | |||||||
| chr12:89697064 | CAA | C | 288 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(285): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-222+11530_-222+11 others(8): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89697064 | |||||||
| chr12:89697090 | A | G | 92 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(89): Show |
92 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.-222+11506T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89697090 | |||||||
| chr12:89697201 | G | C | 1 | a0001c0001t0001g0037 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-222+11395C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89697201 | |||||||
| chr12:89697267 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-222+11329G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89697267 | |||||||
| chr12:89697412 | G | C | 1 | a0001c0001t0001g0216 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-222+11184C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89697412 | |||||||
| chr12:89697669 | G | A | 88 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(85): Show |
88 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.-222+10927C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89697669 | |||||||
| chr12:89697670 | C | CT | 62 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(59): Show |
62 | HG00642.hp1 HG01167.hp1 HG01256.hp1 others(59): Show |
intron_variant | MODIFIER | c.-222+10925dupA | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89697670 | |||||||
| chr12:89697670 | CT | C | 6 | a0001c0001t0005g0116 a0001c0001t0005g0117 a0001c0001t0016g0274 others(3): Show |
7 | HG00735.hp1 HG01884.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-222+10925delA | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89697670 | |||||||
| chr12:89697670 | CTT | C | 36 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(33): Show |
38 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.-222+10924_-222+10 others(8): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89697670 | |||||||
| chr12:89697670 | CTTT | C | 180 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0102 others(177): Show |
180 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.-222+10923_-222+10 others(9): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89697670 | |||||||
| chr12:89697729 | C | A | 7 | a0001c0001t0005g0319 a0001c0001t0005g0321 a0001c0001t0005g0322 others(4): Show |
7 | HG02257.hp1 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-222+10867G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89697729 | |||||||
| chr12:89697881 | TC | T | 4 | a0001c0001t0001g0121 a0001c0001t0001g0150 a0001c0001t0001g0151 others(1): Show |
4 | HG00642.hp1 HG01256.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.-222+10714delG | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89697881 | |||||||
| chr12:89698002 | T | C | 1 | a0001c0001t0001g0309 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-222+10594A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89698002 | |||||||
| chr12:89698005 | G | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(216): Show |
222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.-222+10591C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89698005 | |||||||
| chr12:89698059 | C | T | 8 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(5): Show |
8 | HG02109.hp1 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-222+10537G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89698059 | |||||||
| chr12:89698060 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-222+10536C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89698060 | |||||||
| chr12:89698159 | C | G | 2 | a0001c0002t0001g0136 a0001c0002t0001g0137 |
2 | HG01346.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-222+10437G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89698159 | |||||||
| chr12:89698164 | A | G | 2 | a0001c0006t0001g0032 a0001c0006t0001g0033 |
2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-222+10432T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89698164 | |||||||
| chr12:89698240 | G | T | 6 | a0001c0001t0020g0048 a0001c0003t0001g0050 a0001c0003t0001g0051 others(3): Show |
6 | HG01192.hp1 HG01884.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-222+10356C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89698240 | |||||||
| chr12:89698324 | C | T | 301 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(298): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.-222+10272G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89698324 | |||||||
| chr12:89698332 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-222+10264G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89698332 | |||||||
| chr12:89698421 | A | C | 1 | a0001c0001t0003g0015 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-222+10175T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89698421 | |||||||
| chr12:89698554 | C | T | 5 | a0001c0001t0003g0005 a0001c0001t0003g0009 a0001c0001t0003g0010 others(2): Show |
5 | HG02451.hp1 HG02895.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-222+10042G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89698554 | |||||||
| chr12:89698663 | GA | G | 13 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0001c0002t0001g0041 others(10): Show |
14 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.-222+9932delT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89698663 | |||||||
| chr12:89698828 | G | A | 1 | a0001c0001t0004g0024 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-222+9768C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89698828 | |||||||
| chr12:89699079 | C | A | 2 | a0001c0002t0001g0114 a0001c0002t0001g0115 |
2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-222+9517G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89699079 | |||||||
| chr12:89699215 | G | T | 1 | a0001c0001t0001g0067 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-222+9381C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89699215 | |||||||
| chr12:89699417 | G | A | 4 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0250 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.-222+9179C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89699417 | |||||||
| chr12:89699440 | A | T | 1 | a0001c0001t0001g0133 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-222+9156T>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89699440 | |||||||
| chr12:89699694 | G | A | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-222+8902C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89699694 | |||||||
| chr12:89699829 | T | G | 1 | a0001c0001t0004g0023 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-222+8767A>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89699829 | |||||||
| chr12:89700005 | T | C | 1 | a0001c0001t0001g0126 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-222+8591A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89700005 | |||||||
| chr12:89700006 | G | T | 1 | a0001c0002t0001g0039 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-222+8590C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89700006 | |||||||
| chr12:89700012 | A | AT | 28 | a0001c0001t0001g0133 a0001c0001t0001g0138 a0001c0001t0001g0139 others(25): Show |
28 | HG00423.hp2 HG00738.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.-222+8583dupA | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89700012 | |||||||
| chr12:89700012 | AT | A | 11 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(8): Show |
11 | HG01081.hp1 HG01168.hp2 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.-222+8583delA | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89700012 | |||||||
| chr12:89700145 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-222+8451G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89700145 | |||||||
| chr12:89700150 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-222+8446C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89700150 | |||||||
| chr12:89700259 | G | T | 2 | a0001c0001t0005g0116 a0001c0001t0005g0117 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-222+8337C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89700259 | |||||||
| chr12:89700266 | G | A | 1 | a0001c0002t0003g0025 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-222+8330C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89700266 | |||||||
| chr12:89700402 | C | T | 294 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(291): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.-222+8194G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89700402 | |||||||
| chr12:89700733 | C | A | 1 | a0001c0001t0001g0307 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-222+7863G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89700733 | |||||||
| chr12:89701341 | T | C | 1 | a0001c0002t0001g0055 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-222+7255A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89701341 | |||||||
| chr12:89701396 | T | C | 53 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(50): Show |
53 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.-222+7200A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89701396 | |||||||
| chr12:89701648 | A | G | 6 | a0001c0002t0001g0110 a0001c0002t0001g0111 a0001c0002t0001g0112 others(3): Show |
6 | HG00639.hp1 HG01109.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-222+6948T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89701648 | |||||||
| chr12:89701785 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-222+6811C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89701785 | |||||||
| chr12:89701872 | G | GA | 8 | a0001c0001t0005g0116 a0001c0001t0005g0117 a0001c0002t0001g0110 others(5): Show |
8 | HG00639.hp1 HG01109.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.-222+6723dupT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89701872 | |||||||
| chr12:89701894 | A | G | 1 | a0001c0001t0004g0008 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-222+6702T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89701894 | |||||||
| chr12:89701929 | T | C | 2 | a0001c0001t0005g0116 a0001c0001t0005g0117 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-222+6667A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89701929 | |||||||
| chr12:89702019 | A | G | 294 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(291): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.-222+6577T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89702019 | |||||||
| chr12:89702020 | T | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0222 a0001c0001t0001g0224 others(77): Show |
82 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.-222+6576A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89702020 | |||||||
| chr12:89702042 | G | T | 1 | a0001c0001t0001g0066 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-222+6554C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89702042 | |||||||
| chr12:89702343 | A | G | 1 | a0001c0001t0004g0007 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-222+6253T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89702343 | |||||||
| chr12:89702379 | A | G | 1 | a0001c0002t0012g0002 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-222+6217T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89702379 | |||||||
| chr12:89702568 | T | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0120 a0001c0001t0001g0121 others(200): Show |
205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.-222+6028A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89702568 | |||||||
| chr12:89703205 | T | C | 5 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0011g0125 others(2): Show |
5 | HG00140.hp2 HG00280.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.-222+5391A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89703205 | |||||||
| chr12:89703609 | T | C | 5 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(2): Show |
5 | HG01081.hp2 HG01192.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.-222+4987A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89703609 | |||||||
| chr12:89703741 | G | A | 1 | a0001c0001t0006g0246 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-222+4855C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89703741 | |||||||
| chr12:89703890 | G | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0120 a0001c0001t0001g0121 others(227): Show |
233 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.-222+4706C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89703890 | |||||||
| chr12:89704005 | A | G | 5 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(2): Show |
5 | HG01433.hp2 HG02055.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.-222+4591T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89704005 | |||||||
| chr12:89704120 | G | T | 1 | a0001c0001t0003g0006 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-222+4476C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89704120 | |||||||
| chr12:89704243 | G | A | 8 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0244 others(5): Show |
8 | HG01106.hp1 HG01168.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.-222+4353C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89704243 | |||||||
| chr12:89704256 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-222+4340A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89704256 | |||||||
| chr12:89704322 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-222+4274G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89704322 | |||||||
| chr12:89704538 | A | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0247 |
2 | NA18747.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-222+4058T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89704538 | |||||||
| chr12:89704856 | C | T | 295 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(292): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-222+3740G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89704856 | |||||||
| chr12:89704906 | T | C | 1 | a0001c0001t0001g0307 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-222+3690A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89704906 | |||||||
| chr12:89704932 | C | G | 8 | a0001c0001t0001g0320 a0001c0001t0005g0319 a0001c0001t0005g0321 others(5): Show |
8 | HG02257.hp1 HG02258.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-222+3664G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89704932 | |||||||
| chr12:89705026 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-222+3570T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89705026 | |||||||
| chr12:89705152 | T | C | 1 | a0001c0001t0007g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-222+3444A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89705152 | |||||||
| chr12:89705620 | T | A | 230 | a0001c0001t0001g0001 a0001c0001t0001g0120 a0001c0001t0001g0121 others(227): Show |
233 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.-222+2976A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89705620 | |||||||
| chr12:89705758 | CAGAGAAC others(4): Show |
C | 1 | a0001c0001t0001g0263 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-222+2827_-222+283 others(15): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89705758 | |||||||
| chr12:89705952 | T | C | 1 | a0001c0001t0001g0247 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-222+2644A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89705952 | |||||||
| chr12:89705997 | C | T | 1 | a0001c0002t0012g0002 | 2 | HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-222+2599G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89705997 | |||||||
| chr12:89706118 | T | C | 4 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0250 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.-222+2478A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89706118 | |||||||
| chr12:89706166 | G | T | 1 | a0001c0001t0011g0125 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-222+2430C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89706166 | |||||||
| chr12:89706378 | T | TA | 10 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(7): Show |
10 | HG01081.hp2 HG01192.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.-222+2217dupT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89706378 | |||||||
| chr12:89706378 | TA | T | 18 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(15): Show |
18 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.-222+2217delT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89706378 | |||||||
| chr12:89706509 | T | A | 2 | a0001c0001t0001g0258 a0001c0001t0001g0328 |
2 | HG01081.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-222+2087A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89706509 | |||||||
| chr12:89706688 | CAAT | C | 6 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(3): Show |
6 | HG02280.hp2 HG02809.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-222+1905_-222+190 others(7): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89706688 | |||||||
| chr12:89707019 | TA | T | 230 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0036 others(227): Show |
233 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.-222+1576delT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89707019 | |||||||
| chr12:89707114 | G | C | 1 | a0001c0001t0003g0027 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-222+1482C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89707114 | |||||||
| chr12:89707126 | G | A | 2 | a0001c0001t0001g0308 a0001c0001t0001g0309 |
2 | HG02015.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-222+1470C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89707126 | |||||||
| chr12:89707618 | G | A | 9 | a0001c0001t0001g0320 a0001c0001t0001g0327 a0001c0001t0005g0319 others(6): Show |
9 | HG02257.hp1 HG02258.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-222+978C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89707618 | |||||||
| chr12:89707708 | C | G | 1 | a0001c0001t0001g0120 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-222+888G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89707708 | |||||||
| chr12:89707720 | T | C | 1 | a0001c0002t0001g0118 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-222+876A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89707720 | |||||||
| chr12:89707788 | AGAACCAG others(38): Show |
A | 1 | a0001c0001t0013g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-222+763_-222+807d others(47): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89707788 | |||||||
| chr12:89708010 | T | C | 1 | a0001c0004t0001g0119 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-222+586A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89708010 | |||||||
| chr12:89708055 | T | C | 1 | a0001c0001t0003g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-222+541A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89708055 | |||||||
| chr12:89708115 | T | A | 203 | a0001c0001t0001g0001 a0001c0001t0001g0120 a0001c0001t0001g0121 others(200): Show |
205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.-222+481A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89708115 | |||||||
| chr12:89708140 | G | A | 2 | a0001c0001t0001g0264 a0001c0001t0001g0265 |
2 | HG01168.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.-222+456C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89708140 | |||||||
| chr12:89708162 | C | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0266 a0001c0001t0001g0267 others(42): Show |
47 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(44): Show |
intron_variant | MODIFIER | c.-222+434G>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89708162 | |||||||
| chr12:89708210 | T | A | 9 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0312 others(6): Show |
9 | HG02040.hp1 NA18941.hp2 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.-222+386A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89708210 | |||||||
| chr12:89708316 | A | G | 293 | a0001c0001t0001g0001 a0001c0001t0001g0036 a0001c0001t0001g0037 others(290): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-222+280T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89708316 | |||||||
| chr12:89708335 | C | G | 1 | a0001c0001t0001g0029 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-222+261G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89708335 | |||||||
| chr12:89708494 | G | A | 1 | a0001c0001t0001g0328 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-222+102C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89708494 |