Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and 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 | copy fasta | chr12 | 89583049 | 89713838 |
| a0002 | 0/0 | 1220 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0003 | 0/0 | 1220 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0004 | 0/0 | 1220 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 3663 | 285 | 65 | 44 | 126 | 13 | 36 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| c0002 | 0/1 | 3663 | 26 | 8 | 11 | 1 | 1 | 4 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| c0003 | 0/0 | 3663 | 5 | 4 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| c0004 | 0/0 | 3663 | 5 | 4 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| c0005 | 0/0 | 3663 | 3 | 1 | 2 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| c0006 | 0/0 | 3663 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| c0007 | 0/0 | 3663 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| c0008 | 0/0 | 3663 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| c0009 | 0/0 | 3663 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| c0010 | 0/0 | 3663 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| c0011 | 0/0 | 3663 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 3400 | 256 | 48 | 52 | 109 | 12 | 34 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| t0002 | 0/0 | 3400 | 18 | 2 | 3 | 11 | 0 | 2 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| t0003 | 1/0 | 3400 | 10 | 8 | 0 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| t0004 | 0/0 | 3399 | 9 | 8 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| t0005 | 0/0 | 3400 | 9 | 9 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| t0006 | 0/0 | 3399 | 5 | 0 | 1 | 3 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| t0007 | 0/0 | 3399 | 3 | 3 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| t0008 | 0/0 | 3400 | 3 | 0 | 0 | 2 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| t0009 | 0/0 | 3400 | 2 | 0 | 1 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| t0010 | 0/0 | 3400 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| t0011 | 0/0 | 3400 | 2 | 0 | 0 | 1 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| t0012 | 0/0 | 3399 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| t0013 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| t0014 | 0/0 | 3400 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| t0015 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| t0016 | 0/0 | 3400 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| t0017 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| t0018 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| t0019 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| t0020 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| t0021 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| t0022 | 0/0 | 3400 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| t0023 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0016 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0047 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3663 | 285 | 65 | 44 | 126 | 13 | 36 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0002 | 0/1 | 3663 | 26 | 8 | 11 | 1 | 1 | 4 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0003 | 0/0 | 3663 | 5 | 4 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0004 | 0/0 | 3663 | 5 | 4 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0005 | 0/0 | 3663 | 3 | 1 | 2 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0006 | 0/0 | 3663 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0007 | 0/0 | 3663 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0009 | 0/0 | 3663 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0002c0011 | 0/0 | 3663 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0003c0010 | 0/0 | 3663 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0004c0008 | 0/0 | 3663 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | 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 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0001t0002 | 0/0 | 7062 | 18 | 2 | 3 | 11 | 0 | 2 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0001t0003 | 1/0 | 7062 | 9 | 8 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0001t0004 | 0/0 | 7061 | 9 | 8 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0001t0005 | 0/0 | 7062 | 9 | 9 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0001t0006 | 0/0 | 7061 | 5 | 0 | 1 | 3 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0001t0007 | 0/0 | 7061 | 3 | 3 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0001t0008 | 0/0 | 7062 | 3 | 0 | 0 | 2 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0001t0009 | 0/0 | 7062 | 2 | 0 | 1 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0001t0011 | 0/0 | 7062 | 2 | 0 | 0 | 1 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0001t0013 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0001t0014 | 0/0 | 7062 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0001t0016 | 0/0 | 7062 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0001t0017 | 0/0 | 7062 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0001t0018 | 0/0 | 7062 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0001t0019 | 0/0 | 7062 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0001t0020 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0001t0022 | 0/0 | 7062 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0001t0023 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0002t0001 | 0/1 | 7062 | 22 | 6 | 11 | 0 | 0 | 4 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0002t0003 | 0/0 | 7062 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0002t0012 | 0/0 | 7061 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0002t0015 | 0/0 | 7062 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0003t0001 | 0/0 | 7062 | 4 | 3 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0003t0021 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0004t0001 | 0/0 | 7062 | 5 | 4 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0005t0001 | 0/0 | 7062 | 3 | 1 | 2 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0006t0001 | 0/0 | 7062 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0007t0010 | 0/0 | 7062 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0001c0009t0001 | 0/0 | 7062 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0002c0011t0001 | 0/0 | 7062 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0003c0010t0001 | 0/0 | 7062 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| a0004c0008t0001 | 0/0 | 7062 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | copy fasta | chr12 | 89583049 | 89713838 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0239 | 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 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0001g0329 | 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 |
| a0001c0001t0003g0012 | 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 |
| a0001c0001t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0004g0021 | 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 |
| a0001c0001t0005g0320 | 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 |
| a0001c0001t0005g0327 | 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 |
| a0001c0001t0007g0019 | 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 |
| a0001c0001t0009g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0009g0014 | 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 |
| a0001c0001t0011g0193 | 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 |
| a0001c0001t0014g0015 | 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 |
| a0001c0001t0017g0303 | 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 |
| a0001c0001t0019g0206 | 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 |
| a0001c0001t0022g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0001t0023g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 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 |
| a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 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 |
| 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 | 0/1 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0002t0012g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| a0001c0002t0015g0044 | 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 | g0239 | EUR | GBR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | 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 | g0194 | 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 | g0206 | 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 | g0226 | EAS | CHS | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0110 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0294 | 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 | g0014 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0045 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG00738 | hp2 | a0001 | c0001 | t0014 | g0015 | 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 | g0040 | 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 | g0041 | 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 | g0329 | AMR | PUR | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0190 | 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 | g0043 | 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 | g0021 | 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 | g0013 | EUR | IBS | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0291 | 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 | g0001 | 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 | g0195 | 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 | g0077 | AMR | PEL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0196 | 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 | g0297 | AMR | PEL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0309 | 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 | g0317 | EAS | KHV | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0227 | 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 | g0304 | 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 | g0299 | EAS | KHV | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02080 | hp2 | a0001 | c0001 | t0017 | g0303 | 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 | g0042 | 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 | g0191 | EAS | CDX | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0322 | AFR | ACB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0020 | 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 | g0325 | 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 | g0198 | 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 | g0260 | 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 | g0307 | AMR | PEL | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0305 | 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 | g0308 | EAS | KHV | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0201 | 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 | g0019 | AFR | GWD | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0327 | 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 | g0328 | 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 | g0259 | 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 | g0321 | 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 | g0324 | AFR | ESN | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0111 | 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 | g0261 | 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 | g0001 | AFR | ESN | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0262 | 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 | g0012 | 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 | g0323 | 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 | g0002 | 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 | g0203 | 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 | g0302 | 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 | g0039 | SAS | BEB | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0295 | 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 | g0038 | 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 | g0199 | 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 | g0298 | 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 | g0148 | AFR | YRI | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0169 | 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 | g0311 | 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 | g0315 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0205 | 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 | g0316 | 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 | g0079 | 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 | g0078 | 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 | g0197 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0080 | 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 | g0301 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0155 | 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 | g0319 | 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 | g0178 | 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 | g0193 | 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 | g0154 | 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 | g0207 | 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 | g0293 | 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 | g0044 | 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 | g0192 | 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 | g0292 | 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 | g0310 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0153 | 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 | g0170 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0313 | 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 | g0312 | 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 | g0177 | 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 | g0172 | 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 | g0314 | 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 | g0300 | 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 | g0202 | EAS | JPT | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0318 | 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 | g0320 | 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 | g0240 | SAS | GIH | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | GIH | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0149 | 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 | g0330 | 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 | hp1 | a0001 | c0002 | t0001 | g0047 | REF | REF | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0016 | REF | REF | ATP2B1_chr12_89583049_89713838 | ATP2B1 | chr12 | 89583049 | 89713838 |
| 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 |
| 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 | a0001c0006a0001c0007 | 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 | a0001c0002a0001c0007a0002c0011 | 29 | HG00639.hp1 HG00738.hp1 HG01070.hp1 others(26): 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 |
| 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 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(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 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(24): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): 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 |
| 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 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0066others(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 | a0001c0001t0005g0323 | 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 | a0001c0001t0003g0012 | 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 | a0001c0003t0001g0050a0001c0003t0001g0051a0001c0003t0001g0054others(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 | a0001c0001t0001g0309 | 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 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(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 | a0001c0003t0001g0050a0001c0003t0001g0051a0001c0003t0001g0052others(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 | 22 | a0001c0001t0001g0002a0001c0001t0001g0180a0001c0001t0001g0278others(19): 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 | a0001c0001t0001g0292 | 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 | a0001c0001t0005g0116a0001c0001t0005g0117 | 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 | a0001c0002t0012g0001 | 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 | 29 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(26): 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 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0112others(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 | 314 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): 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 | 314 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.3352-3184T>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89594479 | ||||||
| chr12:89594594
|
G | GA | 303 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(300): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.3352-3300dupT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89594594 | ||||||
| chr12:89594606
|
C | A | 4 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0112others(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 | a0001c0001t0009g0013a0001c0001t0009g0014 | 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 | 314 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): 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 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0112others(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 | 314 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): 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 | 177 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(174): 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 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0112others(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 | a0001c0003t0001g0050a0001c0003t0001g0051a0001c0003t0001g0052others(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 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0001g0213others(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 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0301 | 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 | 314 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.3351+1810T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 20/20 | chr12 | 89597307 | ||||||
| chr12:89597381
|
A | G | 308 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(305): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): 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 | a0001c0001t0001g0286a0001c0001t0001g0294a0001c0001t0001g0310 | 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 | 279 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(276): 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 | 322 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(319): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): 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 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0067others(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 | 279 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(276): 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 | a0001c0001t0001g0205 | 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 | a0001c0001t0005g0320a0001c0001t0005g0322a0001c0001t0005g0323others(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 | 313 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(310): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): 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 | a0001c0001t0001g0295 | 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 | a0001c0001t0001g0069a0001c0001t0006g0217a0001c0002t0001g0110others(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 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(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 | 122 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(119): 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 | 35 | a0001c0001t0001g0076a0001c0001t0001g0093a0001c0001t0001g0094others(32): Show | 35 | HG00423.hp1 HG00558.hp2 HG00642.hp2 others(32): 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 | a0001c0001t0005g0324a0001c0002t0001g0042a0001c0002t0001g0046others(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 | a0001c0001t0001g0103a0001c0001t0001g0108 | 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 | a0001c0001t0001g0283a0001c0001t0001g0288a0001c0001t0001g0292others(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 | a0001c0002t0001g0110 | 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 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0112others(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 | a0001c0001t0001g0157a0001c0001t0001g0218a0001c0001t0001g0273 | 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 | a0001c0006t0001g0032a0001c0006t0001g0033a0001c0007t0010g0135others(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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0001t0005g0116a0001c0001t0005g0117a0001c0001t0005g0320others(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 | 25 | a0001c0001t0001g0162a0001c0001t0001g0321a0001c0002t0001g0038others(22): Show | 25 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(22): 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 | a0001c0002t0001g0114a0001c0002t0001g0115 | 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 | a0001c0002t0001g0114a0001c0002t0001g0115 | 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 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147 | 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 | a0001c0001t0001g0202 | 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 | a0001c0001t0001g0097a0001c0001t0001g0103a0001c0001t0001g0108others(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 | a0001c0001t0002g0053a0001c0001t0002g0160 | 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 | 314 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.3061-522T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 18/20 | chr12 | 89601955 | ||||||
| chr12:89602313
|
T | C | 313 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(310): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): 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 | a0001c0001t0001g0298 | 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 | 19 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0040others(16): Show | 19 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(16): 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 | a0001c0002t0001g0114a0001c0002t0001g0115 | 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 | a0001c0003t0001g0050a0001c0003t0001g0051a0001c0003t0001g0052others(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 | a0001c0002t0012g0001 | 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 | a0001c0001t0001g0259 | 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 | 314 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): 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 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0003g0028 | 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 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(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 | 313 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(310): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): 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 | 314 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): 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 | 314 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): 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 | a0001c0001t0001g0314 | 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 | a0001c0001t0005g0116a0001c0001t0005g0117a0001c0001t0005g0320others(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 | 283 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(280): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.2443-2227dupA | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89606572 | ||||||
| chr12:89606572
|
C | CTT | 17 | a0001c0001t0001g0127a0001c0001t0001g0143a0001c0001t0001g0163others(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 | 19 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0040others(16): Show | 19 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(16): 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 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(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 | 19 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0040others(16): Show | 19 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2443-2560G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89606906 | ||||||
| chr12:89606984
|
C | A | 305 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(302): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): 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 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0102others(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 | a0001c0006t0001g0032a0001c0006t0001g0033a0001c0007t0010g0135others(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 | a0001c0001t0001g0305a0001c0001t0001g0307 | 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 | 304 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(301): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): 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 | a0001c0001t0002g0122a0001c0001t0002g0174a0001c0001t0002g0176others(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 | a0001c0001t0001g0286a0001c0001t0001g0294 | 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 | a0001c0001t0007g0019a0001c0001t0007g0022a0001c0001t0007g0026 | 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 | 305 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(302): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.2442+1797G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 15/20 | chr12 | 89608140 | ||||||
| chr12:89608288
|
A | C | 314 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): 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 | a0001c0002t0012g0001 | 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 | 304 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(301): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): 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 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(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 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(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 | a0001c0002t0012g0001 | 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 | a0001c0002t0001g0114a0001c0002t0001g0115 | 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 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0300others(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 | a0001c0001t0001g0199 | 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 | a0001c0001t0001g0302 | 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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227 | 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 | a0001c0001t0001g0143a0001c0001t0003g0028 | 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 | 28 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(25): 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 | a0001c0001t0001g0209a0004c0008t0001g0208 | 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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0001t0001g0200 | 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 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(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 | a0001c0001t0001g0200 | 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 | 314 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): 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 | a0001c0001t0004g0021 | 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 | a0001c0001t0005g0116a0001c0001t0005g0117a0001c0001t0005g0320others(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 | a0001c0001t0001g0258a0001c0001t0001g0329 | 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 | 28 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(25): 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 | a0001c0001t0001g0305 | 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 | a0001c0001t0001g0106a0001c0001t0001g0166a0001c0001t0001g0167 | 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 | a0001c0001t0005g0320 | 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 | a0001c0002t0012g0001 | 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 | 20 | a0001c0001t0001g0107a0001c0002t0001g0038a0001c0002t0001g0039others(17): Show | 20 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(17): 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 | a0001c0001t0001g0300 | 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 | a0001c0003t0001g0051a0001c0003t0001g0054 | 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 | a0001c0001t0001g0263a0001c0001t0001g0329 | 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 | a0001c0001t0001g0271a0001c0001t0001g0272 | 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 | 314 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): 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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0001t0001g0310 | 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 | 19 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0040others(16): Show | 19 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(16): 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 | 300 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(297): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.2067+855delT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 12/20 | chr12 | 89615946 | ||||||
| chr12:89615988
|
C | T | 1 | a0001c0001t0001g0302 | 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 | a0001c0002t0012g0001 | 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 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227 | 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 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(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 | a0001c0005t0001g0083a0001c0005t0001g0084a0001c0005t0001g0101 | 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 | a0001c0001t0001g0205 | 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 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0222 | 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 | a0001c0002t0001g0038a0001c0002t0001g0040a0001c0002t0001g0041others(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 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(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 | 314 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): 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 | a0001c0001t0001g0080 | 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 | a0001c0001t0005g0116a0001c0001t0005g0117a0001c0001t0005g0320others(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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0001t0001g0090a0001c0001t0001g0105 | 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 | 19 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0040others(16): Show | 19 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(16): 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 | a0001c0004t0001g0034a0001c0004t0001g0035a0001c0004t0001g0119 | 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 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0066others(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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0002t0001g0055a0001c0002t0001g0110a0001c0002t0001g0111others(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 | a0001c0001t0001g0199 | 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 | a0001c0001t0001g0103a0001c0001t0001g0108 | 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 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0112others(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 | 19 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0040others(16): Show | 19 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.1587+56C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 10/20 | chr12 | 89621493 | ||||||
| chr12:89621802
|
C | CA | 305 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(302): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.1345-12dupT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 9/20 | chr12 | 89621802 | ||||||
| chr12:89621847
|
A | T | 2 | a0001c0001t0001g0267a0001c0001t0001g0301 | 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 | a0001c0003t0001g0050a0001c0003t0001g0051a0001c0003t0001g0054others(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 | a0001c0001t0001g0318 | 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 | 245 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(242): Show | 247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.1345-509dupA | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 9/20 | chr12 | 89622299 | ||||||
| chr12:89622447
|
A | C | 1 | a0001c0001t0001g0297 | 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 | 314 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1344+1158T>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 9/20 | chr12 | 89623025 | ||||||
| chr12:89623073
|
T | TACC | 314 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): 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 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(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 | a0001c0002t0012g0001 | 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 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0097others(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 | a0001c0002t0001g0114a0001c0002t0001g0115 | 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 | a0001c0001t0001g0146a0001c0001t0001g0147 | 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 | 21 | a0001c0001t0001g0002a0001c0001t0001g0278a0001c0001t0001g0279others(18): 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 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0001g0186others(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 | 309 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(306): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1130-597C>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 8/20 | chr12 | 89624994 | ||||||
| chr12:89625081
|
A | G | 314 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): 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 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0066others(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 | 201 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(198): 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 | 53 | a0001c0001t0001g0066a0001c0001t0001g0143a0001c0001t0001g0153others(50): Show | 54 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.1129+869delT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 8/20 | chr12 | 89625584 | ||||||
| chr12:89625584
|
CAA | C | 267 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(264): 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 | a0001c0002t0001g0114a0001c0002t0001g0115 | 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 | a0001c0001t0001g0120a0001c0001t0001g0128a0001c0001t0001g0129others(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 | a0001c0002t0001g0114a0001c0002t0001g0115 | 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 | a0001c0003t0001g0051a0001c0003t0001g0054 | 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 | a0001c0002t0001g0039 | 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 | 305 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(302): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): 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 | a0001c0003t0001g0050a0001c0003t0001g0051a0001c0003t0001g0052others(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 | a0001c0001t0001g0124a0001c0001t0001g0190a0001c0001t0001g0191others(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 | a0001c0001t0001g0199 | 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 | a0001c0002t0001g0114a0001c0002t0001g0115 | 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 | a0001c0001t0001g0079a0001c0001t0001g0089a0001c0001t0001g0138others(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 | a0001c0001t0001g0190a0001c0001t0001g0234a0001c0001t0001g0248others(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 | a0001c0001t0001g0124a0001c0001t0001g0190a0001c0001t0001g0191others(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 | a0001c0001t0001g0321 | 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 | a0001c0001t0001g0202 | 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 | a0001c0002t0001g0039 | 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 | 314 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): 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 | a0001c0001t0001g0097a0001c0001t0001g0103a0001c0001t0001g0108others(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 | a0001c0001t0001g0281a0001c0001t0001g0287 | 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 | a0001c0001t0004g0004a0001c0001t0004g0008a0001c0001t0004g0017others(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 | a0001c0001t0004g0007a0001c0001t0004g0020a0001c0001t0006g0142others(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 | a0001c0001t0001g0143a0001c0001t0001g0153a0001c0001t0001g0258others(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 | 266 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(263): 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 | 29 | a0001c0001t0001g0095a0001c0001t0001g0197a0001c0001t0001g0225others(26): Show | 29 | HG00099.hp1 HG00558.hp1 HG00738.hp1 others(26): 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 | a0001c0002t0001g0118a0001c0002t0001g0134 | 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 | a0001c0003t0001g0050a0001c0003t0001g0051a0001c0003t0001g0052others(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 | a0001c0003t0001g0050a0001c0003t0001g0051a0001c0003t0001g0054others(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 | 314 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.929-883T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 6/20 | chr12 | 89628599 | ||||||
| chr12:89629001
|
A | T | 309 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(306): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): 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 | a0001c0001t0001g0103a0001c0001t0001g0108 | 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 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0037 | 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 | a0001c0002t0001g0040a0001c0002t0001g0041a0001c0002t0001g0055 | 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 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0098others(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 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(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 | a0001c0001t0005g0116a0001c0001t0005g0117a0001c0001t0005g0320others(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 | 19 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0040others(16): Show | 19 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(16): 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 | a0001c0001t0005g0116a0001c0001t0005g0117a0001c0001t0005g0320others(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 |
281 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(278): 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 |
32 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0040others(29): Show | 32 | HG00639.hp1 HG00738.hp1 HG01070.hp1 others(29): 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 | a0001c0002t0012g0001 | 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 | a0001c0001t0019g0206 | 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 | a0001c0001t0001g0311a0001c0001t0001g0314 | 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 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(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 | 280 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(277): 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 | a0001c0001t0001g0180a0001c0001t0002g0053a0001c0001t0002g0122others(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 | 314 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.788-1113C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89631758 | ||||||
| chr12:89631845
|
G | A | 177 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(174): 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 | a0001c0001t0011g0193 | 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 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(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 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0293others(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 | 25 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0040others(22): Show | 25 | HG00639.hp1 HG00738.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.788-1497delA | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89632141 | ||||||
| chr12:89632236
|
T | C | 1 | a0001c0001t0001g0300 | 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 | a0001c0002t0001g0039a0001c0002t0015g0044 | 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 | 19 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0040others(16): Show | 19 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(16): 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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | 310 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(307): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.787+1297delA | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 5/20 | chr12 | 89633480 | ||||||
| chr12:89633546
|
T | G | 2 | a0001c0001t0005g0326a0001c0001t0005g0327 | 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 | a0001c0001t0001g0328 | 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 | a0001c0003t0001g0050a0001c0003t0001g0051a0001c0003t0001g0052others(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 | a0001c0001t0001g0310 | 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 | a0001c0002t0001g0040a0001c0002t0001g0041 | 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 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0287 | 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 | 305 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(302): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): 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 | 305 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(302): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.407-952C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89636203 | ||||||
| chr12:89636234
|
G | C | 314 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.407-983C>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89636234 | ||||||
| chr12:89636371
|
C | G | 19 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0040others(16): Show | 19 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.407-1120G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89636371 | ||||||
| chr12:89636376
|
CAA | C | 37 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(34): 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 | 314 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): 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 | 311 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(308): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): 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 | 314 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): 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 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0102others(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 | 307 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(304): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): 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 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(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 | a0001c0001t0005g0116a0001c0001t0005g0117a0001c0001t0005g0320others(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 | ||||||
| chr12:89638815
|
T | C | 329 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(326): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.406+3343A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 3/20 | chr12 | 89638815 | ||||||
| chr12:89638821
|
C | T | 3 | a0001c0001t0007g0019a0001c0001t0007g0022a0001c0001t0007g0026 | 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 | a0001c0003t0001g0050a0001c0003t0001g0051a0001c0003t0001g0052others(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 | a0001c0002t0001g0038a0001c0002t0001g0040a0001c0002t0001g0041others(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 | a0001c0003t0001g0050a0001c0003t0001g0051a0001c0003t0001g0054others(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 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0219others(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 | a0001c0001t0001g0090a0001c0001t0001g0105 | 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 | a0001c0001t0005g0116a0001c0001t0005g0117a0001c0001t0005g0320others(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 | a0001c0001t0009g0013a0001c0001t0009g0014 | 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 | a0001c0001t0001g0202 | 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 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0112others(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 | a0001c0001t0005g0116a0001c0001t0005g0117a0001c0001t0005g0320others(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 | 202 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(199): 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 | 202 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(199): 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 | a0001c0003t0001g0050a0001c0003t0001g0051a0001c0003t0001g0052others(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 | a0001c0001t0002g0123a0001c0001t0002g0175 | 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 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(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 | a0001c0001t0001g0278a0003c0010t0001g0306 | 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 | 299 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(296): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): 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 | a0001c0001t0001g0080 | 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 | a0001c0002t0012g0001 | 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 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0275others(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 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0092 | 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 | a0001c0001t0001g0244a0001c0001t0001g0264a0001c0001t0001g0265 | 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 | 19 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0040others(16): Show | 19 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.209-479dupT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89642833 | ||||||
| chr12:89642933
|
C | T | 314 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): 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 | a0001c0001t0005g0116a0001c0001t0005g0117a0001c0001t0005g0320others(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 | a0001c0001t0001g0063a0001c0001t0001g0140a0001c0001t0001g0149others(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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0001t0001g0159a0001c0004t0001g0034a0001c0004t0001g0119 | 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 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(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 | a0001c0002t0001g0110a0001c0002t0001g0114a0001c0002t0001g0115others(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 | a0001c0002t0001g0038a0001c0002t0001g0040a0001c0002t0001g0041others(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 |
2 | a0001c0002t0001g0047a0001c0002t0001g0134 | 2 | HG02602.hp1 homoSapiens_chm13v2.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 | a0001c0002t0001g0039a0001c0002t0001g0118 | 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 | a0001c0003t0001g0050a0001c0003t0001g0051a0001c0003t0001g0054others(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 | a0001c0001t0001g0283a0001c0001t0005g0116a0001c0001t0005g0117others(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 | 28 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(25): 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 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0275others(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 | a0001c0001t0020g0048a0001c0002t0001g0110a0001c0002t0001g0111others(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 | a0001c0003t0001g0050a0001c0003t0001g0051a0001c0003t0001g0054others(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 | a0001c0001t0003g0012 | 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 | a0001c0001t0001g0124a0001c0001t0001g0197 | 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 | 304 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(301): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): 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 | a0001c0001t0001g0082a0001c0001t0001g0095 | 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 | a0001c0004t0001g0034a0001c0004t0001g0035a0001c0004t0001g0119 | 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 | 314 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): 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 | 38 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(35): 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 | a0001c0001t0002g0122a0001c0001t0002g0174a0001c0001t0002g0176others(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 | 314 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): 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 | a0001c0001t0001g0300 | 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 | a0001c0003t0001g0050a0001c0003t0001g0051a0001c0003t0001g0054others(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 | a0001c0001t0001g0268a0001c0001t0001g0269 | 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 | a0001c0001t0007g0019a0001c0001t0007g0022a0001c0001t0007g0026 | 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 | a0001c0001t0002g0169a0001c0001t0002g0170a0001c0001t0002g0171others(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 | a0001c0001t0004g0021 | 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0005g0320a0001c0001t0005g0322a0001c0001t0005g0323others(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 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(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 | 38 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(35): 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 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0102others(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 | 298 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(295): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): 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 | a0001c0001t0005g0320a0001c0001t0005g0322a0001c0001t0005g0323others(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 | a0001c0001t0001g0298 | 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 | a0001c0001t0001g0091a0001c0002t0001g0038a0001c0002t0001g0039others(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 | a0001c0001t0001g0259 | 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 | a0001c0001t0001g0060a0001c0001t0001g0078a0001c0001t0001g0079others(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 | 298 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(295): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.209-4875G>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89647230 | ||||||
| chr12:89647231
|
T | A | 298 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(295): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): 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 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0112others(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 | a0001c0001t0001g0224a0001c0001t0001g0231 | 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 | a0001c0001t0005g0116a0001c0001t0005g0117a0001c0001t0005g0320others(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 | a0001c0003t0001g0050a0001c0003t0001g0051a0001c0003t0001g0052others(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 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(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 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(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 | 307 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(304): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): 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 | 204 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(201): 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 | a0001c0001t0001g0252a0001c0001t0001g0253 | 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 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0112others(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 | a0001c0002t0012g0001 | 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 | a0001c0002t0012g0001 | 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 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131 | 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 | a0001c0002t0001g0038a0001c0002t0001g0040a0001c0002t0001g0041others(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 | a0001c0002t0001g0114a0001c0002t0001g0115 | 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 | a0001c0001t0001g0086a0001c0001t0001g0087 | 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 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0222others(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 | a0001c0002t0001g0038a0001c0002t0001g0040a0001c0002t0001g0041others(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 | a0001c0002t0012g0001 | 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 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(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 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(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 | a0001c0001t0005g0116a0001c0001t0005g0117 | 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 | a0001c0001t0001g0191a0001c0001t0001g0192 | 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 | a0001c0001t0001g0189a0001c0001t0001g0219a0001c0001t0008g0161others(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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0001t0001g0201a0001c0001t0001g0207a0001c0009t0001g0220 | 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 | a0001c0001t0001g0328 | 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 | a0001c0001t0001g0104a0001c0001t0001g0211a0001c0001t0011g0193 | 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 | a0001c0001t0006g0246a0001c0007t0010g0232 | 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 | 314 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.208+3358delG | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 2/20 | chr12 | 89652320 | ||||||
| chr12:89652352
|
T | C | 1 | a0001c0001t0023g0330 | 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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0001t0001g0309 | 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 | a0001c0001t0001g0078a0001c0001t0001g0079 | 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 | 314 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): 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 | a0001c0001t0005g0320 | 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 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(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 | a0001c0001t0001g0036a0001c0001t0001g0070a0001c0001t0001g0129others(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 | 266 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0037others(263): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): 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 | 19 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0040others(16): Show | 19 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(16): 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 | a0001c0003t0001g0050a0001c0003t0001g0051a0001c0003t0001g0052others(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 | a0001c0001t0005g0116a0001c0001t0005g0117a0001c0001t0005g0320others(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 | a0001c0001t0001g0328 | 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 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0300others(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 | 19 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0040others(16): Show | 19 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(16): 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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | 19 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0040others(16): Show | 19 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(16): 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 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(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 | a0001c0001t0014g0015 | 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 | a0001c0003t0001g0050a0001c0003t0001g0051a0001c0003t0001g0052others(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 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0244others(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 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0138others(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 | a0001c0001t0001g0075a0001c0001t0001g0081 | 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 | a0001c0001t0005g0116a0001c0001t0005g0117a0001c0001t0005g0320others(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 | a0001c0002t0001g0042 | 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 | a0001c0001t0001g0198 | 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 | a0001c0001t0001g0060a0001c0001t0001g0076a0001c0001t0001g0081others(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 | a0001c0001t0001g0064a0001c0001t0001g0068a0001c0001t0001g0069others(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 | a0001c0001t0001g0036a0001c0001t0001g0063a0001c0001t0001g0065others(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 | a0001c0001t0001g0037a0001c0001t0001g0066a0001c0001t0001g0073others(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 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0001g0091others(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 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0001t0001g0127others(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 | a0001c0001t0001g0074a0001c0001t0001g0124a0001c0001t0001g0192others(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 | a0001c0001t0001g0164a0001c0001t0001g0190a0001c0001t0001g0195others(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 | a0001c0001t0001g0191a0001c0001t0001g0196a0001c0001t0001g0237others(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 | a0001c0001t0001g0197a0001c0001t0001g0284a0001c0001t0001g0305others(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 | a0001c0001t0001g0293 | 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 | 31 | a0001c0001t0001g0002a0001c0001t0001g0139a0001c0001t0001g0141others(28): Show | 32 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(29): 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 | a0001c0001t0001g0097a0001c0001t0001g0107a0001c0001t0001g0138others(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 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(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 | a0001c0001t0001g0085a0001c0002t0001g0110a0001c0002t0001g0111others(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 | a0001c0001t0001g0316 | 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 | a0001c0001t0001g0095a0001c0001t0001g0187a0001c0001t0001g0288others(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 | 35 | a0001c0001t0001g0067a0001c0001t0001g0163a0001c0001t0001g0165others(32): Show | 36 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(33): 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 | a0001c0001t0001g0077a0001c0001t0001g0098a0001c0001t0001g0269others(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 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(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 | a0001c0001t0001g0057a0001c0001t0001g0078a0001c0001t0001g0127 | 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 | 34 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(31): 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 | 307 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(304): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): 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 | a0001c0001t0001g0059a0001c0001t0001g0063a0001c0001t0001g0075others(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 | a0001c0001t0001g0082a0001c0001t0001g0128a0001c0001t0001g0221 | 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 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0001g0129others(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 | a0001c0001t0001g0085a0001c0001t0001g0124a0001c0001t0001g0190others(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 | ||||||
| chr12:89660375
|
T | C | 1 | a0001c0002t0001g0047 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-221-4268A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89660375 | ||||||
| chr12:89660678
|
A | C | 1 | a0001c0001t0001g0316 | 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 | a0001c0002t0001g0114a0001c0002t0001g0115 | 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 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0112others(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 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0066others(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 | a0001c0002t0012g0001 | 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 | 22 | a0001c0001t0001g0002a0001c0001t0001g0277a0001c0001t0001g0278others(19): 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 | a0001c0001t0001g0094a0001c0001t0001g0099a0001c0001t0001g0100others(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 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(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 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(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 | a0001c0001t0005g0116a0001c0001t0005g0117a0001c0001t0005g0320others(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 | a0001c0001t0001g0079a0001c0001t0001g0121a0001c0001t0001g0133others(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 | a0001c0002t0001g0114a0001c0002t0001g0115 | 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 | 304 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(301): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): 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 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0112others(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 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(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 | a0001c0001t0005g0320a0001c0001t0005g0322a0001c0001t0005g0323others(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 | a0001c0001t0011g0193 | 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 | ||||||
| chr12:89663522
|
A | AAGT | 329 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(326): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.-221-7416_-221-741 others(7): Show |
ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89663522 | ||||||
| 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 | a0001c0001t0001g0120a0001c0001t0001g0200 | 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 | a0001c0001t0001g0309 | 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 | 321 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(318): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): 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 | 37 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(34): 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 | a0001c0003t0001g0050a0001c0003t0001g0051a0001c0003t0001g0052others(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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | 298 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(295): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): 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 | a0001c0001t0001g0157a0001c0001t0001g0218a0001c0001t0001g0273 | 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 | a0001c0001t0014g0015 | 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 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0112others(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 | a0001c0001t0001g0121a0001c0001t0001g0127a0001c0001t0001g0150others(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 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0098others(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 | a0001c0001t0001g0149 | 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 | a0001c0002t0012g0001 | 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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0001t0001g0277a0001c0001t0016g0274 | 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 | a0001c0002t0012g0001 | 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 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(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 | a0001c0001t0007g0019a0001c0001t0007g0022a0001c0001t0007g0026 | 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 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0112others(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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0112others(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 | a0001c0002t0001g0039a0001c0002t0015g0044a0001c0003t0001g0050others(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 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0181others(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 | a0001c0001t0011g0193 | 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 | a0001c0002t0012g0001 | 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 | a0001c0002t0012g0001 | 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 | a0001c0001t0001g0146a0001c0001t0001g0147 | 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 | a0001c0001t0002g0123a0001c0001t0002g0175a0001c0001t0002g0184 | 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 | a0001c0001t0005g0326a0001c0001t0005g0327 | 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 | a0001c0001t0001g0261 | 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 | 19 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0040others(16): Show | 19 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-221-14201A>G | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89670308 | ||||||
| chr12:89670371
|
A | AT | 178 | a0001c0001t0001g0063a0001c0001t0001g0102a0001c0001t0001g0103others(175): Show | 178 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(175): 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 | a0001c0002t0012g0001 | 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 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0112others(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 | 313 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(310): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): 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 | a0001c0002t0012g0001 | 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 | a0001c0001t0001g0157a0001c0001t0001g0218a0001c0001t0001g0273 | 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 | 298 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(295): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-221-14846dupT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89670952 | ||||||
| chr12:89670952
|
T | TAA | 9 | a0001c0001t0001g0128a0001c0001t0001g0143a0001c0001t0001g0187others(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 | a0001c0001t0003g0012 | 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 | a0001c0001t0005g0327 | 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 | 307 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(304): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): 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 | a0001c0002t0001g0114a0001c0002t0001g0115 | 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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | 161 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(158): 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 | 23 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0213others(20): Show | 23 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(20): 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 | a0001c0001t0005g0116a0001c0001t0005g0117 | 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 | a0001c0001t0001g0309a0001c0001t0001g0310 | 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 | a0001c0001t0005g0116a0001c0001t0005g0117a0001c0001t0005g0320others(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 | a0001c0001t0001g0188a0001c0001t0001g0315 | 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 | 272 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(269): 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 | a0001c0001t0005g0320a0001c0001t0005g0322a0001c0001t0005g0324others(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 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0009g0013others(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 | a0001c0003t0001g0050a0001c0003t0001g0051a0001c0003t0001g0052others(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 | a0001c0001t0005g0116a0001c0001t0005g0117 | 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 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0112others(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 | 19 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0040others(16): Show | 19 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(16): 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 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(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 | a0001c0001t0001g0328 | 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 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(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 | a0001c0001t0014g0015 | 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 | a0001c0001t0004g0008a0001c0001t0004g0024 | 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 | 19 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0040others(16): Show | 19 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(16): 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 | 298 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(295): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): 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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0001t0001g0090a0001c0001t0001g0105 | 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 | a0001c0001t0003g0005a0001c0001t0003g0011 | 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 | 271 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(268): 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 | 298 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(295): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): 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 | a0001c0001t0001g0318 | 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 | 176 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(173): 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 | a0001c0002t0001g0045 | 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 | a0001c0001t0001g0305a0001c0001t0001g0307 | 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 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(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 | a0001c0002t0001g0110 | 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 | a0001c0002t0001g0113a0001c0003t0021g0049 | 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 | a0001c0002t0001g0111 | 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 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(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 | a0001c0001t0001g0075a0001c0001t0001g0085a0001c0001t0001g0087others(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 | a0001c0001t0001g0069a0001c0001t0020g0048a0001c0002t0001g0114others(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 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0070others(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 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0006g0056others(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 | a0001c0001t0001g0080a0001c0002t0001g0136a0001c0002t0001g0137others(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 | a0001c0002t0001g0038a0001c0002t0001g0040a0001c0002t0001g0041others(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 | a0001c0002t0001g0043 | 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 | a0001c0001t0005g0322 | 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 | a0001c0001t0001g0314 | 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 | a0001c0001t0001g0151a0001c0001t0001g0152 | 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 | a0001c0001t0001g0063a0001c0001t0001g0143a0001c0001t0001g0144others(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 | a0001c0001t0001g0102a0001c0001t0001g0128a0001c0001t0001g0129others(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 | a0001c0001t0001g0124a0001c0001t0001g0145a0001c0001t0001g0163others(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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0066others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0097others(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 | a0001c0001t0001g0076a0001c0001t0001g0089a0001c0006t0001g0032 | 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 | a0001c0001t0001g0245a0001c0001t0001g0308 | 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 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0295others(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 | a0001c0001t0001g0064a0001c0001t0001g0164a0001c0001t0001g0205others(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 | a0001c0001t0001g0133a0001c0001t0008g0212a0001c0001t0019g0206 | 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 | a0001c0001t0001g0126a0001c0001t0001g0185a0001c0001t0001g0207others(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 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0122others(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 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254 | 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 | a0001c0001t0001g0187a0001c0001t0001g0248a0001c0001t0001g0249 | 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 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(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 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(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 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0103others(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 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(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 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0037others(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 | 10 | a0001c0001t0005g0320a0001c0001t0005g0323a0001c0001t0005g0324others(7): Show | 10 | HG00738.hp1 HG01109.hp1 HG02258.hp2 others(7): 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 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0102others(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 | a0001c0001t0001g0002a0001c0001t0001g0238a0001c0001t0001g0289others(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 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0102others(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 | a0001c0001t0004g0004a0001c0001t0004g0008a0001c0001t0004g0017others(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 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0006g0246others(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 | a0001c0002t0012g0001 | 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 | a0001c0002t0001g0045 | 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(23): Show |
1 | a0001c0002t0001g0047 | 1 | homoSapiens_chm13v2.hp1 | 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(21): Show |
1 | a0001c0002t0015g0044 | 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 | a0001c0002t0001g0039a0001c0002t0001g0046 | 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 | a0001c0001t0005g0324 | 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 | a0001c0001t0005g0325 | 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 | a0001c0001t0005g0327 | 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 | a0001c0001t0005g0320 | 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 | a0001c0001t0005g0323 | 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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0001t0001g0097a0001c0001t0001g0318a0001c0007t0010g0135others(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 | a0001c0001t0001g0097a0001c0007t0010g0135a0001c0007t0010g0232 | 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 | a0001c0007t0010g0135a0001c0007t0010g0232 | 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 | a0001c0007t0010g0135a0001c0007t0010g0232 | 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 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0112others(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 | 298 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(295): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): 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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0002t0001g0114a0001c0002t0001g0115 | 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 | a0001c0002t0001g0114a0001c0002t0001g0115 | 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 | a0001c0001t0005g0116a0001c0001t0005g0117a0001c0001t0005g0320others(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 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0001t0005g0320a0001c0001t0005g0322a0001c0001t0005g0323others(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 | 307 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(304): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): 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 | a0001c0001t0001g0189a0001c0001t0008g0161a0001c0001t0008g0210 | 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 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0112others(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 | a0001c0001t0001g0209a0001c0002t0001g0113a0004c0008t0001g0208 | 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 | a0001c0001t0001g0295 | 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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0001t0001g0315 | 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 | a0001c0001t0001g0271a0001c0001t0001g0272 | 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 | a0001c0001t0005g0323a0001c0001t0005g0324a0001c0001t0005g0325 | 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 | 171 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(168): 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 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(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 | 297 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(294): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): 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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | 19 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0040others(16): Show | 19 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(16): 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 | a0001c0001t0001g0316 | 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 | 19 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0040others(16): Show | 19 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(16): 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 | a0001c0002t0012g0001 | 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 | a0001c0001t0002g0169a0001c0001t0002g0170a0001c0001t0002g0171others(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 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0001g0186others(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 | a0001c0003t0001g0050a0001c0003t0001g0051a0001c0003t0001g0054others(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 | a0001c0001t0005g0116a0001c0001t0005g0117a0001c0001t0005g0320others(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 | a0001c0001t0001g0312 | 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 | a0001c0001t0001g0299 | 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 | a0001c0001t0005g0322 | 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 | a0001c0001t0005g0116a0001c0001t0005g0117a0001c0001t0005g0320others(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 | 304 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(301): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): 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 | 314 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.-222+24342A>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89684254 | ||||||
| chr12:89684273
|
T | G | 314 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): 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 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147 | 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 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0001g0186others(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 | a0001c0001t0005g0116a0001c0001t0005g0117a0001c0001t0005g0320others(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 | a0001c0002t0001g0114a0001c0002t0001g0115 | 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 | 271 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(268): 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 | a0001c0002t0012g0001 | 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 | 308 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(305): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.-222+23388dupT | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89685207 | ||||||
| chr12:89685239
|
T | C | 5 | a0001c0003t0001g0050a0001c0003t0001g0051a0001c0003t0001g0052others(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 | a0001c0002t0012g0001 | 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 | a0001c0001t0002g0053a0001c0001t0002g0160 | 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 | a0001c0001t0001g0248a0001c0001t0001g0249 | 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 | a0001c0001t0001g0312 | 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 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0222 | 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 | a0001c0002t0001g0114a0001c0002t0001g0115 | 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 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(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 | 296 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(293): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): 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 | a0001c0001t0001g0292 | 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 | a0001c0002t0012g0001 | 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 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(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 | a0001c0001t0001g0304 | 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 | 176 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(173): 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 | a0001c0001t0008g0161a0001c0001t0008g0210 | 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 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0102others(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 | a0001c0001t0003g0012 | 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 | a0001c0002t0012g0001 | 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 | a0001c0001t0001g0298 | 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 | 294 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(291): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): 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 | a0001c0001t0005g0116a0001c0001t0005g0117 | 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 | a0001c0002t0001g0114a0001c0002t0001g0115 | 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 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(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 | a0001c0001t0001g0277a0001c0002t0001g0110a0001c0002t0001g0111others(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 | a0001c0002t0012g0001 | 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 | a0001c0005t0001g0083a0001c0005t0001g0084a0001c0005t0001g0101 | 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 | 314 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): 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 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(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 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0112others(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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0001t0001g0321 | 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 | a0001c0002t0012g0001 | 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 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319 | 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 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(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 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131 | 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 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227 | 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 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(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 | a0001c0001t0005g0116a0001c0001t0005g0117a0001c0001t0005g0320others(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 | a0001c0002t0001g0114a0001c0002t0001g0115 | 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 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0112others(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 | 306 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(303): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.-222+14982delG | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89693613 | ||||||
| chr12:89693855
|
C | T | 9 | a0001c0001t0005g0116a0001c0001t0005g0117a0001c0001t0005g0320others(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 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0112others(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 | a0001c0002t0001g0114a0001c0002t0001g0115 | 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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | 204 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(201): Show | 205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.-222+13583C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89695013 | ||||||
| chr12:89695052
|
C | T | 182 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(179): 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 | a0001c0001t0001g0068a0001c0001t0001g0090a0001c0001t0001g0091others(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 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0037others(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 |
49 | a0001c0001t0001g0002a0001c0001t0001g0085a0001c0001t0001g0086others(46): Show | 50 | HG00140.hp1 HG00280.hp1 HG00738.hp1 others(47): 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 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0181others(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 | a0001c0001t0001g0180a0001c0001t0001g0214a0001c0001t0001g0224others(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 | a0001c0001t0002g0169a0001c0001t0002g0170a0001c0001t0002g0171others(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 | a0001c0003t0001g0050a0001c0003t0001g0051a0001c0003t0001g0052others(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 | a0001c0001t0001g0293 | 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 | 306 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(303): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.-222+12492G>A | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89696104 | ||||||
| chr12:89696509
|
CAA | C | 211 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(208): Show | 212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): 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 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254 | 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 | a0001c0001t0001g0222a0001c0001t0001g0236 | 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 | a0001c0001t0001g0264a0001c0001t0001g0265 | 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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0001t0005g0116a0001c0001t0005g0117a0001c0001t0005g0320others(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 | a0001c0001t0001g0089a0001c0001t0001g0098a0001c0001t0001g0099others(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 | 290 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(287): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): 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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(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 | a0001c0001t0005g0116a0001c0001t0005g0117a0001c0001t0016g0274others(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 | 37 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(34): 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 | 181 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0102others(178): Show | 181 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(178): 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 | a0001c0001t0005g0320a0001c0001t0005g0322a0001c0001t0005g0323others(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 | a0001c0001t0001g0121a0001c0001t0001g0150a0001c0001t0001g0151others(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 | a0001c0001t0001g0310 | 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 | 221 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(218): Show | 223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): 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 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(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 | a0001c0002t0001g0136a0001c0002t0001g0137 | 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 | a0001c0006t0001g0032a0001c0006t0001g0033 | 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 | a0001c0001t0020g0048a0001c0003t0001g0050a0001c0003t0001g0051others(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 | 303 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(300): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): 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 | a0001c0001t0003g0012 | 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 | a0001c0001t0003g0005a0001c0001t0003g0009a0001c0001t0003g0010others(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 | 14 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0040others(11): Show | 15 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(12): 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 | a0001c0002t0001g0114a0001c0002t0001g0115 | 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 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(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 | a0001c0001t0001g0234a0001c0001t0001g0235 | 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 | a0001c0002t0001g0038 | 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 | a0001c0001t0001g0133a0001c0001t0001g0138a0001c0001t0001g0139others(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 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(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 | a0001c0001t0001g0328 | 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 | a0001c0001t0005g0116a0001c0001t0005g0117 | 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 | 296 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(293): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): 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 | a0001c0001t0001g0308 | 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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0112others(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 | a0001c0001t0005g0116a0001c0001t0005g0117a0001c0002t0001g0110others(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 | a0001c0001t0005g0116a0001c0001t0005g0117 | 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 | 296 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(293): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-222+6577T>C | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89702019 | ||||||
| chr12:89702020
|
T | A | 81 | a0001c0001t0001g0002a0001c0001t0001g0222a0001c0001t0001g0224others(78): 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 | a0001c0002t0012g0001 | 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 | 204 | a0001c0001t0001g0002a0001c0001t0001g0120a0001c0001t0001g0121others(201): 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 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0011g0125others(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 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(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 | 232 | a0001c0001t0001g0002a0001c0001t0001g0120a0001c0001t0001g0121others(229): Show | 234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): 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 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(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 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0244others(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 | a0001c0001t0001g0126a0001c0001t0001g0247 | 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 | 297 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): 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 | a0001c0001t0001g0308 | 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 | a0001c0001t0001g0321a0001c0001t0005g0320a0001c0001t0005g0322others(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 | 232 | a0001c0001t0001g0002a0001c0001t0001g0120a0001c0001t0001g0121others(229): Show | 234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): 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 | a0001c0002t0012g0001 | 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 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(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 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254others(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 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0001t0001g0258a0001c0001t0001g0329 | 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 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(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 | 232 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0036others(229): Show | 234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): 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 | a0001c0001t0001g0309a0001c0001t0001g0310 | 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 | a0001c0001t0001g0321a0001c0001t0001g0328a0001c0001t0005g0320others(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 | 204 | a0001c0001t0001g0002a0001c0001t0001g0120a0001c0001t0001g0121others(201): 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 | a0001c0001t0001g0264a0001c0001t0001g0265 | 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 | 46 | a0001c0001t0001g0002a0001c0001t0001g0266a0001c0001t0001g0267others(43): 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 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0001g0313others(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 | 295 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0037others(292): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): 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 | a0001c0001t0001g0329 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-222+102C>T | ATP2B1 | ENSG00000070961.17 | transcript | ENST00000428670.8 | protein_coding | 1/20 | chr12 | 89708494 |