Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 488 |
|---|---|
| ensemblid | ENSG00000174437.18 |
| hgncid | 812 |
| symbol | ATP2A2 |
| name | ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2 |
| refseq_nuc | NM_170665.4 |
| refseq_prot | NP_733765.1 |
| ensembl_nuc | ENST00000539276.7 |
| ensembl_prot | ENSP00000440045.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 110281247 |
| end | 110351093 |
| strand | + |
| ver | v1.2 |
| region | chr12:110281247-110351093 |
| region5000 | chr12:110276247-110356093 |
| regionname0 | ATP2A2_chr12_110281247_110351093 |
| regionname5000 | ATP2A2_chr12_110276247_110356093 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1042 | 225 | 88 | 61 | 34 | 16 | 24 | 28 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0002 | 0/0 | 1042 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0003 | 0/0 | 1042 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 3129 | 211 | 82 | 58 | 33 | 13 | 23 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| c0002 | 0/0 | 3129 | 4 | 0 | 1 | 0 | 3 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| c0003 | 0/0 | 3129 | 4 | 4 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| c0004 | 0/0 | 3129 | 2 | 0 | 0 | 0 | 0 | 2 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| c0005 | 0/0 | 3129 | 2 | 0 | 2 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| c0006 | 0/0 | 3129 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| c0007 | 0/0 | 3129 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| c0008 | 0/0 | 3129 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| c0009 | 0/0 | 3129 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| c0010 | 0/0 | 3129 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 5167 | 110 | 42 | 24 | 21 | 8 | 14 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| t0002 | 0/0 | 5171 | 29 | 17 | 3 | 5 | 1 | 3 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| t0003 | 0/1 | 5167 | 29 | 1 | 18 | 0 | 5 | 4 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| t0004 | 0/0 | 5171 | 10 | 9 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| t0005 | 0/0 | 5167 | 8 | 1 | 4 | 0 | 1 | 2 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| t0006 | 0/0 | 5167 | 6 | 5 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| t0007 | 0/0 | 5167 | 5 | 0 | 4 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| t0008 | 0/0 | 5167 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| t0009 | 0/0 | 5167 | 2 | 0 | 2 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| t0010 | 0/0 | 5167 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| t0011 | 0/0 | 5171 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| t0012 | 0/0 | 5171 | 2 | 1 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| t0013 | 0/0 | 5167 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| t0014 | 0/0 | 5167 | 2 | 1 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| t0015 | 0/0 | 5167 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| t0016 | 0/0 | 5167 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| t0017 | 0/0 | 5171 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| t0018 | 0/0 | 5171 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| t0019 | 0/0 | 5171 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| t0020 | 0/0 | 5171 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| t0021 | 0/0 | 5167 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| t0022 | 0/0 | 5167 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| t0023 | 0/0 | 5167 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| t0024 | 0/0 | 5167 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| t0025 | 0/0 | 5167 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| t0026 | 0/0 | 5167 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| t0027 | 0/0 | 5167 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| t0028 | 0/0 | 5167 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| t0029 | 0/0 | 5167 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| t0030 | 0/0 | 5167 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0065 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0180 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3129 | 211 | 82 | 58 | 33 | 13 | 23 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0002 | 0/0 | 3129 | 4 | 0 | 1 | 0 | 3 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0003 | 0/0 | 3129 | 4 | 4 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0005 | 0/0 | 3129 | 2 | 0 | 2 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0006 | 0/0 | 3129 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0007 | 0/0 | 3129 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0008 | 0/0 | 3129 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0010 | 0/0 | 3129 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0002c0004 | 0/0 | 3129 | 2 | 0 | 0 | 0 | 0 | 2 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0003c0009 | 0/0 | 3129 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 8295 | 103 | 42 | 22 | 20 | 5 | 13 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0001t0002 | 0/0 | 8299 | 26 | 14 | 3 | 5 | 1 | 3 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0001t0003 | 0/1 | 8295 | 27 | 1 | 18 | 0 | 5 | 2 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0001t0004 | 0/0 | 8299 | 9 | 8 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0001t0005 | 0/0 | 8295 | 8 | 1 | 4 | 0 | 1 | 2 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0001t0006 | 0/0 | 8295 | 6 | 5 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0001t0007 | 0/0 | 8295 | 5 | 0 | 4 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0001t0008 | 0/0 | 8295 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0001t0010 | 0/0 | 8295 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0001t0011 | 0/0 | 8299 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0001t0012 | 0/0 | 8299 | 2 | 1 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0001t0013 | 0/0 | 8295 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0001t0014 | 0/0 | 8295 | 2 | 1 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0001t0015 | 0/0 | 8295 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0001t0016 | 0/0 | 8295 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0001t0017 | 0/0 | 8299 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0001t0018 | 0/0 | 8299 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0001t0019 | 0/0 | 8299 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0001t0021 | 0/0 | 8295 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0001t0022 | 0/0 | 8295 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0001t0023 | 0/0 | 8295 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0001t0024 | 0/0 | 8295 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0001t0025 | 0/0 | 8295 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0001t0026 | 0/0 | 8295 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0001t0027 | 0/0 | 8295 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0001t0028 | 0/0 | 8295 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0001t0029 | 0/0 | 8295 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0002t0001 | 0/0 | 8295 | 4 | 0 | 1 | 0 | 3 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0003t0002 | 0/0 | 8299 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0003t0004 | 0/0 | 8299 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0003t0020 | 0/0 | 8299 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0005t0009 | 0/0 | 8295 | 2 | 0 | 2 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0006t0001 | 0/0 | 8295 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0007t0002 | 0/0 | 8299 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0008t0030 | 0/0 | 8295 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0001c0010t0001 | 0/0 | 8295 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0002c0004t0003 | 0/0 | 8295 | 2 | 0 | 0 | 0 | 0 | 2 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| a0003c0009t0001 | 0/0 | 8295 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | copy fasta | chr12 | 110276247 | 110356093 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0065 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0180 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0005g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0005g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0005g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0005g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0006g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0006g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0006g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0007g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0007g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0007g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0007g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0007g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0008g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0008g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0010g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0010g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0011g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0011g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0012g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0012g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0013g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0013g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0014g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0014g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0015g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0015g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0016g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0017g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0018g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0019g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0021g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0022g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0023g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0024g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0025g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0026g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0027g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0028g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0001t0029g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0003t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0003t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0003t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0003t0020g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0005t0009g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0005t0009g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0006t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0007t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0008t0030g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0001c0010t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0002c0004t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0002c0004t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| a0003c0009t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | GBR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | GBR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0209 | EUR | FIN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0048 | EUR | FIN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0192 | EUR | FIN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00423 | hp1 | a0001 | c0001 | t0023 | g0139 | EAS | CHS | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0188 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0210 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00738 | hp1 | a0001 | c0005 | t0009 | g0221 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0124 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01069 | hp1 | a0001 | c0001 | t0007 | g0051 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01069 | hp2 | a0001 | c0005 | t0009 | g0220 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01071 | hp1 | a0001 | c0001 | t0007 | g0049 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0190 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0159 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01074 | hp2 | a0001 | c0001 | t0028 | g0207 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0189 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01099 | hp1 | a0001 | c0001 | t0012 | g0223 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01109 | hp1 | a0001 | c0001 | t0014 | g0177 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0169 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01175 | hp1 | a0001 | c0001 | t0005 | g0162 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0181 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0185 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01255 | hp2 | a0001 | c0001 | t0005 | g0120 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0195 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0225 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01346 | hp1 | a0001 | c0001 | t0029 | g0198 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0203 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0187 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | IBS | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0114 | EUR | IBS | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0118 | EUR | IBS | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0200 | EUR | IBS | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0176 | EUR | IBS | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0117 | EUR | IBS | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01884 | hp1 | a0001 | c0001 | t0015 | g0078 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01891 | hp2 | a0001 | c0003 | t0020 | g0018 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0186 | AMR | PEL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01928 | hp2 | a0001 | c0001 | t0026 | g0115 | AMR | PEL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0191 | AMR | PEL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01943 | hp1 | a0001 | c0001 | t0006 | g0016 | AMR | PEL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01943 | hp2 | a0001 | c0001 | t0007 | g0050 | AMR | PEL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0197 | AMR | PEL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0179 | AMR | PEL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0193 | AMR | PEL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0213 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02145 | hp1 | a0001 | c0001 | t0012 | g0224 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02145 | hp2 | a0001 | c0008 | t0030 | g0184 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02257 | hp2 | a0001 | c0001 | t0018 | g0025 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0199 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0173 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02293 | hp1 | a0001 | c0001 | t0007 | g0052 | AMR | PEL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0201 | AMR | PEL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0122 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02615 | hp1 | a0001 | c0001 | t0021 | g0028 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0168 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0171 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0174 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0012 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0219 | SAS | PJL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02717 | hp2 | a0001 | c0007 | t0002 | g0024 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02735 | hp2 | a0001 | c0001 | t0005 | g0111 | SAS | PJL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0170 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02922 | hp1 | a0001 | c0003 | t0002 | g0019 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02970 | hp1 | a0001 | c0001 | t0015 | g0077 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02970 | hp2 | a0001 | c0001 | t0011 | g0057 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02976 | hp2 | a0001 | c0001 | t0017 | g0003 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0013 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0175 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0014 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03195 | hp1 | a0001 | c0003 | t0002 | g0020 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | MSL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | MSL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03490 | hp2 | a0002 | c0004 | t0003 | g0182 | SAS | PJL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03492 | hp1 | a0002 | c0004 | t0003 | g0183 | SAS | PJL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03516 | hp1 | a0001 | c0001 | t0011 | g0058 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0212 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | MSL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | STU | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | STU | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | STU | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG04115 | hp2 | a0001 | c0001 | t0016 | g0216 | SAS | STU | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0194 | SAS | BEB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0045 | SAS | BEB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | STU | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG04199 | hp2 | a0001 | c0001 | t0025 | g0075 | SAS | STU | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG04204 | hp1 | a0001 | c0001 | t0027 | g0202 | SAS | STU | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | STU | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | STU | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG04228 | hp2 | a0001 | c0010 | t0001 | g0104 | SAS | STU | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | YRI | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | YRI | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | YRI | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0172 | AFR | YRI | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18946 | hp1 | a0001 | c0001 | t0013 | g0086 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18946 | hp2 | a0001 | c0001 | t0008 | g0164 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18959 | hp2 | a0001 | c0001 | t0013 | g0084 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18973 | hp1 | a0001 | c0001 | t0022 | g0142 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18995 | hp1 | a0001 | c0006 | t0001 | g0163 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18998 | hp1 | a0001 | c0001 | t0008 | g0166 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | LWK | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | LWK | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | LWK | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19062 | hp2 | a0001 | c0001 | t0010 | g0136 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19077 | hp2 | a0001 | c0001 | t0010 | g0137 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | YRI | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ASW | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ASW | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0204 | EUR | TSI | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | TSI | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA20805 | hp1 | a0001 | c0001 | t0007 | g0053 | EUR | TSI | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0125 | EUR | TSI | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | GIH | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0110 | SAS | GIH | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01123 | hp1 | a0003 | c0009 | t0001 | g0064 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0196 | AMR | CLM | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02109 | hp2 | a0001 | c0001 | t0014 | g0178 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02486 | hp1 | a0001 | c0003 | t0004 | g0217 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03471 | hp1 | a0001 | c0001 | t0019 | g0046 | AFR | MSL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | MSL | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA21309 | hp1 | a0001 | c0001 | t0024 | g0093 | AFR | LWK | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | LWK | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0180 | REF | REF | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0065 | REF | REF | ATP2A2_chr12_110276247_110356093 | ATP2A2 | chr12 | 110276247 | 110356093 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110332597
|
A | G | 1 | a0003 | 1 | HG01123.hp1 | missense_variant&splice_region_variant | MODERATE | c.1096A>G | p.Met366Val | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 9/20 | 1639/8295 | 1096/3129 | 366/1042 | chr12 | 110332597 | ||
| chr12:110346405
|
A | G | 1 | a0002 | 2 | HG03490.hp2 HG03492.hp1 |
missense_variant | MODERATE | c.3064A>G | p.Ile1022Val | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 3607/8295 | 3064/3129 | 1022/1042 | chr12 | 110346405 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110281870
|
A | G | 1 | a0001c0005 | 2 | HG00738.hp1 HG01069.hp2 |
synonymous_variant | LOW | c.81A>G | p.Glu27Glu | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 1/20 | 624/8295 | 81/3129 | 27/1042 | chr12 | 110281870 | ||
| chr12:110296601
|
A | G | 1 | a0001c0005 | 2 | HG00738.hp1 HG01069.hp2 |
splice_region_variant&synonymous_variant | LOW | c.327A>G | p.Glu109Glu | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/20 | 870/8295 | 327/3129 | 109/1042 | chr12 | 110296601 | ||
| chr12:110326424
|
C | T | 1 | a0001c0010 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.579C>T | p.Pro193Pro | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 7/20 | 1122/8295 | 579/3129 | 193/1042 | chr12 | 110326424 | ||
| chr12:110342302
|
G | A | 1 | a0001c0002 | 4 | HG01261.hp2 HG01515.hp2 HG01516.hp1 others(1): Show |
synonymous_variant | LOW | c.2172G>A | p.Ala724Ala | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 15/20 | 2715/8295 | 2172/3129 | 724/1042 | chr12 | 110342302 | ||
| chr12:110342440
|
A | G | 1 | a0001c0008 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.2310A>G | p.Glu770Glu | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 15/20 | 2853/8295 | 2310/3129 | 770/1042 | chr12 | 110342440 | ||
| chr12:110345269
|
A | G | 1 | a0001c0003 | 4 | HG01891.hp2 HG02486.hp1 HG02922.hp1 others(1): Show |
synonymous_variant | LOW | c.2628A>G | p.Lys876Lys | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 18/20 | 3171/8295 | 2628/3129 | 876/1042 | chr12 | 110345269 | ||
| chr12:110346007
|
C | T | 1 | a0001c0007 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.2748C>T | p.Ser916Ser | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 19/20 | 3291/8295 | 2748/3129 | 916/1042 | chr12 | 110346007 | ||
| chr12:110346266
|
C | G | 1 | a0001c0006 | 1 | NA18995.hp1 | synonymous_variant | LOW | c.2925C>G | p.Pro975Pro | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 3468/8295 | 2925/3129 | 975/1042 | chr12 | 110346266 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110281270
|
G | C | 1 | a0001c0001t0008 | 2 | NA18946.hp2 NA18998.hp1 |
5_prime_UTR_variant | MODIFIER | c.-520G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 1/20 | 520 | chr12 | 110281270 | |||||
| chr12:110281290
|
T | C | 1 | a0001c0005t0009 | 2 | HG00738.hp1 HG01069.hp2 |
5_prime_UTR_variant | MODIFIER | c.-500T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 1/20 | 500 | chr12 | 110281290 | |||||
| chr12:110281387
|
C | G | 6 | a0001c0001t0003a0001c0001t0027a0001c0001t0028others(3): Show | 33 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(30): Show |
5_prime_UTR_variant | MODIFIER | c.-403C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 1/20 | 403 | chr12 | 110281387 | |||||
| chr12:110281516
|
G | C | 2 | a0001c0001t0008a0001c0001t0010 | 4 | NA18946.hp2 NA18998.hp1 NA19062.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-274G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 1/20 | 274 | chr12 | 110281516 | |||||
| chr12:110281550
|
G | A | 1 | a0001c0001t0016 | 1 | HG04115.hp2 | 5_prime_UTR_variant | MODIFIER | c.-240G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 1/20 | 240 | chr12 | 110281550 | |||||
| chr12:110281569
|
A | G | 1 | a0001c0001t0026 | 1 | HG01928.hp2 | 5_prime_UTR_variant | MODIFIER | c.-221A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 1/20 | 221 | chr12 | 110281569 | |||||
| chr12:110281780
|
C | G | 1 | a0001c0005t0009 | 2 | HG00738.hp1 HG01069.hp2 |
5_prime_UTR_variant | MODIFIER | c.-10C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 1/20 | 10 | chr12 | 110281780 | |||||
| chr12:110346773
|
T | C | 1 | a0001c0001t0005 | 8 | HG00738.hp2 HG01074.hp1 HG01175.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*303T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 303 | chr12 | 110346773 | |||||
| chr12:110346847
|
T | C | 1 | a0001c0001t0027 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*377T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 377 | chr12 | 110346847 | |||||
| chr12:110347055
|
G | A | 1 | a0001c0001t0011 | 2 | HG02970.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*585G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 585 | chr12 | 110347055 | |||||
| chr12:110347102
|
C | CATCA | 11 | a0001c0001t0002a0001c0001t0004a0001c0001t0011others(8): Show | 47 | HG00323.hp1 HG01081.hp1 HG01099.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*633_*636dupATCA | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 637 | INFO_REALIGN_3_PRIME | chr12 | 110347102 | ||||
| chr12:110347162
|
C | G | 1 | a0001c0001t0025 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*692C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 692 | chr12 | 110347162 | |||||
| chr12:110347254
|
A | T | 1 | a0001c0001t0012 | 2 | HG01099.hp1 HG02145.hp1 |
3_prime_UTR_variant | MODIFIER | c.*784A>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 784 | chr12 | 110347254 | |||||
| chr12:110347557
|
G | A | 1 | a0001c0001t0028 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1087G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 1087 | chr12 | 110347557 | |||||
| chr12:110347704
|
G | A | 3 | a0001c0001t0004a0001c0001t0017a0001c0003t0004 | 11 | HG01167.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1234G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 1234 | chr12 | 110347704 | |||||
| chr12:110347755
|
G | A | 1 | a0001c0001t0013 | 2 | NA18946.hp1 NA18959.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1285G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 1285 | chr12 | 110347755 | |||||
| chr12:110348131
|
G | A | 1 | a0001c0001t0014 | 2 | HG01109.hp1 HG02109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1661G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 1661 | chr12 | 110348131 | |||||
| chr12:110348237
|
G | A | 2 | a0001c0001t0017a0001c0001t0021 | 2 | HG02615.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1767G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 1767 | chr12 | 110348237 | |||||
| chr12:110348249
|
C | T | 1 | a0001c0001t0007 | 5 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1779C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 1779 | chr12 | 110348249 | |||||
| chr12:110348411
|
C | G | 1 | a0001c0005t0009 | 2 | HG00738.hp1 HG01069.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1941C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 1941 | chr12 | 110348411 | |||||
| chr12:110348445
|
C | T | 1 | a0001c0001t0006 | 6 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1975C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 1975 | chr12 | 110348445 | |||||
| chr12:110348750
|
G | T | 1 | a0001c0008t0030 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2280G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 2280 | chr12 | 110348750 | |||||
| chr12:110348804
|
G | A | 1 | a0001c0005t0009 | 2 | HG00738.hp1 HG01069.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2334G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 2334 | chr12 | 110348804 | |||||
| chr12:110348832
|
A | T | 1 | a0001c0005t0009 | 2 | HG00738.hp1 HG01069.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2362A>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 2362 | chr12 | 110348832 | |||||
| chr12:110349070
|
G | C | 1 | a0001c0001t0022 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2600G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 2600 | chr12 | 110349070 | |||||
| chr12:110349170
|
G | A | 1 | a0001c0001t0029 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2700G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 2700 | chr12 | 110349170 | |||||
| chr12:110349170
|
G | C | 1 | a0001c0001t0015 | 2 | HG01884.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2700G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 2700 | chr12 | 110349170 | |||||
| chr12:110349507
|
T | G | 1 | a0001c0001t0018 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3037T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 3037 | chr12 | 110349507 | |||||
| chr12:110349778
|
G | A | 1 | a0001c0001t0019 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3308G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 3308 | chr12 | 110349778 | |||||
| chr12:110350028
|
C | G | 1 | a0001c0001t0022 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3558C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 3558 | chr12 | 110350028 | |||||
| chr12:110350072
|
C | T | 1 | a0001c0001t0007 | 5 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3602C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 3602 | chr12 | 110350072 | |||||
| chr12:110350517
|
A | G | 1 | a0001c0005t0009 | 2 | HG00738.hp1 HG01069.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4047A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 4047 | chr12 | 110350517 | |||||
| chr12:110350582
|
C | T | 1 | a0001c0003t0020 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4112C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 4112 | chr12 | 110350582 | |||||
| chr12:110350673
|
A | G | 1 | a0001c0001t0024 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4203A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 4203 | chr12 | 110350673 | |||||
| chr12:110350941
|
G | A | 1 | a0001c0001t0023 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4471G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 20/20 | 4471 | chr12 | 110350941 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:110282363
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.119-241C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 1/19 | chr12 | 110282363 | ||||||
| chr12:110282390
|
A | C | 1 | a0001c0002t0001g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.119-214A>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 1/19 | chr12 | 110282390 | ||||||
| chr12:110282421
|
C | T | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG01099.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.119-183C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 1/19 | chr12 | 110282421 | ||||||
| chr12:110282508
|
G | A | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG01099.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.119-96G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 1/19 | chr12 | 110282508 | ||||||
| chr12:110282517
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.119-87A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 1/19 | chr12 | 110282517 | ||||||
| chr12:110282522
|
A | G | 3 | a0001c0001t0001g0222a0001c0005t0009g0220a0001c0005t0009g0221 | 3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.119-82A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 1/19 | chr12 | 110282522 | ||||||
| chr12:110282538
|
GTC | G | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.119-58_119-57delCT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr12 | 110282538 | |||||
| chr12:110282917
|
T | C | 1 | a0001c0001t0017g0003 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.219+122T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110282917 | ||||||
| chr12:110282970
|
A | G | 1 | a0001c0001t0003g0219 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.219+175A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110282970 | ||||||
| chr12:110283698
|
G | A | 1 | a0001c0001t0004g0004 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.219+903G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110283698 | ||||||
| chr12:110283801
|
A | G | 2 | a0001c0001t0001g0218a0001c0003t0004g0217 | 2 | HG02486.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.219+1006A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110283801 | ||||||
| chr12:110283957
|
G | A | 1 | a0001c0001t0002g0005 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.219+1162G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110283957 | ||||||
| chr12:110284107
|
G | A | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.219+1312G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110284107 | ||||||
| chr12:110284147
|
T | C | 1 | a0001c0001t0001g0006 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.219+1352T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110284147 | ||||||
| chr12:110284342
|
A | G | 1 | a0001c0001t0016g0216 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.219+1547A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110284342 | ||||||
| chr12:110284387
|
C | T | 2 | a0001c0001t0002g0214a0001c0001t0002g0215 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.219+1592C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110284387 | ||||||
| chr12:110284494
|
T | G | 1 | a0001c0001t0001g0007 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219+1699T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110284494 | ||||||
| chr12:110284530
|
T | C | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02717.hp1 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.219+1735T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110284530 | ||||||
| chr12:110284583
|
A | G | 3 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0213 | 3 | HG02055.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.219+1788A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110284583 | ||||||
| chr12:110284827
|
A | G | 41 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(38): Show | 42 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.219+2032A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110284827 | ||||||
| chr12:110285123
|
GACTT | G | 9 | a0001c0001t0004g0004a0001c0001t0004g0168a0001c0001t0004g0169others(6): Show | 9 | HG01167.hp1 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.219+2333_219+2336d others(6): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr12 | 110285123 | |||||
| chr12:110285169
|
T | A | 6 | a0001c0001t0006g0012a0001c0001t0006g0013a0001c0001t0006g0014others(3): Show | 6 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.219+2374T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110285169 | ||||||
| chr12:110285345
|
C | A | 3 | a0001c0003t0002g0019a0001c0003t0002g0020a0001c0003t0020g0018 | 3 | HG01891.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219+2550C>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110285345 | ||||||
| chr12:110285397
|
G | A | 1 | a0001c0001t0006g0012 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.219+2602G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110285397 | ||||||
| chr12:110285398
|
T | C | 115 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(112): Show | 116 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.219+2603T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110285398 | ||||||
| chr12:110285440
|
C | T | 77 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0095others(74): Show | 77 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.219+2645C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110285440 | ||||||
| chr12:110285915
|
C | CT | 32 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(29): Show | 32 | HG00423.hp2 HG00558.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.219+3140dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr12 | 110285915 | |||||
| chr12:110285915
|
CT | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0095others(5): Show | 8 | HG00738.hp1 HG01069.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.219+3140delT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr12 | 110285915 | |||||
| chr12:110285936
|
A | T | 1 | a0001c0001t0002g0062 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.219+3141A>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110285936 | ||||||
| chr12:110285993
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.219+3198G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110285993 | ||||||
| chr12:110286118
|
T | A | 1 | a0001c0001t0001g0097 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.219+3323T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110286118 | ||||||
| chr12:110286193
|
G | T | 1 | a0001c0001t0004g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.219+3398G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110286193 | ||||||
| chr12:110286246
|
A | G | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.219+3451A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110286246 | ||||||
| chr12:110286316
|
A | T | 7 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0211others(4): Show | 7 | HG02055.hp2 HG02809.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.219+3521A>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110286316 | ||||||
| chr12:110286394
|
T | C | 4 | a0001c0001t0002g0005a0001c0001t0002g0026a0001c0001t0018g0025others(1): Show | 4 | HG02257.hp2 HG02559.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.219+3599T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110286394 | ||||||
| chr12:110286467
|
C | T | 53 | a0001c0001t0001g0222a0001c0001t0002g0005a0001c0001t0002g0022others(50): Show | 53 | HG00323.hp1 HG00738.hp1 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.219+3672C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110286467 | ||||||
| chr12:110286614
|
A | G | 1 | a0001c0001t0001g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.219+3819A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110286614 | ||||||
| chr12:110286700
|
T | TA | 9 | a0001c0001t0002g0061a0001c0001t0006g0012a0001c0001t0006g0013others(6): Show | 9 | HG01081.hp1 HG01099.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.219+3920dupA | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr12 | 110286700 | |||||
| chr12:110286701
|
A | T | 1 | a0001c0001t0002g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.219+3906A>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110286701 | ||||||
| chr12:110286868
|
A | G | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.219+4073A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110286868 | ||||||
| chr12:110286910
|
G | C | 1 | a0001c0001t0001g0098 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.219+4115G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110286910 | ||||||
| chr12:110287050
|
C | T | 1 | a0001c0001t0002g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.219+4255C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110287050 | ||||||
| chr12:110287262
|
T | A | 3 | a0001c0001t0001g0222a0001c0005t0009g0220a0001c0005t0009g0221 | 3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.219+4467T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110287262 | ||||||
| chr12:110287300
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.219+4505G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110287300 | ||||||
| chr12:110287613
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.220-4407C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110287613 | ||||||
| chr12:110287749
|
G | A | 3 | a0001c0003t0002g0019a0001c0003t0002g0020a0001c0003t0020g0018 | 3 | HG01891.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.220-4271G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110287749 | ||||||
| chr12:110287764
|
A | G | 3 | a0001c0001t0001g0222a0001c0005t0009g0220a0001c0005t0009g0221 | 3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.220-4256A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110287764 | ||||||
| chr12:110287865
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.220-4155C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110287865 | ||||||
| chr12:110287978
|
G | A | 1 | a0001c0001t0002g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.220-4042G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110287978 | ||||||
| chr12:110288101
|
C | CT | 94 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0030others(91): Show | 94 | HG00323.hp1 HG00558.hp1 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.220-3895dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr12 | 110288101 | |||||
| chr12:110288101
|
C | CTT | 11 | a0001c0001t0001g0074a0001c0001t0001g0092a0001c0001t0002g0005others(8): Show | 11 | HG00423.hp2 HG01175.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-3896_220-3895d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr12 | 110288101 | |||||
| chr12:110288174
|
G | A | 1 | a0001c0001t0002g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.220-3846G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110288174 | ||||||
| chr12:110288266
|
T | TA | 9 | a0001c0001t0002g0005a0001c0001t0002g0026a0001c0001t0002g0038others(6): Show | 9 | HG01099.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.220-3745dupA | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr12 | 110288266 | |||||
| chr12:110288276
|
T | A | 37 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0039others(34): Show | 37 | HG00323.hp1 HG01167.hp1 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.220-3744T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110288276 | ||||||
| chr12:110288404
|
C | CT | 6 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(3): Show | 6 | HG00558.hp1 HG00738.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.220-3603dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr12 | 110288404 | |||||
| chr12:110288415
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.220-3605T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110288415 | ||||||
| chr12:110288438
|
C | G | 1 | a0001c0001t0001g0088 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.220-3582C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110288438 | ||||||
| chr12:110288497
|
C | T | 2 | a0001c0001t0002g0048a0001c0001t0002g0055 | 2 | HG00323.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.220-3523C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110288497 | ||||||
| chr12:110288653
|
C | A | 1 | a0001c0001t0002g0062 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.220-3367C>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110288653 | ||||||
| chr12:110288741
|
A | G | 3 | a0001c0003t0002g0019a0001c0003t0002g0020a0001c0003t0020g0018 | 3 | HG01891.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.220-3279A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110288741 | ||||||
| chr12:110288860
|
G | A | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.220-3160G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110288860 | ||||||
| chr12:110289012
|
A | G | 1 | a0001c0006t0001g0163 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.220-3008A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110289012 | ||||||
| chr12:110289386
|
T | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0150 | 2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.220-2634T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110289386 | ||||||
| chr12:110289450
|
C | T | 1 | a0001c0001t0003g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.220-2570C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110289450 | ||||||
| chr12:110289608
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.220-2412G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110289608 | ||||||
| chr12:110289615
|
A | G | 2 | a0001c0001t0002g0047a0001c0001t0002g0054 | 2 | NA18952.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.220-2405A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110289615 | ||||||
| chr12:110289805
|
G | T | 6 | a0001c0001t0006g0012a0001c0001t0006g0013a0001c0001t0006g0014others(3): Show | 6 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.220-2215G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110289805 | ||||||
| chr12:110290044
|
A | G | 17 | a0001c0001t0001g0069a0001c0001t0001g0073a0001c0001t0001g0082others(14): Show | 17 | HG00423.hp2 HG00558.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.220-1976A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110290044 | ||||||
| chr12:110290196
|
C | G | 39 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(36): Show | 40 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.220-1824C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110290196 | ||||||
| chr12:110290294
|
C | G | 7 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0041others(4): Show | 7 | HG01099.hp1 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.220-1726C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110290294 | ||||||
| chr12:110290391
|
T | C | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.220-1629T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110290391 | ||||||
| chr12:110290560
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.220-1460A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110290560 | ||||||
| chr12:110290700
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.220-1320G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110290700 | ||||||
| chr12:110291002
|
G | A | 2 | a0001c0001t0001g0151a0001c0001t0002g0056 | 2 | HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.220-1018G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110291002 | ||||||
| chr12:110291034
|
G | C | 1 | a0001c0001t0003g0179 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.220-986G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110291034 | ||||||
| chr12:110291044
|
G | A | 9 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(6): Show | 9 | HG01168.hp2 HG01169.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.220-976G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110291044 | ||||||
| chr12:110291204
|
G | A | 11 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0030others(8): Show | 11 | HG01168.hp2 HG01169.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.220-816G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110291204 | ||||||
| chr12:110291328
|
C | T | 2 | a0001c0001t0003g0002a0001c0001t0028g0207 | 3 | HG00741.hp1 HG01074.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.220-692C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110291328 | ||||||
| chr12:110291593
|
A | C | 1 | a0001c0001t0001g0206 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.220-427A>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110291593 | ||||||
| chr12:110291640
|
CT | C | 143 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0021others(140): Show | 143 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.220-360delT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr12 | 110291640 | |||||
| chr12:110291640
|
CTT | C | 11 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0226others(8): Show | 11 | HG00323.hp1 HG01169.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-361_220-360del others(2): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr12 | 110291640 | |||||
| chr12:110291808
|
A | G | 3 | a0001c0001t0001g0222a0001c0005t0009g0220a0001c0005t0009g0221 | 3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.220-212A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | chr12 | 110291808 | ||||||
| chr12:110291942
|
C | CG | 10 | a0001c0001t0001g0069a0001c0001t0004g0004a0001c0001t0004g0168others(7): Show | 10 | HG01167.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.220-76dupG | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr12 | 110291942 | |||||
| chr12:110292273
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.324+149A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110292273 | ||||||
| chr12:110292808
|
C | T | 6 | a0001c0001t0006g0012a0001c0001t0006g0013a0001c0001t0006g0014others(3): Show | 6 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.324+684C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110292808 | ||||||
| chr12:110292903
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.324+779A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110292903 | ||||||
| chr12:110292904
|
A | G | 5 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0001t0007g0051others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.324+780A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110292904 | ||||||
| chr12:110293046
|
G | A | 1 | a0001c0001t0002g0055 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.324+922G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293046 | ||||||
| chr12:110293367
|
C | CT | 19 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0069others(16): Show | 19 | HG00423.hp1 HG00558.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.324+1264dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293367 | |||||
| chr12:110293367
|
CTT | C | 5 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0001t0007g0051others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.324+1263_324+1264d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293367 | |||||
| chr12:110293373
|
T | G | 3 | a0001c0001t0001g0009a0001c0001t0003g0179a0001c0001t0003g0219 | 3 | HG01978.hp2 HG02683.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.324+1249T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293373 | ||||||
| chr12:110293377
|
T | G | 36 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(33): Show | 37 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.324+1253T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293377 | ||||||
| chr12:110293378
|
TTTTTTTT others(4): Show |
T | 1 | a0001c0001t0001g0101 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.324+1258_324+1268d others(13): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293378 | |||||
| chr12:110293381
|
T | G | 41 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(38): Show | 42 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.324+1257T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293381 | ||||||
| chr12:110293385
|
T | G | 45 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(42): Show | 46 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.324+1261T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293385 | ||||||
| chr12:110293385
|
T | TTTTG | 6 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(3): Show | 6 | HG01168.hp2 HG01169.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.324+1285_324+1288d others(6): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293385 | |||||
| chr12:110293386
|
TTTG | T | 14 | a0001c0001t0002g0048a0001c0001t0004g0004a0001c0001t0004g0168others(11): Show | 14 | HG00323.hp1 HG01167.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.324+1265_324+1267d others(5): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293386 | |||||
| chr12:110293387
|
TTG | T | 17 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0039others(14): Show | 17 | HG01175.hp2 HG02630.hp1 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.324+1265_324+1266d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293387 | |||||
| chr12:110293388
|
TG | T | 23 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(20): Show | 23 | HG00140.hp1 HG01069.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.324+1265delG | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293388 | ||||||
| chr12:110293389
|
G | T | 59 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0095others(56): Show | 59 | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.324+1265G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293389 | ||||||
| chr12:110293393
|
G | T | 3 | a0001c0001t0001g0133a0001c0005t0009g0220a0001c0005t0009g0221 | 3 | HG00738.hp1 HG01069.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.324+1269G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293393 | ||||||
| chr12:110293475
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.324+1351A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293475 | ||||||
| chr12:110293485
|
C | G | 6 | a0001c0001t0006g0012a0001c0001t0006g0013a0001c0001t0006g0014others(3): Show | 6 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.324+1361C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293485 | ||||||
| chr12:110293570
|
C | T | 48 | a0001c0001t0001g0222a0001c0001t0002g0005a0001c0001t0002g0022others(45): Show | 48 | HG00323.hp1 HG00738.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.324+1446C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293570 | ||||||
| chr12:110293619
|
T | C | 2 | a0001c0001t0001g0148a0001c0001t0001g0152 | 2 | HG01934.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.324+1495T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293619 | ||||||
| chr12:110293657
|
A | G | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.324+1533A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293657 | ||||||
| chr12:110293680
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.324+1556G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293680 | ||||||
| chr12:110293691
|
C | T | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.324+1567C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293691 | ||||||
| chr12:110293819
|
CAT | C | 3 | a0001c0001t0001g0095a0001c0001t0001g0155a0001c0001t0003g0203 | 3 | HG01167.hp2 HG01169.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.324+1702_324+1703d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293819 | |||||
| chr12:110293824
|
A | ATGTGTG | 2 | a0001c0001t0001g0072a0001c0001t0001g0092 | 2 | HG00423.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.324+1701_324+1702i others(8): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293824 | |||||
| chr12:110293826
|
A | ATG | 34 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(31): Show | 35 | HG00558.hp2 HG00741.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.324+1740_324+1741d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293826 | |||||
| chr12:110293826
|
A | ATGTG | 29 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(26): Show | 29 | HG00558.hp1 HG00738.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.324+1738_324+1741d others(6): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293826 | |||||
| chr12:110293826
|
A | ATGTGTG | 23 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0037others(20): Show | 23 | HG00423.hp1 HG01099.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.324+1736_324+1741d others(8): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293826 | |||||
| chr12:110293826
|
A | ATGTGTGT others(1): Show |
5 | a0001c0001t0001g0073a0001c0001t0001g0079a0001c0001t0004g0004others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.324+1734_324+1741d others(10): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293826 | |||||
| chr12:110293826
|
A | ATGTGTGT others(3): Show |
2 | a0001c0001t0001g0148a0001c0001t0006g0016 | 2 | HG01934.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.324+1732_324+1741d others(12): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293826 | |||||
| chr12:110293826
|
A | ATGTGTGT others(5): Show |
2 | a0001c0001t0001g0080a0001c0001t0002g0038 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.324+1730_324+1741d others(14): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293826 | |||||
| chr12:110293826
|
A | G | 10 | a0001c0001t0001g0072a0001c0001t0001g0092a0001c0001t0001g0132others(7): Show | 10 | HG00423.hp2 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.324+1702A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293826 | ||||||
| chr12:110293826
|
ATG | A | 9 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0105others(6): Show | 9 | HG00140.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.324+1740_324+1741d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293826 | |||||
| chr12:110293826
|
ATGTG | A | 5 | a0001c0001t0001g0106a0001c0001t0002g0005a0001c0001t0002g0048others(2): Show | 5 | HG00323.hp1 HG02922.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.324+1738_324+1741d others(6): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293826 | |||||
| chr12:110293826
|
ATGTGTG | A | 4 | a0001c0001t0002g0056a0001c0001t0018g0025a0001c0001t0022g0142others(1): Show | 4 | HG02257.hp2 HG02717.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+1736_324+1741d others(8): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293826 | |||||
| chr12:110293826
|
ATGTGTGT others(3): Show |
A | 1 | a0001c0001t0001g0089 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.324+1732_324+1741d others(12): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293826 | |||||
| chr12:110293826
|
ATGTGTGT others(7): Show |
A | 1 | a0001c0001t0001g0205 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.324+1728_324+1741d others(16): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293826 | |||||
| chr12:110293850
|
G | GTATATAT others(13): Show |
1 | a0001c0005t0009g0221 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.324+1727_324+1728i others(22): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293850 | |||||
| chr12:110293852
|
G | A | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.324+1728G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293852 | ||||||
| chr12:110293854
|
G | A | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.324+1730G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293854 | ||||||
| chr12:110293856
|
G | A | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.324+1732G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293856 | ||||||
| chr12:110293858
|
G | A | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.324+1734G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293858 | ||||||
| chr12:110293860
|
G | A | 18 | a0001c0001t0002g0022a0001c0001t0002g0042a0001c0001t0002g0043others(15): Show | 18 | HG00738.hp1 HG01069.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.324+1736G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293860 | ||||||
| chr12:110293862
|
G | A | 21 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0042others(18): Show | 21 | HG00738.hp1 HG01069.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.324+1738G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293862 | ||||||
| chr12:110293864
|
G | A | 27 | a0001c0001t0002g0005a0001c0001t0002g0022a0001c0001t0002g0023others(24): Show | 27 | HG00323.hp1 HG00738.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.324+1740G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293864 | ||||||
| chr12:110293864
|
G | GTGTGTGT others(1): Show |
2 | a0001c0001t0004g0168a0001c0001t0004g0174 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.324+1741_324+1742i others(10): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293864 | |||||
| chr12:110293864
|
G | GTGTGTGT others(7): Show |
1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.324+1741_324+1742i others(16): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293864 | |||||
| chr12:110293866
|
A | G | 1 | a0001c0001t0027g0202 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.324+1742A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293866 | ||||||
| chr12:110293870
|
A | AT | 7 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0126others(4): Show | 7 | HG01175.hp1 HG02698.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+1771dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293870 | |||||
| chr12:110293870
|
A | ATT | 7 | a0001c0001t0004g0004a0001c0001t0004g0169a0001c0001t0004g0170others(4): Show | 7 | HG01167.hp1 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.324+1770_324+1771d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293870 | |||||
| chr12:110293870
|
A | T | 1 | a0001c0001t0001g0146 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.324+1746A>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293870 | ||||||
| chr12:110293870
|
AT | A | 13 | a0001c0001t0001g0092a0001c0001t0001g0096a0001c0001t0001g0140others(10): Show | 13 | HG00423.hp2 HG01071.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.324+1771delT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293870 | |||||
| chr12:110293870
|
ATT | A | 22 | a0001c0001t0001g0021a0001c0001t0001g0073a0001c0001t0001g0082others(19): Show | 22 | HG00558.hp1 HG01943.hp1 HG02071.hp1 others(19): Show |
intron_variant | MODIFIER | c.324+1770_324+1771d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293870 | |||||
| chr12:110293870
|
ATTT | A | 18 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0042others(15): Show | 18 | HG01074.hp2 HG01175.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.324+1769_324+1771d others(5): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110293870 | |||||
| chr12:110293871
|
T | TA | 10 | a0001c0001t0001g0081a0001c0001t0001g0222a0001c0001t0003g0180others(7): Show | 10 | HG01099.hp1 HG01109.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.324+1747_324+1748i others(3): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293871 | ||||||
| chr12:110293871
|
T | TATATATA others(12): Show |
1 | a0001c0005t0009g0220 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.324+1747_324+1748i others(21): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293871 | ||||||
| chr12:110293872
|
T | A | 58 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(55): Show | 59 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.324+1748T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293872 | ||||||
| chr12:110293873
|
T | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0222 | 2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.324+1749T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293873 | ||||||
| chr12:110293874
|
T | A | 15 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(12): Show | 15 | HG00323.hp1 HG01168.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.324+1750T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293874 | ||||||
| chr12:110293875
|
T | A | 7 | a0001c0001t0001g0222a0001c0001t0002g0023a0001c0001t0002g0042others(4): Show | 7 | HG03579.hp1 NA18948.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+1751T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293875 | ||||||
| chr12:110293877
|
T | A | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.324+1753T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293877 | ||||||
| chr12:110293940
|
G | A | 9 | a0001c0001t0001g0097a0001c0001t0001g0116a0001c0001t0001g0126others(6): Show | 9 | HG01261.hp2 HG01515.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.324+1816G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110293940 | ||||||
| chr12:110294056
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.324+1932T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110294056 | ||||||
| chr12:110294201
|
G | A | 6 | a0001c0001t0006g0012a0001c0001t0006g0013a0001c0001t0006g0014others(3): Show | 6 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.324+2077G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110294201 | ||||||
| chr12:110294233
|
C | T | 6 | a0001c0001t0006g0012a0001c0001t0006g0013a0001c0001t0006g0014others(3): Show | 6 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.324+2109C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110294233 | ||||||
| chr12:110294244
|
C | T | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.324+2120C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110294244 | ||||||
| chr12:110294311
|
G | A | 4 | a0001c0001t0001g0165a0001c0001t0002g0039a0001c0001t0002g0040others(1): Show | 4 | HG02280.hp2 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+2187G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110294311 | ||||||
| chr12:110294321
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.324+2197G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110294321 | ||||||
| chr12:110294571
|
C | A | 1 | a0001c0001t0002g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.325-2028C>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110294571 | ||||||
| chr12:110294635
|
C | T | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.325-1964C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110294635 | ||||||
| chr12:110294652
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.325-1947A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110294652 | ||||||
| chr12:110294663
|
C | T | 4 | a0001c0001t0001g0095a0001c0001t0001g0154a0001c0001t0001g0155others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.325-1936C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110294663 | ||||||
| chr12:110294686
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.325-1913C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110294686 | ||||||
| chr12:110294976
|
C | T | 20 | a0001c0001t0001g0069a0001c0001t0001g0073a0001c0001t0001g0076others(17): Show | 20 | HG00423.hp2 HG00558.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.325-1623C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110294976 | ||||||
| chr12:110294977
|
G | A | 1 | a0001c0001t0002g0062 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.325-1622G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110294977 | ||||||
| chr12:110295063
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.325-1536C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110295063 | ||||||
| chr12:110295313
|
C | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.325-1286C>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110295313 | ||||||
| chr12:110295374
|
G | C | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.325-1225G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110295374 | ||||||
| chr12:110295540
|
C | G | 7 | a0001c0001t0002g0061a0001c0001t0006g0012a0001c0001t0006g0013others(4): Show | 7 | HG01081.hp1 HG01943.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.325-1059C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110295540 | ||||||
| chr12:110295546
|
T | C | 3 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0041 | 3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.325-1053T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110295546 | ||||||
| chr12:110295547
|
G | C | 1 | a0001c0001t0002g0026 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.325-1052G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110295547 | ||||||
| chr12:110295718
|
A | G | 1 | a0001c0007t0002g0024 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.325-881A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110295718 | ||||||
| chr12:110296080
|
G | T | 3 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091 | 3 | HG00558.hp1 NA18948.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.325-519G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110296080 | ||||||
| chr12:110296127
|
G | GT | 5 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-465dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr12 | 110296127 | |||||
| chr12:110296208
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.325-391G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110296208 | ||||||
| chr12:110296413
|
C | T | 32 | a0001c0001t0003g0002a0001c0001t0003g0176a0001c0001t0003g0179others(29): Show | 33 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.325-186C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110296413 | ||||||
| chr12:110296414
|
G | A | 1 | a0001c0010t0001g0104 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.325-185G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110296414 | ||||||
| chr12:110296568
|
C | G | 7 | a0001c0001t0002g0061a0001c0001t0006g0012a0001c0001t0006g0013others(4): Show | 7 | HG01081.hp1 HG01943.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.325-31C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110296568 | ||||||
| chr12:110296578
|
C | A | 1 | a0001c0001t0001g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.325-21C>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 4/19 | chr12 | 110296578 | ||||||
| chr12:110297132
|
A | G | 1 | a0001c0001t0017g0003 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.463+395A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110297132 | ||||||
| chr12:110297205
|
C | T | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.463+468C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110297205 | ||||||
| chr12:110297238
|
G | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.463+501G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110297238 | ||||||
| chr12:110297292
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.463+555G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110297292 | ||||||
| chr12:110297327
|
T | C | 6 | a0001c0001t0001g0073a0001c0001t0001g0082a0001c0001t0001g0087others(3): Show | 6 | HG04115.hp2 NA18946.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.463+590T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110297327 | ||||||
| chr12:110297394
|
C | T | 6 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0171others(3): Show | 6 | HG01167.hp1 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.463+657C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110297394 | ||||||
| chr12:110297434
|
C | CA | 27 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(24): Show | 27 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.463+715dupA | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110297434 | |||||
| chr12:110297434
|
CA | C | 22 | a0001c0001t0001g0134a0001c0001t0002g0005a0001c0001t0002g0026others(19): Show | 22 | HG00735.hp1 HG01099.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.463+715delA | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110297434 | |||||
| chr12:110297446
|
A | C | 1 | a0001c0001t0001g0113 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.463+709A>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110297446 | ||||||
| chr12:110297474
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.463+737T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110297474 | ||||||
| chr12:110297870
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.463+1133G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110297870 | ||||||
| chr12:110297892
|
GGTGTGCC others(8): Show |
G | 1 | a0001c0001t0001g0143 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.463+1156_463+1170d others(17): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110297892 | ||||||
| chr12:110298010
|
G | A | 3 | a0001c0001t0001g0222a0001c0005t0009g0220a0001c0005t0009g0221 | 3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.463+1273G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110298010 | ||||||
| chr12:110298299
|
A | G | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.463+1562A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110298299 | ||||||
| chr12:110298300
|
A | G | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.463+1563A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110298300 | ||||||
| chr12:110298323
|
T | TGTGTGTA others(4): Show |
6 | a0001c0001t0006g0012a0001c0001t0006g0013a0001c0001t0006g0014others(3): Show | 6 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.463+1593_463+1603d others(13): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110298323 | |||||
| chr12:110298814
|
G | C | 5 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0001t0007g0051others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.463+2077G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110298814 | ||||||
| chr12:110298874
|
T | C | 7 | a0001c0001t0002g0061a0001c0001t0006g0012a0001c0001t0006g0013others(4): Show | 7 | HG01081.hp1 HG01943.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.463+2137T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110298874 | ||||||
| chr12:110298875
|
C | A | 7 | a0001c0001t0002g0061a0001c0001t0006g0012a0001c0001t0006g0013others(4): Show | 7 | HG01081.hp1 HG01943.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.463+2138C>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110298875 | ||||||
| chr12:110298987
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.463+2250G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110298987 | ||||||
| chr12:110299037
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.463+2300A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110299037 | ||||||
| chr12:110299086
|
C | CAG | 12 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0098others(9): Show | 12 | HG00735.hp1 HG01106.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.463+2350_463+2351d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110299086 | |||||
| chr12:110299361
|
T | C | 1 | a0001c0001t0006g0014 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.463+2624T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110299361 | ||||||
| chr12:110299612
|
C | T | 3 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0041 | 3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.463+2875C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110299612 | ||||||
| chr12:110299650
|
G | A | 1 | a0001c0001t0002g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.463+2913G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110299650 | ||||||
| chr12:110299975
|
C | T | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.463+3238C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110299975 | ||||||
| chr12:110300002
|
C | T | 1 | a0001c0001t0004g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.463+3265C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110300002 | ||||||
| chr12:110300008
|
A | G | 2 | a0001c0001t0001g0147a0001c0006t0001g0163 | 2 | NA18995.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.463+3271A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110300008 | ||||||
| chr12:110300031
|
C | T | 36 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(33): Show | 37 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.463+3294C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110300031 | ||||||
| chr12:110300052
|
G | A | 1 | a0001c0001t0003g0002 | 2 | HG00741.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.463+3315G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110300052 | ||||||
| chr12:110300092
|
G | GTCCT | 7 | a0001c0001t0001g0027a0001c0001t0006g0012a0001c0001t0006g0013others(4): Show | 7 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.463+3368_463+3371d others(6): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110300092 | |||||
| chr12:110300116
|
T | TCCCTC | 27 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0085others(24): Show | 27 | HG00423.hp2 HG00558.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.463+3406_463+3410d others(7): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110300116 | |||||
| chr12:110300116
|
T | TCCCTCCC others(3): Show |
9 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(6): Show | 9 | HG01168.hp2 HG01169.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.463+3401_463+3410d others(12): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110300116 | |||||
| chr12:110300116
|
TCCCTC | T | 17 | a0001c0001t0001g0222a0001c0001t0004g0004a0001c0001t0004g0168others(14): Show | 17 | HG00738.hp1 HG01069.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.463+3406_463+3410d others(7): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110300116 | |||||
| chr12:110300141
|
C | A | 1 | a0001c0001t0001g0113 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.463+3404C>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110300141 | ||||||
| chr12:110300176
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.463+3439C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110300176 | ||||||
| chr12:110300179
|
T | G | 1 | a0001c0001t0001g0101 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.463+3442T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110300179 | ||||||
| chr12:110300184
|
C | CT | 57 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(54): Show | 58 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.463+3467dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110300184 | |||||
| chr12:110300184
|
C | CTT | 22 | a0001c0001t0001g0069a0001c0001t0001g0079a0001c0001t0001g0080others(19): Show | 22 | HG00423.hp2 HG00558.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.463+3466_463+3467d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110300184 | |||||
| chr12:110300184
|
CT | C | 35 | a0001c0001t0001g0119a0001c0001t0001g0135a0001c0001t0001g0147others(32): Show | 35 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.463+3467delT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110300184 | |||||
| chr12:110300184
|
CTT | C | 17 | a0001c0001t0002g0044a0001c0001t0002g0056a0001c0001t0004g0004others(14): Show | 17 | HG01069.hp2 HG01167.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.463+3466_463+3467d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110300184 | |||||
| chr12:110300340
|
A | G | 1 | a0001c0001t0005g0159 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.463+3603A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110300340 | ||||||
| chr12:110300351
|
C | CT | 122 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 123 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.463+3634dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110300351 | |||||
| chr12:110300351
|
C | CTT | 10 | a0001c0001t0003g0194a0001c0001t0003g0195a0001c0001t0003g0209others(7): Show | 10 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.463+3633_463+3634d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110300351 | |||||
| chr12:110300377
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.463+3640C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110300377 | ||||||
| chr12:110300423
|
C | T | 3 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0041 | 3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.463+3686C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110300423 | ||||||
| chr12:110300440
|
C | T | 2 | a0001c0001t0014g0177a0001c0001t0014g0178 | 2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.463+3703C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110300440 | ||||||
| chr12:110300643
|
C | CT | 28 | a0001c0001t0001g0087a0001c0001t0002g0005a0001c0001t0002g0022others(25): Show | 28 | HG00323.hp1 HG01175.hp2 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.463+3925dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110300643 | |||||
| chr12:110300643
|
C | CTT | 6 | a0001c0001t0001g0222a0001c0001t0012g0223a0001c0001t0012g0224others(3): Show | 6 | HG01099.hp1 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.463+3924_463+3925d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110300643 | |||||
| chr12:110300643
|
CT | C | 9 | a0001c0001t0001g0109a0001c0001t0001g0134a0001c0001t0001g0140others(6): Show | 9 | HG00735.hp1 HG01069.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.463+3925delT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110300643 | |||||
| chr12:110300643
|
CTTTTTT | C | 12 | a0001c0001t0002g0056a0001c0001t0004g0004a0001c0001t0004g0168others(9): Show | 12 | HG01167.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.463+3920_463+3925d others(8): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110300643 | |||||
| chr12:110300849
|
A | G | 3 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0041 | 3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.463+4112A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110300849 | ||||||
| chr12:110301041
|
T | A | 3 | a0001c0001t0001g0222a0001c0005t0009g0220a0001c0005t0009g0221 | 3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.463+4304T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110301041 | ||||||
| chr12:110301072
|
G | A | 3 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0041 | 3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.463+4335G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110301072 | ||||||
| chr12:110301174
|
G | A | 2 | a0001c0001t0011g0057a0001c0001t0011g0058 | 2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.463+4437G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110301174 | ||||||
| chr12:110301199
|
T | C | 4 | a0001c0003t0002g0019a0001c0003t0002g0020a0001c0003t0004g0217others(1): Show | 4 | HG01891.hp2 HG02486.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.463+4462T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110301199 | ||||||
| chr12:110301289
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.463+4552C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110301289 | ||||||
| chr12:110301461
|
A | AT | 5 | a0001c0001t0002g0005a0001c0001t0002g0026a0001c0001t0003g0193others(2): Show | 5 | HG02004.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.463+4730dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110301461 | |||||
| chr12:110301461
|
AT | A | 3 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0041 | 3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.463+4730delT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110301461 | |||||
| chr12:110301473
|
C | G | 1 | a0001c0001t0001g0145 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.463+4736C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110301473 | ||||||
| chr12:110301562
|
T | C | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.463+4825T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110301562 | ||||||
| chr12:110301610
|
G | T | 1 | a0001c0001t0003g0192 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.463+4873G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110301610 | ||||||
| chr12:110301642
|
C | T | 1 | a0001c0001t0014g0177 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.463+4905C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110301642 | ||||||
| chr12:110301722
|
C | T | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.463+4985C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110301722 | ||||||
| chr12:110302013
|
A | G | 3 | a0001c0001t0001g0109a0001c0001t0001g0119a0001c0001t0001g0121 | 3 | HG03491.hp2 HG03492.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.463+5276A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110302013 | ||||||
| chr12:110302228
|
CT | C | 3 | a0001c0001t0001g0222a0001c0005t0009g0220a0001c0005t0009g0221 | 3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.463+5495delT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110302228 | |||||
| chr12:110302357
|
C | T | 2 | a0001c0001t0002g0005a0001c0001t0002g0026 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.463+5620C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110302357 | ||||||
| chr12:110302567
|
AATTTTTA others(5): Show |
A | 2 | a0001c0001t0001g0069a0001c0001t0024g0093 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.463+5834_463+5845d others(14): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110302567 | |||||
| chr12:110302581
|
T | C | 2 | a0001c0001t0001g0069a0001c0001t0024g0093 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.463+5844T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110302581 | ||||||
| chr12:110302584
|
C | CTAT | 106 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(103): Show | 107 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.463+5871_463+5873d others(5): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110302584 | |||||
| chr12:110302584
|
C | CTATTAT | 14 | a0001c0001t0001g0007a0001c0001t0001g0105a0001c0001t0001g0108others(11): Show | 14 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.463+5868_463+5873d others(8): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110302584 | |||||
| chr12:110302584
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0024g0093 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.463+5847C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110302584 | ||||||
| chr12:110302584
|
CTAT | C | 65 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(62): Show | 65 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.463+5871_463+5873d others(5): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110302584 | |||||
| chr12:110302665
|
T | G | 1 | a0001c0001t0001g0105 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.463+5928T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110302665 | ||||||
| chr12:110303039
|
T | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0150 | 2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.463+6302T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110303039 | ||||||
| chr12:110303350
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.463+6613C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110303350 | ||||||
| chr12:110303551
|
T | C | 219 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(216): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.463+6814T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110303551 | ||||||
| chr12:110303567
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.463+6830C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110303567 | ||||||
| chr12:110303705
|
C | T | 5 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0001t0007g0051others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.463+6968C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110303705 | ||||||
| chr12:110303840
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.463+7103C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110303840 | ||||||
| chr12:110303936
|
G | C | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.463+7199G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110303936 | ||||||
| chr12:110304082
|
A | G | 2 | a0001c0001t0001g0037a0001c0001t0005g0125 | 2 | HG02818.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.463+7345A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110304082 | ||||||
| chr12:110304273
|
C | T | 2 | a0001c0001t0013g0084a0001c0001t0013g0086 | 2 | NA18946.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.463+7536C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110304273 | ||||||
| chr12:110304291
|
T | G | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.463+7554T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110304291 | ||||||
| chr12:110304297
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.463+7560A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110304297 | ||||||
| chr12:110304353
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.463+7616G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110304353 | ||||||
| chr12:110304459
|
G | C | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG01099.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.463+7722G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110304459 | ||||||
| chr12:110304510
|
C | A | 2 | a0001c0001t0002g0214a0001c0001t0002g0215 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.463+7773C>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110304510 | ||||||
| chr12:110304590
|
A | C | 5 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.463+7853A>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110304590 | ||||||
| chr12:110304605
|
A | G | 3 | a0001c0001t0001g0222a0001c0005t0009g0220a0001c0005t0009g0221 | 3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.463+7868A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110304605 | ||||||
| chr12:110304952
|
C | T | 3 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0208 | 3 | HG02559.hp2 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.463+8215C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110304952 | ||||||
| chr12:110304988
|
G | A | 1 | a0001c0001t0005g0125 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.463+8251G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110304988 | ||||||
| chr12:110305112
|
T | G | 1 | a0001c0001t0001g0007 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.463+8375T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110305112 | ||||||
| chr12:110305120
|
A | G | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.463+8383A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110305120 | ||||||
| chr12:110305176
|
C | T | 1 | a0001c0001t0001g0009 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.463+8439C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110305176 | ||||||
| chr12:110305186
|
A | G | 61 | a0001c0001t0001g0222a0001c0001t0001g0226a0001c0001t0002g0005others(58): Show | 61 | HG00323.hp1 HG00738.hp1 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.463+8449A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110305186 | ||||||
| chr12:110305598
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.463+8861G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110305598 | ||||||
| chr12:110305632
|
G | C | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.463+8895G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110305632 | ||||||
| chr12:110305765
|
G | A | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.463+9028G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110305765 | ||||||
| chr12:110305856
|
A | T | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.463+9119A>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110305856 | ||||||
| chr12:110305872
|
T | G | 11 | a0001c0001t0002g0005a0001c0001t0002g0026a0001c0001t0002g0039others(8): Show | 11 | HG01099.hp1 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.463+9135T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110305872 | ||||||
| chr12:110305873
|
T | G | 8 | a0001c0001t0002g0005a0001c0001t0002g0026a0001c0001t0002g0214others(5): Show | 8 | HG01099.hp1 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.463+9136T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110305873 | ||||||
| chr12:110305882
|
G | GT | 8 | a0001c0001t0002g0023a0001c0001t0002g0042a0001c0001t0002g0043others(5): Show | 8 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.463+9157dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110305882 | |||||
| chr12:110305882
|
GT | G | 11 | a0001c0001t0001g0074a0001c0001t0001g0095a0001c0001t0001g0153others(8): Show | 11 | HG00642.hp1 HG00735.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.463+9157delT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110305882 | |||||
| chr12:110305931
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.463+9194T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110305931 | ||||||
| chr12:110305970
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.463+9233G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110305970 | ||||||
| chr12:110306179
|
G | C | 195 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(192): Show | 196 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.463+9442G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110306179 | ||||||
| chr12:110306184
|
G | A | 1 | a0001c0001t0017g0003 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.463+9447G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110306184 | ||||||
| chr12:110306200
|
A | G | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.463+9463A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110306200 | ||||||
| chr12:110306239
|
C | T | 19 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0042others(16): Show | 19 | HG00323.hp1 HG01175.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.463+9502C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110306239 | ||||||
| chr12:110306253
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.463+9516A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110306253 | ||||||
| chr12:110306464
|
AGAT | A | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG01099.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.463+9733_463+9735d others(5): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110306464 | |||||
| chr12:110306877
|
C | T | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.463+10140C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110306877 | ||||||
| chr12:110306950
|
G | A | 1 | a0001c0001t0001g0076 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.463+10213G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110306950 | ||||||
| chr12:110307004
|
C | A | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.463+10267C>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110307004 | ||||||
| chr12:110307017
|
C | T | 1 | a0001c0001t0018g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.463+10280C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110307017 | ||||||
| chr12:110307067
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.463+10330T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110307067 | ||||||
| chr12:110307100
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.463+10363G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110307100 | ||||||
| chr12:110307222
|
C | CT | 186 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(183): Show | 188 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.463+10502dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110307222 | |||||
| chr12:110307222
|
C | CTT | 27 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0001g0069others(24): Show | 27 | HG00558.hp1 HG01243.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.463+10501_463+1050 others(6): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110307222 | |||||
| chr12:110307240
|
C | T | 8 | a0001c0001t0001g0100a0001c0001t0001g0107a0001c0001t0001g0129others(5): Show | 8 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.463+10503C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110307240 | ||||||
| chr12:110307241
|
T | C | 1 | a0001c0001t0001g0147 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.463+10504T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110307241 | ||||||
| chr12:110307271
|
G | T | 2 | a0001c0001t0001g0205a0001c0001t0001g0208 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.463+10534G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110307271 | ||||||
| chr12:110307716
|
A | G | 2 | a0001c0001t0002g0047a0001c0001t0002g0054 | 2 | NA18952.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.463+10979A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110307716 | ||||||
| chr12:110307792
|
AG | A | 39 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(36): Show | 40 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.463+11057delG | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110307792 | |||||
| chr12:110307810
|
G | T | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.463+11073G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110307810 | ||||||
| chr12:110307967
|
C | T | 2 | a0001c0002t0001g0114a0001c0002t0001g0117 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.463+11230C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110307967 | ||||||
| chr12:110308227
|
C | T | 6 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0171others(3): Show | 6 | HG01167.hp1 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.463+11490C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110308227 | ||||||
| chr12:110308242
|
A | C | 2 | a0001c0003t0002g0020a0001c0003t0020g0018 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.463+11505A>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110308242 | ||||||
| chr12:110308303
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.463+11566G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110308303 | ||||||
| chr12:110308347
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.463+11610G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110308347 | ||||||
| chr12:110308427
|
G | A | 3 | a0001c0001t0005g0110a0001c0001t0005g0111a0001c0001t0005g0120 | 3 | HG01255.hp2 HG02735.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.463+11690G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110308427 | ||||||
| chr12:110308627
|
C | T | 2 | a0001c0001t0002g0005a0001c0001t0002g0026 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.463+11890C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110308627 | ||||||
| chr12:110308639
|
T | G | 2 | a0001c0001t0014g0177a0001c0001t0014g0178 | 2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.463+11902T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110308639 | ||||||
| chr12:110308759
|
G | A | 1 | a0001c0001t0002g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.463+12022G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110308759 | ||||||
| chr12:110308776
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.463+12039C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110308776 | ||||||
| chr12:110309004
|
T | C | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.463+12267T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110309004 | ||||||
| chr12:110309021
|
A | T | 1 | a0001c0001t0003g0192 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.463+12284A>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110309021 | ||||||
| chr12:110309083
|
T | C | 1 | a0001c0003t0004g0217 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.463+12346T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110309083 | ||||||
| chr12:110309133
|
G | A | 1 | a0001c0001t0003g0181 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.463+12396G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110309133 | ||||||
| chr12:110309139
|
A | T | 2 | a0001c0001t0003g0176a0001c0001t0003g0200 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.463+12402A>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110309139 | ||||||
| chr12:110309140
|
A | AT | 35 | a0001c0001t0001g0009a0001c0001t0001g0066a0001c0001t0001g0068others(32): Show | 35 | HG00558.hp2 HG00642.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.463+12438dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | |||||
| chr12:110309140
|
A | ATT | 23 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0082others(20): Show | 23 | HG00323.hp2 HG01361.hp1 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.463+12437_463+1243 others(6): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | |||||
| chr12:110309140
|
A | ATTT | 14 | a0001c0001t0001g0069a0001c0001t0001g0073a0001c0001t0001g0079others(11): Show | 14 | HG00558.hp1 HG01081.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.463+12436_463+1243 others(7): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | |||||
| chr12:110309140
|
A | ATTTT | 9 | a0001c0001t0001g0091a0001c0001t0001g0218a0001c0001t0002g0023others(6): Show | 9 | HG00423.hp1 HG02055.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.463+12435_463+1243 others(8): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | |||||
| chr12:110309140
|
A | ATTTTTTT others(4): Show |
1 | a0001c0008t0030g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.463+12428_463+1243 others(15): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | |||||
| chr12:110309140
|
A | ATTTTTTT others(7): Show |
2 | a0001c0001t0003g0189a0001c0001t0003g0196 | 2 | HG01081.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.463+12425_463+1243 others(18): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | |||||
| chr12:110309140
|
A | ATTTTTTT others(8): Show |
1 | a0001c0001t0003g0190 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.463+12424_463+1243 others(19): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | |||||
| chr12:110309140
|
A | ATTTTTTT others(9): Show |
5 | a0001c0001t0003g0193a0001c0001t0003g0204a0001c0001t0028g0207others(2): Show | 5 | HG01074.hp2 HG02004.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.463+12423_463+1243 others(20): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | |||||
| chr12:110309140
|
A | ATTTTTTT others(12): Show |
2 | a0001c0001t0003g0191a0001c0001t0003g0203 | 2 | HG01358.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.463+12420_463+1243 others(23): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | |||||
| chr12:110309140
|
A | ATTTTTTT others(14): Show |
2 | a0001c0001t0003g0197a0001c0001t0029g0198 | 2 | HG01346.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.463+12418_463+1243 others(25): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | |||||
| chr12:110309140
|
A | ATTTTTTT others(17): Show |
1 | a0001c0001t0027g0202 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.463+12415_463+1243 others(28): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | |||||
| chr12:110309140
|
A | T | 2 | a0001c0001t0003g0176a0001c0001t0003g0200 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.463+12403A>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110309140 | ||||||
| chr12:110309140
|
AT | A | 38 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0101others(35): Show | 38 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.463+12438delT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | |||||
| chr12:110309140
|
ATTTTTTT others(2): Show |
A | 6 | a0001c0001t0003g0219a0001c0001t0007g0049a0001c0001t0007g0050others(3): Show | 6 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.463+12430_463+1243 others(13): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | |||||
| chr12:110309140
|
ATTTTTTT others(3): Show |
A | 5 | a0001c0001t0001g0095a0001c0001t0001g0155a0001c0001t0002g0039others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.463+12429_463+1243 others(14): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | |||||
| chr12:110309140
|
ATTTTTTT others(5): Show |
A | 13 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(10): Show | 13 | HG01169.hp2 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.463+12427_463+1243 others(16): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | |||||
| chr12:110309140
|
ATTTTTTT others(6): Show |
A | 3 | a0001c0001t0001g0032a0001c0001t0001g0222a0001c0001t0003g0185 | 3 | HG01168.hp2 HG01255.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.463+12426_463+1243 others(17): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | |||||
| chr12:110309140
|
ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0018g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.463+12425_463+1243 others(18): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | |||||
| chr12:110309140
|
ATTTTTTT others(9): Show |
A | 1 | a0001c0001t0001g0205 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.463+12423_463+1243 others(20): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309140 | |||||
| chr12:110309567
|
G | A | 2 | a0001c0001t0014g0177a0001c0001t0014g0178 | 2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.463+12830G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110309567 | ||||||
| chr12:110309614
|
G | A | 112 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(109): Show | 113 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.463+12877G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110309614 | ||||||
| chr12:110309638
|
C | T | 5 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0001t0007g0051others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.463+12901C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110309638 | ||||||
| chr12:110309882
|
G | C | 1 | a0001c0001t0017g0003 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.464-13110G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110309882 | ||||||
| chr12:110309908
|
CA | C | 75 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(72): Show | 76 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.464-13070delA | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309908 | |||||
| chr12:110309908
|
CAA | C | 34 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0042others(31): Show | 34 | HG00323.hp1 HG01167.hp1 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.464-13071_464-1307 others(6): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110309908 | |||||
| chr12:110310282
|
C | T | 1 | a0001c0001t0002g0061 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.464-12710C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110310282 | ||||||
| chr12:110310283
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0152 | 2 | HG01934.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.464-12709G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110310283 | ||||||
| chr12:110310337
|
C | G | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.464-12655C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110310337 | ||||||
| chr12:110310369
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.464-12623T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110310369 | ||||||
| chr12:110310458
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.464-12534A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110310458 | ||||||
| chr12:110310647
|
G | C | 1 | a0001c0001t0001g0088 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.464-12345G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110310647 | ||||||
| chr12:110310658
|
T | TTAACA | 3 | a0001c0001t0001g0222a0001c0005t0009g0220a0001c0005t0009g0221 | 3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.464-12331_464-1233 others(9): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110310658 | |||||
| chr12:110310759
|
C | T | 3 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091 | 3 | HG00558.hp1 NA18948.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.464-12233C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110310759 | ||||||
| chr12:110310831
|
G | A | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.464-12161G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110310831 | ||||||
| chr12:110310930
|
G | C | 19 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0042others(16): Show | 19 | HG00323.hp1 HG01175.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.464-12062G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110310930 | ||||||
| chr12:110310981
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.464-12011A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110310981 | ||||||
| chr12:110310982
|
T | C | 1 | a0001c0003t0004g0217 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.464-12010T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110310982 | ||||||
| chr12:110311310
|
A | G | 3 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0041 | 3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.464-11682A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110311310 | ||||||
| chr12:110311535
|
G | A | 1 | a0001c0001t0010g0137 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.464-11457G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110311535 | ||||||
| chr12:110311551
|
G | A | 7 | a0001c0001t0004g0170a0001c0001t0004g0171a0001c0001t0007g0049others(4): Show | 7 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.464-11441G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110311551 | ||||||
| chr12:110311552
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.464-11440C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110311552 | ||||||
| chr12:110311595
|
C | CA | 32 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0031others(29): Show | 32 | HG00423.hp1 HG01109.hp1 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.464-11370dupA | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110311595 | |||||
| chr12:110311595
|
C | CAA | 18 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0030others(15): Show | 18 | HG01069.hp1 HG01071.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.464-11371_464-1137 others(6): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110311595 | |||||
| chr12:110311595
|
C | CAAA | 19 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(16): Show | 19 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.464-11372_464-1137 others(7): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110311595 | |||||
| chr12:110311595
|
C | CAAAA | 16 | a0001c0001t0001g0205a0001c0001t0003g0179a0001c0001t0003g0180others(13): Show | 16 | HG01074.hp2 HG01081.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.464-11373_464-1137 others(8): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110311595 | |||||
| chr12:110311595
|
CA | C | 30 | a0001c0001t0001g0096a0001c0001t0001g0102a0001c0001t0001g0103others(27): Show | 30 | HG00642.hp1 HG00738.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.464-11370delA | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110311595 | |||||
| chr12:110311595
|
CAAAAA | C | 6 | a0001c0001t0002g0045a0001c0001t0002g0054a0001c0001t0002g0055others(3): Show | 6 | HG01099.hp1 HG01175.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.464-11374_464-1137 others(9): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110311595 | |||||
| chr12:110311595
|
CAAAAAA | C | 14 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0042others(11): Show | 14 | HG00323.hp1 HG01361.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.464-11375_464-1137 others(10): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110311595 | |||||
| chr12:110311611
|
A | C | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.464-11381A>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110311611 | ||||||
| chr12:110311613
|
A | AC | 19 | a0001c0001t0001g0069a0001c0001t0001g0073a0001c0001t0001g0076others(16): Show | 19 | HG00558.hp1 HG01884.hp1 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.464-11379_464-1137 others(5): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110311613 | ||||||
| chr12:110311732
|
TA | T | 96 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(93): Show | 97 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.464-11243delA | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110311732 | |||||
| chr12:110311732
|
TAA | T | 17 | a0001c0001t0002g0044a0001c0001t0002g0214a0001c0001t0002g0215others(14): Show | 17 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.464-11244_464-1124 others(6): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110311732 | |||||
| chr12:110311828
|
A | G | 3 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0041 | 3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.464-11164A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110311828 | ||||||
| chr12:110311962
|
C | A | 1 | a0001c0001t0002g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.464-11030C>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110311962 | ||||||
| chr12:110312073
|
G | A | 1 | a0001c0001t0028g0207 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.464-10919G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110312073 | ||||||
| chr12:110312113
|
G | A | 48 | a0001c0001t0001g0222a0001c0001t0002g0005a0001c0001t0002g0022others(45): Show | 48 | HG00323.hp1 HG00738.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.464-10879G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110312113 | ||||||
| chr12:110312289
|
T | A | 5 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0001t0007g0051others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-10703T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110312289 | ||||||
| chr12:110312498
|
T | G | 1 | a0001c0001t0001g0083 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.464-10494T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110312498 | ||||||
| chr12:110312553
|
G | A | 3 | a0001c0001t0001g0222a0001c0005t0009g0220a0001c0005t0009g0221 | 3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.464-10439G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110312553 | ||||||
| chr12:110312706
|
C | T | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.464-10286C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110312706 | ||||||
| chr12:110312753
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.464-10239G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110312753 | ||||||
| chr12:110312849
|
C | CA | 7 | a0001c0001t0001g0021a0001c0001t0001g0096a0001c0001t0001g0144others(4): Show | 7 | HG00735.hp2 HG01106.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.464-10127dupA | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110312849 | |||||
| chr12:110312866
|
G | C | 3 | a0001c0001t0001g0098a0001c0001t0013g0084a0001c0001t0013g0086 | 3 | HG02622.hp1 NA18946.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.464-10126G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110312866 | ||||||
| chr12:110313062
|
A | C | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.464-9930A>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110313062 | ||||||
| chr12:110313206
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.464-9786G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110313206 | ||||||
| chr12:110313213
|
T | C | 2 | a0001c0003t0002g0020a0001c0003t0020g0018 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.464-9779T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110313213 | ||||||
| chr12:110313223
|
AG | A | 9 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(6): Show | 9 | HG01168.hp2 HG01169.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.464-9767delG | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110313223 | |||||
| chr12:110313310
|
C | CT | 97 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(94): Show | 98 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.464-9660dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110313310 | |||||
| chr12:110313310
|
C | CTT | 5 | a0001c0001t0001g0007a0001c0001t0001g0107a0001c0001t0003g0181others(2): Show | 5 | HG01192.hp1 HG01258.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.464-9661_464-9660d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110313310 | |||||
| chr12:110313310
|
C | CTTT | 5 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0001t0007g0051others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-9662_464-9660d others(5): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110313310 | |||||
| chr12:110313310
|
CTTTT | C | 24 | a0001c0001t0001g0222a0001c0001t0002g0005a0001c0001t0002g0026others(21): Show | 24 | HG01099.hp1 HG01167.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.464-9663_464-9660d others(6): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110313310 | |||||
| chr12:110313310
|
CTTTTT | C | 21 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0042others(18): Show | 21 | HG00323.hp1 HG00738.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.464-9664_464-9660d others(7): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110313310 | |||||
| chr12:110313314
|
T | C | 1 | a0001c0001t0012g0224 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.464-9678T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110313314 | ||||||
| chr12:110313339
|
G | A | 1 | a0001c0001t0002g0041 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.464-9653G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110313339 | ||||||
| chr12:110313344
|
G | A | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.464-9648G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110313344 | ||||||
| chr12:110313501
|
G | C | 1 | a0001c0001t0017g0003 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.464-9491G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110313501 | ||||||
| chr12:110313569
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.464-9423C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110313569 | ||||||
| chr12:110313705
|
C | CT | 8 | a0001c0001t0001g0101a0001c0001t0001g0160a0001c0001t0001g0167others(5): Show | 8 | HG00738.hp1 HG01069.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.464-9265dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110313705 | |||||
| chr12:110313705
|
CT | C | 41 | a0001c0001t0001g0032a0001c0001t0001g0102a0001c0001t0001g0119others(38): Show | 41 | HG00558.hp2 HG01071.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.464-9265delT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110313705 | |||||
| chr12:110313705
|
CTT | C | 16 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0098others(13): Show | 16 | HG00735.hp1 HG01106.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.464-9266_464-9265d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110313705 | |||||
| chr12:110313856
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.464-9136G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110313856 | ||||||
| chr12:110313883
|
A | AT | 7 | a0001c0001t0001g0222a0001c0001t0006g0012a0001c0001t0006g0013others(4): Show | 7 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.464-9099dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110313883 | |||||
| chr12:110314094
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.464-8898C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110314094 | ||||||
| chr12:110314127
|
G | A | 3 | a0001c0001t0003g0180a0001c0001t0027g0202a0001c0001t0029g0198 | 3 | HG01346.hp1 HG04204.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.464-8865G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110314127 | ||||||
| chr12:110314283
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.464-8709G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110314283 | ||||||
| chr12:110314336
|
G | GA | 129 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(126): Show | 130 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.464-8641dupA | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110314336 | |||||
| chr12:110314336
|
G | GAA | 6 | a0001c0001t0001g0072a0001c0001t0001g0081a0001c0001t0002g0005others(3): Show | 6 | HG01884.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.464-8642_464-8641d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110314336 | |||||
| chr12:110314598
|
C | T | 1 | a0001c0001t0004g0169 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.464-8394C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110314598 | ||||||
| chr12:110314674
|
G | A | 3 | a0001c0003t0002g0019a0001c0003t0002g0020a0001c0003t0020g0018 | 3 | HG01891.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.464-8318G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110314674 | ||||||
| chr12:110314708
|
G | C | 1 | a0001c0001t0003g0190 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.464-8284G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110314708 | ||||||
| chr12:110314750
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.464-8242T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110314750 | ||||||
| chr12:110314820
|
G | A | 3 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0041 | 3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.464-8172G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110314820 | ||||||
| chr12:110314918
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.464-8074G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110314918 | ||||||
| chr12:110314952
|
C | T | 2 | a0001c0001t0006g0015a0001c0001t0006g0016 | 2 | HG01943.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.464-8040C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110314952 | ||||||
| chr12:110315011
|
C | T | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.464-7981C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110315011 | ||||||
| chr12:110315079
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.464-7913G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110315079 | ||||||
| chr12:110315119
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.464-7873G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110315119 | ||||||
| chr12:110315129
|
G | T | 1 | a0001c0001t0002g0039 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.464-7863G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110315129 | ||||||
| chr12:110315150
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.464-7842G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110315150 | ||||||
| chr12:110315161
|
C | T | 2 | a0001c0001t0003g0203a0001c0001t0003g0204 | 2 | HG01358.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.464-7831C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110315161 | ||||||
| chr12:110315393
|
T | C | 22 | a0001c0001t0001g0069a0001c0001t0001g0073a0001c0001t0001g0076others(19): Show | 22 | HG00423.hp2 HG00558.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.464-7599T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110315393 | ||||||
| chr12:110315519
|
G | A | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.464-7473G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110315519 | ||||||
| chr12:110315627
|
G | A | 1 | a0001c0001t0019g0046 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.464-7365G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110315627 | ||||||
| chr12:110315908
|
C | T | 2 | a0002c0004t0003g0182a0002c0004t0003g0183 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.464-7084C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110315908 | ||||||
| chr12:110316216
|
A | G | 4 | a0001c0001t0003g0179a0001c0001t0003g0181a0001c0001t0003g0187others(1): Show | 4 | HG01192.hp1 HG01433.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-6776A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110316216 | ||||||
| chr12:110316292
|
A | G | 23 | a0001c0001t0001g0069a0001c0001t0001g0073a0001c0001t0001g0076others(20): Show | 23 | HG00423.hp2 HG00558.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.464-6700A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110316292 | ||||||
| chr12:110316561
|
A | G | 1 | a0001c0001t0002g0061 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.464-6431A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110316561 | ||||||
| chr12:110316887
|
G | A | 4 | a0001c0001t0008g0164a0001c0001t0008g0166a0001c0001t0010g0136others(1): Show | 4 | NA18946.hp2 NA18998.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-6105G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110316887 | ||||||
| chr12:110317097
|
C | T | 2 | a0001c0001t0002g0214a0001c0001t0002g0215 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.464-5895C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110317097 | ||||||
| chr12:110317299
|
C | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.464-5693C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110317299 | ||||||
| chr12:110317420
|
G | GT | 44 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(41): Show | 45 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.464-5564dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110317420 | |||||
| chr12:110317432
|
A | G | 1 | a0001c0001t0002g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.464-5560A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110317432 | ||||||
| chr12:110317593
|
G | T | 1 | a0001c0001t0001g0099 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.464-5399G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110317593 | ||||||
| chr12:110317679
|
G | C | 5 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0001t0007g0051others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-5313G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110317679 | ||||||
| chr12:110318067
|
A | G | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.464-4925A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110318067 | ||||||
| chr12:110318170
|
C | T | 2 | a0001c0001t0013g0084a0001c0001t0013g0086 | 2 | NA18946.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.464-4822C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110318170 | ||||||
| chr12:110318534
|
C | T | 2 | a0001c0001t0014g0177a0001c0001t0014g0178 | 2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.464-4458C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110318534 | ||||||
| chr12:110318608
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.464-4384G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110318608 | ||||||
| chr12:110318737
|
G | C | 1 | a0001c0001t0017g0003 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.464-4255G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110318737 | ||||||
| chr12:110318754
|
A | G | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.464-4238A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110318754 | ||||||
| chr12:110318763
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.464-4229C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110318763 | ||||||
| chr12:110318764
|
G | A | 34 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0042others(31): Show | 34 | HG00323.hp1 HG01167.hp1 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.464-4228G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110318764 | ||||||
| chr12:110318859
|
C | G | 1 | a0001c0001t0001g0138 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.464-4133C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110318859 | ||||||
| chr12:110318933
|
A | G | 9 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(6): Show | 9 | HG01168.hp2 HG01169.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.464-4059A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110318933 | ||||||
| chr12:110319215
|
T | TA | 4 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0001t0007g0051others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-3771dupA | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110319215 | |||||
| chr12:110319222
|
T | A | 1 | a0001c0001t0007g0053 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.464-3770T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110319222 | ||||||
| chr12:110319223
|
G | GA | 7 | a0001c0001t0001g0021a0001c0001t0001g0123a0001c0001t0001g0147others(4): Show | 7 | HG01891.hp1 HG02293.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.464-3746dupA | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110319223 | |||||
| chr12:110319223
|
G | T | 1 | a0001c0001t0007g0053 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.464-3769G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110319223 | ||||||
| chr12:110319223
|
GA | G | 108 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0027others(105): Show | 108 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.464-3746delA | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110319223 | |||||
| chr12:110319223
|
GAA | G | 7 | a0001c0001t0001g0088a0001c0001t0001g0108a0001c0001t0001g0133others(4): Show | 7 | HG01106.hp2 HG02572.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.464-3747_464-3746d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110319223 | |||||
| chr12:110319223
|
GAAAAAAA others(4): Show |
G | 1 | a0001c0008t0030g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.464-3756_464-3746d others(13): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110319223 | |||||
| chr12:110319224
|
A | G | 1 | a0001c0001t0007g0053 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.464-3768A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110319224 | ||||||
| chr12:110319496
|
A | G | 2 | a0001c0001t0001g0126a0001c0001t0001g0218 | 2 | HG02698.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.464-3496A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110319496 | ||||||
| chr12:110319679
|
T | C | 1 | a0001c0001t0002g0054 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.464-3313T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110319679 | ||||||
| chr12:110319780
|
A | G | 20 | a0001c0001t0001g0006a0001c0001t0001g0096a0001c0001t0001g0099others(17): Show | 20 | HG00140.hp1 HG00738.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.464-3212A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110319780 | ||||||
| chr12:110320237
|
T | A | 9 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(6): Show | 9 | HG01168.hp2 HG01169.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.464-2755T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110320237 | ||||||
| chr12:110320276
|
T | A | 19 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0042others(16): Show | 19 | HG00323.hp1 HG01175.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.464-2716T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110320276 | ||||||
| chr12:110320337
|
C | T | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.464-2655C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110320337 | ||||||
| chr12:110320393
|
C | T | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.464-2599C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110320393 | ||||||
| chr12:110320409
|
A | G | 1 | a0001c0001t0001g0097 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.464-2583A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110320409 | ||||||
| chr12:110320428
|
G | C | 2 | a0001c0001t0002g0022a0001c0001t0002g0045 | 2 | HG03491.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.464-2564G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110320428 | ||||||
| chr12:110320546
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.464-2446G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110320546 | ||||||
| chr12:110320719
|
G | A | 1 | a0001c0002t0001g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.464-2273G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110320719 | ||||||
| chr12:110320777
|
TGA | T | 5 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0112others(2): Show | 5 | HG02647.hp1 HG03516.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.464-2212_464-2211d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr12 | 110320777 | |||||
| chr12:110320950
|
T | C | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.464-2042T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110320950 | ||||||
| chr12:110321114
|
G | A | 3 | a0001c0001t0005g0110a0001c0001t0005g0111a0001c0001t0005g0120 | 3 | HG01255.hp2 HG02735.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.464-1878G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110321114 | ||||||
| chr12:110321145
|
T | C | 3 | a0001c0001t0001g0108a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG00735.hp1 HG01106.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.464-1847T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110321145 | ||||||
| chr12:110321277
|
A | G | 3 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0041 | 3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.464-1715A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110321277 | ||||||
| chr12:110321387
|
T | G | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.464-1605T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110321387 | ||||||
| chr12:110321475
|
A | G | 5 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.464-1517A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110321475 | ||||||
| chr12:110321544
|
C | T | 1 | a0001c0001t0017g0003 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.464-1448C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110321544 | ||||||
| chr12:110321550
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.464-1442A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110321550 | ||||||
| chr12:110321632
|
G | A | 1 | a0001c0005t0009g0221 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.464-1360G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110321632 | ||||||
| chr12:110322034
|
A | T | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG01099.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.464-958A>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110322034 | ||||||
| chr12:110322038
|
T | G | 19 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0042others(16): Show | 19 | HG00323.hp1 HG01175.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.464-954T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110322038 | ||||||
| chr12:110322054
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0021g0028 | 2 | HG02615.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.464-938G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110322054 | ||||||
| chr12:110322076
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.464-916C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110322076 | ||||||
| chr12:110322268
|
G | A | 2 | a0001c0001t0004g0168a0001c0001t0004g0174 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.464-724G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110322268 | ||||||
| chr12:110322305
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.464-687T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 5/19 | chr12 | 110322305 | ||||||
| chr12:110323196
|
T | C | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG01099.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.544+124T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110323196 | ||||||
| chr12:110323216
|
G | A | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.544+144G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110323216 | ||||||
| chr12:110323246
|
G | A | 10 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0030others(7): Show | 10 | HG01168.hp2 HG01169.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.544+174G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110323246 | ||||||
| chr12:110323255
|
G | T | 6 | a0001c0001t0006g0012a0001c0001t0006g0013a0001c0001t0006g0014others(3): Show | 6 | HG01943.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.544+183G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110323255 | ||||||
| chr12:110323270
|
C | T | 2 | a0001c0001t0002g0048a0001c0001t0002g0055 | 2 | HG00323.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.544+198C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110323270 | ||||||
| chr12:110323524
|
A | G | 4 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0151others(1): Show | 4 | HG02615.hp1 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.544+452A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110323524 | ||||||
| chr12:110324038
|
A | G | 2 | a0001c0002t0001g0114a0001c0002t0001g0117 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.544+966A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110324038 | ||||||
| chr12:110324181
|
A | G | 1 | a0001c0001t0012g0223 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.544+1109A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110324181 | ||||||
| chr12:110324254
|
T | TG | 3 | a0001c0001t0001g0222a0001c0005t0009g0220a0001c0005t0009g0221 | 3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.544+1184dupG | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 110324254 | |||||
| chr12:110324288
|
A | G | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.544+1216A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110324288 | ||||||
| chr12:110324426
|
A | T | 2 | a0002c0004t0003g0182a0002c0004t0003g0183 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.544+1354A>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110324426 | ||||||
| chr12:110324427
|
T | A | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.544+1355T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110324427 | ||||||
| chr12:110324452
|
C | T | 2 | a0001c0001t0002g0005a0001c0001t0002g0026 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.544+1380C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110324452 | ||||||
| chr12:110324570
|
C | T | 6 | a0001c0001t0002g0005a0001c0001t0002g0026a0001c0001t0012g0223others(3): Show | 6 | HG01099.hp1 HG02145.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.544+1498C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110324570 | ||||||
| chr12:110324601
|
T | A | 1 | a0001c0007t0002g0024 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.544+1529T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110324601 | ||||||
| chr12:110324611
|
G | A | 1 | a0001c0001t0005g0110 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.544+1539G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110324611 | ||||||
| chr12:110324704
|
A | T | 2 | a0001c0001t0001g0069a0001c0001t0024g0093 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.544+1632A>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110324704 | ||||||
| chr12:110324803
|
C | A | 15 | a0001c0001t0002g0056a0001c0001t0004g0004a0001c0001t0004g0168others(12): Show | 15 | HG01167.hp1 HG01891.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.545-1587C>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110324803 | ||||||
| chr12:110324828
|
C | CT | 7 | a0001c0001t0001g0021a0001c0001t0001g0128a0001c0001t0002g0039others(4): Show | 7 | HG02622.hp2 HG02630.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.545-1545dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr12 | 110324828 | |||||
| chr12:110324951
|
A | G | 62 | a0001c0001t0001g0222a0001c0001t0001g0226a0001c0001t0002g0005others(59): Show | 62 | HG00323.hp1 HG00738.hp1 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.545-1439A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110324951 | ||||||
| chr12:110325303
|
C | T | 2 | a0001c0001t0002g0212a0001c0001t0002g0213 | 2 | HG02055.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.545-1087C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110325303 | ||||||
| chr12:110325409
|
G | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02717.hp1 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.545-981G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110325409 | ||||||
| chr12:110325449
|
A | G | 3 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0041 | 3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.545-941A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110325449 | ||||||
| chr12:110325549
|
G | C | 22 | a0001c0001t0001g0069a0001c0001t0001g0073a0001c0001t0001g0076others(19): Show | 22 | HG00423.hp2 HG00558.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.545-841G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110325549 | ||||||
| chr12:110325552
|
C | T | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.545-838C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110325552 | ||||||
| chr12:110325632
|
A | C | 1 | a0001c0001t0002g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.545-758A>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110325632 | ||||||
| chr12:110326120
|
C | G | 3 | a0001c0001t0003g0180a0001c0001t0027g0202a0001c0001t0029g0198 | 3 | HG01346.hp1 HG04204.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.545-270C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110326120 | ||||||
| chr12:110326229
|
G | A | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.545-161G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110326229 | ||||||
| chr12:110326313
|
G | A | 1 | a0001c0001t0006g0015 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.545-77G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110326313 | ||||||
| chr12:110326317
|
G | T | 1 | a0001c0001t0001g0116 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.545-73G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 6/19 | chr12 | 110326317 | ||||||
| chr12:110327193
|
C | A | 2 | a0001c0001t0002g0022a0001c0001t0002g0045 | 2 | HG03491.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.631-360C>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 7/19 | chr12 | 110327193 | ||||||
| chr12:110327255
|
C | CTA | 46 | a0001c0001t0002g0005a0001c0001t0002g0022a0001c0001t0002g0023others(43): Show | 46 | HG00323.hp1 HG01099.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.631-294_631-293dup others(2): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr12 | 110327255 | |||||
| chr12:110327349
|
C | G | 1 | a0001c0001t0001g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.631-204C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 7/19 | chr12 | 110327349 | ||||||
| chr12:110327495
|
G | A | 3 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0041 | 3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.631-58G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 7/19 | chr12 | 110327495 | ||||||
| chr12:110328361
|
C | A | 113 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(110): Show | 114 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.1095+344C>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110328361 | ||||||
| chr12:110328423
|
T | C | 1 | a0001c0001t0010g0136 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1095+406T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110328423 | ||||||
| chr12:110328458
|
A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0021g0028 | 3 | HG02615.hp1 HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1095+441A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110328458 | ||||||
| chr12:110328460
|
T | G | 1 | a0001c0001t0001g0102 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1095+443T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110328460 | ||||||
| chr12:110328516
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1095+499C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110328516 | ||||||
| chr12:110328714
|
T | C | 1 | a0001c0001t0003g0197 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1095+697T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110328714 | ||||||
| chr12:110328740
|
A | AT | 5 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1095+732dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr12 | 110328740 | |||||
| chr12:110328912
|
T | C | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1095+895T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110328912 | ||||||
| chr12:110328962
|
A | G | 19 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0042others(16): Show | 19 | HG00323.hp1 HG01175.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.1095+945A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110328962 | ||||||
| chr12:110329224
|
T | C | 2 | a0001c0001t0014g0177a0001c0001t0014g0178 | 2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1095+1207T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110329224 | ||||||
| chr12:110329848
|
G | A | 3 | a0001c0003t0002g0019a0001c0003t0002g0020a0001c0003t0020g0018 | 3 | HG01891.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1095+1831G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110329848 | ||||||
| chr12:110329887
|
G | A | 3 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091 | 3 | HG00558.hp1 NA18948.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1095+1870G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110329887 | ||||||
| chr12:110329902
|
T | C | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1095+1885T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110329902 | ||||||
| chr12:110329916
|
T | A | 48 | a0001c0001t0001g0222a0001c0001t0002g0005a0001c0001t0002g0022others(45): Show | 48 | HG00323.hp1 HG00738.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.1095+1899T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110329916 | ||||||
| chr12:110330147
|
G | T | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1095+2130G>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110330147 | ||||||
| chr12:110330380
|
A | C | 3 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0041 | 3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1096-2217A>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110330380 | ||||||
| chr12:110330422
|
G | C | 10 | a0001c0001t0004g0004a0001c0001t0004g0168a0001c0001t0004g0169others(7): Show | 10 | HG01167.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1096-2175G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110330422 | ||||||
| chr12:110330571
|
TAAGCCAT others(5): Show |
T | 3 | a0001c0001t0001g0222a0001c0005t0009g0220a0001c0005t0009g0221 | 3 | HG00738.hp1 HG01069.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1096-2011_1096-200 others(16): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr12 | 110330571 | |||||
| chr12:110330575
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1096-2022C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110330575 | ||||||
| chr12:110330637
|
A | T | 3 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091 | 3 | HG00558.hp1 NA18948.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1096-1960A>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110330637 | ||||||
| chr12:110331192
|
C | T | 1 | a0001c0007t0002g0024 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1096-1405C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110331192 | ||||||
| chr12:110331208
|
A | G | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1096-1389A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110331208 | ||||||
| chr12:110331221
|
G | A | 1 | a0001c0001t0002g0215 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1096-1376G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110331221 | ||||||
| chr12:110331496
|
C | T | 45 | a0001c0001t0002g0005a0001c0001t0002g0022a0001c0001t0002g0023others(42): Show | 45 | HG00323.hp1 HG01099.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.1096-1101C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110331496 | ||||||
| chr12:110332291
|
A | G | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1096-306A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110332291 | ||||||
| chr12:110332581
|
C | T | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1096-16C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110332581 | ||||||
| chr12:110332585
|
C | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0092 | 2 | HG00423.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.1096-12C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 8/19 | chr12 | 110332585 | ||||||
| chr12:110332783
|
T | C | 11 | a0001c0001t0002g0005a0001c0001t0002g0026a0001c0001t0002g0039others(8): Show | 11 | HG01099.hp1 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1184+98T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 9/19 | chr12 | 110332783 | ||||||
| chr12:110332792
|
A | G | 11 | a0001c0001t0002g0005a0001c0001t0002g0026a0001c0001t0002g0039others(8): Show | 11 | HG01099.hp1 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1184+107A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 9/19 | chr12 | 110332792 | ||||||
| chr12:110333051
|
T | C | 1 | a0001c0001t0001g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1185-130T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 9/19 | chr12 | 110333051 | ||||||
| chr12:110333107
|
CG | C | 13 | a0001c0001t0002g0005a0001c0001t0002g0026a0001c0001t0002g0214others(10): Show | 13 | HG00738.hp1 HG01069.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.1185-67delG | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr12 | 110333107 | |||||
| chr12:110333134
|
A | G | 1 | a0001c0001t0003g0188 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1185-47A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 9/19 | chr12 | 110333134 | ||||||
| chr12:110333370
|
C | G | 1 | a0001c0001t0018g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1287+87C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 10/19 | chr12 | 110333370 | ||||||
| chr12:110333458
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1287+175G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 10/19 | chr12 | 110333458 | ||||||
| chr12:110333559
|
A | G | 9 | a0001c0001t0002g0005a0001c0001t0002g0026a0001c0001t0002g0038others(6): Show | 9 | HG01099.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1287+276A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 10/19 | chr12 | 110333559 | ||||||
| chr12:110333624
|
T | A | 5 | a0001c0001t0007g0049a0001c0001t0007g0050a0001c0001t0007g0051others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1287+341T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 10/19 | chr12 | 110333624 | ||||||
| chr12:110333707
|
C | G | 1 | a0001c0001t0001g0130 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1288-305C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 10/19 | chr12 | 110333707 | ||||||
| chr12:110333783
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1288-229A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 10/19 | chr12 | 110333783 | ||||||
| chr12:110333861
|
T | C | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1288-151T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 10/19 | chr12 | 110333861 | ||||||
| chr12:110333890
|
A | AAATGGCC others(15): Show |
2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1288-120_1288-99du others(23): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr12 | 110333890 | |||||
| chr12:110333940
|
A | G | 1 | a0001c0001t0002g0044 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1288-72A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 10/19 | chr12 | 110333940 | ||||||
| chr12:110334486
|
C | T | 6 | a0001c0001t0002g0005a0001c0001t0002g0026a0001c0001t0012g0223others(3): Show | 6 | HG01099.hp1 HG02145.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1419+343C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110334486 | ||||||
| chr12:110334586
|
C | CT | 69 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0027others(66): Show | 69 | HG00140.hp1 HG00140.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.1419+463dupT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr12 | 110334586 | |||||
| chr12:110334586
|
C | CTT | 15 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0112others(12): Show | 15 | HG01081.hp1 HG01099.hp1 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.1419+462_1419+463d others(4): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr12 | 110334586 | |||||
| chr12:110334586
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1419+453_1419+463d others(13): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr12 | 110334586 | |||||
| chr12:110334621
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1419+478C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110334621 | ||||||
| chr12:110334651
|
G | A | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1419+508G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110334651 | ||||||
| chr12:110334831
|
G | A | 3 | a0001c0001t0005g0110a0001c0001t0005g0111a0001c0001t0005g0120 | 3 | HG01255.hp2 HG02735.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1419+688G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110334831 | ||||||
| chr12:110335040
|
T | C | 1 | a0001c0001t0015g0077 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1419+897T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110335040 | ||||||
| chr12:110335432
|
G | C | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1419+1289G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110335432 | ||||||
| chr12:110335529
|
G | A | 2 | a0001c0001t0002g0047a0001c0001t0002g0054 | 2 | NA18952.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1419+1386G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110335529 | ||||||
| chr12:110335765
|
T | C | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1419+1622T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110335765 | ||||||
| chr12:110335798
|
T | C | 2 | a0001c0001t0012g0223a0001c0001t0012g0224 | 2 | HG01099.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1419+1655T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110335798 | ||||||
| chr12:110335933
|
T | A | 1 | a0001c0001t0002g0026 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1419+1790T>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110335933 | ||||||
| chr12:110336013
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0024g0093 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1419+1870C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110336013 | ||||||
| chr12:110336015
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1419+1872C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110336015 | ||||||
| chr12:110336030
|
G | A | 1 | a0001c0001t0002g0062 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1419+1887G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110336030 | ||||||
| chr12:110336206
|
G | A | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1419+2063G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110336206 | ||||||
| chr12:110336363
|
GA | G | 2 | a0001c0001t0014g0177a0001c0001t0014g0178 | 2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1419+2221delA | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110336363 | ||||||
| chr12:110336428
|
T | G | 1 | a0001c0001t0001g0021 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1419+2285T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110336428 | ||||||
| chr12:110336751
|
A | G | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1420-2530A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110336751 | ||||||
| chr12:110337256
|
T | C | 1 | a0001c0001t0002g0055 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1420-2025T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110337256 | ||||||
| chr12:110337439
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1420-1842A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110337439 | ||||||
| chr12:110337567
|
T | C | 7 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0171others(4): Show | 7 | HG01167.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1420-1714T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110337567 | ||||||
| chr12:110337775
|
CT | C | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1420-1504delT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr12 | 110337775 | |||||
| chr12:110337804
|
T | C | 50 | a0001c0001t0001g0222a0001c0001t0001g0226a0001c0001t0002g0005others(47): Show | 50 | HG00323.hp1 HG00738.hp1 HG01069.hp2 others(47): Show |
intron_variant | MODIFIER | c.1420-1477T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110337804 | ||||||
| chr12:110337805
|
G | A | 19 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0042others(16): Show | 19 | HG00323.hp1 HG01175.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.1420-1476G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110337805 | ||||||
| chr12:110337816
|
G | A | 2 | a0001c0001t0010g0136a0001c0001t0010g0137 | 2 | NA19062.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1420-1465G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110337816 | ||||||
| chr12:110337969
|
A | C | 22 | a0001c0001t0001g0069a0001c0001t0001g0073a0001c0001t0001g0076others(19): Show | 22 | HG00423.hp2 HG00558.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1420-1312A>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110337969 | ||||||
| chr12:110338141
|
A | G | 10 | a0001c0001t0004g0004a0001c0001t0004g0168a0001c0001t0004g0169others(7): Show | 10 | HG01167.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1420-1140A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110338141 | ||||||
| chr12:110338184
|
A | G | 4 | a0001c0001t0005g0122a0001c0001t0005g0124a0001c0001t0005g0125others(1): Show | 4 | HG00738.hp2 HG01175.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-1097A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110338184 | ||||||
| chr12:110338191
|
C | G | 3 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0041 | 3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1420-1090C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110338191 | ||||||
| chr12:110338275
|
G | A | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1420-1006G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110338275 | ||||||
| chr12:110338397
|
C | T | 1 | a0001c0001t0002g0062 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1420-884C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110338397 | ||||||
| chr12:110338443
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1420-838C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110338443 | ||||||
| chr12:110338456
|
C | T | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1420-825C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110338456 | ||||||
| chr12:110338758
|
T | C | 1 | a0001c0001t0002g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1420-523T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110338758 | ||||||
| chr12:110338978
|
G | A | 1 | a0001c0001t0001g0206 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1420-303G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110338978 | ||||||
| chr12:110339219
|
T | G | 9 | a0001c0001t0002g0005a0001c0001t0002g0026a0001c0001t0002g0038others(6): Show | 9 | HG01099.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1420-62T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110339219 | ||||||
| chr12:110339273
|
C | G | 7 | a0001c0001t0002g0061a0001c0001t0006g0012a0001c0001t0006g0013others(4): Show | 7 | HG01081.hp1 HG01943.hp1 HG02647.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1420-8C>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 11/19 | chr12 | 110339273 | ||||||
| chr12:110340004
|
A | G | 1 | a0001c0001t0025g0075 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1761+283A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 13/19 | chr12 | 110340004 | ||||||
| chr12:110340577
|
A | G | 1 | a0001c0001t0002g0060 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1762-82A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 13/19 | chr12 | 110340577 | ||||||
| chr12:110340578
|
A | G | 34 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0042others(31): Show | 34 | HG00323.hp1 HG01167.hp1 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.1762-81A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 13/19 | chr12 | 110340578 | ||||||
| chr12:110341229
|
A | G | 5 | a0001c0001t0002g0022a0001c0001t0002g0045a0001c0001t0002g0048others(2): Show | 5 | HG00323.hp1 HG01175.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.2097+235A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 14/19 | chr12 | 110341229 | ||||||
| chr12:110341611
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2097+617T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 14/19 | chr12 | 110341611 | ||||||
| chr12:110341824
|
C | T | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.2098-404C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 14/19 | chr12 | 110341824 | ||||||
| chr12:110341846
|
C | A | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.2098-382C>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 14/19 | chr12 | 110341846 | ||||||
| chr12:110342135
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2098-93A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 14/19 | chr12 | 110342135 | ||||||
| chr12:110342496
|
G | A | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.2318+48G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 15/19 | chr12 | 110342496 | ||||||
| chr12:110342649
|
T | C | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.2318+201T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 15/19 | chr12 | 110342649 | ||||||
| chr12:110342735
|
A | T | 32 | a0001c0001t0003g0002a0001c0001t0003g0176a0001c0001t0003g0179others(29): Show | 33 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.2318+287A>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 15/19 | chr12 | 110342735 | ||||||
| chr12:110342787
|
C | T | 7 | a0001c0001t0002g0061a0001c0001t0006g0012a0001c0001t0006g0013others(4): Show | 7 | HG01081.hp1 HG01943.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2318+339C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 15/19 | chr12 | 110342787 | ||||||
| chr12:110342807
|
G | A | 19 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0042others(16): Show | 19 | HG00323.hp1 HG01175.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.2318+359G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 15/19 | chr12 | 110342807 | ||||||
| chr12:110342864
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2319-368G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 15/19 | chr12 | 110342864 | ||||||
| chr12:110342977
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2319-255C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 15/19 | chr12 | 110342977 | ||||||
| chr12:110343100
|
A | G | 46 | a0001c0001t0002g0005a0001c0001t0002g0022a0001c0001t0002g0023others(43): Show | 46 | HG00323.hp1 HG01099.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.2319-132A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 15/19 | chr12 | 110343100 | ||||||
| chr12:110343124
|
AGTT | A | 3 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0041 | 3 | HG02630.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2319-102_2319-100d others(5): Show |
ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr12 | 110343124 | |||||
| chr12:110343159
|
T | G | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.2319-73T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 15/19 | chr12 | 110343159 | ||||||
| chr12:110343823
|
G | A | 19 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0042others(16): Show | 19 | HG00323.hp1 HG01175.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.2521+389G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 16/19 | chr12 | 110343823 | ||||||
| chr12:110344188
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2522-698C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 16/19 | chr12 | 110344188 | ||||||
| chr12:110344222
|
T | C | 9 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(6): Show | 9 | HG01168.hp2 HG01169.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.2522-664T>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 16/19 | chr12 | 110344222 | ||||||
| chr12:110344394
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2522-492C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 16/19 | chr12 | 110344394 | ||||||
| chr12:110344644
|
A | G | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.2522-242A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 16/19 | chr12 | 110344644 | ||||||
| chr12:110344727
|
C | T | 19 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0042others(16): Show | 19 | HG00323.hp1 HG01175.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.2522-159C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 16/19 | chr12 | 110344727 | ||||||
| chr12:110344736
|
G | C | 3 | a0001c0003t0002g0019a0001c0003t0002g0020a0001c0003t0020g0018 | 3 | HG01891.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2522-150G>C | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 16/19 | chr12 | 110344736 | ||||||
| chr12:110345070
|
G | A | 2 | a0001c0005t0009g0220a0001c0005t0009g0221 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.2607+99G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 17/19 | chr12 | 110345070 | ||||||
| chr12:110345412
|
G | A | 1 | a0001c0001t0006g0014 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2741+30G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 18/19 | chr12 | 110345412 | ||||||
| chr12:110345436
|
G | A | 41 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(38): Show | 42 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.2741+54G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 18/19 | chr12 | 110345436 | ||||||
| chr12:110345883
|
G | A | 1 | a0001c0003t0004g0217 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2742-118G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 18/19 | chr12 | 110345883 | ||||||
| chr12:110345885
|
G | A | 6 | a0001c0001t0002g0005a0001c0001t0002g0026a0001c0001t0012g0223others(3): Show | 6 | HG01099.hp1 HG02145.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.2742-116G>A | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 18/19 | chr12 | 110345885 | ||||||
| chr12:110345899
|
T | G | 9 | a0001c0001t0004g0004a0001c0001t0004g0168a0001c0001t0004g0169others(6): Show | 9 | HG01167.hp1 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2742-102T>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 18/19 | chr12 | 110345899 | ||||||
| chr12:110345917
|
A | G | 2 | a0001c0001t0001g0095a0001c0001t0001g0155 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2742-84A>G | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 18/19 | chr12 | 110345917 | ||||||
| chr12:110346180
|
C | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0218 | 2 | HG02698.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2860-21C>T | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 19/19 | chr12 | 110346180 | ||||||
| chr12:110346190
|
CTG | C | 6 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0171others(3): Show | 6 | HG01167.hp1 HG02280.hp1 HG02622.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.2860-5_2860-4delGT | ATP2A2 | ENSG00000174437.18 | transcript | ENST00000539276.7 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr12 | 110346190 |